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CATCCGACTCTGTAGTGTCCCACTC[A/G]ATAAAGAAAAATGGTATCCATTAGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 609001 MIM: 608075 | ||||||||||||||||||||
Literature Links: |
PIK3C2G PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
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 |
PIK3C2G - phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 gamma | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001288772.1 | 4536 | Missense Mutation | AAT,GAT | N,D 1474 | NP_001275701.1 | |
NM_001288774.1 | 4536 | Missense Mutation | AAT,GAT | N,D 1252 | NP_001275703.1 | |
NM_004570.5 | 4536 | Missense Mutation | AAT,GAT | N,D 1433 | NP_004561.3 | |
XM_011520696.2 | 4536 | Intron | XP_011518998.1 | |||
XM_011520697.2 | 4536 | Intron | XP_011518999.1 | |||
XM_011520700.2 | 4536 | Intron | XP_011519002.1 | |||
XM_011520701.2 | 4536 | Intron | XP_011519003.1 | |||
XM_017019470.1 | 4536 | Intron | XP_016874959.1 | |||
XM_017019471.1 | 4536 | Intron | XP_016874960.1 | |||
XM_017019472.1 | 4536 | Intron | XP_016874961.1 | |||
XM_017019473.1 | 4536 | Intron | XP_016874962.1 | |||
XM_017019474.1 | 4536 | Intron | XP_016874963.1 | |||
XM_017019475.1 | 4536 | Intron | XP_016874964.1 | |||
XM_017019476.1 | 4536 | Intron | XP_016874965.1 | |||
XM_017019477.1 | 4536 | Intron | XP_016874966.1 | |||
XM_017019478.1 | 4536 | Intron | XP_016874967.1 | |||
XM_017019479.1 | 4536 | Intron | XP_016874968.1 |
PLCZ1 - phospholipase C zeta 1 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_033123.3 | 4536 | Intron | NP_149114.2 | |||
XM_005253519.2 | 4536 | Intron | XP_005253576.1 | |||
XM_011520883.1 | 4536 | Intron | XP_011519185.1 | |||
XM_017020176.1 | 4536 | Intron | XP_016875665.1 | |||
XM_017020177.1 | 4536 | Intron | XP_016875666.1 | |||
XM_017020178.1 | 4536 | Intron | XP_016875667.1 | |||
XM_017020179.1 | 4536 | Intron | XP_016875668.1 | |||
XM_017020180.1 | 4536 | Intron | XP_016875669.1 | |||
XM_017020181.1 | 4536 | Intron | XP_016875670.1 | |||
XM_017020182.1 | 4536 | Intron | XP_016875671.1 | |||
XM_017020183.1 | 4536 | Intron | XP_016875672.1 | |||
XM_017020184.1 | 4536 | Intron | XP_016875673.1 | |||
XM_017020185.1 | 4536 | Intron | XP_016875674.1 | |||
XM_017020186.1 | 4536 | Intron | XP_016875675.1 |