Variant #0001063973 (NC_000003.11:g.49759334_49759338dup, NC_000003.11(NM_021971.2):c.952-21_952-17dup (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.49759334_49759338dup
DNA change (hg38) -
Published as -
ISCN -
DB-ID AMIGO3_000058
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2026-01-20 18:57:21 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GMPPB NM_021971.2 ?/. - c.952-21_952-17dup r.(=) p.(=)
RNF123 NM_022064.3 ?/. - c.*596_*600dup r.(=) p.(=)
IP6K1 NM_153273.3 ?/. - c.*5218_*5222dup r.(=) p.(=)
AMIGO3 NM_198722.2 ?/. - c.-2439_-2435dup r.(?) p.(=)


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