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Search Thermo Fisher Scientific
GGCACACAGGTGATGGTGACCTCGC[C/T]GATAAGCTCAAAGCCCTCATAGCAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616667 | ||||||||||||||||||||
Literature Links: |
CDIPT-AS1 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 |
CDIPT-AS1 - CDIPT antisense RNA 1 (head to head) | ||||||
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There are no transcripts associated with this gene. |
SEZ6L2 - seizure related 6 homolog like 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001114099.2 | 2421 | Missense Mutation | AGC,GGC | S,G 737 | NP_001107571.1 | |
NM_001114100.2 | 2421 | Missense Mutation | AGC,GGC | S,G 693 | NP_001107572.1 | |
NM_001243332.1 | 2421 | Missense Mutation | AGC,GGC | S,G 807 | NP_001230261.1 | |
NM_001243333.1 | 2421 | Missense Mutation | AGC,GGC | S,G 763 | NP_001230262.1 | |
NM_012410.3 | 2421 | Missense Mutation | AGC,GGC | S,G 737 | NP_036542.1 | |
NM_201575.3 | 2421 | Missense Mutation | AGC,GGC | S,G 807 | NP_963869.2 | |
XM_005255252.2 | 2421 | Intron | XP_005255309.1 | |||
XM_017023135.1 | 2421 | Missense Mutation | AGC,GGC | S,G 623 | XP_016878624.1 |