Variant #0000302382 (NC_000006.11:g.160106070T>A, NM_005891.2:c.-77050T>A (ACAT2))

Chromosome 6
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.160106070T>A
DNA change (hg38) g.159685038T>A
Published as SOD2(NM_000636.4):c.344-5A>T
ISCN -
DB-ID SOD2_000001
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
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     
SOD2 NM_000636.2 -/. - c.344-5A>T r.spl? p.?
ACAT2 NM_005891.2 -/. - c.-77050T>A r.(?) p.(=)
WTAP NM_152857.2 -/. - c.-42674T>A r.(?) p.(=)


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