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CTGCAACTCGTAGACTGGGAGGGAC[A/G]TGATGAATCTCACAGTTTTGGAAGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609593 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
CARMIL1 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
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CEPH (CEU)
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EAS
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African American
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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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CARMIL1 - capping protein regulator and myosin 1 linker 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001173977.1 | Intron | NP_001167448.1 | ||||
NM_017640.5 | Intron | NP_060110.4 | ||||
XM_005249218.1 | Intron | XP_005249275.1 | ||||
XM_017011008.1 | Intron | XP_016866497.1 | ||||
XM_017011009.1 | Intron | XP_016866498.1 | ||||
XM_017011010.1 | Intron | XP_016866499.1 | ||||
XM_017011011.1 | Intron | XP_016866500.1 | ||||
XM_017011012.1 | Intron | XP_016866501.1 | ||||
XM_017011013.1 | Intron | XP_016866502.1 | ||||
XM_017011014.1 | Intron | XP_016866503.1 | ||||
XM_017011015.1 | Intron | XP_016866504.1 | ||||
XM_017011016.1 | Intron | XP_016866505.1 | ||||
XM_017011017.1 | Intron | XP_016866506.1 |
LOC105375106 - uncharacterized LOC105375106 | ||||||
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There are no transcripts associated with this gene. |