Product Details

SNP ID

rs115375801

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.10:101588419 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CAGGACGGTAACTCGAGGGTCCCCA[C/G]GGGCTCCTTCGTTTTTTTCCCTCAG

Phenotype

MIM: 616467 MIM: 606343

Polymorphism

C/G, Transversion 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

POLL

Gene Name

polymerase (DNA) lambda

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001174084.1		Intron			NP_001167555.1
NM_001174085.1		Intron			NP_001167556.1
NM_001308382.1		Intron			NP_001295311.1
NM_013274.3		Intron			NP_037406.1
XM_006717775.1		Intron			XP_006717838.1
XM_006717776.1		Intron			XP_006717839.1
XM_006717777.1		Intron			XP_006717840.1
XM_011539650.1		Intron			XP_011537952.1
XM_011539651.1		Intron			XP_011537953.1
XM_011539652.1		Intron			XP_011537954.1
XM_011539653.1		Intron			XP_011537955.1
XM_011539654.1		Intron			XP_011537956.1
XM_011539655.1		Intron			XP_011537957.1
XM_011539656.1		Intron			XP_011537958.1
XM_011539657.1		Intron			XP_011537959.1
XM_011539659.1		Intron			XP_011537961.1
XM_011539660.1		Intron			XP_011537962.1
XM_011539662.1		Intron			XP_011537964.1
XM_011539663.1		Intron			XP_011537965.1
XM_011539664.1		Intron			XP_011537966.1
XM_011539665.2		Intron			XP_011537967.1
XM_011539666.1		Intron			XP_011537968.1
XM_011539667.1		Intron			XP_011537969.1
XM_017016084.1		Intron			XP_016871573.1
XM_017016085.1		Intron			XP_016871574.1
XM_017016086.1		Intron			XP_016871575.1
XM_017016087.1		Intron			XP_016871576.1
XM_017016088.1		Intron			XP_016871577.1
XM_017016089.1		Intron			XP_016871578.1
XM_017016090.1		Intron			XP_016871579.1
XM_017016091.1		Intron			XP_016871580.1
XM_017016092.1		Intron			XP_016871581.1
XM_017016093.1		Intron			XP_016871582.1

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