Product Details

SNP ID

rs17081095

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.13:24748394 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AGAAATGGGTTTGAATAGAAAATCT[A/G]CAAAAGTATGTTAGCTGTAACTGCC

Phenotype

MIM: 605793

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

RNF17 PubMed Links

Gene Details

Gene

RNF17

Gene Name

ring finger protein 17

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001184993.1		Intron			NP_001171922.1
NM_031277.2		Intron			NP_112567.2
XM_006719846.3		Intron			XP_006719909.1
XM_006719849.2		Intron			XP_006719912.1
XM_006719852.2		Intron			XP_006719915.1
XM_011535152.2		Intron			XP_011533454.1
XM_011535155.2		Intron			XP_011533457.1
XM_011535156.2		Intron			XP_011533458.1
XM_011535157.2		Intron			XP_011533459.1
XM_011535158.2		Intron			XP_011533460.1
XM_011535159.2		Intron			XP_011533461.1
XM_011535160.2		Intron			XP_011533462.1
XM_011535162.1		Intron			XP_011533464.1
XM_011535163.1		Intron			XP_011533465.1
XM_011535164.2		Intron			XP_011533466.1
XM_017020676.1		Intron			XP_016876165.1

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