Product Details

SNP ID
rs142454996
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.6:22287550 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGCCATCTGCAGGGATGGAAGTCCC[A/G]ACCAGACAGGGTAGATCTCATTTTC
Phenotype
MIM: 176760
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
PRL PubMed Links

Gene Details

Gene
PRL
Gene Name
prolactin
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000948.5 774 Missense Mutation TCG,TTG S179L NP_000939.1
NM_001163558.2 774 Missense Mutation TCG,TTG S179L NP_001157030.1
XM_011514753.2 774 Missense Mutation TCG,TTG S180L XP_011513055.1
XM_011514754.2 774 Missense Mutation TCG,TTG S180L XP_011513056.1

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