Variant #0001056501 (NC_000019.9:g.13002774C>G, NM_000159.3:c.257C>G (GCDH))

Chromosome 19
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.13002774C>G
DNA change (hg38) -
Published as GCDH(NM_000159.4):c.257C>G (p.(Ala86Gly))
ISCN -
DB-ID KLF1_000002
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GCDH NM_000159.3 +?/. - c.257C>G r.(?) p.(Ala86Gly)
SYCE2 NM_001105578.1 +?/. - c.*7381G>C r.(=) p.(=)
KLF1 NM_006563.3 +?/. - c.-4820G>C r.(?) p.(=)


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