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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
SPAG16_chr2_213279464_214415501 | 213665373 | CACACACA others(5): Show |
C | intron_variant | MODIFIER | HG02976.hp1 NA20129.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0002 a0001c0001t0002g0001 |
2 | 86 | 0.0233 | -12 | c.107 others(35): Show |
SPAG16 | ENSG00000144451.20 | transcript | ENST00000331683.10 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SPAG16_chr2_213279464_214415501 | 213802395 | CTCTATCT others(5): Show |
C | intron_variant | MODIFIER | HG01361.hp2 HG01891.hp2 NA19086.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0014 a0001c0001t0001g0040 a0001c0001t0001g0068 others(1): Show |
4 | 86 | 0.0465 | -12 | c.107 others(33): Show |
SPAG16 | ENSG00000144451.20 | transcript | ENST00000331683.10 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SPAG16_chr2_213279464_214415501 | 213859178 | CAAAAAAA others(5): Show |
C | intron_variant | MODIFIER | NA19043.hp2 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0018 | 1 | 86 | 0.0116 | -12 | c.107 others(31): Show |
SPAG16 | ENSG00000144451.20 | transcript | ENST00000331683.10 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SPAG16_chr2_213279464_214415501 | 213859205 | AAAAAAAA others(5): Show |
A | intron_variant | MODIFIER | HG02293.hp2 | a0003 | a0003c0003 | a0003c0003t0001 | a0003c0003t0001g0031 | 1 | 86 | 0.0116 | -12 | c.107 others(31): Show |
SPAG16 | ENSG00000144451.20 | transcript | ENST00000331683.10 | protein_coding | 10/15 | chr2 | TogoVar | |||||||
SPAG16_chr2_213279464_214415501 | 213884129 | TTGTGGTA others(5): Show |
T | intron_variant | MODIFIER | HG00673.hp2 HG00735.hp2 HG01256.hp2 others(36): Show |
a0001a0002a0003others(4): Show | a0001c0001a0002c0002a0003c0003others(4): Show | a0001c0001t0001a0001c0001t0002a0002c0002t0002others(7): Show | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(36): Show |
39 | 86 | 0.4535 | -12 | c.121 others(33): Show |
SPAG16 | ENSG00000144451.20 | transcript | ENST00000331683.10 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SPAG16_chr2_213279464_214415501 | 213894987 | CAAAAAAA others(5): Show |
C | intron_variant | MODIFIER | HG02109.hp1 | a0003 | a0003c0003 | a0003c0003t0003 | a0003c0003t0003g0019 | 1 | 86 | 0.0116 | -12 | c.121 others(33): Show |
SPAG16 | ENSG00000144451.20 | transcript | ENST00000331683.10 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SPAG16_chr2_213279464_214415501 | 213932147 | CATATATA others(5): Show |
C | intron_variant | MODIFIER | HG02559.hp1 NA18522.hp2 NA19030.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0078 a0001c0001t0002g0008 a0001c0001t0002g0009 |
3 | 86 | 0.0349 | -12 | c.140 others(31): Show |
SPAG16 | ENSG00000144451.20 | transcript | ENST00000331683.10 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SPAG16_chr2_213279464_214415501 | 214037864 | GGTGTGTG others(5): Show |
G | intron_variant | MODIFIER | HG01256.hp1 HG01496.hp2 NA18522.hp2 others(1): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0002c0002t0001 | a0001c0001t0001g0069 a0001c0001t0002g0009 a0002c0002t0001g0053 others(1): Show |
4 | 86 | 0.0465 | -12 | c.152 others(33): Show |
SPAG16 | ENSG00000144451.20 | transcript | ENST00000331683.10 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SPAG16_chr2_213279464_214415501 | 214041974 | GTGTGTAT others(5): Show |
G | intron_variant | MODIFIER | HG02717.hp1 NA19043.hp1 |
a0003a0006 | a0003c0003a0006c0006 | a0003c0003t0001a0006c0006t0001 | a0003c0003t0001g0080 a0006c0006t0001g0024 |
2 | 86 | 0.0233 | -12 | c.152 others(33): Show |
SPAG16 | ENSG00000144451.20 | transcript | ENST00000331683.10 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SPAG16_chr2_213279464_214415501 | 214059186 | CTATATAT others(5): Show |
C | intron_variant | MODIFIER | HG01256.hp1 HG01361.hp2 HG01496.hp2 others(13): Show |
a0001a0002a0004 | a0001c0001a0002c0002a0004c0004 | a0001c0001t0001a0001c0001t0002a0002c0002t0001others(2): Show | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0071 others(13): Show |
16 | 86 | 0.1861 | -12 | c.152 others(33): Show |
SPAG16 | ENSG00000144451.20 | transcript | ENST00000331683.10 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SPAG16_chr2_213279464_214415501 | 214059234 | ATATATAT others(5): Show |
A | intron_variant | MODIFIER | NA19000.hp1 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0057 | 1 | 86 | 0.0116 | -12 | c.152 others(33): Show |
SPAG16 | ENSG00000144451.20 | transcript | ENST00000331683.10 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SPAG16_chr2_213279464_214415501 | 214059248 | ATATATAT others(5): Show |
A | intron_variant | MODIFIER | HG01496.hp2 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0053 | 1 | 86 | 0.0116 | -12 | c.152 others(33): Show |
SPAG16 | ENSG00000144451.20 | transcript | ENST00000331683.10 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SPAG16_chr2_213279464_214415501 | 214108439 | TCACACAC others(5): Show |
T | intron_variant | MODIFIER | HG01256.hp2 HG02647.hp1 HG02886.hp2 others(2): Show |
a0001a0003a0005others(1): Show | a0001c0001a0003c0003a0005c0005others(1): Show | a0001c0001t0001a0003c0003t0001a0005c0005t0001others(1): Show | a0001c0001t0001g0065 a0001c0001t0001g0066 a0003c0003t0001g0032 others(2): Show |
5 | 86 | 0.0581 | -12 | c.159 others(29): Show |
SPAG16 | ENSG00000144451.20 | transcript | ENST00000331683.10 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SPAG16_chr2_213279464_214415501 | 214108469 | ACACACAC others(5): Show |
A | intron_variant | MODIFIER | HG03130.hp2 HG03195.hp2 NA19030.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0001 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0002c0002t0001g0011 |
3 | 86 | 0.0349 | -12 | c.159 others(29): Show |
SPAG16 | ENSG00000144451.20 | transcript | ENST00000331683.10 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SPAG16_chr2_213279464_214415501 | 214165469 | CTTTTTTT others(5): Show |
C | intron_variant | MODIFIER | HG02015.hp1 HG03490.hp1 |
a0001a0007 | a0001c0001a0007c0007 | a0001c0001t0001a0007c0007t0001 | a0001c0001t0001g0015 a0007c0007t0001g0083 |
2 | 86 | 0.0233 | -12 | c.172 others(33): Show |
SPAG16 | ENSG00000144451.20 | transcript | ENST00000331683.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SPAG16_chr2_213279464_214415501 | 214177971 | GTATATAT others(5): Show |
G | intron_variant | MODIFIER | HG01496.hp2 HG02559.hp1 HG03098.hp1 others(3): Show |
a0001a0002a0005 | a0001c0001a0002c0002a0005c0005 | a0001c0001t0001a0001c0001t0002a0002c0002t0001others(1): Show | a0001c0001t0001g0013 a0001c0001t0001g0040 a0001c0001t0002g0007 others(3): Show |
6 | 86 | 0.0698 | -12 | c.172 others(33): Show |
SPAG16 | ENSG00000144451.20 | transcript | ENST00000331683.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SPAG16_chr2_213279464_214415501 | 214193426 | TGAGAGAG others(5): Show |
T | intron_variant | MODIFIER | HG01256.hp1 HG02293.hp1 HG02647.hp1 others(2): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0001 | a0001c0001t0001g0066 a0001c0001t0001g0071 a0002c0002t0001g0003 others(2): Show |
5 | 86 | 0.0581 | -12 | c.172 others(33): Show |
SPAG16 | ENSG00000144451.20 | transcript | ENST00000331683.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SPAG16_chr2_213279464_214415501 | 214248287 | ATATTATT others(5): Show |
A | intron_variant | MODIFIER | HG02615.hp1 HG02886.hp2 NA19043.hp1 |
a0001a0005a0006 | a0001c0001a0005c0005a0006c0006 | a0001c0001t0002a0005c0005t0001a0006c0006t0001 | a0001c0001t0002g0067 a0005c0005t0001g0081 a0006c0006t0001g0024 |
3 | 86 | 0.0349 | -12 | c.172 others(33): Show |
SPAG16 | ENSG00000144451.20 | transcript | ENST00000331683.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SPAG16_chr2_213279464_214415501 | 214250749 | TATATATA others(5): Show |
T | intron_variant | MODIFIER | HG02109.hp1 HG03130.hp1 |
a0002a0003 | a0002c0002a0003c0003 | a0002c0002t0001a0003c0003t0003 | a0002c0002t0001g0075 a0003c0003t0003g0019 |
2 | 86 | 0.0233 | -12 | c.172 others(35): Show |
SPAG16 | ENSG00000144451.20 | transcript | ENST00000331683.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SPAG16_chr2_213279464_214415501 | 214250751 | TATATATA others(5): Show |
T | intron_variant | MODIFIER | HG03225.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0072 | 1 | 86 | 0.0116 | -12 | c.172 others(35): Show |
SPAG16 | ENSG00000144451.20 | transcript | ENST00000331683.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SPAG16_chr2_213279464_214415501 | 214250753 | TATATAGA others(5): Show |
T | intron_variant | MODIFIER | HG00735.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0027 | 1 | 86 | 0.0116 | -12 | c.172 others(35): Show |
SPAG16 | ENSG00000144451.20 | transcript | ENST00000331683.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SPAG16_chr2_213279464_214415501 | 214284797 | CTGTGTGT others(5): Show |
C | intron_variant | MODIFIER | HG00673.hp1 HG01256.hp2 HG01361.hp2 others(10): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0003c0003others(1): Show | a0001c0001t0001a0002c0002t0001a0003c0003t0001others(1): Show | a0001c0001t0001g0014 a0001c0001t0001g0040 a0001c0001t0001g0048 others(10): Show |
13 | 86 | 0.1512 | -12 | c.172 others(35): Show |
SPAG16 | ENSG00000144451.20 | transcript | ENST00000331683.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SPAG16_chr2_213279464_214415501 | 214315501 | TTTTATTT others(5): Show |
T | intron_variant | MODIFIER | HG01361.hp1 HG02109.hp1 HG03098.hp2 others(5): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0003 | a0001c0001t0001a0001c0001t0002a0002c0002t0001others(2): Show | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(5): Show |
8 | 86 | 0.0930 | -12 | c.172 others(33): Show |
SPAG16 | ENSG00000144451.20 | transcript | ENST00000331683.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SPAG16_chr2_213279464_214415501 | 214323328 | ATATATAT others(5): Show |
A | intron_variant | MODIFIER | NA19086.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0040 | 1 | 86 | 0.0116 | -12 | c.172 others(33): Show |
SPAG16 | ENSG00000144451.20 | transcript | ENST00000331683.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SPAG17_chr1_117948590_118190228 | 118051692 | GTATGTAT others(5): Show |
G | intron_variant | MODIFIER | NA20300.hp1 | a0004 | a0004c0005 | a0004c0005t0001 | a0004c0005t0001g0080 | 1 | 266 | 0.0038 | -12 | c.281 others(31): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | TogoVar | |||||||
SPAG17_chr1_117948590_118190228 | 118073255 | CTAGCTTC others(5): Show |
C | intron_variant | MODIFIER | HG03710.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0178 | 1 | 266 | 0.0038 | -12 | c.238 others(29): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | TogoVar | |||||||
SPAG1_chr8_100153587_100246904 | 100170800 | CATTTATT others(5): Show |
C | intron_variant | MODIFIER | HG01243.hp1 HG01257.hp2 HG01258.hp1 others(11): Show |
a0002a0003 | a0002c0001a0003c0004a0003c0018 | a0002c0001t0001a0003c0004t0001a0003c0018t0001 | a0002c0001t0001g0007 a0002c0001t0001g0008 a0002c0001t0001g0010 others(11): Show |
14 | 366 | 0.0383 | -12 | c.300 others(29): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SPAG1_chr8_100153587_100246904 | 100202709 | CAAAAAAA others(5): Show |
C | intron_variant | MODIFIER | HG02258.hp2 HG02818.hp2 NA20300.hp1 |
a0002 | a0002c0007 | a0002c0007t0001 | a0002c0007t0001g0194 a0002c0007t0001g0195 a0002c0007t0001g0196 |
3 | 366 | 0.0082 | -12 | c.109 others(31): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SPAG1_chr8_100153587_100246904 | 100214988 | CATATATA others(5): Show |
C | intron_variant | MODIFIER | HG00673.hp2 HG01109.hp1 HG02015.hp1 others(4): Show |
a0001a0002 | a0001c0002a0001c0003a0002c0001 | a0001c0002t0001a0001c0003t0001a0002c0001t0001 | a0001c0002t0001g0098 a0001c0002t0001g0124 a0001c0002t0001g0169 others(4): Show |
7 | 366 | 0.0191 | -12 | c.153 others(31): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SPAG4_chr20_35610829_35626094 | 35615424 | AAAAGAAA others(5): Show |
A | upstream_gene_variant | MODIFIER | HG00642.hp2 HG01515.hp2 HG02723.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0042 |
3 | 320 | 0.0094 | -12 | c.-57 others(21): Show |
SPAG4 | ENSG00000061656.11 | transcript | ENST00000374273.8 | protein_coding | 404 | chr20 | TogoVar | |||||||
SPAG6_chr10_22340496_22422610 | 22346430 | GTTCTTCT others(5): Show |
G | intron_variant | MODIFIER | HG02602.hp1 HG02698.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0008 | a0001c0001t0001g0127 a0002c0002t0008g0007 |
2 | 142 | 0.0141 | -12 | c.121 others(27): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | ||||||
SPAG8_chr9_35804795_35817262 | 35811488 | ACCAGGAC others(5): Show |
A | disruptive_inframe_deletion | MODERATE | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(144): Show |
a0002a0006a0007 | a0002c0002a0002c0005a0002c0006others(7): Show | a0002c0002t0001a0002c0005t0001a0002c0006t0001others(7): Show | a0002c0002t0001g0002 a0002c0002t0001g0010 a0002c0005t0001g0005 others(8): Show |
147 | 420 | 0.3500 | -12 | c.546 others(19): Show |
p.Ser others(13): Show |
SPAG8 | ENSG00000137098.14 | transcript | ENST00000396638.7 | protein_coding | 2/7 | 672/1716 | 546/1458 | 182/485 | chr9 | TogoVar | |||
SPAG9_chr17_50957174_51125868 | 50981390 | GTGGATGG others(5): Show |
G | intron_variant | MODIFIER | HG01069.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0020 | 1 | 292 | 0.0034 | -12 | c.323 others(31): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 25/29 | chr17 | TogoVar | |||||||
SPAG9_chr17_50957174_51125868 | 50981483 | AAGATAGA others(5): Show |
A | intron_variant | MODIFIER | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(40): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0005others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(5): Show | a0001c0001t0001g0200 a0001c0001t0001g0204 a0001c0001t0001g0212 others(40): Show |
43 | 292 | 0.1473 | -12 | c.323 others(31): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 25/29 | chr17 | TogoVar | |||||||
SPAG9_chr17_50957174_51125868 | 50998022 | ATTTTTTT others(5): Show |
A | intron_variant | MODIFIER | HG03239.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0147 | 1 | 292 | 0.0034 | -12 | c.183 others(29): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 15/29 | chr17 | TogoVar | |||||||
SPAG9_chr17_50957174_51125868 | 51000743 | CAATAAAT others(5): Show |
C | intron_variant | MODIFIER | HG01891.hp2 HG02809.hp1 HG02896.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0151 others(2): Show |
5 | 292 | 0.0171 | -12 | c.160 others(29): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 13/29 | chr17 | TogoVar | |||||||
SPAG9_chr17_50957174_51125868 | 51000751 | GAATGAAT others(5): Show |
G | intron_variant | MODIFIER | HG02615.hp1 HG02895.hp1 HG02896.hp1 others(3): Show |
a0002 | a0002c0003 | a0002c0003t0010a0002c0003t0011a0002c0003t0018 | a0002c0003t0010g0194 a0002c0003t0010g0195 a0002c0003t0010g0196 others(3): Show |
6 | 292 | 0.0206 | -12 | c.160 others(29): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 13/29 | chr17 | TogoVar | |||||||
SPAG9_chr17_50957174_51125868 | 51007110 | GGTGTGTG others(5): Show |
G | intron_variant | MODIFIER | HG04204.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0191 | 1 | 292 | 0.0034 | -12 | c.127 others(29): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 10/29 | chr17 | TogoVar | |||||||
SPAG9_chr17_50957174_51125868 | 51012722 | CTTTATTT others(5): Show |
C | intron_variant | MODIFIER | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(65): Show |
a0001a0002 | a0001c0001a0001c0005a0001c0007others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(4): Show | a0001c0001t0001g0200 a0001c0001t0001g0202 a0001c0001t0001g0204 others(65): Show |
68 | 292 | 0.2329 | -12 | c.121 others(31): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 9/29 | chr17 | TogoVar | |||||||
SPAG9_chr17_50957174_51125868 | 51013907 | CACACACA others(5): Show |
C | intron_variant | MODIFIER | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(8): Show |
a0001 | a0001c0002 | a0001c0002t0001a0001c0002t0004 | a0001c0002t0001g0267 a0001c0002t0001g0268 a0001c0002t0001g0269 others(8): Show |
11 | 292 | 0.0377 | -12 | c.121 others(29): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 9/29 | chr17 | TogoVar | |||||||
SPAG9_chr17_50957174_51125868 | 51053850 | AAAAAGTA others(5): Show |
A | intron_variant | MODIFIER | HG03195.hp1 HG03486.hp2 |
a0002 | a0002c0003 | a0002c0003t0008 | a0002c0003t0008g0170 a0002c0003t0008g0257 |
2 | 292 | 0.0069 | -12 | c.495 others(29): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | TogoVar | |||||||
SPAG9_chr17_50957174_51125868 | 51053855 | GTATATAT others(5): Show |
G | intron_variant | MODIFIER | HG02683.hp2 HG03654.hp2 NA18970.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0006a0001c0001t0009 | a0001c0001t0002g0082 a0001c0001t0002g0172 a0001c0001t0006g0106 others(2): Show |
5 | 292 | 0.0171 | -12 | c.495 others(29): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | TogoVar | |||||||
SPAG9_chr17_50957174_51125868 | 51075195 | CAAAAAAA others(5): Show |
C | intron_variant | MODIFIER | NA20300.hp1 | a0001 | a0001c0005 | a0001c0005t0001 | a0001c0005t0001g0241 | 1 | 292 | 0.0034 | -12 | c.424 others(29): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | TogoVar | |||||||
SPAG9_chr17_50957174_51125868 | 51077017 | GCTATCTA others(5): Show |
G | intron_variant | MODIFIER | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(10): Show |
a0001 | a0001c0002 | a0001c0002t0001a0001c0002t0004 | a0001c0002t0001g0267 a0001c0002t0001g0268 a0001c0002t0001g0269 others(10): Show |
13 | 292 | 0.0445 | -12 | c.424 others(29): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | TogoVar | |||||||
SPAG9_chr17_50957174_51125868 | 51077041 | TCTAGCTA others(5): Show |
T | intron_variant | MODIFIER | HG02572.hp2 HG02723.hp1 NA18994.hp1 others(2): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0003a0001c0002t0023a0001c0002t0024 | a0001c0001t0003g0042 a0001c0001t0003g0046 a0001c0001t0003g0048 others(2): Show |
5 | 292 | 0.0171 | -12 | c.424 others(29): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | TogoVar | |||||||
SPAG9_chr17_50957174_51125868 | 51077093 | TCTATCTA others(5): Show |
T | intron_variant | MODIFIER | HG02965.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0159 | 1 | 292 | 0.0034 | -12 | c.424 others(29): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | TogoVar | |||||||
SPAG9_chr17_50957174_51125868 | 51089618 | TTTTATAT others(5): Show |
T | intron_variant | MODIFIER | NA21309.hp1 | a0002 | a0002c0003 | a0002c0003t0011 | a0002c0003t0011g0193 | 1 | 292 | 0.0034 | -12 | c.304 others(29): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | TogoVar | |||||||
SPAG9_chr17_50957174_51125868 | 51089620 | TTATATAT others(5): Show |
T | intron_variant | MODIFIER | NA18955.hp1 | a0001 | a0001c0005 | a0001c0005t0001 | a0001c0005t0001g0264 | 1 | 292 | 0.0034 | -12 | c.304 others(29): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | TogoVar | |||||||
SPAG9_chr17_50957174_51125868 | 51089653 | TATATATA others(5): Show |
T | intron_variant | MODIFIER | homoSapiens_chm13v2.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0260 | 1 | 292 | 0.0034 | -12 | c.304 others(29): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | TogoVar | |||||||
SPAG9_chr17_50957174_51125868 | 51095296 | TAAAAAAA others(5): Show |
T | intron_variant | MODIFIER | HG01515.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0217 | 1 | 292 | 0.0034 | -12 | c.304 others(31): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | TogoVar |