Variant #0000980957 (NC_000014.8:g.64694278_64694281dup, NM_182914.2:c.*2034_*2037dup (SYNE2))

Chromosome 14
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.64694278_64694281dup
DNA change (hg38) -
Published as ESR2(NM_001040275.1):c.1459_1462dup (p.(Leu488SerfsTer4))
ISCN -
DB-ID SYNE2_000359
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 2024-04-19 20:27:30 +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     
ESR2 NM_001040275.1 ?/. - c.1459_1462dup r.(?) p.(Leu488Serfs*4)
SYNE2 NM_182914.2 ?/. - c.*2034_*2037dup r.(=) p.(=)


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