Transcript #00017632 (NM_144775.2, SMCR8 gene)

Transcript name Smith-Magenis syndrome chromosome region, candidate 8
Gene name SMCR8 (Smith-Magenis syndrome chromosome region, candidate 8)
Chromosome 17
Transcript - NCBI ID NM_144775.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_658988.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

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

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.13C>A r.(?) p.(Pro5Thr)
?/? c.78G>A r.(=) p.(=)
?/? c.107C>A r.(?) p.(Pro36His)
?/? c.108C>T r.(=) p.(=)
?/? c.156G>C r.(?) p.(Lys52Asn)
?/? c.158T>A r.(?) p.(Phe53Tyr)
?/? c.172A>G r.(?) p.(Ile58Val)
?/? c.237C>G r.(=) p.(=)
?/? c.239A>T r.(?) p.(Lys80Ile)
?/? c.313G>T r.(?) p.(Gly105Cys)
?/? c.322C>T r.(?) p.(Pro108Ser)
?/? c.354G>C r.(=) p.(=)
?/? c.365A>G r.(?) p.(Lys122Arg)
?/? c.408G>A r.(=) p.(=)
?/? c.467_468insCGT r.(?) p.(Ala156_Tyr157insVal)
?/? c.488A>G r.(?) p.(His163Arg)
?/? c.504G>A r.(=) p.(=)
?/? c.520G>A r.(?) p.(Ala174Thr)
?/? c.554C>T r.(?) p.(Thr185Ile)
?/? c.558C>T r.(=) p.(=)
?/? c.639G>A r.(=) p.(=)
?/? c.660C>A r.(?) p.(Asn220Lys)
?/? c.665A>G r.(?) p.(Lys222Arg)
?/? c.732T>C r.(=) p.(=)
?/? c.769C>T r.(?) p.(Pro257Ser)
?/? c.780G>A r.(=) p.(=)
?/? c.783G>A r.(=) p.(=)
?/? c.805G>C r.(?) p.(Gly269Arg)
?/? c.819C>T r.(=) p.(=)
?/? c.829C>G r.(?) p.(Gln277Glu)
?/? c.845C>T r.(?) p.(Ser282Phe)
?/? c.859C>G r.(?) p.(Pro287Ala)
?/? c.873C>T r.(=) p.(=)
?/? c.921_925del r.(?) p.(Ala309Valfs*6)
?/? c.998A>G r.(?) p.(Gln333Arg)
?/? c.1045C>G r.(?) p.(Leu349Val)
?/? c.1110T>G r.(?) p.(Phe370Leu)
?/? c.1113C>T r.(=) p.(=)
?/? c.1122C>T r.(=) p.(=)
?/? c.1130A>G r.(?) p.(Glu377Gly)
?/? c.1140C>T r.(=) p.(=)
?/? c.1147G>A r.(?) p.(Val383Met)
?/? c.1165A>G r.(?) p.(Ile389Val)
?/? c.1194G>A r.(=) p.(=)
?/? c.1206T>C r.(=) p.(=)
?/? c.1250C>G r.(?) p.(Ser417Cys)
?/? c.1254C>A r.(?) p.(Tyr418*)
?/? c.1260C>T r.(=) p.(=)
?/? c.1292A>G r.(?) p.(Gln431Arg)
?/? c.1299G>A r.(=) p.(=)
?/? c.1308G>A r.(=) p.(=)
?/? c.1347C>T r.(=) p.(=)
?/? c.1446C>T r.(=) p.(=)
?/? c.1447G>T r.(?) p.(Val483Leu)
?/? c.1466G>A r.(?) p.(Ser489Asn)
?/? c.1472C>T r.(?) p.(Ala491Val)
?/? c.1480A>T r.(?) p.(Thr494Ser)
?/? c.1552G>A r.(?) p.(Glu518Lys)
?/? c.1557C>T r.(=) p.(=)
?/? c.1571C>T r.(?) p.(Pro524Leu)
?/? c.1580C>T r.(?) p.(Ala527Val)
?/? c.1599T>C r.(=) p.(=)
?/? c.1604C>T r.(?) p.(Ala535Val)
?/? c.1618G>T r.(?) p.(Ala540Ser)
?/? c.1643C>T r.(?) p.(Pro548Leu)
?/? c.1658G>A r.(?) p.(Gly553Glu)
?/? c.1667G>A r.(?) p.(Arg556His)
?/? c.1671C>A r.(?) p.(Phe557Leu)
?/? c.1696C>T r.(=) p.(=)
?/? c.1703A>C r.(?) p.(Glu568Ala)
?/? c.1714G>A r.(?) p.(Gly572Ser)
?/? c.1751C>T r.(?) p.(Ser584Phe)
?/? c.1752C>A r.(=) p.(=)
?/? c.1756T>C r.(?) p.(Cys586Arg)
?/? c.1761T>C r.(=) p.(=)
?/? c.1773C>T r.(=) p.(=)
?/? c.1777G>T r.(?) p.(Gly593Cys)
?/? c.1778G>A r.(?) p.(Gly593Asp)
?/? c.1880G>A r.(?) p.(Arg627His)
?/? c.1884A>G r.(=) p.(=)
?/? c.1907A>G r.(?) p.(Asn636Ser)
?/? c.1918C>T r.(?) p.(Arg640*)
?/? c.1919G>A r.(?) p.(Arg640Gln)
?/? c.1937G>T r.(?) p.(Gly646Val)
?/? c.1945G>A r.(?) p.(Ala649Thr)
?/? c.1959C>T r.(=) p.(=)
?/? c.1961C>T r.(?) p.(Pro654Leu)
?/? c.2000G>T r.(?) p.(Ser667Ile)
?/? c.2014T>G r.(?) p.(Ser672Ala)
?/? c.2024C>T r.(?) p.(Thr675Ile)
?/? c.2029T>C r.(?) p.(Tyr677His)
?/? c.2030A>G r.(?) p.(Tyr677Cys)
?/? c.2031C>T r.(=) p.(=)
?/? c.2039G>A r.(?) p.(Ser680Asn)
?/? c.2065A>T r.(?) p.(Ile689Phe)
?/? c.2098G>C r.(?) p.(Asp700His)
?/? c.2128G>A r.(?) p.(Ala710Thr)
?/? c.2154C>T r.(=) p.(=)
?/? c.2181G>C r.(=) p.(=)
?/? c.2227G>A r.(?) p.(Val743Ile)
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