Variant #0000561092 (NC_000017.10:g.35478362T>C, NM_198834.1:c.6189= (ACACA))

Chromosome 17
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.35478362T>C
DNA change (hg38) g.37121440=
Published as ACACA(NM_198839.3):c.6078A>G (p.R2026=)
ISCN -
DB-ID C17orf78_000002
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) 0.99947 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C17orf78 NM_173625.3 -/. - c.-254673T>C r.(?) p.(=)
ACACA NM_198834.1 -/. - c.6189= r.(=) p.(Thr2063=)


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