Variant #0001007087 (NC_000014.8:g.55312502C>T, NM_000161.2:c.610G>A (GCH1))

Chromosome 14
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.55312502C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID GCH1_000003 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs200891969
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00021 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2024-09-05 10:25:01 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GCH1 NM_000161.2 ?/. - c.610G>A r.(?) p.(Val204Ile)


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