Variant #0000543070 (NC_000011.9:g.134127032del, NM_014384.2:c.261del (ACAD8))

Chromosome 11
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.134127032del
DNA change (hg38) g.134257138del
Published as ACAD8(NM_014384.2):c.261delA (p.V89Sfs*35)
ISCN -
DB-ID ACAD8_000034
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 2020-07-01 16:46:23 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
THYN1 NM_014174.2 ?/. - c.-4256del r.(?) p.(=)
ACAD8 NM_014384.2 ?/. - c.261del r.(?) p.(Val89SerfsTer35)


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