Product Details

SNP ID
rs142898915
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:123772894 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCACATGCTCTGTACCCCTCTTCCC[A/G]AGGAGTTCCTGGACCAAAACGTGGT
Phenotype
MIM: 605884
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
DNAH10 PubMed Links

Gene Details

Gene
DNAH10
Gene Name
dynein axonemal heavy chain 10
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_207437.3 791 Missense Mutation AAG,GAG K92E NP_997320.2
XM_005253555.3 791 Missense Mutation AAG,GAG K153E XP_005253612.1
XM_011538014.2 791 Missense Mutation AAG,GAG K153E XP_011536316.1
XM_011538015.2 791 Missense Mutation AAG,GAG K153E XP_011536317.1
XM_011538016.2 791 Missense Mutation AAG,GAG K153E XP_011536318.1
XM_011538017.2 791 Missense Mutation AAG,GAG K153E XP_011536319.1
XM_011538019.2 791 Intron XP_011536321.1
XM_011538020.2 791 Missense Mutation AAG,GAG K153E XP_011536322.1
XM_017018960.1 791 Missense Mutation AAG,GAG K153E XP_016874449.1
XM_017018961.1 791 Missense Mutation AAG,GAG K153E XP_016874450.1
XM_017018962.1 791 Intron XP_016874451.1

View Full Product Details