rs889871814 Rat Genome Database

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Variant: rs889871814 -  Homo sapiens

RGD ID: 151736528
RS ID: rs889871814
ClinVar ID: CV1463594
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MNX1  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 7 156,802,369
GRCh38 7 157,009,675
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_005515.4:c.676A>G
NG_013212.1:g.5979A>G
NC_000007.14:g.157009675T>C
NC_000007.13:g.156802369T>C
More... 		02/20/2023 missense variant uncertain significance none provided

Variant Details
Variant Transcripts
Gene Symbol:MNX1
Accession:NM_005515
Location:EXON
Amino Acid Prediction: M to V (nonsynonymous)
Amino Acid Position: 226
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MEKSKNFRIDALLAVDPPRAASAQSAPLALVTSLAAAASGTGGGGGGGGASGGTSGSCSPASSEPPAAPADRLRAESPSP
PRLLAAHCALLPKPGFLGAGGGGGGTGGGHGGPHHHAHPGAAAAAAAAAAAAAAGGLALGLHPGGAQGGAGLPAQAALYG
HPVYGYSAAAAAAALAGQHPALSYSYPQVQGAHPAHPADPIKLGAGTFQLDQWLRASTAGMILPKVPDFNSQAQSNLLGK
CRRPRTAFTSQQLLELEHQFKLNKYLSRPKRFEVATSLMLTETQVKIWFQNRRMKWKRSKKAKEQAAQEAEKQKGGGGGA
GKGGAEEPGAEELLGPPAPGDKGSGRRLRDLRDSDPEEDEDEDDEDHFPYSNGASVHAASSDCSSEDDSPPPRPSHQPAP
Q*

Gene Symbol:MNX1
Accession:NM_001165255
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001911468 CLINVAR
dbSNP (RS) rs889871814 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene MNX1 CLINVAR
OMIM 142994 CLINVAR