Variant #0000277331 (NC_000003.11:g.49760477G>A, GMPPB(NM_021971.2):c.330C>T)

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.49760477G>A
DNA change (hg38) g.49723044G>A
Published as GMPPB(NM_013334.3):c.330C>T (p.D110=)
ISCN -
DB-ID GMPPB_000027
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 0.01316 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GMPPB NM_021971.2 -?/. - c.330C>T r.(?) p.(Asp110=)
RNF123 NM_022064.3 -?/. - c.*1739G>A r.(=) p.(=)
IP6K1 NM_153273.3 -?/. - c.*4078C>T r.(=) p.(=)
AMIGO3 NM_198722.2 -?/. - c.-3579C>T r.(?) p.(=)