Product Details

SNP ID

rs76774458

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:40129482 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTCCCCAAAAGGGACCCAGCACCCA[C/T]CCCAAGGAGAAAGCCTTCTCAAGTG

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	782	Silent Mutation	CAC,CAT	H147H	NP_001012241.1
XM_005257298.4	782	Silent Mutation	CAC,CAT	H410H	XP_005257355.1
XM_005257299.4	782	Silent Mutation	CAC,CAT	H410H	XP_005257356.3

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