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TATTAATAGGGGACCCTATTACCAC[A/C]TGTCTTTCTCCCTCAGTGTATGATA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 615532 MIM: 186977 | ||||||||||||||||||||
Literature Links: |
ERMARD 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 |
ERMARD - ER membrane associated RNA degradation | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001278531.1 | 1159 | Silent Mutation | ACA,ACC | T,T 11 | NP_001265460.1 | |
NM_001278532.1 | 1159 | Intron | NP_001265461.1 | |||
NM_001278533.1 | 1159 | Silent Mutation | ACA,ACC | T,T 11 | NP_001265462.1 | |
NM_018341.2 | 1159 | Silent Mutation | ACA,ACC | T,T 11 | NP_060811.1 | |
XM_011535938.2 | 1159 | Silent Mutation | ACA,ACC | T,T 11 | XP_011534240.1 | |
XM_011535939.2 | 1159 | UTR 5 | XP_011534241.1 | |||
XM_011535940.2 | 1159 | UTR 5 | XP_011534242.1 | |||
XM_017011027.1 | 1159 | UTR 5 | XP_016866516.1 | |||
XM_017011028.1 | 1159 | UTR 5 | XP_016866517.1 | |||
XM_017011029.1 | 1159 | UTR 5 | XP_016866518.1 | |||
XM_017011030.1 | 1159 | Intron | XP_016866519.1 | |||
XM_017011031.1 | 1159 | Intron | XP_016866520.1 | |||
XM_017011032.1 | 1159 | UTR 5 | XP_016866521.1 | |||
XM_017011033.1 | 1159 | UTR 5 | XP_016866522.1 |
TCTE3 - t-complex-associated-testis-expressed 3 | ||||||
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There are no transcripts associated with this gene. |