Variant #0001038562 (NC_000011.9:g.62458753T>G, NM_001122955.3:c.1004A>C (BSCL2))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.62458753T>G
DNA change (hg38) -
Published as BSCL2(NM_001122955.4):c.1004A>C (p.(Gln335Pro))
ISCN -
DB-ID GNG3_000024
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) 1.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +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.*24018A>C r.(=) p.(=)
BSCL2 NM_001122955.3 +?/. - c.1004A>C r.(?) p.(Gln335Pro)
GNG3 NM_012202.4 +?/. - c.-16636T>G r.(?) p.(=)
HNRNPUL2-BSCL2 NR_037946.1 +?/. - n.3524A>C r.(?) -


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