Variant #0000527628 (NC_000006.11:g.152757224G>A, NM_182961.3:c.4162C>T (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.152757224G>A
DNA change (hg38) g.152436089G>A
Published as SYNE1(NM_033071.5):c.4183C>T (p.R1395W), SYNE1(NM_182961.3):c.4162C>T (p.R1388W), SYNE1(NM_182961.4):c.4162C>T (p.R1388W)
ISCN -
DB-ID SYNE1_000799 See all 9 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) 0.0028 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SYNE1 NM_182961.3 -?/. - c.4162C>T r.(?) p.(Arg1388Trp)


Screenscraping/webscraping (interacting with LOVD using scripts to download data) is strictly prohibited.
Use our APIs to retrieve data.