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Search Thermo Fisher Scientific
GGCCAGGCCATTTTCGCTTCATTTT[C/T]TTCTGTTTGCCATTCTTGTGACCAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 611551 | ||||||||||||||||||||
Literature Links: |
FBLN7 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 |
FBLN7 - fibulin 7 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001128165.1 | 485 | Intron | NP_001121637.1 | |||
NM_153214.2 | 485 | Intron | NP_694946.2 | |||
XM_006712260.3 | 485 | Intron | XP_006712323.1 | |||
XM_011510585.2 | 485 | Intron | XP_011508887.1 | |||
XM_011510587.2 | 485 | Intron | XP_011508889.1 | |||
XM_017003317.1 | 485 | Intron | XP_016858806.1 | |||
XM_017003318.1 | 485 | Intron | XP_016858807.1 | |||
XM_017003319.1 | 485 | Intron | XP_016858808.1 |
ZC3H8 - zinc finger CCCH-type containing 8 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_032494.2 | 485 | Silent Mutation | AAA,AAG | K,K 142 | NP_115883.2 | |
XM_011511998.1 | 485 | Silent Mutation | AAA,AAG | K,K 40 | XP_011510300.1 | |
XM_017005107.1 | 485 | Silent Mutation | AAA,AAG | K,K 40 | XP_016860596.1 |