Transcript #00021037 (NM_003227.3, TFR2 gene)

Transcript name transcript variant 1
Gene name TFR2 (transferrin receptor 2)
Chromosome 7
Transcript - NCBI ID NM_003227.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_003218.2
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

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.-6003C>T r.(?) p.(=)
?/. - c.-5970C>T r.(?) p.(=)
?/. - c.-5575G>A r.(?) p.(=)
-/. - c.-5546C>T r.(?) p.(=)
?/. - c.-5246G>T r.(?) p.(=)
?/. - c.-5128G>A r.(?) p.(=)
?/. - c.-4805G>A r.(?) p.(=)
?/. - c.-1804A>T r.(?) p.(=)
+/. - c.-1751C>T r.(?) p.(=)
?/. 2 c.64G>A r.(?) p.(Val22Ile)
?/. 2 c.64G>A r.(?) p.(Val22Ile)
?/. 2 c.64G>A r.(?) p.(Val22Ile)
+/. 2 c.88dup r.(?) p.(Arg30Profs*31)
+/. 2 c.88dup r.88dup p.Arg30Profs*31
-?/. 2 c.97C>A r.(?) p.(His33Asn)
?/. - c.109G>A r.(?) p.(Glu37Lys)
+/. 2 c.178G>T r.(?) p.(Glu60*)
-/. 2 c.224C>T r.(?) p.(Ala75Val)
?/. - c.235C>T r.(?) p.(Arg79Trp)
+/. 2_2i c.254_286+9del r.spl p.(Leu85_Ala96delinsPro)
?/. 3i c.286+10G>A r.(=) p.(=)
-/. 2i c.286+15C>T r.(?) p.(=)
?/. 3i c.286+15C>T r.(=) p.(=)
-/. 3 c.295C>G r.(?) p.(Leu99Val)
+/. 3 c.313C>T r.(?) p.(Arg105*)
+/. 3 c.313C>T r.(?) p.(Arg105*)
-?/. - c.447G>A r.(?) p.(Gly149=)
-/. 3i c.473+49C>A r.(?) p.(=)
+/. 4 c.515T>A r.(?) p.(Met172Lys)
+/. 4 c.515T>A r.(?) p.(Met172Lys)
+/. 4 c.515T>A r.515u>a p.Met172Lys
+?/. 4 c.565G>A r.(?) p.(Asp189Asn)
+/. 4i c.614+4A>G r.spl p.?
+/+ 4i c.614+4A>G r.474_614del p.Gln159_Pro205del
-/. - c.714C>G r.(?) p.(Ile238Met)
-?/. 5 c.714C>G r.(?) p.(Ile238Met)
-/. 5 c.714C>G r.(?) p.(Ile238Met)
-/. 5 c.714C>G r.(?) p.(Ile238Met)
-?/. 5 c.714C>G r.(?) p.(Ile238Met)
-/. 5i c.727-24G>C r.(?) p.(=)
?/. 5i c.727-24G>C r.(=) p.(=)
?/. 5i c.727-24G>C r.(=) p.(=)
?/. 5i c.727-9T>A r.(spl?) p.(?)
-?/. 5i c.727-9T>A r.(spl?) p.(?)
+/. 6 c.750C>G r.(?) p.(Tyr250*)
+/. 6 c.750C>G r.(?) p.(Tyr250*)
+/. 6 c.750C>G r.0 p.0
+/. 6 c.750C>G r.0 p.0
-/. 6 c.829G>C r.(?) p.(Val277Leu)
+?/. 6 c.840C>G r.(?) p.(Phe280Leu)
?/. 6 c.840C>G r.(?) p.(Phe280Leu)
-?/. - c.849+8T>C r.(=) p.(=)
?/. - c.850-3C>G r.spl? p.?
?/. - c.915C>G r.(?) p.(Ser305=)
+/. 7 c.916C>T r.(?) p.(Gln306*)
+/. 7 c.949C>T r.(?) p.(Gln317*)
-?/. - c.1094C>T r.(?) p.(Ser365Phe)
-?/. - c.1098C>T r.(?) p.(=)
?/. 9 c.1118G>A r.(?) p.(Gly373Asp)
?/. 9 c.1118G>A r.(?) p.(Gly373Asp)
?/. - c.1118G>A r.(?) p.(Gly373Asp)
?/. - c.1127C>A r.(?) p.(Ala376Asp)
?/. - c.1127C>A r.(?) p.(Ala376Asp)
?/. 9 c.1127C>A r.(?) p.(Ala376Asp)
?/. 9 c.1127C>A r.(?) p.(Ala376Asp)
?/. 9 c.1127C>A r.(?) p.(Ala376Asp)
-/. 9 c.1127C>A r.(?) p.(Ala376Asp)
+?/. 9 c.1186C>T r.(?) p.(Arg396*)
+/. 9 c.1186C>T r.(?) p.(Arg396*)
+?/. 9 c.1186C>T r.(?) p.(Arg396*)
+/. 9 c.1235A>T r.(?) p.(Asn412Ile)
+?/. 9 c.1235_1237del r.(?) p.(Asn412del)
?/. - c.1259G>A r.(?) p.(Arg420His)
+?/. 9 c.1259G>A r.(?) p.(Arg420His)
+/. 10 c.1288G>A r.(?) p.(Gly430Arg)
+/. 10 c.1288G>A r.(?) p.(Gly430Arg)
?/. 10 c.1330G>A r.(?) p.(Ala444Thr)
?/. 10 c.1330G>A r.(?) p.(Ala444Thr)
?/. - c.1345A>G r.(?) p.(Ile449Val)
?/. - c.1364G>A r.(?) p.(Arg455Gln)
?/. 10 c.1364G>A r.(?) p.(Arg455Gln)
+?/-? 10 c.1364G>A r.(?) p.(Arg455Gln)
+?/-? 10 c.1364G>A r.(?) p.(Arg455Gln)
+?/-? 10 c.1364G>A r.(?) p.(Arg455Gln)
+?/-? 10 c.1364G>A r.(?) p.(Arg455Gln)
?/. 10 c.1364G>A r.(?) p.(Arg455Gln)
?/. - c.1364G>A r.(?) p.(Arg455Gln)
-?/. - c.1377C>T r.(?) p.(Ser459=)
+/. 11 c.1403G>A r.(?) p.(Arg468His)
-?/. - c.1420A>G r.(?) p.(Ile474Val)
-?/. - c.1449C>T r.(?) p.(Ser483=)
?/. - c.1450G>A r.(?) p.(Val484Met)
+/. 11 c.1469T>G r.(?) p.(Leu490Arg)
?/. 11 c.1473G>A r.1473g>a p.Glu491=
?/. 11 c.1473G>A r.spl? p.(=)
?/. 11 c.1473G>A r.1473g>a p.Glu491=
?/. - c.1473G>A r.(?) p.(Glu491=)
?/. - c.1473G>A r.(?) p.(Glu491=)
?/. 12 c.1473G>A r.0? p.0?
?/. - c.1473G>A r.(?) p.(Glu491=)
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