Product Details

SNP ID

rs145952459

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:122885902 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTCTCTATTCAATCTCCTGTCCTTC[A/C]TACCAACTTAAATGTCCAGTCCACA

Phenotype

Polymorphism

A/C, Transversion 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	937	Missense Mutation	CAT,CCT	H18P	NP_079082.2
NM_199124.2	937	Missense Mutation	CAT,CCT	H18P	NP_954575.1
XM_005271680.4	937	Missense Mutation	CAT,CCT	H18P	XP_005271737.1
XM_006718915.2	937	Missense Mutation	CAT,CCT	H18P	XP_006718978.1
XM_011543009.2	937	Missense Mutation	CAT,CCT	H18P	XP_011541311.1
XM_017018338.1	937	Missense Mutation	CAT,CCT	H18P	XP_016873827.1
XM_017018339.1	937	Missense Mutation	CAT,CCT	H18P	XP_016873828.1
XM_017018340.1	937	Missense Mutation	CAT,CCT	H18P	XP_016873829.1
XM_017018341.1	937	Missense Mutation	CAT,CCT	H18P	XP_016873830.1
XM_017018342.1	937	Missense Mutation	CAT,CCT	H18P	XP_016873831.1
XM_017018343.1	937	Missense Mutation	CAT,CCT	H18P	XP_016873832.1
XM_017018344.1	937	Intron			XP_016873833.1

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