Transcript #00010188 (NM_002206.2, ITGA7 gene)

Transcript name transcript variant 2
Gene name ITGA7 (integrin, alpha 7)
Chromosome 12
Transcript - NCBI ID NM_002206.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_002197.2
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

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.-4466T>G r.(?) p.(=)
?/. _1 c.-4428C>T r.(?) p.(Thr139-29Ile)
-?/. - c.-4428C>T r.(?) p.(=)
-/. - c.-4428C>T r.(?) p.(=)
-/- _25 c.= r.= p.=
-/- _25 c.= r.= p.=
+/. 1_25 c.? r.? p.?
+/. 1_25 c.? r.? p.?
?/. _25 c.? r.? p.?
+?/. - c.34dup r.(?) p.(Ala12Glyfs*91)
-?/. - c.46T>G r.(?) p.(Cys16Gly)
-?/. - c.46T>G r.(?) p.(Cys16Gly)
?/. - c.49T>C r.(?) p.(Tyr17His)
+/. - c.132_133insA r.(?) p.(Glu45Argfs*58)
?/. 1 c.187C>A r.(?) p.(Gln63Lys)
?/. - c.206+2T>A r.spl? p.?
-/. - c.206+180C>G r.(=) p.(=)
-/. - c.207-63T>G r.(=) p.(=)
-/. 2 c.285G>T r.(?) p.(=)
-/. 2 c.285G>T r.(?) p.(=)
-?/. - c.285G>T r.(?) p.(Pro95=)
-?/. - c.311A>T r.(?) p.(Tyr104Phe)
-/. 2i c.334+19A>G r.(?) p.(=)
-/. - c.334+19A>G r.(=) p.(=)
-/. - c.334+19A>G r.(=) p.(=)
-/. 3 c.351A>G r.(?) p.(=)
-/. 3 c.366G>A r.(?) p.(=)
-/. - c.415-430del r.(=) p.(=)
-/. 3i c.415-10C>T r.(?) p.(=)
-/. - c.415-10C>T r.(=) p.(=)
?/. - c.427C>T r.(?) p.(Arg143Ter)
+/. - c.445C>T r.(?) p.(Arg149*)
-?/. - c.459C>G r.(?) p.(Ile153Met)
-?/. - c.459C>G r.(?) p.(Ile153Met)
-?/. - c.537G>A r.(?) p.(Gly179=)
?/. 4 c.610G>A r.(?) p.(Ala204Thr)
?/. 4 c.616T>C r.(?) p.(Ser206Pro)
-?/. - c.671-366G>T r.(=) p.(=)
?/. - c.671-305G>A r.(=) p.(=)
-/. 4i c.671-44A>C r.(?) p.(=)
-?/. - c.671-5C>T r.spl? p.?
?/. - c.671G>C r.(?) p.(Gly224Ala)
-?/. - c.671G>C r.(?) p.(Gly224Ala)
-/. 6 c.810G>A r.(?) p.(=)
-/. 6 c.810G>A r.(?) p.(=)
?/. 6 c.824G>A r.(?) p.(Arg275His)
-?/. - c.824G>A r.(?) p.(Arg275His)
?/. 6 c.882G>A r.(?) p.(=)
-?/. - c.882G>A r.(?) p.(Val294=)
-/. - c.999-4A>G r.spl? p.?
?/. - c.1011-4A>G r.spl? p.?
?/. - c.1039C>T r.(?) p.(Arg347Cys)
+/. 8 c.1205del r.(?) p.Glu402Valfs*104
-/. - c.1281+13G>A r.(=) p.(=)
-?/. - c.1281+13G>A r.(=) p.(=)
-/. 8i c.1282-11T>C r.(?) p.(=)
-/. - c.1282-11T>C r.(=) p.(=)
-?/. - c.1294G>A r.(?) p.(Glu432Lys)
?/. 9 c.1317C>T r.(?) p.(=)
-?/. - c.1317C>T r.(?) p.(Phe439=)
-/. - c.1410-3del r.spl? p.?
-?/. - c.1410-3del r.spl? p.?
-?/. - c.1506-14C>T r.(=) p.(=)
+/. 10i c.1506-2A>G r.1505_1506ins1506-21_1506-1 p.Cys502delinsWSHLCPRS
-/. 11i c.1567+12C>T r.(?) p.(=)
?/. 11i c.1567+16C>G r.(?) p.(=)
-?/. - c.1567+16C>G r.(=) p.(=)
?/. - c.1606C>T r.(?) p.(Leu536Phe)
-/. 12 c.1609C>T r.(?) p.(Arg537Trp)
-?/. - c.1609C>T r.(?) p.(Arg537Trp)
?/. - c.1610G>A r.(?) p.(Arg537Gln)
-/. 12 c.1617G>T r.(?) p.(Gln539His)
?/. - c.1625G>A r.(?) p.(Arg542His)
-?/. - c.1659C>G r.(?) p.(Pro553=)
?/. - c.1765A>C r.(?) p.(Ile589Leu)
-?/. - c.1786A>G r.(?) p.(Ser596Gly)
?/. - c.1828G>A r.(?) p.(Gly610Arg)
-/. 13i c.1887+29G>A r.(?) p.(=)
-/. 14 c.1952G>A r.(?) p.(Arg651His)
-/. 14 c.1952G>A r.(?) p.(Arg651His)
-/. 14 c.1952G>A r.(?) p.(Arg651His)
-/. 14 c.1952G>A r.(?) p.(Arg651His)
-/. 14 c.1952G>A r.(?) p.(Arg651His)
+?/. 14 c.1952G>A r.(?) p.(Arg651His)
-/. 14 c.1952G>A r.(?) p.(Arg651His)
-/. - c.1952G>A r.(?) p.(Arg651His)
?/. 14 c.1965T>C r.(?) p.(=)
-?/. - c.1965T>C r.(?) p.(Cys655=)
+?/. 14 c.1969C>G r.1969g>c p.Arg657Gly
-/. 14i c.2004-19G>A r.(?) p.(=)
-/. - c.2004-19G>A r.(=) p.(=)
-?/. - c.2035C>A r.(?) p.(Leu679Met)
?/. 15 c.2087C>T r.(?) p.(Ser696Leu)
?/. - c.2087C>T r.(?) p.(Ser696Leu)
?/. - c.2155G>A r.(?) p.(Asp719Asn)
?/. - c.2179C>T r.(?) p.(Arg727Trp)
+?/. - c.2196G>A r.(?) p.(=)
?/. 16 c.2199G>A r.(?) p.(=)
-/. 16i c.2278-43G>A r.(?) p.(=)
+/. - c.2278-1G>A r.spl? p.?
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