PMID: 15084988

Naruse S, Ishiguro H, Suzuki Y, Fujiki K, Ko SB, Mizuno N, Takemura T, Yamamoto A, Yoshikawa T, Jin C, Suzuki R, Kitagawa M, Tsuda T, Kondo T, Hayakawa T
A finger sweat chloride test for the detection of a high-risk group of chronic pancreatitis.
Pancreas. 2004 Apr;28(3):e80-5., [PubMed]
Sentences
No. Mutations Sentence Comment
50 ABCC7 p.Gly551Asp
X
ABCC7 p.Gly551Asp 15084988:50:189
status: NEW
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ABCC7 p.Arg117His
X
ABCC7 p.Arg117His 15084988:50:126
status: NEW
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ABCC7 p.Ala455Glu
X
ABCC7 p.Ala455Glu 15084988:50:147
status: NEW
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ABCC7 p.Trp1282*
X
ABCC7 p.Trp1282* 15084988:50:239
status: NEW
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ABCC7 p.Arg553*
X
ABCC7 p.Arg553* 15084988:50:196
status: NEW
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ABCC7 p.Arg334Trp
X
ABCC7 p.Arg334Trp 15084988:50:133
status: NEW
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ABCC7 p.Arg347Pro
X
ABCC7 p.Arg347Pro 15084988:50:140
status: NEW
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ABCC7 p.Asn1303Lys
X
ABCC7 p.Asn1303Lys 15084988:50:247
status: NEW
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ABCC7 p.Gly542*
X
ABCC7 p.Gly542* 15084988:50:182
status: NEW
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ABCC7 p.Arg1162*
X
ABCC7 p.Arg1162* 15084988:50:223
status: NEW
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ABCC7 p.Ser1251Asn
X
ABCC7 p.Ser1251Asn 15084988:50:231
status: NEW
view ABCC7 p.Ser1251Asn details
ABCC7 p.Glu60*
X
ABCC7 p.Glu60* 15084988:50:120
status: NEW
view ABCC7 p.Glu60* details
The DNA samples were analyzed using an amplification refractory mutation system kit for 20 common major CFTR mutations (E60X, R117H, R334W, R347P, A455E, ⌬I507, ⌬F508, G542X, G551D, R553X, 621+1G>T, 1078delT, R1162X, S1251N, W1282X, N1303K, 1717-1G>A, 2183AA>G, 3659delC, 3849+10kbC>T) (Elucigene CF 20, AstraZeneca Diagnostics, Abingdon, UK) following the standard procedures recommended by the manufacturer. Login to comment
51 ABCC7 p.Arg347His
X
ABCC7 p.Arg347His 15084988:51:47
status: NEW
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ABCC7 p.Asp979Ala
X
ABCC7 p.Asp979Ala 15084988:51:68
status: NEW
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ABCC7 p.His1085Arg
X
ABCC7 p.His1085Arg 15084988:51:75
status: NEW
view ABCC7 p.His1085Arg details
ABCC7 p.Arg75*
X
ABCC7 p.Arg75* 15084988:51:28
status: NEW
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ABCC7 p.Gln98Arg
X
ABCC7 p.Gln98Arg 15084988:51:34
status: NEW
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ABCC7 p.Leu571Ser
X
ABCC7 p.Leu571Ser 15084988:51:61
status: NEW
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ABCC7 p.Thr1086Ile
X
ABCC7 p.Thr1086Ile 15084988:51:87
status: NEW
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ABCC7 p.Met152Arg
X
ABCC7 p.Met152Arg 15084988:51:40
status: NEW
view ABCC7 p.Met152Arg details
ABCC7 p.Leu441Pro
X
ABCC7 p.Leu441Pro 15084988:51:54
status: NEW
view ABCC7 p.Leu441Pro details
The 9 CF-causing mutations (R75X, Q98R, M152R, R347H, L441P, L571S, D979A, H1085R, and T1086I) in Japa- nese20,25-28 were screened by SNP typing with Masscode System (Shimadzu, Kyoto, Japan). Login to comment