Product Details

SNP ID

rs7322

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.15:64963363 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

TGGTGAAGACTTTTGGTAGCAAAAT[C/T]TGCACGGTTCTTAAAATGGGAGTCT

Phenotype

MIM: 608181

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

ANKDD1A PubMed Links

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	1409	UTR 3			NP_001121361.1
NM_001127890.4	1409	UTR 3			NP_001121362.1
NM_016630.6	1409	UTR 3			NP_057714.1
XM_005254437.4	1409	UTR 3			XP_005254494.1
XM_017022297.1	1409	UTR 3			XP_016877786.1
XM_017022298.1	1409	UTR 3			XP_016877787.1

View Full Product Details