Product Details

SNP ID
rs138968448
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.10:27675330 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTAGTTCCCTGCAGTTTGTCCTTTC[C/T]CTGTGCAAGATTTGTTAAGGCCATA
Phenotype
MIM: 601332
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
MKX PubMed Links

Gene Details

Gene
MKX
Gene Name
mohawk homeobox
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001242702.1 1183 Missense Mutation AGA,GGA R320G NP_001229631.1
NM_173576.2 1183 Missense Mutation AGA,GGA R320G NP_775847.2
XM_017016105.1 1183 Missense Mutation AGA,GGA R320G XP_016871594.1
XM_017016106.1 1183 Missense Mutation AGA,GGA R320G XP_016871595.1
XM_017016107.1 1183 Intron XP_016871596.1
XM_017016108.1 1183 UTR 3 XP_016871597.1

View Full Product Details