Variant #0000528282 (NC_000006.11:g.31868136C>A, NM_000063.4:c.-27394C>A (C2))

Chromosome 6
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.31868136C>A
DNA change (hg38) g.31900359C>A
Published as ZBTB12(NM_181842.2):c.947G>T (p.S316I)
ISCN -
DB-ID C2_000009
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C2 NM_000063.4 -?/. - c.-27394C>A r.(?) p.(=)
EHMT2 NM_006709.3 -?/. - c.-2682G>T r.(?) p.(=)
ZBTB12 NM_181842.2 -?/. - c.947G>T r.(?) p.(Ser316Ile)


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