Variant #0001035392 (NC_000006.11:g.107050773G>A, NM_032730.4:c.645C>T (RTN4IP1))

Chromosome 6
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.107050773G>A
DNA change (hg38) -
Published as RTN4IP1(NM_032730.5):c.645C>T (p.(Gly215=))
ISCN -
DB-ID QRSL1_000020
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) 0.00109 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +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.-26784G>A r.(?) p.(=)
RTN4IP1 NM_032730.4 -?/. - c.645C>T r.(?) p.(=)


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