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TGAGGGCCACCATCGTGAACGTGGT[A/G]GTCAGGAGCCCAGCATGAACCGGAC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 609499 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
MCF2L 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
|
MCF2L - MCF.2 cell line derived transforming sequence like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001112732.2 | Intron | NP_001106203.2 | ||||
NM_001320815.1 | Intron | NP_001307744.1 | ||||
NM_001320816.1 | Intron | NP_001307745.1 | ||||
NM_001320817.1 | Intron | NP_001307746.1 | ||||
NM_024979.4 | Intron | NP_079255.4 | ||||
XM_011537482.1 | Intron | XP_011535784.1 | ||||
XM_011537483.2 | Intron | XP_011535785.1 | ||||
XM_011537484.1 | Intron | XP_011535786.1 | ||||
XM_011537485.1 | Intron | XP_011535787.1 | ||||
XM_011537486.2 | Intron | XP_011535788.2 | ||||
XM_011537487.1 | Intron | XP_011535789.1 | ||||
XM_011537488.1 | Intron | XP_011535790.1 | ||||
XM_011537490.1 | Intron | XP_011535792.1 | ||||
XM_011537491.1 | Intron | XP_011535793.1 | ||||
XM_017020493.1 | Intron | XP_016875982.1 | ||||
XM_017020494.1 | Intron | XP_016875983.1 | ||||
XM_017020495.1 | Intron | XP_016875984.1 | ||||
XM_017020496.1 | Intron | XP_016875985.1 | ||||
XM_017020497.1 | Intron | XP_016875986.1 | ||||
XM_017020498.1 | Intron | XP_016875987.1 | ||||
XM_017020499.1 | Intron | XP_016875988.1 |