Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616555 | |||||||||||||||||||||||
Literature Links: |
ARL17B PubMed Links | |||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU)
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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 |
ARL17B - ADP ribosylation factor like GTPase 17B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001039083.3 | Intron | NP_001034172.3 | ||||
NM_001103154.1 | Intron | NP_001096624.1 | ||||
XM_005256918.4 | Intron | XP_005256975.1 | ||||
XM_011524160.2 | Intron | XP_011522462.1 | ||||
XM_011524161.2 | Intron | XP_011522463.1 | ||||
XM_011524162.2 | Intron | XP_011522464.1 | ||||
XM_011524163.2 | Intron | XP_011522465.1 | ||||
XM_011524164.2 | Intron | XP_011522466.1 | ||||
XM_011524165.2 | Intron | XP_011522467.1 | ||||
XM_011524166.2 | Intron | XP_011522468.1 | ||||
XM_011524167.2 | Intron | XP_011522469.1 |
LRRC37A - leucine rich repeat containing 37A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_014834.4 | Intron | NP_055649.4 | ||||
XM_005257879.4 | Intron | XP_005257936.1 | ||||
XM_005257880.4 | Intron | XP_005257937.1 | ||||
XM_005257882.4 | Intron | XP_005257939.1 | ||||
XM_005257883.4 | Intron | XP_005257940.1 | ||||
XM_005257884.4 | Intron | XP_005257941.1 | ||||
XM_006722210.3 | Intron | XP_006722273.1 | ||||
XM_006722211.3 | Intron | XP_006722274.1 | ||||
XM_011525539.2 | Intron | XP_011523841.1 | ||||
XM_017025472.1 | Intron | XP_016880961.1 | ||||
XM_017025473.1 | Intron | XP_016880962.1 |
Set Membership: |
HapMap |