Variant #0000681013 (NC_000017.10:g.73518276G>A, NM_207346.2:c.1114G>A (TSEN54))

Chromosome 17
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.73518276G>A
DNA change (hg38) -
Published as TSEN54(NM_207346.2):c.1114G>A (p.V372M), TSEN54(NM_207346.3):c.1114G>A (p.V372M)
ISCN -
DB-ID TSEN54_000025 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) 0.00048 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
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     
LLGL2 NM_004524.2 ?/. - c.-3661G>A r.(?) p.(=)
TSEN54 NM_207346.2 ?/. - c.1114G>A r.(?) p.(Val372Met)


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