Variant #0000330834 (NC_000006.11:g.24698178A>G, NM_018473.3:c.149A>G (ACOT13))

Chromosome 6
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.24698178A>G
DNA change (hg38) g.24697950A>G
Published as ACOT13(NM_001160094.1):c.80A>G (p.(Asn27Ser))
ISCN -
DB-ID ACOT13_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) 0.00054 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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     
ACOT13 NM_018473.3 ?/. - c.149A>G r.(?) p.(Asn50Ser)
C6orf62 NM_030939.4 ?/. - c.*8187T>C r.(=) p.(=)


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