RGD:150413104 Rat Genome Database

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Variant: RGD:150413104 -  Homo sapiens

RGD ID: 150413104
RS ID: rs59863978
ClinVar ID: CV1198913
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FOXN1  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 17 26,850,905
GRCh38 17 28,523,887
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_007260.1:g.4947G>T
NC_000017.11:g.28523887G>T
NM_001369369.1:c.-14-69G>T
LRG_61:g.4947G>T
More... 		09/02/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:FOXN1
Accession:XM_011525358
Location:5UTRS;INTRON

Gene Symbol:FOXN1
Accession:NM_001369369
Location:5UTRS;INTRON

Gene Symbol:FOXN1
Accession:XM_011525368
Location:5UTRS;INTRON

Gene Symbol:FOXN1
Accession:XM_017025229
Location:5UTRS;INTRON

Gene Symbol:FOXN1
Accession:XM_017025230
Location:5UTRS;INTRON

Gene Symbol:FOXN1
Accession:XM_011525362
Location:5UTRS;INTRON

Gene Symbol:FOXN1
Accession:XM_011525359
Location:5UTRS;INTRON

Gene Symbol:FOXN1
Accession:XM_017025231
Location:5UTRS;INTRON

Gene Symbol:FOXN1
Accession:XM_047436939
Location:INTRON

Gene Symbol:FOXN1
Accession:XM_011525369
Location:INTRON

Gene Symbol:FOXN1
Accession:XM_011525367
Location:INTRON

Gene Symbol:FOXN1
Accession:NM_003593
Location:INTRON

Gene Symbol:FOXN1
Accession:XM_011525370
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001574522 CLINVAR
dbSNP (RS) rs59863978 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene FOXN1 CLINVAR
OMIM 600838 CLINVAR