Variant #0000980932 (NC_000014.8:g.55310817T>C, NM_000161.2:c.671A>G (GCH1))

Chromosome 14
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.55310817T>C
DNA change (hg38) -
Published as GCH1(NM_000161.2):c.671A>G (p.K224R), GCH1(NM_000161.3):c.671A>G (p.(Lys224Arg))
ISCN -
DB-ID GCH1_000014 See all 3 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) 0.00038 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 2024-04-19 20:27:30 +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.671A>G r.(?) p.(Lys224Arg)


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