Product Details

SNP ID

rs141577275

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.15:64968538 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AACCGTTGATTATCAGAGGCCGGGG[A/G]AAGAAAGGGAACAGGAGTTATTGTT

Phenotype

MIM: 608181

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

ANKDD1A PubMed Links

Additional Information

For this assay, SNP(s) [rs112449052] 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

ANKDD1A

Gene Name

ankyrin repeat and death domain containing 1A

There are no transcripts associated with this gene.

Gene

SPG21

Gene Name

spastic paraplegia 21 (autosomal recessive, Mast syndrome)

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001127889.4		Intron			NP_001121361.1
NM_001127890.4		Intron			NP_001121362.1
NM_016630.6		Intron			NP_057714.1
XM_005254437.4		Intron			XP_005254494.1
XM_017022297.1		Intron			XP_016877786.1
XM_017022298.1		Intron			XP_016877787.1

View Full Product Details