rs61753777 Rat Genome Database

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Variant: rs61753777 -  Homo sapiens

RGD ID: 15189207
RS ID: rs61753777
ClinVar ID: CV724167
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MMP7  
Reference Nucleotide: T
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 11 102,398,672
GRCh38 11 102,527,941
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000011.10:g.102527941T>G
NM_002423.4:c.151A>C
NM_002423.5:c.151A>C
NC_000011.9:g.102398672T>G
More... 		08/05/2018 missense variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:MMP7
Accession:NM_002423
Location:EXON
Amino Acid Prediction: N to H (nonsynonymous)
Amino Acid Position: 51
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MRLTVLCAVCLLPGSLALPLPQEAGGMSELQWEQAQDYLKRFYLYDSETKHANSLEAKLKEMQKFFGLPITGMLNSRVIE
IMQKPRCGVPDVAEYSLFPNSPKWTSKVVTYRIVSYTRDLPHITVDRLVSKALNMWGKEIPLHFRKVVWGTADIMIGFAR
GAHGDSYPFDGPGNTLAHAFAPGTGLGGDAHFDEDERWTDGSSLGINFLYAATHELGHSLGMGHSSDPNAVMYPTYGNGD
PQNFKLSQDDIKGIQKLYGKRSNSRKK*
Variant Samples
Additional References at PubMed
PMID:25741868   PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000887754 CLINVAR
dbSNP (RS) rs61753777 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene MMP7 CLINVAR
OMIM 178990 CLINVAR