Variant #0000326686 (NC_000019.9:g.49335923G>A, NM_001161354.1:c.*4915C>T (PLEKHA4))

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.49335923G>A
DNA change (hg38) g.48832666G>A
Published as HSD17B14(NM_016246.2):c.277C>T (p.?)
ISCN -
DB-ID HSD17B14_000001
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) 0.00027 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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PLEKHA4 NM_001161354.1 ?/. - c.*4915C>T r.(=) p.(=)
HSD17B14 NM_016246.2 ?/. - c.277C>T r.(?) p.(His93Tyr)


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