Variant #0000620479 (NC_000001.10:g.203767429C>T, NM_001174108.1:c.779C>T (ZBED6))

Chromosome 1
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.203767429C>T
DNA change (hg38) g.203798301C>T
Published as ZBED6(NM_001174108.2):c.779C>T (p.P260L)
ISCN -
DB-ID ZBED6_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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZBED6 NM_001174108.1 ?/. - c.779C>T r.(?) p.(Pro260Leu)
ZC3H11A NM_014827.4 ?/. - c.-260+1805C>T r.(=) p.(=)


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