Product Details

SNP ID
rs6624595
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.X:72130283 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TCATCTTCATCTTCTTCATCCTTAC[G/T]CTCTCCTTCCTCCTCATTCTTGTTC
Phenotype
Polymorphism
G/T, Transversion 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 1619 Intron NP_001013649.2
XM_011530932.1 1619 Intron XP_011529234.1
XM_011530933.1 1619 Intron XP_011529235.1
XM_011530934.2 1619 Intron XP_011529236.1
XM_017029473.1 1619 Intron XP_016884962.1
XM_017029474.1 1619 Intron XP_016884963.1
XM_017029475.1 1619 Intron XP_016884964.1
XM_017029476.1 1619 Intron XP_016884965.1
XM_017029477.1 1619 Intron XP_016884966.1
Gene
RGAG4
Gene Name
retrotransposon gag domain containing 4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001024455.3 1619 Missense Mutation NP_001019626.1

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