Product Details

SNP ID

rs6735969

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.2:96882654 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

CTTACCTGCTTCCTCTCCCTTTGGG[A/T]GCACAAGGTGGCCCTTCTATACGCC

Phenotype

Polymorphism

A/T, Transversion substitution

Allele Nomenclature

Literature Links

FAM178B PubMed Links

Gene Details

Gene

FAM178B

Gene Name

family with sequence similarity 178 member B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001122646.2		Intron			NP_001116118.2
NM_001172667.1		Intron			NP_001166138.1
NM_016490.4		Intron			NP_057574.2
XM_011511294.2		Intron			XP_011509596.1
XM_011511297.2		Intron			XP_011509599.1
XM_017004263.1		Intron			XP_016859752.1
XM_017004264.1		Intron			XP_016859753.1
XM_017004265.1		Intron			XP_016859754.1
XM_017004266.1		Intron			XP_016859755.1
XM_017004267.1		Intron			XP_016859756.1
XM_017004268.1		Intron			XP_016859757.1

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