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AGTGCCATGAGTCTTGTAATTCTTA[G/T]CCCCAAGGAAGGGAGGATAACAGCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 603668 | ||||||||||||||||||||
Literature Links: |
SCAF11 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 |
SCAF11 - SR-related CTD associated factor 11 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_004719.2 | 7385 | UTR 3 | NP_004710.2 | |||
XM_005269230.2 | 7385 | UTR 3 | XP_005269287.2 | |||
XM_011538984.2 | 7385 | UTR 3 | XP_011537286.1 | |||
XM_011538985.1 | 7385 | UTR 3 | XP_011537287.1 | |||
XM_017020217.1 | 7385 | UTR 3 | XP_016875706.1 | |||
XM_017020218.1 | 7385 | Intron | XP_016875707.1 | |||
XM_017020219.1 | 7385 | UTR 3 | XP_016875708.1 | |||
XM_017020220.1 | 7385 | UTR 3 | XP_016875709.1 | |||
XM_017020221.1 | 7385 | UTR 3 | XP_016875710.1 | |||
XM_017020222.1 | 7385 | UTR 3 | XP_016875711.1 | |||
XM_017020223.1 | 7385 | UTR 3 | XP_016875712.1 |