Variant #0001014854 (NC_000011.9:g.62460120G>A, NC_000011.9(NM_001122955.3):c.765+15C>T (BSCL2))

Chromosome 11
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.62460120G>A
DNA change (hg38) -
Published as BSCL2(NM_001122955.3):c.765+15C>T (p.(=)), BSCL2(NM_001122955.4):c.765+15C>T
ISCN -
DB-ID BSCL2_000069 See all 2 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) 0.00946 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 2024-10-29 21:08:56 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HNRNPUL2 NM_001079559.2 -/. - c.*22651C>T r.(=) p.(=)
BSCL2 NM_001122955.3 -/. - c.765+15C>T r.(=) p.(=)
GNG3 NM_012202.4 -/. - c.-15269G>A r.(?) p.(=)
LRRN4CL NM_203422.2 -/. - c.-3227C>T r.(?) p.(=)
HNRNPUL2-BSCL2 NR_037946.1 -/. - n.3285+15C>T r.(?) -


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