Variant #0000527444 (NC_000006.11:g.152443667T>C, NM_182961.3:c.26298A>G (SYNE1))

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.152443667T>C
DNA change (hg38) g.152122532T>C
Published as SYNE1(NM_182961.3):c.26298A>G (p.P8766=)
ISCN -
DB-ID SYNE1_000906
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) 0.00057 View details
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 2020-06-22 10:59:26 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ESR1 NM_000125.3 -?/. - c.*23566T>C r.(=) p.(=)
SYNE1 NM_182961.3 -?/. - c.26298A>G r.(?) p.(Pro8766=)


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