Transcript #00011989 (NM_001410.2, MEGF8 gene)

Transcript name multiple EGF-like-domains 8
Gene name MEGF8 (multiple EGF-like-domains 8)
Chromosome 19
Transcript - NCBI ID NM_001410.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_001401.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.-1488C>G r.(?) p.(=)
?/. - c.124G>C r.(?) p.(Gly42Arg)
+?/. - c.136G>T r.(?) p.(Asp46Tyr)
?/. - c.281C>T r.(?) p.(Pro94Leu)
?/. - c.283C>T r.(?) p.(Arg95Ter)
?/. - c.284G>A r.(?) p.(Arg95Gln)
-?/. - c.357G>A r.(?) p.(=)
-?/. - c.428C>G r.(?) p.(Pro143Arg)
?/. - c.466G>A r.(?) p.(Gly156Ser)
?/. - c.496G>A r.(?) p.(Gly166Ser)
-?/. - c.558+7C>T r.(=) p.(=)
?/. - c.574C>T r.(?) p.(Arg192Cys)
-?/. - c.740-6C>T r.(=) p.(=)
-?/. - c.829-10T>C r.(=) p.(=)
-?/. - c.853G>A r.(?) p.(Val285Met)
?/. - c.1031A>G r.(?) p.(Asp344Gly)
?/. - c.1057C>T r.(?) p.(Arg353Cys)
-/. - c.1197C>T r.(?) p.(=)
+?/. - c.1214T>C r.(?) p.(Val405Ala)
?/. - c.1343G>A r.(?) p.(Arg448Gln)
?/. - c.1393G>A r.(?) p.(Gly465Ser)
?/. - c.1600G>A r.(?) p.(Gly534Ser)
?/. - c.1816G>C r.(?) p.(Gly606Arg)
-?/. - c.1902C>T r.(?) p.(Cys634=)
-?/. - c.2098-1185G>A r.(=) p.(=)
-?/. - c.2098-6C>T r.(=) p.(=)
?/. - c.2234C>T r.(?) p.(Ser745Leu)
-?/. - c.2249A>G r.(?) p.(His750Arg)
-?/. - c.2253C>T r.(?) p.(Ser751=)
?/. - c.2276G>A r.(?) p.(Arg759Gln)
?/. - c.2276G>A r.(?) p.(Arg759Gln)
-?/. - c.2336C>T r.(?) p.(Ser779Leu)
-?/. - c.2336C>T r.(?) p.(Ser779Leu)
?/. - c.2372T>C r.(?) p.(Leu791Ser)
?/. - c.2405G>A r.(?) p.(Ser802Asn)
-?/. - c.2431G>A r.(?) p.(Gly811Arg)
?/. - c.2495C>T r.(?) p.(Pro832Leu)
?/. - c.2749C>T r.(?) p.(Arg917Trp)
?/. - c.2809C>T r.(?) p.(Arg937Trp)
-?/. - c.2832C>T r.(?) p.(Thr944=)
?/. - c.2870G>A r.(?) p.(Cys957Tyr)
-?/. - c.3150-3C>T r.spl? p.?
?/. - c.3191C>T r.(?) p.(Pro1064Leu)
?/. - c.3255G>A r.(?) p.(Pro1085=)
?/. - c.3255G>A r.(?) p.(Pro1085=)
?/. - c.3280C>T r.(?) p.(Arg1094Trp)
-?/. - c.3561G>C r.(?) p.(Arg1187=)
?/. - c.3810G>A r.(?) p.(=)
-?/. - c.3878G>A r.(?) p.(Arg1293His)
-?/. - c.3943+4C>G r.spl? p.?
?/. - c.3943+4C>T r.spl? p.?
-?/. - c.4192-5C>A r.spl? p.?
?/. - c.4240G>A r.(?) p.(Ala1414Thr)
-?/. - c.4302C>T r.(?) p.(=)
?/. - c.4328G>A r.(?) p.(Arg1443His)
+?/. - c.4421+1G>A r.spl? p.?
-?/. - c.4422-10C>T r.(=) p.(=)
?/. - c.4532G>A r.(?) p.(Arg1511His)
-?/. - c.4563C>T r.(?) p.(Thr1521=)
-?/. - c.4580G>A r.(?) p.(Arg1527His)
-?/. - c.4580G>A r.(?) p.(Arg1527His)
+?/. - c.4629+2T>C r.spl p.?
-?/. - c.4629+5G>T r.spl? p.?
?/. - c.4636C>A r.(?) p.(Gln1546Lys)
+?/. - c.4846A>C r.(?) p.(Thr1616Pro)
?/. - c.4911G>T r.(?) p.(Glu1637Asp)
-?/. - c.5074A>G r.(?) p.(Met1692Val)
-?/. - c.5080C>G r.(?) p.(Leu1694Val)
-?/. - c.5115G>A r.(?) p.(=)
-?/. - c.5119G>C r.(?) p.(Glu1707Gln)
?/. - c.5170G>T r.(?) p.(Ala1724Ser)
-?/. - c.5211G>A r.(?) p.(Ser1737=)
?/. - c.5251G>C r.(?) p.(Val1751Leu)
-?/. - c.5433C>T r.(?) p.(=)
?/. - c.5503G>C r.(?) p.(Gly1835Arg)
-?/. - c.5506G>C r.(?) p.(Asp1836His)
-?/. - c.5532G>A r.(?) p.(Gly1844=)
?/. - c.5609G>A r.(?) p.(Arg1870His)
-?/. - c.5622C>T r.(?) p.(Thr1874=)
?/. - c.5644-3C>G r.spl? p.?
-?/. - c.5857+5G>T r.spl? p.?
-?/. - c.5857+5G>T r.spl? p.?
?/. - c.5942C>T r.(?) p.(Pro1981Leu)
-?/. - c.6073-8C>G r.(=) p.(=)
-?/. - c.6158G>C r.(?) p.(Gly2053Ala)
?/. - c.6194G>A r.(?) p.(Arg2065Gln)
-/. - c.6375G>A r.(?) p.(=)
?/. - c.6514C>T r.(?) p.(Arg2172Cys)
-?/. - c.6634-8G>T r.(=) p.(=)
+?/. - c.6659C>T r.(?) p.(Pro2220Leu)
-?/. - c.6733A>G r.(?) p.(Ile2245Val)
-?/. - c.6840C>T r.(?) p.(Asp2280=)
-?/. - c.6847G>A r.(?) p.(Val2283Met)
-/. - c.6852C>T r.(?) p.(=)
-?/. - c.6853G>A r.(?) p.(Val2285Met)
-/. - c.6853G>A r.(?) p.(Val2285Met)
-/. - c.6853G>A r.(?) p.(Val2285Met)
+?/. - c.6935+1G>A r.spl? p.?
-?/. - c.6935+10A>T r.(=) p.(=)
-?/. - c.6935+36_6935+41del r.(=) p.(=)
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