Product Details

SNP ID

rs147453724

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:64858828 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CAAAATCGTTAGTATTCCAGTCACA[A/G]TTAACGCCAAGATGAGTTTTTTGGT

Phenotype

MIM: 616557

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

LRRC37A3 PubMed Links

Gene Details

Gene

LRRC37A3

Gene Name

leucine rich repeat containing 37 member A3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001303255.1	5426	Missense Mutation			NP_001290184.1
NM_199340.3	5426	Missense Mutation			NP_955372.2
XM_011524776.1	5426	Intron			XP_011523078.1
XM_011524777.1	5426	Intron			XP_011523079.1
XM_011524778.2	5426	Intron			XP_011523080.2
XM_017024593.1	5426	Intron			XP_016880082.1
XM_017024594.1	5426	Intron			XP_016880083.1
XM_017024595.1	5426	Intron			XP_016880084.1
XM_017024596.1	5426	Intron			XP_016880085.1
XM_017024597.1	5426	Intron			XP_016880086.1
XM_017024598.1	5426	Intron			XP_016880087.1
XM_017024599.1	5426	Intron			XP_016880088.1
XM_017024600.1	5426	Intron			XP_016880089.1
XM_017024601.1	5426	Missense Mutation	ACT,ATT	T851I	XP_016880090.1
XM_017024602.1	5426	Missense Mutation	ACT,ATT	T776I	XP_016880091.1
XM_017024603.1	5426	Intron			XP_016880092.1
XM_017024604.1	5426	Intron			XP_016880093.1
XM_017024605.1	5426	Intron			XP_016880094.1
XM_017024606.1	5426	Intron			XP_016880095.1
XM_017024607.1	5426	Intron			XP_016880096.1
XM_017024608.1	5426	Intron			XP_016880097.1

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