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TAAGGTTTCAATTTGTTTTTT[CTCTAGTC/-]CATTTGATCATTGTCTCTGGTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613629 | ||||||||||||||||||||
Literature Links: |
LOC101927410 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 |
LOC101927410 - uncharacterized LOC101927410 | ||||||
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There are no transcripts associated with this gene. |
PIEZO2 - piezo type mechanosensitive ion channel component 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_022068.3 | 9342 | Frame Shift Delete | TGACAA,TGGACTAGAGAA | *,E Q2746WTR | NP_071351.2 | |
XM_011525723.2 | 9342 | Missense Mutation | TGGACTAGAGAA,TGGACTAGAGAC | W,D TRE2790WTR | XP_011524025.1 | |
XM_011525724.2 | 9342 | Missense Mutation | TGGACTAGAGAA,TGGACTAGAGAC | W,D TRE2771WTR | XP_011524026.1 | |
XM_011525725.2 | 9342 | Missense Mutation | TGGACTAGAGAA,TGGACTAGAGAC | W,D TRE2760WTR | XP_011524027.1 | |
XM_011525726.2 | 9342 | Missense Mutation | TGGACTAGAGAA,TGGACTAGAGAC | W,D TRE2729WTR | XP_011524028.1 | |
XM_017025918.1 | 9342 | Missense Mutation | TGGACTAGAGAA,TGGACTAGAGAC | W,D TRE2777WTR | XP_016881407.1 |