Variant #0000253371 (NC_000017.10:g.73513677A>C, NM_207346.2:c.409A>C (TSEN54))

Chromosome 17
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.73513677A>C
DNA change (hg38) g.75517596A>C
Published as TSEN54(NM_207346.2):c.409A>C (p.I137L), TSEN54(NM_207346.3):c.409A>C (p.I137L)
ISCN -
DB-ID TSEN54_000011 See all 3 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) 0.07257 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 2018-01-15 20:58:59 +01:00 (CET)
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.*18262A>C r.(=) p.(=)
CASKIN2 NM_020753.3 -/. - c.-2600T>G r.(?) p.(=)
TSEN54 NM_207346.2 -/. - c.409A>C r.(?) p.(Ile137Leu)


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