Variant #0000322252 (NC_000011.9:g.60701965C>A, NM_016582.2:c.*2726G>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.60701965C>A
DNA change (hg38) g.60934493C>A
Published as TMEM132A(NM_017870.3):c.1568C>A (p.A523E, p.(Ala523Glu))
ISCN -
DB-ID TMEM132A_000002 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) 0.00705 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)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC15A3 NM_016582.2 ?/. - c.*2726G>T r.(=) p.(=)
TMEM132A NM_017870.3 ?/. - c.1568C>A r.(?) p.(Ala523Glu)


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