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TTTAAATCAAGCTCCACTGCCTAAA[A/G]TATTAATTGGAGCAAGGGGTTCCCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608532 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
NCAPG2 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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NCAPG2 - non-SMC condensin II complex subunit G2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001281932.1 | Intron | NP_001268861.1 | ||||
NM_001281933.1 | Intron | NP_001268862.1 | ||||
NM_017760.6 | Intron | NP_060230.5 | ||||
XM_005249547.2 | Intron | XP_005249604.1 | ||||
XM_011516356.2 | Intron | XP_011514658.1 | ||||
XM_011516357.2 | Intron | XP_011514659.1 | ||||
XM_011516358.2 | Intron | XP_011514660.1 | ||||
XM_011516362.1 | Intron | XP_011514664.1 | ||||
XM_017012374.1 | Intron | XP_016867863.1 | ||||
XM_017012375.1 | Intron | XP_016867864.1 | ||||
XM_017012376.1 | Intron | XP_016867865.1 | ||||
XM_017012377.1 | Intron | XP_016867866.1 | ||||
XM_017012378.1 | Intron | XP_016867867.1 |