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SNP ID

rs138481361

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.16:1691806 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTGGGGTGGGGTGGGGTCCGGTGGA[C/T]GTCTGGTTGCTCAGTGTTCTGTGAT

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

HN1L PubMed Links

Gene Details

Gene

HN1L

Gene Name

hematological and neurological expressed 1-like

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_144570.2		Intron			NP_653171.1

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