Variant #0000723540 (NC_000011.9:g.62457861C>T, NM_001122955.3:c.1367G>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.62457861C>T
DNA change (hg38) -
Published as BSCL2(NM_001122955.3):c.1367G>A (p.R456H), BSCL2(NM_032667.6):c.1175G>A (p.R392H)
ISCN -
DB-ID BSCL2_000036 See all 3 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) 0.00032 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2024-10-29 21:08:56 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HNRNPUL2 NM_001079559.2 ?/. - c.*24910G>A r.(=) p.(=)
BSCL2 NM_001122955.3 ?/. - c.1367G>A r.(?) p.(Arg456His)
GNG3 NM_012202.4 ?/. - c.-17528C>T r.(?) p.(=)
LRRN4CL NM_203422.2 ?/. - c.-968G>A r.(?) p.(=)
HNRNPUL2-BSCL2 NR_037946.1 ?/. - n.3887G>A r.(?) -


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.