Variant #0000563001 (NC_000017.10:g.73500519G>A, NM_014738.4:c.*5104G>A (KIAA0195))

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.73500519G>A
DNA change (hg38) g.75504438G>A
Published as CASKIN2(NM_001142643.1):c.1111C>T (p.(His371Tyr))
ISCN -
DB-ID KIAA0195_000017
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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.*5104G>A r.(=) p.(=)
CASKIN2 NM_020753.3 -?/. - c.1357C>T r.(?) p.(His453Tyr)


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