Transcript #00016885 (NM_006017.2, PROM1 gene)

Transcript name transcript variant 1
Gene name PROM1 (prominin 1)
Chromosome 4
Transcript - NCBI ID NM_006017.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_006008.1
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

744 entries on 8 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+?/. - c.436>T r.(?) p.(Arg146*)
+?/. - c.630_c.630+8del r.(?) p.?
+?/. - c.? r.? p.?
?/. - c.? r.spl p.(?)
+/. - c.? r.? p.?
+/. 3 c.? r.(?) p.?
+?/. - c.3G>A r.(?) p.(Met1?)
+?/. 1 c.7dup r.(?) p.(Leu3Profs*28)
-/. - c.15C>T r.(?) p.(Leu5=)
-?/. - c.15C>T r.(=) p.(=)
+?/. - c.22del r.(?) p.(Leu8Cysfs*51)
?/. 1 c.55T>A r.(?) p.(Ser19Thr)
?/. - c.55T>G r.(?) p.(Ser19Ala)
-?/. 1 c.55T>G r.(?) p.(Ser19Ala)
-/. - c.129C>T r.(?) p.(Thr43=)
-?/. - c.129C>T r.(=) p.(=)
+/. - c.139del r.(?) p.(His47Ilefs*12)
+?/. 1 c.139del r.(?) p.(His47Ilefs*12)
+/. - c.139del r.(?) p.(His47Ilefs*12)
+/. - c.139del r.(?) p.(His47IlefsTer12)
+?/. - c.139del r.(?) p.(His47IlefsTer12)
+?/. - c.139del r.(?) p.(His47Ilefs*12)
+?/. - c.139del r.(?) p.(His47IlefsTer12)
+?/. 1 c.139del r.(?) p.(His47Ilefs*12)
+/. - c.139del r.(?) p.(His47Ilefs*12)
+/. - c.139delC r.(?) p.(His47IlefsTer12)
+/. - c.139delC r.(?) p.(His47IlefsTer12)
+/. - c.139delC r.(?) p.(His47IlefsTer12)
-?/. - c.152C>T r.(?) p.(Pro51Leu)
+?/. - c.155T>C r.(?) p.(Ile52Thr)
?/. 2 c.158G>A r.(?) p.(Gly53Asp)
?/. - c.158G>A r.(?) p.(Gly53Asp)
+/. - c.181A>G r.(?) p.(Ile61Val)
?/. - c.199C>G r.(?) p.(Gln67Glu)
?/. - c.199C>G r.(?) p.(Gln67Glu)
+?/. - c.199C>T r.(?) p.(Gln67*)
+/. - c.199C>T r.(?) p.(Gln67Ter)
+/. 1 c.199C>T r.(?) p.(Gln67*)
-?/. - c.206G>A r.(?) p.(Arg69His)
-?/. - c.206G>A r.(?) p.(Arg69His)
+/. - c.220+1G>C r.spl p.?
+/. - c.220+1G>T r.spl? p.?
+/. - c.221-20T>G r.221_276del p.Asp74Alafs*14
+/. - c.221-20T>G r.221_276del p.Asp74Alafs*14
+?/. - c.223A>G r.(?) p.(Thr75Ala)
+/. - c.242dup r.(?) p.(Lys82Glufs*4)
+/. - c.242dupA r.(?) p.(Lys82GlufsTer4)
+/. - c.262dup r.(?) p.(Ile88Asnfs*2)
+/. - c.262dup r.(?) p.(Ile88Asnfs*2)
-/. - c.276+15G>A r.(=) p.(=)
+/. - c.277-1G>A r.spl p.?
+?/. - c.303G>C r.(?) p.(Lys101Asn)
+?/. - c.303G>C r.(?) p.(Lys101Asn)
+/. - c.303+1G>A r.spl? p.?
+?/. - c.303+1G>A r.spl p.?
+?/. - c.303+1G>A r.spl p.(?)
+?/. 3i c.303+1G>A r.spl p.(?)
+?/. 3i c.303+1G>A r.spl p.(?)
+?/. 3i c.303+1G>A r.spl p.(?)
+?/. 3i c.303+2T>C r.(?) p.(?)
+?/. - c.303+2T>C r.spl p.(?)
+?/. 3i c.303+2T>C r.spl p.(?)
-/. - c.303+6G>A r.(=) p.(=)
-/. - c.303+6G>A r.(=) p.(=)
?/. 4 c.314A>G r.(?) p.(Tyr105Cys)
+?/. 5 c.334T>C r.(?) p.(Cys112Arg)
?/. 3 c.376G>A r.(?) p.(Val292Met)
?/. - c.376G>A r.(?) p.(Val126Met)
+/. - c.380G>A r.(?) p.(Gly127Glu)
+?/. 3 c.380G>A r.(?) p.(Cys127Tyr)
+?/. 3 c.380G>A r.(?) p.(Cys127Tyr)
+?/. - c.400C>T r.(?) p.(Arg134Cys)
+?/? - c.400C>T r.(?) p.(Arg134Cys)
?/. - c.421G>A r.(?) p.(Gly141Arg)
?/. - c.430C>T r.(?) p.(His144Tyr)
+/. - c.436C>T r.(?) p.(Arg146*)
+/. - c.436C>T r.(?) p.(Arg146*)
+?/. - c.436C>T r.(?) p.(Arg146*)
+?/. 4,12 c.436C>T r.(?) p.(Arg146*)
+?/. - c.436C>T r.(?) p.(Arg146Ter)
+/. 4 c.436C>T r.(?) p.(Arg146*)
?/. 4 c.437G>A r.(?) p.(Arg146Gln)
?/. - c.437G>A r.(?) p.(Arg146Gln)
+/. 6 c.439C>T r.spl? p.(Gln147*)
+/. - c.442A>T r.(?) p.(Lys148*)
+?/. - c.442A>T r.(?) p.(Lys148*)
?/. - c.454C>T r.(?) p.(Pro152Ser)
+?/. - c.485del r.(?) p.(Leu162Argfs*3)
-?/. - c.489G>A r.(?) p.(Leu163=)
+/. 4i c.510-1G>A r.spl p.?
+?/. 3i c.510-1G>A r.spl? p.(?)
+/. 3i c.510-1G>A r.(?) p.?
+?/. 6 c.524A>C r.(?) p.(Tyr175Ser)
+?/. 4 c.544C>T r.(?) p.(Gln182*)
?/. - c.604C>G r.(?) p.(Arg202Gly)
-?/. - c.604C>G r.(?) p.(Arg202Gly)
?/. 6 c.604C>G r.(?) p.(Arg202Gly)
+?/. - c.604C>G r.(?) p.(Arg202Gly)
?/. - c.604C>G r.(?) p.(Arg202Gly)
?/. 5 c.604C>G r.(?) p.(Arg202Gly)
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