Variant #0000616812 (NC_000017.10:g.73512642A>T, NM_207346.2:c.1A>T (TSEN54))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.73512642A>T
DNA change (hg38) g.75516561A>T
Published as TSEN54(NM_207346.3):c.1A>T (p.M1?)
ISCN -
DB-ID KIAA0195_000036
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KIAA0195 NM_014738.4 +?/. - c.*17227A>T r.(=) p.(=)
CASKIN2 NM_020753.3 +?/. - c.-1565T>A r.(?) p.(=)
TSEN54 NM_207346.2 +?/. - c.1A>T r.(?) p.(Met1?)


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