Variant #0000720613 (NC_000006.11:g.107031213T>A, NM_032730.4:c.1073A>T (RTN4IP1))

Chromosome 6
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.107031213T>A
DNA change (hg38) -
Published as RTN4IP1(NM_032730.5):c.1073A>T (p.D358V)
ISCN -
DB-ID QRSL1_000010
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) 0.00072 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
QRSL1 NM_018292.4 ?/. - c.-46344T>A r.(?) p.(=)
RTN4IP1 NM_032730.4 ?/. - c.1073A>T r.(?) p.(Asp358Val)


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