Variant #0000266339 (NC_000011.9:g.62457894C>T, NM_001122955.3:c.1334G>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.62457894C>T
DNA change (hg38) g.62690422C>T
Published as BSCL2(NM_001122955.4):c.1334G>A (p.S445N)
ISCN -
DB-ID BSCL2_000064
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 2018-01-15 20:58:59 +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.*24877G>A r.(=) p.(=)
BSCL2 NM_001122955.3 ?/. - c.1334G>A r.(?) p.(Ser445Asn)
GNG3 NM_012202.4 ?/. - c.-17495C>T r.(?) p.(=)
LRRN4CL NM_203422.2 ?/. - c.-1001G>A r.(?) p.(=)
HNRNPUL2-BSCL2 NR_037946.1 ?/. - n.3854G>A r.(?) -


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