Product Details

SNP ID

rs2501079

Assay Type

Functionally tested

NCBI dbSNP Submissions

17

Location

Chr.1:224929520 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CAACACCCCCCTTACCCCCAGCACC[A/G]TCGGTGTCACATCGGGGGCCGCCGC

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	1098	Intron			NP_001138626.1
NM_001373.1	1098	Intron			NP_001364.1
NM_144989.2	1098	Intron			NP_659426.2
XM_006711735.3	1098	UTR 5			XP_006711798.1
XM_011544057.2	1098	UTR 5			XP_011542359.1
XM_011544058.2	1098	UTR 5			XP_011542360.1
XM_011544059.2	1098	UTR 5			XP_011542361.1
XM_011544061.2	1098	UTR 5			XP_011542363.1
XM_011544062.2	1098	UTR 5			XP_011542364.1
XM_011544063.2	1098	UTR 5			XP_011542365.1
XM_011544064.2	1098	UTR 5			XP_011542366.1
XM_011544065.2	1098	UTR 5			XP_011542367.1
XM_011544066.2	1098	UTR 5			XP_011542368.1
XM_011544067.2	1098	UTR 5			XP_011542369.1
XM_011544069.2	1098	UTR 5			XP_011542371.1
XM_011544070.2	1098	UTR 5			XP_011542372.1
XM_011544071.2	1098	UTR 5			XP_011542373.1
XM_011544072.2	1098	UTR 5			XP_011542374.1
XM_011544073.2	1098	Intron			XP_011542375.1
XM_011544074.2	1098	Intron			XP_011542376.1
XM_011544076.1	1098	Intron			XP_011542378.1
XM_011544079.1	1098	Intron			XP_011542381.1
XM_011544081.1	1098	Intron			XP_011542383.1
XM_017000295.1	1098	UTR 5			XP_016855784.1
XM_017000296.1	1098	UTR 5			XP_016855785.1
XM_017000297.1	1098	UTR 5			XP_016855786.1
XM_017000298.1	1098	UTR 5			XP_016855787.1
XM_017000299.1	1098	Intron			XP_016855788.1
XM_017000300.1	1098	UTR 5			XP_016855789.1

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