Product Details

SNP ID

rs2449272

Assay Type

Validated

NCBI dbSNP Submissions

34

Location

Chr.1:224929311 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

ACGCCCACGAGTTGTGAAAATCTTA[C/A]GTGTAAGTCACCTCTTTCAGAGGTC

Phenotype

MIM: 603341

Polymorphism

C/A, Transversion 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	889	Intron			NP_001138626.1
NM_001373.1	889	Intron			NP_001364.1
NM_144989.2	889	Intron			NP_659426.2
XM_006711735.3	889	UTR 5			XP_006711798.1
XM_011544057.2	889	UTR 5			XP_011542359.1
XM_011544058.2	889	UTR 5			XP_011542360.1
XM_011544059.2	889	UTR 5			XP_011542361.1
XM_011544061.2	889	UTR 5			XP_011542363.1
XM_011544062.2	889	UTR 5			XP_011542364.1
XM_011544063.2	889	UTR 5			XP_011542365.1
XM_011544064.2	889	UTR 5			XP_011542366.1
XM_011544065.2	889	UTR 5			XP_011542367.1
XM_011544066.2	889	UTR 5			XP_011542368.1
XM_011544067.2	889	UTR 5			XP_011542369.1
XM_011544069.2	889	UTR 5			XP_011542371.1
XM_011544070.2	889	UTR 5			XP_011542372.1
XM_011544071.2	889	UTR 5			XP_011542373.1
XM_011544072.2	889	UTR 5			XP_011542374.1
XM_011544073.2	889	Intron			XP_011542375.1
XM_011544074.2	889	Intron			XP_011542376.1
XM_011544076.1	889	Intron			XP_011542378.1
XM_011544079.1	889	Intron			XP_011542381.1
XM_011544081.1	889	Intron			XP_011542383.1
XM_017000295.1	889	UTR 5			XP_016855784.1
XM_017000296.1	889	UTR 5			XP_016855785.1
XM_017000297.1	889	UTR 5			XP_016855786.1
XM_017000298.1	889	UTR 5			XP_016855787.1
XM_017000299.1	889	Intron			XP_016855788.1
XM_017000300.1	889	UTR 5			XP_016855789.1

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