Variant #0000520631 (NC_000003.11:g.69998275A>G, NM_198159.2:c.836A>G (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.69998275A>G
DNA change (hg38) g.69949124A>G
Published as MITF(NM_198159.2):c.836A>G (p.N279S)
ISCN -
DB-ID MITF_000097
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) 7.0E-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 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.515A>G r.(?) p.(Asn172Ser)
MITF NM_198159.2 -?/. - c.836A>G r.(?) p.(Asn279Ser)


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