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CTCTCATCGAATGATGGGTGCCGAG[C/T]GATCATTCGTCACAGTCGGGCGGAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611877 MIM: 615628 | ||||||||||||||||||||
Literature Links: |
BAIAP2L1 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 |
BAIAP2L1 - BAI1 associated protein 2 like 1 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_018842.4 | 1777 | Missense Mutation | CAC,CGC | H,R 505 | NP_061330.2 |
BRI3 - brain protein I3 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001159491.1 | 1777 | Intron | NP_001152963.1 | |||
NM_015379.4 | 1777 | Intron | NP_056194.1 | |||
XM_017011931.1 | 1777 | Intron | XP_016867420.1 | |||
XM_017011932.1 | 1777 | Intron | XP_016867421.1 | |||
XM_017011933.1 | 1777 | Intron | XP_016867422.1 | |||
XM_017011934.1 | 1777 | Intron | XP_016867423.1 | |||
XM_017011935.1 | 1777 | Intron | XP_016867424.1 | |||
XM_017011936.1 | 1777 | Intron | XP_016867425.1 |