Product Details

SNP ID
rs141737883
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.18:46477832 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTGTTGTCACGATGACTTCGTACTT[C/G]ACGGGCACCAGGCTCTGGACCTTGC
Phenotype
MIM: 613072
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
LOXHD1 PubMed Links

Gene Details

Gene
LOXHD1
Gene Name
lipoxygenase homology domains 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001145472.2 3082 Silent Mutation GTC,GTG V1043V NP_001138944.1
NM_001145473.2 3082 Silent Mutation GTC,GTG V393V NP_001138945.1
NM_001173129.1 3082 Silent Mutation GTC,GTG V393V NP_001166600.1
NM_001308013.1 3082 Silent Mutation GTC,GTG V947V NP_001294942.1
NM_144612.6 3082 Silent Mutation GTC,GTG V2092V NP_653213.6
XM_006722388.3 3082 Silent Mutation GTC,GTG V1087V XP_006722451.1
XM_006722389.3 3082 Silent Mutation GTC,GTG V1043V XP_006722452.1
XM_006722390.3 3082 Silent Mutation GTC,GTG V1043V XP_006722453.1
XM_006722391.3 3082 Silent Mutation GTC,GTG V1025V XP_006722454.1
XM_011525804.2 3082 Silent Mutation GTC,GTG V1541V XP_011524106.1
XM_011525807.2 3082 Silent Mutation GTC,GTG V947V XP_011524109.1
XM_011525810.2 3082 Silent Mutation GTC,GTG V410V XP_011524112.1
XM_011525811.2 3082 Silent Mutation GTC,GTG V393V XP_011524113.1
XM_017025540.1 3082 Silent Mutation GTC,GTG V1806V XP_016881029.1
XM_017025541.1 3082 Silent Mutation GTC,GTG V1835V XP_016881030.1
XM_017025542.1 3082 Intron XP_016881031.1
XM_017025543.1 3082 Intron XP_016881032.1
XM_017025544.1 3082 Intron XP_016881033.1
XM_017025545.1 3082 Intron XP_016881034.1
XM_017025546.1 3082 Intron XP_016881035.1
XM_017025547.1 3082 Intron XP_016881036.1
XM_017025548.1 3082 Silent Mutation GTC,GTG V1948V XP_016881037.1

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