Product Details

SNP ID

hCV25926487

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:136226151 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AACCTTTTGAATGAGGGTTCCTATA[C/T]CATGATATTTGCGGATTGTCAATTT

Phenotype

MIM: 300930

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

MAP7D3 PubMed Links

Gene Details

Gene

MAP7D3

Gene Name

MAP7 domain containing 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001173516.1		Intron			NP_001166987.1
NM_001173517.1		Intron			NP_001166988.1
NM_024597.3		Intron			NP_078873.2

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