Variant #0000610272 (NC_000006.11:g.31901976C>G, NM_000063.4:c.749C>G (C2))

Chromosome 6
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.31901976C>G
DNA change (hg38) g.31934199C>G
Published as C2(NM_001282458.1):c.662C>G (p.S221C), C2(NM_001282458.2):c.662C>G (p.S221C)
ISCN -
DB-ID C2_000013 See all 3 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) 0.00024 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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C2 NM_000063.4 ?/. - c.749C>G r.(?) p.(Ser250Cys)
ZBTB12 NM_181842.2 ?/. - c.-32383G>C r.(?) p.(=)


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