RGD:12846238 Rat Genome Database

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Variant: RGD:12846238 -  Homo sapiens

RGD ID: 12846238
RS ID: rs1057522504
ClinVar ID: CV367607
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC127401499  MFSD8  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 4 128,886,356
GRCh38 4 127,965,201
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_152778.2:c.-68C>T
NG_008657.1:g.5784C>T
NC_000004.12:g.127965201G>A
NC_000004.11:g.128886356G>A
More... 		05/26/2016 5 prime utr variant likely benign AllHighlyPenetrant

Variant Details
Variant Transcripts
Gene Symbol:MFSD8
Accession:XM_017007989
Location:5UTRS;EXON

Gene Symbol:MFSD8
Accession:XM_047449997
Location:5UTRS;EXON

Gene Symbol:MFSD8
Accession:NM_152778
Location:5UTRS;EXON

Gene Symbol:MFSD8
Accession:XM_005262898
Location:5UTRS;EXON

Gene Symbol:
Accession:
Location:5UTRS;EXON

Gene Symbol:MFSD8
Accession:XM_047449994
Location:5UTRS;EXON

Gene Symbol:MFSD8
Accession:XM_047449999
Location:5UTRS;INTRON

Gene Symbol:
Accession:
Location:5UTRS;INTRON

Gene Symbol:MFSD8
Accession:XM_024453982
Location:5UTRS;INTRON

Gene Symbol:MFSD8
Accession:NM_001371590
Location:5UTRS;INTRON

Gene Symbol:MFSD8
Accession:NM_001410765
Location:5UTRS;INTRON

Gene Symbol:MFSD8
Accession:XM_047449995
Location:5UTRS;INTRON

Gene Symbol:MFSD8
Accession:XM_047449992
Location:5UTRS;INTRON

Gene Symbol:MFSD8
Accession:XM_047449993
Location:5UTRS;INTRON

Gene Symbol:MFSD8
Accession:XM_047449998
Location:5UTRS;INTRON

Gene Symbol:MFSD8
Accession:NM_001371593
Location:INTRON

Gene Symbol:MFSD8
Accession:NM_001363520
Location:INTRON

Gene Symbol:MFSD8
Accession:NM_001371596
Location:INTRON

Gene Symbol:MFSD8
Accession:NM_001371591
Location:INTRON

Gene Symbol:MFSD8
Accession:NM_001371592
Location:INTRON

Gene Symbol:MFSD8
Accession:NM_001363521
Location:INTRON

Gene Symbol:MFSD8
Accession:NM_001371594
Location:INTRON

Gene Symbol:MFSD8
Accession:NM_001371595
Location:INTRON

Gene Symbol:MFSD8
Accession:NM_001410766
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000441264 CLINVAR
dbSNP (RS) rs1057522504 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene MFSD8 CLINVAR
OMIM 611124 CLINVAR