Variant #0000810684 (NC_000023.10:g.77528924A>T, CYSLTR1(NM_006639.2):c.320T>A)

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.77528924A>T
DNA change (hg38) -
Published as CYSLTR1(NM_001282187.1):c.320T>A (p.L107H)
ISCN -
DB-ID CYSLTR1_000011
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) Variant not found in online data sets
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CYSLTR1 NM_006639.2 ?/. - c.320T>A r.(?) p.(Leu107His)