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GGGTGCCCTTGGGCATCCGGGCCTC[A/G]GGCCTGGGTCTGACGCCTGGGAAGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606091 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
LOC100129083 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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LOC100129083 - uncharacterized LOC100129083 | ||||||
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There are no transcripts associated with this gene. |
SIGLEC10 - sialic acid binding Ig like lectin 10 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001171156.1 | 1800 | Silent Mutation | CCC,CCT | P,P 621 | NP_001164627.1 | |
NM_001171157.1 | 1800 | Intron | NP_001164628.1 | |||
NM_001171158.1 | 1800 | Silent Mutation | CCC,CCT | P,P 536 | NP_001164629.1 | |
NM_001171159.1 | 1800 | Silent Mutation | CCC,CCT | P,P 526 | NP_001164630.1 | |
NM_001171161.1 | 1800 | Silent Mutation | CCC,CCT | P,P 436 | NP_001164632.1 | |
NM_001322105.1 | 1800 | Silent Mutation | CCC,CCT | P,P 494 | NP_001309034.1 | |
NM_033130.4 | 1800 | Silent Mutation | CCC,CCT | P,P 679 | NP_149121.2 | |
XM_005259366.4 | 1800 | Silent Mutation | CCC,CCT | P,P 589 | XP_005259423.1 | |
XM_005259367.3 | 1800 | Silent Mutation | CCC,CCT | P,P 531 | XP_005259424.1 | |
XM_011527439.1 | 1800 | Silent Mutation | CCC,CCT | P,P 631 | XP_011525741.1 |