Variant #0000981139 (NC_000015.9:g.28538063A>G, NM_004667.5:c.293T>C (HERC2))

Chromosome 15
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.28538063A>G
DNA change (hg38) -
Published as HERC2(NM_004667.5):c.293T>C (p.L98P), HERC2(NM_004667.6):c.293T>C (p.(Leu98Pro), p.L98P)
ISCN -
DB-ID HERC2_000101 See all 4 reported entries
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HERC2 NM_004667.5 ?/. - c.293T>C r.(?) p.(Leu98Pro)


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