Variant #0000723049 (NC_000010.10:g.97626000G>C, NM_001776.5:c.1393G>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.97626000G>C
DNA change (hg38) -
Published as ENTPD1(NM_001164179.1):c.1270G>C (p.E424Q)
ISCN -
DB-ID C10orf131_000009
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) 4.0E-5 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     
CC2D2B NM_001001732.3 ?/. - c.-134047G>C r.(?) p.(=)
C10orf131 NM_001130446.2 ?/. - c.-41918G>C r.(?) p.(=)
ENTPD1 NM_001776.5 ?/. - c.1393G>C r.(?) p.(Glu465Gln)
CCNJ NM_019084.4 ?/. - c.-177518G>C r.(?) p.(=)
ENTPD1-AS1 NR_038444.1 ?/. - n.439+10275C>G r.(?) -


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