Variant 18-49823132-A-ACTTT details in Genebe, Genetics Data Aggregator

Variant summary

Our verdict is Uncertain significance. Variant got 0 ACMG points: 0P and 0B.

The ENST00000285039.12(MYO5B):c.*3338_*3339insAAAG variant causes a 3 prime UTR change involving the alteration of a non-conserved nucleotide. Variant has been reported in ClinVar as Uncertain significance (★).

Frequency

Genomes: 𝑓 0.076 ( 0 hom., cov: 28)

Failed GnomAD Quality Control

Consequence

MYO5B
ENST00000285039.12 3_prime_UTR

Scores

Not classified

Clinical Significance

Uncertain significance criteria provided, single submitter U:1

Conservation

PhyloP100: 0.415

Variant links:

Genes affected

MYO5B (HGNC:7603): (myosin VB) The protein encoded by this gene, together with other proteins, may be involved in plasma membrane recycling. Mutations in this gene are associated with microvillous inclusion disease. [provided by RefSeq, Sep 2009]

MYO5B links:

SNHG22 (HGNC:50285): (small nucleolar RNA host gene 22)

SNHG22 links:

Genome browser will be placed here

ACMG classification

Classification made for transcript

Verdict is Uncertain_significance. Variant got 0 ACMG points.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
MYO5B	NM_001080467.3 linkuse as main transcript	c.3338_3339insAAAG		3_prime_UTR_variant	40/40	ENST00000285039.12	NP_001073936.1
SNHG22	NR_117096.1 linkuse as main transcript	n.40+9070_40+9071insCTTT		intron_variant, non_coding_transcript_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
MYO5B	ENST00000285039.12 linkuse as main transcript	c.3338_3339insAAAG		3_prime_UTR_variant	40/40	1	NM_001080467.3	ENSP00000285039	P1	Q9ULV0-1
SNHG22	ENST00000589499.1 linkuse as main transcript	n.40+9070_40+9071insCTTT		intron_variant, non_coding_transcript_variant		2

Frequencies

GnomAD3 genomes

AF:

0.00

AC:

3696

AN:

48552

Hom.:

Cov.:

FAILED QC

Gnomad AFR

AF:

0.0672

Gnomad AMI

AF:

0.0522

Gnomad AMR

AF:

0.0921

Gnomad ASJ

AF:

0.0705

Gnomad EAS

AF:

0.103

Gnomad SAS

AF:

0.0756

Gnomad FIN

AF:

0.102

Gnomad MID

AF:

0.139

Gnomad NFE

AF:

0.0719

Gnomad OTH

AF:

0.0824

GnomAD4 exome

Data not reliable, filtered out with message: AC0;AS_VQSR

AC:

AN:

Hom.:

Cov.:

AC XY:

AN XY:

GnomAD4 genome

Data not reliable, filtered out with message: AS_VQSR;InbreedingCoeff

AF:

0.0762

AC:

3700

AN:

48578

Hom.:

Cov.:

AF XY:

0.0779

AC XY:

1910

AN XY:

24528

show subpopulations

Gnomad4 AFR

AF:

0.0675

Gnomad4 AMR

AF:

0.0924

Gnomad4 ASJ

AF:

0.0705

Gnomad4 EAS

AF:

0.102

Gnomad4 SAS

AF:

0.0773

Gnomad4 FIN

AF:

0.102

Gnomad4 NFE

AF:

0.0718

Gnomad4 OTH

AF:

0.0809

Alfa

AF:

0.243

Hom.:

ClinVar

Significance: Uncertain significance

Submissions summary: Uncertain:1

Revision: criteria provided, single submitter

LINK: link

Submissions by phenotype

Diarrhea with Microvillus Atrophy

Uncertain:1

Uncertain significance, criteria provided, single submitter

clinical testing

Illumina Laboratory Services, Illumina

Jun 14, 2016

- -

Computational scores

Source: dbNSFP v4.3

Name

Calibrated prediction

Score

Prediction

Splicing

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

Publications

LitVar

Below is the list of publications found by LitVar. It may be empty.

Variant summary

Frequency

Consequence

Scores

Clinical Significance

Conservation

ACMG classification

Transcripts

RefSeq

Ensembl

Frequencies

ClinVar

Submissions by phenotype

Computational scores

Splicing

Publications

LitVar

Other links and lift over