Product Details

SNP ID

rs1983764

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.14:50725941 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

GTGAGGTGGGTGAACAGAGATGACC[A/G]GGTAGGCTCACTTGTTCTTTGAGCT

Phenotype

MIM: 608684

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

NIN PubMed Links

Gene Details

Gene

NIN

Gene Name

ninein

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_016350.4	6246	Silent Mutation	CCC,CCT	P1355P	NP_057434.4
NM_020921.3	6246	Intron			NP_065972.3
NM_182944.2	6246	Intron			NP_891989.2
NM_182946.1	6246	Silent Mutation	CCC,CCT	P2068P	NP_891991.1
XM_011536817.1	6246	Intron			XP_011535119.1
XM_011536819.2	6246	Intron			XP_011535121.1
XM_011536822.1	6246	Intron			XP_011535124.1
XM_011536823.2	6246	Silent Mutation	CCC,CCT	P2074P	XP_011535125.1

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