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GACTCGCTGGTGCAGTTTCGCTCAC[C/T]CCACGCCGGCTGCGGTTGGCCGGGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608826 MIM: 176268 MIM: 162662 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CGB7 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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CGB7 - chorionic gonadotropin beta subunit 7 | ||||||
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There are no transcripts associated with this gene. |
KCNA7 - potassium voltage-gated channel subfamily A member 7 | ||||||
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There are no transcripts associated with this gene. |
NTF4 - neurotrophin 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_006179.4 | 505 | Silent Mutation | GGA,GGG | G,G 81 | NP_006170.1 | |
XM_005258962.3 | 505 | Silent Mutation | GGA,GGG | G,G 81 | XP_005259019.1 | |
XM_006723232.3 | 505 | Intron | XP_006723295.1 | |||
XM_011527008.2 | 505 | Intron | XP_011525310.1 | |||
XM_011527009.2 | 505 | Intron | XP_011525311.1 | |||
XM_011527010.2 | 505 | Intron | XP_011525312.1 |