Variant #0000249447 (NC_000014.8:g.64604650A>G, NM_182914.2:c.14792A>G (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.64604650A>G
DNA change (hg38) g.64137932A>G
Published as SYNE2(NM_182914.2):c.14792A>G (p.K4931R), SYNE2(NM_182914.3):c.14792A>G (p.K4931R)
ISCN -
DB-ID SYNE2_000133 See all 4 reported entries
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) 0.00088 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 2018-01-15 20:58:59 +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     
SYNE2 NM_182914.2 -?/. - c.14792A>G r.(?) p.(Lys4931Arg)


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