Variant #0000719516 (NC_000003.11:g.49759296dup, NM_021971.2:c.972dup (GMPPB))

Chromosome 3
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.49759296dup
DNA change (hg38) -
Published as GMPPB(NM_013334.4):c.1053dupA (p.V352Sfs*4)
ISCN -
DB-ID AMIGO3_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_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)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GMPPB NM_021971.2 +?/. - c.972dup r.(?) p.(Val325SerfsTer4)
RNF123 NM_022064.3 +?/. - c.*558dup r.(?) p.(=)
IP6K1 NM_153273.3 +?/. - c.*5259dup r.(?) p.(=)
AMIGO3 NM_198722.2 +?/. - c.-2398dup r.(?) p.(=)


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