Variant #0000563023 (NC_000017.10:g.73517536G>A, NM_207346.2:c.568G>A (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.73517536G>A
DNA change (hg38) g.75521455G>A
Published as TSEN54(NM_207346.2):c.568G>A (p.V190M), TSEN54(NM_207346.3):c.568G>A (p.V190M)
ISCN -
DB-ID TSEN54_000016 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) 0.04741 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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     
LLGL2 NM_004524.2 -/. - c.-4401G>A r.(?) p.(=)
TSEN54 NM_207346.2 -/. - c.568G>A r.(?) p.(Val190Met)


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