Variant #0000527653 (NC_000006.11:g.152784621T>C, NM_182961.3:c.1964A>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.152784621T>C
DNA change (hg38) g.152463486T>C
Published as SYNE1(NM_033071.3):c.1985A>G (p.(Gln662Arg)), SYNE1(NM_182961.3):c.1964A>G (p.Q655R), SYNE1(NM_182961.4):c.1964A>G (p.Q655R)
ISCN -
DB-ID SYNE1_000342 See all 4 reported entries
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) 0.0063 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 2021-09-17 14:40:49 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SYNE1 NM_182961.3 -?/. - c.1964A>G r.(?) p.(Gln655Arg)


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