RGD:156043468 Rat Genome Database

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Variant: RGD:156043468 -  Homo sapiens

RGD ID: 156043468
ClinVar ID: CV2127072
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: IGSF10  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 3 151,162,702
GRCh38 3 151,444,914
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001385060.1:c.5062+5G>A
NM_001385062.1:c.5062+5G>A
NM_001385063.1:c.5062+5G>A
NM_178822.5:c.5062+5G>A
More... 		01/15/2024 intron variant benign IGSF10-related condition; none provided

Variant Details
Variant Transcripts
Gene Symbol:IGSF10
Accession:NM_178822
Location:INTRON

Gene Symbol:IGSF10
Accession:NM_001178145
Location:INTRON

Gene Symbol:IGSF10
Accession:NM_001178146
Location:INTRON

Gene Symbol:IGSF10
Accession:XM_011512709
Location:INTRON

Gene Symbol:IGSF10
Accession:XM_011512708
Location:INTRON

Gene Symbol:IGSF10
Accession:NM_001385061
Location:INTRON

Gene Symbol:IGSF10
Accession:NM_001385060
Location:INTRON

Gene Symbol:IGSF10
Accession:NM_001385062
Location:INTRON

Gene Symbol:IGSF10
Accession:NM_001385063
Location:INTRON

Gene Symbol:IGSF10
Accession:XM_047448015
Location:INTRON

Gene Symbol:IGSF10
Accession:XM_047448013
Location:INTRON

Gene Symbol:IGSF10
Accession:XM_047448011
Location:INTRON

Gene Symbol:IGSF10
Accession:XM_047448016
Location:INTRON

Gene Symbol:IGSF10
Accession:XM_047448014
Location:INTRON

Gene Symbol:IGSF10
Accession:XM_047448012
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002949710 CLINVAR
  RCV003906413 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene IGSF10 CLINVAR
OMIM 617351 CLINVAR