rs7294518 Rat Genome Database
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Summary
ClinVar Data
Variant Details
Variant Transcripts
Variant Samples
Additional Information
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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
Annotation
Click to see Annotation Summary View
ClinVar Data
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
NM_001319999.2:c.1339+44G>A
NM_001320000.2:c.1339+44G>A
NM_001320001.2:c.1339+44G>A
NM_001320002.2:c.1339+44G>A
NM_001320003.2:c.1339+44G>A
NM_001320004.2:c.1339+44G>A
NM_013277.5:c.1339+44G>A
NM_001320006.2:c.1375+44G>A
NC_000012.12:g.49994087C>T
NC_000012.11:g.50387870C>T
More...
06/21/2021
intron variant
benign
none provided
Variant Details
Variant Transcripts
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
.
Variant Samples
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ClinVar GRCh37
ClinVar GRCh38
1 to 1 of 1 rows
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Additional Information
External Database Links
1 to 5 of 5 rows
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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
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