Transcript #00018032 (NM_002941.3, ROBO1 gene)

Transcript name transcript variant 1
Gene name ROBO1 (roundabout, axon guidance receptor, homolog 1 (Drosophila))
Chromosome 3
Transcript - NCBI ID NM_002941.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_002932.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.? r.(?) p.(Ala1414Asp)
-/. - c.89-20T>C r.(=) p.(=)
?/. - c.108G>T r.(?) p.(Arg36Ser)
-?/. - c.159G>A r.(?) p.(Ser53=)
?/. - c.214G>A r.(?) p.(Glu72Lys)
?/. - c.214G>A r.(?) p.(Glu72Lys)
-/. - c.499+15C>T r.(=) p.(=)
-?/. - c.537C>T r.(?) p.(Val179=)
?/. - c.584G>A r.(?) p.(Arg195Gln)
-/. - c.658-7T>C r.(=) p.(=)
+/. - c.686dup r.(?) p.(Tyr229*)
-?/. - c.699T>C r.(?) p.(Ser233=)
-/. - c.699T>C r.(?) p.(Ser233=)
-?/. - c.798G>A r.(?) p.(Lys266=)
-?/. - c.798G>A r.(?) p.(Lys266=)
+/. - c.928C>T r.(?) p.(Arg310Ter)
+/. - c.928C>T r.(?) p.(Arg310*)
+/. - c.928C>T r.(?) p.(Arg310Ter)
?/. - c.941C>G r.(?) p.(Thr314Ser)
-/. - c.1071C>A r.(?) p.(Pro357=)
?/. - c.1126G>A r.(?) p.(Gly376Arg)
?/. - c.1138C>T r.(?) p.(Pro380Ser)
-/. - c.1206C>T r.(?) p.(Ser402=)
-?/. - c.1224C>T r.(?) p.(=)
-?/. - c.1224C>T r.(?) p.(=)
-?/. - c.1224C>T r.(?) p.(=)
?/. - c.1394C>T r.(?) p.(Thr465Ile)
-?/. - c.1565G>A r.(?) p.(Arg522Gln)
?/. - c.1619T>C r.(?) p.(Ile540Thr)
?/. - c.1693T>A r.(?) p.(Ser565Thr)
-/. - c.1740G>A r.(?) p.(Ser580=)
-?/. - c.1828G>A r.(?) p.(Val610Ile)
-?/. - c.1828G>A r.(?) p.(Val610Ile)
?/. - c.1967-1G>A r.spl? p.?
?/. - c.2051C>A r.(?) p.(Thr684Asn)
-?/. - c.2088+7T>G r.(=) p.(=)
-?/. - c.2088+7T>G r.(=) p.(=)
-/. - c.2088+7T>G r.(=) p.(=)
-/. - c.2088+7T>G r.(=) p.(=)
-?/. - c.2088+18T>C r.(=) p.(=)
-?/. - c.2088+18T>C r.(=) p.(=)
?/. - c.2189C>T r.(?) p.(Thr730Met)
-?/. - c.2190G>A r.(?) p.(=)
-/. - c.2211A>T r.(?) p.(Val737=)
-?/. - c.2306A>G r.(?) p.(Lys769Arg)
?/. - c.2321-604G>A r.(=) p.(=)
?/. - c.2428G>A r.(?) p.(Val810Ile)
?/. - c.2442G>T r.(?) p.(Lys814Asn)
-?/. - c.2442+7G>A r.(=) p.(=)
-?/. - c.2442+20_2442+25dup r.(=) p.(=)
-?/. - c.2442+22_2442+25dup r.(=) p.(=)
-?/. - c.2615-10G>A r.(=) p.(=)
?/. - c.2630C>G r.(?) p.(Pro877Arg)
?/. - c.2665C>G r.(?) p.(Gln889Glu)
?/. - c.2665C>G r.(?) p.(Gln889Glu)
?/. - c.2708T>C r.(?) p.(Ile903Thr)
-?/. - c.2765G>A r.(?) p.(Arg922His)
-/. - c.2765G>A r.(?) p.(Arg922His)
-/. - c.2793C>A r.(?) p.(Thr931=)
?/. - c.2812+2T>G r.spl? p.?
-/. - c.2840-12G>A r.(=) p.(=)
-/. - c.2859C>T r.(?) p.(Gly953=)
-?/. - c.2859C>T r.(?) p.(Gly953=)
-?/. - c.2882+7A>C r.(=) p.(=)
?/. - c.2883-7del r.(=) p.(=)
-/. - c.2883-7dup r.(=) p.(=)
?/. - c.2944A>G r.(?) p.(Asn982Asp)
-/. - c.2973C>T r.(?) p.(Ser991=)
-/. - c.2973C>T r.(?) p.(Ser991=)
-?/. - c.3007G>A r.(?) p.(Asp1003Asn)
?/. - c.3178G>T r.(?) p.(Asp1060Tyr)
-?/. - c.3185G>A r.(?) p.(Arg1062His)
-?/. - c.3272G>A r.(?) p.(Ser1091Asn)
-/. - c.3272G>A r.(?) p.(Ser1091Asn)
-?/. - c.3373+15A>G r.(=) p.(=)
-/. - c.3373+15A>G r.(=) p.(=)
?/. - c.3503_3505dup r.(?) p.(Gly1168dup)
-?/. - c.3503_3505dup r.(?) p.(Gly1168dup)
-?/. - c.3503_3505dup r.(?) p.(Gly1168dup)
?/. - c.3620A>C r.(?) p.(Asp1207Ala)
?/. - c.3620A>C r.(?) p.(Asp1207Ala)
-?/. - c.3652G>A r.(?) p.(Val1218Met)
?/. - c.3652G>A r.(?) p.(Val1218Met)
-/. - c.3823T>C r.(?) p.(=)
-/. - c.3875+4T>C r.spl? p.?
?/. - c.3986A>G r.(?) p.(Glu1329Gly)
?/. - c.3986A>G r.(?) p.(Glu1329Gly)
?/. - c.4100C>T r.(?) p.(Thr1367Met)
-?/. - c.4131C>T r.(?) p.(=)
?/. - c.4172G>A r.(?) p.(Ser1391Asn)
-/. - c.4282+20A>G r.(=) p.(=)
-/. - c.4283-9del r.(=) p.(=)
-/. - c.4283-6C>T r.(=) p.(=)
-/. - c.4284C>T r.(?) p.(Gly1428=)
-/. - c.4284C>T r.(?) p.(Gly1428=)
?/. - c.4565C>T r.(?) p.(Ser1522Leu)
?/. - c.4565C>T r.(?) p.(Ser1522Leu)
?/. - c.4565C>T r.(?) p.(Ser1522Leu)
-?/. - c.4608T>C r.(?) p.(Asp1536=)
-?/. - c.4610G>A r.(?) p.(Gly1537Glu)
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