Product Details

SNP ID

rs7445128

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:177701035 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ATTTTCTCATGAATGGTTTAGTACA[A/G]TCCCCTTGGTGGTGGTCTCGTGATA

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

FAM153A PubMed Links

Gene Details

Gene

FAM153A

Gene Name

family with sequence similarity 153 member A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_173663.3		Intron			NP_775934.3
XM_005265889.3		Intron			XP_005265946.1
XM_006714848.3		Intron			XP_006714911.1
XM_006714849.3		Intron			XP_006714912.1
XM_011534520.2		Intron			XP_011532822.1
XM_011534521.2		Intron			XP_011532823.1
XM_011534522.2		Intron			XP_011532824.1
XM_011534523.2		Intron			XP_011532825.1
XM_011534528.2		Intron			XP_011532830.1
XM_017009352.1		Intron			XP_016864841.1
XM_017009353.1		Intron			XP_016864842.1
XM_017009354.1		Intron			XP_016864843.1
XM_017009355.1		Intron			XP_016864844.1
XM_017009356.1		Intron			XP_016864845.1
XM_017009357.1		Intron			XP_016864846.1
XM_017009358.1		Intron			XP_016864847.1
XM_017009359.1		Intron			XP_016864848.1
XM_017009360.1		Intron			XP_016864849.1
XM_017009361.1		Intron			XP_016864850.1
XM_017009362.1		Intron			XP_016864851.1
XM_017009363.1		Intron			XP_016864852.1
XM_017009364.1		Intron			XP_016864853.1
XM_017009365.1		Intron			XP_016864854.1
XM_017009366.1		Intron			XP_016864855.1
XM_017009367.1		Intron			XP_016864856.1
XM_017009368.1		Intron			XP_016864857.1
XM_017009369.1		Intron			XP_016864858.1
XM_017009370.1		Intron			XP_016864859.1
XM_017009371.1		Intron			XP_016864860.1

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