rs372834388 Rat Genome Database

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Variant: rs372834388 -  Homo sapiens

RGD ID: 15145639
RS ID: rs372834388
ClinVar ID: CV787865
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: KIF21A  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 12 39,751,042
GRCh38 12 39,357,240
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001173463.2:c.1405+8G>C
NM_001173464.2:c.1405+8G>C
NM_001173465.2:c.1405+8G>C
NM_017641.4:c.1405+8G>C
More...
12/31/2019 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:KIF21A
Accession:XM_047429120
Location:INTRON

Gene Symbol:KIF21A
Accession:XM_047429119
Location:INTRON

Gene Symbol:KIF21A
Accession:NM_001378440
Location:INTRON

Gene Symbol:KIF21A
Accession:XM_047429128
Location:INTRON

Gene Symbol:KIF21A
Accession:NM_001173463
Location:INTRON

Gene Symbol:KIF21A
Accession:XM_017019608
Location:INTRON

Gene Symbol:KIF21A
Accession:XM_005269014
Location:INTRON

Gene Symbol:KIF21A
Accession:XM_017019609
Location:INTRON

Gene Symbol:KIF21A
Accession:XM_047429125
Location:INTRON

Gene Symbol:KIF21A
Accession:XM_005269009
Location:INTRON

Gene Symbol:KIF21A
Accession:XM_005269012
Location:INTRON

Gene Symbol:KIF21A
Accession:NM_001378441
Location:INTRON

Gene Symbol:KIF21A
Accession:XM_047429132
Location:INTRON

Gene Symbol:KIF21A
Accession:NM_017641
Location:INTRON

Gene Symbol:KIF21A
Accession:NM_001173464
Location:INTRON

Gene Symbol:KIF21A
Accession:XM_011538556
Location:INTRON

Gene Symbol:KIF21A
Accession:XM_017019607
Location:INTRON

Gene Symbol:KIF21A
Accession:XM_047429126
Location:INTRON

Gene Symbol:KIF21A
Accession:NM_001173465
Location:INTRON

Gene Symbol:KIF21A
Accession:XM_017019611
Location:INTRON

Gene Symbol:KIF21A
Accession:XM_047429133
Location:INTRON

Gene Symbol:KIF21A
Accession:XM_006719494
Location:INTRON

Gene Symbol:KIF21A
Accession:XM_005269013
Location:INTRON

Gene Symbol:KIF21A
Accession:NM_001378439
Location:INTRON

Gene Symbol:KIF21A
Accession:XM_047429123
Location:INTRON

Gene Symbol:KIF21A
Accession:XM_047429129
Location:INTRON

Gene Symbol:KIF21A
Accession:XM_047429130
Location:INTRON

Gene Symbol:KIF21A
Accession:XM_047429121
Location:INTRON

Gene Symbol:KIF21A
Accession:XM_006719493
Location:INTRON

Gene Symbol:KIF21A
Accession:XM_017019610
Location:INTRON

Gene Symbol:KIF21A
Accession:XM_005269011
Location:INTRON

Gene Symbol:KIF21A
Accession:XM_047429127
Location:INTRON

Gene Symbol:KIF21A
Accession:XM_047429122
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000983699 CLINVAR
dbSNP (RS) rs372834388 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene KIF21A CLINVAR
OMIM 608283 CLINVAR