Variant #0000616811 (NC_000017.10:g.73501734_73501735insTC, NM_014738.4:c.*6319_*6320insTC (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.73501734_73501735insTC
DNA change (hg38) g.75505653_75505654insTC
Published as CASKIN2(NM_001142643.1):c.590-3_590-2insGA (p.?)
ISCN -
DB-ID KIAA0195_000035
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-12-04 15:24:38 +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.*6319_*6320insTC r.(=) p.(=)
CASKIN2 NM_020753.3 ?/. - c.836-3_836-2insGA r.spl? p.?


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