Product Details

SNP ID

rs16824007

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:183123805 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GGCACATGCAGAAGCACGCAAGATT[C/T]CGCGGTGTGGAGGGTTCGTGGGTGC

Phenotype

MIM: 608140

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

NUP35 PubMed Links

Gene Details

Gene

NUP35

Gene Name

nucleoporin 35

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001287584.1	278	Intron			NP_001274513.1
NM_001287585.1	278	Intron			NP_001274514.1
NM_138285.4	278	Intron			NP_612142.2
XM_006712254.2	278	Intron			XP_006712317.1
XM_011510576.2	278	Intron			XP_011508878.1
XM_011510577.2	278	Intron			XP_011508879.1
XM_017003308.1	278	Missense Mutation	CCG,TCG	P10S	XP_016858797.1

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