Transcript #00025546 (NM_001024858.2, SPTB gene)

Transcript name transcript variant 1
Gene name SPTB (spectrin, beta, erythrocytic)
Chromosome 14
Transcript - NCBI ID NM_001024858.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_001020029.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2020-08-27 15:20:23 +02:00 (CEST)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.148+56G>A r.(=) p.(=)
-/. - c.148+130T>C r.(=) p.(=)
-/. - c.148+131C>T r.(=) p.(=)
-/. - c.177C>T r.(?) p.(Thr59=)
-?/. - c.204G>A r.(?) p.(Leu68=)
-/. - c.300+7T>C r.(=) p.(=)
-/. - c.300+23C>T r.(=) p.(=)
-/. - c.300+24G>A r.(=) p.(=)
-/. - c.300+57G>T r.(=) p.(=)
-/. - c.300+140G>A r.(=) p.(=)
-/. - c.300+177T>C r.(=) p.(=)
-/. - c.301-29T>C r.(=) p.(=)
-/. - c.301-18G>A r.(=) p.(=)
-/. - c.345T>C r.(?) p.(Asn115=)
-/. - c.408C>T r.(?) p.(His136=)
-/. - c.474+53G>T r.(=) p.(=)
-/. - c.474+103T>C r.(=) p.(=)
-/. - c.474+110del r.(=) p.(=)
+/. - c.544T>G r.(?) p.(Trp182Gly)
?/. - c.560C>T r.(?) p.(Thr187Met)
-/. - c.567-166T>C r.(=) p.(=)
-/. - c.567-53T>C r.(=) p.(=)
?/. - c.580A>T r.(?) p.(Asn194Tyr)
+/. - c.606G>A r.(?) p.(Trp202*)
-/. - c.609G>A r.(?) p.(Lys203=)
-/. - c.647+21G>A r.(=) p.(=)
-/. - c.647+68C>A r.(=) p.(=)
-/. - c.647+148T>A r.(=) p.(=)
-/. - c.648-113C>T r.(=) p.(=)
-/. - c.648-49G>A r.(=) p.(=)
-/. - c.666T>C r.(?) p.(Phe222=)
-?/. - c.696C>T r.(?) p.(His232=)
-/. - c.764-24dup r.(=) p.(=)
-/. - c.876+5A>G r.spl? p.?
?/. - c.964A>G r.(?) p.(Ile322Val)
-?/. - c.964A>G r.(?) p.(Ile322Val)
-/. - c.996C>T r.(?) p.(Asn332=)
-?/. - c.1008C>T r.(?) p.(=)
?/. - c.1064A>C r.(?) p.(Lys355Thr)
+?/. 8 c.1064+1G>A r.877_1064del p.Ile294Serlfs*35
+?/. - c.1179_1182+17del r.(?) p.(Leu388_Arg394del)
-/. - c.1182+225C>T r.(=) p.(=)
-/. - c.1183-158dup r.(=) p.(=)
-/. - c.1269G>A r.(?) p.(Leu423=)
-?/. - c.1293C>T r.(?) p.(Ala431=)
?/. - c.1303G>C r.(?) p.(Glu435Gln)
-/. - c.1316G>A r.(?) p.(Ser439Asn)
-/. - c.1341+101C>T r.(=) p.(=)
-/. - c.1342-68G>T r.(=) p.(=)
+/. - c.1508del r.(?) p.(Lys503Argfs*70)
?/. - c.1606G>A r.(?) p.(Asp536Asn)
-?/. - c.1623C>T r.(?) p.(Ile541=)
-/. - c.1645-68G>T r.(=) p.(=)
+/. - c.1714_1723del r.(?) p.(Met573ThrfsTer9)
-?/. - c.1740A>G r.(?) p.(Gln580=)
-/. - c.1765G>A r.(?) p.(Ala589Thr)
-?/. - c.1773C>G r.(?) p.(Thr591=)
-?/. - c.1786G>A r.(?) p.(Glu596Lys)
-/. - c.1838G>T r.(?) p.(Ser613Ile)
-?/. - c.1838G>T r.(?) p.(Ser613Ile)
+/. - c.1912C>T r.(?) p.(Arg638*)
-?/. - c.2060G>A r.(?) p.(Arg687His)
-?/. - c.2136G>A r.(?) p.(Pro712=)
+/. - c.2137C>T r.(?) p.(Gln713Ter)
-/. - c.2154A>C r.(?) p.(Ile718=)
?/. - c.2243C>T r.(?) p.(Ser748Leu)
?/. - c.2387G>A r.(?) p.(Arg796His)
?/. - c.2464C>T r.(?) p.(Arg822Trp)
?/. - c.2480G>A r.(?) p.(Arg827Gln)
-/. - c.2562C>T r.(?) p.(Phe854=)
+/. - c.2562_2563insCTGTACAC r.(?) p.(Gly855Leufs*46)
-/. - c.2666+94G>T r.(=) p.(=)
-/. - c.2666+134C>A r.(=) p.(=)
-/. - c.2667-70G>C r.(=) p.(=)
?/. - c.2758C>A r.(?) p.(Pro920Thr)
-/. - c.2805-129del r.(=) p.(=)
-?/. - c.2805-22G>A r.(=) p.(=)
-/. - c.2934G>A r.(?) p.(Glu978=)
-?/. - c.2934G>A r.(=) p.(=)
+/. - c.2967dup r.(?) p.(Ile990TyrfsTer14)
?/. - c.3103C>T r.(?) p.(Arg1035Trp)
-?/. - c.3103C>T r.(?) p.(Arg1035Trp)
-?/. - c.3334G>A r.(?) p.(Gly1112Arg)
+/. - c.3449G>A r.(?) p.(Trp1150Ter)
-/. - c.3451A>G r.(?) p.(Asn1151Asp)
?/. - c.3479G>A r.(?) p.(Arg1160His)
?/. - c.3479G>A r.(?) p.(Arg1160His)
-/. - c.3562-179G>A r.(=) p.(=)
-?/. - c.3562-64G>T r.(=) p.(=)
-/. - c.3562-63G>T r.(=) p.(=)
-/. - c.3764+24G>A r.(=) p.(=)
?/. - c.3764+42C>T r.(?) p.(?)
-/. - c.3855+67G>A r.(=) p.(=)
-/. - c.3855+140A>G r.(=) p.(=)
-/. - c.3855+160C>A r.(=) p.(=)
-/. - c.3855+184_3855+185del r.(=) p.(=)
-/. - c.3855+185del r.(=) p.(=)
-/. - c.3856-120_3856-119del r.(=) p.(=)
+/. - c.3916C>T r.(?) p.(Arg1306*)
?/. - c.3917G>A r.(?) p.(Arg1306Gln)
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