Variant #0000862612 (NC_000011.9:g.62473053G>A, NM_001122955.3:c.124C>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.62473053G>A
DNA change (hg38) -
Published as BSCL2(NM_001122955.3):c.124C>T (p.R42C), BSCL2(NM_001122955.4):c.124C>T (p.R42C), BSCL2(NM_032667.6):c.-69C>T
ISCN -
DB-ID BSCL2_000028 See all 5 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) 0.00059 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited 2024-04-19 20:27:30 +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.*9718C>T r.(=) p.(=)
BSCL2 NM_001122955.3 -?/. - c.124C>T r.(?) p.(Arg42Cys)
GNG3 NM_012202.4 -?/. - c.-2336G>A r.(?) p.(=)
HNRNPUL2-BSCL2 NR_037946.1 -?/. - n.2644C>T r.(?) -


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