Variant #0000925236 (NC_000010.10:g.97602230C>T, NM_001776.5:c.392C>T (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.97602230C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID C10orf131_000013
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CC2D2B NM_001001732.3 ?/. - c.-157817C>T r.(?) p.(=)
C10orf131 NM_001130446.2 ?/. - c.-65688C>T r.(?) p.(=)
ENTPD1 NM_001776.5 ?/. - c.392C>T r.(?) p.(Thr131Met)
CCNJ NM_019084.4 ?/. - c.-201288C>T r.(?) p.(=)
ENTPD1-AS1 NR_038444.1 ?/. - n.533+4919G>A r.(?) -


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