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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