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TTGACCTCTTAGCTCCTCCAGGTCC[C/T]GGGGCTCTGCATCCTGAGCTATCCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610215 MIM: 601873 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ARHGEF25 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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ARHGEF25 - Rho guanine nucleotide exchange factor 25 | ||||||
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There are no transcripts associated with this gene. |
B4GALNT1 - beta-1,4-N-acetyl-galactosaminyltransferase 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001276468.1 | 1552 | Intron | NP_001263397.1 | |||
NM_001276469.1 | 1552 | Intron | NP_001263398.1 | |||
NM_001478.4 | 1552 | Intron | NP_001469.1 | |||
XM_005268773.4 | 1552 | UTR 3 | XP_005268830.1 | |||
XM_011538147.2 | 1552 | UTR 3 | XP_011536449.1 | |||
XM_011538148.2 | 1552 | UTR 3 | XP_011536450.1 | |||
XM_017019140.1 | 1552 | UTR 3 | XP_016874629.1 | |||
XM_017019141.1 | 1552 | UTR 3 | XP_016874630.1 | |||
XM_017019142.1 | 1552 | UTR 3 | XP_016874631.1 |
LOC101927583 - uncharacterized LOC101927583 | ||||||
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There are no transcripts associated with this gene. |
SLC26A10 - solute carrier family 26 member 10 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_133489.2 | 1552 | Missense Mutation | CCG,CTG | P,L 414 | NP_597996.2 |