Product Details

SNP ID

rs139745814

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:122886019 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGCCTCACGCAAGAGATTATGTGCC[A/G]TTCTGAGTTTGATGATCGAATCCGG

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

C11orf63 PubMed Links

Gene Details

Gene

C11orf63

Gene Name

chromosome 11 open reading frame 63

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_024806.3	1054	Missense Mutation	CAT,CGT	H57R	NP_079082.2
NM_199124.2	1054	Missense Mutation	CAT,CGT	H57R	NP_954575.1
XM_005271680.4	1054	Missense Mutation	CAT,CGT	H57R	XP_005271737.1
XM_006718915.2	1054	Missense Mutation	CAT,CGT	H57R	XP_006718978.1
XM_011543009.2	1054	Missense Mutation	CAT,CGT	H57R	XP_011541311.1
XM_017018338.1	1054	Missense Mutation	CAT,CGT	H57R	XP_016873827.1
XM_017018339.1	1054	Missense Mutation	CAT,CGT	H57R	XP_016873828.1
XM_017018340.1	1054	Missense Mutation	CAT,CGT	H57R	XP_016873829.1
XM_017018341.1	1054	Missense Mutation	CAT,CGT	H57R	XP_016873830.1
XM_017018342.1	1054	Missense Mutation	CAT,CGT	H57R	XP_016873831.1
XM_017018343.1	1054	Missense Mutation	CAT,CGT	H57R	XP_016873832.1
XM_017018344.1	1054	Intron			XP_016873833.1

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