Variant #0000802358 (NC_000006.11:g.152451909C>T, NM_182961.3:c.26099G>A (SYNE1))

Chromosome 6
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.152451909C>T
DNA change (hg38) -
Published as SYNE1(NM_182961.3):c.26099G>A (p.R8700Q)
ISCN -
DB-ID SYNE1_001129
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) 1.0E-5 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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ESR1 NM_000125.3 ?/. - c.*31808C>T r.(=) p.(=)
SYNE1 NM_182961.3 ?/. - c.26099G>A r.(?) p.(Arg8700Gln)


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