Product Details

SNP ID

rs35614606

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.10:101612369 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGGTGCGGAGGTCCCAGTAGCGAAC[A/G]TAGGTGTCATAGCCACAGGACAGCA

Phenotype

MIM: 616467 MIM: 608071

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

DPCD PubMed Links

Gene Details

Gene

DPCD

Gene Name

deleted in primary ciliary dyskinesia homolog (mouse)

There are no transcripts associated with this gene.

Gene

FBXW4

Gene Name

F-box and WD repeat domain containing 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001323541.1		Intron			NP_001310470.1
NM_022039.3		Intron			NP_071322.1
XM_005270053.2		Intron			XP_005270110.2
XM_017016570.1		Intron			XP_016872059.1

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