Variant #0000689116 (NC_000003.11:g.51429147C>T, NM_006010.4:c.*2627C>T (MANF))

Chromosome 3
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.51429147C>T
DNA change (hg38) -
Published as RBM15B(NM_013286.5):c.317C>T (p.S106F)
ISCN -
DB-ID MANF_000003
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MANF NM_006010.4 ?/. - c.*2627C>T r.(=) p.(=)
RBM15B NM_013286.4 ?/. - c.317C>T r.(?) p.(Ser106Phe)
VPRBP NM_014703.2 ?/. - c.*5443G>A r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.