rs767760567 Rat Genome Database

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Variant: rs767760567 -  Homo sapiens

RGD ID: 28870725
RS ID: rs767760567
ClinVar ID: CV869741
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: KIF21A  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 12 39,687,644
GRCh38 12 39,293,842
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001378439.1:c.*582G>A
NG_017067.1:g.154549G>A
NM_001378441.1:c.*582G>A
NM_017641.4:c.*582G>A
More... 		01/13/2018 3 prime utr variant uncertain significance BLEPHAROPTOSIS WITH ABSENT EYE MOVEMENTS; FEOM1 LOCUS; OPHTHALMOPLEGIA, CONGENITAL
Disease Annotations     Click to see Annotation Detail View

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype

Variant Details
Variant Transcripts
Gene Symbol:KIF21A
Accession:NM_001173465
Location:3UTRS;EXON

Gene Symbol:KIF21A
Accession:XM_047429128
Location:3UTRS;EXON

Gene Symbol:KIF21A
Accession:XM_005269011
Location:3UTRS;EXON

Gene Symbol:KIF21A
Accession:XM_011538556
Location:3UTRS;EXON

Gene Symbol:KIF21A
Accession:XM_017019609
Location:3UTRS;EXON

Gene Symbol:KIF21A
Accession:XM_017019607
Location:3UTRS;EXON

Gene Symbol:KIF21A
Accession:XM_047429123
Location:3UTRS;EXON

Gene Symbol:KIF21A
Accession:XM_047429120
Location:3UTRS;EXON

Gene Symbol:KIF21A
Accession:XM_047429125
Location:3UTRS;EXON

Gene Symbol:KIF21A
Accession:NM_017641
Location:3UTRS;EXON

Gene Symbol:KIF21A
Accession:XM_006719493
Location:3UTRS;EXON

Gene Symbol:KIF21A
Accession:XM_047429133
Location:3UTRS;EXON

Gene Symbol:KIF21A
Accession:XM_047429122
Location:3UTRS;EXON

Gene Symbol:KIF21A
Accession:XM_047429121
Location:3UTRS;EXON

Gene Symbol:KIF21A
Accession:XM_005269014
Location:3UTRS;EXON

Gene Symbol:KIF21A
Accession:XM_047429132
Location:3UTRS;EXON

Gene Symbol:KIF21A
Accession:NM_001378441
Location:3UTRS;EXON

Gene Symbol:KIF21A
Accession:XM_047429127
Location:3UTRS;EXON

Gene Symbol:KIF21A
Accession:XM_047429119
Location:3UTRS;EXON

Gene Symbol:KIF21A
Accession:XM_017019611
Location:3UTRS;EXON

Gene Symbol:KIF21A
Accession:XM_017019610
Location:3UTRS;EXON

Gene Symbol:KIF21A
Accession:NM_001378439
Location:3UTRS;EXON

Gene Symbol:KIF21A
Accession:XM_005269012
Location:3UTRS;EXON

Gene Symbol:KIF21A
Accession:XM_005269009
Location:3UTRS;EXON

Gene Symbol:KIF21A
Accession:XM_006719494
Location:3UTRS;EXON

Gene Symbol:KIF21A
Accession:XM_047429129
Location:3UTRS;EXON

Gene Symbol:KIF21A
Accession:XM_005269013
Location:3UTRS;EXON

Gene Symbol:KIF21A
Accession:XM_017019608
Location:3UTRS;EXON

Gene Symbol:KIF21A
Accession:NM_001378440
Location:3UTRS;EXON

Gene Symbol:KIF21A
Accession:XM_047429130
Location:3UTRS;EXON

Gene Symbol:KIF21A
Accession:XM_047429126
Location:3UTRS;EXON

Gene Symbol:KIF21A
Accession:NM_001173463
Location:3UTRS;EXON

Gene Symbol:KIF21A
Accession:NM_001173464
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001113698 CLINVAR
dbSNP (RS) rs767760567 CLINVAR
MedGen C1851102 CLINVAR
NCBI Gene KIF21A CLINVAR
OMIM 135700 CLINVAR
  608283 CLINVAR