Transcript #00000633 (NM_000369.5, TSHR gene)

Transcript name transcript variant 1
Gene name TSHR (thyroid stimulating hormone receptor)
Chromosome 14
Transcript - NCBI ID NM_000369.5
Transcript - Ensembl ID -
Protein - NCBI ID NP_000360.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

32 entries on 1 page. Showing entries 1 - 32.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

Published as     

RNA change     

Protein     

Clinical classification     
+/. 1 c.154C>A 253C>A, P52T r.(?) p.(Pro52Thr) Benign
+/. 1 c.154C>A 253C>A, P52T r.(?) p.(Pro52Thr) Benign
+/. 1 c.154C>A 253C>A , P25T r.(?) p.(Pro52Thr) Benign
+/. 5i c.468-31C>T IVS5-31C>T r.(=) p.(=) -
+/. 5i c.468-31C>T IVS5-31C>T r.(=) p.(=) -
+/. 5i c.468-31C>T IVS5-31C>T r.(=) p.(=) -
+/. 5i c.468-31C>T IVS5-31C>T r.(=) p.(=) -
+/. 5i c.468-31C>T IVS5-31C>T r.(=) p.(=) -
+/. 5i c.468-31C>T IVS5-31C>T r.(=) p.(=) -
+/. 5i c.468-31C>T IVS5-31C>T r.(=) p.(=) -
+/. 5i c.468-31C>T IVS5-31C>T r.(=) p.(=) -
+/. 6i c.545+13A>G IVS6+13A>G r.(=) p.(=) Benign
+/. 6i c.545+13A>G IVS6+13A>G r.(=) p.(=) Benign
+/. 6i c.545+13A>G IVS6+13A>G r.(=) p.(=) Benign
+/. 6i c.545+13A>G IVS6+13A>G r.(=) p.(=) Benign
+/. 6i c.545+13A>G IVS6+13A>G r.(=) p.(=) Benign
+/. 6i c.545+13A>G IVS6+13A>G r.(=) p.(=) Benign
+/. 6i c.545+13A>G IVS6+13A>G r.(=) p.(=) Benign
+/. 6i c.545+13A>G IVS6+13A>G r.(=) p.(=) Benign
+/. 7 c.561T>C 561T>C, N187N r.(=) p.(=) Benign
+/. 7 c.561T>C 561T>C, N187N r.(=) p.(=) Benign
+/. 7 c.561T>C 561T>C, N187N r.(=) p.(=) Benign
+/. 7 c.561T>C 561T>C, N187N r.(=) p.(=) Benign
+/. 7 c.561T>C N187N, 561T>C r.(=) p.(=) Benign
+/. 9i c.881+3A>G IVS9+3A>G r.spl? p.? Uncertain significance
+/. 10 c.1377G>A 1377G>A, A459A r.(=) p.(=) Benign/Likely benign​
+/. 10 c.1377G>A 1377G>A, A459A r.(=) p.(=) Benign/Likely benign
+/. 10 c.2181G>C 2181C>G, D727E r.(?) p.(Glu727Asp) Benign/Likely benign
+/. 10 c.2181G>C D727E, 2181C>G r.(?) p.(Glu727Asp) Benign/Likely benign
+/. 10 c.2181G>C D727E r.(?) p.(Glu727Asp) Benign/Likely benign
+/. 10 c.2181G>C D727E r.(?) p.(Glu727Asp) Benign/Likely benign
+/. 10 c.2181G>C D727E r.(?) p.(Glu727Asp) Benign/Likely benign​
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