Variant #0000723971 (NC_000012.11:g.21689928G>A, NM_021957.3:c.2072C>T (GYS2))

Chromosome 12
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.21689928G>A
DNA change (hg38) -
Published as GYS2(NM_021957.4):c.2072C>T (p.P691L)
ISCN -
DB-ID C12orf39_000002
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) 0.00014 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +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     
GYS2 NM_021957.3 ?/. - c.2072C>T r.(?) p.(Pro691Leu)
C12orf39 NM_030572.2 ?/. - c.*5799G>A r.(=) p.(=)


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