Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGCTGTTCAGACCTGAATTCCTCTC[A/C]CAGCCTGCTTTATATTTTCCAGTAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613084 | ||||||||||||||||||||
Literature Links: |
MYT1L 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 |
MYT1L - myelin transcription factor 1 like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001303052.1 | 4650 | Missense Mutation | GGG,GTG | G,V 1181 | NP_001289981.1 | |
NM_015025.3 | 4650 | Missense Mutation | GGG,GTG | G,V 1179 | NP_055840.2 | |
XM_011510318.1 | 4650 | Missense Mutation | GGG,GTG | G,V 1204 | XP_011508620.1 | |
XM_011510319.1 | 4650 | Missense Mutation | GGG,GTG | G,V 1204 | XP_011508621.1 | |
XM_011510320.2 | 4650 | Missense Mutation | GGG,GTG | G,V 1204 | XP_011508622.1 | |
XM_011510321.2 | 4650 | Missense Mutation | GGG,GTG | G,V 1204 | XP_011508623.1 | |
XM_011510322.2 | 4650 | Missense Mutation | GGG,GTG | G,V 1204 | XP_011508624.1 | |
XM_011510323.1 | 4650 | Missense Mutation | GGG,GTG | G,V 1204 | XP_011508625.1 | |
XM_011510324.1 | 4650 | Missense Mutation | GGG,GTG | G,V 1202 | XP_011508626.1 | |
XM_011510325.1 | 4650 | Missense Mutation | GGG,GTG | G,V 1202 | XP_011508627.1 | |
XM_011510326.1 | 4650 | Missense Mutation | GGG,GTG | G,V 1183 | XP_011508628.1 | |
XM_011510327.1 | 4650 | Intron | XP_011508629.1 | |||
XM_011510328.2 | 4650 | Intron | XP_011508630.1 | |||
XM_011510331.2 | 4650 | Intron | XP_011508633.1 | |||
XM_011510332.2 | 4650 | Intron | XP_011508634.1 | |||
XM_017003604.1 | 4650 | Missense Mutation | GGG,GTG | G,V 1204 | XP_016859093.1 | |
XM_017003605.1 | 4650 | Missense Mutation | GGG,GTG | G,V 1204 | XP_016859094.1 | |
XM_017003606.1 | 4650 | Missense Mutation | GGG,GTG | G,V 1202 | XP_016859095.1 | |
XM_017003607.1 | 4650 | Missense Mutation | GGG,GTG | G,V 1202 | XP_016859096.1 | |
XM_017003608.1 | 4650 | Intron | XP_016859097.1 | |||
XM_017003609.1 | 4650 | Missense Mutation | GGG,GTG | G,V 1181 | XP_016859098.1 | |
XM_017003610.1 | 4650 | Missense Mutation | GGG,GTG | G,V 1181 | XP_016859099.1 | |
XM_017003611.1 | 4650 | Missense Mutation | GGG,GTG | G,V 1181 | XP_016859100.1 | |
XM_017003612.1 | 4650 | Missense Mutation | GGG,GTG | G,V 1181 | XP_016859101.1 | |
XM_017003613.1 | 4650 | Missense Mutation | GGG,GTG | G,V 1179 | XP_016859102.1 | |
XM_017003614.1 | 4650 | Missense Mutation | GGG,GTG | G,V 1179 | XP_016859103.1 | |
XM_017003615.1 | 4650 | Intron | XP_016859104.1 | |||
XM_017003616.1 | 4650 | Intron | XP_016859105.1 | |||
XM_017003617.1 | 4650 | Intron | XP_016859106.1 | |||
XM_017003618.1 | 4650 | Intron | XP_016859107.1 | |||
XM_017003619.1 | 4650 | Intron | XP_016859108.1 | |||
XM_017003620.1 | 4650 | Missense Mutation | GGG,GTG | G,V 1106 | XP_016859109.1 | |
XM_017003621.1 | 4650 | Intron | XP_016859110.1 | |||
XM_017003622.1 | 4650 | Intron | XP_016859111.1 |