Product Details

SNP ID: rs6970749
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.7:77797306 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: TTCATTTTTTTCTTACATTTGGCTG[C/T]ACTTACCACAGGTGCTTTAGGGCTG
Phenotype: MIM: 616785
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: PHTF2 PubMed Links

Gene Details

There are no transcripts associated with this gene.

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_032936.3		Intron			NP_116325.1