Variant #0001046475 (NC_000014.8:g.64692115_64692132del, NM_182914.2:c.20595_20612del (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.64692115_64692132del
DNA change (hg38) -
Published as SYNE2(NM_182914.3):c.20595_20612delCCTGCTGCTGCTGCTCCT (p.L6866_L6871del)
ISCN -
DB-ID SYNE2_000377
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2025-07-08 13:22:38 +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.*2128_*2145del r.(=) p.(=)
SYNE2 NM_182914.2 ?/. - c.20595_20612del r.(?) p.(Leu6866_Leu6871del)


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