Product Details

SNP ID
rs138044522
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:2794575 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGGACCGTGATGACGGACGCTACCC[A/G]CCCAGGCCCAGGCCACGGCCGCCTG
Phenotype
MIM: 300879
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
XG PubMed Links

Gene Details

Gene
XG
Gene Name
Xg blood group
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001141919.1 1448 Intron NP_001135391.1
NM_001141920.1 1448 Intron NP_001135392.1
NM_175569.2 1448 Intron NP_780778.1
XM_005274587.3 1448 Silent Mutation CCA,CCG P99P XP_005274644.1
XM_011545575.2 1448 Silent Mutation CCA,CCG P99P XP_011543877.1
XM_017029787.1 1448 Silent Mutation CCA,CCG P85P XP_016885276.1

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