Transcript #00025962 (NM_001271938.1, MEGF8 gene)

Transcript name transcript variant 1
Gene name MEGF8 (multiple EGF-like-domains 8)
Chromosome 19
Transcript - NCBI ID NM_001271938.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001258867.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2024-12-19 15:58:48 +01:00 (CET)
Date last edited N/A


Variants

130 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.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.2140G>A r.(?) p.(Ala714Thr)
-?/. - c.2299-6C>T r.(=) p.(=)
?/. - c.2435C>T r.(?) p.(Ser812Leu)
-?/. - c.2450A>G r.(?) p.(His817Arg)
-?/. - c.2454C>T r.(?) p.(Ser818=)
?/. - c.2477G>A r.(?) p.(Arg826Gln)
?/. - c.2477G>A r.(?) p.(Arg826Gln)
-?/. - c.2537C>T r.(?) p.(Ser846Leu)
-?/. - c.2537C>T r.(?) p.(Ser846Leu)
?/. - c.2573T>C r.(?) p.(Leu858Ser)
?/. - c.2606G>A r.(?) p.(Ser869Asn)
-?/. - c.2632G>A r.(?) p.(Gly878Arg)
?/. - c.2696C>T r.(?) p.(Pro899Leu)
?/. - c.2950C>T r.(?) p.(Arg984Trp)
?/. - c.3010C>T r.(?) p.(Arg1004Trp)
-?/. - c.3033C>T r.(?) p.(Thr1011=)
?/. - c.3071G>A r.(?) p.(Cys1024Tyr)
-?/. - c.3351-3C>T r.spl? p.?
?/. - c.3392C>T r.(?) p.(Pro1131Leu)
?/. - c.3456G>A r.(?) p.(Pro1152=)
?/. - c.3456G>A r.(?) p.(Pro1152=)
?/. - c.3481C>T r.(?) p.(Arg1161Trp)
-?/. - c.3762G>C r.(?) p.(Arg1254=)
?/. - c.4011G>A r.(?) p.(=)
-?/. - c.4079G>A r.(?) p.(Arg1360His)
-?/. - c.4144+4C>G r.spl? p.?
?/. - c.4144+4C>T r.spl? p.?
-?/. - c.4393-5C>A r.spl? p.?
?/. - c.4441G>A r.(?) p.(Ala1481Thr)
-?/. - c.4503C>T r.(?) p.(=)
?/. - c.4529G>A r.(?) p.(Arg1510His)
+?/. - c.4622+1G>A r.spl? p.?
-?/. - c.4623-10C>T r.(=) p.(=)
?/. - c.4733G>A r.(?) p.(Arg1578His)
-?/. - c.4764C>T r.(?) p.(Thr1588=)
-?/. - c.4781G>A r.(?) p.(Arg1594His)
-?/. - c.4781G>A r.(?) p.(Arg1594His)
-?/. - c.4830+5G>T r.spl? p.?
?/. - c.4837C>A r.(?) p.(Gln1613Lys)
?/. - c.5112G>T r.(?) p.(Glu1704Asp)
-?/. - c.5275A>G r.(?) p.(Met1759Val)
-?/. - c.5281C>G r.(?) p.(Leu1761Val)
-?/. - c.5316G>A r.(?) p.(=)
-?/. - c.5320G>C r.(?) p.(Glu1774Gln)
?/. - c.5371G>T r.(?) p.(Ala1791Ser)
-?/. - c.5412G>A r.(?) p.(Ser1804=)
?/. - c.5452G>C r.(?) p.(Val1818Leu)
-?/. - c.5634C>T r.(?) p.(=)
?/. - c.5704G>C r.(?) p.(Gly1902Arg)
-?/. - c.5707G>C r.(?) p.(Asp1903His)
-?/. - c.5733G>A r.(?) p.(Gly1911=)
?/. - c.5810G>A r.(?) p.(Arg1937His)
-?/. - c.5823C>T r.(?) p.(Thr1941=)
?/. - c.5845-3C>G r.spl? p.?
-?/. - c.6058+5G>T r.spl? p.?
-?/. - c.6058+5G>T r.spl? p.?
?/. - c.6143C>T r.(?) p.(Pro2048Leu)
-?/. - c.6274-8C>G r.(=) p.(=)
-?/. - c.6359G>C r.(?) p.(Gly2120Ala)
?/. 36 c.6395G>A r.6395G>A p.Arg2132Gln
?/. - c.6395G>A r.(?) p.(Arg2132Gln)
-/. - c.6576G>A r.(?) p.(=)
?/. - c.6715C>T r.(?) p.(Arg2239Cys)
-?/. - c.6835-8G>T r.(=) p.(=)
-?/. - c.6934A>G r.(?) p.(Ile2312Val)
-?/. - c.7041C>T r.(?) p.(Asp2347=)
-?/. - c.7048G>A r.(?) p.(Val2350Met)
-/. - c.7053C>T r.(?) p.(=)
-?/. - c.7054G>A r.(?) p.(Val2352Met)
-/. - c.7054G>A r.(?) p.(Val2352Met)
-/. - c.7054G>A r.(?) p.(Val2352Met)
+?/. - c.7136+1G>A r.spl? p.?
-?/. - c.7136+10A>T r.(=) p.(=)
-?/. - c.7136+36_7136+41del r.(=) p.(=)
?/. - c.7184C>T r.(?) p.(Thr2395Met)
?/. - c.7213A>T r.(?) p.(Thr2405Ser)
?/. - c.7420C>T r.(?) p.(Arg2474Cys)
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