Variant #0000689649 (NC_000006.11:g.152201899G>C, NM_182961.3:c.*241672C>G (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.152201899G>C
DNA change (hg38) -
Published as ESR1(NM_001122742.1):c.753G>C (p.M251I)
ISCN -
DB-ID SYNE1_001094
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) 4.0E-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 2020-09-15 15:50:26 +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.753G>C r.(?) p.(Met251Ile)
SYNE1 NM_182961.3 ?/. - c.*241672C>G r.(=) p.(=)


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