Variant #0000993054 (NC_000002.11:g.85770005G>A, NM_000821.5:c.*7052C>T (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.85770005G>A
DNA change (hg38) -
Published as MAT2A(NM_005911.6):c.952-19G>A
ISCN -
DB-ID GGCX_000032
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) 0.00056 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GGCX NM_000821.5 -/. - c.*7052C>T r.(=) p.(=)
MAT2A NM_005911.5 -/. - c.952-19G>A r.(=) p.(=)


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