Variant #0000617698 (NC_000019.9:g.45997490G>T, NM_005619.4:c.748C>A (RTN2))

Chromosome 19
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.45997490G>T
DNA change (hg38) g.45494232G>T
Published as RTN2(NM_005619.5):c.748C>A (p.P250T)
ISCN -
DB-ID PPM1N_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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PPM1N NM_001080401.1 ?/. - c.-4241G>T r.(?) p.(=)
RTN2 NM_005619.4 ?/. - c.748C>A r.(?) p.(Pro250Thr)


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