Variant #0000726629 (NC_000017.10:g.6524121C>T, NM_014804.2:c.1302G>A (KIAA0753))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.6524121C>T
DNA change (hg38) -
Published as KIAA0753(NM_001351225.1):c.405G>A (p.K135=)
ISCN -
DB-ID KIAA0753_000010
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 2021-02-08 18:36:18 +01:00 (CET)
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.1302G>A r.(?) p.(Lys434=)
TXNDC17 NM_032731.3 -?/. - c.-20282C>T r.(?) p.(=)


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