Product Details

SNP ID
rs144137484
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:71923041 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TATTTTGTGTCTGTAGCTTCCAGAC[C/T]ACCTAATGCACATGGGGTGTGGGGT
Phenotype
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
NHSL2 PubMed Links

Gene Details

Gene
NHSL2
Gene Name
NHS like 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001013627.2 Intron NP_001013649.2
XM_011530932.1 Intron XP_011529234.1
XM_011530933.1 Intron XP_011529235.1
XM_011530934.2 Intron XP_011529236.1
XM_017029473.1 Intron XP_016884962.1
XM_017029474.1 Intron XP_016884963.1
XM_017029475.1 Intron XP_016884964.1
XM_017029476.1 Intron XP_016884965.1
XM_017029477.1 Intron XP_016884966.1

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