Variant #0000719518 (NC_000003.11:g.49759384_49759388dup, NC_000003.11(NM_021971.2):c.951+19_951+23dup (GMPPB))

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.49759384_49759388dup
DNA change (hg38) -
Published as GMPPB(NM_013334.4):c.970_974dupCTGGG (p.G326Wfs*27)
ISCN -
DB-ID AMIGO3_000023
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GMPPB NM_021971.2 ?/. - c.951+19_951+23dup r.(=) p.(=)
RNF123 NM_022064.3 ?/. - c.*646_*650dup r.(=) p.(=)
IP6K1 NM_153273.3 ?/. - c.*5176_*5180dup r.(=) p.(=)
AMIGO3 NM_198722.2 ?/. - c.-2481_-2477dup r.(?) p.(=)


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