Variant #0000527806 (NC_000006.11:g.160103652C>A, NM_005891.2:c.-79468C>A (ACAT2))

Chromosome 6
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.160103652C>A
DNA change (hg38) g.159682620C>A
Published as SOD2(NM_000636.4):c.542G>T (p.G181V)
ISCN -
DB-ID ACAT2_000004 See all 2 reported entries
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 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 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     
SOD2 NM_000636.2 +?/. - c.542G>T r.(?) p.(Gly181Val)
ACAT2 NM_005891.2 +?/. - c.-79468C>A r.(?) p.(=)
WTAP NM_152857.2 +?/. - c.-45092C>A r.(?) p.(=)


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