Variant #0000528112 (NC_000006.11:g.24714548G>A, NM_018473.3:c.*12705G>A (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.24714548G>A
DNA change (hg38) g.24714320G>A
Published as C6orf62(NM_030939.5):c.427C>T (p.Q143*)
ISCN -
DB-ID ACOT13_000002
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-18 15:04:07 +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.*12705G>A r.(=) p.(=)
C6orf62 NM_030939.4 ?/. - c.427C>T r.(?) p.(Gln143Ter)


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