Product Details

SNP ID

rs141628955

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:154506857 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CGGGATACAGCCTTCCATCTCCAGC[A/G]CCTCGGGCCAGCCTTCGTACTTGTT

Phenotype

MIM: 300492

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

FAM3A PubMed Links

Gene Details

Gene

FAM3A

Gene Name

family with sequence similarity 3 member A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001171132.2	1362	Missense Mutation	GCG,GTG	A216V	NP_001164603.1
NM_001171133.2	1362	Missense Mutation	GCG,GTG	A178V	NP_001164604.1
NM_001171134.2	1362	Missense Mutation	GCG,GTG	A199V	NP_001164605.1
NM_001282311.1	1362	Missense Mutation	GCG,GTG	A230V	NP_001269240.1
NM_001282312.1	1362	Missense Mutation	GCG,GTG	A216V	NP_001269241.1
NM_021806.3	1362	Missense Mutation	GCG,GTG	A216V	NP_068578.2
XM_005274714.3	1362	Missense Mutation	GCG,GTG	A237V	XP_005274771.1
XM_005274716.3	1362	Missense Mutation	GCG,GTG	A230V	XP_005274773.1
XM_005277879.4	1362	Missense Mutation	GCG,GTG	A199V	XP_005277936.1
XM_006724831.2	1362	Missense Mutation	GCG,GTG	A238V	XP_006724894.1
XM_006724832.3	1362	Missense Mutation	GCG,GTG	A224V	XP_006724895.1
XM_006724833.2	1362	Missense Mutation	GCG,GTG	A213V	XP_006724896.1
XM_006724834.2	1362	Missense Mutation	GCG,GTG	A183V	XP_006724897.1
XM_011531185.2	1362	Missense Mutation	GCG,GTG	A183V	XP_011529487.1
XM_017029699.1	1362	Missense Mutation	GCG,GTG	A183V	XP_016885188.1
XM_017029700.1	1362	Missense Mutation	GCG,GTG	A175V	XP_016885189.1
XM_017029701.1	1362	Missense Mutation	GCG,GTG	A175V	XP_016885190.1
XM_017029702.1	1362	Missense Mutation	GCG,GTG	A175V	XP_016885191.1

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