Predicted mutation | |||||||
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evidence | seq id | position | mutation | freq | annotation | gene | description |
RA | NC_014034 | 1,721,519 | +GG | 100% | intergenic (‑414/+32) | RCAP_rcc01588 ← / ← RCAP_rcc01589 | GSCFA family protein/ErfK/YbiS/YcfS/YnhG family protein |
Read alignment evidence... | ||||||||||
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seq id | position | change | freq | score | reads | annotation | genes | product | ||
* | NC_014034 | 1,721,519 | 1 | .→G | 100.0% | 36.5 | 14 | intergenic (‑414/+32) | RCAP_rcc01588/RCAP_rcc01589 | GSCFA family protein/ErfK/YbiS/YcfS/YnhG family protein |
Reads supporting (aligned to +/- strand): new base (5/9): ref base (0/0): total (5/9) | ||||||||||
* | NC_014034 | 1,721,519 | 2 | .→G | 100.0% | 35.0 | 14 | intergenic (‑414/+32) | RCAP_rcc01588/RCAP_rcc01589 | GSCFA family protein/ErfK/YbiS/YcfS/YnhG family protein |
Reads supporting (aligned to +/- strand): new base (5/9): ref base (0/0): total (5/9) |
GGGTTCCAAATAACGCGCTGCGGGCCTCCCTCCCGCAGCGCTTTATTTTTGGCC.GG.TCGCCTTGGGGATTT.CGCCTCGGCTGCGCCGAGGCGACCCGCC....GGGCTGCGCCCCCGGACCCCCCCCGAAGATCTCAGATCACCTTGACCTGCGTGCCGACCGGGCAGAGCGGATAAAGTT > NC_014034/1721421‑1721597
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gggTTCCAAATAACGCGCTGCGGGCCTCCCTCCCGCAGCGCTTTATTTTTGGCC.GG.TCGCCTTGGGGATTT.CGCCTCGGCTGCGCCGAGGCGACccgcccg > 1:653740/1‑99 (MQ=255)
tCCAAATAACGCGCTGCGGGCCTCCCTCCCGCAGCGCTTTATTTTTGGCC.GG.TCGCCTTGGGGATTT.CGCCTCGGCTGCGCCGAGGCGACccgccccgggg > 1:1669547/1‑95 (MQ=255)
aaaTAACGCGCTGCGGGCCTCCCTCCCGCAGCGCTTTATTTTTGGCC.GG.TCGCCTTGGGGATTT.CGCCTCGGCTGCGCCGAGGCGACCCGCC....cgggggggg > 2:2300277/1‑95 (MQ=255)
aaTAACGCGCTGCGGGCCTCCCTCCCGCAGCGCTTTATTTTTGGCC.GG.TCGCCTTGGGGATTT.CGCCTCGGCTGCGCCGAGGCGACCCGCC....ggggggtgcg > 2:4109217/1‑94 (MQ=255)
gggCCTCCCTCCCGCAGCGCTTTATTTTTGGCC.GG.TCGCCTTGGGGATTT.CGCCTCGGCTGCGCCGAGGCGACCCGCCCG..GGGCCGGGCCCCCCGGccccc > 2:2699279/1‑101 (MQ=25)
gCCTCCCTCCCGCAGCGCTTTATTTTTGGCC.GG.TCGCCTTGGGGATTT.CGCCTCGGCTGCGCCGAGGCGACCCGCCGG..GGGGTGGGCCCCCCGGccccccc > 2:2024375/1‑101 (MQ=25)
cccccccGCGTCGTTTTTTTTTTGGCG.GG.CCCCCTGGGGTTTTC.CGCCCCGGCCCCCCCGGGGCCCCCCGCCGG..GGGCTGCGCCCCCGGACCCCCCCCGaa < 1:1998221/101‑1 (MQ=2)
ctcccGCAGCGCTTTATTTTTGGCC.GG.TCGCCTTGGGGATTT.CGCCTCGGCTGCGCCGAGGCGACCCGCCGG..GGGCTGGGCCCCCGGACCCCCCCCGCAGa > 2:537195/1‑101 (MQ=21)
ctcccGCAGCGCTTTATTTTTGGCC.GG.TCGCCTTGGGGATTT.CGCCTCGGCTGCGCCGAGGCGACCCGCCGG..GGGCGGCGCCCCCGGGccccccccccaga > 2:2471561/1‑96 (MQ=21)
ccccGCGGCTTTTTTTTTTGGGCC.GG..CCCCTTGGGGGTTTCCCCCGCGGCCGCGCCGGGGCCCCCCGCCGG..GGGCTGCGCCCCCGGACCCCCCCCGAAGAt < 1:2472855/100‑1 (MQ=9)
cGCAGCGCTTTATTTTTGGCC.GG.TCGCCTTGGGGATTT.CGCCTCGGCTGCGCCGAGGCGACCCGCCCGGGGGGGGGCGCCCCCGGCccccccccccccatc > 1:1393939/1‑94 (MQ=21)
ggtttttTTTTTGGGCC.GG.CCTCCGGGGGGTTTC.CCCCTGGGCCGCGCAGGGGCGCCCCGCCGG..GGGCTGCGCCCCCGGACCCCCCCCGAAGATCTCAGAt < 1:1288228/97‑1 (MQ=255)
cgtttttTTTTTTGGGC.GGTTCGCTTTGGGGTTTC.CCCCGCGGCGCCCCCGGGGCCCCCCGCCGG..GGGCTGCGCCCCCGGACCCCCCCCGAAGATCTCAGa < 1:3416447/97‑1 (MQ=9)
cTTTATTTTTGGCC.GG.TCGCCTTGGGGATTT.CGCCTCGGCTGCGCCGAGGCGACCCGCCGG..GGGCTGCGCCCCCCGACCCCCCCCGAAGATCTCAGATCAc > 2:2065036/1‑101 (MQ=25)
tttttttGGCCGGG.TGGGTTTGGGGTTTT.CGCCGCGGCCGCGCCGGGCCCCCCCGCCGG..GGGCTGCGCCCCCGGACCCCCCCCGAAGATCTCAGATCACCt < 2:3891594/99‑1 (MQ=12)
ttgtGGCC.GC.TCGCGTTGGCGTTTC.CGCCGGGGCGGCGCGGAGGCCCCCCGCCGG..GGGCTGCGCCCCCGGACCCCCCCCGAAGATCTCAGATCACCTTGAc < 2:255739/98‑1 (MQ=255)
ggCG.GG.TCGCCTGGGGGTTCC.CGCCCGGGCGGCCCCGGGCCGCCCCGCCGG..GGGCTGCGCCCCCGGACCCCCCCCGAAGATCTCAGATCACCTTGACCTGc < 1:2699485/101‑1 (MQ=255)
gggttttccGCCGCGGCCGCGCGGAGGCCCCCCGCCGG..GGGCTGCGCCCCCGGACCCCCCCCGAAGATCTCAGATCACCTTGACCTGCGTGCCGACCGGGc < 1:4217529/93‑1 (MQ=21)
ccGCCGCGGCGGCCCCGAGGCCCCCCGCCGG..GGGCTGCGCCCCCGGACCCCCCCCGAAGATCTCAGATCACCTTGACCTGCGTGCCGACCGGGCAGAGCgg < 2:3426966/100‑1 (MQ=255)
gCTGCGCCGAGGCGACCCGCCGG..GGGCTGGGCCCCCGGACCCCCCCCCCAGAACTCAGATAACCCTGGCCTCCGTGCCGCCCGGGCAGAGCGGACAAAggt > 1:1908908/1‑99 (MQ=12)
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GGGTTCCAAATAACGCGCTGCGGGCCTCCCTCCCGCAGCGCTTTATTTTTGGCC.GG.TCGCCTTGGGGATTT.CGCCTCGGCTGCGCCGAGGCGACCCGCC....GGGCTGCGCCCCCGGACCCCCCCCGAAGATCTCAGATCACCTTGACCTGCGTGCCGACCGGGCAGAGCGGATAAAGTT > NC_014034/1721421‑1721597
Base quality scores:
ATCG
< 3 ≤
ATCG
< 15 ≤
ATCG
< 31 ≤
ATCG
< 35 ≤
ATCG
< 41 ≤
ATCG
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