Variant #0000689991 (NC_000007.13:g.33060885_33060886dup, NM_016489.12:c.336_337dup (NT5C3))

Chromosome 7
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.33060885_33060886dup
DNA change (hg38) -
Published as NT5C3A(NM_001166118.2):c.300_301dupAT (p.W101Yfs*60)
ISCN -
DB-ID NT5C3_000002
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NT5C3 NM_016489.12 +/. - c.336_337dup r.(?) p.(Trp113TyrfsTer60)


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