Variant #0000858989 (NC_000003.11:g.38180452C>T, NM_001607.3:c.-1926G>A (ACAA1))

Chromosome 3
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.38180452C>T
DNA change (hg38) -
Published as MYD88(NM_001172567.1):c.300C>T (p.G100=)
ISCN -
DB-ID ACAA1_000017
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) 0.00035 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ACAA1 NM_001607.3 -?/. - c.-1926G>A r.(?) p.(=)
MYD88 NM_002468.4 -?/. - c.300C>T r.(?) p.(Gly100=)
DLEC1 NM_007337.2 -?/. - c.*16356C>T r.(=) p.(=)


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