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AGCAGCTCTCTGCACTATCTTCTCA[A/T]TTTTTTCTGCAACTCTAAAACTATT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
C19orf47 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 |
C19orf47 - chromosome 19 open reading frame 47 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001256440.1 | 7153 | Intron | NP_001243369.1 | |||
NM_001256441.1 | 7153 | Intron | NP_001243370.1 | |||
XM_005258520.2 | 7153 | Intron | XP_005258577.1 | |||
XM_011526460.2 | 7153 | Intron | XP_011524762.1 | |||
XM_017026291.1 | 7153 | Intron | XP_016881780.1 | |||
XM_017026292.1 | 7153 | UTR 3 | XP_016881781.1 | |||
XM_017026293.1 | 7153 | UTR 3 | XP_016881782.1 | |||
XM_017026294.1 | 7153 | Intron | XP_016881783.1 | |||
XM_017026295.1 | 7153 | Intron | XP_016881784.1 |