Transcript #00025895 (NM_022367.3, SEMA4A gene)

Transcript name transcript variant 1
Gene name SEMA4A (sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A)
Chromosome 1
Transcript - NCBI ID NM_022367.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_071762.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2024-01-25 12:21:04 +01:00 (CET)
Date last edited N/A


Variants

71 entries on 1 page. Showing entries 1 - 71.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.20G>A r.(?) p.(Gly7Asp)
?/. - c.38T>C r.(?) p.(Leu13Pro)
?/. - c.140-3C>G r.spl? p.?
?/. - c.149G>A r.(?) p.(Arg50His)
?/. - c.247G>C r.(?) p.(Ala83Pro)
?/. - c.274C>T r.(?) p.(Pro92Ser)
+?/. - c.300G>A r.(?) p.(Met100Ile)
-?/. - c.300+3G>A r.spl? p.?
-?/. - c.300+3G>A r.spl? p.?
-?/. - c.301-11_301-7del r.(=) p.(=)
?/. - c.305C>T r.(?) p.(Pro102Leu)
?/. - c.369G>C r.(?) p.(Gln123His)
-/. - c.435C>T r.(?) p.(Phe145=)
?/. - c.473A>G r.(?) p.(Asp158Gly)
-?/. - c.492C>T r.(?) p.(Ile164=)
-?/. - c.494C>T r.(?) p.(Ser165Leu)
-?/. - c.592A>G r.(?) p.(Met198Val)
-/. - c.615G>A r.(?) p.(Glu205=)
?/. - c.686-5C>T r.spl? p.?
-?/. - c.686-5C>T r.spl? p.?
?/. - c.712C>T r.(?) p.(Pro238Ser)
+?/. - c.745dup r.(?) p.(Glu249Glyfs*7)
-?/. - c.811-6C>A r.(=) p.(=)
?/. - c.829A>G r.(?) p.(Lys277Glu)
?/. - c.932C>T r.(?) p.(Pro311Leu)
+?/. - c.985C>T r.(?) p.(Gln329*)
-/. - c.1011G>A r.(?) p.(Ala337=)
-?/. - c.1011G>A r.(?) p.(Ala337=)
?/. - c.1012G>A r.(?) p.(Val338Ile)
-?/. - c.1086A>C r.(?) p.(Ser362=)
-?/. - c.1167G>C r.(?) p.(Leu389=)
-?/. - c.1215G>T r.(?) p.(Thr405=)
?/. - c.1300A>C r.(?) p.(Met434Leu)
?/. - c.1301T>C r.(?) p.(Met434Thr)
?/. - c.1306C>A r.(?) p.(Leu436Met)
-?/. - c.1314C>A r.(?) p.(Thr438=)
?/. - c.1376A>G r.(?) p.(Glu459Gly)
-?/. - c.1420C>T r.(?) p.(Leu474=)
?/. - c.1433A>G r.(?) p.(Gln478Arg)
-/. - c.1434+12C>A r.(=) p.(=)
-?/. - c.1435-18T>G r.(=) p.(=)
?/. - c.1474G>A r.(?) p.(Val492Met)
-/. - c.1529G>A r.(?) p.(Arg510Gln)
-/. - c.1529G>A r.(?) p.(Arg510Gln)
+/. - c.1561C>T r.(?) p.(Arg521*)
-?/. - c.1618C>A r.(?) p.(Arg540=)
?/. - c.1619G>C r.(?) p.(Arg540Pro)
?/. - c.1646G>A r.(?) p.(Ser549Asn)
-?/. - c.1670G>A r.(?) p.(Arg557Gln)
-?/. - c.1682G>A r.(?) p.(Arg561His)
-?/. - c.1694-8T>C r.(=) p.(=)
-/. - c.1716C>T r.(?) p.(Pro572=)
-/. - c.1716C>T r.(?) p.(Pro572=)
?/. - c.1876G>T r.(?) p.(Ala626Ser)
?/. - c.1969C>G r.(?) p.(Pro657Ala)
?/. - c.1973G>A r.(?) p.(Arg658Gln)
?/. - c.2038T>C r.(?) p.(Tyr680His)
?/. - c.2038T>C r.(?) p.(Tyr680His)
-/. - c.2044C>T r.(?) p.(Pro682Ser)
?/. - c.2135C>T r.(?) p.(Ala712Val)
-?/. - c.2138G>A r.(?) p.(Arg713Gln)
-/. - c.2138G>A r.(?) p.(Arg713Gln)
-/. - c.2138G>A r.(?) p.(Arg713Gln)
-?/. - c.2138G>A r.(?) p.(Arg713Gln)
?/. - c.2167C>A r.(?) p.(Arg723Ser)
+?/. - c.2167C>A r.(?) p.(Arg723Ser)
-?/. - c.2167C>T r.(?) p.(Arg723Cys)
?/. - c.2182G>A r.(?) p.(Ala728Thr)
-?/. - c.2187G>A r.(?) p.(Pro729=)
+?/. - c.2231C>T r.(?) p.(Thr744Ile)
+?/. - c.2231C>T r.(?) p.(Thr744Ile)
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