Transcript #00005487 (NM_004370.5, COL12A1 gene)

Transcript name transcript variant long
Gene name COL12A1 (collagen, type XII, alpha 1)
Chromosome 6
Transcript - NCBI ID NM_004370.5
Transcript - Ensembl ID -
Protein - NCBI ID NP_004361.3
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

252 entries on 3 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
./. - c.-899792_*2087198del r.0? p.0?
+/. _1_28_ c.0 r.0 p.0
-?/. - c.108A>C r.(?) p.(Ile36=)
-?/. - c.132A>G r.(?) p.(Ser44=)
-?/. - c.132A>G r.(?) p.(Ser44=)
?/. - c.196C>T r.(?) p.(Pro66Ser)
?/. - c.236C>T r.(?) p.(Thr79Ile)
?/. 5 c.350C>T r.(?) p.(Ser117Leu)
-?/. - c.394+133C>T r.(=) p.(=)
+/. - c.395-2A>C r.spl p.?
?/. - c.469A>G r.(?) p.(Lys157Glu)
-?/. - c.489T>C r.(?) p.(Ile163=)
?/. - c.511G>C r.(?) p.(Asp171His)
?/. - c.511G>C r.(?) p.(Asp171His)
-?/. - c.597A>G r.(?) p.(Gln199=)
?/. - c.607C>A r.(?) p.(Leu203Ile)
?/. - c.607C>A r.(?) p.(Leu203Ile)
-/. - c.626A>C r.(?) p.(Lys209Thr)
-?/. - c.673T>G r.(?) p.(Tyr225Asp)
-?/. - c.695C>T r.(?) p.(Thr232Met)
?/. 7 c.796A>C r.(?) p.(Asn266His)
-/. - c.834T>G r.(?) p.(Ala278=)
?/. 8 c.922A>T r.(?) p.(Ile308Phe)
?/. 8 c.922A>T r.(?) p.(Ile308Phe)
-?/. - c.922A>T r.(?) p.(Ile308Phe)
-?/. - c.997+14G>A r.(=) p.(=)
?/. - c.1006C>T r.(?) p.Pro336Ser
-?/. - c.1015A>G r.(?) p.(Asn339Asp)
?/. - c.1043A>T r.(?) p.(Lys348Ile)
?/. 9 c.1112T>C r.(?) p.(Met371Thr)
-?/. - c.1117G>T r.(?) p.(Ala373Ser)
-?/. - c.1117G>T r.(?) p.(Ala373Ser)
?/. - c.1150C>T r.(?) p.(Pro384Ser)
-?/. - c.1152T>C r.(?) p.(Pro384=)
-?/. - c.1152T>C r.(?) p.(Pro384=)
?/. - c.1171G>T r.(?) p.(Val391Phe)
?/. - c.1181T>C r.(?) p.(Leu394Pro)
-?/. - c.1275G>A r.(?) p.(Met425Ile)
-?/. - c.1326G>A r.(?) p.(Val442=)
?/. 10 c.1483A>G r.(?) p.(Lys495Glu)
?/. - c.1531C>T r.(?) p.(Pro511Ser)
-/. - c.1551A>G r.(?) p.(Thr517=)
-?/. - c.1644C>A r.(?) p.(=)
-?/. - c.1821G>A r.(?) p.(Arg607=)
?/. - c.1871T>G r.(?) p.(Leu624Trp)
-/. - c.1892-8_1892-7dup r.(=) p.(=)
-/. - c.1892-8_1892-7dup r.(=) p.(=)
-/. - c.1892-8_1892-7dup r.(=) p.(=)
-?/. - c.1892-8_1892-7dup r.(=) p.(=)
-/. - c.1892-8_1892-6del r.(=) p.(=)
-/. - c.1892-7del r.(=) p.(=)
-/. - c.1892-7dup r.(=) p.(=)
-?/. - c.1892-7dup r.(=) p.(=)
-/. - c.1892-7dup r.(=) p.(=)
-/. - c.1892-7dup r.(=) p.(=)
-?/. - c.1892-7_1892-6del r.(=) p.(=)
-?/. - c.1892-7_1892-6insC r.(=) p.(=)
-/. - c.2007G>A r.(?) p.(Ala669=)
?/. - c.2038C>G r.(?) p.(Pro680Ala)
?/. 11 c.2062C>G r.(?) p.(Leu688Val)
-/. - c.2086T>C r.(?) p.(Leu696=)
-/. - c.2164+18C>A r.(=) p.(=)
-?/. - c.2165-146C>T r.(=) p.(=)
?/. - c.2260C>T r.(?) p.(Arg754*)
?/. - c.2275C>T r.(?) p.(Pro759Ser)
?/. - c.2393C>T r.(?) p.(Ser798Leu)
-/. - c.2437+13T>C r.(=) p.(=)
?/. - c.2481G>A r.(?) p.(Thr827=)
-/. - c.2481G>A r.(?) p.(Thr827=)
?/. 13 c.2496A>T r.(?) p.(Leu832Phe)
?/. 13 c.2510C>T r.(?) p.(Ala837Val)
?/. 13 c.2510C>T r.(?) p.(Ala837Val)
-?/. - c.2637C>T r.(?) p.(Tyr879=)
-?/. - c.2676A>C r.(?) p.(Gly892=)
?/. - c.2696G>A r.(?) p.(Gly899Glu)
-/. - c.2711-15T>C r.(=) p.(=)
-/. - c.2772T>C r.(?) p.(Tyr924=)
-?/. - c.2965G>A r.(?) p.(Gly989Arg)
?/. - c.2984-2A>G r.spl? p.?
-?/. - c.3070G>A r.(?) p.(Val1024Ile)
-?/. - c.3079C>T r.(?) p.(Arg1027Cys)
+?/. - c.3160C>T r.(?) p.(Arg1054Ter)
?/. 15 c.3168G>T r.(?) p.(Gln1056His)
-?/. - c.3231G>A r.(?) p.(Arg1077=)
?/. 15 c.3247A>G r.(?) p.(Thr1083Ala)
-?/. - c.3251-74G>T r.(=) p.(=)
-?/. - c.3251-66A>G r.(=) p.(=)
?/. - c.3340G>A r.(?) p.(Val1114Met)
?/. - c.3376G>C r.(?) p.(Asp1126His)
-?/. - c.3444-98T>C r.(=) p.(=)
?/. - c.3467A>T r.(?) p.(Asn1156Ile)
?/. - c.3631G>A r.(?) p.(Gly1211Ser)
-?/. - c.3652G>A r.(?) p.(Val1218Met)
-?/. - c.3652G>A r.(?) p.(Val1218Met)
?/. - c.3753G>A r.(?) p.(Trp1251Ter)
?/. - c.3767A>G r.(?) p.(His1256Arg)
-?/. - c.3831C>G r.(?) p.(Leu1277=)
?/. 20 c.3881C>G r.(?) p.(Ala1294Gly)
-?/. - c.4000+5G>A r.spl? p.?
-?/. - c.4000+5G>A r.spl? p.?
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