RGD:11663531 Rat Genome Database

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Variant: RGD:11663531 -  Homo sapiens

RGD ID: 11663531
RS ID: rs886059063
ClinVar ID: CV293665
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MFSD8  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 4 128,839,102
GRCh38 4 127,917,947
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_008657.1:g.53038C>T
NC_000004.12:g.127917947G>A
NC_000004.11:g.128839102G>A
NM_152778.4:c.*2683C>T
More... 		01/12/2018 3 prime utr variant uncertain significance MFSD8-Related Neuronal Ceroid-Lipofuscinosis
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:MFSD8
Accession:NM_001371593
Location:3UTRS;EXON

Gene Symbol:MFSD8
Accession:XM_047449993
Location:3UTRS;EXON

Gene Symbol:MFSD8
Accession:XM_047449992
Location:3UTRS;EXON

Gene Symbol:MFSD8
Accession:NM_152778
Location:3UTRS;EXON

Gene Symbol:MFSD8
Accession:NM_001363521
Location:3UTRS;EXON

Gene Symbol:MFSD8
Accession:NM_001363520
Location:3UTRS;EXON

Gene Symbol:MFSD8
Accession:NM_001371595
Location:3UTRS;EXON

Gene Symbol:MFSD8
Accession:NM_001410766
Location:3UTRS;EXON

Gene Symbol:MFSD8
Accession:NM_001371594
Location:3UTRS;EXON

Gene Symbol:
Accession:
Location:3UTRS;EXON

Gene Symbol:MFSD8
Accession:XM_024453982
Location:3UTRS;EXON

Gene Symbol:MFSD8
Accession:NM_001371590
Location:3UTRS;EXON

Gene Symbol:MFSD8
Accession:NM_001371591
Location:3UTRS;EXON

Gene Symbol:MFSD8
Accession:NM_001371596
Location:3UTRS;EXON

Gene Symbol:MFSD8
Accession:NM_001410765
Location:3UTRS;EXON

Gene Symbol:MFSD8
Accession:NM_001371592
Location:3UTRS;EXON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:MFSD8
Accession:XM_047449999
Location:INTRON

Gene Symbol:MFSD8
Accession:XM_047449997
Location:INTRON

Gene Symbol:MFSD8
Accession:XM_017007989
Location:INTRON

Gene Symbol:MFSD8
Accession:XM_047449994
Location:INTRON

Gene Symbol:MFSD8
Accession:XM_047449995
Location:INTRON

Gene Symbol:MFSD8
Accession:XM_047449998
Location:INTRON

Gene Symbol:MFSD8
Accession:XM_005262898
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000396699 CLINVAR
dbSNP (RS) rs886059063 CLINVAR
MedGen C1838571 CLINVAR
NCBI Gene MFSD8 CLINVAR
OMIM 610951 CLINVAR
  611124 CLINVAR