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GCCAGCAACATCAGGTCAATCCTCC[C/T]GTGCTGCTGTCCCTCTGACTCTCTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616380 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
LAMB4 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
|
LAMB4 - laminin subunit beta 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001318046.1 | 5905 | Intron | NP_001304975.1 | |||
NM_001318047.1 | 5905 | Intron | NP_001304976.1 | |||
NM_001318048.1 | 5905 | Intron | NP_001304977.1 | |||
NM_007356.2 | 5905 | Intron | NP_031382.2 | |||
XM_011515975.1 | 5905 | Intron | XP_011514277.1 | |||
XM_011515978.1 | 5905 | Intron | XP_011514280.1 | |||
XM_011515979.2 | 5905 | Intron | XP_011514281.1 | |||
XM_011515980.2 | 5905 | Intron | XP_011514282.1 | |||
XM_017011879.1 | 5905 | UTR 3 | XP_016867368.1 | |||
XM_017011880.1 | 5905 | Intron | XP_016867369.1 |