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GTTTTCCTTGAAGCTCTTACTATGC[C/T]TGCACTTGAACTCCAGCACCATCCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
FAM234B 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 |
FAM234B - family with sequence similarity 234 member B | ||||||
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There are no transcripts associated with this gene. |
GSG1 - germ cell associated 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001080554.2 | 1074 | Silent Mutation | CAA,CAG | Q,Q 320 | NP_001074023.1 | |
NM_001080555.2 | 1074 | Missense Mutation | AAG,AGG | K,R 279 | NP_001074024.1 | |
NM_001206842.1 | 1074 | Missense Mutation | AAG,AGG | K,R 256 | NP_001193771.1 | |
NM_001206843.1 | 1074 | Missense Mutation | AAG,AGG | K,R 215 | NP_001193772.1 | |
NM_001206845.1 | 1074 | Missense Mutation | AAG,AGG | K,R 192 | NP_001193774.1 | |
NM_031289.3 | 1074 | Silent Mutation | CAA,CAG | Q,Q 284 | NP_112579.2 | |
NM_153823.3 | 1074 | Missense Mutation | AAG,AGG | K,R 243 | NP_722545.2 | |
XM_005253493.2 | 1074 | Missense Mutation | AAG,AGG | K,R 303 | XP_005253550.1 | |
XM_005253495.1 | 1074 | Silent Mutation | CAA,CAG | Q,Q 344 | XP_005253552.1 | |
XM_011520858.1 | 1074 | Missense Mutation | AAG,AGG | K,R 312 | XP_011519160.1 | |
XM_011520859.1 | 1074 | Missense Mutation | AAG,AGG | K,R 288 | XP_011519161.1 | |
XM_011520860.1 | 1074 | Silent Mutation | CAA,CAG | Q,Q 353 | XP_011519162.1 | |
XM_011520861.1 | 1074 | Missense Mutation | AAG,AGG | K,R 265 | XP_011519163.1 | |
XM_011520862.1 | 1074 | Silent Mutation | CAA,CAG | Q,Q 329 | XP_011519164.1 | |
XM_011520863.1 | 1074 | Silent Mutation | CAA,CAG | Q,Q 306 | XP_011519165.1 |