Search Thermo Fisher Scientific
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CCCCAGCAAGAAGATGTGGATTAAG[C/G]TTCGGTCTCTGTAAGTCCCCGGCCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 141180 MIM: 171891 | ||||||||||||||||||||
Literature Links: |
NCKAP1L 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 |
NCKAP1L - NCK associated protein 1 like | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
PDE1B - phosphodiesterase 1B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000924.3 | 496 | Missense Mutation | CTT,GTT | L,V 35 | NP_000915.1 | |
NM_001165975.2 | 496 | Intron | NP_001159447.1 | |||
NM_001288768.1 | 496 | UTR 5 | NP_001275697.1 | |||
NM_001288769.1 | 496 | Intron | NP_001275698.1 | |||
NM_001315534.1 | 496 | Intron | NP_001302463.1 | |||
NM_001315535.1 | 496 | Intron | NP_001302464.1 | |||
XM_011538456.1 | 496 | UTR 5 | XP_011536758.1 | |||
XM_017019432.1 | 496 | Intron | XP_016874921.1 | |||
XM_017019433.1 | 496 | Intron | XP_016874922.1 |