Variant #0000656828 (NC_000011.9:g.62472993G>A, NM_001122955.3:c.184C>T (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.62472993G>A
DNA change (hg38) g.62705521G>A
Published as BSCL2(NM_001122955.4):c.184C>T (p.L62F)
ISCN -
DB-ID GNG3_000008
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HNRNPUL2 NM_001079559.2 ?/. - c.*9778C>T r.(=) p.(=)
BSCL2 NM_001122955.3 ?/. - c.184C>T r.(?) p.(Leu62Phe)
GNG3 NM_012202.4 ?/. - c.-2396G>A r.(?) p.(=)
HNRNPUL2-BSCL2 NR_037946.1 ?/. - n.2704C>T r.(?) -


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