Variant #0000517025 (NC_000002.11:g.85781318T>G, NM_000821.5:c.837= (GGCX))

Chromosome 2
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.85781318T>G
DNA change (hg38) -
Published as GGCX(NM_000821.7):c.837A>C (p.G279=)
ISCN -
DB-ID GGCX_000014
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) 0.98874 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GGCX NM_000821.5 -/. - c.837= r.(=) p.(Gly279=)
MAT2A NM_005911.5 -/. - c.*10423T>G r.(=) p.(=)


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