Variant #0000568993 (NC_000019.9:g.920746T>A, NM_032551.4:c.1195T>A (KISS1R))

Chromosome 19
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.920746T>A
DNA change (hg38) g.920746T>A
Published as -
ISCN -
DB-ID ARID3A_000001
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_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 2020-07-15 09:17:35 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARID3A NM_005224.2 +/. - c.-5581T>A r.(?) p.(=)
KISS1R NM_032551.4 +/. - c.1195T>A r.(?) p.(Ter399ArgextTer?)


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