Product Details

SNP ID

rs199520780

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:64858883 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCATATCCTGGAAGTTCTTTTGTGA[A/G]CTAAAAAAAAAAAAACCAGAATGAG

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	5371	Missense Mutation			NP_001290184.1
NM_199340.3	5371	Missense Mutation			NP_955372.2
XM_011524776.1	5371	Intron			XP_011523078.1
XM_011524777.1	5371	Intron			XP_011523079.1
XM_011524778.2	5371	Intron			XP_011523080.2
XM_017024593.1	5371	Intron			XP_016880082.1
XM_017024594.1	5371	Intron			XP_016880083.1
XM_017024595.1	5371	Intron			XP_016880084.1
XM_017024596.1	5371	Intron			XP_016880085.1
XM_017024597.1	5371	Intron			XP_016880086.1
XM_017024598.1	5371	Intron			XP_016880087.1
XM_017024599.1	5371	Intron			XP_016880088.1
XM_017024600.1	5371	Intron			XP_016880089.1
XM_017024601.1	5371	Missense Mutation	CTC,TTC	L833F	XP_016880090.1
XM_017024602.1	5371	Missense Mutation	CTC,TTC	L758F	XP_016880091.1
XM_017024603.1	5371	Intron			XP_016880092.1
XM_017024604.1	5371	Intron			XP_016880093.1
XM_017024605.1	5371	Intron			XP_016880094.1
XM_017024606.1	5371	Intron			XP_016880095.1
XM_017024607.1	5371	Intron			XP_016880096.1
XM_017024608.1	5371	Intron			XP_016880097.1

View Full Product Details