Product Details

SNP ID

rs59160527

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.18:63588878 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTCCTTGTTTCCTATGCACAAATTC[A/T]TTTGGCGGGGGGGTTGTCAGCCCTC

Phenotype

MIM: 604445

Polymorphism

A/T, Transversion Substitution

Allele Nomenclature

Literature Links

SERPINB13 PubMed Links

Additional Information

For this assay, SNP(s) [rs562269359] are located under a probe 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

SERPINB13

Gene Name

serpin family B member 13

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001307923.1		Intron			NP_001294852.1
NM_012397.3		Intron			NP_036529.1
XM_005266707.3		Intron			XP_005266764.1
XM_011526029.2		Intron			XP_011524331.1

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