Product Details

SNP ID

rs145138816

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.14:74408685 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CATTAACAATCACCTCTCAGGAATA[C/T]ATTAAATTACATGGAGCAATACTAA

Phenotype

MIM: 609999

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

SYNDIG1L PubMed Links

Gene Details

Gene

SYNDIG1L

Gene Name

synapse differentiation inducing 1 like

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001105579.1		Intron			NP_001099049.1
XM_017021600.1		Intron			XP_016877089.1

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