Product Details

SNP ID

rs17856754

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:165290034 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTCAACCTTCTCAGTAAGAGTAAGT[C/T]GGTTTTCATCAATTATATGTTTCTC

Phenotype

Polymorphism

C/T, Transition 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	1317	Missense Mutation			NP_659417.2
XM_005266838.2	1317	Missense Mutation			XP_005266895.1
XM_011535509.2	1317	Missense Mutation			XP_011533811.1
XM_011535510.2	1317	Missense Mutation			XP_011533812.1
XM_011535511.2	1317	Missense Mutation			XP_011533813.1
XM_011535512.2	1317	Missense Mutation			XP_011533814.1
XM_011535513.2	1317	Missense Mutation			XP_011533815.1
XM_017010323.1	1317	Missense Mutation			XP_016865812.1
XM_017010324.1	1317	Missense Mutation			XP_016865813.1

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