Variant #0000520232 (NC_000003.11:g.49759369_49759370insGCC, NC_000003.11(NM_021971.2):c.951+28_951+29insGGC (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.49759369_49759370insGCC
DNA change (hg38) g.49721936_49721937insGCC
Published as GMPPB(NM_013334.3):c.979_980insGGC (p.(Glu327delinsGlyGln)), GMPPB(NM_013334.3):c.979_980insGGC (p.E327delinsGQ)
ISCN -
DB-ID AMIGO3_000014 See all 2 reported entries
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-05-09 15:24:52 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GMPPB NM_021971.2 ?/. - c.951+28_951+29insGGC r.(=) p.(=)
RNF123 NM_022064.3 ?/. - c.*631_*632insGCC r.(=) p.(=)
IP6K1 NM_153273.3 ?/. - c.*5185_*5186insGGC r.(=) p.(=)
AMIGO3 NM_198722.2 ?/. - c.-2472_-2471insGGC r.(?) p.(=)


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