Variant #0001068897 (NC_000023.10:g.48891667T>C, NM_006521.4:c.985A>G (TFE3))

Chromosome X
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.48891667T>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID TFE3_000043
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1277025733
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2026-03-02 15:18:02 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TFE3 NM_006521.4 -?/. - c.985A>G r.(?) p.(Ile329Val)


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