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SNP ID

rs4496294

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:186696385 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTCCTTTGAATGCATTGTGATCTCT[A/C]CATTGAACTGGTCTTCCTGTTTCAA

Phenotype

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

FAM171B PubMed Links

Gene Details

Gene

FAM171B

Gene Name

family with sequence similarity 171 member B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_177454.3		Intron			NP_803237.3

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