15-89648269-C-T

Variant names:

Variant summary

Our verdict is Benign. The variant received -20 ACMG points: 0P and 20B. BP4_StrongBP6_Very_StrongBS1BS2

The NM_198525.3(KIF7):c.1429G>A(p.Ala477Thr) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.000549 in 1,516,588 control chromosomes in the GnomAD database, including 3 homozygotes. In-silico tool predicts a benign outcome for this variant. 15/21 in silico tools predict a benign outcome for this variant. Variant has been reported in ClinVar as Likely benign (★★).

Frequency

Genomes: 𝑓 0.0028 ( 2 hom., cov: 32)

Exomes 𝑓: 0.00030 ( 1 hom. )

Consequence

KIF7
NM_198525.3 missense

Scores

Clinical Significance

Benign/Likely benign criteria provided, multiple submitters, no conflicts B:7

Conservation

PhyloP100: 0.00900

Publications

1 publications found

Variant links:

Genes affected

KIF7 (HGNC:30497): (kinesin family member 7) This gene encodes a cilia-associated protein belonging to the kinesin family. This protein plays a role in the sonic hedgehog (SHH) signaling pathway through the regulation of GLI transcription factors. It functions as a negative regulator of the SHH pathway by preventing inappropriate activation of GLI2 in the absence of ligand, and as a positive regulator by preventing the processing of GLI3 into its repressor form. Mutations in this gene have been associated with various ciliopathies. [provided by RefSeq, Oct 2011]

KIF7 Gene-Disease associations (from GenCC):

acrocallosal syndrome
Inheritance: AR Classification: DEFINITIVE, STRONG, MODERATE, SUPPORTIVE Submitted by: G2P, Ambry Genetics, Orphanet, Labcorp Genetics (formerly Invitae)
neurodevelopmental disorder
Inheritance: AR Classification: DEFINITIVE Submitted by: G2P
hydrolethalus syndrome 2
Inheritance: AR Classification: STRONG, MODERATE Submitted by: Labcorp Genetics (formerly Invitae), Genomics England PanelApp
hydrolethalus syndrome
Inheritance: AR Classification: SUPPORTIVE Submitted by: Orphanet
multiple epiphyseal dysplasia, Al-Gazali type
Inheritance: AR Classification: SUPPORTIVE Submitted by: Orphanet
orofaciodigital syndrome type 6
Inheritance: AR Classification: SUPPORTIVE Submitted by: Orphanet

KIF7 links:

Genome browser will be placed here

ACMG classification

Classification was made for transcript

Our verdict: Benign. The variant received -20 ACMG points.

BP4

Computational evidence support a benign effect (MetaRNN=0.003024429).

BP6

Variant 15-89648269-C-T is Benign according to our data. Variant chr15-89648269-C-T is described in CliVar as Benign/Likely_benign. Clinvar id is 197899.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr15-89648269-C-T is described in CliVar as Benign/Likely_benign. Clinvar id is 197899.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr15-89648269-C-T is described in CliVar as Benign/Likely_benign. Clinvar id is 197899.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr15-89648269-C-T is described in CliVar as Benign/Likely_benign. Clinvar id is 197899.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr15-89648269-C-T is described in CliVar as Benign/Likely_benign. Clinvar id is 197899.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr15-89648269-C-T is described in CliVar as Benign/Likely_benign. Clinvar id is 197899.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr15-89648269-C-T is described in CliVar as Benign/Likely_benign. Clinvar id is 197899.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr15-89648269-C-T is described in CliVar as Benign/Likely_benign. Clinvar id is 197899.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr15-89648269-C-T is described in CliVar as Benign/Likely_benign. Clinvar id is 197899.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr15-89648269-C-T is described in CliVar as Benign/Likely_benign. Clinvar id is 197899.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr15-89648269-C-T is described in CliVar as Benign/Likely_benign. Clinvar id is 197899.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr15-89648269-C-T is described in CliVar as Benign/Likely_benign. Clinvar id is 197899.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr15-89648269-C-T is described in CliVar as Benign/Likely_benign. Clinvar id is 197899.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr15-89648269-C-T is described in CliVar as Benign/Likely_benign. Clinvar id is 197899.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr15-89648269-C-T is described in CliVar as Benign/Likely_benign. Clinvar id is 197899.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr15-89648269-C-T is described in CliVar as Benign/Likely_benign. Clinvar id is 197899.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr15-89648269-C-T is described in CliVar as Benign/Likely_benign. Clinvar id is 197899.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr15-89648269-C-T is described in CliVar as Benign/Likely_benign. Clinvar id is 197899.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr15-89648269-C-T is described in CliVar as Benign/Likely_benign. Clinvar id is 197899.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr15-89648269-C-T is described in CliVar as Benign/Likely_benign. Clinvar id is 197899.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr15-89648269-C-T is described in CliVar as Benign/Likely_benign. Clinvar id is 197899.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr15-89648269-C-T is described in CliVar as Benign/Likely_benign. Clinvar id is 197899.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr15-89648269-C-T is described in CliVar as Benign/Likely_benign. Clinvar id is 197899.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr15-89648269-C-T is described in CliVar as Benign/Likely_benign. Clinvar id is 197899.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr15-89648269-C-T is described in CliVar as Benign/Likely_benign. Clinvar id is 197899.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars.

BS1

Variant frequency is greater than expected in population afr. GnomAd4 allele frequency = 0.00278 (423/152276) while in subpopulation AFR AF = 0.00986 (410/41576). AF 95% confidence interval is 0.00907. There are 2 homozygotes in GnomAd4. There are 171 alleles in the male GnomAd4 subpopulation. Median coverage is 32. This position passed quality control check.

BS2

High Homozygotes in GnomAd4 at 2 AR gene

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
KIF7	NM_198525.3 link	c.1429G>A	p.Ala477Thr	missense_variant	Exon 5 of 19	ENST00000394412.8	NP_940927.2	Q2M1P5

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	UniProt
KIF7	ENST00000394412.8 link	c.1429G>A	p.Ala477Thr	missense_variant	Exon 5 of 19	5	NM_198525.3	ENSP00000377934.3	Q2M1P5
KIF7	ENST00000696512.1 link	c.1552G>A	p.Ala518Thr	missense_variant	Exon 5 of 19			ENSP00000512678.1	A0A8Q3SIQ8
KIF7	ENST00000445906.1 link	n.*1088G>A		downstream_gene_variant		1		ENSP00000395906.1	F8WD21

Frequencies

GnomAD3 genomes

AF:

0.00277

AC:

421

AN:

152162

Hom.:

Cov.:

show subpopulations

Gnomad AFR

AF:

0.00984

Gnomad AMI

AF:

0.00

Gnomad AMR

AF:

0.000654

Gnomad ASJ

AF:

0.00

Gnomad EAS

AF:

0.00

Gnomad SAS

AF:

0.00

Gnomad FIN

AF:

0.00

Gnomad MID

AF:

0.00

Gnomad NFE

AF:

0.0000294

Gnomad OTH

AF:

0.000478

GnomAD2 exomes

AF:

0.000587

AC:

AN:

126170

AF XY:

0.000422

show subpopulations

Gnomad AFR exome

AF:

0.0110

Gnomad AMR exome

AF:

0.000296

Gnomad ASJ exome

AF:

0.00

Gnomad EAS exome

AF:

0.00

Gnomad FIN exome

AF:

0.00

Gnomad NFE exome

AF:

0.0000429

Gnomad OTH exome

AF:

0.000513

GnomAD4 exome

AF:

0.000301

AC:

410

AN:

1364312

Hom.:

Cov.:

AF XY:

0.000259

AC XY:

174

AN XY:

670932

show subpopulations

African (AFR)

AF:

0.0113

AC:

347

AN:

30658

American (AMR)

AF:

0.000490

AC:

AN:

34724

Ashkenazi Jewish (ASJ)

AF:

0.00

AC:

AN:

24764

East Asian (EAS)

AF:

0.00

AC:

AN:

34498

South Asian (SAS)

AF:

0.0000128

AC:

AN:

78354

European-Finnish (FIN)

AF:

0.00

AC:

AN:

33570

Middle Eastern (MID)

AF:

0.000500

AC:

AN:

3998

European-Non Finnish (NFE)

AF:

0.00000656

AC:

AN:

1067000

Other (OTH)

AF:

0.000634

AC:

AN:

56746

Allele Balance Distribution

Red line indicates average allele balance

Average allele balance: 0.495

Heterozygous variant carriers

102

0.00

0.20

0.40

0.60

0.80

0.95

Allele balance

Age Distribution

Exome Het

Variant carriers

100

<30

30-35

35-40

40-45

45-50

50-55

55-60

60-65

65-70

70-75

75-80

>80

Age

GnomAD4 genome

AF:

0.00278

AC:

423

AN:

152276

Hom.:

Cov.:

AF XY:

0.00230

AC XY:

171

AN XY:

74464

show subpopulations

African (AFR)

AF:

0.00986

AC:

410

AN:

41576

American (AMR)

AF:

0.000654

AC:

AN:

15302

Ashkenazi Jewish (ASJ)

AF:

0.00

AC:

AN:

3472

East Asian (EAS)

AF:

0.00

AC:

AN:

5180

South Asian (SAS)

AF:

0.00

AC:

AN:

4834

European-Finnish (FIN)

AF:

0.00

AC:

AN:

10594

Middle Eastern (MID)

AF:

0.00

AC:

AN:

294

European-Non Finnish (NFE)

AF:

0.0000294

AC:

AN:

68000

Other (OTH)

AF:

0.000473

AC:

AN:

2112

Allele Balance Distribution

Red line indicates average allele balance

Average allele balance: 0.507

Heterozygous variant carriers

108

0.00

0.20

0.40

0.60

0.80

0.95

Allele balance

Age Distribution

Genome Het

Genome Hom

Variant carriers

<30

30-35

35-40

40-45

45-50

50-55

55-60

60-65

65-70

70-75

75-80

>80

Age

Alfa

AF:

0.00187

Hom.:

Bravo

AF:

0.00326

ExAC

AF:

0.000150

AC:

ClinVar

Significance: Benign/Likely benign

Submissions summary: Benign:7

Revision: criteria provided, multiple submitters, no conflicts

LINK: link

Submissions by phenotype

not provided

Benign:3

Breakthrough Genomics, Breakthrough Genomics

Significance:Likely benign

Review Status:criteria provided, single submitter

Collection Method:not provided

- -

Oct 13, 2020

GeneDx

Significance:Likely benign

Review Status:criteria provided, single submitter

Collection Method:clinical testing

- -

Aug 31, 2017

Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics

Significance:Likely benign

Review Status:criteria provided, single submitter

Collection Method:clinical testing

- -

not specified

Benign:2

May 23, 2017

Eurofins Ntd Llc (ga)

Significance:Likely benign

Review Status:criteria provided, single submitter

Collection Method:clinical testing

- -

PreventionGenetics, part of Exact Sciences

Significance:Benign

Review Status:criteria provided, single submitter

Collection Method:clinical testing

- -

Acrocallosal syndrome;C1846722:Multiple epiphyseal dysplasia, Al-Gazali type;C3279899:Hydrolethalus syndrome 2

Benign:1

May 03, 2022

Fulgent Genetics, Fulgent Genetics

Significance:Likely benign

Review Status:criteria provided, single submitter

Collection Method:clinical testing

- -

Acrocallosal syndrome

Benign:1

Jan 20, 2025

Labcorp Genetics (formerly Invitae), Labcorp

Significance:Benign

Review Status:criteria provided, single submitter

Collection Method:clinical testing

- -

Computational scores

Source: dbNSFP v4.3

Name

Calibrated prediction

Score

Prediction

AlphaMissense

Benign

0.063

BayesDel_addAF

Benign

-0.59

BayesDel_noAF

Benign

-0.62

CADD

Benign

0.95

(source)

DANN

Benign

0.92

DEOGEN2

Benign

0.11

Eigen

Benign

-1.8

Eigen_PC

Benign

-1.8

FATHMM_MKL

Benign

0.0075

LIST_S2

Benign

0.29

MetaRNN

Benign

0.0030

MetaSVM

Benign

-1.0

MutationAssessor

Benign

-0.76

PhyloP100

0.0090

PrimateAI

Uncertain

0.57

PROVEAN

Benign

-1.2

REVEL

Benign

0.12

Sift

Benign

0.56

Sift4G

Benign

0.57

Polyphen

0.0

Vest4

0.025

MVP

0.055

MPC

0.018

ClinPred

0.0034

GERP RS

-6.8

Varity_R

0.031

gMVP

0.20

Mutation Taster

=100/0

polymorphism

(source)

Splicing

Name

Calibrated prediction

Score

Prediction

SpliceAI score (max)

0.0

Details are displayed if max score is > 0.2

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Publications

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Variant summary

Frequency

Consequence

Scores

Clinical Significance

Conservation

Publications

ACMG classification

Transcripts

RefSeq

Ensembl

Frequencies

Age Distribution

Age Distribution

ClinVar

Submissions by phenotype

Computational scores

Splicing

Publications

Other links and lift over