Product Details

SNP ID

rs35702111

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:80264902 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGGATACACCAGGTGTGCTTCCACC[A/G]CAGGGCCTTTGCACCACCCTTCCCC

Phenotype

MIM: 613768

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

RNF213 PubMed Links

Gene Details

Gene

RNF213

Gene Name

ring finger protein 213

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001256071.2		Intron			NP_001243000.2
NM_020954.3		Intron			NP_066005.2
XM_005257545.4		Intron			XP_005257602.2
XM_005257546.4		Intron			XP_005257603.2
XM_006721995.3		Intron			XP_006722058.1
XM_011525084.2		Intron			XP_011523386.1
XM_011525086.2		Intron			XP_011523388.1
XM_011525087.2		Intron			XP_011523389.1
XM_017024905.1		Intron			XP_016880394.1

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