Product Details

SNP ID

rs79965149

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:31071430 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGTCTCTTTGACGCGGCCGCCCAGG[C/G]TGAGCTTGTCGAACAGGTACTCAGC

Phenotype

MIM: 300308

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

FTHL17 PubMed Links

Gene Details

Gene

FTHL17

Gene Name

ferritin heavy chain like 17

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_031894.2		Intron			NP_114100.1

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