Variant #0000562832 (NC_000017.10:g.6528125G>A, NM_014804.2:c.775C>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.6528125G>A
DNA change (hg38) g.6624805G>A
Published as -
ISCN -
DB-ID KIAA0753_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) 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-11 14:18:56 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KIAA0753 NM_014804.2 +/. - c.775C>T r.(?) p.(Gln259Ter)
TXNDC17 NM_032731.3 +/. - c.-16278G>A r.(?) p.(=)


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