Variant #0000885757 (NC_000003.11:g.38182230C>G, NM_001607.3:c.-3704G>C (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.38182230C>G
DNA change (hg38) -
Published as MYD88(NM_002468.5):c.645-18C>G
ISCN -
DB-ID ACAA1_000018
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) 0.0002 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:01:21 +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.-3704G>C r.(?) p.(=)
MYD88 NM_002468.4 -?/. - c.684-18C>G r.(=) p.(=)
DLEC1 NM_007337.2 -?/. - c.*18134C>G r.(=) p.(=)


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