Variant #0000676508 (NC_000002.11:g.219526966C>T, NM_004328.4:c.702C>T (BCS1L))

Chromosome 2
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.219526966C>T
DNA change (hg38) -
Published as BCS1L(NM_004328.4):c.702C>T (p.C234=)
ISCN -
DB-ID BCS1L_000031
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) 0.00011 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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZNF142 NM_001105537.1 -?/. - c.-3141G>A r.(?) p.(=)
BCS1L NM_004328.4 -?/. - c.702C>T r.(?) p.(Cys234=)
STK36 NM_015690.4 -?/. - c.-10062C>T r.(?) p.(=)
RNF25 NM_022453.2 -?/. - c.*1714G>A r.(=) p.(=)


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