chr14:23899810:C>T Detail (hg19) (MYH7)

Information

Genome

Assembly Position
hg19 chr14:23,899,810-23,899,810
hg38 chr14:23,430,601-23,430,601 View the variant detail on this assembly version.

HGVS

Type Transcript Protein
RefSeq NM_000257.3:c.958G>A NP_000248.2:p.Val320Met
Ensemble ENST00000713769.1:c.958G>A ENST00000713769.1:p.Val320Met
ENST00000355349.4:c.958G>A ENST00000355349.4:p.Val320Met
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 Pathogenic Likely pathogenic
Review star
Show details
Links
Type Database ID Link
Gene MIM 160760 OMIM
HGNC 7577 HGNC
Ensembl ENSG00000092054 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar
COSMIC COSM2031871 COSMIC
MONDO
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance Last evaluated Review status Condition Origin Links
Conflicting interpretations of pathogenicity 2014-06-09 no assertion criteria provided Primary familial hypertrophic cardiomyopathy germline Detail
Likely pathogenic 2020-03-10 criteria provided, multiple submitters, no conflicts hypertrophic cardiomyopathy 1 germline unknown Detail
Likely pathogenic 2022-11-23 criteria provided, multiple submitters, no conflicts not provided germline Detail
Pathogenic Likely pathogenic 2023-11-19 criteria provided, multiple submitters, no conflicts hypertrophic cardiomyopathy germline Detail
Likely pathogenic 2023-11-28 criteria provided, single submitter germline Detail
Likely pathogenic 2022-04-19 criteria provided, single submitter cardiomyopathy germline Detail
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.360 Cardiomyopathy, Familial Hypertrophic, 1 (disorder) NA CLINVAR Detail
0.252 Cardiomyopathy, Hypertrophic, Familial NA CLINVAR Detail
Annotation

Annotations

DescrptionSourceLinks
NM_000257.4(MYH7):c.958G>A (p.Val320Met) AND Primary familial hypertrophic cardiomyopathy ClinVar Detail
NM_000257.4(MYH7):c.958G>A (p.Val320Met) AND Hypertrophic cardiomyopathy 1 ClinVar Detail
NM_000257.4(MYH7):c.958G>A (p.Val320Met) AND not provided ClinVar Detail
NM_000257.4(MYH7):c.958G>A (p.Val320Met) AND Hypertrophic cardiomyopathy ClinVar Detail
NM_000257.4(MYH7):c.958G>A (p.Val320Met) AND Cardiovascular phenotype ClinVar Detail
NM_000257.4(MYH7):c.958G>A (p.Val320Met) AND Cardiomyopathy ClinVar Detail
NA DisGeNET 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
rs376897125 dbSNP
Genome
hg19
Position
chr14:23,899,810-23,899,810
Variant Type
snv
Reference Allele
C
Alternative Allele
T
East Asian Chromosome Counts (ExAC)
8604
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)
119812
Allele Counts in All Race (ExAC)
1
Heterozygous Counts in All Race (ExAC)
1
Homozygous Counts in All Race (ExAC)
0
Allele Frequency in All Race (ExAC)
8.34640937468701E-6
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