Transcript #00025674 (NM_182895.2, SCARF2 gene)

Transcript name transcript variant 2
Gene name SCARF2 (scavenger receptor class F, member 2)
Chromosome 22
Transcript - NCBI ID NM_182895.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_878315.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2022-01-01 11:44:40 +01:00 (CET)
Date last edited N/A


Variants

74 entries on 1 page. Showing entries 1 - 74.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+/. - c.-1038521_*1940378dup r.0? p.0?
+/. - c.-672078_*1756502del r.0? p.0?
+/. - c.-672078_*1886102del r.0? p.0?
+/. - c.-672078_*1890626del r.0? p.0?
-?/. - c.-4556C>T r.(?) p.(=)
+/. _1_11_ c.-105_*791{0} r.0 p.0
-?/. - c.99G>A r.(?) p.(Leu33=)
?/. - c.99_101dup r.(?) p.(Leu34dup)
-?/. - c.186C>G r.(?) p.(Pro62=)
+/. - c.190T>C r.(?) p.(Cys64Arg)
-?/. - c.240C>T r.(?) p.(Cys80=)
?/. - c.240C>T r.(?) p.(Cys80=)
+/. - c.465_470del r.(?) p.(Cys158_Gln159del)
-/. - c.520C>T r.(?) p.(Pro174Ser)
-?/. - c.595G>T r.(?) p.(Ala199Ser)
+/. - c.654C>G r.(?) p.(Asn218Lys)
?/. - c.700C>G r.(?) p.(Arg234Gly)
-?/. - c.921C>T r.(?) p.(Pro307=)
?/. - c.1072C>T r.(?) p.(Arg358Trp)
?/. - c.1214C>A r.(?) p.(Thr405Lys)
-?/. - c.1230C>G r.(?) p.(Leu410=)
-/. - c.1273A>T r.(?) p.(Thr425Ser)
-?/. - c.1307-9C>T r.(=) p.(=)
-?/. - c.1350C>G r.(?) p.(Leu450=)
-?/. - c.1425-35_1425-25del r.(=) p.(=)
-?/. - c.1425-35_1425-25del r.(=) p.(=)
-?/. - c.1646C>T r.(?) p.(Ser549Leu)
?/. - c.1646C>T r.(?) p.(Ser549Leu)
-/. - c.1693+15A>G r.(=) p.(=)
-?/. - c.1788C>T r.(?) p.(Ala596=)
+/. - c.1796C>T r.(?) p.(Ala599Val)
?/. - c.1865T>G r.(?) p.(Leu622Arg)
?/. - c.1907C>T r.(?) p.(Ala636Val)
-?/. - c.1967C>T r.(?) p.(Pro656Leu)
-/. - c.1967C>T r.(?) p.(Pro656Leu)
-?/. - c.1967C>T r.(?) p.(Pro656Leu)
-/. - c.1967C>T r.(?) p.(Pro656Leu)
-?/. - c.1967C>T r.(?) p.(Pro656Leu)
?/. - c.1978G>T r.(?) p.(Ala660Ser)
?/. - c.1994T>C r.(?) p.(Val665Ala)
-?/. - c.2010C>A r.(?) p.(Gly670=)
-?/. - c.2123C>A r.(?) p.(Thr708Lys)
-/. - c.2166C>G r.(?) p.(Arg722=)
-/. - c.2166C>G r.(?) p.(Arg722=)
-/. - c.2166C>G r.(?) p.(Arg722=)
-/. - c.2172G>C r.(?) p.(Pro724=)
-/. - c.2172G>C r.(?) p.(Pro724=)
-/. - c.2172G>C r.(?) p.(Pro724=)
-/. - c.2184G>A r.(?) p.(Glu728=)
?/. - c.2186A>T r.(?) p.(Glu729Val)
-?/. - c.2232C>G r.(?) p.(Arg744=)
-?/. - c.2232C>G r.(?) p.(Arg744=)
-/. - c.2232C>G r.(?) p.(Arg744=)
-/. - c.2232delinsGG r.(?) p.(Ala745GlyfsTer28)
-?/. - c.2233dup r.(?) p.(Ala745GlyfsTer28)
-?/. - c.2238dup r.(?) p.(Pro747AlafsTer26)
-/. - c.2238dup r.(?) p.(Pro747AlafsTer26)
-?/. - c.2289dup r.(?) p.(Glu764ArgfsTer9)
-/. - c.2289dup r.(?) p.(Glu764ArgfsTer9)
-/. - c.2316C>G r.(?) p.(Asp772Glu)
-/. - c.2316C>G r.(?) p.(Asp772Glu)
-/. - c.2317G>C r.(?) p.(Val773Leu)
-/. - c.2317G>C r.(?) p.(Val773Leu)
-/. - c.2441C>G r.(?) p.(Ala814Gly)
-/. - c.2441C>G r.(?) p.(Ala814Gly)
-/. - c.2441C>G r.(?) p.(Ala814Gly)
-/. - c.2495C>G r.(?) p.(Ala832Gly)
-/. - c.2495C>G r.(?) p.(Ala832Gly)
?/. - c.2519C>T r.(?) p.(Thr840Ile)
-/. - c.2522C>T r.(?) p.(Thr841Ile)
+/. - c.2528del r.(?) p.(Gln843Argfs*95)
?/. - c.2555A>G r.(?) p.(Glu852Gly)
?/. - c.2564G>T r.(?) p.(Gly855Val)
-?/. - c.*61A>C r.(=) p.(=)
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