Product Details

SNP ID

rs13336534

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.16:20933391 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GCAGTGGGTCATAGAGGATTTTGGG[A/G]AGAGATTCCCCAATCTGCATCGTTT

Phenotype

MIM: 603334 MIM: 614709

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

DNAH3 PubMed Links

Gene Details

Gene

DNAH3

Gene Name

dynein axonemal heavy chain 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_017539.2	12692	Silent Mutation	CTC,CTT	L4038L	NP_060009.1
XM_006721062.1	12692	Silent Mutation	CTC,CTT	L3992L	XP_006721125.1
XM_011545882.2	12692	Silent Mutation	CTC,CTT	L3999L	XP_011544184.1
XM_011545883.1	12692	Silent Mutation	CTC,CTT	L3999L	XP_011544185.1
XM_011545885.2	12692	Intron			XP_011544187.1
XM_011545886.2	12692	Silent Mutation	CTC,CTT	L3662L	XP_011544188.1
XM_011545888.2	12692	Silent Mutation	CTC,CTT	L3133L	XP_011544190.1
XM_011545889.2	12692	Silent Mutation	CTC,CTT	L3133L	XP_011544191.1
XM_017023426.1	12692	Silent Mutation	CTC,CTT	L3954L	XP_016878915.1
XM_017023427.1	12692	Silent Mutation	CTC,CTT	L3918L	XP_016878916.1
XM_017023428.1	12692	Silent Mutation	CTC,CTT	L3806L	XP_016878917.1
XM_017023429.1	12692	Intron			XP_016878918.1
XM_017023430.1	12692	Silent Mutation	CTC,CTT	L2017L	XP_016878919.1
XM_017023431.1	12692	Intron			XP_016878920.1
XM_017023432.1	12692	Silent Mutation	CTC,CTT	L4052L	XP_016878921.1

Gene

LYRM1

Gene Name

LYR motif containing 1

There are no transcripts associated with this gene.

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