Variant #0000290168 (NC_000008.10:g.126079895T>C, NM_014846.3:c.1217A>G (KIAA0196))

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.126079895T>C
DNA change (hg38) g.125067653T>C
Published as KIAA0196(NM_014846.3):c.1217A>G (p.N406S, p.(Asn406Ser)), WASHC5(NM_014846.4):c.1217A>G (p.N406S)
ISCN -
DB-ID KIAA0196_000020 See all 3 reported entries
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) 0.00011 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KIAA0196 NM_014846.3 ?/. - c.1217A>G r.(?) p.(Asn406Ser)


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