view | regionname | pos | ref | alt | annotation | impact | samples | ahapids | chapids | thapids | thapids | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
SPATS2_chr12_49362462_49532425 | 49418108 | GT | G | intron_variant | MODIFIER | HG01069.hp2 HG01123.hp2 HG01346.hp1 others(25): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(1): Show | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(25): Show |
28 | 158 | 0.1772 | -1 | c.-24 others(11): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
SPATS2_chr12_49362462_49532425 | 49421416 | CA | C | intron_variant | MODIFIER | HG00280.hp1 HG00280.hp2 HG00639.hp1 others(83): Show |
a0001a0003 | a0001c0001a0001c0003a0001c0005others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(8): Show | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(83): Show |
86 | 158 | 0.5443 | -1 | c.-24 others(11): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
SPATS2_chr12_49362462_49532425 | 49423689 | CT | C | intron_variant | MODIFIER | HG01071.hp2 homoSapiens_chm13v2.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0009 a0001c0001t0001g0015 |
2 | 158 | 0.0127 | -1 | c.-24 others(11): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | TogoVar | |||||||
SPATS2_chr12_49362462_49532425 | 49428273 | CA | C | intron_variant | MODIFIER | HG00280.hp1 HG00741.hp1 HG01069.hp2 others(29): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(1): Show | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(29): Show |
32 | 158 | 0.2025 | -1 | c.-24 others(11): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
SPATS2_chr12_49362462_49532425 | 49429786 | CT | C | intron_variant | MODIFIER | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(67): Show |
a0001a0004 | a0001c0001a0001c0003a0001c0005others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(10): Show | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(67): Show |
70 | 158 | 0.4430 | -1 | c.-24 others(11): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
SPATS2_chr12_49362462_49532425 | 49435638 | CT | C | intron_variant | MODIFIER | HG00099.hp2 HG01515.hp2 HG02055.hp2 others(6): Show |
a0001a0002 | a0001c0001a0002c0006 | a0001c0001t0001a0001c0001t0003a0002c0006t0001 | a0001c0001t0001g0004 a0001c0001t0001g0080 a0001c0001t0001g0111 others(6): Show |
9 | 158 | 0.0570 | -1 | c.-24 others(11): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
SPATS2_chr12_49362462_49532425 | 49444215 | TG | T | intron_variant | MODIFIER | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(50): Show |
a0001a0004 | a0001c0001a0001c0003a0001c0005others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(8): Show | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(50): Show |
53 | 158 | 0.3354 | -1 | c.-24 others(11): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | TogoVar | |||||||
SPATS2_chr12_49362462_49532425 | 49453856 | CT | C | intron_variant | MODIFIER | HG00280.hp1 HG01071.hp2 HG01123.hp2 others(14): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(14): Show |
17 | 158 | 0.1076 | -1 | c.-24 others(10): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
SPATS2_chr12_49362462_49532425 | 49454880 | TA | T | intron_variant | MODIFIER | HG02080.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0006 | a0001c0001t0001g0092 a0001c0001t0001g0098 a0001c0001t0006g0043 others(2): Show |
5 | 158 | 0.0317 | -1 | c.-24 others(10): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
SPATS2_chr12_49362462_49532425 | 49458483 | GA | G | intron_variant | MODIFIER | HG02080.hp2 HG02647.hp2 HG02723.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0006a0001c0001t0011 | a0001c0001t0001g0144 a0001c0001t0006g0043 a0001c0001t0006g0044 others(3): Show |
6 | 158 | 0.0380 | -1 | c.-24 others(10): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
SPATS2_chr12_49362462_49532425 | 49459740 | TC | T | intron_variant | MODIFIER | HG00099.hp2 HG01074.hp1 HG01074.hp2 others(16): Show |
a0001a0002 | a0001c0001a0002c0006 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(4): Show | a0001c0001t0001g0019 a0001c0001t0001g0073 a0001c0001t0001g0076 others(16): Show |
19 | 158 | 0.1203 | -1 | c.-24 others(10): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
SPATS2_chr12_49362462_49532425 | 49459940 | GA | G | intron_variant | MODIFIER | HG00639.hp2 HG01167.hp1 HG01175.hp1 others(50): Show |
a0001a0004 | a0001c0001a0001c0003a0001c0005others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(9): Show | a0001c0001t0001g0033 a0001c0001t0001g0040 a0001c0001t0001g0058 others(50): Show |
53 | 158 | 0.3354 | -1 | c.-24 others(9): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
SPATS2_chr12_49362462_49532425 | 49460455 | CA | C | intron_variant | MODIFIER | HG00099.hp2 HG01069.hp1 HG01071.hp1 others(18): Show |
a0001a0002 | a0001c0001a0002c0006 | a0001c0001t0001a0001c0001t0003a0002c0006t0001 | a0001c0001t0001g0036 a0001c0001t0001g0070 a0001c0001t0001g0086 others(18): Show |
21 | 158 | 0.1329 | -1 | c.-24 others(9): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
SPATS2_chr12_49362462_49532425 | 49463249 | CA | C | intron_variant | MODIFIER | HG01884.hp2 HG01943.hp1 HG02451.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0115 a0001c0001t0002g0149 a0001c0001t0002g0150 others(3): Show |
6 | 158 | 0.0380 | -1 | c.25+ others(8): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
SPATS2_chr12_49362462_49532425 | 49463412 | CA | C | intron_variant | MODIFIER | HG01069.hp2 HG01071.hp2 HG01515.hp1 others(7): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0006a0001c0001t0011others(1): Show | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(7): Show |
10 | 158 | 0.0633 | -1 | c.25+ others(8): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
SPATS2_chr12_49362462_49532425 | 49464225 | TG | T | intron_variant | MODIFIER | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(1): Show | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(28): Show |
31 | 158 | 0.1962 | -1 | c.25+ others(8): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
SPATS2_chr12_49362462_49532425 | 49464627 | TA | T | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp1 HG01069.hp1 others(79): Show |
a0001a0002a0004 | a0001c0001a0002c0006a0004c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(9): Show | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(79): Show |
82 | 158 | 0.5190 | -1 | c.25+ others(8): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
SPATS2_chr12_49362462_49532425 | 49467044 | GT | G | intron_variant | MODIFIER | HG02572.hp2 HG02647.hp1 HG02647.hp2 others(2): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0006a0001c0001t0012a0001c0003t0001 | a0001c0001t0006g0043 a0001c0001t0006g0044 a0001c0001t0006g0045 others(2): Show |
5 | 158 | 0.0317 | -1 | c.25+ others(8): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
SPATS2_chr12_49362462_49532425 | 49467215 | AT | A | intron_variant | MODIFIER | HG01069.hp1 HG01071.hp1 HG02055.hp2 others(10): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0006 | a0001c0001t0001g0036 a0001c0001t0001g0117 a0001c0001t0001g0137 others(10): Show |
13 | 158 | 0.0823 | -1 | c.25+ others(8): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
SPATS2_chr12_49362462_49532425 | 49469542 | TA | T | intron_variant | MODIFIER | HG00639.hp2 HG01167.hp1 HG02293.hp1 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0004 | a0001c0001t0001g0122 a0001c0001t0002g0053 a0001c0001t0004g0068 others(5): Show |
8 | 158 | 0.0506 | -1 | c.25+ others(8): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
SPATS2_chr12_49362462_49532425 | 49473048 | CA | C | intron_variant | MODIFIER | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(18): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(18): Show |
21 | 158 | 0.1329 | -1 | c.26- others(9): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
SPATS2_chr12_49362462_49532425 | 49477102 | TA | T | intron_variant | MODIFIER | HG01167.hp1 HG01884.hp2 HG03225.hp1 others(2): Show |
a0001a0004 | a0001c0001a0004c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(2): Show | a0001c0001t0001g0143 a0001c0001t0002g0151 a0001c0001t0003g0030 others(2): Show |
5 | 158 | 0.0317 | -1 | c.26- others(8): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
SPATS2_chr12_49362462_49532425 | 49477962 | CT | C | intron_variant | MODIFIER | HG01069.hp1 HG01167.hp2 HG01346.hp1 others(25): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(3): Show | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(25): Show |
28 | 158 | 0.1772 | -1 | c.26- others(8): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
SPATS2_chr12_49362462_49532425 | 49480795 | GT | G | intron_variant | MODIFIER | HG00639.hp2 HG01167.hp2 HG01175.hp1 others(17): Show |
a0001a0004 | a0001c0001a0004c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0008others(2): Show | a0001c0001t0001g0082 a0001c0001t0002g0047 a0001c0001t0002g0048 others(17): Show |
20 | 158 | 0.1266 | -1 | c.26- others(8): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
SPATS2_chr12_49362462_49532425 | 49481457 | CA | C | intron_variant | MODIFIER | HG01884.hp1 HG02055.hp1 HG02976.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(3): Show |
6 | 158 | 0.0380 | -1 | c.26- others(8): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | TogoVar | |||||||
SPATS2_chr12_49362462_49532425 | 49481458 | AT | A | intron_variant | MODIFIER | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(60): Show |
a0001a0004 | a0001c0001a0001c0005a0004c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(8): Show | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(60): Show |
63 | 158 | 0.3987 | -1 | c.26- others(8): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
SPATS2_chr12_49362462_49532425 | 49483770 | TG | T | intron_variant | MODIFIER | HG01167.hp1 HG02486.hp1 HG02896.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0068 a0001c0001t0004g0123 a0001c0001t0004g0124 others(3): Show |
6 | 158 | 0.0380 | -1 | c.26- others(7): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | TogoVar | |||||||
SPATS2_chr12_49362462_49532425 | 49493099 | TA | T | intron_variant | MODIFIER | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(81): Show |
a0001a0004 | a0001c0001a0001c0003a0001c0005others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(11): Show | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(81): Show |
84 | 158 | 0.5317 | -1 | c.265 others(9): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
SPATS2_chr12_49362462_49532425 | 49497392 | CT | C | intron_variant | MODIFIER | HG01167.hp1 HG02486.hp1 HG02896.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004 | a0001c0001t0001g0116 a0001c0001t0004g0068 a0001c0001t0004g0123 others(4): Show |
7 | 158 | 0.0443 | -1 | c.703 others(8): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
SPATS2_chr12_49362462_49532425 | 49504734 | GT | G | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(148): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0005a0002c0006others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(14): Show | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(148): Show |
151 | 158 | 0.9557 | -1 | c.839 others(9): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
SPATS2_chr12_49362462_49532425 | 49504770 | CT | C | intron_variant | MODIFIER | HG01943.hp1 HG02451.hp2 HG02896.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0006 | a0001c0001t0001g0065 a0001c0001t0001g0084 a0001c0001t0001g0098 others(3): Show |
6 | 158 | 0.0380 | -1 | c.839 others(9): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
SPATS2_chr12_49362462_49532425 | 49506836 | TA | T | intron_variant | MODIFIER | HG01069.hp1 HG01071.hp1 HG02055.hp2 others(12): Show |
a0001 | a0001c0001a0001c0005 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(1): Show | a0001c0001t0001g0036 a0001c0001t0001g0073 a0001c0001t0001g0108 others(12): Show |
15 | 158 | 0.0949 | -1 | c.839 others(9): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
SPATS2_chr12_49362462_49532425 | 49508745 | CT | C | intron_variant | MODIFIER | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(21): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0005 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(21): Show |
24 | 158 | 0.1519 | -1 | c.840 others(9): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
SPATS2_chr12_49362462_49532425 | 49509273 | CT | C | intron_variant | MODIFIER | HG00099.hp1 HG01167.hp2 HG01175.hp2 others(12): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(1): Show | a0001c0001t0001g0067 a0001c0001t0001g0082 a0001c0001t0001g0114 others(12): Show |
15 | 158 | 0.0949 | -1 | c.840 others(9): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
SPATS2_chr12_49362462_49532425 | 49514154 | CA | C | intron_variant | MODIFIER | HG00280.hp1 HG00639.hp2 HG00741.hp1 others(93): Show |
a0001a0004 | a0001c0001a0001c0003a0001c0005others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(11): Show | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(93): Show |
96 | 158 | 0.6076 | -1 | c.840 others(8): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
SPATS2_chr12_49362462_49532425 | 49516167 | AT | A | intron_variant | MODIFIER | HG02109.hp2 NA18951.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0096 a0001c0001t0001g0118 |
2 | 158 | 0.0127 | -1 | c.898 others(9): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | chr12 | TogoVar | |||||||
SPATS2_chr12_49362462_49532425 | 49516365 | TA | T | intron_variant | MODIFIER | HG00280.hp1 HG00639.hp2 HG01069.hp1 others(94): Show |
a0001a0004 | a0001c0001a0001c0003a0001c0005others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(11): Show | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(94): Show |
97 | 158 | 0.6139 | -1 | c.898 others(9): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
SPATS2_chr12_49362462_49532425 | 49516710 | TA | T | intron_variant | MODIFIER | HG00639.hp2 HG01069.hp1 HG01071.hp1 others(63): Show |
a0001a0004 | a0001c0001a0001c0003a0001c0005others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(10): Show | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0040 others(63): Show |
66 | 158 | 0.4177 | -1 | c.898 others(9): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
SPATS2_chr12_49362462_49532425 | 49519814 | AT | A | intron_variant | MODIFIER | HG01167.hp1 HG01346.hp1 HG02257.hp1 others(19): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(1): Show | a0001c0001t0001g0004 a0001c0001t0001g0069 a0001c0001t0003g0012 others(19): Show |
22 | 158 | 0.1392 | -1 | c.100 others(9): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
SPATS2_chr12_49362462_49532425 | 49522028 | GA | G | intron_variant | MODIFIER | HG00639.hp1 HG01069.hp2 HG01167.hp1 others(16): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(2): Show | a0001c0001t0001g0011 a0001c0001t0001g0102 a0001c0001t0003g0037 others(16): Show |
19 | 158 | 0.1203 | -1 | c.100 others(9): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
SPATS2_chr12_49362462_49532425 | 49529312 | CA | C | downstream_gene_variant | MODIFIER | HG00639.hp2 HG01167.hp1 HG01175.hp1 others(51): Show |
a0001a0004 | a0001c0001a0001c0003a0001c0005others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(9): Show | a0001c0001t0001g0033 a0001c0001t0001g0040 a0001c0001t0001g0058 others(51): Show |
54 | 158 | 0.3418 | -1 | c.*30 others(6): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 1888 | chr12 | TogoVar | |||||||
SPATS2_chr12_49362462_49532425 | 49529833 | CT | C | downstream_gene_variant | MODIFIER | HG00099.hp2 HG02293.hp1 HG02922.hp2 others(5): Show |
a0001a0002 | a0001c0001a0002c0006 | a0001c0001t0001a0001c0001t0007a0002c0006t0001 | a0001c0001t0001g0070 a0001c0001t0001g0086 a0001c0001t0001g0108 others(5): Show |
8 | 158 | 0.0506 | -1 | c.*35 others(6): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2409 | chr12 | TogoVar | |||||||
SPATS2_chr12_49362462_49532425 | 49532144 | TC | T | downstream_gene_variant | MODIFIER | HG00639.hp2 HG01069.hp1 HG01071.hp1 others(54): Show |
a0001a0004 | a0001c0001a0001c0003a0001c0005others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(8): Show | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0040 others(54): Show |
57 | 158 | 0.3608 | -1 | c.*58 others(6): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 4720 | chr12 | TogoVar | |||||||
SPC24_chr19_11140493_11160782 | 11141294 | CT | C | downstream_gene_variant | MODIFIER | HG00099.hp2 HG00558.hp1 HG00621.hp1 others(61): Show |
a0001a0003 | a0001c0001a0003c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(29): Show | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0022 others(45): Show |
64 | 438 | 0.1461 | -1 | c.*58 others(6): Show |
SPC24 | ENSG00000161888.12 | transcript | ENST00000592540.6 | protein_coding | 4198 | chr19 | TogoVar | |||||||
SPC24_chr19_11140493_11160782 | 11141833 | TA | T | downstream_gene_variant | MODIFIER | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(29): Show |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0007a0001c0001t0017a0001c0001t0050others(23): Show | a0001c0001t0007g0023 a0001c0001t0017g0032 a0001c0001t0017g0171 others(26): Show |
32 | 438 | 0.0731 | -1 | c.*53 others(6): Show |
SPC24 | ENSG00000161888.12 | transcript | ENST00000592540.6 | protein_coding | 3659 | chr19 | TogoVar | |||||||
SPC24_chr19_11140493_11160782 | 11143210 | CA | C | downstream_gene_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
a0001a0002 | a0001c0001a0001c0004a0002c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(127): Show | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0022 others(210): Show |
311 | 438 | 0.7101 | -1 | c.*39 others(6): Show |
SPC24 | ENSG00000161888.12 | transcript | ENST00000592540.6 | protein_coding | 2282 | chr19 | TogoVar | |||||||
SPC24_chr19_11140493_11160782 | 11144460 | CT | C | downstream_gene_variant | MODIFIER | HG01168.hp2 HG02896.hp1 HG02965.hp2 others(13): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(12): Show | a0001c0001t0001g0302 a0001c0001t0003g0002 a0001c0001t0004g0007 others(13): Show |
16 | 438 | 0.0365 | -1 | c.*27 others(6): Show |
SPC24 | ENSG00000161888.12 | transcript | ENST00000592540.6 | protein_coding | 1032 | chr19 | TogoVar | |||||||
SPC24_chr19_11140493_11160782 | 11147908 | CA | C | intron_variant | MODIFIER | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(26): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0006a0001c0001t0020others(22): Show | a0001c0001t0001g0253 a0001c0001t0001g0267 a0001c0001t0006g0144 others(24): Show |
29 | 438 | 0.0662 | -1 | c.411 others(7): Show |
SPC24 | ENSG00000161888.12 | transcript | ENST00000592540.6 | protein_coding | 3/4 | chr19 | TogoVar | |||||||
SPC24_chr19_11140493_11160782 | 11149712 | CT | C | intron_variant | MODIFIER | NA18941.hp1 NA18942.hp2 NA18954.hp2 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0006a0001c0001t0019others(4): Show | a0001c0001t0004g0081 a0001c0001t0004g0186 a0001c0001t0006g0080 others(5): Show |
8 | 438 | 0.0183 | -1 | c.161 others(8): Show |
SPC24 | ENSG00000161888.12 | transcript | ENST00000592540.6 | protein_coding | 1/4 | chr19 | TogoVar | |||||||
SPC24_chr19_11140493_11160782 | 11151162 | CA | C | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(208): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(80): Show | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0022 others(131): Show |
211 | 438 | 0.4817 | -1 | c.161 others(9): Show |
SPC24 | ENSG00000161888.12 | transcript | ENST00000592540.6 | protein_coding | 1/4 | chr19 | TogoVar |