chr14:23894612:C>T Detail (hg19) (MYH7, LOC126861898)

Information

Genome

Assembly Position
hg19 chr14:23,894,612-23,894,612
hg38 chr14:23,425,403-23,425,403 View the variant detail on this assembly version.

HGVS

Type Transcript Protein
RefSeq NM_000257.3:c.2302G>A NP_000248.2:p.Gly768Arg
Ensemble ENST00000713769.1:c.2302G>A ENST00000713769.1:p.Gly768Arg
ENST00000713768.1:c.2302G>A ENST00000713768.1:p.Gly768Arg
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

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
MONDO
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance Last evaluated Review status Condition Origin Links
Pathogenic 2017-09-04 criteria provided, single submitter hypertrophic cardiomyopathy,restrictive cardiomyopathy germline Detail
Pathogenic 2017-09-04 criteria provided, single submitter hypertrophic cardiomyopathy,restrictive cardiomyopathy germline Detail
Pathogenic Likely pathogenic 2022-02-17 criteria provided, multiple submitters, no conflicts not provided germline Detail
Pathogenic 2023-12-09 criteria provided, single submitter hypertrophic cardiomyopathy germline Detail
Pathogenic 2017-08-01 criteria provided, single submitter hypertrophic cardiomyopathy 1 germline Detail
Pathogenic 2021-05-04 criteria provided, single submitter germline Detail
Pathogenic 2021-11-25 criteria provided, single submitter cardiomyopathy germline Detail
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.252 Cardiomyopathy, Hypertrophic, Familial NA CLINVAR Detail
0.125 restrictive cardiomyopathy NA CLINVAR Detail
Annotation

Annotations

DescrptionSourceLinks
NM_000257.4(MYH7):c.2302G>A (p.Gly768Arg) AND multiple conditions ClinVar Detail
NM_000257.4(MYH7):c.2302G>A (p.Gly768Arg) AND multiple conditions ClinVar Detail
NM_000257.4(MYH7):c.2302G>A (p.Gly768Arg) AND not provided ClinVar Detail
NM_000257.4(MYH7):c.2302G>A (p.Gly768Arg) AND Hypertrophic cardiomyopathy ClinVar Detail
NM_000257.4(MYH7):c.2302G>A (p.Gly768Arg) AND Hypertrophic cardiomyopathy 1 ClinVar Detail
NM_000257.4(MYH7):c.2302G>A (p.Gly768Arg) AND Cardiovascular phenotype ClinVar Detail
NM_000257.4(MYH7):c.2302G>A (p.Gly768Arg) 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
rs727503260 dbSNP
Genome
hg19
Position
chr14:23,894,612-23,894,612
Variant Type
snv
Reference Allele
C
Alternative Allele
T
Genome browser