Product Details

SNP ID
rs148442580
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:142075884 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGGTTGACACAAGAATTGCCAAAAC[C/T]GAGAACCCGGGCAACTAAGGTGACA
Phenotype
MIM: 162341
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
NMBR PubMed Links

Gene Details

Gene
NMBR
Gene Name
neuromedin B receptor
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001324307.1 614 Missense Mutation AGT,GGT S165G NP_001311236.1
NM_001324308.1 614 Missense Mutation AGT,GGT S165G NP_001311237.1
NM_002511.3 614 Missense Mutation AGT,GGT S313G NP_002502.2
XM_011535846.1 614 Missense Mutation AGT,GGT S206G XP_011534148.1
XM_017010901.1 614 Missense Mutation AGT,GGT S224G XP_016866390.1
XM_017010902.1 614 Missense Mutation AGT,GGT S165G XP_016866391.1

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