Variant #0000718479 (NC_000002.11:g.219525978C>T, NM_004328.4:c.268C>T (BCS1L))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.219525978C>T
DNA change (hg38) -
Published as BCS1L(NM_004328.5):c.268C>T (p.R90C)
ISCN -
DB-ID BCS1L_000009
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) 1.0E-5 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZNF142 NM_001105537.1 +?/. - c.-2153G>A r.(?) p.(=)
BCS1L NM_004328.4 +?/. - c.268C>T r.(?) p.(Arg90Cys)
STK36 NM_015690.4 +?/. - c.-11050C>T r.(?) p.(=)
RNF25 NM_022453.2 +?/. - c.*2702G>A r.(=) p.(=)


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