Variant #0000316076 (NC_000006.11:g.152453291G>A, NM_182961.3:c.26060C>T (SYNE1))

Chromosome 6
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.152453291G>A
DNA change (hg38) g.152132156G>A
Published as SYNE1(NM_182961.3):c.26060C>T (p.T8687I), SYNE1(NM_182961.4):c.26060C>T (p.T8687I)
ISCN -
DB-ID SYNE1_000018 See all 3 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) 0.05102 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ESR1 NM_000125.3 -/. - c.*33190G>A r.(=) p.(=)
SYNE1 NM_182961.3 -/. - c.26060C>T r.(?) p.(Thr8687Ile)


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