Variant #0000622469 (NC_000010.10:g.97728491A>C, NM_001776.5:c.*102351A>C (ENTPD1))

Chromosome 10
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.97728491A>C
DNA change (hg38) g.95968734A>C
Published as CC2D2B(NM_001349008.2):c.1477A>C (p.K493Q)
ISCN -
DB-ID C10orf131_000007
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CC2D2B NM_001001732.3 ?/. - c.-31556A>C r.(?) p.(=)
C10orf131 NM_001130446.2 ?/. - c.*30525A>C r.(=) p.(=)
ENTPD1 NM_001776.5 ?/. - c.*102351A>C r.(=) p.(=)
CCNJ NM_019084.4 ?/. - c.-75027A>C r.(?) p.(=)
ENTPD1-AS1 NR_038444.1 ?/. - n.297-92074T>G r.(?) -


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