Variant #0001014852 (NC_000011.9:g.62457781C>T, NM_001122955.3:c.*58G>A (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.62457781C>T
DNA change (hg38) -
Published as BSCL2(NM_001122955.3):c.*58G>A (p.(=))
ISCN -
DB-ID GNG3_000022
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) 0.00015 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.*24990G>A r.(=) p.(=)
BSCL2 NM_001122955.3 -?/. - c.*58G>A r.(=) p.(=)
GNG3 NM_012202.4 -?/. - c.-17608C>T r.(?) p.(=)
HNRNPUL2-BSCL2 NR_037946.1 -?/. - n.3967G>A r.(?) -


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