Product Details

SNP ID

rs200202390

Assay Type

Functionally tested

NCBI dbSNP Submissions

13

Location

Chr.1:182904205 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTGGGCGCCAGTTATTTCACTGTCT[G/T]TAATTGTCAAAGCAGCCCCTGTAAG

Phenotype

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

SHCBP1L PubMed Links

Gene Details

Gene

SHCBP1L

Gene Name

SHC binding and spindle associated 1 like

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_030933.2	1847	Missense Mutation			NP_112195.2

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