Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ACATCAGGGATGCCATCAGGCACCC[C/T]GTGTCCCACTCTTCCTCGTCCTGTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608326 | ||||||||||||||||||||
Literature Links: |
STOML1 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 |
STOML1 - stomatin like 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001256672.1 | 2051 | Missense Mutation | AGG,GGG | R,G 341 | NP_001243601.1 | |
NM_001256673.1 | 2051 | Missense Mutation | AGG,GGG | R,G 292 | NP_001243602.1 | |
NM_001256674.1 | 2051 | Missense Mutation | AGG,GGG | R,G 291 | NP_001243603.1 | |
NM_001256675.1 | 2051 | Missense Mutation | AGG,GGG | R,G 271 | NP_001243604.1 | |
NM_001256676.1 | 2051 | Missense Mutation | AGG,GGG | R,G 254 | NP_001243605.1 | |
NM_001256677.1 | 2051 | Missense Mutation | AGG,GGG | R,G 299 | NP_001243606.1 | |
NM_001324226.1 | 2051 | Missense Mutation | AGG,GGG | R,G 185 | NP_001311155.1 | |
NM_001324227.1 | 2051 | Missense Mutation | AGG,GGG | R,G 255 | NP_001311156.1 | |
NM_001324228.1 | 2051 | Missense Mutation | AGG,GGG | R,G 255 | NP_001311157.1 | |
NM_001324229.1 | 2051 | Missense Mutation | AGG,GGG | R,G 186 | NP_001311158.1 | |
NM_001324230.1 | 2051 | Missense Mutation | AGG,GGG | R,G 300 | NP_001311159.1 | |
NM_004809.4 | 2051 | Missense Mutation | AGG,GGG | R,G 342 | NP_004800.2 | |
XM_005254792.4 | 2051 | Missense Mutation | AGG,GGG | R,G 300 | XP_005254849.1 | |
XM_006720773.3 | 2051 | Missense Mutation | AGG,GGG | R,G 299 | XP_006720836.1 |