Variant #0000849715 (NC_000002.11:g.219527288T>A, NM_004328.4:c.775T>A (BCS1L))

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.219527288T>A
DNA change (hg38) -
Published as BCS1L(NM_004328.4):c.775T>A (p.S259T)
ISCN -
DB-ID BCS1L_000037
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) 0.00031 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 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BCS1L NM_004328.4 ?/. - c.775T>A r.(?) p.(Ser259Thr)
STK36 NM_015690.4 ?/. - c.-9740T>A r.(?) p.(=)
RNF25 NM_022453.2 ?/. - c.*1392A>T r.(=) p.(=)


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