Variant #0001055974 (NC_000017.10:g.35603872T>C, NM_198834.1:c.2330A>G (ACACA))

Chromosome 17
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.35603872T>C
DNA change (hg38) -
Published as ACACA(NM_198834.3):c.2330A>G (p.(Asn777Ser))
ISCN -
DB-ID C17orf78_000013
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C17orf78 NM_173625.3 ?/. - c.-129163T>C r.(?) p.(=)
ACACA NM_198834.1 ?/. - c.2330A>G r.(?) p.(Asn777Ser)


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