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ATTTGGGCGCCCCTGAGGTGGGGAA[C/T]AGGAAAGCCCGCCGGGCAGGTCAGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602235 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
KCNQ2 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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KCNQ2 - potassium voltage-gated channel subfamily Q member 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_004518.5 | 2787 | UTR 3 | NP_004509.2 | |||
NM_172106.2 | 2787 | UTR 3 | NP_742104.1 | |||
NM_172107.3 | 2787 | UTR 3 | NP_742105.1 | |||
NM_172108.4 | 2787 | UTR 3 | NP_742106.1 | |||
NM_172109.2 | 2787 | Intron | NP_742107.1 | |||
XM_011528810.1 | 2787 | UTR 3 | XP_011527112.1 | |||
XM_011528811.1 | 2787 | UTR 3 | XP_011527113.1 | |||
XM_017027841.1 | 2787 | UTR 3 | XP_016883330.1 | |||
XM_017027842.1 | 2787 | UTR 3 | XP_016883331.1 | |||
XM_017027843.1 | 2787 | UTR 3 | XP_016883332.1 | |||
XM_017027844.1 | 2787 | UTR 3 | XP_016883333.1 | |||
XM_017027845.1 | 2787 | UTR 3 | XP_016883334.1 |
LOC100130152 - uncharacterized LOC100130152 | ||||||
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There are no transcripts associated with this gene. |