Transcript #00000096

Transcript name HNF1 homeobox A
Gene name HNF1A (HNF1 homeobox A)
Chromosome 12
Transcript - NCBI ID NM_000545.5
Transcript - Ensembl ID -
Protein - NCBI ID NP_000536.5
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
./. - c.-4A>G r.(=) p.(=)
./. - c.-4A>G r.(=) p.(=)
./. - c.29C>T r.(?) p.(Thr10Met)
./. - c.92G>A r.(?) p.(Gly31Asp)
./. - c.92G>A r.(?) p.(Gly31Asp)
./. - c.99G>A r.(=) p.(=)
./. - c.99G>A r.(=) p.(=)
./. - c.238G>T r.(?) p.(Asp80Tyr)
./. - c.285G>A r.(=) p.(=)
./. - c.292G>A r.(?) p.(Ala98Thr)
./. - c.326+24G>A r.(=) p.(=)
./. - c.326+25C>T r.(=) p.(=)
./. - c.326+25C>T r.(=) p.(=)
./. - c.327-21C>A r.(=) p.(=)
./. - c.327-21C>A r.(=) p.(=)
./. - c.336G>A r.(=) p.(=)
./. - c.336G>A r.(=) p.(=)
./. - c.336G>A r.(=) p.(=)
./. - c.336G>A r.(=) p.(=)
./. - c.336G>A r.(=) p.(=)
./. - c.336G>A r.(=) p.(=)
./. - c.336G>A r.(=) p.(=)
./. - c.336G>A r.(=) p.(=)
./. - c.336G>A r.(=) p.(=)
./. - c.336G>A r.(=) p.(=)
./. - c.336G>A r.(=) p.(=)
./. - c.336G>A r.(=) p.(=)
./. - c.336G>A r.(=) p.(=)
./. - c.336G>A r.(=) p.(=)
./. - c.341G>A r.(?) p.(Arg114His)
./. - c.355G>C r.(?) p.(Val119Leu)
./. - c.481G>A r.(?) p.(Ala161Thr)
./. - c.481G>A r.(?) p.(Ala161Thr)
./. - c.481G>A r.(?) p.(Ala161Thr)
./. - c.481G>A r.(?) p.(Ala161Thr)
./. - c.481G>A r.(?) p.(Ala161Thr)
./. - c.481G>A r.(?) p.(Ala161Thr)
./. - c.526+18C>G r.(=) p.(=)
./. - c.527-6C>T r.(=) p.(=)
./. - c.693G>A r.(=) p.(=)
./. - c.693G>A r.(=) p.(=)
./. - c.693G>A r.(=) p.(=)
./. - c.693G>A r.(=) p.(=)
./. - c.693G>A r.(=) p.(=)
./. - c.713+14C>T r.(=) p.(=)
./. - c.713+50G>A r.(=) p.(=)
./. - c.716C>T r.(?) p.(Ala239Val)
./. - c.716C>T r.(?) p.(Ala239Val)
./. - c.716C>T r.(?) p.(Ala239Val)
./. - c.716C>T r.(?) p.(Ala239Val)
./. - c.716C>T r.(?) p.(Ala239Val)
./. - c.716C>T r.(?) p.(Ala239Val)
./. - c.716C>T r.(?) p.(Ala239Val)
./. - c.775G>A r.(?) p.(Val259Ile)
./. - c.862G>T r.(?) p.(Gly288Trp)
./. - c.862G>T r.(?) p.(Gly288Trp)
./. - c.865C>T r.(?) p.(Pro289Ser)
./. - c.867C>A r.(=) p.(=)
./. - c.873A>G r.(=) p.(=)
./. - c.942C>T r.(=) p.(=)
./. - c.956-31T>C r.(=) p.(=)
./. - c.956-24G>A r.(=) p.(=)
./. - c.962G>A r.(?) p.(Arg321His)
./. - c.984T>G r.(?) p.(Ser328Arg)
./. - c.1061C>T r.(?) p.(Thr354Met)
./. - c.1108-36C>T r.(=) p.(=)
./. - c.1108-36C>T r.(=) p.(=)
./. - c.1108-34G>A r.(=) p.(=)
./. - c.1108-34G>A r.(=) p.(=)
./. - c.1108-27C>T r.(=) p.(=)
./. - c.1108-27C>T r.(=) p.(=)
./. - c.1108-27C>T r.(=) p.(=)
./. - c.1108-27C>T r.(=) p.(=)
./. - c.1108-27C>T r.(=) p.(=)
./. - c.1108-27C>T r.(=) p.(=)
./. - c.1108-27C>T r.(=) p.(=)
./. - c.1108-27C>T r.(=) p.(=)
./. - c.1108-27C>T r.(=) p.(=)
./. - c.1108-27C>T r.(=) p.(=)
./. - c.1108-27C>T r.(=) p.(=)
./. - c.1108-27C>T r.(=) p.(=)
./. - c.1108-27C>T r.(=) p.(=)
./. - c.1108-27C>T r.(=) p.(=)
./. - c.1108-27C>T r.(=) p.(=)
./. - c.1108-27C>T r.(=) p.(=)
./. - c.1108-27C>T r.(=) p.(=)
./. - c.1108-27C>T r.(=) p.(=)
./. - c.1108-27C>T r.(=) p.(=)
./. - c.1108-27C>T r.(=) p.(=)
./. - c.1108-27C>T r.(=) p.(=)
./. - c.1108-27C>T r.(=) p.(=)
./. - c.1108-27C>T r.(=) p.(=)
./. - c.1108-27C>T r.(=) p.(=)
./. - c.1108-27C>T r.(=) p.(=)
./. - c.1108-27C>T r.(=) p.(=)
./. - c.1108-27C>T r.(=) p.(=)
./. - c.1108-27C>T r.(=) p.(=)
./. - c.1108-27C>T r.(=) p.(=)
./. - c.1108-27C>T r.(=) p.(=)
./. - c.1108-27C>T r.(=) p.(=)
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