Transcript #00020164 (NM_005876.4, SPEG gene)

Transcript name transcript variant 1
Gene name SPEG (SPEG complex locus)
Chromosome 2
Transcript - NCBI ID NM_005876.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_005867.3
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

93 entries on 1 page. Showing entries 1 - 93.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.52C>T r.(?) p.(Pro18Ser)
-?/. - c.153C>T r.(?) p.(=)
?/. - c.182G>A r.(?) p.(Arg61Gln)
?/. - c.182G>A r.(?) p.(Arg61Gln)
-?/. - c.182G>A r.(?) p.(Arg61Gln)
?/. - c.202G>A r.(?) p.(Gly68Arg)
?/. - c.322T>C r.(?) p.(Cys108Arg)
-?/. - c.617G>A r.(?) p.(Arg206His)
-/. - c.620G>A r.(?) p.(Arg207His)
?/. - c.749C>T r.(?) p.(Ser250Phe)
-?/. - c.769G>A r.(?) p.(Gly257Ser)
-?/. - c.815+9C>T r.(=) p.(=)
-?/. - c.815+9C>T r.(=) p.(=)
-?/. - c.1046C>T r.(?) p.(Thr349Ile)
-?/. - c.1434C>T r.(?) p.(=)
-?/. - c.1753G>A r.(?) p.(Gly585Ser)
-?/. - c.1841C>A r.(?) p.(Pro614His)
?/. - c.2053C>G r.(?) p.(Arg685Gly)
?/. - c.2276G>A r.(?) p.(Gly759Glu)
-?/. - c.2287C>T r.(?) p.(Arg763Cys)
?/. - c.2492T>A r.(?) p.(Leu831Gln)
?/. - c.2717G>A r.(?) p.(Arg906His)
+/. 10 c.2915_2916delinsA r.(?) p.(Ala972Aspfs*79)
-?/. - c.3142+6T>C r.(=) p.(=)
+/. - c.3143-2A>C r.(?) p.(?)
-/. - c.3164G>A r.(?) p.(Arg1055Gln)
-?/. - c.3183G>T r.(?) p.(Ser1061=)
?/. - c.3212A>G r.(?) p.(Glu1071Gly)
-?/. - c.3491+9G>A r.(=) p.(=)
-?/. - c.3571C>T r.(?) p.(Leu1191=)
?/. - c.3595G>T r.(?) p.(Val1199Leu)
?/. - c.3595G>T r.(?) p.(Val1199Leu)
?/. - c.3700C>T r.(?) p.Arg1234Trp
+/. 13_13i c.3709_3715+29del r.spl p.?
-?/. - c.3941-6C>T r.(=) p.(=)
?/. - c.3969G>T r.(?) p.(Gln1323His)
-?/. - c.3999G>A r.(?) p.(Thr1333=)
-?/. - c.4019G>A r.(?) p.(Arg1340Gln)
?/. - c.4048C>T r.(?) p.(Arg1350Cys)
-?/. - c.4146C>T r.(?) p.(=)
-?/. - c.4148-7C>T r.(=) p.(=)
+/. 18 c.4276C>T r.(?) p.(Arg1426*)
?/. - c.4298G>A r.(?) p.(Arg1433Gln)
-?/. - c.4400G>A r.(?) p.(Arg1467Gln)
?/. - c.4447+3G>C r.spl? p.?
-?/. - c.4688C>T r.(?) p.(Ala1563Val)
?/. - c.4700C>T r.(?) p.(Ser1567Phe)
-?/. - c.4730-4C>T r.spl? p.?
?/. - c.4822G>A r.(?) p.(Gly1608Ser)
?/. - c.4822G>A r.(?) p.(Gly1608Ser)
-?/. - c.4928G>T r.(?) p.(Arg1643Leu)
-?/. - c.5289T>C r.(?) p.(Phe1763=)
-?/. - c.5289T>C r.(?) p.(Phe1763=)
?/. - c.5485C>T r.(?) p.(Arg1829Trp)
-?/. - c.5635C>T r.(?) p.(Arg1879Cys)
?/. - c.5724G>T r.(?) p.(Met1908Ile)
+?/. - c.5823dup r.(?) p.(Glu1942Argfs*15)
-?/. - c.5891A>G r.(?) p.(Glu1964Gly)
-/. - c.6076C>G r.(?) p.(Arg2026Gly)
-?/. - c.6076C>G r.(?) p.(Arg2026Gly)
-?/. - c.6163C>T r.(?) p.(Arg2055Trp)
-/. - c.6692C>A r.(?) p.(Pro2231His)
+/. 30 c.6697C>T r.(?) p.(Gln2233*)
?/. - c.6971T>A r.(?) p.(Ile2324Asn)
-?/. - c.7200C>A r.(?) p.(=)
-?/. - c.7202G>A r.(?) p.(Gly2401Glu)
?/. - c.7598C>T r.(?) p.(Ser2533Leu)
+?/. - c.7685del r.(?) p.(Asn2562Thrfs*57)
-?/. - c.7810C>T r.(?) p.(Leu2604Phe)
?/. - c.8078C>A r.(?) p.(Thr2693Lys)
?/. - c.8099C>T r.(?) p.(Pro2700Leu)
-?/. - c.8111G>A r.(?) p.(Arg2704Gln)
?/. - c.8141G>A r.(?) p.(Arg2714Gln)
?/. - c.8167C>T r.(?) p.(Pro2723Ser)
+/. 35 c.8270G>T r.(?) p.(Gly2757Val)
?/. - c.8503C>G r.(?) p.(Leu2835Val)
-?/. - c.8508G>A r.(?) p.(=)
+?/. - c.8539C>T r.(?) p.(Arg2847*)
-?/. - c.8573C>T r.(?) p.(Ala2858Val)
-?/. - c.8695C>T r.(?) p.(Pro2899Ser)
+/. - c.8872C>T r.(?) p.(Arg2958Ter)
?/. - c.9133C>T r.(?) p.(Arg3045Trp)
+/. - c.9185_9187del r.(?) p.(Val3062del)
?/. - c.9323A>G r.(?) p.(Gln3108Arg)
-?/. - c.9361C>T r.(?) p.(Arg3121Cys)
?/. - c.9385+6G>A r.(=) p.(=)
?/. - c.9443G>C r.(?) p.(Gly3148Ala)
?/. - c.9571G>A r.(?) p.(Ala3191Thr)
+/. - c.9586C>T r.(?) p.(Arg3196Ter)
-?/. - c.*4277A>G r.(=) p.(=)
-?/. - c.*5080G>A r.(=) p.(=)
-?/. - c.*5085G>C r.(=) p.(=)
?/. - c.*5383G>C r.(=) p.(=)
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