Variant #0000291825 (NC_000003.11:g.69928298C>T, NM_198159.2:c.118C>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.69928298C>T
DNA change (hg38) g.69879147C>T
Published as MITF(NM_198159.2):c.118C>T (p.H40Y)
ISCN -
DB-ID MITF_000059
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_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 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.-57576C>T r.(?) p.(=)
MITF NM_198159.2 ?/. - c.118C>T r.(?) p.(His40Tyr)


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