Variant #0000320777 (NC_000001.10:g.44169743C>T, NM_174963.3:c.-3652C>T (ST3GAL3))

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.44169743C>T
DNA change (hg38) g.43704072C>T
Published as KDM4A(NM_014663.2):c.3014C>T (p.(Thr1005Ile))
ISCN -
DB-ID KDM4A_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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-04 13:07:32 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KDM4A NM_014663.2 ?/. - c.3014C>T r.(?) p.(Thr1005Ile)
ST3GAL3 NM_174963.3 ?/. - c.-3652C>T r.(?) p.(=)
KDM4A-AS1 NR_033827.1 ?/. - n.388+281G>A r.(?) -


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.