Variant #0000517018 (NC_000002.11:g.85769711C>G, NM_000821.5:c.*7346G>C (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.85769711C>G
DNA change (hg38) g.85542588C>G
Published as MAT2A(NM_005911.5):c.792_793delCAinsGA (p.R264_K265=)
ISCN -
DB-ID GGCX_000008
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) 0.44218 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +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.*7346G>C r.(=) p.(=)
MAT2A NM_005911.5 -/. - c.792C>G r.(?) p.(Arg264=)


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