Variant #0001033924 (NC_000003.11:g.38181994G>A, NM_001607.3:c.-3468C>T (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.38181994G>A
DNA change (hg38) -
Published as MYD88(NM_002468.5):c.579G>A (p.(Val193=))
ISCN -
DB-ID ACAA1_000020
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) 0.00047 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 2025-05-05 21:14:00 +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.-3468C>T r.(?) p.(=)
MYD88 NM_002468.4 -?/. - c.618G>A r.(?) p.(=)
DLEC1 NM_007337.2 -?/. - c.*17898G>A r.(=) p.(=)


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