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GTTTCTCATGCCCTTCCCACCCAAG[C/T]CATGCGCAACGCTAGGCGCACACTG
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 608760 | |||||||||||||||||||||||
Literature Links: |
ATG7 PubMed Links | |||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
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 |
VGLL4 - vestigial like family member 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001128219.2 | Intron | NP_001121691.1 | ||||
NM_001128220.2 | Intron | NP_001121692.1 | ||||
NM_001128221.2 | Intron | NP_001121693.1 | ||||
NM_001284390.1 | Intron | NP_001271319.1 | ||||
NM_001284391.1 | Intron | NP_001271320.1 | ||||
NM_014667.3 | Intron | NP_055482.2 | ||||
XM_011534267.2 | Intron | XP_011532569.1 | ||||
XM_011534268.1 | Intron | XP_011532570.1 | ||||
XM_011534269.1 | Intron | XP_011532571.1 | ||||
XM_017007541.1 | Intron | XP_016863030.1 | ||||
XM_017007542.1 | Intron | XP_016863031.1 |