ABCC7 p.Gly314Gln

ClinVar: c.940G>C , p.Gly314Arg ? , not provided
c.941G>T , p.Gly314Val ? , not provided
c.941G>A , p.Gly314Glu ? , not provided
CF databases: c.941G>T , p.Gly314Val (CFTR1) D , This mutation was found in a CF patient homozygous for this mutation. He was diagnosed as CF at 32 years.
c.940G>C , p.Gly314Arg (CFTR1) D , This mutation was detected by chemical mismatch and sequencing. The mutation is a G to C change at nucleotide 1072. This results in a glycine to arginine substitution at amino acid 314 (G314R). It is in exon 7 and it eliminates a DdeI restriction site. This mutation was found in a patient with an American Indian/Caucasian mother and Dutch/French father. This patient has a [delta]F508 mutation on the other chromosomes and is pancreatic insufficient. This mutation was not found in 25 normal chromosomes and 25 CF chromosomes.
c.941G>A , p.Gly314Glu (CFTR1) ? , This mutation, in exon 7 of the CFTR gene, was found by direct sequencing and the second mutation is [delta]F508. The patient is 7 years old. Diagnosis of CF was established at the age of five after severe lung infection. Sweat gland tests were positive. She is receiveing pancreatic enzyme supplements and long-term antibiotic treatment.
Predicted by SNAP2: A: D (85%), C: D (91%), D: D (95%), E: D (66%), F: D (95%), H: D (95%), I: D (95%), K: D (95%), L: D (95%), M: D (95%), N: D (91%), P: D (95%), Q: D (95%), R: D (71%), S: D (80%), T: D (91%), V: D (95%), W: D (95%), Y: D (95%),
Predicted by PROVEAN: A: N, C: N, D: N, E: N, F: N, H: N, I: N, K: N, L: N, M: N, N: N, P: N, Q: N, R: N, S: N, T: N, V: N, W: N, Y: N,

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[hide] Dawson DC, Smith SS, Mansoura MK
CFTR: mechanism of anion conduction.
Physiol Rev. 1999 Jan;79(1 Suppl):S47-75., [PMID:9922376]

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[hide] Mansoura MK, Smith SS, Choi AD, Richards NW, Strong TV, Drumm ML, Collins FS, Dawson DC
Cystic fibrosis transmembrane conductance regulator (CFTR) anion binding as a probe of the pore.
Biophys J. 1998 Mar;74(3):1320-32., [PMID:9512029]

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