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TCTGAGGGTTCCGGGGCACGGCTAT[A/G]GGTTCTGAAGGGGGTGCTCCTACTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608715 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
LOC101060391 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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LOC101060391 - uncharacterized LOC101060391 | ||||||
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There are no transcripts associated with this gene. |
SNTG2 - syntrophin gamma 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_018968.3 | Intron | NP_061841.2 | ||||
XM_011510366.2 | Intron | XP_011508668.1 | ||||
XM_017004361.1 | Intron | XP_016859850.1 | ||||
XM_017004362.1 | Intron | XP_016859851.1 | ||||
XM_017004363.1 | Intron | XP_016859852.1 | ||||
XM_017004364.1 | Intron | XP_016859853.1 | ||||
XM_017004365.1 | Intron | XP_016859854.1 | ||||
XM_017004366.1 | Intron | XP_016859855.1 | ||||
XM_017004367.1 | Intron | XP_016859856.1 | ||||
XM_017004368.1 | Intron | XP_016859857.1 | ||||
XM_017004369.1 | Intron | XP_016859858.1 | ||||
XM_017004370.1 | Intron | XP_016859859.1 | ||||
XM_017004371.1 | Intron | XP_016859860.1 | ||||
XM_017004372.1 | Intron | XP_016859861.1 | ||||
XM_017004373.1 | Intron | XP_016859862.1 | ||||
XM_017004374.1 | Intron | XP_016859863.1 |