Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CCTGCCTGGCGCGCGGGGCTAGTCC[G/T]TGCCGTCCACCAGCTCGCACAGCAT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 615124 | ||||||||||||||||||||
Literature Links: |
ANKRD13B 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 |
ANKRD13B - ankyrin repeat domain 13B | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_152345.4 | 1354 | Intron | NP_689558.4 | |||
XM_005257920.4 | 1354 | Intron | XP_005257977.1 | |||
XM_011524319.2 | 1354 | Intron | XP_011522621.1 | |||
XM_011524320.2 | 1354 | Intron | XP_011522622.1 | |||
XM_011524321.2 | 1354 | Intron | XP_011522623.1 | |||
XM_017024174.1 | 1354 | Intron | XP_016879663.1 | |||
XM_017024175.1 | 1354 | Intron | XP_016879664.1 | |||
XM_017024176.1 | 1354 | Intron | XP_016879665.1 |
CORO6 - coronin 6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_032854.3 | 1354 | Missense Mutation | AAG,ACG | K,T 471 | NP_116243.2 | |
XM_005258047.3 | 1354 | Missense Mutation | AAG,ACG | K,T 471 | XP_005258104.1 | |
XM_005258048.4 | 1354 | Missense Mutation | AAG,ACG | K,T 542 | XP_005258105.2 | |
XM_005258056.4 | 1354 | Missense Mutation | AAG,ACG | K,T 236 | XP_005258113.1 | |
XM_011525385.2 | 1354 | Missense Mutation | AAG,ACG | K,T 541 | XP_011523687.1 | |
XM_011525386.2 | 1354 | Missense Mutation | AAG,ACG | K,T 507 | XP_011523688.1 | |
XM_011525387.2 | 1354 | Missense Mutation | AAG,ACG | K,T 501 | XP_011523689.1 | |
XM_011525388.2 | 1354 | Intron | XP_011523690.1 | |||
XM_011525389.2 | 1354 | Intron | XP_011523691.1 | |||
XM_011525390.2 | 1354 | Missense Mutation | AAG,ACG | K,T 237 | XP_011523692.1 | |
XM_011525391.2 | 1354 | Missense Mutation | AAG,ACG | K,T 237 | XP_011523693.1 | |
XM_017025235.1 | 1354 | Missense Mutation | AAG,ACG | K,T 430 | XP_016880724.1 |