Variant #0000279788 (NC_000003.11:g.70000956T>A, NC_000003.11(NM_198159.2):c.881-25T>A (MITF))

Chromosome 3
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.70000956T>A
DNA change (hg38) g.69951805T>A
Published as MITF(NM_198159.3):c.881-25T>A
ISCN -
DB-ID MITF_000069
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) 0.00033 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
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.560-7T>A r.(=) p.(=)
MITF NM_198159.2 -/. - c.881-25T>A r.(=) p.(=)


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