Variant #0001052515 (NC_000006.11:g.152265322C>T, NM_182961.3:c.*178249G>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.152265322C>T
DNA change (hg38) -
Published as ESR1(NM_000125.4):c.775C>T (p.(Arg259*))
ISCN -
DB-ID SYNE1_001290
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ESR1 NM_000125.3 ?/. - c.775C>T r.(?) p.(Arg259*)
SYNE1 NM_182961.3 ?/. - c.*178249G>A r.(=) p.(=)


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