Variant #0000520634 (NC_000003.11:g.70008488C>T, NM_198159.2:c.1078C>T (MITF))

Chromosome 3
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.70008488C>T
DNA change (hg38) g.69959337C>T
Published as MITF(NM_198159.3):c.1078C>T (p.R360*)
ISCN -
DB-ID MITF_000018 See all 6 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) Retrieve
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-10-28 14:15:03 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MITF NM_000248.3 +?/. - c.775C>T r.(?) p.(Arg259Ter)
MITF NM_198159.2 +?/. - c.1078C>T r.(?) p.(Arg360Ter)


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