Product Details

SNP ID

rs10915744

Assay Type

Functionally tested

NCBI dbSNP Submissions

20

Location

Chr.1:224929112 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GCTCAATAAATATTGTAGTTGTTGC[A/G]TGAGTGAAATATAGAACATTAACTT

Phenotype

MIM: 603341

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

DNAH14 PubMed Links

Gene Details

Gene

DNAH14

Gene Name

dynein axonemal heavy chain 14

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001145154.1	690	Intron			NP_001138626.1
NM_001373.1	690	Intron			NP_001364.1
NM_144989.2	690	Intron			NP_659426.2
XM_006711735.3	690	UTR 5			XP_006711798.1
XM_011544057.2	690	UTR 5			XP_011542359.1
XM_011544058.2	690	UTR 5			XP_011542360.1
XM_011544059.2	690	UTR 5			XP_011542361.1
XM_011544061.2	690	UTR 5			XP_011542363.1
XM_011544062.2	690	UTR 5			XP_011542364.1
XM_011544063.2	690	UTR 5			XP_011542365.1
XM_011544064.2	690	UTR 5			XP_011542366.1
XM_011544065.2	690	UTR 5			XP_011542367.1
XM_011544066.2	690	UTR 5			XP_011542368.1
XM_011544067.2	690	UTR 5			XP_011542369.1
XM_011544069.2	690	UTR 5			XP_011542371.1
XM_011544070.2	690	UTR 5			XP_011542372.1
XM_011544071.2	690	UTR 5			XP_011542373.1
XM_011544072.2	690	UTR 5			XP_011542374.1
XM_011544073.2	690	Intron			XP_011542375.1
XM_011544074.2	690	Intron			XP_011542376.1
XM_011544076.1	690	Intron			XP_011542378.1
XM_011544079.1	690	Intron			XP_011542381.1
XM_011544081.1	690	Intron			XP_011542383.1
XM_017000295.1	690	UTR 5			XP_016855784.1
XM_017000296.1	690	UTR 5			XP_016855785.1
XM_017000297.1	690	UTR 5			XP_016855786.1
XM_017000298.1	690	UTR 5			XP_016855787.1
XM_017000299.1	690	Intron			XP_016855788.1
XM_017000300.1	690	UTR 5			XP_016855789.1

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