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GGTATGTGGAGAGCACACTTTGTTT[G/T]TGAGACAGGATCTCACTCTGTTGCC
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 |
---|---|---|
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 |
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 | 6872 | UTR 3 | NP_001098676.2 | |||
NM_001105207.2 | 6872 | UTR 3 | NP_001098677.2 | |||
NM_001105208.2 | 6872 | Intron | NP_001098678.1 | |||
NM_001105209.2 | 6872 | Intron | NP_001098679.1 | |||
NM_002290.4 | 6872 | UTR 3 | NP_002281.3 | |||
XM_005266983.3 | 6872 | Intron | XP_005267040.2 | |||
XM_005266984.3 | 6872 | Intron | XP_005267041.2 | |||
XM_017010854.1 | 6872 | Intron | XP_016866343.1 |