Variant #0000514586 (NC_000002.11:g.219526634G>A, NM_004328.4:c.613G>A (BCS1L))

Chromosome 2
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.219526634G>A
DNA change (hg38) g.218661911G>A
Published as BCS1L(NM_004328.4):c.613G>A (p.V205I)
ISCN -
DB-ID BCS1L_000016
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) 0.00759 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 2019-07-18 18:22:55 +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.-2809C>T r.(?) p.(=)
BCS1L NM_004328.4 -/. - c.613G>A r.(?) p.(Val205Ile)
STK36 NM_015690.4 -/. - c.-10394G>A r.(?) p.(=)
RNF25 NM_022453.2 -/. - c.*2046C>T r.(=) p.(=)


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