Variant #0000681397 (NC_000019.9:g.38810745C>T, NM_033520.1:c.*15141C>T (C19orf33))

Chromosome 19
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.38810745C>T
DNA change (hg38) -
Published as KCNK6(NM_004823.3):c.155C>T (p.P52L)
ISCN -
DB-ID C19orf33_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) 1.0E-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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KCNK6 NM_004823.1 ?/. - c.155C>T r.(?) p.(Pro52Leu)
C19orf33 NM_033520.1 ?/. - c.*15141C>T r.(=) p.(=)
YIF1B NM_033557.3 ?/. - c.-10497G>A r.(?) p.(=)


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