Variant #0000948135 (NC_000003.11:g.38180410G>C, NM_001607.3:c.-1884C>G (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.38180410G>C
DNA change (hg38) -
Published as MYD88(NM_002468.5):c.219G>C (p.R73S)
ISCN -
DB-ID ACAA1_000019
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-11-27 17:35:39 +01:00 (CET)
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.-1884C>G r.(?) p.(=)
MYD88 NM_002468.4 -?/. - c.258G>C r.(?) p.(Arg86Ser)
DLEC1 NM_007337.2 -?/. - c.*16314G>C r.(=) p.(=)


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