Variant #0000561104 (NC_000017.10:g.35767584G>A, NM_198834.1:c.-1195C>T (ACACA))

Chromosome 17
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.35767584G>A
DNA change (hg38) g.37407497G>A
Published as TADA2A(NM_001488.4):c.-98+1G>A
ISCN -
DB-ID C17orf78_000006
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 2020-07-13 12:24:40 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TADA2A NM_001488.3 -?/. - c.-98+1G>A r.spl? p.?
C17orf78 NM_173625.3 -?/. - c.*18906G>A r.(=) p.(=)
ACACA NM_198834.1 -?/. - c.-1195C>T r.(?) p.(=)


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