Product Details

SNP ID

rs4650035

Assay Type

Functionally Tested

NCBI dbSNP Submissions

27

Location

Chr.1:70268176 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AGTCACTCATACAGCTAGCTTCCCC[C/G]CCCCCACCTTGAGACAGAGTCTTGC

Phenotype

MIM: 615125

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

ANKRD13C PubMed Links

Additional Information

For this assay, SNP(s) [rs142997780] are located under a probe and SNP(s) [rs368839551] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

ANKRD13C

Gene Name

ankyrin repeat domain 13C

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_030816.4		Intron			NP_110443.3
XM_005271234.3		Intron			XP_005271291.1
XM_005271235.3		Intron			XP_005271292.1
XM_006710929.3		Intron			XP_006710992.1
XM_017002413.1		Intron			XP_016857902.1
XM_017002414.1		Intron			XP_016857903.1
XM_017002415.1		Intron			XP_016857904.1
XM_017002416.1		Intron			XP_016857905.1

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