Variant #0000527624 (NC_000006.11:g.152746682C>A, NM_182961.3:c.5101G>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.152746682C>A
DNA change (hg38) g.152425547C>A
Published as SYNE1(NM_033071.3):c.5122G>T (p.(Ala1708Ser)), SYNE1(NM_182961.3):c.5101G>T (p.A1701S), SYNE1(NM_182961.4):c.5101G>T (p.A1701S)
ISCN -
DB-ID SYNE1_000244 See all 10 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) 0.00247 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SYNE1 NM_182961.3 -?/. - c.5101G>T r.(?) p.(Ala1701Ser)


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