Variant #0000679260 (NC_000011.9:g.64853934C>T, NM_006782.3:c.262C>T (ZFPL1))

Chromosome 11
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.64853934C>T
DNA change (hg38) -
Published as ZFPL1(NM_006782.3):c.262C>T (p.(Arg88Ter))
ISCN -
DB-ID CDCA5_000001
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZFPL1 NM_006782.3 ?/. - c.262C>T r.(?) p.(Arg88Ter)
CDCA5 NM_080668.3 ?/. - c.-2484G>A r.(?) p.(=)


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