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ACATTTCAGGAATTAACAGAAGTCG[G/T]ATCAAATTCTCTTGCTAGATGTTCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 300163 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FHL1 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
|
FHL1 - four and a half LIM domains 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001159699.1 | Intron | NP_001153171.1 | ||||
NM_001159700.1 | Intron | NP_001153172.1 | ||||
NM_001159701.1 | Intron | NP_001153173.1 | ||||
NM_001159702.2 | Intron | NP_001153174.1 | ||||
NM_001159703.1 | Intron | NP_001153175.1 | ||||
NM_001159704.1 | Intron | NP_001153176.1 | ||||
NM_001167819.1 | Intron | NP_001161291.1 | ||||
NM_001449.4 | Intron | NP_001440.2 | ||||
XM_006724743.2 | Intron | XP_006724806.1 | ||||
XM_006724744.2 | Intron | XP_006724807.1 | ||||
XM_006724745.3 | Intron | XP_006724808.1 | ||||
XM_006724746.2 | Intron | XP_006724809.1 | ||||
XM_006724747.2 | Intron | XP_006724810.1 | ||||
XM_011531316.1 | Intron | XP_011529618.1 | ||||
XM_017029357.1 | Intron | XP_016884846.1 |