Variant #0000681012 (NC_000017.10:g.73515117A>T, NM_207346.2:c.510A>T (TSEN54))

Chromosome 17
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.73515117A>T
DNA change (hg38) -
Published as TSEN54(NM_207346.2):c.510A>T (p.R170=)
ISCN -
DB-ID KIAA0195_000038
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KIAA0195 NM_014738.4 -?/. - c.*19702A>T r.(=) p.(=)
CASKIN2 NM_020753.3 -?/. - c.-4040T>A r.(?) p.(=)
TSEN54 NM_207346.2 -?/. - c.510A>T r.(?) p.(Arg170=)


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