Variant #0000334194 (NC_000023.10:g.53112212_53112217del, NM_022117.3:c.532_537del (TSPYL2))

Chromosome X
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.53112212_53112217del
DNA change (hg38) g.53083030_53083035del
Published as TSPYL2(NM_022117.3):c.517_522del (p.(Asp174_Glu175del))
ISCN -
DB-ID TSPYL2_000003
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GPR173 NM_018969.5 ?/. - c.*5287_*5292del r.(=) p.(=)
TSPYL2 NM_022117.3 ?/. - c.532_537del r.(?) p.(Asp178_Glu179del)


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