Variant #0000679629 (NC_000012.11:g.6639060C>A, NM_014865.3:c.3773C>A (NCAPD2))

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.6639060C>A
DNA change (hg38) -
Published as NCAPD2(NM_014865.4):c.3773C>A (p.S1258Y)
ISCN -
DB-ID GAPDH_000005
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) 0.00061 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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GAPDH NM_002046.4 ?/. - c.-4699C>A r.(?) p.(=)
NCAPD2 NM_014865.3 ?/. - c.3773C>A r.(?) p.(Ser1258Tyr)


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