Variant #0000655015 (NC_000003.11:g.70008542G>A, NM_198159.2:c.1132G>A (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.70008542G>A
DNA change (hg38) g.69959391G>A
Published as MITF(NM_001354607.1):c.1081G>A (p.A361T), MITF(NM_198159.3):c.1132G>A (p.A378T)
ISCN -
DB-ID MITF_000073 See all 2 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) 0.00013 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 2020-03-23 16:13:27 +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.829G>A r.(?) p.(Ala277Thr)
MITF NM_198159.2 -?/. - c.1132G>A r.(?) p.(Ala378Thr)


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