Variant #0000890026 (NC_000011.9:g.62472981C>T, NM_001122955.3:c.196G>A (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.62472981C>T
DNA change (hg38) -
Published as BSCL2(NM_032667.6):c.4G>A (p.V2I)
ISCN -
DB-ID GNG3_000017
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 2022-11-01 13:01:21 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HNRNPUL2 NM_001079559.2 ?/. - c.*9790G>A r.(=) p.(=)
BSCL2 NM_001122955.3 ?/. - c.196G>A r.(?) p.(Val66Ile)
GNG3 NM_012202.4 ?/. - c.-2408C>T r.(?) p.(=)
HNRNPUL2-BSCL2 NR_037946.1 ?/. - n.2716G>A r.(?) -


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