Variant #0000560176 (NC_000017.10:g.10426810C>A, NC_000017.10(NM_017534.5):c.5472+3G>T (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.10426810C>A
DNA change (hg38) g.10523493C>A
Published as MYH2(NM_001100112.2):c.5472+3G>T
ISCN -
DB-ID MYH1_000006
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) 8.0E-5 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYH1 NM_005963.3 -?/. - c.-5045G>T r.(?) p.(=)
MYH2 NM_017534.5 -?/. - c.5472+3G>T r.spl? p.?


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