Variant #0001061498 (NC_000017.10:g.10438464_10438471del, NM_017534.5:c.2104_2111del (MYH2))

Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.10438464_10438471del
DNA change (hg38) -
Published as -
ISCN -
DB-ID MYH2_000105
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs757940256
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-12-16 13:38:02 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYH2 NM_017534.5 +/. - c.2104_2111del r.(?) p.(Asn702AlafsTer8)


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