Variant #0000979701 (NC_000011.9:g.62494472_62494492dup, NM_001122955.3:c.-19818_-19798dup (BSCL2))

Chromosome 11
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.62494472_62494492dup
DNA change (hg38) -
Published as HNRNPUL2(NM_001079559.3):c.144_164dup (p.(Gly49_Gly55dup))
ISCN -
DB-ID GNG3_000019
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HNRNPUL2 NM_001079559.2 ?/. - c.144_164dup r.(?) p.(Gly49_Gly55dup)
BSCL2 NM_001122955.3 ?/. - c.-19818_-19798dup r.(?) p.(=)
GNG3 NM_012202.4 ?/. - c.*18194_*18214dup r.(=) p.(=)
TTC9C NM_173810.3 ?/. - c.-1849_-1829dup r.(?) p.(=)
HNRNPUL2-BSCL2 NR_037946.1 ?/. - n.372_392dup r.(?) -


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