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ACGCCGGAGAGCCTCACCTGCTCAA[A/G]GAGGAAAGGCAGTTCGTGACCGTCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600240 MIM: 602346 MIM: 605785 | ||||||||||||||||||||
Literature Links: |
CCR10 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
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Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
CCR10 - C-C motif chemokine receptor 10 | ||||||
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There are no transcripts associated with this gene. |
CNTNAP1 - contactin associated protein 1 | ||||||
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There are no transcripts associated with this gene. |
PLEKHH3 - pleckstrin homology, MyTH4 and FERM domain containing H3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_024927.4 | 1849 | Missense Mutation | CTT,TTT | L,F 516 | NP_079203.3 | |
XM_017025113.1 | 1849 | Missense Mutation | CTT,TTT | L,F 605 | XP_016880602.1 | |
XM_017025114.1 | 1849 | Missense Mutation | CTT,TTT | L,F 602 | XP_016880603.1 | |
XM_017025115.1 | 1849 | Missense Mutation | CTT,TTT | L,F 561 | XP_016880604.1 | |
XM_017025116.1 | 1849 | Missense Mutation | CTT,TTT | L,F 560 | XP_016880605.1 | |
XM_017025117.1 | 1849 | Missense Mutation | CTT,TTT | L,F 545 | XP_016880606.1 | |
XM_017025118.1 | 1849 | Missense Mutation | CTT,TTT | L,F 513 | XP_016880607.1 |
TUBG2 - tubulin gamma 2 | ||||||
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There are no transcripts associated with this gene. |