Transcript #00009624

Transcript name lectin, mannose-binding, 1 like
Gene name LMAN1L (lectin, mannose-binding, 1 like)
Chromosome 15
Transcript - NCBI ID NM_021819.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_068591.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

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

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.5C>T r.(?) p.(Pro2Leu)
?/? c.29T>C r.(?) p.(Leu10Ser)
?/? c.59C>G r.(?) p.(Pro20Arg)
?/? c.78G>C r.(=) p.(=)
?/? c.92G>A r.(?) p.(Arg31His)
?/? c.145G>A r.(?) p.(Ala49Thr)
?/? c.162G>A r.(?) p.(Trp54*)
?/? c.175+32C>T r.(=) p.(=)
?/? c.175+35G>C r.(=) p.(=)
?/? c.176-35G>A r.(=) p.(=)
?/? c.230G>C r.(?) p.(Ser77Thr)
?/? c.279A>G r.(=) p.(=)
?/? c.289A>G r.(?) p.(Met97Val)
?/? c.305T>G r.(?) p.(Leu102Arg)
?/? c.314G>A r.(?) p.(Arg105Gln)
?/? c.330+25C>T r.(=) p.(=)
?/? c.330+30C>T r.(=) p.(=)
?/? c.330+31G>C r.(=) p.(=)
?/? c.330+48C>T r.(=) p.(=)
?/? c.334G>A r.(?) p.(Val112Met)
?/? c.345C>G r.(=) p.(=)
?/? c.366C>T r.(=) p.(=)
?/? c.377G>C r.(?) p.(Gly126Ala)
?/? c.438+11G>C r.(=) p.(=)
?/? c.438+37C>G r.(=) p.(=)
?/? c.438+48_438+49insC r.(=) p.(=)
?/? c.439-33C>G r.(=) p.(=)
?/? c.439-30C>T r.(=) p.(=)
?/? c.439-25C>G r.(=) p.(=)
?/? c.439-11C>T r.(=) p.(=)
?/? c.498-52C>T r.(=) p.(=)
?/? c.498-42G>A r.(=) p.(=)
?/? c.537C>T r.(=) p.(=)
?/? c.568C>T r.(?) p.(Arg190Trp)
?/? c.569G>A r.(?) p.(Arg190Gln)
?/? c.591G>A r.(=) p.(=)
?/? c.595C>T r.(?) p.(Arg199Cys)
?/? c.596G>T r.(?) p.(Arg199Leu)
?/? c.597+3G>C r.spl? p.?
?/? c.597+23G>C r.(=) p.(=)
?/? c.597+26A>G r.(=) p.(=)
?/? c.598-52G>A r.(=) p.(=)
?/? c.598-35_598-34insC r.(=) p.(=)
?/? c.598-34C>G r.(=) p.(=)
?/? c.598-29C>G r.(=) p.(=)
?/? c.619A>C r.(?) p.(Thr207Pro)
?/? c.635G>A r.(?) p.(Gly212Asp)
?/? c.680G>A r.(?) p.(Gly227Asp)
?/? c.690G>A r.(=) p.(=)
?/? c.711C>A r.(=) p.(=)
?/? c.719-48G>A r.(=) p.(=)
?/? c.719-25T>C r.(=) p.(=)
?/? c.765C>T r.(=) p.(=)
?/? c.774+3G>A r.spl? p.?
?/? c.774+19T>A r.(=) p.(=)
?/? c.775-17C>T r.(=) p.(=)
?/? c.775-15G>C r.(=) p.(=)
?/? c.775-2A>G r.spl? p.?
?/? c.810C>T r.(=) p.(=)
?/? c.811C>T r.(?) p.(Arg271Cys)
?/? c.822G>A r.(=) p.(=)
?/? c.824A>C r.(?) p.(Gln275Pro)
?/? c.839G>A r.(?) p.(Trp280*)
?/? c.879_880del r.(?) p.(Lys294Ilefs*4)
?/? c.882A>G r.(=) p.(=)
?/? c.895G>A r.(?) p.(Ala299Thr)
?/? c.907+9C>T r.(=) p.(=)
?/? c.907+28C>T r.(=) p.(=)
?/? c.907+29G>A r.(=) p.(=)
?/? c.907+52C>T r.(=) p.(=)
?/? c.952C>T r.(?) p.(Arg318Trp)
?/? c.953G>A r.(?) p.(Arg318Gln)
?/? c.970C>T r.(?) p.(Arg324Trp)
?/? c.997G>A r.(?) p.(Ala333Thr)
?/? c.1009T>C r.(?) p.(Trp337Arg)
?/? c.1050C>T r.(=) p.(=)
?/? c.1055G>T r.(?) p.(Gly352Val)
?/? c.1060-41A>C r.(=) p.(=)
?/? c.1060-15T>C r.(=) p.(=)
?/? c.1131+1G>A r.spl? p.?
?/? c.1131+9C>G r.(=) p.(=)
?/? c.1132-46G>A r.(=) p.(=)
?/? c.1132-38A>G r.(=) p.(=)
?/? c.1199+32C>A r.(=) p.(=)
?/? c.1200-45A>T r.(=) p.(=)
?/? c.1200-7C>T r.(=) p.(=)
?/? c.1200-6G>A r.(=) p.(=)
?/? c.1200-5G>A r.spl? p.?
?/? c.1200-2A>G r.spl? p.?
?/? c.1217T>A r.(?) p.(Met406Lys)
?/? c.1220C>T r.(?) p.(Ala407Val)
?/? c.1222G>A r.(?) p.(Ala408Thr)
?/? c.1234G>A r.(?) p.(Val412Ile)
?/? c.1236C>A r.(=) p.(=)
?/? c.1242C>T r.(=) p.(=)
?/? c.1279G>T r.(?) p.(Asp427Tyr)
?/? c.1280A>G r.(?) p.(Asp427Gly)
?/? c.1284C>T r.(=) p.(=)
?/? c.1293C>G r.(=) p.(=)
?/? c.1309C>T r.(?) p.(Leu437Phe)
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