Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GTCCAGGCCTCACCTTCCCCGATGG[C/T]GCAGGTACCAGGGGAAGTGGACAAC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600941 MIM: 606214 | ||||||||||||||||||||
Literature Links: |
BLVRB 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 |
BLVRB - biliverdin reductase B | ||||||
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There are no transcripts associated with this gene. |
SPTBN4 - spectrin beta, non-erythrocytic 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_020971.2 | 173 | Missense Mutation | GCG,GTG | A,V 2 | NP_066022.2 | |
NM_025213.2 | 173 | Intron | NP_079489.2 | |||
XM_011527173.2 | 173 | Missense Mutation | GCG,GTG | A,V 2 | XP_011525475.1 | |
XM_017027049.1 | 173 | Missense Mutation | GCG,GTG | A,V 2 | XP_016882538.1 | |
XM_017027050.1 | 173 | Intron | XP_016882539.1 | |||
XM_017027051.1 | 173 | Missense Mutation | GCG,GTG | A,V 2 | XP_016882540.1 | |
XM_017027052.1 | 173 | Missense Mutation | GCG,GTG | A,V 2 | XP_016882541.1 |