rs7294518 Rat Genome Database

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Variant: rs7294518 -  Homo sapiens

RGD ID: 150512568
RS ID: rs7294518
ClinVar ID: CV1284952
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: RACGAP1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 12 50,387,870
GRCh38 12 49,994,087
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001320007.2:c.1117+44G>A
NM_001320005.2:c.1165+44G>A
NM_001126103.3:c.1339+44G>A
NM_001126104.3:c.1339+44G>A
More...
06/21/2021 intron variant benign none provided

Gene Symbol:RACGAP1
Accession:NM_001126103
Location:INTRON

Gene Symbol:RACGAP1
Accession:NM_013277
Location:INTRON

Gene Symbol:RACGAP1
Accession:NM_001126104
Location:INTRON

Gene Symbol:RACGAP1
Accession:XM_006719359
Location:INTRON

Gene Symbol:RACGAP1
Accession:XM_011538238
Location:INTRON

Gene Symbol:RACGAP1
Accession:NM_001320004
Location:INTRON

Gene Symbol:RACGAP1
Accession:NM_001320005
Location:INTRON

Gene Symbol:RACGAP1
Accession:NM_001320003
Location:INTRON

Gene Symbol:RACGAP1
Accession:NM_001320007
Location:INTRON

Gene Symbol:RACGAP1
Accession:NM_001319999
Location:INTRON

Gene Symbol:RACGAP1
Accession:NM_001320006
Location:INTRON

Gene Symbol:RACGAP1
Accession:NM_001320000
Location:INTRON

Gene Symbol:RACGAP1
Accession:NM_001320002
Location:INTRON

Gene Symbol:RACGAP1
Accession:NM_001320001
Location:INTRON

Gene Symbol:RACGAP1
Accession:XM_017019227
Location:INTRON

Gene Symbol:RACGAP1
Accession:XM_017019224
Location:INTRON

Gene Symbol:RACGAP1
Accession:XM_017019222
Location:INTRON

Gene Symbol:RACGAP1
Accession:XM_017019223
Location:INTRON

Gene Symbol:RACGAP1
Accession:XM_017019221
Location:INTRON

Gene Symbol:RACGAP1
Accession:XM_017019225
Location:INTRON

Gene Symbol:RACGAP1
Accession:XM_017019226
Location:INTRON

Gene Symbol:RACGAP1
Accession:XM_024448958
Location:INTRON

Gene Symbol:RACGAP1
Accession:XM_047428750
Location:INTRON

Gene Symbol:RACGAP1
Accession:XM_047428748
Location:INTRON

Gene Symbol:RACGAP1
Accession:XM_047428747
Location:INTRON

Gene Symbol:RACGAP1
Accession:XM_047428751
Location:INTRON

Gene Symbol:RACGAP1
Accession:XM_047428746
Location:INTRON

Gene Symbol:RACGAP1
Accession:XM_047428749
Location:INTRON

Gene Symbol:RACGAP1
Accession:XM_047428745
Location:INTRON

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Database
Acc Id
Source(s)
ClinVar RCV001721821 CLINVAR
dbSNP (RS) rs7294518 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene RACGAP1 CLINVAR
OMIM 604980 CLINVAR