Product Details

SNP ID

rs1419041

Assay Type

Validated

NCBI dbSNP Submissions

49

Location

Chr.1:112395518 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

ATAATGAGGCCAAGGAAAGAAAAAA[C/G]TCGCCTCAGCTGGCAAGCATAGGGT

Phenotype

MIM: 615100

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

CTTNBP2NL PubMed Links

Gene Details

Gene

CTTNBP2NL

Gene Name

CTTNBP2 N-terminal like

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_018704.2		Intron			NP_061174.1
XM_011541781.2		Intron			XP_011540083.1
XM_017001806.1		Intron			XP_016857295.1

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