Variant #0000860057 (NC_000006.11:g.107070811C>T, NM_032730.4:c.308G>A (RTN4IP1))

Chromosome 6
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.107070811C>T
DNA change (hg38) -
Published as RTN4IP1(NM_032730.5):c.308G>A (p.R103H)
ISCN -
DB-ID RTN4IP1_000001 See all 25 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) 3.0E-5 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2022-05-09 15:51:19 +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     
QRSL1 NM_018292.4 +/. - c.-6746C>T r.(?) p.(=)
RTN4IP1 NM_032730.4 +/. - c.308G>A r.(?) p.(Arg103His)


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