Variant #0000329373 (NC_000003.11:g.47164459_47164471del, NM_014159.6:c.1655_1667del (SETD2))

Chromosome 3
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.47164459_47164471del
DNA change (hg38) g.47122969_47122981del
Published as SETD2(NM_014159.6):c.1655_1667del (p.(Ala552AspfsTer23))
ISCN -
DB-ID SETD2_000008
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-15 08:55:18 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SETD2 NM_014159.6 ?/. - c.1655_1667del r.(?) p.(Ala552AspfsTer23)


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