Variant #0000612832 (NC_000010.10:g.97620237T>C, NM_001776.5:c.1086T>C (ENTPD1))

Chromosome 10
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.97620237T>C
DNA change (hg38) g.95860480T>C
Published as ENTPD1(NM_001776.6):c.1086T>C (p.A362=)
ISCN -
DB-ID C10orf131_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) 3.0E-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 2019-12-04 15:24:38 +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.-139810T>C r.(?) p.(=)
C10orf131 NM_001130446.2 -?/. - c.-47681T>C r.(?) p.(=)
ENTPD1 NM_001776.5 -?/. - c.1086T>C r.(?) p.(Ala362=)
CCNJ NM_019084.4 -?/. - c.-183281T>C r.(?) p.(=)
ENTPD1-AS1 NR_038444.1 -?/. - n.440-12995A>G r.(?) -


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