RGD:405177642 Rat Genome Database
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Summary
ClinVar Data
Variant Details
Variant Transcripts
Variant Samples
PubMed References
Additional Information
External Database Links
Variant: RGD:405177642 - Homo sapiens
RGD ID:
405177642
ClinVar ID:
CV2912930
Genic Status:
GENIC
Type:
SNV
(SO:0001483)
Associated Genes:
ADGRG1
Reference Nucleotide:
C
Variant Nucleotide:
G
Position
Assembly
Chr
Position
GRCh37
16
57,691,267
GRCh38
16
57,657,355
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
NC_000016.9:g.57691267C>G
NM_001370442.1:c.1012-18C>G
NM_001370434.1:c.1165-18C>G
NM_001370441.1:c.1165-18C>G
NM_001145770.3:c.1168-18C>G
NM_001145771.3:c.1168-18C>G
NM_001145772.3:c.1168-18C>G
NM_001145774.3:c.1168-18C>G
NM_001370428.1:c.1168-18C>G
NM_001370429.1:c.1168-18C>G
NM_001370430.1:c.1168-18C>G
NM_001370431.1:c.1168-18C>G
NM_001370432.1:c.1168-18C>G
NM_001370435.1:c.1168-18C>G
NM_001370436.1:c.1168-18C>G
NM_001370437.1:c.1168-18C>G
NM_005682.7:c.1168-18C>G
NM_001370438.1:c.1168-18C>G
NM_001370439.1:c.1168-18C>G
NM_001370440.1:c.1168-18C>G
NM_201524.4:c.1168-18C>G
NM_201525.4:c.1168-18C>G
NM_001290144.2:c.643-18C>G
NM_001145773.3:c.1183-18C>G
NM_001370433.1:c.1183-18C>G
NM_001290143.2:c.643-18C>G
NM_001370451.1:c.643-18C>G
NM_001370453.1:c.643-18C>G
NM_001370454.1:c.643-18C>G
NM_001290142.2:c.658-18C>G
NG_011643.1:g.42358C>G
NC_000016.10:g.57657355C>G
More...
08/07/2023
intron variant
likely benign
none provided
Variant Details
Variant Transcripts
Gene Symbol:
ADGRG1
Accession:
NM_001145770
Location:
INTRON
Gene Symbol:
ADGRG1
Accession:
XM_005256242
Location:
INTRON
Gene Symbol:
ADGRG1
Accession:
XM_011523468
Location:
INTRON
Gene Symbol:
ADGRG1
Accession:
NM_001370437
Location:
INTRON
Gene Symbol:
ADGRG1
Accession:
XM_006721342
Location:
INTRON
Gene Symbol:
ADGRG1
Accession:
NM_001370429
Location:
INTRON
Gene Symbol:
ADGRG1
Accession:
XM_047434907
Location:
INTRON
Gene Symbol:
ADGRG1
Accession:
XM_047434909
Location:
INTRON
Gene Symbol:
ADGRG1
Accession:
XM_047434913
Location:
INTRON
Gene Symbol:
ADGRG1
Accession:
XM_005256237
Location:
INTRON
Gene Symbol:
ADGRG1
Accession:
XM_005256248
Location:
INTRON
Gene Symbol:
ADGRG1
Accession:
XM_006721340
Location:
INTRON
Gene Symbol:
ADGRG1
Accession:
XM_006721338
Location:
INTRON
Gene Symbol:
ADGRG1
Accession:
NM_001370440
Location:
INTRON
Gene Symbol:
ADGRG1
Accession:
NM_001370432
Location:
INTRON
Gene Symbol:
ADGRG1
Accession:
XM_047434916
Location:
INTRON
Gene Symbol:
ADGRG1
Accession:
NM_005682
Location:
INTRON
Gene Symbol:
ADGRG1
Accession:
NM_001290144
Location:
INTRON
Gene Symbol:
ADGRG1
Accession:
XM_011523462
Location:
INTRON
Gene Symbol:
ADGRG1
Accession:
NM_001370428
Location:
INTRON
Gene Symbol:
ADGRG1
Accession:
NM_201525
Location:
INTRON
Gene Symbol:
ADGRG1
Accession:
XM_005256238
Location:
INTRON
Gene Symbol:
ADGRG1
Accession:
NM_001370438
Location:
INTRON
Gene Symbol:
ADGRG1
Accession:
XM_047434906
Location:
INTRON
Gene Symbol:
ADGRG1
Accession:
NM_001370436
Location:
INTRON
Gene Symbol:
ADGRG1
Accession:
NM_001370451
Location:
INTRON
Gene Symbol:
ADGRG1
Accession:
NM_001370441
Location:
INTRON
Gene Symbol:
ADGRG1
Accession:
NM_001370430
Location:
INTRON
Gene Symbol:
ADGRG1
Accession:
XM_006721347
Location:
INTRON
Gene Symbol:
ADGRG1
Accession:
NM_001290143
Location:
INTRON
Gene Symbol:
ADGRG1
Accession:
XM_011523466
Location:
INTRON
Gene Symbol:
ADGRG1
Accession:
NM_001370439
Location:
INTRON
Gene Symbol:
ADGRG1
Accession:
XM_005256255
Location:
INTRON
Gene Symbol:
ADGRG1
Accession:
XM_005256244
Location:
INTRON
Gene Symbol:
ADGRG1
Accession:
NM_001370454
Location:
INTRON
Gene Symbol:
ADGRG1
Accession:
XM_005256245
Location:
INTRON
Gene Symbol:
ADGRG1
Accession:
XM_005256254
Location:
INTRON
Gene Symbol:
ADGRG1
Accession:
NM_201524
Location:
INTRON
Gene Symbol:
ADGRG1
Accession:
NM_001145771
Location:
INTRON
Gene Symbol:
ADGRG1
Accession:
XM_047434912
Location:
INTRON
Gene Symbol:
ADGRG1
Accession:
XM_047434910
Location:
INTRON
Gene Symbol:
ADGRG1
Accession:
XM_047434911
Location:
INTRON
Gene Symbol:
ADGRG1
Accession:
NM_001370442
Location:
INTRON
Gene Symbol:
ADGRG1
Accession:
NM_001370433
Location:
INTRON
Gene Symbol:
ADGRG1
Accession:
NM_001145772
Location:
INTRON
Gene Symbol:
ADGRG1
Accession:
NM_001370435
Location:
INTRON
Gene Symbol:
ADGRG1
Accession:
XM_005256252
Location:
INTRON
Gene Symbol:
ADGRG1
Accession:
XM_006721339
Location:
INTRON
Gene Symbol:
ADGRG1
Accession:
NM_001370453
Location:
INTRON
Gene Symbol:
ADGRG1
Accession:
NM_001370434
Location:
INTRON
Gene Symbol:
ADGRG1
Accession:
XM_047434915
Location:
INTRON
Gene Symbol:
ADGRG1
Accession:
XM_005256240
Location:
INTRON
Gene Symbol:
ADGRG1
Accession:
XM_005256239
Location:
INTRON
Gene Symbol:
ADGRG1
Accession:
XM_005256241
Location:
INTRON
Gene Symbol:
ADGRG1
Accession:
NM_001290142
Location:
INTRON
Gene Symbol:
ADGRG1
Accession:
NM_001370431
Location:
INTRON
Gene Symbol:
ADGRG1
Accession:
XM_047434908
Location:
INTRON
Gene Symbol:
ADGRG1
Accession:
NM_001145773
Location:
INTRON
Gene Symbol:
ADGRG1
Accession:
NM_001145774
Location:
INTRON
Gene Symbol:
ADGRG1
Accession:
XM_005256246
Location:
INTRON
Gene Symbol:
ADGRG1
Accession:
XM_017023892
Location:
INTRON
Gene Symbol:
ADGRG1
Accession:
XM_047434914
Location:
INTRON
.
Variant Samples
1 to 1 of 1 rows
10
20
30
40
100
All Rows
ClinVar GRCh37
ClinVar GRCh38
1 to 1 of 1 rows
10
20
30
40
100
All Rows
Additional References at PubMed
1 to 1 of 1 rows
10
20
30
40
100
All Rows
PMID:
28492532
1 to 1 of 1 rows
10
20
30
40
100
All Rows
Additional Information
External Database Links
1 to 4 of 4 rows
3
5
10
20
40
100
All Rows
Database
Acc Id
Source(s)
ClinVar
RCV003563678
CLINVAR
MedGen
C3661900
CLINVAR
NCBI Gene
ADGRG1
CLINVAR
OMIM
604110
CLINVAR
1 to 4 of 4 rows
3
5
10
20
40
100
All Rows