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GCTGCAGAACTAGCATTTTTGCTCA[C/T]GTTCTGGAAGCTTTCTCCGTTTATT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609870 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ARHGAP21 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) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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ARHGAP21 - Rho GTPase activating protein 21 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_020824.3 | 6534 | Intron | NP_065875.3 | |||
XM_005252542.3 | 6534 | Intron | XP_005252599.1 | |||
XM_005252544.4 | 6534 | Missense Mutation | ATG,GTG | M,V 1919 | XP_005252601.1 | |
XM_011519602.2 | 6534 | Missense Mutation | ATG,GTG | M,V 1963 | XP_011517904.1 | |
XM_011519603.2 | 6534 | Missense Mutation | ATG,GTG | M,V 1963 | XP_011517905.1 | |
XM_011519604.2 | 6534 | Intron | XP_011517906.1 | |||
XM_011519605.2 | 6534 | Missense Mutation | ATG,GTG | M,V 1953 | XP_011517907.1 | |
XM_011519606.2 | 6534 | Missense Mutation | ATG,GTG | M,V 1895 | XP_011517908.1 | |
XM_011519607.2 | 6534 | UTR 3 | XP_011517909.1 | |||
XM_017016459.1 | 6534 | Missense Mutation | ATG,GTG | M,V 1929 | XP_016871948.1 | |
XM_017016460.1 | 6534 | Missense Mutation | ATG,GTG | M,V 1919 | XP_016871949.1 | |
XM_017016461.1 | 6534 | Intron | XP_016871950.1 |