Variant #0000655504 (NC_000006.11:g.152129456A>G, NM_182961.3:c.*314115T>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.152129456A>G
DNA change (hg38) g.151808321A>G
Published as ESR1(NM_001122742.1):c.409A>G (p.S137G)
ISCN -
DB-ID SYNE1_001079
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) 0.00049 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 2020-03-23 16:13:27 +01:00 (CET)
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.409A>G r.(?) p.(Ser137Gly)
SYNE1 NM_182961.3 -?/. - c.*314115T>C r.(=) p.(=)


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