chr11:47360110:C>T Detail (hg19) (MYBPC3)

Information

Genome

Assembly Position
hg19 chr11:47,360,110-47,360,110
hg38 chr11:47,338,559-47,338,559 View the variant detail on this assembly version.

HGVS

Type Transcript Protein
RefSeq NM_000256.3:c.2269G>A NP_000247.2:p.Val757Met
Ensemble ENST00000399249.6:c.2269G>A ENST00000399249.6:p.Val757Met
ENST00000545968.6:c.2269G>A ENST00000545968.6:p.Val757Met
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

JP HGVD:[No Data.]
ToMMo:[No Data.]
NCBN:[No Data.]
NCBN(Hondo):[No Data.]
NCBN(Ryukyu):[No Data.]
East asia ExAC:<0.001

Prediction

ClinVar

Clinical Significance Uncertain significance
Review star
Show details
Links
Type Database ID Link
Gene MIM 600958 OMIM
HGNC 7551 HGNC
Ensembl ENSG00000134571 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar
COSMIC
MONDO
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance Last evaluated Review status Condition Origin Links
Uncertain significance 2014-06-01 no assertion criteria provided Primary familial hypertrophic cardiomyopathy germline Detail
Uncertain significance 2013-02-12 no assertion criteria provided not specified germline Detail
Uncertain significance 2023-12-18 criteria provided, multiple submitters, no conflicts hypertrophic cardiomyopathy germline Detail
Uncertain significance 2022-01-13 criteria provided, single submitter not provided germline Detail
Uncertain significance 2023-11-27 criteria provided, single submitter cardiomyopathy germline Detail
Uncertain significance 2023-12-11 criteria provided, single submitter germline Detail
Uncertain significance 2021-10-29 criteria provided, single submitter Left ventricular noncompaction 10,hypertrophic cardiomyopathy 4 unknown Detail
Uncertain significance 2021-10-29 criteria provided, single submitter Left ventricular noncompaction 10,hypertrophic cardiomyopathy 4 unknown Detail
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.247 Cardiomyopathy, Hypertrophic, Familial NA CLINVAR Detail
Annotation

Annotations

DescrptionSourceLinks
NM_000256.3(MYBPC3):c.2269G>A (p.Val757Met) AND Primary familial hypertrophic cardiomyopathy ClinVar Detail
NM_000256.3(MYBPC3):c.2269G>A (p.Val757Met) AND not specified ClinVar Detail
NM_000256.3(MYBPC3):c.2269G>A (p.Val757Met) AND Hypertrophic cardiomyopathy ClinVar Detail
NM_000256.3(MYBPC3):c.2269G>A (p.Val757Met) AND not provided ClinVar Detail
NM_000256.3(MYBPC3):c.2269G>A (p.Val757Met) AND Cardiomyopathy ClinVar Detail
NM_000256.3(MYBPC3):c.2269G>A (p.Val757Met) AND Cardiovascular phenotype ClinVar Detail
NM_000256.3(MYBPC3):c.2269G>A (p.Val757Met) AND multiple conditions ClinVar Detail
NM_000256.3(MYBPC3):c.2269G>A (p.Val757Met) AND multiple conditions ClinVar Detail
NA DisGeNET Detail

Overlapped Transcript Coordinates

Gene Transcript ID Exon Number Chromosome Start Stop Type Amino Mutation Transcript Position Links

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
dbSNP
rs369790992 dbSNP
Genome
hg19
Position
chr11:47,360,110-47,360,110
Variant Type
snv
Reference Allele
C
Alternative Allele
T
Homozygous Counts in All Race (ExAC)
0
East Asian Chromosome Counts (ExAC)
8624
East Asian Allele Counts (ExAC)
0
East Asian Heterozygous Counts (ExAC)
0
East Asian Homozygous Counts (ExAC)
0
East Asian Allele Frequency (ExAC)
0.0
Chromosome Counts in All Race (ExAC)
120616
Allele Counts in All Race (ExAC)
8
Heterozygous Counts in All Race (ExAC)
8
Allele Frequency in All Race (ExAC)
6.632619221330503E-5
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