Variant #0000322251 (NC_000011.9:g.60701964G>A, NM_016582.2:c.*2727C>T (SLC15A3))

Chromosome 11
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.60701964G>A
DNA change (hg38) g.60934492G>A
Published as TMEM132A(NM_017870.3):c.1567G>A (p.A523T, p.(Ala523Thr))
ISCN -
DB-ID TMEM132A_000001 See all 2 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) 0.00701 View details
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 2022-05-09 15:24:52 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC15A3 NM_016582.2 ?/. - c.*2727C>T r.(=) p.(=)
TMEM132A NM_017870.3 ?/. - c.1567G>A r.(?) p.(Ala523Thr)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.