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AGGGACATGGCCTTGGCTCCCAAGC[C/T]CAGGCACAGCTTCTGTGGAGCACCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600240 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
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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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CCR10 - C-C motif chemokine receptor 10 | ||||||
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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 | 2353 | Missense Mutation | AGC,GGC | S,G 684 | NP_079203.3 | |
XM_017025113.1 | 2353 | Missense Mutation | AGC,GGC | S,G 773 | XP_016880602.1 | |
XM_017025114.1 | 2353 | Missense Mutation | AGC,GGC | S,G 770 | XP_016880603.1 | |
XM_017025115.1 | 2353 | Missense Mutation | AGC,GGC | S,G 729 | XP_016880604.1 | |
XM_017025116.1 | 2353 | Missense Mutation | AGC,GGC | S,G 728 | XP_016880605.1 | |
XM_017025117.1 | 2353 | Missense Mutation | AGC,GGC | S,G 713 | XP_016880606.1 | |
XM_017025118.1 | 2353 | Missense Mutation | AGC,GGC | S,G 681 | XP_016880607.1 |
TUBG2 - tubulin gamma 2 | ||||||
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There are no transcripts associated with this gene. |