Product Details

SNP ID

rs9900154

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:40126946 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CTTACATCATAAAGAGAATGGGCAA[C/T]AAGTATGACAGCTGAGTTTCTTAAA

Phenotype

MIM: 614801

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

MSL1 PubMed Links

Gene Details

Gene

MSL1

Gene Name

male specific lethal 1 homolog

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001012241.1		Intron			NP_001012241.1
XM_005257298.4		Intron			XP_005257355.1
XM_005257299.4		Intron			XP_005257356.3

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