Variant #0000885979 (NC_000003.11:g.69998243A>T, NM_198159.2:c.804A>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.69998243A>T
DNA change (hg38) -
Published as MITF(NM_000248.3):c.483A>T (p.(Gln161His)), MITF(NM_001354607.2):c.753A>T (p.Q251H)
ISCN -
DB-ID MITF_000005 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) Retrieve
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2022-11-01 13:01:21 +01:00 (CET)
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.483A>T r.(?) p.(Gln161His)
MITF NM_198159.2 -?/. - c.804A>T r.(?) p.(Gln268His)


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