Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TTCCCTTCTGATTCCTCCAAGTGTT[A/G]TGATTTCTTCACAGAAGAGTAGATG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
14 submissions
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Phenotype: |
MIM: 606509 | ||||||||||||||||||||
Literature Links: |
FCRL2 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 |
FCRL2 - Fc receptor like 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001159488.1 | 1613 | UTR 3 | NP_001152960.1 | |||
XM_006711535.3 | 1613 | Intron | XP_006711598.1 | |||
XM_011509974.2 | 1613 | UTR 3 | XP_011508276.1 | |||
XM_011509975.2 | 1613 | UTR 3 | XP_011508277.1 | |||
XM_017002316.1 | 1613 | Missense Mutation | ACA,ATA | T,I 499 | XP_016857805.1 | |
XM_017002317.1 | 1613 | Missense Mutation | ACA,ATA | T,I 433 | XP_016857806.1 | |
XM_017002318.1 | 1613 | Missense Mutation | ACA,ATA | T,I 406 | XP_016857807.1 | |
XM_017002319.1 | 1613 | Missense Mutation | ACA,ATA | T,I 404 | XP_016857808.1 |