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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
SPATA17_chr1_217626344_217876696 | 217698579 | TA | T | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(83): Show |
a0001a0002a0005 | a0001c0001a0001c0002a0002c0006others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(29): Show | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(83): Show |
86 | 252 | 0.3413 | -1 | c.395 others(10): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
SPATA17_chr1_217626344_217876696 | 217704230 | CT | C | intron_variant | MODIFIER | HG02486.hp1 HG02976.hp2 HG03041.hp2 others(7): Show |
a0001 | a0001c0002a0001c0003a0001c0004others(1): Show | a0001c0002t0001a0001c0003t0038a0001c0004t0004others(6): Show | a0001c0002t0001g0128 a0001c0003t0038g0244 a0001c0004t0004g0247 others(7): Show |
10 | 252 | 0.0397 | -1 | c.395 others(10): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
SPATA17_chr1_217626344_217876696 | 217705430 | CT | C | intron_variant | MODIFIER | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(5): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0006a0001c0001t0016others(2): Show | a0001c0001t0001g0123 a0001c0001t0006g0201 a0001c0001t0016g0172 others(5): Show |
8 | 252 | 0.0318 | -1 | c.395 others(10): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
SPATA17_chr1_217626344_217876696 | 217706872 | CT | C | intron_variant | MODIFIER | HG01433.hp2 HG02055.hp1 HG02451.hp1 others(20): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0005a0001c0001t0008a0001c0001t0015others(14): Show | a0001c0001t0005g0084 a0001c0001t0008g0045 a0001c0001t0008g0049 others(20): Show |
23 | 252 | 0.0913 | -1 | c.395 others(10): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
SPATA17_chr1_217626344_217876696 | 217715669 | CA | C | intron_variant | MODIFIER | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(24): Show |
a0001 | a0001c0003a0001c0004a0001c0008others(1): Show | a0001c0003t0001a0001c0003t0003a0001c0003t0014others(7): Show | a0001c0003t0001g0215 a0001c0003t0001g0220 a0001c0003t0001g0231 others(24): Show |
27 | 252 | 0.1071 | -1 | c.396 others(10): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
SPATA17_chr1_217626344_217876696 | 217730219 | AT | A | intron_variant | MODIFIER | HG01070.hp1 HG01070.hp2 HG01891.hp1 others(5): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0010a0001c0002t0001others(3): Show | a0001c0001t0001g0008 a0001c0001t0010g0043 a0001c0002t0001g0107 others(5): Show |
8 | 252 | 0.0318 | -1 | c.396 others(10): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
SPATA17_chr1_217626344_217876696 | 217732787 | CT | C | intron_variant | MODIFIER | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(27): Show |
a0001 | a0001c0003a0001c0004a0001c0008others(1): Show | a0001c0003t0001a0001c0003t0003a0001c0003t0014others(10): Show | a0001c0003t0001g0215 a0001c0003t0001g0220 a0001c0003t0001g0231 others(27): Show |
30 | 252 | 0.1191 | -1 | c.396 others(9): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | TogoVar | |||||||
SPATA17_chr1_217626344_217876696 | 217739474 | AT | A | intron_variant | MODIFIER | HG01109.hp2 HG02109.hp1 HG03130.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0005a0001c0001t0008others(2): Show | a0001c0001t0001g0119 a0001c0001t0001g0190 a0001c0001t0005g0118 others(3): Show |
6 | 252 | 0.0238 | -1 | c.396 others(9): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
SPATA17_chr1_217626344_217876696 | 217741638 | TG | T | intron_variant | MODIFIER | HG00099.hp2 HG00438.hp1 HG00642.hp1 others(26): Show |
a0001 | a0001c0002a0001c0008 | a0001c0002t0001a0001c0002t0002a0001c0002t0007others(5): Show | a0001c0002t0001g0064 a0001c0002t0001g0083 a0001c0002t0001g0103 others(26): Show |
29 | 252 | 0.1151 | -1 | c.396 others(8): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
SPATA17_chr1_217626344_217876696 | 217744462 | CA | C | intron_variant | MODIFIER | HG01168.hp1 HG02895.hp1 HG02895.hp2 others(2): Show |
a0001a0005 | a0001c0001a0001c0002a0001c0005others(1): Show | a0001c0001t0056a0001c0002t0013a0001c0002t0044others(2): Show | a0001c0001t0056g0075 a0001c0002t0013g0121 a0001c0002t0044g0091 others(2): Show |
5 | 252 | 0.0198 | -1 | c.519 others(9): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
SPATA17_chr1_217626344_217876696 | 217746458 | GT | G | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(104): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0004others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(34): Show | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(104): Show |
107 | 252 | 0.4246 | -1 | c.519 others(9): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
SPATA17_chr1_217626344_217876696 | 217748743 | CA | C | intron_variant | MODIFIER | HG01167.hp2 HG02109.hp1 HG02615.hp2 others(8): Show |
a0001 | a0001c0001a0001c0002a0001c0004 | a0001c0001t0001a0001c0001t0008a0001c0001t0012others(6): Show | a0001c0001t0001g0119 a0001c0001t0001g0175 a0001c0001t0001g0190 others(8): Show |
11 | 252 | 0.0437 | -1 | c.519 others(9): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
SPATA17_chr1_217626344_217876696 | 217755993 | TA | T | intron_variant | MODIFIER | HG02559.hp1 HG03453.hp2 NA19240.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0005 | a0001c0001t0001g0090 a0001c0001t0005g0084 a0001c0001t0005g0089 |
3 | 252 | 0.0119 | -1 | c.519 others(10): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | TogoVar | |||||||
SPATA17_chr1_217626344_217876696 | 217763397 | GA | G | intron_variant | MODIFIER | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(77): Show |
a0001a0002a0004 | a0001c0001a0001c0004a0001c0005others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(31): Show | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0041 others(77): Show |
80 | 252 | 0.3175 | -1 | c.520 others(10): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
SPATA17_chr1_217626344_217876696 | 217765159 | CT | C | intron_variant | MODIFIER | HG01891.hp1 HG02630.hp2 HG03225.hp1 others(1): Show |
a0001 | a0001c0004 | a0001c0004t0032a0001c0004t0052a0001c0004t0053others(1): Show | a0001c0004t0032g0186 a0001c0004t0052g0238 a0001c0004t0053g0239 others(1): Show |
4 | 252 | 0.0159 | -1 | c.520 others(9): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
SPATA17_chr1_217626344_217876696 | 217766720 | CT | C | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(68): Show |
a0001a0003a0005 | a0001c0002a0001c0004a0001c0008others(3): Show | a0001c0002t0001a0001c0002t0002a0001c0002t0003others(32): Show | a0001c0002t0001g0064 a0001c0002t0001g0083 a0001c0002t0001g0086 others(68): Show |
71 | 252 | 0.2818 | -1 | c.520 others(9): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
SPATA17_chr1_217626344_217876696 | 217768495 | CT | C | intron_variant | MODIFIER | HG00738.hp2 HG02451.hp1 HG02717.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0008 | a0001c0001t0001g0022 a0001c0001t0001g0123 a0001c0001t0001g0140 others(2): Show |
5 | 252 | 0.0198 | -1 | c.520 others(9): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
SPATA17_chr1_217626344_217876696 | 217770978 | AT | A | intron_variant | MODIFIER | HG01168.hp1 HG01261.hp1 HG02895.hp2 others(5): Show |
a0001a0005 | a0001c0002a0001c0003a0001c0005others(1): Show | a0001c0002t0001a0001c0002t0044a0001c0003t0031others(3): Show | a0001c0002t0001g0086 a0001c0002t0044g0091 a0001c0003t0031g0225 others(5): Show |
8 | 252 | 0.0318 | -1 | c.520 others(9): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
SPATA17_chr1_217626344_217876696 | 217772118 | TA | T | intron_variant | MODIFIER | HG00639.hp1 HG01109.hp1 HG02083.hp1 others(21): Show |
a0001a0002 | a0001c0001a0001c0004a0001c0011others(1): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0009others(10): Show | a0001c0001t0001g0087 a0001c0001t0001g0124 a0001c0001t0001g0154 others(21): Show |
24 | 252 | 0.0952 | -1 | c.520 others(9): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | TogoVar | |||||||
SPATA17_chr1_217626344_217876696 | 217776676 | TA | T | intron_variant | MODIFIER | HG01168.hp1 HG02155.hp2 HG02559.hp1 others(10): Show |
a0001a0005 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(5): Show | a0001c0001t0001g0016 a0001c0001t0001g0021 a0001c0001t0001g0044 others(10): Show |
13 | 252 | 0.0516 | -1 | c.723 others(9): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
SPATA17_chr1_217626344_217876696 | 217777042 | AG | A | intron_variant | MODIFIER | HG00323.hp1 HG01099.hp2 HG01106.hp1 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0011a0001c0001t0040 | a0001c0001t0002g0003 a0001c0001t0002g0020 a0001c0001t0002g0033 others(6): Show |
9 | 252 | 0.0357 | -1 | c.723 others(9): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
SPATA17_chr1_217626344_217876696 | 217790001 | CA | C | intron_variant | MODIFIER | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0006 | a0001c0001t0001g0209 a0001c0001t0006g0096 a0001c0001t0006g0161 others(5): Show |
8 | 252 | 0.0318 | -1 | c.872 others(9): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
SPATA17_chr1_217626344_217876696 | 217793220 | TG | T | intron_variant | MODIFIER | HG01109.hp2 HG02109.hp1 HG02451.hp1 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0005a0001c0001t0008others(2): Show | a0001c0001t0001g0119 a0001c0001t0001g0190 a0001c0001t0005g0118 others(6): Show |
9 | 252 | 0.0357 | -1 | c.873 others(9): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | TogoVar | |||||||
SPATA17_chr1_217626344_217876696 | 217794115 | CA | C | intron_variant | MODIFIER | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0006 | a0001c0001t0001g0209 a0001c0001t0006g0096 a0001c0001t0006g0161 others(5): Show |
8 | 252 | 0.0318 | -1 | c.873 others(9): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
SPATA17_chr1_217626344_217876696 | 217797251 | CT | C | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(161): Show |
a0001a0002a0004 | a0001c0001a0001c0003a0001c0004others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(50): Show | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(161): Show |
164 | 252 | 0.6508 | -1 | c.873 others(9): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
SPATA17_chr1_217626344_217876696 | 217798874 | CT | C | intron_variant | MODIFIER | HG01109.hp2 HG02109.hp1 HG02257.hp2 others(6): Show |
a0001 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0001a0001c0001t0005a0001c0002t0001others(5): Show | a0001c0001t0001g0119 a0001c0001t0005g0084 a0001c0001t0005g0118 others(6): Show |
9 | 252 | 0.0357 | -1 | c.873 others(9): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
SPATA17_chr1_217626344_217876696 | 217800265 | CA | C | intron_variant | MODIFIER | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(65): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(28): Show | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0016 others(65): Show |
68 | 252 | 0.2698 | -1 | c.873 others(9): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
SPATA17_chr1_217626344_217876696 | 217802012 | AT | A | intron_variant | MODIFIER | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(9): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(2): Show | a0001c0001t0001g0119 a0001c0001t0001g0190 a0001c0001t0001g0209 others(9): Show |
12 | 252 | 0.0476 | -1 | c.100 others(9): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
SPATA17_chr1_217626344_217876696 | 217804616 | GA | G | intron_variant | MODIFIER | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0006 | a0001c0001t0001g0209 a0001c0001t0006g0096 a0001c0001t0006g0161 others(5): Show |
8 | 252 | 0.0318 | -1 | c.100 others(10): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
SPATA17_chr1_217626344_217876696 | 217808853 | CA | C | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(70): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(29): Show | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0041 others(70): Show |
73 | 252 | 0.2897 | -1 | c.100 others(10): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
SPATA17_chr1_217626344_217876696 | 217810495 | AC | A | intron_variant | MODIFIER | HG00438.hp1 HG00609.hp2 HG00738.hp2 others(29): Show |
a0001a0004 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0001a0001c0001t0005a0001c0002t0001others(6): Show | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0021 others(29): Show |
32 | 252 | 0.1270 | -1 | c.100 others(10): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
SPATA17_chr1_217626344_217876696 | 217811695 | GA | G | intron_variant | MODIFIER | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(30): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0008a0001c0001t0012a0001c0001t0042others(12): Show | a0001c0001t0008g0045 a0001c0001t0008g0049 a0001c0001t0008g0136 others(30): Show |
33 | 252 | 0.1310 | -1 | c.100 others(10): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
SPATA17_chr1_217626344_217876696 | 217816067 | GT | G | intron_variant | MODIFIER | HG02486.hp1 HG02572.hp2 HG02630.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0002t0022a0001c0003t0001others(3): Show | a0001c0001t0001g0123 a0001c0002t0022g0194 a0001c0002t0022g0196 others(4): Show |
7 | 252 | 0.0278 | -1 | c.100 others(11): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
SPATA17_chr1_217626344_217876696 | 217818882 | CT | C | intron_variant | MODIFIER | HG01109.hp1 HG01261.hp1 HG02055.hp1 others(13): Show |
a0001 | a0001c0001a0001c0002a0001c0004others(2): Show | a0001c0001t0004a0001c0001t0008a0001c0001t0018others(9): Show | a0001c0001t0004g0143 a0001c0001t0008g0045 a0001c0001t0018g0183 others(13): Show |
16 | 252 | 0.0635 | -1 | c.100 others(11): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
SPATA17_chr1_217626344_217876696 | 217820847 | CG | C | intron_variant | MODIFIER | HG02486.hp1 HG02572.hp2 HG02630.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0002t0022a0001c0003t0001others(3): Show | a0001c0001t0001g0123 a0001c0002t0022g0194 a0001c0002t0022g0196 others(4): Show |
7 | 252 | 0.0278 | -1 | c.100 others(11): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
SPATA17_chr1_217626344_217876696 | 217821685 | AT | A | intron_variant | MODIFIER | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0006 | a0001c0001t0001g0209 a0001c0001t0006g0096 a0001c0001t0006g0161 others(5): Show |
8 | 252 | 0.0318 | -1 | c.100 others(11): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
SPATA17_chr1_217626344_217876696 | 217822368 | TG | T | intron_variant | MODIFIER | HG00438.hp1 HG00609.hp2 HG00738.hp2 others(22): Show |
a0001a0004 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0001a0001c0002t0001a0001c0004t0001others(1): Show | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0021 others(22): Show |
25 | 252 | 0.0992 | -1 | c.100 others(11): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | TogoVar | |||||||
SPATA17_chr1_217626344_217876696 | 217822785 | AT | A | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(43): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(7): Show | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(43): Show |
46 | 252 | 0.1825 | -1 | c.100 others(11): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
SPATA17_chr1_217626344_217876696 | 217823265 | AG | A | intron_variant | MODIFIER | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0006 | a0001c0001t0001g0209 a0001c0001t0006g0096 a0001c0001t0006g0161 others(5): Show |
8 | 252 | 0.0318 | -1 | c.100 others(11): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
SPATA17_chr1_217626344_217876696 | 217823463 | AT | A | intron_variant | MODIFIER | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0006 | a0001c0001t0001g0209 a0001c0001t0006g0096 a0001c0001t0006g0161 others(5): Show |
8 | 252 | 0.0318 | -1 | c.100 others(11): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | TogoVar | |||||||
SPATA17_chr1_217626344_217876696 | 217827411 | CT | C | intron_variant | MODIFIER | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0006 | a0001c0001t0001g0209 a0001c0001t0006g0096 a0001c0001t0006g0161 others(5): Show |
8 | 252 | 0.0318 | -1 | c.100 others(11): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
SPATA17_chr1_217626344_217876696 | 217829627 | CA | C | intron_variant | MODIFIER | HG00140.hp2 HG01261.hp2 HG02055.hp1 others(19): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0004others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(15): Show | a0001c0001t0001g0037 a0001c0001t0001g0177 a0001c0001t0002g0038 others(19): Show |
22 | 252 | 0.0873 | -1 | c.100 others(11): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
SPATA17_chr1_217626344_217876696 | 217835728 | CT | C | intron_variant | MODIFIER | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0006 | a0001c0001t0001g0209 a0001c0001t0006g0096 a0001c0001t0006g0161 others(5): Show |
8 | 252 | 0.0318 | -1 | c.100 others(11): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | TogoVar | |||||||
SPATA17_chr1_217626344_217876696 | 217839706 | CT | C | intron_variant | MODIFIER | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(34): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0008a0001c0001t0012others(14): Show | a0001c0001t0001g0190 a0001c0001t0008g0045 a0001c0001t0008g0049 others(34): Show |
37 | 252 | 0.1468 | -1 | c.100 others(11): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
SPATA17_chr1_217626344_217876696 | 217842953 | CT | C | intron_variant | MODIFIER | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(31): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0008a0001c0001t0042others(13): Show | a0001c0001t0001g0148 a0001c0001t0008g0045 a0001c0001t0008g0049 others(31): Show |
34 | 252 | 0.1349 | -1 | c.100 others(11): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
SPATA17_chr1_217626344_217876696 | 217858708 | CA | C | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(63): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0016a0001c0001t0041others(13): Show | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(63): Show |
66 | 252 | 0.2619 | -1 | c.100 others(10): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
SPATA17_chr1_217626344_217876696 | 217863119 | CT | C | intron_variant | MODIFIER | HG01070.hp1 HG01074.hp1 HG01099.hp1 others(21): Show |
a0001a0003a0005 | a0001c0001a0001c0002a0001c0004others(2): Show | a0001c0001t0001a0001c0001t0006a0001c0001t0008others(12): Show | a0001c0001t0001g0154 a0001c0001t0006g0096 a0001c0001t0006g0161 others(21): Show |
24 | 252 | 0.0952 | -1 | c.*2+ others(7): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
SPATA17_chr1_217626344_217876696 | 217866840 | CT | C | intron_variant | MODIFIER | HG02015.hp1 HG02630.hp1 HG02965.hp2 others(3): Show |
a0001 | a0001c0001a0001c0002a0001c0011 | a0001c0001t0001a0001c0001t0002a0001c0001t0008others(3): Show | a0001c0001t0001g0041 a0001c0001t0002g0026 a0001c0001t0008g0045 others(3): Show |
6 | 252 | 0.0238 | -1 | c.*3- others(7): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
SPATA17_chr1_217626344_217876696 | 217868664 | GT | G | 3_prime_UTR_variant | MODIFIER | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(116): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0001a0001c0001t0010a0001c0001t0012others(32): Show | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(116): Show |
119 | 252 | 0.4722 | -1 | c.*16 others(6): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 11/11 | 5836 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
SPATA17_chr1_217626344_217876696 | 217876418 | TG | T | downstream_gene_variant | MODIFIER | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(21): Show |
a0001a0004 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0001a0001c0002t0001a0001c0004t0001others(1): Show | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(21): Show |
24 | 252 | 0.0952 | -1 | c.*94 others(6): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4723 | chr1 | TogoVar |