Product Details

SNP ID
rs144217156
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.15:70882769 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GAAGAGTCAAAACATACCCACACTA[C/T]GGTGACGGGGCCTTTTCAAAGAAAT
Phenotype
MIM: 612538
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
LRRC49 PubMed Links

Gene Details

Gene
LRRC49
Gene Name
leucine rich repeat containing 49
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001199017.2 730 Intron NP_001185946.1
NM_001199018.2 730 Intron NP_001185947.1
NM_001284357.1 730 Intron NP_001271286.1
NM_017691.4 730 Intron NP_060161.2
XM_005254492.4 730 Intron XP_005254549.1
XM_011521715.2 730 Intron XP_011520017.1
XM_011521717.2 730 Intron XP_011520019.1
XM_011521718.2 730 Intron XP_011520020.1
XM_017022357.1 730 Intron XP_016877846.1
XM_017022358.1 730 Intron XP_016877847.1
XM_017022359.1 730 Intron XP_016877848.1
Gene
THAP10
Gene Name
THAP domain containing 10
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_020147.3 730 Missense Mutation NP_064532.1

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