RGD:11089556 Rat Genome Database

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Variant: RGD:11089556 -  Homo sapiens

RGD ID: 11089556
RS ID: rs766938558
ClinVar ID: CV229150
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MITF  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 3 70,000,954
GRCh38 3 69,951,803
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_776t1:c.560-9C>G
LRG_776:g.217322C>G
NG_011631.1:g.217322C>G
NC_000003.12:g.69951803C>G
More... 		07/13/2021 intron variant uncertain significance Albinism-deafness of Tietz; AllHighlyPenetrant; Cancer predisposition; Coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, and deafness; COMMAD syndrome; Cutaneous malignant melanoma 8; Hereditary Cancer Syndrome; Hereditary neoplastic syndrome; Hypopigmentation/deafness of Tietz; MELANOMA AND RENAL CELL CARCINOMA, SUSCEPTIBILITY TO; Melanoma, cutaneous malignant, susceptibility to, 8; Neoplastic Syndromes, Hereditary; none provided; Tietz albinism-deafness syndrome; Tumor predisposition; Waardenburg syndrome type 2A; WAARDENBURG SYNDROME WITHOUT DYSTOPIA CANTHORUM
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:MITF
Accession:NM_001354604
Location:INTRON

Gene Symbol:MITF
Accession:NM_198159
Location:INTRON

Gene Symbol:MITF
Accession:NM_001184967
Location:INTRON

Gene Symbol:MITF
Accession:NM_198177
Location:INTRON

Gene Symbol:MITF
Accession:NM_001354608
Location:INTRON

Gene Symbol:MITF
Accession:NM_198178
Location:INTRON

Gene Symbol:MITF
Accession:NM_000248
Location:INTRON

Gene Symbol:MITF
Accession:NM_001354607
Location:INTRON

Gene Symbol:MITF
Accession:NM_001184968
Location:INTRON

Gene Symbol:MITF
Accession:NM_001354606
Location:INTRON

Gene Symbol:MITF
Accession:NM_001354605
Location:INTRON

Gene Symbol:MITF
Accession:NM_198158
Location:INTRON

Gene Symbol:MITF
Accession:NM_006722
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:24033266   PMID:25741868   PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000214959 CLINVAR
  RCV001596994 CLINVAR
  RCV002256126 CLINVAR
  RCV002485390 CLINVAR
  RCV002519640 CLINVAR
dbSNP (RS) rs766938558 CLINVAR
MedGen C0027672 CLINVAR
  C0391816 CLINVAR
  C3661900 CLINVAR
  CN169374 CLINVAR
NCBI Gene MITF CLINVAR
OMIM 103500 CLINVAR
  156845 CLINVAR
  193510 CLINVAR
  614456 CLINVAR
  617306 CLINVAR
SNOMED CT 699346009 CLINVAR