Variant #0000982273 (NC_000017.10:g.10433181C>T, NM_017534.5:c.2908G>A (MYH2))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.10433181C>T
DNA change (hg38) -
Published as MYH2(NM_001100112.1):c.2908G>A (p.(Val970Ile)), MYH2(NM_017534.6):c.2908G>A (p.V970I)
ISCN -
DB-ID MYH2_000083 See all 2 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00532 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYH2 NM_017534.5 -?/. - c.2908G>A r.(?) p.(Val970Ile)


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