Product Details

SNP ID

rs61760876

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:74595873 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AATCTTCTTCACTCAGGTTATTTAC[A/G]AATTGATAGAAAGCTTCTTCTCGAT

Phenotype

MIM: 300379

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

RLIM PubMed Links

Gene Details

Gene

RLIM

Gene Name

ring finger protein, LIM domain interacting

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_016120.3	395	Silent Mutation	TTC,TTT	F35F	NP_057204.2
NM_183353.2	395	Silent Mutation	TTC,TTT	F35F	NP_899196.1

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