Product Details

SNP ID

rs11655643

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.17:60426840 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

CTGGTGAGGCGCAAGACATTCCGCC[T/C]GAGCACAGCTGAGGGTTGGTTGATG

Phenotype

MIM: 607740

Polymorphism

T/C, Transition substitution

Allele Nomenclature

Literature Links

C17orf64 PubMed Links

Gene Details

Gene

C17orf64

Gene Name

chromosome 17 open reading frame 64

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_181707.2	543	Intron			NP_859058.2
XM_005257033.4	543	Missense Mutation	CCG,CTG	P184L	XP_005257090.1
XM_005257034.4	543	Intron			XP_005257091.1
XM_005257035.4	543	Missense Mutation	CCG,CTG	P114L	XP_005257092.1
XM_005257036.2	543	Missense Mutation	CCG,CTG	P151L	XP_005257093.1
XM_017024166.1	543	Intron			XP_016879655.1

Gene

RPL12P38

Gene Name

ribosomal protein L12 pseudogene 38

There are no transcripts associated with this gene.

Gene

USP32

Gene Name

ubiquitin specific peptidase 32

There are no transcripts associated with this gene.

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