Product Details

SNP ID

rs199817589

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:122886057 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGATCGAATCCGGGGCAACGGTATG[A/G]AGCCCGACAGCTTAGACGAGGAGGA

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	1092	Missense Mutation	AAG,GAG	K70E	NP_079082.2
NM_199124.2	1092	Missense Mutation	AAG,GAG	K70E	NP_954575.1
XM_005271680.4	1092	Missense Mutation	AAG,GAG	K70E	XP_005271737.1
XM_006718915.2	1092	Missense Mutation	AAG,GAG	K70E	XP_006718978.1
XM_011543009.2	1092	Missense Mutation	AAG,GAG	K70E	XP_011541311.1
XM_017018338.1	1092	Missense Mutation	AAG,GAG	K70E	XP_016873827.1
XM_017018339.1	1092	Missense Mutation	AAG,GAG	K70E	XP_016873828.1
XM_017018340.1	1092	Missense Mutation	AAG,GAG	K70E	XP_016873829.1
XM_017018341.1	1092	Missense Mutation	AAG,GAG	K70E	XP_016873830.1
XM_017018342.1	1092	Missense Mutation	AAG,GAG	K70E	XP_016873831.1
XM_017018343.1	1092	Missense Mutation	AAG,GAG	K70E	XP_016873832.1
XM_017018344.1	1092	Intron			XP_016873833.1

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