Variant #0000291542 (NC_000002.11:g.85768369T>A, NM_000821.5:c.*8688A>T (GGCX))

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.85768369T>A
DNA change (hg38) g.85541246T>A
Published as MAT2A(NM_005911.5):c.170-9T>A
ISCN -
DB-ID MAT2A_000004
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) Retrieve
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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GGCX NM_000821.5 ?/. - c.*8688A>T r.(=) p.(=)
MAT2A NM_005911.5 ?/. - c.170-9T>A r.(=) p.(=)


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