Variant #0000681292 (NC_000019.9:g.13002983A>G, NM_000159.3:c.325A>G (GCDH))

Chromosome 19
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.13002983A>G
DNA change (hg38) g.12892169A>G
Published as GCDH(NM_000159.3):c.325A>G (p.T109A)
ISCN -
DB-ID GCDH_000269 See all 2 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 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GCDH NM_000159.3 ?/? 5 c.325A>G r.(?) p.(Thr109Ala)
SYCE2 NM_001105578.1 ?/? - c.*7172T>C r.(=) p.(=)
KLF1 NM_006563.3 ?/? - c.-5029T>C r.(?) p.(=)


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