Variant #0000329277 (NC_000003.11:g.16343180_16343182del, NM_015150.1:c.*15158_*15160del (RFTN1))

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.16343180_16343182del
DNA change (hg38) g.16301673_16301675del
Published as OXNAD1(NM_138381.3):c.475_477del (p.(Phe159del))
ISCN -
DB-ID OXNAD1_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_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     
RFTN1 NM_015150.1 ?/. - c.*15158_*15160del r.(=) p.(=)
OXNAD1 NM_138381.3 ?/. - c.480_482del r.(?) p.(Phe161del)


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