Variant #0000552818 (NC_000014.8:g.64691744G>A, NM_182914.2:c.20497G>A (SYNE2))

Chromosome 14
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.64691744G>A
DNA change (hg38) g.64225026G>A
Published as SYNE2(NM_182914.2):c.20497G>A (p.E6833K)
ISCN -
DB-ID SYNE2_000239
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) 0.00102 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ESR2 NM_001040275.1 -/. - c.*2507C>T r.(=) p.(=)
SYNE2 NM_182914.2 -/. - c.20497G>A r.(?) p.(Glu6833Lys)


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