Variant #0000719517 (NC_000003.11:g.49759383A>C, NC_000003.11(NM_021971.2):c.951+15T>G (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.49759383A>C
DNA change (hg38) -
Published as GMPPB(NM_013334.3):c.966T>G (p.A322=)
ISCN -
DB-ID AMIGO3_000045
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 2021-02-08 18:36:18 +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+15T>G r.(=) p.(=)
RNF123 NM_022064.3 -?/. - c.*645A>C r.(=) p.(=)
IP6K1 NM_153273.3 -?/. - c.*5172T>G r.(=) p.(=)
AMIGO3 NM_198722.2 -?/. - c.-2485T>G r.(?) p.(=)


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