Variant #0000891842 (NC_000014.8:g.64692056C>T, NM_182914.2:c.20536C>T (SYNE2))

Chromosome 14
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.64692056C>T
DNA change (hg38) -
Published as SYNE2(NM_182914.3):c.20536C>T (p.P6846S)
ISCN -
DB-ID SYNE2_000344
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) 0.0005 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +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.*2195G>A r.(=) p.(=)
SYNE2 NM_182914.2 -?/. - c.20536C>T r.(?) p.(Pro6846Ser)


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