Product Details

SNP ID

rs202133035

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.14:74407662 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCGGCGGGAGGTGGTGCTGGCCAGG[C/T]GGAAGTCCCCTTTGGAGATGGCCTT

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	3424	Missense Mutation	CAC,CGC	H197R	NP_001099049.1
XM_017021600.1	3424	Missense Mutation	CAC,CGC	H197R	XP_016877089.1

View Full Product Details