Variant #0000514584 (NC_000002.11:g.219520930T>G, NM_004328.4:c.-3795T>G (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.219520930T>G
DNA change (hg38) g.218656207T>G
Published as ZNF142(NM_001105537.2):c.223A>C (p.I75L)
ISCN -
DB-ID BCS1L_000014
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) Retrieve
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 2020-08-06 14:59:34 +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.223A>C r.(?) p.(Ile75Leu)
BCS1L NM_004328.4 -?/. - c.-3795T>G r.(?) p.(=)


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