Product Details

SNP ID

rs201251694

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:158663288 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GAAGAAATGGCCCAAGAAATAGATC[A/T]GAGTGCTCTCAAGGAGTTAGAACGC

Phenotype

Polymorphism

A/T, Transversion substitution

Allele Nomenclature

Literature Links

SYTL3 PubMed Links

Gene Details

Gene

SYTL3

Gene Name

synaptotagmin like 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001009991.3	690	Missense Mutation	CAG,CTG	Q7L	NP_001009991.2
NM_001242384.1	690	Missense Mutation	CAG,CTG	Q7L	NP_001229313.1
NM_001242394.1	690	Missense Mutation	CAG,CTG	Q7L	NP_001229323.1
NM_001242395.1	690	Missense Mutation	CAG,CTG	Q7L	NP_001229324.1
NM_001318745.1	690	Intron			NP_001305674.1
XM_005267215.4	690	Missense Mutation	CAG,CTG	Q7L	XP_005267272.1
XM_005267218.4	690	Intron			XP_005267275.1
XM_005267222.4	690	Intron			XP_005267279.1
XM_006715605.3	690	Missense Mutation	CAG,CTG	Q7L	XP_006715668.1
XM_006715606.3	690	Missense Mutation	CAG,CTG	Q7L	XP_006715669.1
XM_006715611.3	690	Intron			XP_006715674.1
XM_011536254.2	690	Missense Mutation	CAG,CTG	Q7L	XP_011534556.1
XM_011536255.2	690	Intron			XP_011534557.1
XM_017011495.1	690	Missense Mutation	CAG,CTG	Q7L	XP_016866984.1
XM_017011496.1	690	UTR 5			XP_016866985.1
XM_017011497.1	690	UTR 5			XP_016866986.1
XM_017011498.1	690	Intron			XP_016866987.1
XM_017011499.1	690	Missense Mutation	CAG,CTG	Q7L	XP_016866988.1

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