Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TAATTTTATTGCTCACCTCTTATGC[C/T]TGCTTTAAGCATTTTACTAGTTGAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 188840 | ||||||||||||||||||||
Literature Links: |
TTN 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 |
TTN - titin | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001256850.1 | 106789 | Missense Mutation | AGC,GGC | S,G 34250 | NP_001243779.1 | |
NM_001267550.2 | 106789 | Missense Mutation | AGC,GGC | S,G 35891 | NP_001254479.2 | |
NM_003319.4 | 106789 | Missense Mutation | AGC,GGC | S,G 26826 | NP_003310.4 | |
NM_133378.4 | 106789 | Missense Mutation | AGC,GGC | S,G 33323 | NP_596869.4 | |
NM_133379.4 | 106789 | Intron | NP_596870.2 | |||
NM_133432.3 | 106789 | Missense Mutation | AGC,GGC | S,G 26951 | NP_597676.3 | |
NM_133437.4 | 106789 | Missense Mutation | AGC,GGC | S,G 27018 | NP_597681.4 | |
XM_017004819.1 | 106789 | Missense Mutation | AGC,GGC | S,G 35522 | XP_016860308.1 | |
XM_017004820.1 | 106789 | Missense Mutation | AGC,GGC | S,G 33988 | XP_016860309.1 | |
XM_017004821.1 | 106789 | Missense Mutation | AGC,GGC | S,G 33987 | XP_016860310.1 | |
XM_017004822.1 | 106789 | Missense Mutation | AGC,GGC | S,G 33001 | XP_016860311.1 | |
XM_017004823.1 | 106789 | Missense Mutation | AGC,GGC | S,G 26873 | XP_016860312.1 |
TTN-AS1 - TTN antisense RNA 1 | ||||||
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There are no transcripts associated with this gene. |