Variant #0000975983 (NC_000003.11:g.69845665_69845668del, NC_000003.11(NM_198159.2):c.104+56813_104+56816del (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.69845665_69845668del
DNA change (hg38) -
Published as MITF(NM_001184967.1):c.-53+32804_-53+32807del (p.(=))
ISCN -
DB-ID MITF_000136
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MITF NM_000248.3 -?/. - c.-140209_-140206del r.(?) p.(=)
MITF NM_198159.2 -?/. - c.104+56813_104+56816del r.(=) p.(=)


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