Variant #0000808226 (NC_000017.10:g.6493199G>A, NM_014804.2:c.2686C>T (KIAA0753))

Chromosome 17
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.6493199G>A
DNA change (hg38) -
Published as KIAA0753(NM_001351225.1):c.1789C>T (p.Q597*)
ISCN -
DB-ID KIAA0753_000012
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) 0.00059 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +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     
KIAA0753 NM_014804.2 +/. - c.2686C>T r.(?) p.(Gln896*)
TXNDC17 NM_032731.3 +/. - c.-51204G>A r.(?) p.(=)


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