Product Details

SNP ID
rs199710459
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:77667048 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTGGAGGCTAGGCTTGCACTGGCTG[T/G]GCTGTTGTCCTTGGGGGTCTGAGAC
Phenotype
MIM: 608522
Polymorphism
T/G, Transversion substitution
Allele Nomenclature
Literature Links
RSF1 PubMed Links

Gene Details

Gene
RSF1
Gene Name
remodeling and spacing factor 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_016578.3 4089 Missense Mutation ACA,CCA T1399P NP_057662.3
XM_005274051.2 4089 Missense Mutation ACA,CCA T1396P XP_005274108.1
XM_017017923.1 4089 Missense Mutation ACA,CCA T1358P XP_016873412.1

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