Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GAGACTGGCTCAGGTTCGCCAGCTC[A/G]TGGAGGAGAGACTCGTTCTGCTGCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 613084 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
MYT1L 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
|
MYT1L - myelin transcription factor 1 like | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001303052.1 | 4465 | Silent Mutation | CAC,CAT | H,H 1119 | NP_001289981.1 | |
NM_015025.3 | 4465 | Silent Mutation | CAC,CAT | H,H 1117 | NP_055840.2 | |
XM_011510318.1 | 4465 | Silent Mutation | CAC,CAT | H,H 1142 | XP_011508620.1 | |
XM_011510319.1 | 4465 | Silent Mutation | CAC,CAT | H,H 1142 | XP_011508621.1 | |
XM_011510320.2 | 4465 | Silent Mutation | CAC,CAT | H,H 1142 | XP_011508622.1 | |
XM_011510321.2 | 4465 | Silent Mutation | CAC,CAT | H,H 1142 | XP_011508623.1 | |
XM_011510322.2 | 4465 | Silent Mutation | CAC,CAT | H,H 1142 | XP_011508624.1 | |
XM_011510323.1 | 4465 | Silent Mutation | CAC,CAT | H,H 1142 | XP_011508625.1 | |
XM_011510324.1 | 4465 | Silent Mutation | CAC,CAT | H,H 1140 | XP_011508626.1 | |
XM_011510325.1 | 4465 | Silent Mutation | CAC,CAT | H,H 1140 | XP_011508627.1 | |
XM_011510326.1 | 4465 | Silent Mutation | CAC,CAT | H,H 1121 | XP_011508628.1 | |
XM_011510327.1 | 4465 | Silent Mutation | CAC,CAT | H,H 1142 | XP_011508629.1 | |
XM_011510328.2 | 4465 | Silent Mutation | CAC,CAT | H,H 1140 | XP_011508630.1 | |
XM_011510331.2 | 4465 | Intron | XP_011508633.1 | |||
XM_011510332.2 | 4465 | Intron | XP_011508634.1 | |||
XM_017003604.1 | 4465 | Silent Mutation | CAC,CAT | H,H 1142 | XP_016859093.1 | |
XM_017003605.1 | 4465 | Silent Mutation | CAC,CAT | H,H 1142 | XP_016859094.1 | |
XM_017003606.1 | 4465 | Silent Mutation | CAC,CAT | H,H 1140 | XP_016859095.1 | |
XM_017003607.1 | 4465 | Silent Mutation | CAC,CAT | H,H 1140 | XP_016859096.1 | |
XM_017003608.1 | 4465 | Intron | XP_016859097.1 | |||
XM_017003609.1 | 4465 | Silent Mutation | CAC,CAT | H,H 1119 | XP_016859098.1 | |
XM_017003610.1 | 4465 | Silent Mutation | CAC,CAT | H,H 1119 | XP_016859099.1 | |
XM_017003611.1 | 4465 | Silent Mutation | CAC,CAT | H,H 1119 | XP_016859100.1 | |
XM_017003612.1 | 4465 | Silent Mutation | CAC,CAT | H,H 1119 | XP_016859101.1 | |
XM_017003613.1 | 4465 | Silent Mutation | CAC,CAT | H,H 1117 | XP_016859102.1 | |
XM_017003614.1 | 4465 | Silent Mutation | CAC,CAT | H,H 1117 | XP_016859103.1 | |
XM_017003615.1 | 4465 | Silent Mutation | CAC,CAT | H,H 1121 | XP_016859104.1 | |
XM_017003616.1 | 4465 | Silent Mutation | CAC,CAT | H,H 1119 | XP_016859105.1 | |
XM_017003617.1 | 4465 | Silent Mutation | CAC,CAT | H,H 1119 | XP_016859106.1 | |
XM_017003618.1 | 4465 | Silent Mutation | CAC,CAT | H,H 1117 | XP_016859107.1 | |
XM_017003619.1 | 4465 | Silent Mutation | CAC,CAT | H,H 1117 | XP_016859108.1 | |
XM_017003620.1 | 4465 | Silent Mutation | CAC,CAT | H,H 1044 | XP_016859109.1 | |
XM_017003621.1 | 4465 | Intron | XP_016859110.1 | |||
XM_017003622.1 | 4465 | Intron | XP_016859111.1 |