Variant #0000298432 (NC_000006.11:g.160114157C>G, NM_005891.2:c.-68963C>G (ACAT2))

Chromosome 6
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.160114157C>G
DNA change (hg38) g.159693125C>G
Published as SOD2(NM_000636.4):c.23+20G>C
ISCN -
DB-ID SOD2_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) 0.00098 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 2018-01-15 20:58:59 +01:00 (CET)
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.23+20G>C r.(=) p.(=)
ACAT2 NM_005891.2 -?/. - c.-68963C>G r.(?) p.(=)
WTAP NM_152857.2 -?/. - c.-34587C>G r.(?) p.(=)


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