Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GCAGAATTGTCTTTCAGTGGCAGGG[C/T]CTCAGCTACTCATCACAATCAGAAA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 182144 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SHMT1 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
|||||
AMR
|
SHMT1 - serine hydroxymethyltransferase 1 | ||||||
---|---|---|---|---|---|---|
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 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |