Product Details

SNP ID

rs1764627

Assay Type

Functionally Tested

NCBI dbSNP Submissions

11

Location

Chr.1:197217071 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AAACAACCCAATTTTTAAAGTGTAC[A/G]TCGAATTGAAATAGATATTTTTCCA

Phenotype

MIM: 604210

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

CRB1 PubMed Links

Additional Information

For this assay, SNP(s) [rs143487822,rs78471047] 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

CRB1

Gene Name

crumbs 1, cell polarity complex component

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001193640.1		Intron			NP_001180569.1
NM_001257965.1		Intron			NP_001244894.1
NM_001257966.1		Intron			NP_001244895.1
NM_201253.2		Intron			NP_957705.1
XM_011509365.2		Intron			XP_011507667.1
XM_011509367.1		Intron			XP_011507669.1
XM_011509369.2		Intron			XP_011507671.1
XM_017000851.1		Intron			XP_016856340.1
XM_017000852.1		Intron			XP_016856341.1

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