Variant #0000291827 (NC_000003.11:g.69988319C>T, NM_198159.2:c.653C>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.69988319C>T
DNA change (hg38) g.69939168C>T
Published as MITF(NM_000248.4):c.332C>T (p.A111V), MITF(NM_001354604.2):c.653C>T (p.(Ala218Val)), MITF(NM_198159.2):c.653C>T (p.A218V)
ISCN -
DB-ID MITF_000043 See all 4 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) 2.0E-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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MITF NM_000248.3 ?/. - c.332C>T r.(?) p.(Ala111Val)
MITF NM_198159.2 ?/. - c.653C>T r.(?) p.(Ala218Val)


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