Variant #0000895961 (NC_000023.10:g.144906400C>A, NM_032539.4:c.2457C>A (SLITRK2))

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.144906400C>A
DNA change (hg38) -
Published as SLITRK2(NM_001144005.3):c.2457C>A (p.H819Q)
ISCN -
DB-ID CXorf1_000017
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2022-11-01 13:41:49 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CXorf1 NM_004709.2 ?/. - c.-2796C>A r.(?) p.(=)
SLITRK2 NM_032539.4 ?/. - c.2457C>A r.(?) p.(His819Gln)


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