Variant #0000611517 (NC_000008.10:g.145164678G>A, NR_024207.1:n.1466G>A (KIAA1875))

Chromosome 8
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.145164678G>A
DNA change (hg38) g.144109775G>A
Published as WDR97(NM_001316309.1):c.1441G>A (p.A481T)
ISCN -
DB-ID KIAA1875_000001
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) 2.0E-5 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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-06-24 19:00:59 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MAF1 NM_032272.4 ?/. - c.*2666G>A r.(=) p.(=)
KIAA1875 NR_024207.1 ?/. - n.1466G>A r.(?) -


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