Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AAAACCAGATACCATCTTTACATCA[A/T]CAATCACCATATTGGAAGCAGGACG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604874 MIM: 176420 | ||||||||||||||||||||
Literature Links: |
KLRG1 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
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 |
KLRG1 - killer cell lectin like receptor G1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_005810.3 | 4185 | Intron | NP_005801.3 | |||
XM_017018682.1 | 4185 | Intron | XP_016874171.1 | |||
XM_017018683.1 | 4185 | Intron | XP_016874172.1 | |||
XM_017018684.1 | 4185 | Intron | XP_016874173.1 | |||
XM_017018685.1 | 4185 | Intron | XP_016874174.1 |
PZP - PZP, alpha-2-macroglobulin like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_002864.2 | 4185 | Missense Mutation | GAT,GTT | D,V 1387 | NP_002855.2 | |
XM_011520804.2 | 4185 | Missense Mutation | GAT,GTT | D,V 1387 | XP_011519106.1 | |
XM_011520805.2 | 4185 | Missense Mutation | GAT,GTT | D,V 1386 | XP_011519107.1 | |
XM_011520806.1 | 4185 | Intron | XP_011519108.1 | |||
XM_011520807.2 | 4185 | Intron | XP_011519109.1 | |||
XM_017019763.1 | 4185 | Missense Mutation | GAT,GTT | D,V 1387 | XP_016875252.1 | |
XM_017019764.1 | 4185 | Missense Mutation | GAT,GTT | D,V 1387 | XP_016875253.1 | |
XM_017019765.1 | 4185 | Missense Mutation | GAT,GTT | D,V 1304 | XP_016875254.1 | |
XM_017019766.1 | 4185 | Missense Mutation | GAT,GTT | D,V 1173 | XP_016875255.1 | |
XM_017019767.1 | 4185 | Intron | XP_016875256.1 |