Variant #0000990753 (NC_000001.10:g.203766895C>T, NM_001174108.1:c.245C>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.203766895C>T
DNA change (hg38) -
Published as ZBED6(NM_001174108.1):c.245C>T (p.(Ala82Val))
ISCN -
DB-ID ZBED6_000004
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) 0.0028 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:07:21 +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     
ZBED6 NM_001174108.1 ?/. - c.245C>T r.(?) p.(Ala82Val)
ZC3H11A NM_014827.4 ?/. - c.-260+1271C>T r.(=) p.(=)


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