Product Details

SNP ID
rs199630099
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:165280066 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTCAGCCACTTGAGCGTTATCTTCT[C/G]TTTCCTCTGATTTTACAAATTCCTT
Phenotype
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
C6orf118 PubMed Links

Gene Details

Gene
C6orf118
Gene Name
chromosome 6 open reading frame 118
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_144980.3 1620 Missense Mutation AAC,AAG N467K NP_659417.2
XM_005266838.2 1620 Missense Mutation ACA,AGA T486R XP_005266895.1
XM_011535509.2 1620 Missense Mutation ACA,AGA T521R XP_011533811.1
XM_011535510.2 1620 Missense Mutation ACA,AGA T501R XP_011533812.1
XM_011535511.2 1620 Missense Mutation AAC,AAG N502K XP_011533813.1
XM_011535512.2 1620 Missense Mutation ACA,AGA T382R XP_011533814.1
XM_011535513.2 1620 Missense Mutation ACA,AGA T382R XP_011533815.1
XM_017010323.1 1620 Intron XP_016865812.1
XM_017010324.1 1620 Missense Mutation ACA,AGA T382R XP_016865813.1

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