Variant #0000258868 (NC_000017.10:g.35696822_35696825del, NC_000017.10(NM_198834.1):c.39-14_39-11del (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.35696822_35696825del
DNA change (hg38) -
Published as ACACA(NM_198839.3):c.-73-14_-73-11delCTTT
ISCN -
DB-ID ACACA_000004
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
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.-36213_-36210del r.(?) p.(=)
ACACA NM_198834.1 -/. - c.39-14_39-11del r.(=) p.(=)


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