Transcript #00024236 (NM_016642.3, SPTBN5 gene)

Transcript name spectrin, beta, non-erythrocytic 5
Gene name SPTBN5 (spectrin, beta, non-erythrocytic 5)
Chromosome 15
Transcript - NCBI ID NM_016642.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_057726.4
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2017-03-05 17:50:19 +01:00 (CET)
Date last edited N/A


Variants

90 entries on 1 page. Showing entries 1 - 90.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. 46 c.? r.(?) p.?
?/. - c.37G>A r.(?) p.(Gly13Arg)
?/. - c.218C>T r.(?) p.(Ala73Val)
-?/. - c.1018G>A r.(?) p.(Ala340Thr)
-?/. - c.1076G>A r.(?) p.(Arg359Gln)
+?/. - c.1144C>T r.(?) p.(Arg382Cys)
?/. - c.1199G>C r.(?) p.(Trp400Ser)
-?/. - c.1286G>A r.(?) p.(Arg429Gln)
-?/. - c.1289G>A r.(?) p.(Arg430His)
?/. - c.1330G>A r.(?) p.(Asp444Asn)
?/. - c.1445G>A r.(?) p.(Arg482His)
?/. - c.1540C>T r.(?) p.(Arg514Cys)
?/. - c.1984G>A r.(?) p.(Val662Met)
-?/. - c.1985T>C r.(?) p.(Val662Ala)
-?/. - c.2166C>A r.(?) p.(Ala722=)
-?/. - c.2320G>C r.(?) p.(Gly774Arg)
-?/. - c.3752G>A r.(?) p.(Arg1251Gln)
?/. - c.3828_3850del r.(?) p.(Gln1276HisfsTer21)
-?/. - c.4016A>T r.(?) p.(His1339Leu)
-?/. - c.4016A>T r.(?) p.(His1339Leu)
-?/. - c.4031C>T r.(?) p.(Ala1344Val)
-?/. - c.4100G>C r.(?) p.(Arg1367Thr)
-?/. - c.4160A>G r.(?) p.(Gln1387Arg)
-?/. - c.4667A>G r.(?) p.(Gln1556Arg)
?/. - c.5078C>T r.(?) p.(Thr1693Ile)
-?/. - c.5138G>A r.(?) p.(Arg1713Gln)
?/. 31 c.5647C>T r.(?) p.(Arg1883*)
?/. - c.5822G>A r.(?) p.(Arg1941Gln)
-?/. - c.5867C>T r.(?) p.(Ala1956Val)
-?/. - c.6119G>A r.(?) p.(Arg2040Gln)
?/. 38 c.6751C>A r.(?) p.(Leu2251Met)
-?/. - c.7050T>C r.(?) p.(His2350=)
?/. - c.7081G>A r.(?) p.(Glu2361Lys)
-?/. - c.7317C>T r.(?) p.(His2439=)
-?/. - c.7437G>A r.(?) p.(Leu2479=)
?/. - c.7856A>G r.(?) p.(Lys2619Arg)
-?/. - c.7917C>T r.(?) p.(Ala2639=)
?/. - c.7921G>A r.(?) p.(Gly2641Ser)
?/. - c.7921G>A r.(?) p.(Gly2641Ser)
?/. - c.8181G>C r.(?) p.(Gln2727His)
?/. - c.8809A>T r.(?) p.(Asn2937Tyr)
?/. - c.9089G>T r.(?) p.(Ser3030Ile)
-?/. - c.9094G>A r.(?) p.(Glu3032Lys)
+?/. - c.9334C>T r.(?) p.(Arg3112Ter)
-?/. - c.9355G>A r.(?) p.(Ala3119Thr)
-?/. - c.9500A>G r.(?) p.(Lys3167Arg)
./. 56 c.9520dup r.(?) p.(Arg3174Profs*18)
?/. - c.9520dup r.(?) p.(Arg3174Profs*18)
?/. - c.9566G>T r.(?) p.(Arg3189Leu)
-?/. - c.9594C>G r.(?) p.(Asp3198Glu)
?/. - c.9595C>T r.(?) p.(Gln3199*)
-?/. - c.9695C>T r.(?) p.(Thr3232Met)
-?/. - c.9784G>A r.(?) p.(Glu3262Lys)
-?/. - c.9830G>A r.(?) p.(Arg3277Gln)
-?/. - c.10033G>A r.(?) p.(Asp3345Asn)
?/. - c.10202G>A r.(?) p.(Arg3401Gln)
-?/. - c.10263C>T r.(?) p.(Gly3421=)
?/. - c.10286T>C r.(?) p.(Leu3429Pro)
?/. - c.10765C>G r.(?) p.(Leu3589Val)
-?/. - c.10875C>T r.(?) p.(Ser3625=)
-/. - c.*939T>C r.(=) p.(=)
-/. - c.*951G>A r.(=) p.(=)
-/. - c.*2242G>A r.(=) p.(=)
?/. - c.*2392A>C r.(=) p.(=)
?/. - c.*2404T>C r.(=) p.(=)
-/. - c.*2557C>T r.(=) p.(=)
-/. - c.*2684G>A r.(=) p.(=)
-/. - c.*3428G>A r.(=) p.(=)
-/. - c.*3598C>G r.(=) p.(=)
-/. - c.*3613C>T r.(=) p.(=)
?/. - c.*3662C>A r.(=) p.(=)
-?/. - c.*3693G>C r.(=) p.(=)
-/. - c.*6398G>A r.(=) p.(=)
-/. - c.*7096G>A r.(=) p.(=)
?/. - c.*8023G>A r.(=) p.(=)
?/. - c.*8033G>A r.(=) p.(=)
-?/. - c.*8089G>A r.(=) p.(=)
-/. - c.*8373G>A r.(=) p.(=)
?/. - c.*11507A>G r.(=) p.(=)
-/. - c.*13394C>A r.(=) p.(=)
-/. - c.*13708C>G r.(=) p.(=)
-/. - c.*13858G>C r.(=) p.(=)
-/. - c.*13875C>A r.(=) p.(=)
-?/. - c.*23187T>C r.(=) p.(=)
?/. - c.*24060C>T r.(=) p.(=)
-?/. - c.*24077G>A r.(=) p.(=)
-?/. - c.*24077G>A r.(=) p.(=)
-/. - c.*24143C>T r.(=) p.(=)
-?/. - c.*24738C>A r.(=) p.(=)
?/. - c.*25119G>A r.(=) p.(=)
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