Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TCCCTGTTCAGCTCTCTGGCCTCGC[C/T]CTGCCCCGGGTCCCCAACGCCAAGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609240 MIM: 604682 | ||||||||||||||||||||
Literature Links: |
GSG2 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 |
GSG2 - germ cell associated 2, haspin | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_031965.2 | 557 | Missense Mutation | CCC,CTC | P,L 175 | NP_114171.2 |
ITGAE - integrin subunit alpha E | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_002208.4 | 557 | Intron | NP_002199.3 | |||
XM_011523823.2 | 557 | Intron | XP_011522125.1 | |||
XM_011523825.2 | 557 | Intron | XP_011522127.1 | |||
XM_011523827.2 | 557 | Intron | XP_011522129.1 | |||
XM_011523828.2 | 557 | Intron | XP_011522130.1 | |||
XM_017024586.1 | 557 | Intron | XP_016880075.1 | |||
XM_017024587.1 | 557 | Intron | XP_016880076.1 |