Product Details

SNP ID

rs3930740

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:8391641 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CCATTGAAAGGTGTTGGTTGACTTA[C/T]GGACCTCAATAAACAGCCAATAGCT

Phenotype

MIM: 603704

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

RNF222 PubMed Links

Gene Details

Gene

RNF222

Gene Name

ring finger protein 222

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001146684.2	2130	UTR 3			NP_001140156.1
XM_011523978.2	2130	Intron			XP_011522280.1
XM_011523979.2	2130	Intron			XP_011522281.1
XM_011523980.2	2130	Intron			XP_011522282.1
XM_011523981.2	2130	Intron			XP_011522283.1

Gene

RPL26

Gene Name

ribosomal protein L26

There are no transcripts associated with this gene.

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