Product Details

SNP ID

rs147428832

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.15:64963704 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGACCATTGATGGGTCAATGGCCGC[A/G]TATTTGGTTCCATGGAATTGCAGCA

Phenotype

MIM: 608181

Polymorphism

A/G, 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	1068	Silent Mutation	TAC,TAT	Y281Y	NP_001121361.1
NM_001127890.4	1068	Silent Mutation	TAC,TAT	Y254Y	NP_001121362.1
NM_016630.6	1068	Silent Mutation	TAC,TAT	Y281Y	NP_057714.1
XM_005254437.4	1068	Silent Mutation	TAC,TAT	Y281Y	XP_005254494.1
XM_017022297.1	1068	Silent Mutation	TAC,TAT	Y281Y	XP_016877786.1
XM_017022298.1	1068	Silent Mutation	TAC,TAT	Y281Y	XP_016877787.1

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