Variant #0000567047 (NC_000019.9:g.36497439C>T, NM_001039876.1:c.753G>A (SYNE4))

Chromosome 19
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.36497439C>T
DNA change (hg38) g.36006537C>T
Published as SYNE4(NM_001039876.2):c.753G>A (p.P251=)
ISCN -
DB-ID ALKBH6_000002
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) 0.00013 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 2020-07-15 17:38:43 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SYNE4 NM_001039876.1 -?/. - c.753G>A r.(?) p.(Pro251=)
ALKBH6 NM_032878.3 -?/. - c.*2753G>A r.(=) p.(=)


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