Variant #0000281009 (NC_000019.9:g.13002356C>T, NC_000019.9(NM_000159.3):c.127+20C>T (GCDH))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.13002356C>T
DNA change (hg38) g.12891542C>T
Published as GCDH(NM_000159.4):c.127+20C>T
ISCN -
DB-ID GCDH_000178 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_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 -?/. - c.127+20C>T r.(=) p.(=)
SYCE2 NM_001105578.1 -?/. - c.*7799G>A r.(=) p.(=)
KLF1 NM_006563.3 -?/. - c.-4402G>A r.(?) p.(=)


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