Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TCGGCCAGGCCCCACCTTGCAGCCA[C/T]GGGTGTTCCGGACCACAGCAGTGCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616467 MIM: 606343 | ||||||||||||||||||||
Literature Links: |
DPCD PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
DPCD - deleted in primary ciliary dyskinesia homolog (mouse) | ||||||
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There are no transcripts associated with this gene. |
POLL - polymerase (DNA) lambda | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001174084.1 | 2117 | Missense Mutation | CAT,CGT | H,R 541 | NP_001167555.1 | |
NM_001174085.1 | 2117 | Missense Mutation | CAT,CGT | H,R 449 | NP_001167556.1 | |
NM_001308382.1 | 2117 | Missense Mutation | CAT,CGT | H,R 266 | NP_001295311.1 | |
NM_013274.3 | 2117 | Missense Mutation | CAT,CGT | H,R 541 | NP_037406.1 | |
XM_006717775.1 | 2117 | Missense Mutation | CAT,CGT | H,R 280 | XP_006717838.1 | |
XM_006717776.1 | 2117 | Missense Mutation | CAT,CGT | H,R 280 | XP_006717839.1 | |
XM_006717777.1 | 2117 | Missense Mutation | CAT,CGT | H,R 266 | XP_006717840.1 | |
XM_011539650.1 | 2117 | Missense Mutation | CAT,CGT | H,R 548 | XP_011537952.1 | |
XM_011539651.1 | 2117 | Missense Mutation | CAT,CGT | H,R 541 | XP_011537953.1 | |
XM_011539652.1 | 2117 | Missense Mutation | CAT,CGT | H,R 548 | XP_011537954.1 | |
XM_011539653.1 | 2117 | Missense Mutation | CAT,CGT | H,R 548 | XP_011537955.1 | |
XM_011539654.1 | 2117 | Missense Mutation | CAT,CGT | H,R 456 | XP_011537956.1 | |
XM_011539655.1 | 2117 | Missense Mutation | CAT,CGT | H,R 449 | XP_011537957.1 | |
XM_011539656.1 | 2117 | Missense Mutation | CAT,CGT | H,R 442 | XP_011537958.1 | |
XM_011539657.1 | 2117 | Missense Mutation | CAT,CGT | H,R 460 | XP_011537959.1 | |
XM_011539659.1 | 2117 | Missense Mutation | CAT,CGT | H,R 379 | XP_011537961.1 | |
XM_011539660.1 | 2117 | Missense Mutation | CAT,CGT | H,R 379 | XP_011537962.1 | |
XM_011539662.1 | 2117 | Missense Mutation | CAT,CGT | H,R 287 | XP_011537964.1 | |
XM_011539663.1 | 2117 | Missense Mutation | CAT,CGT | H,R 287 | XP_011537965.1 | |
XM_011539664.1 | 2117 | Missense Mutation | CAT,CGT | H,R 273 | XP_011537966.1 | |
XM_011539665.2 | 2117 | Missense Mutation | CAT,CGT | H,R 273 | XP_011537967.1 | |
XM_011539666.1 | 2117 | Missense Mutation | CAT,CGT | H,R 273 | XP_011537968.1 | |
XM_011539667.1 | 2117 | Missense Mutation | CAT,CGT | H,R 233 | XP_011537969.1 | |
XM_017016084.1 | 2117 | Missense Mutation | CAT,CGT | H,R 447 | XP_016871573.1 | |
XM_017016085.1 | 2117 | Missense Mutation | CAT,CGT | H,R 440 | XP_016871574.1 | |
XM_017016086.1 | 2117 | Missense Mutation | CAT,CGT | H,R 435 | XP_016871575.1 | |
XM_017016087.1 | 2117 | Missense Mutation | CAT,CGT | H,R 355 | XP_016871576.1 | |
XM_017016088.1 | 2117 | Intron | XP_016871577.1 | |||
XM_017016089.1 | 2117 | Missense Mutation | CAT,CGT | H,R 379 | XP_016871578.1 | |
XM_017016090.1 | 2117 | UTR 3 | XP_016871579.1 | |||
XM_017016091.1 | 2117 | Missense Mutation | CAT,CGT | H,R 372 | XP_016871580.1 | |
XM_017016092.1 | 2117 | Intron | XP_016871581.1 | |||
XM_017016093.1 | 2117 | Missense Mutation | CAT,CGT | H,R 273 | XP_016871582.1 |