Variant #0000982443 (NC_000017.10:g.35549225G>A, NM_198834.1:c.4222C>T (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.35549225G>A
DNA change (hg38) -
Published as ACACA(NM_198834.3):c.4222C>T (p.(Arg1408Cys)), ACACA(NM_198839.2):c.4111C>T (p.L1371F)
ISCN -
DB-ID C17orf78_000004 See all 2 reported entries
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 2024-04-19 20:27:30 +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.-183810G>A r.(?) p.(=)
ACACA NM_198834.1 ?/. - c.4222C>T r.(?) p.(Arg1408Cys)


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