Variant #0000620775 (NC_000002.11:g.172671648A>C, NM_003705.4:c.995T>G (SLC25A12))

Chromosome 2
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.172671648A>C
DNA change (hg38) g.171815138A>C
Published as SLC25A12(NM_003705.4):c.995T>G (p.L332R), SLC25A12(NM_003705.5):c.995T>G (p.(Leu332Arg))
ISCN -
DB-ID SLC25A12_000004 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) 8.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2025-11-01 13:22:20 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC25A12 NM_003705.4 ?/. - c.995T>G r.(?) p.(Leu332Arg)


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