Transcript #00002945

Transcript name CD248 molecule, endosialin
Gene name CD248 (CD248 molecule, endosialin)
Chromosome 11
Transcript - NCBI ID NM_020404.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_065137.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

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

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.125G>A r.(?) p.(Arg42His)
?/? c.215G>A r.(?) p.(Ser72Asn)
?/? c.255C>T r.(=) p.(=)
?/? c.281G>A r.(?) p.(Cys94Tyr)
?/? c.303C>T r.(=) p.(=)
?/? c.337G>A r.(?) p.(Ala113Thr)
?/? c.343A>G r.(?) p.(Thr115Ala)
?/? c.344C>A r.(?) p.(Thr115Asn)
?/? c.348C>T r.(=) p.(=)
?/? c.373C>T r.(?) p.(Pro125Ser)
?/? c.374C>T r.(?) p.(Pro125Leu)
?/? c.414C>T r.(=) p.(=)
?/? c.415G>A r.(?) p.(Glu139Lys)
?/? c.443C>T r.(?) p.(Thr148Met)
?/? c.453C>T r.(=) p.(=)
?/? c.480C>G r.(?) p.(Phe160Leu)
?/? c.494C>T r.(?) p.(Pro165Leu)
?/? c.495G>A r.(=) p.(=)
?/? c.506A>T r.(?) p.(Asp169Val)
?/? c.513G>A r.(=) p.(=)
?/? c.532G>A r.(?) p.(Val178Met)
?/? c.560C>A r.(?) p.(Ser187Tyr)
?/? c.586G>A r.(?) p.(Gly196Ser)
?/? c.597C>T r.(=) p.(=)
?/? c.664G>A r.(?) p.(Gly222Ser)
?/? c.683C>T r.(?) p.(Pro228Leu)
?/? c.691C>T r.(=) p.(=)
?/? c.717C>T r.(=) p.(=)
?/? c.726C>T r.(=) p.(=)
?/? c.741G>A r.(=) p.(=)
?/? c.746_748del r.(?) p.(Glu249del)
?/? c.759C>T r.(=) p.(=)
?/? c.760G>A r.(?) p.(Val254Met)
?/? c.776C>G r.(?) p.(Thr259Ser)
?/? c.798A>G r.(=) p.(=)
?/? c.801C>T r.(=) p.(=)
?/? c.806G>A r.(?) p.(Arg269His)
?/? c.827C>T r.(?) p.(Ala276Val)
?/? c.833C>A r.(?) p.(Ala278Asp)
?/? c.836C>T r.(?) p.(Pro279Leu)
?/? c.840C>T r.(=) p.(=)
?/? c.859G>A r.(?) p.(Gly287Ser)
?/? c.864G>A r.(=) p.(=)
?/? c.878G>A r.(?) p.(Ser293Asn)
?/? c.902G>A r.(?) p.(Arg301Gln)
?/? c.908C>T r.(?) p.(Ala303Val)
?/? c.924C>T r.(=) p.(=)
?/? c.931G>A r.(?) p.(Val311Met)
?/? c.951G>A r.(=) p.(=)
?/? c.957C>T r.(=) p.(=)
?/? c.988G>A r.(?) p.(Val330Ile)
?/? c.1014C>T r.(=) p.(=)
?/? c.1015G>A r.(?) p.(Glu339Lys)
?/? c.1093G>A r.(?) p.(Gly365Arg)
?/? c.1125G>A r.(=) p.(=)
?/? c.1137C>T r.(=) p.(=)
?/? c.1142C>A r.(?) p.(Ala381Asp)
?/? c.1159G>A r.(?) p.(Gly387Ser)
?/? c.1169C>T r.(?) p.(Thr390Met)
?/? c.1203G>A r.(=) p.(=)
?/? c.1219G>A r.(?) p.(Ala407Thr)
?/? c.1230T>C r.(=) p.(=)
?/? c.1235C>T r.(?) p.(Pro412Leu)
?/? c.1236G>A r.(=) p.(=)
?/? c.1303G>A r.(?) p.(Ala435Thr)
?/? c.1326_1328del r.(?) p.(Ser443del)
?/? c.1341C>T r.(=) p.(=)
?/? c.1351G>A r.(?) p.(Val451Met)
?/? c.1368G>A r.(=) p.(=)
?/? c.1370A>G r.(?) p.(His457Arg)
?/? c.1388C>G r.(?) p.(Ala463Gly)
?/? c.1417C>T r.(?) p.(His473Tyr)
?/? c.1435G>C r.(?) p.(Asp479His)
?/? c.1450G>A r.(?) p.(Val484Met)
?/? c.1455C>T r.(=) p.(=)
?/? c.1456G>A r.(?) p.(Ala486Thr)
?/? c.1495G>A r.(?) p.(Gly499Ser)
?/? c.1509C>T r.(=) p.(=)
?/? c.1543C>G r.(?) p.(Pro515Ala)
?/? c.1585C>G r.(?) p.(Gln529Glu)
?/? c.1589C>T r.(?) p.(Ser530Phe)
?/? c.1595T>A r.(?) p.(Met532Lys)
?/? c.1609C>T r.(?) p.(Arg537Trp)
?/? c.1610G>A r.(?) p.(Arg537Gln)
?/? c.1620C>T r.(=) p.(=)
?/? c.1632_1634del r.(?) p.(Thr545del)
?/? c.1679C>T r.(?) p.(Thr560Ile)
?/? c.1707C>G r.(=) p.(=)
?/? c.1755C>T r.(=) p.(=)
?/? c.1759A>C r.(?) p.(Thr587Pro)
?/? c.1766A>C r.(?) p.(Gln589Pro)
?/? c.1794C>T r.(=) p.(=)
?/? c.1802C>T r.(?) p.(Ser601Phe)
?/? c.1820C>T r.(?) p.(Ser607Phe)
?/? c.1861C>T r.(=) p.(=)
?/? c.1863G>A r.(=) p.(=)
?/? c.1951C>T r.(?) p.(Pro651Ser)
?/? c.1966G>A r.(?) p.(Ala656Thr)
?/? c.1971G>A r.(=) p.(=)
?/? c.2031C>T r.(=) p.(=)
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