Transcript #00005743 (NM_156039.3, CSF3R gene)

Transcript name transcript variant 3
Gene name CSF3R (colony stimulating factor 3 receptor (granulocyte))
Chromosome 1
Transcript - NCBI ID NM_156039.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_724781.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

63 entries on 1 page. Showing entries 1 - 63.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.108C>T r.(?) p.(Val36=)
-?/. - c.108C>T r.(?) p.(Val36=)
-?/. - c.160C>T r.(?) p.(His54Tyr)
-?/. - c.161A>G r.(?) p.(His54Arg)
-?/. - c.171G>A r.(?) p.(Pro57=)
+/. - c.340C>T r.(?) p.(Gln114*)
-?/. - c.352C>T r.(?) p.(Arg118Cys)
-?/. - c.447G>C r.(?) p.(Glu149Asp)
-?/. - c.447G>C r.(?) p.(Glu149Asp)
-?/. - c.471T>C r.(?) p.(Thr157=)
-?/. - c.486-4G>A r.spl? p.?
-?/. - c.516C>T r.(?) p.(Asp172=)
?/. - c.569G>A r.(?) p.(Arg190His)
-/. - c.692T>C r.(?) p.(Met231Thr)
-/. - c.726C>T r.(?) p.(Ala242=)
-?/. - c.801G>C r.(?) p.(Glu267Asp)
+/. - c.922C>T r.(?) p.(Arg308Cys)
?/. - c.931C>T r.(?) p.(Arg311Cys)
-/. - c.958G>A r.(?) p.(Asp320Asn)
-/. - c.958G>A r.(?) p.(Asp320Asn)
-/. - c.958G>A r.(?) p.(Asp320Asn)
-?/. - c.1028G>A r.(?) p.(Arg343Gln)
-/. - c.1037A>G r.(?) p.(Gln346Arg)
-?/. - c.1213G>A r.(?) p.(Glu405Lys)
-/. - c.1260T>C r.(?) p.(Thr420=)
-?/. - c.1319G>A r.(?) p.(Arg440Gln)
-?/. - c.1319G>A r.(?) p.(Arg440Gln)
-?/. - c.1319G>A r.(?) p.(Arg440Gln)
-?/. - c.1410G>A r.(?) p.(Ala470=)
-?/. - c.1410G>A r.(?) p.(Ala470=)
-?/. - c.1458G>A r.(?) p.(Thr486=)
-/. - c.1528G>C r.(?) p.(Asp510His)
-?/. - c.1638G>T r.(?) p.(Glu546Asp)
+/. - c.1640G>A r.(?) p.(Trp547*)
-/. - c.1684T>C r.(?) p.(Tyr562His)
-/. - c.1684T>C r.(?) p.(Tyr562His)
-?/. - c.1689C>A r.(?) p.(Thr563=)
-?/. - c.1711A>G r.(?) p.(Asn571Asp)
-?/. - c.1748G>A r.(?) p.(Arg583His)
-?/. - c.1761C>T r.(?) p.(Leu587=)
-?/. - c.1794C>T r.(?) p.(Ile598=)
-?/. - c.1897T>C r.(?) p.(Phe633Leu)
-?/. - c.1919C>T r.(?) p.(Thr640Ile)
-?/. - c.1919C>T r.(?) p.(Thr640Ile)
-?/. - c.2076G>A r.(?) p.(Gln692=)
-?/. - c.2087T>C r.(?) p.(Met696Thr)
-?/. - c.2087T>C r.(?) p.(Met696Thr)
-?/. - c.2092C>T r.(?) p.(Arg698Cys)
-?/. - c.2140G>A r.(?) p.(Gly714Ser)
-?/. - c.2211G>C r.(?) p.(Glu737Asp)
-/. - c.2278C>A r.(?) p.(Pro760Thr)
-?/. - c.2278C>A r.(?) p.(Pro760Thr)
-?/. - c.2292C>T r.(?) p.(Ser764=)
-?/. - c.2292C>T r.(?) p.(Ser764=)
-?/. - c.2323G>A r.(?) p.(Asp775Asn)
-?/. - c.2415G>A r.(?) p.(Ala805=)
?/. - c.2448C>T r.(=) p.(=)
?/. - c.2448C>T r.(=) p.(=)
-?/. - c.2503G>A r.(?) p.(Glu835Lys)
-?/. - c.2503G>A r.(?) p.(Glu835Lys)
-?/. - c.2509G>A r.(?) p.(Asp837Asn)
-?/. - c.2565T>C r.(?) p.(His855=)
-?/. - c.2577G>A r.(?) p.(Ala859=)
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