Variant #0000962829 (NC_000003.11:g.49759378_49759379del, NC_000003.11(NM_021971.2):c.951+19_951+20del (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.49759378_49759379del
DNA change (hg38) -
Published as GMPPB(NM_013334.3):c.970_971del (p.(Leu324GlyfsTer13)), GMPPB(NM_013334.3):c.970_971delCT (p.L324Gfs*13)
ISCN -
DB-ID AMIGO3_000019 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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2024-02-26 20:06:56 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GMPPB NM_021971.2 ?/. - c.951+19_951+20del r.(=) p.(=)
RNF123 NM_022064.3 ?/. - c.*640_*641del r.(=) p.(=)
IP6K1 NM_153273.3 ?/. - c.*5176_*5177del r.(=) p.(=)
AMIGO3 NM_198722.2 ?/. - c.-2481_-2480del r.(?) p.(=)


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