Variant #0000267836 (NC_000010.10:g.97602091T>C, NC_000010.10(NM_001776.5):c.263-10T>C (ENTPD1))

Chromosome 10
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.97602091T>C
DNA change (hg38) g.95842334T>C
Published as ENTPD1(NM_001776.6):c.263-10T>C, ENTPD1-AS1(NR_038444.1):n.533+5058A>G
ISCN -
DB-ID ENTPD1_000003
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) 0.53864 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CC2D2B NM_001001732.3 -/. - c.-157956T>C r.(?) p.(=)
C10orf131 NM_001130446.2 -/. - c.-65827T>C r.(?) p.(=)
ENTPD1 NM_001776.5 -/. - c.263-10T>C r.(=) p.(=)
CCNJ NM_019084.4 -/. - c.-201427T>C r.(?) p.(=)
ENTPD1-AS1 NR_038444.1 -/. - n.533+5058A>G r.(?) -


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.