Transcript #00011123 (NM_002310.5, LIFR gene)

Transcript name transcript variant 2
Gene name LIFR (leukemia inhibitory factor receptor alpha)
Chromosome 5
Transcript - NCBI ID NM_002310.5
Transcript - Ensembl ID -
Protein - NCBI ID NP_002301.1
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

65 entries on 1 page. Showing entries 1 - 65.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+/. - c.23del r.(?) p.(Leu8*)
?/. - c.28C>T r.(?) p.(Arg10Ter)
-?/. - c.46G>A r.(?) p.(Asp16Asn)
-?/. - c.78C>T r.(?) p.(Phe26=)
-/. - c.143-13_143-10del r.(=) p.(=)
-/. - c.143-13_143-10del r.(=) p.(=)
-/. - c.143-13_143-10dup r.(=) p.(=)
-/. - c.143-13_143-10dup r.(=) p.(=)
-/. - c.143-11_143-10del r.(=) p.(=)
-/. - c.143-11_143-10del r.(=) p.(=)
-/. - c.143-11_143-10dup r.(=) p.(=)
-/. - c.143-11_143-10dup r.(=) p.(=)
-?/. - c.143-11_143-10dup r.(=) p.(=)
-?/. - c.247A>G r.(?) p.(Ile83Val)
-?/. - c.346C>T r.(?) p.(His116Tyr)
-?/. - c.346C>T r.(?) p.(His116Tyr)
-/. - c.397+17_397+20del r.(=) p.(=)
-/. - c.397+17_397+20del r.(=) p.(=)
+?/. - c.478_479del r.(?) p.(Arg160Glyfs*15)
+/. - c.653dup r.(?) p.(Glu219Glyfs*3)
-?/. - c.736+18G>T r.(=) p.(=)
-/. - c.954C>T r.(?) p.(Thr318=)
+/. - c.1121+1G>A r.spl? p.?
+?/. - c.1121+1G>A r.spl? p.?
-?/. - c.1437+138T>C r.(=) p.(=)
-?/. - c.1438-18T>A r.(=) p.(=)
+?/. 11 c.1438-3T>G r.spl? p.?
+?/. 11 c.1438-3T>G r.spl? p.?
-/. - c.1732G>A r.(?) p.(Asp578Asn)
-?/. - c.1790G>A r.(?) p.(Arg597Gln)
-/. - c.1886-18C>T r.(=) p.(=)
-/. - c.1899A>G r.(?) p.(Ile633Met)
-?/. - c.1899A>G r.(?) p.(Ile633Met)
?/. - c.1903_1904insT r.(?) p.(Gln635Leufs*26)
-?/. - c.1915A>T r.(?) p.(Met639Leu)
-?/. - c.1937C>A r.(?) p.(Thr646Asn)
-/. - c.1937C>A r.(?) p.(Thr646Asn)
-?/. - c.1937C>A r.(?) p.(Thr646Asn)
-?/. - c.1971C>T r.(?) p.(=)
-?/. - c.1991C>T r.(?) p.(Ser664Leu)
-?/. - c.2051C>G r.(?) p.(Thr684Ser)
-?/. - c.2066-10C>T r.(=) p.(=)
+/. - c.2074C>T r.(?) p.(Arg692Ter)
-?/. - c.2221T>G r.(?) p.(Leu741Val)
-?/. - c.2410A>G r.(?) p.(Lys804Glu)
-?/. - c.2447A>G r.(?) p.(Asp816Gly)
-/. - c.2447A>G r.(?) p.(Asp816Gly)
-?/. - c.2447A>G r.(?) p.(Asp816Gly)
-?/. - c.2578C>T r.(?) p.(Arg860Trp)
-?/. - c.2591+10C>T r.(=) p.(=)
-/. - c.2591+17T>C r.(=) p.(=)
?/. - c.2612C>T r.(?) p.(Pro871Leu)
-/. - c.2766T>C r.(?) p.(Asp922=)
-?/. - c.2910A>G r.(?) p.(Ala970=)
-?/. - c.2934G>A r.(?) p.(Gln978=)
-?/. - c.2934G>A r.(?) p.(Gln978=)
?/. - c.2936C>T r.(?) p.(Ser979Leu)
-?/. - c.2937G>A r.(?) p.(=)
?/. - c.2940G>C r.(?) p.(Met980Ile)
-?/. - c.3039G>C r.(?) p.(Val1013=)
-?/. - c.3132T>C r.(?) p.(=)
?/. - c.3221A>G r.(?) p.(Asp1074Gly)
?/. - c.3221A>G r.(?) p.(Asp1074Gly)
?/. - c.3230C>G r.(?) p.(Ser1077Cys)
-?/. - c.3288C>A r.(?) p.(Asn1096Lys)
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