Product Details

SNP ID

rs12009026

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:115190034 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGCTACTCAGGCTTGCAGCCACGGC[A/G]CTGGGCCGGCCCACCCCACAAGAGG

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

LRCH2 PubMed Links

Gene Details

Gene

LRCH2

Gene Name

leucine rich repeats and calponin homology domain containing 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001243963.1	635	Intron			NP_001230892.1
NM_020871.3	635	Intron			NP_065922.3
XM_006724724.3	635	Intron			XP_006724787.2
XM_017029696.1	635	Intron			XP_016885185.1
XM_017029697.1	635	Intron			XP_016885186.1

Gene

RBMXL3

Gene Name

RNA binding motif protein, X-linked like 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001145346.1	635	Missense Mutation	CAC,CGC	H198R	NP_001138818.1

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