Variant #0000223357 (NC_000008.10:g.14095199T>C, NC_000008.10(NM_139167.2):c.337-11A>G (SGCZ))

Chromosome 8
Allele Parent #1
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.14095199T>C
DNA change (hg38) g.14237690T>C
Published as -
ISCN -
DB-ID SGCZ_000004 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs28658359
Origin Germline
Segregation -
Frequency 0.26
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.26399 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2008-02-23 18:19:01 +01:00 (CET)
Date last edited 2012-11-02 20:43:05 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SGCZ NM_139167.2 ?/. 3i c.337-11A>G r.(?) p.(=)


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