Variant #0000520626 (NC_000003.11:g.69986984C>T, NM_198159.2:c.366C>T (MITF))

Chromosome 3
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.69986984C>T
DNA change (hg38) g.69937833C>T
Published as MITF(NM_000248.3):c.45C>T (p.(His15=)), MITF(NM_198159.2):c.366C>T (p.H122=), MITF(NM_198159.3):c.366C>T (p.H122=)
ISCN -
DB-ID MITF_000062 See all 3 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) 0.00289 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +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.45C>T r.(?) p.(His15=)
MITF NM_198159.2 -?/. - c.366C>T r.(?) p.(His122=)


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