Variant #0000608780 (NC_000003.11:g.49759369_49759370insGC, NC_000003.11(NM_021971.2):c.951+28_951+29insGC (GMPPB))

Chromosome 3
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.49759369_49759370insGC
DNA change (hg38) g.49721936_49721937insGC
Published as GMPPB(NM_013334.3):c.979_980insGC (p.(Glu327GlyfsTer25))
ISCN -
DB-ID AMIGO3_000035
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 2019-12-04 14:54:23 +01:00 (CET)
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+29insGC r.(=) p.(=)
RNF123 NM_022064.3 -?/. - c.*631_*632insGC r.(=) p.(=)
IP6K1 NM_153273.3 -?/. - c.*5185_*5186insGC r.(=) p.(=)
AMIGO3 NM_198722.2 -?/. - c.-2472_-2471insGC r.(?) p.(=)


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