Variant #0000329354 (NC_000003.11:g.45017795C>T, NM_016598.2:c.-395G>A (ZDHHC3))

Chromosome 3
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.45017795C>T
DNA change (hg38) g.44976303C>T
Published as EXOSC7(NM_015004.3):c.26C>T (p.(Ala9Val))
ISCN -
DB-ID EXOSC7_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) 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EXOSC7 NM_015004.3 ?/. - c.26C>T r.(?) p.(Ala9Val)
ZDHHC3 NM_016598.2 ?/. - c.-395G>A r.(?) p.(=)


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