Product Details

SNP ID

rs6049715

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.20:24473249 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTTGTATCAGTGGAAAGTTGCATAA[A/G]GTCATTTTGGGGCAGTGCACTGATA

Phenotype

MIM: 614311

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

LOC105372585 PubMed Links

Additional Information

For this assay, SNP(s) [rs116761928] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

LOC105372585

Gene Name

translation initiation factor IF-2-like

There are no transcripts associated with this gene.

Gene

SYNDIG1

Gene Name

synapse differentiation inducing 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001323606.1		Intron			NP_001310535.1
NM_001323607.1		Intron			NP_001310536.1
NM_024893.2		Intron			NP_079169.1
XM_011529347.2		Intron			XP_011527649.1
XM_011529348.2		Intron			XP_011527650.1
XM_011529349.2		Intron			XP_011527651.1
XM_011529350.1		Intron			XP_011527652.1
XM_011529351.1		Intron			XP_011527653.1
XM_011529352.2		Intron			XP_011527654.1
XM_011529353.2		Intron			XP_011527655.1
XM_011529354.2		Intron			XP_011527656.1
XM_011529356.2		Intron			XP_011527658.1
XM_011529358.2		Intron			XP_011527660.1
XM_017028064.1		Intron			XP_016883553.1
XM_017028065.1		Intron			XP_016883554.1
XM_017028066.1		Intron			XP_016883555.1
XM_017028067.1		Intron			XP_016883556.1
XM_017028068.1		Intron			XP_016883557.1
XM_017028069.1		Intron			XP_016883558.1

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