Transcript #00008013 (NM_014053.3, FLVCR1 gene)

Transcript name feline leukemia virus subgroup C cellular receptor 1
Gene name FLVCR1 (feline leukemia virus subgroup C cellular receptor 1)
Chromosome 1
Transcript - NCBI ID NM_014053.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_054772.1
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

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.-15C>G r.(?) p.(=)
+?/. - c.0? r.0? p.(?)
-?/. - c.49C>G r.(?) p.(Pro17Ala)
-/. - c.154G>C r.(?) p.(Ala52Pro)
-/. - c.154G>C r.(?) p.(Ala52Pro)
-/. - c.154G>C r.(?) p.(Ala52Pro)
-/. - c.154G>C r.(?) p.(Ala52Pro)
-?/. - c.163G>T r.(?) p.(Asp55Tyr)
-?/. - c.164A>T r.(?) p.(Asp55Val)
+?/. - c.202C>T r.(?) p.(Gln68*)
-?/. - c.247C>T r.(?) p.(Pro83Ser)
-/. - c.279C>T r.(?) p.(Ala93=)
?/. - c.302C>T r.(?) p.(Thr101Met)
-?/. - c.309C>G r.(?) p.(Leu103=)
-/. - c.346C>T r.(?) p.(Leu116=)
+?/. - c.361A>G r.(?) p.(Asn121Asp)
+?/. - c.361A>G r.(?) p.(Asn121Asp)
?/. - c.375G>C r.(?) p.(Trp125Cys)
+/. - c.479T>C r.(?) p.(Leu160Pro)
-/. - c.543C>T r.(?) p.(Ser181=)
?/. - c.554G>C r.(?) p.(Cys185Ser)
?/. - c.593A>G r.(?) p.(His198Arg)
?/. - c.593A>G r.(?) p.(His198Arg)
?/. - c.595C>T r.(?) p.(Leu199Phe)
?/. - c.595C>T r.(?) p.(Leu199Phe)
?/. - c.595C>T r.(?) p.(Leu199Phe)
?/. - c.661C>T r.(?) p.(Pro221Ser)
+?/. 1 c.719delC r.(?) p.(Ala241Profs*19)
+/. - c.721G>A r.(?) p.(Ala241Thr)
?/. 1 c.733A>G r.(?) p.(Asn245Asp)
?/. 1 c.733A>G r.(?) p.(Asn245Asp)
-?/. - c.738+9T>C r.(=) p.(=)
-?/. - c.738+9T>C r.(=) p.(=)
+/. - c.742G>T r.(?) p.(Gly248Ter)
+/. - c.755del r.(?) p.(Gly252AlafsTer8)
+?/. - c.755del r.(?) p.(Gly252Alafs*8)
+?/. - c.755del r.(?) p.(Gly252Alafs*8)
+/. - c.755del r.(?) p.(Gly252AlafsTer8)
-/. - c.768A>G r.(?) p.(Pro256=)
+?/. - c.774_779dup r.(?) p.(Leu259_Val260dup)
+?/. - c.847G>C r.(?) p.(Ala283Pro)
+?/. - c.847G>C r.(?) p.(Ala283Pro)
+?/. - c.847G>C r.(?) p.(Ala283Pro)
+?/. - c.847G>C r.(?) p.(Ala283Pro)
-?/. - c.880A>G r.(?) p.(Ile294Val)
+/. - c.883+6T>C r.spl? p.?
-?/. - c.930T>C r.(?) p.(Ala310=)
-?/. - c.937G>A r.(?) p.(Asp313Asn)
?/. - c.944C>G r.(?) p.(Pro315Arg)
-?/. - c.952G>A r.(?) p.(Glu318Lys)
?/. - c.952G>A r.(?) p.(Glu318Lys)
-?/. - c.952G>A r.(?) p.(Glu318Lys)
+?/. - c.971C>A r.(?) p.(Ser324*)
+?/. - c.991_992dup r.(?) p.(Asn331LysfsTer9)
+?/. - c.1058C>T r.(?) p.(Thr353Met)
+?/. - c.1058C>T r.(?) p.(Thr353Met)
-?/. - c.1059G>A r.(?) p.(Thr353=)
+/. - c.1092+5G>A r.spl? p.?
?/. - c.1092+5G>A r.spl? p.?
+/. - c.1092+5G>A r.spl? p.?
+?/. - c.1092+5G>A r.spl? p.(?)
+/. - c.1092+5G>A r.spl? p.?
+?/. - c.1092+5G>A r.spl? p.(?)
+?/. - c.1092+5G>A r.spl? p.(?)
+?/. - c.1092+5G>A r.spl? p.(?)
+?/. - c.1092+5G>A r.spl? p.?
+/. - c.1092+5G>A r.spl p.?
+/. - c.1092+5G>A r.spl p.?
+/. - c.1092+5G>A r.spl? p.?
+?/. - c.1092+5G>A r.spl p.?
+?/. - c.1092+5G>A r.spl p.?
+?/. - c.1092+5G>A r.spl? p.(?)
+?/. - c.1092+5G>A r.spl? p.(?)
+?/. - c.1092+5G>A r.spl? p.?
+?/. - c.1092+5G>A r.spl? p.(?)
+?/. - c.1092+5G>A r.spl? p.(?)
+?/. - c.1092+5G>A r.spl? p.(?)
+?/. - c.1092+5G>A r.spl? p.(?)
+/. - c.1150G>C r.(?) p.(Gly384Arg)
?/. - c.1158T>G r.(?) p.(Ile386Met)
?/. - c.1158T>G r.(?) p.(Ile386Met)
+?/. - c.1158T>G r.(?) p.(Ile386Met)
-?/. - c.1191A>C r.(?) p.(Thr397=)
?/. - c.1240G>A r.(?) p.(Val414Ile)
-/. - c.1272T>C r.(?) p.(Tyr424=)
-/. - c.1272T>C r.(?) p.(Tyr424=)
-?/. - c.1302G>C r.(?) p.(Val434=)
+?/. - c.1307+5G>T r.spl p.?
-/. - c.1307+19T>A r.(=) p.(=)
-/. - c.1307+19T>A r.(=) p.(=)
-/. - c.1307+19T>A r.(=) p.(=)
-/. - c.1307+19T>A r.(=) p.(=)
+?/. - c.1318_1321del r.(?) p.(Thr440Valfs*63)
?/. - c.1322G>C r.(?) p.(Gly441Ala)
?/. - c.1327C>T r.(?) p.(Leu443Phe)
?/. - c.1381A>T r.(?) p.(Thr461Ser)
+?/. - c.1477G>A r.(?) p.(Gly493Arg)
?/. - c.1516A>G r.(?) p.(Ile506Val)
-?/. - c.1525+12C>T r.(=) p.(=)
+/. - c.1546C>T r.(?) p.(Arg516*)
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