Product Details

SNP ID

rs104664

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.22:45315973 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CAAACTCACCAGAAACCTATCAGCT[A/G]GATCGCAGATGGTTCATTTGTGGTT

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

FAM118A PubMed Links

Gene Details

Gene

FAM118A

Gene Name

family with sequence similarity 118 member A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001104595.1		Intron			NP_001098065.1
NM_017911.2		Intron			NP_060381.2
XM_011530247.2		Intron			XP_011528549.1
XM_011530254.2		Intron			XP_011528556.1
XM_011530256.1		Intron			XP_011528558.1
XM_017028841.1		Intron			XP_016884330.1
XM_017028842.1		Intron			XP_016884331.1
XM_017028843.1		Intron			XP_016884332.1
XM_017028844.1		Intron			XP_016884333.1
XM_017028845.1		Intron			XP_016884334.1
XM_017028846.1		Intron			XP_016884335.1
XM_017028847.1		Intron			XP_016884336.1
XM_017028848.1		Intron			XP_016884337.1
XM_017028849.1		Intron			XP_016884338.1
XM_017028850.1		Intron			XP_016884339.1
XM_017028851.1		Intron			XP_016884340.1
XM_017028852.1		Intron			XP_016884341.1
XM_017028853.1		Intron			XP_016884342.1
XM_017028854.1		Intron			XP_016884343.1
XM_017028855.1		Intron			XP_016884344.1
XM_017028856.1		Intron			XP_016884345.1
XM_017028857.1		Intron			XP_016884346.1
XM_017028858.1		Intron			XP_016884347.1
XM_017028859.1		Intron			XP_016884348.1
XM_017028860.1		Intron			XP_016884349.1
XM_017028861.1		Intron			XP_016884350.1

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