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GCTTGCTACCAGAGAGGCAGTGGTG[C/T]CAGTTCAACCTTAGCTTATCTACAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 610172 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SPEF2 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
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AMR
|
SPEF2 - sperm flagellar 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_024867.3 | Intron | NP_079143.3 | ||||
NM_144722.3 | Intron | NP_653323.1 | ||||
XM_005248376.3 | Intron | XP_005248433.1 | ||||
XM_005248377.3 | Intron | XP_005248434.1 | ||||
XM_005248378.3 | Intron | XP_005248435.1 | ||||
XM_011514135.2 | Intron | XP_011512437.1 | ||||
XM_011514136.2 | Intron | XP_011512438.1 | ||||
XM_011514137.2 | Intron | XP_011512439.1 | ||||
XM_011514138.2 | Intron | XP_011512440.1 | ||||
XM_011514139.2 | Intron | XP_011512441.1 | ||||
XM_011514140.2 | Intron | XP_011512442.1 | ||||
XM_011514141.2 | Intron | XP_011512443.1 | ||||
XM_011514142.1 | Intron | XP_011512444.1 | ||||
XM_017009880.1 | Intron | XP_016865369.1 | ||||
XM_017009881.1 | Intron | XP_016865370.1 | ||||
XM_017009882.1 | Intron | XP_016865371.1 |