Variant #0000692319 (NC_000017.10:g.35627755T>G, NC_000017.10(NM_198834.1):c.1009-3A>C (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.35627755T>G
DNA change (hg38) -
Published as ACACA(NM_198839.2):c.898-3A>C
ISCN -
DB-ID C17orf78_000008
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 2020-09-15 15:50:26 +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     
C17orf78 NM_173625.3 -?/. - c.-105280T>G r.(?) p.(=)
ACACA NM_198834.1 -?/. - c.1009-3A>C r.spl? p.?


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