Variant #0000802359 (NC_000006.11:g.152454403T>G, NC_000006.11(NM_182961.3):c.26001+8A>C (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.152454403T>G
DNA change (hg38) -
Published as SYNE1(NM_033071.3):c.25857+8A>C (p.(=)), SYNE1(NM_182961.3):c.26001+8A>C
ISCN -
DB-ID SYNE1_000909 See all 2 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) 0.00013 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.*34302T>G r.(=) p.(=)
SYNE1 NM_182961.3 -?/. - c.26001+8A>C r.(=) p.(=)


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