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TTTCCCAAGAATACTGCATCTTGTT[A/C]TCTTGTGCAATATACAGACGTGTGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607160 MIM: 609344 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
ATP6V1F 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)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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ATP6V1F - ATPase H+ transporting V1 subunit F | ||||||
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There are no transcripts associated with this gene. |
KCP - kielin/chordin-like protein | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001135914.1 | 3433 | Intron | NP_001129386.1 | |||
NM_199349.2 | 3433 | Intron | NP_955381.2 | |||
XM_017012184.1 | 3433 | Intron | XP_016867673.1 | |||
XM_017012185.1 | 3433 | Intron | XP_016867674.1 | |||
XM_017012186.1 | 3433 | Intron | XP_016867675.1 | |||
XM_017012187.1 | 3433 | Intron | XP_016867676.1 | |||
XM_017012188.1 | 3433 | Intron | XP_016867677.1 | |||
XM_017012189.1 | 3433 | Intron | XP_016867678.1 | |||
XM_017012190.1 | 3433 | Intron | XP_016867679.1 | |||
XM_017012191.1 | 3433 | Intron | XP_016867680.1 | |||
XM_017012192.1 | 3433 | Intron | XP_016867681.1 | |||
XM_017012193.1 | 3433 | Intron | XP_016867682.1 | |||
XM_017012194.1 | 3433 | Intron | XP_016867683.1 |
LOC100130705 - uncharacterized LOC100130705 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001195150.1 | 3433 | UTR 3 | NP_001182079.1 |