Product Details

SNP ID

rs142225173

Assay Type

Functionally tested

NCBI dbSNP Submissions

5

Location

Chr.1:184794992 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATTGTCCCTTTCACTCCTCTGAGGG[A/C]AGCTCTGGGAAACTCTCCTGACCAC

Phenotype

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

FAM129A PubMed Links

Gene Details

Gene

FAM129A

Gene Name

family with sequence similarity 129 member A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_052966.3	3766	Silent Mutation	CTG,CTT	L924L	NP_443198.1
XM_011509140.2	3766	Silent Mutation	CTG,CTT	L983L	XP_011507442.1
XM_011509141.2	3766	Silent Mutation	CTG,CTT	L946L	XP_011507443.1

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