Product Details

SNP ID
rs200730440
Assay Type
Functionally tested
NCBI dbSNP Submissions
2
Location
Chr.1:222522623 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGGTCAAGGGAGACTTCTGCCAGCT[C/T]GCTTCTGCTCTGCTGATGGCCTCAT
Phenotype
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
HHIPL2 PubMed Links

Gene Details

Gene
HHIPL2
Gene Name
HHIP like 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_024746.3 2213 Missense Mutation NP_079022.2
XM_011509985.2 2213 Missense Mutation XP_011508287.1
XM_011509986.1 2213 Intron XP_011508288.1
XM_017002350.1 2213 Intron XP_016857839.1

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