Genetic Variant NM_018942.3:c.650A>G (chr4-8868090-T-C) – ACMG Classification: Uncertain_significance (4 pts)

Variant summary

Our verdict is Uncertain significance. The variant received 4 ACMG points: 4P and 0B. PM2PM5

The NM_018942.3(HMX1):c.650A>G(p.Gln217Arg) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.00000146 in 1,369,020 control chromosomes in the GnomAD database, with no homozygous occurrence. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar. Another variant affecting the same amino acid position, but resulting in a different missense (i.e. Q217P) has been classified as Pathogenic.

Frequency

Genomes: not found (cov: 33)

Exomes 𝑓: 0.0000015 ( 0 hom. )

Consequence

HMX1
NM_018942.3 missense

Scores

Clinical Significance

Not reported in ClinVar

Conservation

PhyloP100: 2.63

Publications

0 publications found

Variant links:

Genes affected

HMX1 (HGNC:5017): (H6 family homeobox 1) This gene encodes a transcription factor that belongs to the H6 family of homeobox proteins. This protein can bind a 5'-CAAG-3' core DNA sequence, and it is involved in the development of craniofacial structures. Mutations in this gene cause oculoauricular syndrome, a disorder of the eye and external ear. [provided by RefSeq, Oct 2009]

HMX1 Gene-Disease associations (from GenCC):

oculoauricular syndrome
Inheritance: AR Classification: DEFINITIVE, STRONG, SUPPORTIVE Submitted by: Labcorp Genetics (formerly Invitae), PanelApp Australia, G2P, ClinGen, Orphanet

HMX1 links:

Genome browser will be placed here

ACMG classification

Classification was made for transcript

Our verdict: Uncertain_significance. The variant received 4 ACMG points.

PM2

Very rare variant in population databases, with high coverage;

PM5

Other missense variant is known to change same aminoacid residue: Variant chr4-8868090-T-G is described in ClinVar as [Pathogenic]. Clinvar id is 192315.Status of the report is no_assertion_criteria_provided, 0 stars.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
HMX1	NM_018942.3 link	c.650A>G	p.Gln217Arg	missense_variant	Exon 2 of 2	ENST00000400677.5	NP_061815.2	Q9NP08
HMX1	NM_001306142.2 link	c.394+3131A>G		intron_variant	Intron 1 of 1		NP_001293071.1	Q9NP08F1T0J4

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
HMX1	ENST00000400677.5 link	c.650A>G	p.Gln217Arg	missense_variant	Exon 2 of 2	1	NM_018942.3	ENSP00000383516.3		Q9NP08
HMX1	ENST00000506970.2 link	c.394+3131A>G		intron_variant	Intron 1 of 1	1		ENSP00000446997.2		F1T0J4

Frequencies

GnomAD3 genomes

Cov.:

GnomAD4 exome

AF:

0.00000146

AC:

AN:

1369020

Hom.:

Cov.:

AF XY:

0.00

AC XY:

AN XY:

676230

show subpopulations

African (AFR)

AF:

0.00

AC:

AN:

29410

American (AMR)

AF:

0.00

AC:

AN:

34154

Ashkenazi Jewish (ASJ)

AF:

0.00

AC:

AN:

24490

East Asian (EAS)

AF:

0.00

AC:

AN:

33294

South Asian (SAS)

AF:

0.00

AC:

AN:

76360

European-Finnish (FIN)

AF:

0.0000248

AC:

AN:

40260

Middle Eastern (MID)

AF:

0.00

AC:

AN:

5562

European-Non Finnish (NFE)

AF:

9.36e-7

AC:

AN:

1068616

Other (OTH)

AF:

0.00

AC:

AN:

56874

Allele Balance Distribution

Red line indicates average allele balance

Average allele balance: 0.400

Heterozygous variant carriers

0.00

0.20

0.40

0.60

0.80

0.95

Allele balance

GnomAD4 genome

Cov.:

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name

Calibrated prediction

Score

Prediction

AlphaMissense

Pathogenic

0.69

BayesDel_addAF

Uncertain

0.082

BayesDel_noAF

Benign

-0.12

CADD

Pathogenic

(source)

DANN

Uncertain

0.99

DEOGEN2

Uncertain

0.79

Eigen

Benign

-0.10

Eigen_PC

Benign

-0.018

FATHMM_MKL

Uncertain

0.92

LIST_S2

Benign

0.85

M_CAP

Pathogenic

0.91

MetaRNN

Uncertain

0.58

MetaSVM

Uncertain

0.39

MutationAssessor

Benign

0.49

PhyloP100

2.6

PrimateAI

Pathogenic

0.96

PROVEAN

Uncertain

-3.7

REVEL

Uncertain

0.52

Sift

Benign

0.043

Sift4G

Uncertain

0.030

Polyphen

0.21

Vest4

0.38

MutPred

0.59

Gain of MoRF binding (P = 0.0165);

MVP

0.94

MPC

2.0

ClinPred

0.91

GERP RS

2.4

Varity_R

0.41

gMVP

0.64

Mutation Taster

=46/54

disease causing

(source)

Splicing

Name

Calibrated prediction

Score

Prediction

SpliceAI score (max)

0.030

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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NM_018942.3:c.650A>G

Variant summary

Frequency

Consequence

Scores

Clinical Significance

Conservation

Publications

ACMG classification

Transcripts

RefSeq

Ensembl

Frequencies

Age Distribution

ClinVar

Computational scores

Splicing

Publications

Other links and lift over