Variant #0000983959 (NC_000021.8:g.33723115C>T, NM_178817.3:c.*38808C>T (MRAP))

Chromosome 21
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.33723115C>T
DNA change (hg38) -
Published as URB1(NM_014825.3):c.2730G>A (p.(Val910=))
ISCN -
DB-ID MRAP_000012
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
URB1 NM_014825.2 ?/. - c.2730G>A r.(?) p.(=)
MRAP NM_178817.3 ?/. - c.*38808C>T r.(=) p.(=)


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