chr2:219420939:G>A Detail (hg38) (DES)

Information

Genome

Assembly Position
hg19 chr2:220,285,661-220,285,661 View the variant detail on this assembly version.
hg38 chr2:219,420,939-219,420,939

HGVS

Type Transcript Protein
RefSeq NM_001927.3:c.1009G>A NP_001918.3:p.Ala337Thr
Ensemble ENST00000373960.4:c.1009G>A ENST00000373960.4:p.Ala337Thr
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 125660 OMIM
HGNC 2770 HGNC
Ensembl ENSG00000175084 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 2017-10-23 criteria provided, single submitter not provided germline Detail
Uncertain significance 2024-01-09 criteria provided, single submitter Desmin-related myofibrillar myopathy germline Detail
Uncertain significance 2021-12-13 criteria provided, single submitter germline Detail
Uncertain significance 2021-10-12 criteria provided, single submitter dilated cardiomyopathy 1I,Desmin-related myofibrillar myopathy,Neurogenic scapuloperoneal syndrome, Kaeser type unknown Detail
Uncertain significance 2021-10-12 criteria provided, single submitter dilated cardiomyopathy 1I,Desmin-related myofibrillar myopathy,Neurogenic scapuloperoneal syndrome, Kaeser type unknown Detail
Uncertain significance 2021-10-12 criteria provided, single submitter dilated cardiomyopathy 1I,Desmin-related myofibrillar myopathy,Neurogenic scapuloperoneal syndrome, Kaeser type unknown Detail
Uncertain significance 2023-02-14 criteria provided, single submitter dilated cardiomyopathy 1I germline Detail
Uncertain significance 2024-02-27 criteria provided, single submitter not specified germline Detail
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.564 MYOPATHY, MYOFIBRILLAR, DESMIN-RELATED NA CLINVAR Detail
0.564 MYOPATHY, MYOFIBRILLAR, DESMIN-RELATED We examined 22 patients from 8 families with dominantly inherited myofibrillar o... UNIPROT 10717012 Detail
Annotation

Annotations

DescrptionSourceLinks
NM_001927.4(DES):c.1009G>A (p.Ala337Thr) AND not provided ClinVar Detail
NM_001927.4(DES):c.1009G>A (p.Ala337Thr) AND Desmin-related myofibrillar myopathy ClinVar Detail
NM_001927.4(DES):c.1009G>A (p.Ala337Thr) AND Cardiovascular phenotype ClinVar Detail
NM_001927.4(DES):c.1009G>A (p.Ala337Thr) AND multiple conditions ClinVar Detail
NM_001927.4(DES):c.1009G>A (p.Ala337Thr) AND multiple conditions ClinVar Detail
NM_001927.4(DES):c.1009G>A (p.Ala337Thr) AND multiple conditions ClinVar Detail
NM_001927.4(DES):c.1009G>A (p.Ala337Thr) AND Dilated cardiomyopathy 1I ClinVar Detail
NM_001927.4(DES):c.1009G>A (p.Ala337Thr) AND not specified ClinVar Detail
NA DisGeNET Detail
We examined 22 patients from 8 families with dominantly inherited myofibrillar or desmin-related myo... 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
rs59962885 dbSNP
Genome
hg38
Position
chr2:219,420,939-219,420,939
Variant Type
snv
Reference Allele
G
Alternative Allele
A
East Asian Chromosome Counts (ExAC)
8382
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)
118470
Allele Counts in All Race (ExAC)
14
Heterozygous Counts in All Race (ExAC)
14
Homozygous Counts in All Race (ExAC)
0
Allele Frequency in All Race (ExAC)
1.1817337722630202E-4
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