Product Details

SNP ID

rs200119700

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:64860247 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTGAAAGCGGTATTTTTTTCTGGAA[C/T]GTACGATGGGTTTAGATGTCTTCAT

Phenotype

MIM: 616557

Polymorphism

C/T, 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	4565	Missense Mutation			NP_001290184.1
NM_199340.3	4565	Missense Mutation			NP_955372.2
XM_011524776.1	4565	Intron			XP_011523078.1
XM_011524777.1	4565	Intron			XP_011523079.1
XM_011524778.2	4565	Intron			XP_011523080.2
XM_017024593.1	4565	Intron			XP_016880082.1
XM_017024594.1	4565	Intron			XP_016880083.1
XM_017024595.1	4565	Intron			XP_016880084.1
XM_017024596.1	4565	Intron			XP_016880085.1
XM_017024597.1	4565	Intron			XP_016880086.1
XM_017024598.1	4565	Intron			XP_016880087.1
XM_017024599.1	4565	Intron			XP_016880088.1
XM_017024600.1	4565	Intron			XP_016880089.1
XM_017024601.1	4565	Missense Mutation	CAT,CGT	H564R	XP_016880090.1
XM_017024602.1	4565	Missense Mutation	CAT,CGT	H489R	XP_016880091.1
XM_017024603.1	4565	Intron			XP_016880092.1
XM_017024604.1	4565	Intron			XP_016880093.1
XM_017024605.1	4565	Intron			XP_016880094.1
XM_017024606.1	4565	Intron			XP_016880095.1
XM_017024607.1	4565	Intron			XP_016880096.1
XM_017024608.1	4565	Intron			XP_016880097.1

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