Transcript #00003101 (NM_001712.4, CEACAM1 gene)

Transcript name transcript variant 1
Gene name CEACAM1 (carcinoembryonic antigen-related cell adhesion molecule 1 (biliary glycoprotein))
Chromosome 19
Transcript - NCBI ID NM_001712.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_001703.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

99 entries on 1 page. Showing entries 1 - 99.
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Affects function     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.-62C>T r.(=) p.(=)
?/? c.-56G>A r.(=) p.(=)
?/? c.-35C>T r.(=) p.(=)
?/? c.17C>T r.(?) p.(Ala6Val)
?/? c.34C>T r.(?) p.(Arg12Cys)
?/? c.64+3_64+4insG r.spl? p.?
?/? c.64+16C>A r.(=) p.(=)
?/? c.64+29G>A r.(=) p.(=)
?/? c.64+33A>G r.(=) p.(=)
?/? c.64+40G>A r.(=) p.(=)
?/? c.65-41A>T r.(=) p.(=)
?/? c.65-45_65-31del r.(=) p.(=)
?/? c.65-5C>G r.spl? p.?
?/? c.103C>A r.(?) p.(Gln35Lys)
?/? c.134T>A r.(?) p.(Val45Asp)
?/? c.174G>T r.(=) p.(=)
?/? c.203A>G r.(?) p.(Tyr68Cys)
?/? c.219G>A r.(=) p.(=)
?/? c.248C>T r.(?) p.(Ala83Val)
?/? c.262C>A r.(?) p.(Gln88Lys)
?/? c.282A>C r.(=) p.(=)
?/? c.289G>A r.(?) p.(Gly97Ser)
?/? c.309C>T r.(=) p.(=)
?/? c.369A>C r.(?) p.(Gln123His)
?/? c.424C>T r.(?) p.(Pro142Ser)
?/? c.424+29T>C r.(=) p.(=)
?/? c.424+36dup r.(=) p.(=)
?/? c.424+36del r.(=) p.(=)
?/? c.424+40G>A r.(=) p.(=)
?/? c.425-36C>G r.(=) p.(=)
?/? c.425-15_425-14del r.(=) p.(=)
?/? c.425-4A>G r.spl? p.?
?/? c.425C>T r.(?) p.(Pro142Leu)
?/? c.442T>C r.(?) p.(Ser148Pro)
?/? c.553_554insAGGC r.(?) p.(Leu185Glnfs*26)
?/? c.557C>A r.(?) p.(Pro186Gln)
?/? c.558G>A r.(=) p.(=)
?/? c.596C>T r.(?) p.(Thr199Ile)
?/? c.625G>A r.(?) p.(Asp209Asn)
?/? c.657C>G r.(?) p.(Asn219Lys)
?/? c.663G>A r.(=) p.(=)
?/? c.668C>T r.(?) p.(Ala223Val)
?/? c.669G>A r.(=) p.(=)
?/? c.674G>A r.(?) p.(Arg225His)
?/? c.703+26C>T r.(=) p.(=)
?/? c.703+49C>T r.(=) p.(=)
?/? c.704-37G>T r.(=) p.(=)
?/? c.704-7G>A r.(=) p.(=)
?/? c.791_792insG r.(?) p.(Asn264Lysfs*25)
?/? c.856A>G r.(?) p.(Ile286Val)
?/? c.909C>T r.(=) p.(=)
?/? c.944C>T r.(?) p.(Thr315Met)
?/? c.945G>T r.(=) p.(=)
?/? c.946A>C r.(?) p.(Ile316Leu)
?/? c.959-51G>A r.(=) p.(=)
?/? c.971T>C r.(?) p.(Val324Ala)
?/? c.974T>C r.(?) p.(Val325Ala)
?/? c.982C>A r.(?) p.(Pro328Thr)
?/? c.1014A>T r.(=) p.(=)
?/? c.1016G>A r.(?) p.(Gly339Glu)
?/? c.1073G>A r.(?) p.(Arg358His)
?/? c.1091A>G r.(?) p.(Gln364Arg)
?/? c.1100C>T r.(?) p.(Pro367Leu)
?/? c.1101G>A r.(=) p.(=)
?/? c.1127A>G r.(?) p.(Gln376Arg)
?/? c.1152C>T r.(=) p.(=)
?/? c.1178C>T r.(?) p.(Thr393Met)
?/? c.1196T>G r.(?) p.(Phe399Cys)
?/? c.1232T>C r.(?) p.(Met411Thr)
?/? c.1237A>T r.(?) p.(Asn413Tyr)
?/? c.1240G>A r.(?) p.(Val414Ile)
?/? c.1246T>C r.(?) p.(Tyr416His)
?/? c.1246+28T>C r.(=) p.(=)
?/? c.1247-20_1247-18del r.(=) p.(=)
?/? c.1376+41G>T r.(=) p.(=)
?/? c.1376+49T>C r.(=) p.(=)
?/? c.1376+52T>C r.(=) p.(=)
?/? c.1377-56C>A r.(=) p.(=)
?/? c.1377-30T>C r.(=) p.(=)
?/? c.1377-1G>A r.spl? p.?
?/? c.1425C>T r.(=) p.(=)
?/? c.1429+4del r.spl? p.?
?/? c.1429+42A>G r.(=) p.(=)
?/? c.1429+47G>A r.(=) p.(=)
?/? c.1430-67del r.(=) p.(=)
?/? c.1430-25G>A r.(=) p.(=)
?/? c.1453C>T r.(?) p.(Pro485Ser)
?/? c.1461+12C>T r.(=) p.(=)
?/? c.1461+37T>C r.(=) p.(=)
?/? c.1461+58T>C r.(=) p.(=)
?/? c.1462-27T>A r.(=) p.(=)
?/? c.1462-20T>C r.(=) p.(=)
?/? c.1462-14T>C r.(=) p.(=)
?/? c.1463T>G r.(?) p.(Met488Arg)
?/? c.1479T>C r.(=) p.(=)
?/? c.1500C>T r.(=) p.(=)
?/? c.1513C>A r.(?) p.(Gln505Lys)
?/? c.1574del r.(?) p.(Lys525Serfs*23)
?/? c.*42T>A r.(=) p.(=)
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