Variant #0000288259 (NC_000019.9:g.13002791G>A, NC_000019.9(NM_000159.3):c.271+3G>A (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.13002791G>A
DNA change (hg38) g.12891977G>A
Published as GCDH(NM_000159.3):c.271+3G>A, GCDH(NM_000159.4):c.271+3G>A
ISCN -
DB-ID GCDH_000179 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) 0.00035 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-02-26 20:06:56 +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.271+3G>A r.spl? p.?
SYCE2 NM_001105578.1 -?/. - c.*7364C>T r.(=) p.(=)
KLF1 NM_006563.3 -?/. - c.-4837C>T r.(?) p.(=)


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