Variant #0001004888 (NC_000019.9:g.45998233A>C, NM_005619.4:c.110T>G (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.45998233A>C
DNA change (hg38) -
Published as RTN2(NM_005619.4):c.110T>G (p.(Leu37Arg))
ISCN -
DB-ID PPM1N_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) 3.0E-5 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 2024-08-28 13:16:32 +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     
PPM1N NM_001080401.1 ?/. - c.-3498A>C r.(?) p.(=)
RTN2 NM_005619.4 ?/. - c.110T>G r.(?) p.(Leu37Arg)


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