Variant #0000999178 (NC_000011.9:g.60719008C>G, NM_016582.2:c.16G>C (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.60719008C>G
DNA change (hg38) -
Published as SLC15A3(NM_016582.2):c.16G>C (p.(Ala6Pro))
ISCN -
DB-ID SLC15A3_000003
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC15A3 NM_016582.2 ?/. - c.16G>C r.(?) p.(Ala6Pro)
TMEM132A NM_017870.3 ?/. - c.*14629C>G r.(=) p.(=)


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