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TTTTTAGATATAATTCTTTTATTTC[A/T]TTTCTATATTTTAATATTCTACCAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600133 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FAM229B 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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FAM229B - family with sequence similarity 229 member B | ||||||
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There are no transcripts associated with this gene. |
LAMA4 - laminin subunit alpha 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001105206.2 | 7014 | UTR 3 | NP_001098676.2 | |||
NM_001105207.2 | 7014 | UTR 3 | NP_001098677.2 | |||
NM_001105208.2 | 7014 | Intron | NP_001098678.1 | |||
NM_001105209.2 | 7014 | Intron | NP_001098679.1 | |||
NM_002290.4 | 7014 | UTR 3 | NP_002281.3 | |||
XM_005266983.3 | 7014 | Intron | XP_005267040.2 | |||
XM_005266984.3 | 7014 | Intron | XP_005267041.2 | |||
XM_017010854.1 | 7014 | Intron | XP_016866343.1 |