Product Details

SNP ID
rs115665903
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:57293946 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGTAGAGGGGACAGACATAGGCATC[C/T]GACTTTATAATCCGAGATTTTTGAG
Phenotype
MIM: 603340
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
ASB14 PubMed Links

Gene Details

Gene
ASB14
Gene Name
ankyrin repeat and SOCS box containing 14
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001142733.2 11896 Intron NP_001136205.2
NM_130387.5 11896 Intron NP_569058.1
XM_017005736.1 11896 Intron XP_016861225.1
XM_017005737.1 11896 Intron XP_016861226.1
Gene
DNAH12
Gene Name
dynein axonemal heavy chain 12
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001291661.1 11896 Silent Mutation TCA,TCG S3910S NP_001278590.1
NM_198564.3 11896 Intron NP_940966.2
XM_011533466.1 11896 Silent Mutation TCA,TCG S3906S XP_011531768.1
XM_011533467.1 11896 Silent Mutation TCA,TCG S3895S XP_011531769.1
XM_011533468.1 11896 Silent Mutation TCA,TCG S3885S XP_011531770.1
XM_011533469.1 11896 Silent Mutation TCA,TCG S3859S XP_011531771.1
XM_011533471.2 11896 Intron XP_011531773.1
XM_011533474.1 11896 Intron XP_011531776.1
XM_017005860.1 11896 Intron XP_016861349.1
XM_017005861.1 11896 Silent Mutation TCA,TCG S3406S XP_016861350.1
XM_017005862.1 11896 Silent Mutation TCA,TCG S2770S XP_016861351.1
XM_017005863.1 11896 Intron XP_016861352.1

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