Product Details

SNP ID
rs57438358
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.15:64963027 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACAATAATCACAAAAGCGACTCAGT[G/T]AAATTGAATTTTTATTCCAAATGAC
Phenotype
MIM: 608181
Polymorphism
G/T, Transversion 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 1745 UTR 3 NP_001121361.1
NM_001127890.4 1745 UTR 3 NP_001121362.1
NM_016630.6 1745 UTR 3 NP_057714.1
XM_005254437.4 1745 UTR 3 XP_005254494.1
XM_017022297.1 1745 UTR 3 XP_016877786.1
XM_017022298.1 1745 UTR 3 XP_016877787.1

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