Transcript #00024185 (NM_015450.2, POT1 gene)

Transcript name transcript variant 1
Gene name POT1 (protection of telomeres 1)
Chromosome 7
Transcript - NCBI ID NM_015450.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_056265.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2016-10-14 17:05:48 +02:00 (CEST)
Date last edited N/A


Variants

99 entries on 1 page. Showing entries 1 - 99.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
./. - c.-11004523_*3463952del r.0? p.0?
-?/. - c.-480C>T r.(?) p.(=)
-?/. - c.-226-5377C>G r.(=) p.(=)
-?/. - c.-153-9del r.(=) p.(=)
-?/. - c.-153-9del r.(=) p.(=)
-?/. - c.-39-17T>C r.(=) p.(=)
-?/. - c.-39-15_-39-12del r.(=) p.(=)
?/. - c.59G>A r.(?) p.(Gly20Asp)
-?/. - c.64A>G r.(?) p.(Ile22Val)
-?/. - c.64A>G r.(?) p.(Ile22Val)
-?/. - c.64A>G r.(?) p.(Ile22Val)
-?/. - c.70A>G r.(?) p.(Asn24Asp)
+?/. - c.86T>A r.(?) p.(Val29Glu)
?/. - c.104C>T r.(?) p.(Pro35Leu)
-?/. - c.125-7075A>T r.(=) p.(=)
-?/. - c.125-6815_125-6800del r.(=) p.(=)
?/. - c.125-1G>T r.spl? p.?
+?/. - c.255+1G>T r.spl? p.?
?/. - c.281A>G r.(?) p.(Gln94Arg)
+/. - c.289_296del r.(?) p.(Thr97Trpfs*8)
-?/. - c.340A>G r.(?) p.(Ile114Val)
-?/. - c.340A>G r.(?) p.(Ile114Val)
?/. - c.347C>T r.(?) p.(Pro116Leu)
+?/. 8 c.347C>T r.(?) p.(Pro116Leu)
+/. - c.349C>T r.(?) p.(Arg117Cys)
+?/. 8 c.349C>T r.(?) p.(Arg117Cys)
+?/. 8i c.546+1G>A r.spl p.?
-?/. - c.546+17A>C r.(=) p.(=)
-?/. - c.661T>C r.(?) p.(=)
-/. - c.702+8A>T r.(=) p.(=)
-/. - c.702+8_702+9delinsTG r.(=) p.(=)
-?/. - c.702+8_702+9delinsTG r.(=) p.(=)
-/. - c.702+9T>G r.(=) p.(=)
-?/. - c.703-144G>A r.(=) p.(=)
?/. - c.725A>G r.(?) p.(Tyr242Cys)
?/. - c.768G>C r.(?) p.(Gln256His)
-?/. - c.771A>T r.(?) p.(Thr257=)
-?/. - c.771A>T r.(?) p.(Thr257=)
+?/. - c.803G>A r.(?) p.(Gly268Asp)
+/. - c.813C>A r.(?) p.(Tyr271Ter)
+?/. - c.818G>A r.(?) p.(Arg273Gln)
-/. - c.870-33A>G r.(=) p.(=)
-?/. - c.889T>G r.(?) p.(Leu297Val)
+?/. 11 c.901C>T r.(?) p.(Gln301*)
-?/. - c.903G>T r.(?) p.(Gln301His)
-?/. - c.903G>T r.(?) p.(Gln301His)
-?/. - c.903G>T r.(?) p.(Gln301His)
-?/. - c.903G>T r.(?) p.(Gln301His)
-?/. - c.916A>G r.(?) p.(Ile306Val)
-?/. - c.916A>G r.(?) p.(Ile306Val)
-/. - c.924A>G r.(?) p.(Gln308=)
-/. - c.924A>G r.(?) p.(Gln308=)
-?/. - c.937G>A r.(?) p.(Asp313Asn)
?/. - c.938A>T r.(?) p.(Asp313Val)
+?/. - c.950-2A>G r.(?) p.(?)
+/. 12 c.965C>T r.(965c>u) p.(Ser322Leu)
-/. - c.1006+16A>G r.(=) p.(=)
-/. - c.1006+16A>G r.(=) p.(=)
-?/. - c.1007-8C>T r.(=) p.(=)
?/. - c.1056G>C r.(?) p.(Leu352Phe)
?/. - c.1071dup r.(?) p.(Gln358SerfsTer13)
+?/. - c.1071dup r.(?) p.(Gln358SerfsTer13)
?/. - c.1088G>A r.(?) p.(Arg363Gln)
?/. - c.1127A>G r.(?) p.(Gln376Arg)
?/. - c.1127A>G r.(?) p.(Gln376Arg)
?/. - c.1127A>G r.(?) p.(Gln376Arg)
?/. - c.1127A>G r.(?) p.(Gln376Arg)
-/. - c.1164-188A>T r.(=) p.(=)
-/. - c.1164-171A>T r.(=) p.(=)
-/. - c.1164-13C>T r.(=) p.(=)
-/. - c.1211G>T r.(?) p.(Gly404Val)
-/. - c.1211G>T r.(?) p.(Gly404Val)
-/. - c.1211G>T r.(?) p.(Gly404Val)
-/. - c.1211G>T r.(?) p.(Gly404Val)
-/. - c.1211G>T r.(?) p.(Gly404Val)
-?/. - c.1213G>A r.(?) p.(Ala405Thr)
-?/. - c.1228G>C r.(?) p.(Asp410His)
?/. - c.1367A>C r.(?) p.(Glu456Ala)
-/. - c.1369+158A>G r.(=) p.(=)
?/. - c.1416T>G r.(?) p.(Ser472Arg)
+?/. 15 c.1490C>A r.(?) p.(Thr497Lys)
-/. - c.1505+32_1505+36del r.(=) p.(=)
-/. - c.1505+32_1505+36del r.(=) p.(=)
-/. - c.1505+32_1505+36dup r.(=) p.(=)
-?/. - c.1505+32_1505+36dup r.(=) p.(=)
-/. - c.1505+32_1505+36dup r.(=) p.(=)
-?/. - c.1506-43A>G r.(=) p.(=)
+/. - c.1507_1510del r.(?) p.(Cys503AsnfsTer6)
-/. - c.1594+41T>A r.(=) p.(=)
-/. - c.1687-98T>G r.(=) p.(=)
-/. - c.1687-5T>A r.spl? p.?
-/. - c.1687-5T>A r.spl? p.?
-?/. - c.1742A>G r.(?) p.(Lys581Arg)
?/. - c.1761G>T r.(?) p.(Met587Ile)
-/. - c.1792+50A>G r.(=) p.(=)
?/. - c.1793-1G>C r.spl? p.?
-?/. - c.1797A>G r.(?) p.(Ala599=)
?/. - c.1829A>G r.(?) p.(Tyr610Cys)
-/. - c.1884A>C r.(?) p.(Thr628=)
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