Product Details

SNP ID

rs201369085

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:134807614 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CGACCCGGACATGGCACAGGAGAAA[A/G]TGAAACTAGGTTTCAAGTCGCTGCC

Phenotype

Polymorphism

A/G, Transition 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	288	Missense Mutation	ATG,GTG	M6V	NP_001164250.1
NM_001170780.1	288	Missense Mutation	ATG,GTG	M42V	NP_001164251.1
NM_001170781.1	288	Missense Mutation	ATG,GTG	M6V	NP_001164252.1
NM_001170782.1	288	Missense Mutation	ATG,GTG	M6V	NP_001164253.1
NM_001170783.1	288	Missense Mutation	ATG,GTG	M6V	NP_001164254.1
NM_001170784.1	288	Missense Mutation	ATG,GTG	M6V	NP_001164255.1
NM_138819.3	288	Missense Mutation	ATG,GTG	M6V	NP_620174.1
XM_005262382.1	288	Missense Mutation	ATG,GTG	M42V	XP_005262439.1
XM_005262383.2	288	Missense Mutation	ATG,GTG	M42V	XP_005262440.1
XM_005262384.4	288	Missense Mutation	ATG,GTG	M42V	XP_005262441.1
XM_005262386.3	288	Missense Mutation	ATG,GTG	M42V	XP_005262443.1
XM_005262387.3	288	Missense Mutation	ATG,GTG	M42V	XP_005262444.1
XM_006724734.3	288	Missense Mutation	ATG,GTG	M6V	XP_006724797.1
XM_006724735.1	288	Missense Mutation	ATG,GTG	M42V	XP_006724798.1
XM_006724736.2	288	Missense Mutation	ATG,GTG	M42V	XP_006724799.1
XM_011531295.1	288	Missense Mutation	ATG,GTG	M42V	XP_011529597.1
XM_011531296.2	288	Missense Mutation	ATG,GTG	M42V	XP_011529598.1
XM_011531297.2	288	Missense Mutation	ATG,GTG	M42V	XP_011529599.1
XM_011531298.2	288	Missense Mutation	ATG,GTG	M42V	XP_011529600.1
XM_011531299.1	288	Intron			XP_011529601.1
XM_011531300.2	288	Intron			XP_011529602.1
XM_011531301.2	288	Intron			XP_011529603.1
XM_011531302.2	288	Intron			XP_011529604.1
XM_011531305.2	288	Missense Mutation	ATG,GTG	M42V	XP_011529607.1
XM_011531306.2	288	Missense Mutation	ATG,GTG	M42V	XP_011529608.1
XM_017029308.1	288	Missense Mutation	ATG,GTG	M42V	XP_016884797.1
XM_017029309.1	288	Intron			XP_016884798.1
XM_017029310.1	288	Missense Mutation	ATG,GTG	M42V	XP_016884799.1
XM_017029311.1	288	Missense Mutation	ATG,GTG	M6V	XP_016884800.1

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