regionname | pos | ref | alt | annotation | impact | samples | ahapids | achapids | acthapids | actghapids | ac | an | af | len | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length
|
cds cds pos length
|
aa aa pos length
|
distance | status | chr | external |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
AOPEP_chr9_94721699_95092159 | 94796253 | CTG | C | intron_variant | MODIFIER | HG01255.hp1 HG02572.hp1 HG02572.hp2 others(11): Show |
a0002 | a0002c0002a0002c0008 | a0002c0002t0002a0002c0002t0005a0002c0008t0001others(2): Show | a0002c0002t0002g0124a0002c0002t0002g0125a0002c0002t0002g0126others(11): Show | 14 | 182 | 0.0769 | -2 | c.111 others(21): Show |
AOPEP | ENSG00000148120.19 | transcript | ENST00000375315.8 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
AOPEP_chr9_94721699_95092159 | 94797556 | ATT | A | intron_variant | MODIFIER | HG02970.hp1 HG03195.hp1 NA19030.hp2 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0165a0001c0001t0002g0166a0001c0001t0002g0167 | 3 | 182 | 0.0165 | -2 | c.111 others(21): Show |
AOPEP | ENSG00000148120.19 | transcript | ENST00000375315.8 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
AOPEP_chr9_94721699_95092159 | 94799861 | CAA | C | intron_variant | MODIFIER | HG01109.hp1 HG01255.hp1 HG01256.hp2 others(31): Show |
a0001a0002a0006others(2): Show | a0001c0001a0002c0002a0002c0008others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(6): Show | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(31): Show | 34 | 182 | 0.1868 | -2 | c.111 others(19): Show |
AOPEP | ENSG00000148120.19 | transcript | ENST00000375315.8 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
AOPEP_chr9_94721699_95092159 | 94821970 | AAC | A | intron_variant | MODIFIER | HG01081.hp2 HG01243.hp2 HG01256.hp2 others(12): Show |
a0001a0002a0007others(1): Show | a0001c0001a0001c0016a0002c0002others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0016t0001others(4): Show | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0140others(12): Show | 15 | 182 | 0.0824 | -2 | c.136 others(23): Show |
AOPEP | ENSG00000148120.19 | transcript | ENST00000375315.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
AOPEP_chr9_94721699_95092159 | 94836082 | TTG | T | intron_variant | MODIFIER | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(156): Show |
a0001a0002a0003others(7): Show | a0001c0001a0001c0014a0001c0015others(11): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(18): Show | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(156): Show | 159 | 182 | 0.8736 | -2 | c.136 others(23): Show |
AOPEP | ENSG00000148120.19 | transcript | ENST00000375315.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
AOPEP_chr9_94721699_95092159 | 94847161 | GTC | G | intron_variant | MODIFIER | HG01081.hp2 HG01243.hp2 HG01255.hp1 others(23): Show |
a0001a0002a0007 | a0001c0001a0001c0016a0002c0002others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(7): Show | a0001c0001t0001g0111a0001c0001t0001g0120a0001c0001t0001g0122others(23): Show | 26 | 182 | 0.1429 | -2 | c.136 others(23): Show |
AOPEP | ENSG00000148120.19 | transcript | ENST00000375315.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
AOPEP_chr9_94721699_95092159 | 94849504 | TTC | T | intron_variant | MODIFIER | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(74): Show |
a0001a0003a0004others(1): Show | a0001c0001a0001c0014a0003c0003others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(5): Show | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0031others(74): Show | 77 | 182 | 0.4231 | -2 | c.136 others(23): Show |
AOPEP | ENSG00000148120.19 | transcript | ENST00000375315.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
AOPEP_chr9_94721699_95092159 | 94856641 | TAA | T | intron_variant | MODIFIER | HG03041.hp2 HG03516.hp1 HG03654.hp2 others(5): Show |
a0001a0005a0006 | a0001c0001a0005c0005a0006c0007 | a0001c0001t0001a0005c0005t0001a0006c0007t0001 | a0001c0001t0001g0115a0001c0001t0001g0118a0001c0001t0001g0120others(5): Show | 8 | 182 | 0.0440 | -2 | c.136 others(23): Show |
AOPEP | ENSG00000148120.19 | transcript | ENST00000375315.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
AOPEP_chr9_94721699_95092159 | 94875347 | GAA | G | intron_variant | MODIFIER | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(47): Show |
a0001a0004a0012 | a0001c0001a0004c0004a0012c0013 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(3): Show | a0001c0001t0001g0012a0001c0001t0001g0029a0001c0001t0001g0031others(47): Show | 50 | 182 | 0.2747 | -2 | c.136 others(23): Show |
AOPEP | ENSG00000148120.19 | transcript | ENST00000375315.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
AOPEP_chr9_94721699_95092159 | 94877427 | CTT | C | intron_variant | MODIFIER | HG01255.hp1 HG02572.hp1 HG02965.hp1 others(9): Show |
a0001a0002a0005 | a0001c0001a0002c0002a0002c0008others(1): Show | a0001c0001t0001a0002c0002t0002a0002c0008t0001others(3): Show | a0001c0001t0001g0078a0001c0001t0001g0115a0001c0001t0001g0118others(9): Show | 12 | 182 | 0.0659 | -2 | c.136 others(23): Show |
AOPEP | ENSG00000148120.19 | transcript | ENST00000375315.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
AOPEP_chr9_94721699_95092159 | 94885008 | CAA | C | intron_variant | MODIFIER | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(80): Show |
a0001a0004a0006others(2): Show | a0001c0001a0004c0004a0006c0007others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(5): Show | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0029others(80): Show | 83 | 182 | 0.4560 | -2 | c.136 others(23): Show |
AOPEP | ENSG00000148120.19 | transcript | ENST00000375315.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
AOPEP_chr9_94721699_95092159 | 94885348 | CAA | C | intron_variant | MODIFIER | HG02071.hp1 HG02735.hp1 HG02735.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0041a0001c0001t0002g0042a0001c0001t0002g0050others(2): Show | 5 | 182 | 0.0275 | -2 | c.136 others(23): Show |
AOPEP | ENSG00000148120.19 | transcript | ENST00000375315.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
AOPEP_chr9_94721699_95092159 | 94887165 | ACC | A | intron_variant | MODIFIER | HG01255.hp1 HG02257.hp2 HG02572.hp1 others(12): Show |
a0001a0002a0005others(1): Show | a0001c0001a0002c0008a0005c0005others(1): Show | a0001c0001t0001a0002c0008t0001a0002c0008t0002others(3): Show | a0001c0001t0001g0008a0001c0001t0001g0115a0001c0001t0001g0118others(12): Show | 15 | 182 | 0.0824 | -2 | c.136 others(23): Show |
AOPEP | ENSG00000148120.19 | transcript | ENST00000375315.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
AOPEP_chr9_94721699_95092159 | 94888294 | CGT | C | intron_variant | MODIFIER | HG02572.hp2 HG02630.hp1 HG02895.hp2 others(7): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0002a0002c0002t0002a0002c0002t0005 | a0001c0001t0002g0039a0002c0002t0002g0124a0002c0002t0002g0125others(7): Show | 10 | 182 | 0.0550 | -2 | c.136 others(23): Show |
AOPEP | ENSG00000148120.19 | transcript | ENST00000375315.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
AOPEP_chr9_94721699_95092159 | 94896910 | GTT | G | intron_variant | MODIFIER | HG03098.hp2 HG03654.hp2 HG04204.hp1 others(5): Show |
a0001a0005 | a0001c0001a0005c0005 | a0001c0001t0001a0001c0001t0002a0005c0005t0001 | a0001c0001t0001g0115a0001c0001t0001g0118a0001c0001t0002g0105others(5): Show | 8 | 182 | 0.0440 | -2 | c.136 others(23): Show |
AOPEP | ENSG00000148120.19 | transcript | ENST00000375315.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
AOPEP_chr9_94721699_95092159 | 94898648 | GAA | G | intron_variant | MODIFIER | HG01255.hp1 HG02257.hp2 HG02572.hp1 others(13): Show |
a0001a0002a0005others(1): Show | a0001c0001a0002c0002a0002c0008others(2): Show | a0001c0001t0001a0002c0002t0002a0002c0008t0001others(4): Show | a0001c0001t0001g0008a0001c0001t0001g0115a0001c0001t0001g0118others(13): Show | 16 | 182 | 0.0879 | -2 | c.136 others(23): Show |
AOPEP | ENSG00000148120.19 | transcript | ENST00000375315.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
AOPEP_chr9_94721699_95092159 | 94899179 | CTT | C | intron_variant | MODIFIER | HG02572.hp1 HG02965.hp1 HG03654.hp2 others(6): Show |
a0001a0002a0005 | a0001c0001a0002c0008a0005c0005 | a0001c0001t0001a0002c0008t0002a0002c0008t0003others(1): Show | a0001c0001t0001g0115a0001c0001t0001g0118a0002c0008t0002g0135others(6): Show | 9 | 182 | 0.0495 | -2 | c.136 others(23): Show |
AOPEP | ENSG00000148120.19 | transcript | ENST00000375315.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
AOPEP_chr9_94721699_95092159 | 94909820 | TAA | T | intron_variant | MODIFIER | HG02109.hp2 HG02572.hp1 HG02630.hp2 others(15): Show |
a0001a0002a0005others(2): Show | a0001c0001a0002c0008a0005c0005others(2): Show | a0001c0001t0001a0001c0001t0003a0002c0008t0002others(4): Show | a0001c0001t0001g0115a0001c0001t0001g0118a0001c0001t0003g0108others(15): Show | 18 | 182 | 0.0989 | -2 | c.136 others(23): Show |
AOPEP | ENSG00000148120.19 | transcript | ENST00000375315.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
AOPEP_chr9_94721699_95092159 | 94914523 | CGT | C | intron_variant | MODIFIER | HG00741.hp1 HG01975.hp2 HG02165.hp1 others(4): Show |
a0001a0004 | a0001c0001a0004c0004 | a0001c0001t0001a0001c0001t0002a0004c0004t0001others(1): Show | a0001c0001t0001g0041a0001c0001t0002g0103a0004c0004t0001g0153others(4): Show | 7 | 182 | 0.0385 | -2 | c.136 others(21): Show |
AOPEP | ENSG00000148120.19 | transcript | ENST00000375315.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
AOPEP_chr9_94721699_95092159 | 94927323 | CAT | C | intron_variant | MODIFIER | NA18973.hp2 NA18999.hp2 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0007a0001c0001t0002g0019 | 2 | 182 | 0.0110 | -2 | c.155 others(21): Show |
AOPEP | ENSG00000148120.19 | transcript | ENST00000375315.8 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
AOPEP_chr9_94721699_95092159 | 94964635 | CTT | C | intron_variant | MODIFIER | HG02723.hp2 HG02970.hp2 HG03041.hp2 others(9): Show |
a0001a0005a0006 | a0001c0001a0005c0005a0006c0007 | a0001c0001t0001a0001c0001t0004a0005c0005t0001others(1): Show | a0001c0001t0001g0067a0001c0001t0001g0115a0001c0001t0001g0118others(9): Show | 12 | 182 | 0.0659 | -2 | c.187 others(21): Show |
AOPEP | ENSG00000148120.19 | transcript | ENST00000375315.8 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
AOPEP_chr9_94721699_95092159 | 94976293 | CTT | C | intron_variant | MODIFIER | HG02145.hp2 HG02257.hp1 HG02572.hp1 others(13): Show |
a0001a0002a0005others(1): Show | a0001c0001a0002c0002a0002c0008others(2): Show | a0001c0001t0001a0001c0001t0002a0002c0002t0002others(3): Show | a0001c0001t0001g0115a0001c0001t0001g0118a0001c0001t0002g0040others(13): Show | 16 | 182 | 0.0879 | -2 | c.191 others(21): Show |
AOPEP | ENSG00000148120.19 | transcript | ENST00000375315.8 | protein_coding | 10/16 | chr9 | TogoVar | ||||||
AOPEP_chr9_94721699_95092159 | 94982584 | TTG | T | intron_variant | MODIFIER | HG00408.hp1 HG00621.hp2 HG00741.hp2 others(20): Show |
a0001a0003a0012 | a0001c0001a0001c0014a0003c0003others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0014t0001others(2): Show | a0001c0001t0001g0013a0001c0001t0001g0053a0001c0001t0001g0065others(20): Show | 23 | 182 | 0.1264 | -2 | c.197 others(21): Show |
AOPEP | ENSG00000148120.19 | transcript | ENST00000375315.8 | protein_coding | 11/16 | chr9 | TogoVar | ||||||
AOPEP_chr9_94721699_95092159 | 94989124 | CAG | C | intron_variant | MODIFIER | HG03654.hp2 HG04204.hp1 NA18969.hp1 others(4): Show |
a0001a0005 | a0001c0001a0005c0005 | a0001c0001t0001a0005c0005t0001 | a0001c0001t0001g0115a0001c0001t0001g0118a0005c0005t0001g0113others(4): Show | 7 | 182 | 0.0385 | -2 | c.197 others(21): Show |
AOPEP | ENSG00000148120.19 | transcript | ENST00000375315.8 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
AOPEP_chr9_94721699_95092159 | 94989609 | CTT | C | intron_variant | MODIFIER | HG02257.hp1 HG02818.hp2 HG02970.hp2 others(3): Show |
a0003a0006a0010 | a0003c0003a0006c0007a0010c0009 | a0003c0003t0001a0006c0007t0001a0010c0009t0001 | a0003c0003t0001g0178a0006c0007t0001g0099a0006c0007t0001g0100others(3): Show | 6 | 182 | 0.0330 | -2 | c.197 others(23): Show |
AOPEP | ENSG00000148120.19 | transcript | ENST00000375315.8 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
AOPEP_chr9_94721699_95092159 | 94990639 | ATT | A | intron_variant | MODIFIER | HG01515.hp2 HG02647.hp2 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0023a0001c0001t0002g0090 | 2 | 182 | 0.0110 | -2 | c.197 others(23): Show |
AOPEP | ENSG00000148120.19 | transcript | ENST00000375315.8 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
AOPEP_chr9_94721699_95092159 | 94996350 | CTG | C | intron_variant | MODIFIER | HG00408.hp1 HG01515.hp2 HG02572.hp1 others(11): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0002c0008others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(5): Show | a0001c0001t0001g0041a0001c0001t0001g0098a0001c0001t0002g0020others(11): Show | 14 | 182 | 0.0769 | -2 | c.197 others(21): Show |
AOPEP | ENSG00000148120.19 | transcript | ENST00000375315.8 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
AOPEP_chr9_94721699_95092159 | 95003142 | ATG | A | intron_variant | MODIFIER | HG00609.hp2 HG02027.hp2 HG02155.hp2 others(13): Show |
a0001a0009 | a0001c0001a0009c0010 | a0001c0001t0001a0001c0001t0002a0009c0010t0001 | a0001c0001t0001g0008a0001c0001t0001g0031a0001c0001t0001g0143others(13): Show | 16 | 182 | 0.0879 | -2 | c.197 others(21): Show |
AOPEP | ENSG00000148120.19 | transcript | ENST00000375315.8 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
AOPEP_chr9_94721699_95092159 | 95003165 | TGC | T | intron_variant | MODIFIER | HG00408.hp1 HG00621.hp2 HG00741.hp2 others(20): Show |
a0001a0003a0012 | a0001c0001a0001c0014a0003c0003others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0014t0001others(2): Show | a0001c0001t0001g0013a0001c0001t0001g0053a0001c0001t0001g0065others(20): Show | 23 | 182 | 0.1264 | -2 | c.197 others(21): Show |
AOPEP | ENSG00000148120.19 | transcript | ENST00000375315.8 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
AOPEP_chr9_94721699_95092159 | 95003716 | AAC | A | intron_variant | MODIFIER | HG03654.hp2 HG04204.hp1 NA18969.hp1 others(4): Show |
a0001a0005 | a0001c0001a0005c0005 | a0001c0001t0001a0005c0005t0001 | a0001c0001t0001g0115a0001c0001t0001g0118a0005c0005t0001g0113others(4): Show | 7 | 182 | 0.0385 | -2 | c.197 others(21): Show |
AOPEP | ENSG00000148120.19 | transcript | ENST00000375315.8 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
AOPEP_chr9_94721699_95092159 | 95006901 | ATT | A | intron_variant | MODIFIER | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(95): Show |
a0001a0002a0004others(2): Show | a0001c0001a0001c0015a0002c0002others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(7): Show | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0016others(95): Show | 98 | 182 | 0.5385 | -2 | c.211 others(21): Show |
AOPEP | ENSG00000148120.19 | transcript | ENST00000375315.8 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
AOPEP_chr9_94721699_95092159 | 95011211 | ATT | A | intron_variant | MODIFIER | HG00408.hp1 HG00621.hp2 HG00741.hp2 others(33): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0016a0002c0008others(3): Show | a0001c0001t0001a0001c0001t0003a0001c0016t0001others(4): Show | a0001c0001t0001g0013a0001c0001t0001g0065a0001c0001t0001g0076others(33): Show | 36 | 182 | 0.1978 | -2 | c.211 others(21): Show |
AOPEP | ENSG00000148120.19 | transcript | ENST00000375315.8 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
AOPEP_chr9_94721699_95092159 | 95083389 | GCA | G | intron_variant | MODIFIER | HG03654.hp2 HG04204.hp1 NA18969.hp1 others(5): Show |
a0001a0005 | a0001c0001a0005c0005 | a0001c0001t0001a0005c0005t0001 | a0001c0001t0001g0056a0001c0001t0001g0115a0001c0001t0001g0118others(5): Show | 8 | 182 | 0.0440 | -2 | c.*4+ others(15): Show |
AOPEP | ENSG00000148120.19 | transcript | ENST00000375315.8 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
AOPEP_chr9_94721699_95092159 | 95092056 | CTG | C | downstream_gene_variant | MODIFIER | HG00438.hp1 HG02080.hp2 HG02145.hp1 others(27): Show |
a0001a0002a0012 | a0001c0001a0001c0016a0002c0002others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0016t0001others(4): Show | a0001c0001t0001g0067a0001c0001t0001g0095a0001c0001t0001g0111others(27): Show | 30 | 182 | 0.1648 | -2 | c.*53 others(13): Show |
AOPEP | ENSG00000148120.19 | transcript | ENST00000375315.8 | protein_coding | 4898 | chr9 | TogoVar | ||||||
AOPEP_chr9_94721699_95092159 | 95092082 | GCA | G | downstream_gene_variant | MODIFIER | HG03654.hp2 HG04204.hp1 NA18969.hp1 others(1): Show |
a0001a0005 | a0001c0001a0005c0005 | a0001c0001t0001a0005c0005t0001 | a0001c0001t0001g0115a0001c0001t0001g0118a0005c0005t0001g0113others(1): Show | 4 | 182 | 0.0220 | -2 | c.*54 others(13): Show |
AOPEP | ENSG00000148120.19 | transcript | ENST00000375315.8 | protein_coding | 4924 | chr9 | TogoVar | ||||||
AOX1_chr2_200581014_200676495 | 200588726 | CTT | C | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(103): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0008a0001c0019others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(11): Show | a0001c0001t0001g0117a0001c0001t0001g0120a0001c0001t0001g0121others(102): Show | 106 | 370 | 0.2865 | -2 | c.45+ others(17): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
AOX1_chr2_200581014_200676495 | 200589620 | TGG | T | intron_variant | MODIFIER | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(82): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0005a0001c0014others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0008others(9): Show | a0001c0001t0001g0237a0001c0001t0001g0267a0001c0001t0001g0282others(82): Show | 85 | 370 | 0.2297 | -2 | c.45+ others(17): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
AOX1_chr2_200581014_200676495 | 200601073 | CTT | C | intron_variant | MODIFIER | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(84): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0005a0001c0014others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0008others(12): Show | a0001c0001t0001g0237a0001c0001t0001g0267a0001c0001t0001g0282others(84): Show | 87 | 370 | 0.2351 | -2 | c.437 others(19): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
AOX1_chr2_200581014_200676495 | 200605510 | ATT | A | intron_variant | MODIFIER | HG00423.hp2 HG00544.hp2 HG00642.hp1 others(16): Show |
a0001a0004 | a0001c0001a0001c0005a0004c0004 | a0001c0001t0001a0001c0001t0002a0001c0001t0008others(3): Show | a0001c0001t0001g0237a0001c0001t0001g0267a0001c0001t0001g0282others(16): Show | 19 | 370 | 0.0514 | -2 | c.815 others(15): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 9/34 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
AOX1_chr2_200581014_200676495 | 200617481 | CAA | C | intron_variant | MODIFIER | HG01884.hp2 HG02258.hp1 HG02723.hp2 others(7): Show |
a0001a0003 | a0001c0001a0001c0005a0003c0003others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0005t0002others(3): Show | a0001c0001t0001g0121a0001c0001t0002g0123a0001c0001t0002g0161others(7): Show | 10 | 370 | 0.0270 | -2 | c.170 others(21): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
AOX1_chr2_200581014_200676495 | 200620199 | CTT | C | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(103): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0005a0001c0008others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(12): Show | a0001c0001t0001g0117a0001c0001t0001g0121a0001c0001t0001g0124others(102): Show | 106 | 370 | 0.2865 | -2 | c.170 others(19): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
AOX1_chr2_200581014_200676495 | 200630210 | TAA | T | intron_variant | MODIFIER | HG00140.hp1 HG00423.hp2 HG00738.hp2 others(10): Show |
a0001a0003a0010 | a0001c0001a0003c0009a0010c0025 | a0001c0001t0002a0001c0001t0008a0003c0009t0001others(1): Show | a0001c0001t0002g0150a0001c0001t0002g0233a0001c0001t0002g0239others(10): Show | 13 | 370 | 0.0351 | -2 | c.222 others(21): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
AOX1_chr2_200581014_200676495 | 200636117 | CTT | C | intron_variant | MODIFIER | HG00408.hp1 HG01106.hp2 HG01433.hp2 others(11): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0002a0003c0003others(2): Show | a0001c0001t0001a0001c0001t0002a0002c0002t0007others(3): Show | a0001c0001t0001g0238a0001c0001t0001g0241a0001c0001t0001g0357others(11): Show | 14 | 370 | 0.0378 | -2 | c.234 others(19): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 21/34 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
AOX1_chr2_200581014_200676495 | 200648577 | GGT | G | intron_variant | MODIFIER | HG02015.hp2 NA18965.hp2 NA18975.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0221a0001c0001t0001g0224a0001c0001t0001g0227others(1): Show | 4 | 370 | 0.0108 | -2 | c.284 others(21): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
AOX1_chr2_200581014_200676495 | 200659777 | TTC | T | intron_variant | MODIFIER | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(49): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0014a0002c0002others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0014t0001others(3): Show | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(48): Show | 52 | 370 | 0.1405 | -2 | c.330 others(19): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 28/34 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
AOX1_chr2_200581014_200676495 | 200659786 | TCA | T | intron_variant | MODIFIER | HG01192.hp2 HG01358.hp2 HG01361.hp1 others(18): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0031a0002c0002others(2): Show | a0001c0001t0001a0001c0001t0005a0001c0031t0001others(3): Show | a0001c0001t0001g0061a0001c0001t0001g0128a0001c0001t0001g0199others(17): Show | 21 | 370 | 0.0568 | -2 | c.330 others(19): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 28/34 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
AOX1_chr2_200581014_200676495 | 200663545 | AAC | A | intron_variant | MODIFIER | HG01884.hp1 HG02451.hp1 HG02572.hp2 others(4): Show |
a0001a0013 | a0001c0001a0013c0021 | a0001c0001t0001a0013c0021t0001 | a0001c0001t0001g0117a0001c0001t0001g0120a0001c0001t0001g0129others(4): Show | 7 | 370 | 0.0189 | -2 | c.354 others(19): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
AOX1_chr2_200581014_200676495 | 200671272 | CAT | C | 3_prime_UTR_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0005a0001c0008others(11): Show | a0001c0001t0002a0001c0001t0008a0001c0001t0010others(14): Show | a0001c0001t0002g0004a0001c0001t0002g0011a0001c0001t0002g0013others(147): Show | 150 | 370 | 0.4054 | -2 | c.*59 others(11): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 35/35 | 598 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||
AP1AR_chr4_112226787_112278110 | 112227379 | GTT | G | upstream_gene_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(69): Show |
a0001 | a0001c0001a0001c0006 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(12): Show | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0047others(40): Show | 72 | 398 | 0.1809 | -2 | c.-47 others(13): Show |
AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 4407 | chr4 | TogoVar | ||||||
AP1AR_chr4_112226787_112278110 | 112237977 | GGT | G | intron_variant | MODIFIER | HG00408.hp2 HG00558.hp1 HG00609.hp2 others(24): Show |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0001a0001c0001t0021a0001c0001t0033others(1): Show | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0019others(5): Show | 27 | 398 | 0.0678 | -2 | c.83+ others(17): Show |
AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | TogoVar |