Product Details

SNP ID

rs150514257

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.22:26169732 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGATCTCGCTGTTCCTCGCTCTGCT[C/T]CTGGGGAGCCCGGCGGCAGCGCTGG

Phenotype

MIM: 607021

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

SEZ6L PubMed Links

Gene Details

Gene

SEZ6L

Gene Name

seizure related 6 homolog like

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001184773.1	259	Silent Mutation	CTC,CTT	L21L	NP_001171702.1
NM_001184774.1	259	Silent Mutation	CTC,CTT	L21L	NP_001171703.1
NM_001184775.1	259	Silent Mutation	CTC,CTT	L21L	NP_001171704.1
NM_001184776.1	259	Silent Mutation	CTC,CTT	L21L	NP_001171705.1
NM_001184777.1	259	Silent Mutation	CTC,CTT	L21L	NP_001171706.1
NM_021115.4	259	Silent Mutation	CTC,CTT	L21L	NP_066938.2
XM_005261439.3	259	Silent Mutation	CTC,CTT	L21L	XP_005261496.1
XM_005261440.3	259	Silent Mutation	CTC,CTT	L21L	XP_005261497.1
XM_006724195.3	259	Silent Mutation	CTC,CTT	L21L	XP_006724258.1
XM_011530037.2	259	Silent Mutation	CTC,CTT	L21L	XP_011528339.1
XM_011530038.2	259	Silent Mutation	CTC,CTT	L21L	XP_011528340.1
XM_011530039.2	259	Silent Mutation	CTC,CTT	L21L	XP_011528341.1
XM_017028699.1	259	Silent Mutation	CTC,CTT	L21L	XP_016884188.1
XM_017028700.1	259	Silent Mutation	CTC,CTT	L21L	XP_016884189.1

View Full Product Details