Variant #0001064010 (NC_000003.11:g.69990481C>T, NM_198159.2:c.761C>T (MITF))

Chromosome 3
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.69990481C>T
DNA change (hg38) -
Published as MITF(NM_000248.3):c.440C>T (p.(Thr147Met))
ISCN -
DB-ID MITF_000148
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) 0.00013 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 2026-01-20 18:57:21 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MITF NM_000248.3 ?/. - c.440C>T r.(?) p.(Thr147Met)
MITF NM_198159.2 ?/. - c.761C>T r.(?) p.(Thr254Met)


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