Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GTCCCCAGCCGCAGTCCACTGGGCC[A/G]CAGAGCGCTTCTGTCACCTACAAGA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 182144 | ||||||||||||||||||||
Literature Links: |
SHMT1 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 |
SHMT1 - serine hydroxymethyltransferase 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001281786.1 | Intron | NP_001268715.1 | ||||
NM_004169.4 | Intron | NP_004160.3 | ||||
NM_148918.2 | Intron | NP_683718.1 | ||||
XM_005256767.3 | Intron | XP_005256824.1 | ||||
XM_011523992.2 | Intron | XP_011522294.1 | ||||
XM_017024957.1 | Intron | XP_016880446.1 | ||||
XM_017024958.1 | Intron | XP_016880447.1 | ||||
XM_017024959.1 | Intron | XP_016880448.1 | ||||
XM_017024960.1 | Intron | XP_016880449.1 |
SMCR8 - Smith-Magenis syndrome chromosome region, candidate 8 | ||||||
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There are no transcripts associated with this gene. |