Product Details

SNP ID
rs79378995
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.2:102473809 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TACAGTCCTTGGAATTGTTTGCTAC[C/T]GCTAGTGGCTCTTGAGTGTTCTGAA
Phenotype
MIM: 600531
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
SLC9A4 PubMed Links

Gene Details

Gene
SLC9A4
Gene Name
solute carrier family 9 member A4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001011552.3 528 Missense Mutation CCG,CTG P17L NP_001011552.2
XM_011511158.1 528 Missense Mutation CCG,CTG P17L XP_011509460.1

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