Transcript #00032637 (NM_015657.3, ABCA12 gene)

Transcript name ATP-binding cassette, sub-family A (ABC1), member 12, transcript variant 2
Gene name ABCA12 (ATP binding cassette subfamily A member 12)
Chromosome 2
Transcript - NCBI ID NM_015657.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_056472.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2017-08-09 12:19:44 +02:00 (CEST)
Date last edited N/A


Variants

2632 entries on 27 pages. Showing entries 1 - 100.
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Affects function     

AscendingDNA change (cDNA)     

RNA change     

Protein     
./. c.-5154C>T r.(=) p.(=)
./. c.-5146C>G r.(=) p.(=)
./. c.-5143C>A r.(=) p.(=)
./. c.-5138T>A r.(=) p.(=)
./. c.-5137G>A r.(=) p.(=)
./. c.-5136T>G r.(=) p.(=)
./. c.-5131C>G r.(=) p.(=)
./. c.-5126T>G r.(=) p.(=)
./. c.-5123G>A r.(=) p.(=)
./. c.-5117G>A r.(=) p.(=)
./. c.-5115T>G r.(=) p.(=)
./. c.-5112A>G r.(=) p.(=)
./. c.-5109C>T r.(=) p.(=)
./. c.-5108A>G r.(=) p.(=)
./. c.-5107C>T r.(=) p.(=)
./. c.-5099A>G r.(=) p.(=)
./. c.-5097C>T r.(=) p.(=)
./. c.-5093C>T r.(=) p.(=)
./. c.-5092G>A r.(=) p.(=)
./. c.-5088G>C r.(=) p.(=)
./. c.-5064T>A r.(=) p.(=)
./. c.-5059C>T r.(=) p.(=)
./. c.-5058A>G r.(=) p.(=)
./. c.-5051G>A r.(=) p.(=)
./. c.-5049A>G r.(=) p.(=)
./. c.-5047A>C r.(=) p.(=)
./. c.-5047A>G r.(=) p.(=)
./. c.-5040A>G r.(=) p.(=)
./. c.-5039C>A r.(=) p.(=)
./. c.-5037C>T r.(=) p.(=)
./. c.-5037C>G r.(=) p.(=)
./. c.-5035C>G r.(=) p.(=)
./. c.-5035C>T r.(=) p.(=)
./. c.-5024T>C r.(=) p.(=)
./. c.-5019T>C r.(=) p.(=)
./. c.-5010C>G r.(=) p.(=)
./. c.-5008T>C r.(=) p.(=)
./. c.-5005T>C r.(=) p.(=)
./. c.-5001T>A r.(=) p.(=)
./. c.-5000T>G r.(=) p.(=)
./. c.-4992G>A r.(=) p.(=)
./. c.-4980C>T r.(=) p.(=)
./. c.-4978A>G r.(=) p.(=)
./. c.-4977T>C r.(=) p.(=)
./. c.-49C>A r.(=) p.(=)
./. c.-46G>T r.(=) p.(=)
./. c.-42T>C r.(=) p.(=)
./. c.-40delG r.(=) p.(=)
./. c.-31G>A r.(=) p.(=)
./. c.-28G>C r.(=) p.(=)
./. c.-25A>G r.(=) p.(=)
./. c.-22A>G r.(=) p.(=)
./. c.-22A>T r.(=) p.(=)
./. c.-22A>C r.(=) p.(=)
./. c.-21A>G r.(=) p.(=)
./. c.-19C>A r.(=) p.(=)
./. c.-19C>T r.(=) p.(=)
./. c.-17T>C r.(=) p.(=)
./. c.-14A>T r.(=) p.(=)
./. c.-3T>C r.(=) p.(=)
./. c.2067delAinsG r.(?) p.(Pro689=)
./. c.5490delAinsT r.(?) p.(LeuIlePhePro1827=)
./. c.6184delAinsC r.(?) p.(Met2062Leu)
./. c.5490delAinsG r.(?) p.(LeuIlePhePro1827=)
./. c.*8delAinsC r.(=) p.(=)
./. c.5462delCinsT r.(?) p.(Thr1821Ile)
./. c.1228delGinsA r.(?) p.(Ala410Thr)
./. c.4824+6delTinsG r.(=) p.(=)
./. c.4824+6delTinsC r.(=) p.(=)
./. c.5427delGinsA r.(?) p.(Lys1809=)
./. c.4737-44delTinsC r.(=) p.(=)
./. c.6075delTinsC r.(?) p.(Asp2025=)
./. c.4736+13delGinsA r.(=) p.(=)
./. c.4045delGinsA r.(?) p.(Glu1349Lys)
./. c.6008+36delAinsG r.(=) p.(=)
./. c.5279+32delTinsC r.(=) p.(=)
./. c.1730-24delGinsT r.(=) p.(=)
./. c.1730-24delGinsC r.(=) p.(=)
./. c.4609-15delAinsG r.(=) p.(=)
./. c.3152delAinsG r.(?) p.(Tyr1051Cys)
./. c.2487delGinsA r.(?) p.(Leu829=)
./. c.333+6delCinsA r.(=) p.(=)
./. c.6483-8delCinsA r.(=) p.(=)
./. c.1519-12delTinsC r.(=) p.(=)
./. c.4986-49delGinsT r.(=) p.(=)
./. c.6370delGinsA r.(?) p.(Val2124Ile)
./. c.2225+40delCinsT r.(=) p.(=)
./. c.11A>G r.(?) p.(Tyr4Cys)
./. c.14T>A r.(?) p.(Ile5Lys)
./. c.18A>T r.(?) p.(Lys6Asn)
./. c.23T>C r.(?) p.(Ile8Thr)
./. c.26C>T r.(?) p.(Thr9Ile)
./. c.28T>G r.(?) p.(Ser10Ala)
./. c.29C>T r.(?) p.(Ser10Leu)
./. c.33T>C r.(?) p.(Gly11=)
./. c.39C>T r.(?) p.(Ser13=)
./. c.39C>A r.(?) p.(Ser13=)
./. c.40G>A r.(?) p.(Asp14Asn)
./. c.48A>G r.(?) p.(Ile16Met)
./. c.50C>T r.(?) p.(Thr17Met)
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