Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGCAGGCGTGCTTCCGCAGCTGGGG[A/G]CTCCGCTCCATCTCCAGGGGATCCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608759 MIM: 610598 | ||||||||||||||||||||
Literature Links: |
CYGB 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 |
CYGB - cytoglobin | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_134268.4 | 235 | Silent Mutation | AGC,AGT | S,S 75 | NP_599030.1 | |
XM_005257005.2 | 235 | Silent Mutation | AGC,AGT | S,S 75 | XP_005257062.1 | |
XM_017024116.1 | 235 | Silent Mutation | AGC,AGT | S,S 10 | XP_016879605.1 |
PRCD - progressive rod-cone degeneration | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001077620.2 | 235 | Intron | NP_001071088.1 | |||
XM_017025013.1 | 235 | Intron | XP_016880502.1 | |||
XM_017025014.1 | 235 | Intron | XP_016880503.1 | |||
XM_017025015.1 | 235 | Intron | XP_016880504.1 |