Transcript #00000138 (NM_000448.2, RAG1 gene)

Transcript name recombination activating gene 1
Gene name RAG1 (recombination activating gene 1)
Chromosome 11
Transcript - NCBI ID NM_000448.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_000439.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2012-05-11 13:12:13 +02:00 (CEST)
Date last edited N/A


Variants

97 entries on 1 page. Showing entries 1 - 97.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.-15+12A>G r.(=) p.(=)
+/. - c.140del r.(?) p.(Lys47Argfs*35)
+/. - c.140del r.(?) p.(Lys47Argfs*35)
+?/. - c.140del r.(?) p.(Lys47Argfs*35)
-?/. - c.189A>G r.(?) p.(Pro63=)
-/. - c.251A>G r.(?) p.(His84Arg)
-?/. - c.295G>A r.(?) p.(Gly99Ser)
-?/. - c.303G>A r.(=) p.(=)
-?/. - c.303G>A r.(=) p.(=)
+/. - c.322C>T r.(?) p.(Arg108*)
+/. - c.322C>T r.(?) p.(Arg108*)
+/. - c.322C>T r.(?) p.(Arg108*)
?/. - c.378A>G r.(?) p.(Arg126=)
?/. - c.394C>T r.(?) p.(Pro132Ser)
?/. - c.486T>A r.(?) p.(Asp162Glu)
?/. - c.486T>A r.(?) p.(Asp162Glu)
-?/. - c.577G>A r.(?) p.(Glu193Lys)
?/. - c.590C>T r.(?) p.(Pro197Leu)
-?/. - c.725A>G r.(?) p.(Gln242Arg)
-?/. - c.725A>G r.(?) p.(Gln242Arg)
-?/. - c.725A>G r.(?) p.(Gln242Arg)
+/? ? c.730A>G r.(?) p.(Arg244Gly)
+/. 2 c.736del r.(?) p.(Ala246Profs*18)
-?/. - c.746= r.(=) p.(Arg249=)
-/. - c.746= r.(=) p.(Arg249=)
-?/. - c.789G>A r.(?) p.(Met263Ile)
-/. - c.906C>A r.(?) p.(Asp302Glu)
-?/. - c.974G>A r.(?) p.(Gly325Asp)
+/. - c.983G>A r.(?) p.(Cys328Tyr)
-?/. - c.1048G>A r.(?) p.(Val350Ile)
+/. 2 c.1175G>A r.(?) p.(Gly392Glu)
+/? ? c.1186C>T r.(?) p.(Arg396Cys)
+/. - c.1187G>A r.(?) p.(Arg396His)
+/? ? c.1187G>T r.(?) p.(Arg396Leu)
+/? ? c.1201T>C r.(?) p.(Ser401Pro)
+/? ? c.1201T>C r.(?) p.(Ser401Pro)
+/. - c.1211G>A r.(?) p.(Arg404Gln)
+/. 2 c.1211G>A r.(?) p.(Arg404Gln)
+/. - c.1211G>A r.(?) p.(Arg404Gln)
+/. - c.1211G>A r.(?) p.(Arg404Gln)
+/. - c.1211G>A r.(?) p.(Arg404Gln)
+/. - c.1211G>A r.(?) p.(Arg404Gln)
+/? ? c.1229G>A r.(?) p.(Arg410Gln)
+/? ? c.1297G>A r.(?) p.(Val433Met)
+/? ? c.1303A>G r.(?) p.(Met435Val)
+/? ? c.1331C>T r.(?) p.(Ala444Val)
+/. - c.1331C>T r.(?) p.(Ala444Val)
+/. - c.1331C>T r.(?) p.(Ala444Val)
-?/. - c.1346G>A r.(?) p.(Arg449Lys)
-/. - c.1346G>A r.(?) p.(Arg449Lys)
?/. - c.1346G>A r.(?) p.(Arg449Lys)
?/. - c.1346G>A r.(?) p.(Arg449Lys)
+/? ? c.1361T>A r.(?) p.(Leu454Gln)
+/? ? c.1420C>T r.(?) p.(Arg474Cys)
+/? ? c.1421G>A r.(?) p.(Arg474His)
+/. - c.1516C>T r.(?) p.(Leu506Phe)
?/. - c.1520G>A r.(?) p.(Arg507Gln)
?/. - c.1573C>T r.(?) p.(Pro525Ser)
?/. - c.1649A>G r.(?) p.(Asp550Gly)
+/? ? c.1677G>T r.(?) p.(Arg559Ser)
+/? ? c.1677G>T r.(?) p.(Arg559Ser)
+/. - c.1681C>T r.(?) p.(Arg561Cys)
+/. - c.1682G>A r.(?) p.(Arg561His)
?/. - c.1864G>A r.(?) p.(Ala622Thr)
+/? ? c.1870C>T r.(?) p.(Arg624Cys)
+/? ? c.1871G>A r.(?) p.(Arg624His)
+/? ? c.2006A>G r.(?) p.(Glu669Gly)
?/. - c.2009C>T r.(?) p.(Thr670Met)
+/? ? c.2095C>T r.(?) p.(Arg699Trp)
+/? ? c.2095C>T r.(?) p.(Arg699Trp)
+/. - c.2095C>T r.(?) p.(Arg699Trp)
+?/. - c.2147G>A r.(?) p.(Arg716Gln)
./. - c.2196_2197del r.(?) p.(Cys733*)
?/. - c.2207C>T r.(?) p.(Thr736Ile)
+/? ? c.2258A>T r.(?) p.(His753Leu)
+/. - c.2326C>T r.(?) p.(Arg776Trp)
+?/. - c.2332C>G r.(?) p.(Arg778Gly)
+/. - c.2333G>A r.(?) p.(Arg778Gln)
-?/. - c.2451A>G r.(?) p.(Glu817=)
-/. - c.2459A>G r.(?) p.(Lys820Arg)
+/. - c.2522G>A r.(?) p.(Arg841Gln)
+/? ? c.2564A>T r.(?) p.(Asn855Ile)
-?/. - c.2571C>T r.(?) p.(Ala857=)
-?/. - c.2571C>T r.(?) p.(Ala857=)
-/. - c.2638G>A r.(?) p.(Glu880Lys)
+/? ? c.2654T>G r.(?) p.(Leu885Arg)
-?/. - c.2659G>A r.(?) p.(Asp887Asn)
+?/. - c.2690G>A r.(?) p.(Arg897Gln)
-?/. - c.2751G>A r.(?) p.(Gln917=)
-?/. - c.2751G>A r.(?) p.(Gln917=)
?/. - c.2857G>T r.(?) p.(Asp953Tyr)
-/. - c.2880A>G r.(?) p.(Ala960=)
+/? ? c.2924G>A r.(?) p.(Arg975Gln)
?/. - c.2942A>G r.(?) p.(Gln981Arg)
+/. - c.2974A>G r.(?) p.(Lys992Glu)
-?/. - c.3016A>G r.(?) p.(Met1006Val)
-?/. - c.3021T>G r.(?) p.(Asn1007Lys)
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