Product Details

SNP ID
rs202178299
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.20:960428 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCCAGCTTCCTGTCCTTGCGTGGGC[A/G]CCGGTCCTTCCTGCCCTTCTTCTGG
Phenotype
MIM: 610573
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
RSPO4 PubMed Links

Gene Details

Gene
RSPO4
Gene Name
R-spondin 4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001029871.3 548 Missense Mutation CGC,TGC R212C NP_001025042.2
NM_001040007.2 548 Missense Mutation CGC,TGC R150C NP_001035096.1
XM_017027839.1 548 Intron XP_016883328.1

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