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CCTTCCACTGGGAAGTTGGCAATCA[C/G]TTCCTCATCATCCTTGTTGAGCGCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612234 MIM: 612235 MIM: 612333 | ||||||||||||||||||||
Literature Links: |
CALHM1 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 |
CALHM1 - calcium homeostasis modulator 1 | ||||||
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There are no transcripts associated with this gene. |
CALHM2 - calcium homeostasis modulator 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_015916.4 | 1398 | Missense Mutation | CTG,GTG | L,V 263 | NP_057000.2 | |
XM_006717880.2 | 1398 | Missense Mutation | CTG,GTG | L,V 263 | XP_006717943.1 | |
XM_006717883.2 | 1398 | Missense Mutation | CTG,GTG | L,V 263 | XP_006717946.1 | |
XM_006717884.3 | 1398 | UTR 3 | XP_006717947.1 | |||
XM_011539848.2 | 1398 | Missense Mutation | CTG,GTG | L,V 263 | XP_011538150.1 | |
XM_017016306.1 | 1398 | Missense Mutation | CTG,GTG | L,V 263 | XP_016871795.1 | |
XM_017016307.1 | 1398 | Missense Mutation | CTG,GTG | L,V 263 | XP_016871796.1 | |
XM_017016308.1 | 1398 | UTR 3 | XP_016871797.1 | |||
XM_017016309.1 | 1398 | UTR 3 | XP_016871798.1 |
PDCD11 - programmed cell death 11 | ||||||
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There are no transcripts associated with this gene. |