Product Details

SNP ID

rs12008270

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:134814900 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCTGTCTAAGACTTGTGCTTATTGG[A/T]CTCAACCAATGGTCTTCAAACTTGA

Phenotype

Polymorphism

A/T, Transversion substitution

Allele Nomenclature

Literature Links

FAM122C PubMed Links

Gene Details

Gene

FAM122C

Gene Name

family with sequence similarity 122C

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001170779.1		Intron			NP_001164250.1
NM_001170780.1		Intron			NP_001164251.1
NM_001170781.1		Intron			NP_001164252.1
NM_001170782.1		Intron			NP_001164253.1
NM_001170783.1		Intron			NP_001164254.1
NM_001170784.1		Intron			NP_001164255.1
NM_138819.3		Intron			NP_620174.1
XM_005262382.1		Intron			XP_005262439.1
XM_005262383.2		Intron			XP_005262440.1
XM_005262384.4		Intron			XP_005262441.1
XM_005262386.3		Intron			XP_005262443.1
XM_005262387.3		Intron			XP_005262444.1
XM_006724734.3		Intron			XP_006724797.1
XM_006724735.1		Intron			XP_006724798.1
XM_006724736.2		Intron			XP_006724799.1
XM_011531295.1		Intron			XP_011529597.1
XM_011531296.2		Intron			XP_011529598.1
XM_011531297.2		Intron			XP_011529599.1
XM_011531298.2		Intron			XP_011529600.1
XM_011531299.1		Intron			XP_011529601.1
XM_011531300.2		Intron			XP_011529602.1
XM_011531301.2		Intron			XP_011529603.1
XM_011531302.2		Intron			XP_011529604.1
XM_011531305.2		Intron			XP_011529607.1
XM_011531306.2		Intron			XP_011529608.1
XM_017029308.1		Intron			XP_016884797.1
XM_017029309.1		Intron			XP_016884798.1
XM_017029310.1		Intron			XP_016884799.1
XM_017029311.1		Intron			XP_016884800.1

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