Variant #0000979699 (NC_000011.9:g.62459867C>T, NM_001122955.3:c.844G>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.62459867C>T
DNA change (hg38) -
Published as BSCL2(NM_001122955.3):c.844G>A (p.A282T), BSCL2(NM_001122955.4):c.844G>A (p.(Ala282Thr)), BSCL2(NM_001386027.1):c.844G>A (p.A282T)
ISCN -
DB-ID GNG3_000005 See all 4 reported entries
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) 3.0E-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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HNRNPUL2 NM_001079559.2 ?/. - c.*22904G>A r.(=) p.(=)
BSCL2 NM_001122955.3 ?/. - c.844G>A r.(?) p.(Ala282Thr)
GNG3 NM_012202.4 ?/. - c.-15522C>T r.(?) p.(=)
LRRN4CL NM_203422.2 ?/. - c.-2974G>A r.(?) p.(=)
HNRNPUL2-BSCL2 NR_037946.1 ?/. - n.3364G>A r.(?) -


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