Variant #0000528336 (NC_000006.11:g.31948509C>T, NM_005510.3:c.-8810G>A (DOM3Z))

Chromosome 6
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.31948509C>T
DNA change (hg38) g.31980732C>T
Published as STK19(NM_004197.1):c.980C>T (p.(Ala327Val))
ISCN -
DB-ID C4A_000005
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) 0.00024 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
STK19 NM_004197.1 -?/. - c.980C>T r.(?) p.(Ala327Val)
DOM3Z NM_005510.3 -?/. - c.-8810G>A r.(?) p.(=)
C4A NM_007293.2 -?/. - c.-1376C>T r.(?) p.(=)


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