Variant #0000979262 (NC_000010.10:g.97607324del, NM_001776.5:c.935del (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.97607324del
DNA change (hg38) -
Published as -
ISCN -
DB-ID C10orf131_000015
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 2024-04-19 20:27:30 +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.-152723del r.(?) p.(=)
C10orf131 NM_001130446.2 +?/. - c.-60594del r.(?) p.(=)
ENTPD1 NM_001776.5 +?/. - c.935del r.(?) p.(Gln312Argfs*55)
CCNJ NM_019084.4 +?/. - c.-196194del r.(?) p.(=)
ENTPD1-AS1 NR_038444.1 +?/. - n.440-82del r.(?) -


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