Variant #0000613495 (NC_000011.9:g.62458824G>A, NM_001122955.3:c.933C>T (BSCL2))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.62458824G>A
DNA change (hg38) g.62691352G>A
Published as BSCL2(NM_001122955.4):c.933C>T (p.S311=)
ISCN -
DB-ID GNG3_000004
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) 2.0E-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 2019-12-04 15:24:38 +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.*23947C>T r.(=) p.(=)
BSCL2 NM_001122955.3 -?/. - c.933C>T r.(?) p.(Ser311=)
GNG3 NM_012202.4 -?/. - c.-16565G>A r.(?) p.(=)
LRRN4CL NM_203422.2 -?/. - c.-1931C>T r.(?) p.(=)
HNRNPUL2-BSCL2 NR_037946.1 -?/. - n.3453C>T r.(?) -


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