Product Details

SNP ID
rs202232099
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.10:101579568 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCCCACCTTGCAGCCATGGGTGTTC[C/T]GGACCACAGCAGTGCTGAGGGCATG
Phenotype
MIM: 616467 MIM: 606343
Polymorphism
C/T, 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
POLL
Gene Name
polymerase (DNA) lambda
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001174084.1 2108 Missense Mutation NP_001167555.1
NM_001174085.1 2108 Missense Mutation NP_001167556.1
NM_001308382.1 2108 Missense Mutation NP_001295311.1
NM_013274.3 2108 Missense Mutation NP_037406.1
XM_006717775.1 2108 Missense Mutation XP_006717838.1
XM_006717776.1 2108 Missense Mutation XP_006717839.1
XM_006717777.1 2108 Missense Mutation XP_006717840.1
XM_011539650.1 2108 Missense Mutation XP_011537952.1
XM_011539651.1 2108 Missense Mutation XP_011537953.1
XM_011539652.1 2108 Missense Mutation XP_011537954.1
XM_011539653.1 2108 Missense Mutation XP_011537955.1
XM_011539654.1 2108 Missense Mutation XP_011537956.1
XM_011539655.1 2108 Missense Mutation XP_011537957.1
XM_011539656.1 2108 Missense Mutation XP_011537958.1
XM_011539657.1 2108 Missense Mutation XP_011537959.1
XM_011539659.1 2108 Missense Mutation XP_011537961.1
XM_011539660.1 2108 Missense Mutation XP_011537962.1
XM_011539662.1 2108 Missense Mutation XP_011537964.1
XM_011539663.1 2108 Missense Mutation XP_011537965.1
XM_011539664.1 2108 Missense Mutation XP_011537966.1
XM_011539665.2 2108 Missense Mutation XP_011537967.1
XM_011539666.1 2108 Missense Mutation XP_011537968.1
XM_011539667.1 2108 Missense Mutation XP_011537969.1
XM_017016084.1 2108 Missense Mutation XP_016871573.1
XM_017016085.1 2108 Missense Mutation XP_016871574.1
XM_017016086.1 2108 Missense Mutation XP_016871575.1
XM_017016087.1 2108 Missense Mutation XP_016871576.1
XM_017016088.1 2108 Intron XP_016871577.1
XM_017016089.1 2108 Missense Mutation XP_016871578.1
XM_017016090.1 2108 UTR 3 XP_016871579.1
XM_017016091.1 2108 Missense Mutation XP_016871580.1
XM_017016092.1 2108 Intron XP_016871581.1
XM_017016093.1 2108 Missense Mutation XP_016871582.1

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