rs1474139972 Rat Genome Database

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Variant: rs1474139972 -  Homo sapiens

RGD ID: 150481694
RS ID: rs1474139972
ClinVar ID: CV1244147
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TRIM37  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 17 57,152,924
GRCh38 17 59,075,563
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001353083.2:c.-52+67G>T
NM_001353085.2:c.222+84G>T
NM_001320990.3:c.318+84G>T
NM_001320987.3:c.582+84G>T
More... 		02/07/2021 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:TRIM37
Accession:XM_017024673
Location:5UTRS;INTRON

Gene Symbol:TRIM37
Accession:NM_001353083
Location:5UTRS;INTRON

Gene Symbol:TRIM37
Accession:NM_001005207
Location:INTRON

Gene Symbol:TRIM37
Accession:NM_015294
Location:INTRON

Gene Symbol:TRIM37
Accession:XM_005257385
Location:INTRON

Gene Symbol:TRIM37
Accession:XM_011524833
Location:INTRON

Gene Symbol:TRIM37
Accession:XM_011524836
Location:INTRON

Gene Symbol:TRIM37
Accession:XM_011524832
Location:INTRON

Gene Symbol:TRIM37
Accession:XM_011524831
Location:INTRON

Gene Symbol:TRIM37
Accession:XM_011524834
Location:INTRON

Gene Symbol:TRIM37
Accession:NM_001320989
Location:INTRON

Gene Symbol:TRIM37
Accession:NM_001320987
Location:INTRON

Gene Symbol:TRIM37
Accession:NM_001320988
Location:INTRON

Gene Symbol:TRIM37
Accession:NM_001320990
Location:INTRON

Gene Symbol:TRIM37
Accession:XM_017024663
Location:INTRON

Gene Symbol:TRIM37
Accession:XM_017024662
Location:INTRON

Gene Symbol:TRIM37
Accession:XM_017024667
Location:INTRON

Gene Symbol:TRIM37
Accession:XM_017024665
Location:INTRON

Gene Symbol:TRIM37
Accession:XM_017024670
Location:INTRON

Gene Symbol:TRIM37
Accession:XM_017024669
Location:INTRON

Gene Symbol:TRIM37
Accession:NM_001353085
Location:INTRON

Gene Symbol:TRIM37
Accession:NM_001353082
Location:INTRON

Gene Symbol:TRIM37
Accession:NM_001353086
Location:INTRON

Gene Symbol:TRIM37
Accession:NM_001353084
Location:INTRON

Gene Symbol:TRIM37
Accession:XM_047436110
Location:INTRON

Gene Symbol:TRIM37
Accession:XM_047436107
Location:INTRON

Gene Symbol:TRIM37
Accession:XM_047436111
Location:INTRON

Gene Symbol:TRIM37
Accession:XM_047436122
Location:INTRON

Gene Symbol:TRIM37
Accession:XM_047436121
Location:INTRON

Gene Symbol:TRIM37
Accession:XM_047436114
Location:INTRON

Gene Symbol:TRIM37
Accession:XM_047436113
Location:INTRON

Gene Symbol:TRIM37
Accession:XM_047436117
Location:INTRON

Gene Symbol:TRIM37
Accession:XM_047436108
Location:INTRON

Gene Symbol:TRIM37
Accession:XM_047436123
Location:INTRON

Gene Symbol:TRIM37
Accession:XM_047436116
Location:INTRON

Gene Symbol:TRIM37
Accession:XM_047436115
Location:INTRON

Gene Symbol:TRIM37
Accession:XM_047436106
Location:INTRON

Gene Symbol:TRIM37
Accession:XM_047436109
Location:INTRON

Gene Symbol:TRIM37
Accession:XM_047436112
Location:INTRON

Gene Symbol:TRIM37
Accession:XM_047436118
Location:INTRON

Gene Symbol:TRIM37
Accession:XM_047436125
Location:INTRON

Gene Symbol:TRIM37
Accession:XM_047436124
Location:INTRON

Gene Symbol:TRIM37
Accession:XM_047436126
Location:INTRON

Gene Symbol:TRIM37
Accession:XM_047436120
Location:INTRON

Gene Symbol:TRIM37
Accession:XM_047436119
Location:INTRON

Gene Symbol:TRIM37
Accession:NR_148347
Location:INTRON;NON-CODING

Gene Symbol:TRIM37
Accession:NR_148346
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001652993 CLINVAR
dbSNP (RS) rs1474139972 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene TRIM37 CLINVAR
OMIM 605073 CLINVAR