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Search Thermo Fisher Scientific
TTTGCCATATGAGGTCTCAGGAGTA[C/T]GCCTTGATGCCTGTGAGAATCCTGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
ATG16L2 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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ATG16L2 - autophagy related 16 like 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001318766.1 | 2326 | Intron | NP_001305695.1 | |||
NM_033388.1 | 2326 | Intron | NP_203746.1 | |||
XM_005274376.4 | 2326 | Intron | XP_005274433.1 | |||
XM_006718732.2 | 2326 | Intron | XP_006718795.1 | |||
XM_006718733.3 | 2326 | Intron | XP_006718796.1 | |||
XM_006718734.2 | 2326 | Intron | XP_006718797.1 | |||
XM_011545332.1 | 2326 | Intron | XP_011543634.1 | |||
XM_011545333.1 | 2326 | Intron | XP_011543635.1 | |||
XM_011545334.1 | 2326 | Intron | XP_011543636.1 |
FCHSD2 - FCH and double SH3 domains 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_014824.2 | 2326 | Missense Mutation | CAT,CGT | H,R 702 | NP_055639.2 | |
XM_011545409.1 | 2326 | Missense Mutation | CAT,CGT | H,R 681 | XP_011543711.1 | |
XM_011545410.2 | 2326 | Missense Mutation | CAT,CGT | H,R 677 | XP_011543712.1 | |
XM_017018632.1 | 2326 | Missense Mutation | CAT,CGT | H,R 681 | XP_016874121.1 |