RGD:11631556 Rat Genome Database

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Variant: RGD:11631556 -  Homo sapiens

RGD ID: 11631556
RS ID: rs1053751
ClinVar ID: CV346416
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CHRNE  MINK1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 17 4,801,286
GRCh38 17 4,897,991
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_008029.2:g.10085G>A
NC_000017.11:g.4897991C>T
NC_000017.10:g.4801286C>T
LRG_1254:g.10085G>A
More... 		01/12/2018 3 prime utr variant benign
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:MINK1
Accession:XM_017024708
Location:3UTRS;EXON

Gene Symbol:MINK1
Accession:NM_001024937
Location:3UTRS;EXON

Gene Symbol:CHRNE
Accession:NM_000080
Location:3UTRS;EXON

Gene Symbol:MINK1
Accession:NM_001321236
Location:3UTRS;EXON

Gene Symbol:MINK1
Accession:XM_047436172
Location:3UTRS;EXON

Gene Symbol:MINK1
Accession:NM_153827
Location:3UTRS;EXON

Gene Symbol:MINK1
Accession:XM_006721531
Location:3UTRS;EXON

Gene Symbol:MINK1
Accession:XM_047436175
Location:3UTRS;EXON

Gene Symbol:MINK1
Accession:XM_017024704
Location:3UTRS;EXON

Gene Symbol:MINK1
Accession:XM_017024707
Location:3UTRS;EXON

Gene Symbol:MINK1
Accession:XM_047436173
Location:3UTRS;EXON

Gene Symbol:MINK1
Accession:XM_047436178
Location:3UTRS;EXON

Gene Symbol:MINK1
Accession:XM_006721536
Location:3UTRS;EXON

Gene Symbol:MINK1
Accession:XM_047436177
Location:3UTRS;EXON

Gene Symbol:MINK1
Accession:XM_047436171
Location:3UTRS;EXON

Gene Symbol:MINK1
Accession:NM_015716
Location:3UTRS;EXON

Gene Symbol:MINK1
Accession:XM_047436174
Location:3UTRS;EXON

Gene Symbol:MINK1
Accession:NM_170663
Location:3UTRS;EXON

Gene Symbol:MINK1
Accession:XM_006721532
Location:3UTRS;EXON

Gene Symbol:MINK1
Accession:XM_047436166
Location:3UTRS;EXON

Gene Symbol:MINK1
Accession:XM_047436165
Location:3UTRS;EXON

Gene Symbol:MINK1
Accession:XM_047436169
Location:3UTRS;EXON

Gene Symbol:CHRNE
Accession:XM_017024115
Location:3UTRS;EXON

Gene Symbol:MINK1
Accession:XM_047436170
Location:3UTRS;EXON

Gene Symbol:MINK1
Accession:XM_047436167
Location:3UTRS;EXON

Gene Symbol:MINK1
Accession:XM_047436176
Location:3UTRS;EXON

Gene Symbol:MINK1
Accession:XM_011523906
Location:3UTRS;EXON

Gene Symbol:MINK1
Accession:XM_017024705
Location:3UTRS;EXON

Gene Symbol:MINK1
Accession:XM_017024706
Location:3UTRS;EXON

Gene Symbol:MINK1
Accession:XM_047436168
Location:3UTRS;EXON

Gene Symbol:MINK1
Accession:XM_047436179
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000380686 CLINVAR
dbSNP (RS) rs1053751 CLINVAR
MedGen C0751882 CLINVAR
NCBI Gene CHRNE CLINVAR
  MINK1 CLINVAR
OMIM 100725 CLINVAR
  609426 CLINVAR