rs886063410 Rat Genome Database

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Variant: rs886063410 -  Homo sapiens

RGD ID: 11659618
RS ID: rs886063410
ClinVar ID: CV316607
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: GSN  
Reference Nucleotide: -
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 9 124,095,005
GRCh38 9 121,332,727
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000177.5:c.*124_*125insC
NM_001127662.2:c.*124_*125insC
NM_001127663.2:c.*124_*125insC
NM_001353076.2:c.*124_*125insC
More... 		06/14/2016 3 prime utr variant uncertain significance
Disease Annotations     Click to see Annotation Detail View
amyloidosis  (IAGP)

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
Amyloidosis  (IAGP)

Variant Details
Variant Transcripts
Gene Symbol:GSN
Accession:NM_001258029
Location:3UTRS;EXON

Gene Symbol:GSN
Accession:XM_017014645
Location:3UTRS;EXON

Gene Symbol:GSN
Accession:NM_001353060
Location:3UTRS;EXON

Gene Symbol:GSN
Accession:NM_001353074
Location:3UTRS;EXON

Gene Symbol:GSN
Accession:NM_001353071
Location:3UTRS;EXON

Gene Symbol:GSN
Accession:NM_001353055
Location:3UTRS;EXON

Gene Symbol:GSN
Accession:NM_001353063
Location:3UTRS;EXON

Gene Symbol:GSN
Accession:NM_001353077
Location:3UTRS;EXON

Gene Symbol:GSN
Accession:NM_001353069
Location:3UTRS;EXON

Gene Symbol:GSN
Accession:XM_047423265
Location:3UTRS;EXON

Gene Symbol:GSN
Accession:XM_011518594
Location:3UTRS;EXON

Gene Symbol:GSN
Accession:NM_001353068
Location:3UTRS;EXON

Gene Symbol:GSN
Accession:XM_047423269
Location:3UTRS;EXON

Gene Symbol:GSN
Accession:NM_001127667
Location:3UTRS;EXON

Gene Symbol:GSN
Accession:NM_000177
Location:3UTRS;EXON

Gene Symbol:GSN
Accession:NM_001353066
Location:3UTRS;EXON

Gene Symbol:GSN
Accession:XM_047423267
Location:3UTRS;EXON

Gene Symbol:GSN
Accession:XM_005251944
Location:3UTRS;EXON

Gene Symbol:GSN
Accession:NM_001127665
Location:3UTRS;EXON

Gene Symbol:GSN
Accession:NM_001353078
Location:3UTRS;EXON

Gene Symbol:GSN
Accession:NM_001353062
Location:3UTRS;EXON

Gene Symbol:GSN
Accession:XM_047423266
Location:3UTRS;EXON

Gene Symbol:GSN
Accession:NM_001127662
Location:3UTRS;EXON

Gene Symbol:GSN
Accession:NM_001353054
Location:3UTRS;EXON

Gene Symbol:GSN
Accession:NM_001353073
Location:3UTRS;EXON

Gene Symbol:GSN
Accession:NM_001353072
Location:3UTRS;EXON

Gene Symbol:GSN
Accession:NM_001353057
Location:3UTRS;EXON

Gene Symbol:GSN
Accession:XM_047423273
Location:3UTRS;EXON

Gene Symbol:GSN
Accession:NM_001353053
Location:3UTRS;EXON

Gene Symbol:GSN
Accession:NM_001353075
Location:3UTRS;EXON

Gene Symbol:GSN
Accession:NM_001127663
Location:3UTRS;EXON

Gene Symbol:GSN
Accession:NM_001353076
Location:3UTRS;EXON

Gene Symbol:GSN
Accession:XM_047423268
Location:3UTRS;EXON

Gene Symbol:GSN
Accession:NM_001258030
Location:3UTRS;EXON

Gene Symbol:GSN
Accession:NM_001353061
Location:3UTRS;EXON

Gene Symbol:GSN
Accession:NM_001353058
Location:3UTRS;EXON

Gene Symbol:GSN
Accession:NM_001353070
Location:3UTRS;EXON

Gene Symbol:GSN
Accession:NM_001127666
Location:3UTRS;EXON

Gene Symbol:GSN
Accession:NM_001353065
Location:3UTRS;EXON

Gene Symbol:GSN
Accession:XM_047423272
Location:3UTRS;EXON

Gene Symbol:GSN
Accession:NM_001127664
Location:3UTRS;EXON

Gene Symbol:GSN
Accession:NM_198252
Location:3UTRS;EXON

Gene Symbol:GSN
Accession:XM_011518585
Location:3UTRS;EXON

Gene Symbol:GSN
Accession:NM_001353059
Location:3UTRS;EXON

Gene Symbol:GSN
Accession:XM_047423270
Location:3UTRS;EXON

Gene Symbol:GSN
Accession:NM_001353056
Location:3UTRS;EXON

Gene Symbol:GSN
Accession:NM_001353067
Location:3UTRS;EXON

Gene Symbol:GSN
Accession:XM_047423271
Location:3UTRS;EXON

Gene Symbol:GSN
Accession:NM_001353064
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000359858 CLINVAR
dbSNP (RS) rs886063410 CLINVAR
MedGen C0002726 CLINVAR
NCBI Gene GSN CLINVAR
OMIM 137350 CLINVAR