Product Details

SNP ID

rs190459935

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:115190091 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCCCGGTCAAGCCTGGCTCGCATTG[A/G]CGGCAGTGGAATGCCTGGGAAGGCC

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	692	Intron			NP_001230892.1
NM_020871.3	692	Intron			NP_065922.3
XM_006724724.3	692	Intron			XP_006724787.2
XM_017029696.1	692	Intron			XP_016885185.1
XM_017029697.1	692	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	692	Missense Mutation	GAC,GGC	D217G	NP_001138818.1

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