Variant #0000325615 (NC_000017.10:g.73500672A>C, NM_014738.4:c.*5257A>C (KIAA0195))

Chromosome 17
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.73500672A>C
DNA change (hg38) g.75504591A>C
Published as CASKIN2(NM_001142643.1):c.1049T>G (p.(Leu350Arg))
ISCN -
DB-ID CASKIN2_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) 0.00149 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KIAA0195 NM_014738.4 ?/. - c.*5257A>C r.(=) p.(=)
CASKIN2 NM_020753.3 ?/. - c.1295T>G r.(?) p.(Leu432Arg)


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