Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TGCTTTCTTAGTTCTTCTGTCTGTC[C/T]TTCTTTCATCTGCTCTTCGTGCTTT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
1 submissions
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Phenotype: |
MIM: 608692 | ||||||||||||||||||||
Literature Links: |
BLZF1 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 |
BLZF1 - basic leucine zipper nuclear factor 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001320972.1 | 1477 | Intron | NP_001307901.1 | |||
NM_001320973.1 | 1477 | Intron | NP_001307902.1 | |||
NM_003666.3 | 1477 | Intron | NP_003657.1 | |||
XM_005245561.4 | 1477 | Intron | XP_005245618.1 | |||
XM_011510092.2 | 1477 | Intron | XP_011508394.1 | |||
XM_017002645.1 | 1477 | Intron | XP_016858134.1 |
CCDC181 - coiled-coil domain containing 181 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001300968.1 | 1477 | Missense Mutation | AGA,GGA | R,G 429 | NP_001287897.1 | |
NM_001300969.1 | 1477 | Missense Mutation | AGA,GGA | R,G 430 | NP_001287898.1 | |
NM_021179.2 | 1477 | Missense Mutation | AGA,GGA | R,G 429 | NP_067002.1 | |
XM_005245383.1 | 1477 | Missense Mutation | AGA,GGA | R,G 430 | XP_005245440.1 | |
XM_011509827.2 | 1477 | Missense Mutation | AGA,GGA | R,G 430 | XP_011508129.1 | |
XM_017001938.1 | 1477 | Missense Mutation | AGA,GGA | R,G 430 | XP_016857427.1 | |
XM_017001939.1 | 1477 | Missense Mutation | AGA,GGA | R,G 430 | XP_016857428.1 | |
XM_017001940.1 | 1477 | Missense Mutation | AGA,GGA | R,G 429 | XP_016857429.1 |