RGD:28882707 Rat Genome Database

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Variant: RGD:28882707 -  Homo sapiens

RGD ID: 28882707
RS ID: rs2066664856
ClinVar ID: CV889622
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MITF  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 3 70,014,474
GRCh38 3 69,965,323
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001354608.2:c.*75G>T
NM_198177.3:c.*75G>T
NM_198178.3:c.*75G>T
LRG_776:g.230842G>T
More... 		01/15/2018 3 prime utr variant uncertain significance Albinism-deafness of Tietz; Hypopigmentation/deafness of Tietz; Tietz albinism-deafness syndrome; WAARDENBURG SYNDROME WITHOUT DYSTOPIA CANTHORUM
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:MITF
Accession:NM_001354604
Location:3UTRS;EXON

Gene Symbol:MITF
Accession:NM_198177
Location:3UTRS;EXON

Gene Symbol:MITF
Accession:NM_001184967
Location:3UTRS;EXON

Gene Symbol:MITF
Accession:NM_198178
Location:3UTRS;EXON

Gene Symbol:MITF
Accession:NM_001354605
Location:3UTRS;EXON

Gene Symbol:MITF
Accession:NM_198158
Location:3UTRS;EXON

Gene Symbol:MITF
Accession:NM_001354607
Location:3UTRS;EXON

Gene Symbol:MITF
Accession:NM_001354606
Location:3UTRS;EXON

Gene Symbol:MITF
Accession:NM_000248
Location:3UTRS;EXON

Gene Symbol:MITF
Accession:NM_198159
Location:3UTRS;EXON

Gene Symbol:MITF
Accession:NM_006722
Location:3UTRS;EXON

Gene Symbol:MITF
Accession:NM_001354608
Location:3UTRS;EXON

Gene Symbol:MITF
Accession:NM_001184968
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001150049 CLINVAR
  RCV001150050 CLINVAR
dbSNP (RS) rs2066664856 CLINVAR
MedGen C0391816 CLINVAR
  C1860339 CLINVAR
NCBI Gene MITF CLINVAR
OMIM 103500 CLINVAR
  156845 CLINVAR
  193510 CLINVAR