Variant #0000321705 (NC_000010.10:g.97620260T>A, NM_001776.5:c.1109T>A (ENTPD1))

Chromosome 10
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.97620260T>A
DNA change (hg38) g.95860503T>A
Published as ENTPD1(NM_001164178.1):c.1145T>A (p.(Leu382*))
ISCN -
DB-ID ENTPD1_000004
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-08-28 13:16:32 +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.-139787T>A r.(?) p.(=)
C10orf131 NM_001130446.2 +?/. - c.-47658T>A r.(?) p.(=)
ENTPD1 NM_001776.5 +?/. - c.1109T>A r.(?) p.(Leu370Ter)
CCNJ NM_019084.4 +?/. - c.-183258T>A r.(?) p.(=)
ENTPD1-AS1 NR_038444.1 +?/. - n.440-13018A>T r.(?) -


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