Transcript #00006941

Transcript name transcript variant 5
Gene name ABI3BP (ABI family member 3 binding protein)
Chromosome 3
Transcript - NCBI ID NM_015429.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_056244.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

98 entries on 1 page. Showing entries 1 - 98.
Legend  

Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
./. - c.100+568T>C r.(=) p.(=)
./. - c.100+881T>C - -
./. - c.100+3155T>C - -
./. - c.100+3682T>G - -
./. - c.100+10302G>C - -
./. - c.100+12591G>A - -
./. - c.100+13269G>A - -
./. - c.100+13476G>A - -
./. - c.100+14651G>C - -
./. - c.100+20715T>C - -
./. - c.100+25611G>A - -
./. - c.100+30467T>C - -
./. - c.101-33194T>C r.(=) p.(=)
./. - c.101-25213G>A r.(=) p.(=)
./. - c.101-21034T>A r.(=) p.(=)
./. - c.101-18217T>A - -
./. - c.101-17905G>C r.(=) p.(=)
./. - c.280+1340T>C - -
./. - c.280+7276T>C - -
./. - c.280+9709T>C r.(=) p.(=)
./. - c.281-10884G>A - -
./. - c.281-8120T>C r.(=) p.(=)
./. - c.281-4172T>C - -
./. - c.349+1180T>G - -
./. - c.349+1703T>C - -
./. - c.409G>A r.(?) p.(Val137Ile)
./. - c.482+2057G>A - -
./. - c.482+3611T>G r.(=) p.(=)
./. - c.482+4114T>G r.(=) p.(=)
./. - c.482+4314T>C - -
./. - c.482+5154T>G - -
./. - c.483-5864G>A - -
./. - c.483-5668T>A r.(=) p.(=)
./. - c.483-4717G>A - -
./. - c.717+487G>A - -
./. - c.717+927T>C - -
./. - c.717+3210T>C - -
./. - c.718-3270G>A r.(=) p.(=)
./. - c.718-3052T>G r.(=) p.(=)
./. - c.718-2998G>A r.(=) p.(=)
./. - c.718-2584T>G - -
./. - c.718-2273G>C - -
./. - c.718-966T>C r.(=) p.(=)
./. - c.931+832T>G - -
./. - c.931+2680G>A - -
./. - c.931+2761G>A - -
./. - c.932-3529T>G - -
./. - c.932-3142T>A - -
./. - c.932-2266T>C - -
./. - c.1159+3725T>C r.(=) p.(=)
./. - c.1159+4557T>C - -
./. - c.1160-4968G>A - -
./. - c.1160-708T>C - -
./. - c.1160-122G>A - -
./. - c.1376-79T>C - -
./. - c.1523-576G>A - -
./. - c.1597+351G>A - -
./. - c.1597+599C>A - -
./. - c.1597+1451G>A - -
./. - c.1597+2143G>A - -
./. - c.1597+2305C>A r.(=) p.(=)
./. - c.1597+2418G>A - -
./. - c.1597+15081C>A - -
./. - c.1597+18243T>C - -
./. - c.1598-10816T>C r.(=) p.(=)
./. - c.1598-10521G>A - -
./. - c.1598-9484C>A - -
./. - c.1598-9204G>A - -
./. - c.1598-8867T>A - -
./. - c.1598-705G>A - -
./. - c.1672+1033T>C r.(=) p.(=)
./. - c.1672+1136T>C - -
./. - c.1673-238G>A r.(=) p.(=)
./. - c.1748-3337G>C - -
./. - c.1748-3154T>C - -
./. - c.1888+974T>C r.(=) p.(=)
./. - c.1966+90T>A - -
./. - c.2029+570T>G - -
./. - c.2030-2800T>C - -
./. - c.2030-636T>C - -
./. - c.2030-311G>A - -
./. - c.2030-267C>A r.(=) p.(=)
./. - c.2200+449G>C r.(=) p.(=)
./. - c.2200+514T>C r.(=) p.(=)
./. - c.2201-998G>C - -
./. - c.2329+28C>A - -
./. - c.2398+388G>A - -
./. - c.2608+613G>C - -
./. - c.2609-657G>A - -
./. - c.2717+5259G>A r.(=) p.(=)
./. - c.2717+5302G>A - -
./. - c.2717+5421G>A r.(=) p.(=)
./. - c.2718-5215T>C r.(=) p.(=)
./. - c.2718-3177G>A - -
./. - c.2718-2032G>A - -
./. - c.2718-1781G>A - -
./. - c.2798-155T>C - -
./. - c.*840T>C - -
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