rs10849 Rat Genome Database

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Variant: rs10849 -  Homo sapiens

RGD ID: 8592250
RS ID: rs10849
ClinVar ID: CV95059
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LRRFIP2  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 3 37,095,070
GRCh38 3 37,053,579
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_216t1:c.*2926C>T
LRG_216:g.65230C>T
NG_007109.2:g.65230C>T
NC_000003.12:g.37053579C>T
More... 		09/05/2013 3 prime utr variant benign none provided
Disease Annotations     Click to see Annotation Detail View
Lynch syndrome  (IAGP)


Variant Details
Variant Transcripts
Gene Symbol:LRRFIP2
Accession:XM_005265540
Location:3UTRS;EXON

Gene Symbol:LRRFIP2
Accession:XM_047449202
Location:3UTRS;EXON

Gene Symbol:LRRFIP2
Accession:XM_011534217
Location:3UTRS;EXON

Gene Symbol:LRRFIP2
Accession:XM_017007472
Location:3UTRS;EXON

Gene Symbol:LRRFIP2
Accession:NM_001348310
Location:3UTRS;EXON

Gene Symbol:LRRFIP2
Accession:XM_024453826
Location:3UTRS;EXON

Gene Symbol:LRRFIP2
Accession:XM_047449204
Location:3UTRS;EXON

Gene Symbol:LRRFIP2
Accession:XM_005265539
Location:3UTRS;EXON

Gene Symbol:LRRFIP2
Accession:XM_006713389
Location:3UTRS;EXON

Gene Symbol:LRRFIP2
Accession:XM_011534219
Location:3UTRS;EXON

Gene Symbol:LRRFIP2
Accession:NM_001348297
Location:3UTRS;EXON

Gene Symbol:LRRFIP2
Accession:NM_001348300
Location:3UTRS;EXON

Gene Symbol:LRRFIP2
Accession:NM_001348298
Location:3UTRS;EXON

Gene Symbol:LRRFIP2
Accession:NM_001348302
Location:3UTRS;EXON

Gene Symbol:LRRFIP2
Accession:XM_024453824
Location:3UTRS;EXON

Gene Symbol:LRRFIP2
Accession:XM_024453820
Location:3UTRS;EXON

Gene Symbol:LRRFIP2
Accession:XM_047449206
Location:3UTRS;EXON

Gene Symbol:LRRFIP2
Accession:XM_005265551
Location:3UTRS;EXON

Gene Symbol:LRRFIP2
Accession:XM_006713393
Location:3UTRS;EXON

Gene Symbol:LRRFIP2
Accession:XM_006713392
Location:3UTRS;EXON

Gene Symbol:LRRFIP2
Accession:XM_017007476
Location:3UTRS;EXON

Gene Symbol:LRRFIP2
Accession:NM_001282691
Location:3UTRS;EXON

Gene Symbol:LRRFIP2
Accession:XM_006713396
Location:3UTRS;EXON

Gene Symbol:LRRFIP2
Accession:XM_017007469
Location:3UTRS;EXON

Gene Symbol:LRRFIP2
Accession:NM_001348305
Location:3UTRS;EXON

Gene Symbol:LRRFIP2
Accession:XM_024453821
Location:3UTRS;EXON

Gene Symbol:LRRFIP2
Accession:XM_047449207
Location:3UTRS;EXON

Gene Symbol:LRRFIP2
Accession:XM_017007473
Location:3UTRS;EXON

Gene Symbol:LRRFIP2
Accession:NM_001348304
Location:3UTRS;EXON

Gene Symbol:LRRFIP2
Accession:XM_047449203
Location:3UTRS;EXON

Gene Symbol:LRRFIP2
Accession:XM_006713388
Location:3UTRS;EXON

Gene Symbol:LRRFIP2
Accession:XM_006713397
Location:3UTRS;EXON

Gene Symbol:LRRFIP2
Accession:XM_006713390
Location:3UTRS;EXON

Gene Symbol:LRRFIP2
Accession:XM_017007479
Location:3UTRS;EXON

Gene Symbol:LRRFIP2
Accession:XM_017007467
Location:3UTRS;EXON

Gene Symbol:LRRFIP2
Accession:NM_001348303
Location:3UTRS;EXON

Gene Symbol:LRRFIP2
Accession:XM_011534218
Location:3UTRS;EXON

Gene Symbol:LRRFIP2
Accession:NM_001348299
Location:3UTRS;EXON

Gene Symbol:LRRFIP2
Accession:NM_001348309
Location:3UTRS;EXON

Gene Symbol:LRRFIP2
Accession:NM_001348306
Location:3UTRS;EXON

Gene Symbol:LRRFIP2
Accession:XM_047449205
Location:3UTRS;EXON

Gene Symbol:LRRFIP2
Accession:NM_001348301
Location:3UTRS;EXON

Gene Symbol:LRRFIP2
Accession:NM_006309
Location:3UTRS;EXON

Gene Symbol:LRRFIP2
Accession:XM_011534222
Location:3UTRS;EXON

Gene Symbol:LRRFIP2
Accession:NM_001134369
Location:3UTRS;EXON

Gene Symbol:LRRFIP2
Accession:NM_001348311
Location:3UTRS;EXON

Gene Symbol:LRRFIP2
Accession:NM_001348307
Location:3UTRS;EXON

Gene Symbol:LRRFIP2
Accession:NM_017724
Location:3UTRS;EXON

Gene Symbol:LRRFIP2
Accession:XM_017007471
Location:3UTRS;EXON

Gene Symbol:LRRFIP2
Accession:XM_047449208
Location:3UTRS;EXON

Gene Symbol:LRRFIP2
Accession:XM_006713385
Location:3UTRS;EXON

Gene Symbol:LRRFIP2
Accession:XM_006713387
Location:3UTRS;EXON

Gene Symbol:LRRFIP2
Accession:XM_047449201
Location:3UTRS;EXON

Gene Symbol:LRRFIP2
Accession:XM_006713395
Location:3UTRS;EXON

Gene Symbol:LRRFIP2
Accession:NM_001348308
Location:3UTRS;EXON

Gene Symbol:LRRFIP2
Accession:NR_145514
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:25741868  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000075054 CLINVAR
  RCV004707904 CLINVAR
dbSNP (RS) rs10849 CLINVAR
MedGen C3661900 CLINVAR
  C4552100 CLINVAR
NCBI Gene LRRFIP2 CLINVAR
  MLH1 CLINVAR
OMIM 120436 CLINVAR
  614043 CLINVAR