Product Details

SNP ID
rs146795138
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:16552981 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCTGTTTGGAAGTTGATTCATCGTT[C/T]AAGTGCTTTGTAGTGAACCTGGATG
Phenotype
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
FAM49A PubMed Links

Gene Details

Gene
FAM49A
Gene Name
family with sequence similarity 49 member A
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_030797.3 1180 Silent Mutation TTA,TTG L309L NP_110424.1
XM_005262630.3 1180 Silent Mutation TTA,TTG L309L XP_005262687.1
XM_006712108.3 1180 Silent Mutation TTA,TTG L309L XP_006712171.1

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