Transcript #00000371 (NM_000369.2, TSHR gene)

Transcript name transcript variant 1
Gene name TSHR (thyroid stimulating hormone receptor)
Chromosome 14
Transcript - NCBI ID NM_000369.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_000360.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2012-09-13 12:10:21 +02:00 (CEST)
Date last edited N/A


Variants

101 entries on 2 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+?/. - c.22C>T r.(?) p.(Gln8*)
?/. - c.100G>A r.(?) p.(Glu34Lys)
?/. - c.100G>A r.(?) p.(Glu34Lys)
-/. - c.106G>C r.(?) p.(Asp36His)
-/. - c.154C>A r.(?) p.(Pro52Thr)
-/. - c.154C>A r.(?) p.(Pro52Thr)
?/. - c.170+25902G>A r.(=) p.(=)
?/. - c.170+25902G>A r.(=) p.(=)
?/. - c.170+26088C>G r.(=) p.(=)
?/. - c.170+26088C>G r.(=) p.(=)
?/. - c.170+26188T>G r.(=) p.(=)
?/. - c.170+26188T>G r.(=) p.(=)
?/. - c.170+26317G>A r.(=) p.(=)
?/. - c.170+26317G>A r.(=) p.(=)
?/. - c.170+26408G>A r.(=) p.(=)
?/. - c.170+26408G>A r.(=) p.(=)
?/. - c.170+26426A>G r.(=) p.(=)
?/. - c.170+26426A>G r.(=) p.(=)
?/. - c.170+26767dup r.(=) p.(=)
?/. - c.170+26767dup r.(=) p.(=)
?/. - c.170+27169G>A r.(=) p.(=)
?/. - c.170+27169G>A r.(=) p.(=)
?/. - c.170+27340T>C r.(=) p.(=)
?/. - c.170+27496C>G r.(=) p.(=)
?/. - c.170+28052G>A r.(=) p.(=)
?/. - c.170+28062G>A r.(=) p.(=)
?/. - c.170+28858C>T r.(=) p.(=)
?/. - c.170+28908G>A r.(=) p.(=)
?/. - c.170+29035C>T r.(=) p.(=)
?/. - c.170+29136C>G r.(=) p.(=)
?/. - c.170+29762G>A r.(=) p.(=)
-?/. - c.171-11T>C r.(=) p.(=)
?/. - c.202C>T r.(?) p.(Pro68Ser)
+?/. - c.202C>T r.(?) p.(Pro68Ser)
+?/. - c.202C>T r.(?) p.(Pro68Ser)
+?/. - c.202C>T r.(?) p.(Pro68Ser)
-?/. - c.262A>C r.(?) p.(Thr88Pro)
+?/. - c.326G>A r.(?) p.(Arg109Gln)
?/. 4 c.352G>A r.(?) p.(Asp118Asn)
-/. - c.375C>T r.(?) p.(Leu125=)
?/. - c.431T>C r.(?) p.(Leu144Pro)
+/. - c.484C>G r.(?) p.(Pro162Ala)
+/. - c.484C>G r.(?) p.(Pro162Ala)
-/. - c.545+13A>G r.(=) p.(=)
-/. - c.545+13A>G r.(=) p.(=)
-/. - c.561T>C r.(?) p.(Asn187=)
-/. - c.561T>C r.(?) p.(Asn187=)
-/. - c.606G>T r.(?) p.(Leu202=)
?/. - c.635A>G r.(?) p.(Tyr212Cys)
?/. - c.692+3G>A r.spl? p.?
-/. - c.692+20G>C r.(=) p.(=)
-?/. - c.692+118G>A r.(=) p.(=)
-/. - c.692+163A>G r.(=) p.(=)
-/. - c.692+163A>G r.(=) p.(=)
-/. - c.692+209C>A r.(=) p.(=)
-/. - c.692+209C>A r.(=) p.(=)
?/. - c.847T>C r.(?) p.(Cys283Arg)
-/. - c.881+3A>G r.spl? p.?
?/. - c.902G>A r.(?) p.(Cys301Tyr)
?/. - c.962C>G r.(?) p.(Pro321Arg)
?/. - c.1078G>C r.(?) p.(Glu360Gln)
?/. - c.1090A>T r.(?) p.(Ile364Phe)
-?/. - c.1192T>G r.(?) p.(Cys398Gly)
?/. - c.1207G>A r.(?) p.(Asp403Asn)
+?/. 10 c.1264T>C r.(?) p.(Trp422Arg)
+?/. - c.1348C>T r.(?) p.(Arg450Cys)
+/. - c.1349G>A r.(?) p.(Arg450His)
-/. - c.1377G>A r.(?) p.(Ala459=)
-/. - c.1488G>A r.(?) p.(Thr496=)
+?/. - c.1504G>T r.(?) p.(Val502Phe)
+?/. - c.1532C>A r.(?) p.(Thr511Lys)
+?/. - c.1555C>T r.(?) p.(Arg519Cys)
?/. - c.1556G>A r.(?) p.(Arg519His)
-/. - c.1572C>G r.(?) p.(Thr524=)
?/. - c.1582C>T r.(?) p.(Arg528Cys)
?/. - c.1591C>T r.(?) p.(Arg531Trp)
?/. - c.1600C>T r.(?) p.(Arg534Cys)
+?/. - c.1631G>A r.(?) p.(Gly544Glu)
+/. - c.1657G>A r.(?) p.(Ala553Thr)
?/. - c.1667C>G r.(?) p.(Pro556Arg)
?/. - c.1727C>T r.(?) p.(Thr576Ile)
?/. - c.1778C>T r.(?) p.(Ala593Val)
+/. - c.1826G>A r.(?) p.(Arg609Gln)
-/. - c.1908C>T r.(?) p.(Cys636=)
?/. - c.1946T>C r.(?) p.(Leu649Pro)
+?/. - c.1963_1964del r.(?) p.(Thr655CysfsTer2)
?/. - c.2002C>T r.(?) p.(Pro668Ser)
?/. - c.2002C>T r.(?) p.(Pro668Ser)
?/. - c.2062G>A r.(?) p.(Asp688Asn)
?/. - c.2096G>A r.(?) p.(Cys699Tyr)
?/. - c.2101C>T r.(?) p.(Arg701Cys)
?/. - c.2104C>G r.(?) p.(Gln702Glu)
-?/. - c.2161G>T r.(?) p.(Val721Phe)
-/. - c.2181G>C r.(?) p.(Glu727Asp)
-/. - c.2181G>C r.(?) p.(Glu727Asp)
-/. - c.2181G>C r.(?) p.(Glu727Asp)
?/. - c.2183T>C r.(?) p.(Met728Thr)
-/. - c.2232C>G r.(?) p.(Asn744Lys)
?/. - c.2285C>T r.(?) p.(Thr762Met)
-?/. - c.*4A>G r.(=) p.(=)
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