Variant #0000862105 (NC_000010.10:g.97620257T>A, NM_001776.5:c.1106T>A (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.97620257T>A
DNA change (hg38) -
Published as ENTPD1(NM_001776.6):c.1106T>A (p.F369Y)
ISCN -
DB-ID C10orf131_000012
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) 1.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-05-09 15:51:19 +02:00 (CEST)
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.-139790T>A r.(?) p.(=)
C10orf131 NM_001130446.2 ?/. - c.-47661T>A r.(?) p.(=)
ENTPD1 NM_001776.5 ?/. - c.1106T>A r.(?) p.(Phe369Tyr)
CCNJ NM_019084.4 ?/. - c.-183261T>A r.(?) p.(=)
ENTPD1-AS1 NR_038444.1 ?/. - n.440-13015A>T r.(?) -


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