Variant #0000249661 (NC_000019.9:g.13008647A>G, NM_000159.3:c.1213A>G (GCDH))

Chromosome 19
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.13008647A>G
DNA change (hg38) g.12897833A>G
Published as GCDH(NM_000159.4):c.1213A>G (p.M405V)
ISCN -
DB-ID GCDH_000012 See all 18 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) 5.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GCDH NM_000159.3 +/+ 11 c.1213A>G r.(?) p.(Met405Val)
SYCE2 NM_001105578.1 +/+ - c.*1508T>C r.(=) p.(=)


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