Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CCCTTGATCAAGGCCGCACTCACCA[A/G]GCAGGCCCCCGAGGTACAGAGGGGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610650 MIM: 601033 | ||||||||||||||||||||
Literature Links: |
ADRM1 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 |
ADRM1 - adhesion regulating molecule 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001281437.1 | 10893 | Intron | NP_001268366.1 | |||
NM_001281438.1 | 10893 | Intron | NP_001268367.1 | |||
NM_007002.3 | 10893 | Intron | NP_008933.2 | |||
NM_175573.2 | 10893 | Intron | NP_783163.1 | |||
XM_005260257.1 | 10893 | Intron | XP_005260314.1 | |||
XM_011528503.1 | 10893 | Intron | XP_011526805.1 | |||
XM_017027602.1 | 10893 | Intron | XP_016883091.1 | |||
XM_017027603.1 | 10893 | Intron | XP_016883092.1 | |||
XM_017027604.1 | 10893 | Intron | XP_016883093.1 | |||
XM_017027605.1 | 10893 | Intron | XP_016883094.1 | |||
XM_017027606.1 | 10893 | Intron | XP_016883095.1 | |||
XM_017027607.1 | 10893 | Intron | XP_016883096.1 | |||
XM_017027608.1 | 10893 | Intron | XP_016883097.1 | |||
XM_017027609.1 | 10893 | Intron | XP_016883098.1 | |||
XM_017027610.1 | 10893 | Intron | XP_016883099.1 |
LAMA5 - laminin subunit alpha 5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_005560.4 | 10893 | Missense Mutation | CCT,CTT | P,L 3649 | NP_005551.3 | |
XM_006723796.3 | 10893 | Missense Mutation | CCT,CTT | P,L 3654 | XP_006723859.1 | |
XM_006723798.3 | 10893 | Intron | XP_006723861.1 | |||
XM_011528818.2 | 10893 | Missense Mutation | CCT,CTT | P,L 3608 | XP_011527120.1 | |
XM_011528819.2 | 10893 | Missense Mutation | CCT,CTT | P,L 3563 | XP_011527121.1 |