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AAGTTCAAGATGGCCGCCGCGGAGA[C/G]CCAGTCGCTACGGGAGCAGCCAGAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602338 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
PRPF4B PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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PRPF4B - pre-mRNA processing factor 4B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_003913.4 | 2041 | Missense Mutation | ACC,AGC | T,S 6 | NP_003904.3 | |
XM_011514970.2 | 2041 | Missense Mutation | ACC,AGC | T,S 6 | XP_011513272.1 | |
XM_017011410.1 | 2041 | Missense Mutation | ACC,AGC | T,S 6 | XP_016866899.1 | |
XM_017011411.1 | 2041 | Missense Mutation | ACC,AGC | T,S 6 | XP_016866900.1 | |
XM_017011412.1 | 2041 | Missense Mutation | ACC,AGC | T,S 6 | XP_016866901.1 | |
XM_017011413.1 | 2041 | Missense Mutation | ACC,AGC | T,S 6 | XP_016866902.1 | |
XM_017011414.1 | 2041 | Missense Mutation | ACC,AGC | T,S 6 | XP_016866903.1 | |
XM_017011415.1 | 2041 | Missense Mutation | ACC,AGC | T,S 6 | XP_016866904.1 | |
XM_017011416.1 | 2041 | Missense Mutation | ACC,AGC | T,S 6 | XP_016866905.1 | |
XM_017011417.1 | 2041 | Missense Mutation | ACC,AGC | T,S 6 | XP_016866906.1 | |
XM_017011418.1 | 2041 | Missense Mutation | ACC,AGC | T,S 6 | XP_016866907.1 | |
XM_017011419.1 | 2041 | Missense Mutation | ACC,AGC | T,S 6 | XP_016866908.1 | |
XM_017011420.1 | 2041 | Missense Mutation | ACC,AGC | T,S 6 | XP_016866909.1 | |
XM_017011421.1 | 2041 | Missense Mutation | ACC,AGC | T,S 6 | XP_016866910.1 | |
XM_017011422.1 | 2041 | Missense Mutation | ACC,AGC | T,S 6 | XP_016866911.1 | |
XM_017011423.1 | 2041 | Missense Mutation | ACC,AGC | T,S 6 | XP_016866912.1 | |
XM_017011424.1 | 2041 | Missense Mutation | ACC,AGC | T,S 6 | XP_016866913.1 | |
XM_017011425.1 | 2041 | Missense Mutation | ACC,AGC | T,S 6 | XP_016866914.1 | |
XM_017011426.1 | 2041 | Missense Mutation | ACC,AGC | T,S 6 | XP_016866915.1 | |
XM_017011427.1 | 2041 | Missense Mutation | ACC,AGC | T,S 6 | XP_016866916.1 | |
XM_017011428.1 | 2041 | Missense Mutation | ACC,AGC | T,S 6 | XP_016866917.1 | |
XM_017011429.1 | 2041 | Missense Mutation | ACC,AGC | T,S 6 | XP_016866918.1 | |
XM_017011430.1 | 2041 | Missense Mutation | ACC,AGC | T,S 6 | XP_016866919.1 | |
XM_017011431.1 | 2041 | Missense Mutation | ACC,AGC | T,S 6 | XP_016866920.1 | |
XM_017011432.1 | 2041 | Missense Mutation | ACC,AGC | T,S 6 | XP_016866921.1 | |
XM_017011433.1 | 2041 | Missense Mutation | ACC,AGC | T,S 6 | XP_016866922.1 | |
XM_017011434.1 | 2041 | Missense Mutation | ACC,AGC | T,S 6 | XP_016866923.1 | |
XM_017011435.1 | 2041 | Missense Mutation | ACC,AGC | T,S 6 | XP_016866924.1 |