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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
TMEM135_chr11_87032934_87333824 | 87122357 | AAAT | A | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00597.hp2 others(111): Show |
a0001a0002a0003others(3): Show | a0001c0001a0002c0002a0003c0003others(3): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(25): Show | a0001c0001t0002g0002 a0001c0001t0002g0029 a0001c0001t0002g0032 others(111): Show |
114 | 274 | 0.4161 | -3 | c.396 others(22): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TMEM135_chr11_87032934_87333824 | 87130119 | TTTA | T | intron_variant | MODIFIER | HG02056.hp2 HG02132.hp2 HG02155.hp1 others(1): Show |
a0001a0005 | a0001c0001a0005c0004 | a0001c0001t0002a0005c0004t0043 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0134 others(1): Show |
4 | 274 | 0.0146 | -3 | c.397 others(22): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 4/14 | chr11 | TogoVar | |||||||
TMEM135_chr11_87032934_87333824 | 87131631 | GAAT | G | intron_variant | MODIFIER | HG00544.hp1 HG01081.hp2 HG01978.hp2 others(17): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0007a0001c0001t0008a0001c0001t0012others(6): Show | a0001c0001t0007g0025 a0001c0001t0007g0223 a0001c0001t0008g0241 others(17): Show |
20 | 274 | 0.0730 | -3 | c.397 others(22): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TMEM135_chr11_87032934_87333824 | 87132673 | TAAC | T | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00597.hp2 others(93): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0002a0003c0003others(2): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(20): Show | a0001c0001t0002g0002 a0001c0001t0002g0029 a0001c0001t0002g0032 others(93): Show |
96 | 274 | 0.3504 | -3 | c.397 others(22): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TMEM135_chr11_87032934_87333824 | 87137724 | TGGG | T | intron_variant | MODIFIER | HG00544.hp1 HG00609.hp1 HG01081.hp2 others(31): Show |
a0001a0002a0006 | a0001c0001a0002c0002a0006c0006 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(12): Show | a0001c0001t0002g0229 a0001c0001t0004g0143 a0001c0001t0006g0144 others(31): Show |
34 | 274 | 0.1241 | -3 | c.397 others(22): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TMEM135_chr11_87032934_87333824 | 87150215 | CAAA | C | intron_variant | MODIFIER | HG00280.hp2 HG00597.hp2 HG00621.hp2 others(106): Show |
a0001a0002a0003others(3): Show | a0001c0001a0002c0002a0003c0003others(3): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(24): Show | a0001c0001t0002g0029 a0001c0001t0002g0032 a0001c0001t0002g0037 others(106): Show |
109 | 274 | 0.3978 | -3 | c.397 others(20): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TMEM135_chr11_87032934_87333824 | 87175354 | CTGA | C | intron_variant | MODIFIER | HG00544.hp1 HG00609.hp1 HG01081.hp2 others(30): Show |
a0001a0002a0006 | a0001c0001a0002c0002a0006c0006 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(12): Show | a0001c0001t0002g0229 a0001c0001t0004g0143 a0001c0001t0006g0144 others(30): Show |
33 | 274 | 0.1204 | -3 | c.462 others(22): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TMEM135_chr11_87032934_87333824 | 87179938 | CTGT | C | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(57): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0003c0003others(1): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(14): Show | a0001c0001t0002g0029 a0001c0001t0002g0064 a0001c0001t0002g0065 others(57): Show |
60 | 274 | 0.2190 | -3 | c.462 others(22): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TMEM135_chr11_87032934_87333824 | 87183135 | ATTT | A | intron_variant | MODIFIER | HG00544.hp1 HG00609.hp1 HG01081.hp2 others(29): Show |
a0001a0002a0006 | a0001c0001a0002c0002a0006c0006 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(11): Show | a0001c0001t0002g0229 a0001c0001t0004g0143 a0001c0001t0006g0144 others(29): Show |
32 | 274 | 0.1168 | -3 | c.462 others(22): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TMEM135_chr11_87032934_87333824 | 87183955 | CAAA | C | intron_variant | MODIFIER | HG00140.hp1 HG01081.hp2 HG01123.hp1 others(20): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0002a0001c0001t0007a0001c0001t0008others(9): Show | a0001c0001t0002g0229 a0001c0001t0007g0025 a0001c0001t0007g0223 others(20): Show |
23 | 274 | 0.0839 | -3 | c.462 others(22): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TMEM135_chr11_87032934_87333824 | 87212824 | GAAA | G | intron_variant | MODIFIER | HG00544.hp1 HG00609.hp1 HG01081.hp2 others(28): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(10): Show | a0001c0001t0002g0229 a0001c0001t0004g0143 a0001c0001t0006g0144 others(28): Show |
31 | 274 | 0.1131 | -3 | c.463 others(22): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TMEM135_chr11_87032934_87333824 | 87222687 | CCAG | C | intron_variant | MODIFIER | HG00544.hp1 HG01081.hp2 HG01978.hp2 others(15): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0007a0001c0001t0008a0001c0001t0012others(5): Show | a0001c0001t0007g0025 a0001c0001t0007g0223 a0001c0001t0008g0241 others(15): Show |
18 | 274 | 0.0657 | -3 | c.463 others(22): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TMEM135_chr11_87032934_87333824 | 87222822 | AAAG | A | intron_variant | MODIFIER | HG00609.hp1 HG01243.hp1 HG01346.hp1 others(11): Show |
a0001a0002a0006 | a0001c0001a0002c0002a0006c0006 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(4): Show | a0001c0001t0002g0229 a0001c0001t0004g0143 a0001c0001t0006g0144 others(11): Show |
14 | 274 | 0.0511 | -3 | c.463 others(22): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TMEM135_chr11_87032934_87333824 | 87278984 | ATTT | A | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(46): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0003 | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(14): Show | a0001c0001t0002g0002 a0001c0001t0002g0029 a0001c0001t0002g0032 others(46): Show |
49 | 274 | 0.1788 | -3 | c.510 others(22): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TMEM135_chr11_87032934_87333824 | 87280052 | GTTA | G | intron_variant | MODIFIER | HG02818.hp1 HG03540.hp1 |
a0001a0003 | a0001c0001a0003c0003 | a0001c0001t0052a0003c0003t0041 | a0001c0001t0052g0262 a0003c0003t0041g0268 |
2 | 274 | 0.0073 | -3 | c.510 others(22): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TMEM135_chr11_87032934_87333824 | 87284523 | ATCG | A | intron_variant | MODIFIER | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(67): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0003c0003others(1): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(17): Show | a0001c0001t0002g0114 a0001c0001t0003g0015 a0001c0001t0003g0053 others(67): Show |
70 | 274 | 0.2555 | -3 | c.510 others(22): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TMEM135_chr11_87032934_87333824 | 87289437 | CTTT | C | intron_variant | MODIFIER | HG00544.hp2 HG00673.hp1 HG01081.hp2 others(36): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0003c0003others(1): Show | a0001c0001t0004a0001c0001t0005a0001c0001t0007others(13): Show | a0001c0001t0004g0001 a0001c0001t0004g0107 a0001c0001t0004g0109 others(36): Show |
39 | 274 | 0.1423 | -3 | c.510 others(20): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TMEM135_chr11_87032934_87333824 | 87291515 | ATTT | A | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp1 HG01109.hp1 others(26): Show |
a0001a0002a0004 | a0001c0001a0002c0002a0004c0008 | a0001c0001t0002a0001c0001t0005a0001c0001t0007others(10): Show | a0001c0001t0002g0029 a0001c0001t0002g0086 a0001c0001t0002g0097 others(26): Show |
29 | 274 | 0.1058 | -3 | c.510 others(20): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TMEM135_chr11_87032934_87333824 | 87315146 | TTCC | T | intron_variant | MODIFIER | NA18951.hp2 NA18990.hp2 NA18994.hp1 others(2): Show |
a0002a0003 | a0002c0002a0003c0003 | a0002c0002t0001a0003c0003t0035 | a0002c0002t0001g0132 a0002c0002t0001g0136 a0002c0002t0001g0137 others(2): Show |
5 | 274 | 0.0183 | -3 | c.107 others(20): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TMEM135_chr11_87032934_87333824 | 87332225 | AAGT | A | downstream_gene_variant | MODIFIER | HG00099.hp2 HG00280.hp1 HG00735.hp2 others(41): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0009a0001c0001t0012others(2): Show | a0001c0001t0002g0002 a0001c0001t0002g0029 a0001c0001t0002g0032 others(41): Show |
44 | 274 | 0.1606 | -3 | c.*10 others(16): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 3402 | chr11 | TogoVar | |||||||
TMEM139_chr7_143279958_143293048 | 143282161 | GTAT | G | upstream_gene_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
a0001a0002a0005 | a0001c0001a0001c0002a0002c0003others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(3): Show | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0003g0001 others(4): Show |
188 | 304 | 0.6184 | -3 | c.-33 others(14): Show |
TMEM139 | ENSG00000178826.11 | transcript | ENST00000359333.8 | protein_coding | 2796 | chr7 | TogoVar | |||||||
TMEM140_chr7_135143072_135171215 | 135144938 | TAAA | T | upstream_gene_variant | MODIFIER | HG00639.hp2 HG00735.hp2 HG01261.hp2 others(20): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0004a0001c0001t0009others(1): Show | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0010 others(9): Show |
23 | 388 | 0.0593 | -3 | c.-33 others(14): Show |
TMEM140 | ENSG00000146859.6 | transcript | ENST00000275767.3 | protein_coding | 3133 | chr7 | TogoVar | |||||||
TMEM140_chr7_135143072_135171215 | 135158704 | AAAG | A | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(162): Show |
a0001a0005 | a0001c0001a0005c0006 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(3): Show | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0006 others(46): Show |
165 | 388 | 0.4253 | -3 | c.-24 others(20): Show |
TMEM140 | ENSG00000146859.6 | transcript | ENST00000275767.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
TMEM143_chr19_48327356_48368940 | 48338850 | CGGG | C | intron_variant | MODIFIER | HG02257.hp2 HG02280.hp2 HG02717.hp1 |
a0001 | a0001c0002 | a0001c0002t0004 | a0001c0002t0004g0012 a0001c0002t0004g0319 |
3 | 350 | 0.0086 | -3 | c.975 others(20): Show |
TMEM143 | ENSG00000161558.11 | transcript | ENST00000293261.8 | protein_coding | 6/7 | chr19 | TogoVar | |||||||
TMEM143_chr19_48327356_48368940 | 48340121 | ATTT | A | intron_variant | MODIFIER | HG00099.hp2 HG00423.hp1 HG00642.hp1 others(40): Show |
a0001 | a0001c0003a0001c0004 | a0001c0003t0003a0001c0004t0003 | a0001c0003t0003g0001 a0001c0003t0003g0003 a0001c0003t0003g0004 others(32): Show |
43 | 350 | 0.1229 | -3 | c.975 others(20): Show |
TMEM143 | ENSG00000161558.11 | transcript | ENST00000293261.8 | protein_coding | 6/7 | chr19 | TogoVar | |||||||
TMEM143_chr19_48327356_48368940 | 48350919 | CAAA | C | intron_variant | MODIFIER | HG00673.hp2 HG01168.hp2 HG01169.hp1 others(14): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0002t0004a0001c0003t0002others(2): Show | a0001c0001t0001g0154 a0001c0001t0001g0161 a0001c0001t0001g0187 others(14): Show |
17 | 350 | 0.0486 | -3 | c.370 others(20): Show |
TMEM143 | ENSG00000161558.11 | transcript | ENST00000293261.8 | protein_coding | 3/7 | chr19 | TogoVar | |||||||
TMEM143_chr19_48327356_48368940 | 48354264 | CTTT | C | intron_variant | MODIFIER | HG01884.hp1 HG02486.hp2 HG02630.hp2 others(5): Show |
a0001 | a0001c0002 | a0001c0002t0001a0001c0002t0005 | a0001c0002t0001g0071 a0001c0002t0005g0065 a0001c0002t0005g0066 others(5): Show |
8 | 350 | 0.0229 | -3 | c.369 others(20): Show |
TMEM143 | ENSG00000161558.11 | transcript | ENST00000293261.8 | protein_coding | 3/7 | chr19 | TogoVar | |||||||
TMEM144_chr4_158205486_158260416 | 158209901 | TACA | T | upstream_gene_variant | MODIFIER | HG02145.hp2 HG02486.hp1 HG02572.hp2 |
a0001 | a0001c0001 | a0001c0001t0016 | a0001c0001t0016g0056 a0001c0001t0016g0057 a0001c0001t0016g0117 |
3 | 274 | 0.0110 | -3 | c.-86 others(12): Show |
TMEM144 | ENSG00000164124.11 | transcript | ENST00000296529.11 | protein_coding | 584 | chr4 | TogoVar | |||||||
TMEM144_chr4_158205486_158260416 | 158254435 | GTTT | G | 3_prime_UTR_variant | MODIFIER | HG00639.hp1 HG01070.hp1 HG01081.hp2 others(35): Show |
a0001a0005 | a0001c0001a0005c0007 | a0001c0001t0003a0001c0001t0014a0001c0001t0016others(12): Show | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0016 others(34): Show |
38 | 274 | 0.1387 | -3 | c.*93 others(12): Show |
TMEM144 | ENSG00000164124.11 | transcript | ENST00000296529.11 | protein_coding | 13/13 | 930 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
TMEM147_chr19_35540626_35552526 | 35546186 | CAGT | C | intron_variant | MODIFIER | HG00609.hp2 HG02071.hp2 HG02080.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0008 | 5 | 424 | 0.0118 | -3 | c.147 others(18): Show |
TMEM147 | ENSG00000105677.12 | transcript | ENST00000222284.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
TMEM14A_chr6_52666113_52691588 | 52670030 | CCTT | C | upstream_gene_variant | MODIFIER | HG00280.hp2 HG00597.hp2 HG01081.hp2 others(26): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0004 a0001c0001t0002g0037 a0001c0001t0002g0038 others(23): Show |
29 | 426 | 0.0681 | -3 | c.-12 others(14): Show |
TMEM14A | ENSG00000096092.6 | transcript | ENST00000211314.5 | protein_coding | 1082 | chr6 | TogoVar | |||||||
TMEM14A_chr6_52666113_52691588 | 52674889 | CTTT | C | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(212): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(2): Show | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(167): Show |
215 | 426 | 0.5047 | -3 | c.-16 others(20): Show |
TMEM14A | ENSG00000096092.6 | transcript | ENST00000211314.5 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
TMEM14A_chr6_52666113_52691588 | 52690592 | TATC | T | downstream_gene_variant | MODIFIER | HG01106.hp2 HG02572.hp2 HG02895.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0045 a0001c0001t0001g0197 a0001c0001t0001g0242 |
4 | 426 | 0.0094 | -3 | c.*45 others(14): Show |
TMEM14A | ENSG00000096092.6 | transcript | ENST00000211314.5 | protein_coding | 4005 | chr6 | TogoVar | |||||||
TMEM14B_chr6_10742805_10761981 | 10747097 | AGAG | A | upstream_gene_variant | MODIFIER | HG01884.hp1 HG02451.hp1 HG02723.hp2 others(12): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0004 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0028 others(3): Show |
15 | 440 | 0.0341 | -3 | c.-82 others(12): Show |
TMEM14B | ENSG00000137210.14 | transcript | ENST00000379542.10 | protein_coding | 707 | chr6 | TogoVar | |||||||
TMEM14C_chr6_10718070_10736127 | 10734856 | AAAC | A | downstream_gene_variant | MODIFIER | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(20): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(2): Show | a0001c0001t0002g0038 a0001c0001t0003g0004 a0001c0001t0003g0038 others(6): Show |
23 | 438 | 0.0525 | -3 | c.*41 others(14): Show |
TMEM14C | ENSG00000111843.14 | transcript | ENST00000229563.6 | protein_coding | 3730 | chr6 | TogoVar | |||||||
TMEM150A_chr2_85593547_85607698 | 85599771 | TCTC | T | intron_variant | MODIFIER | HG00741.hp1 HG01081.hp2 HG01168.hp1 others(8): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0001 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0032 others(1): Show |
11 | 386 | 0.0285 | -3 | c.397 others(16): Show |
TMEM150A | ENSG00000168890.14 | transcript | ENST00000334462.10 | protein_coding | 6/7 | chr2 | TogoVar | |||||||
TMEM150C_chr4_82478176_82566988 | 82480365 | CTTT | C | downstream_gene_variant | MODIFIER | HG01891.hp2 HG02572.hp1 HG02630.hp2 others(8): Show |
a0001 | a0001c0001 | a0001c0001t0006a0001c0001t0034 | a0001c0001t0006g0005 a0001c0001t0006g0025 a0001c0001t0006g0081 others(8): Show |
11 | 256 | 0.0430 | -3 | c.*51 others(14): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 2810 | chr4 | TogoVar | |||||||
TMEM150C_chr4_82478176_82566988 | 82489411 | ACCT | A | intron_variant | MODIFIER | HG02165.hp1 HG03098.hp2 NA18961.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0035 others(4): Show |
7 | 256 | 0.0273 | -3 | c.541 others(18): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | TogoVar | |||||||
TMEM150C_chr4_82478176_82566988 | 82492117 | TTTG | T | intron_variant | MODIFIER | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(132): Show |
a0001a0002a0003 | a0001c0001a0002c0003a0003c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(28): Show | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0035 others(131): Show |
135 | 256 | 0.5273 | -3 | c.364 others(20): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | TogoVar | |||||||
TMEM150C_chr4_82478176_82566988 | 82499424 | AAAG | A | intron_variant | MODIFIER | HG02818.hp1 HG02886.hp1 HG03195.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0017a0001c0001t0034 | a0001c0001t0004g0114 a0001c0001t0017g0145 a0001c0001t0017g0147 others(1): Show |
4 | 256 | 0.0156 | -3 | c.236 others(20): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | TogoVar | |||||||
TMEM150C_chr4_82478176_82566988 | 82539357 | AATT | A | intron_variant | MODIFIER | HG02895.hp2 HG03225.hp1 |
a0001 | a0001c0001 | a0001c0001t0007a0001c0001t0031 | a0001c0001t0007g0077 a0001c0001t0031g0028 |
2 | 256 | 0.0078 | -3 | c.-11 others(22): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | TogoVar | |||||||
TMEM151A_chr11_66286894_66301664 | 66295720 | ATTG | A | 3_prime_UTR_variant | MODIFIER | HG02145.hp1 HG02572.hp2 HG02615.hp1 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0011a0001c0001t0012 | a0001c0001t0011g0004 a0001c0001t0011g0029 a0001c0001t0012g0002 others(1): Show |
8 | 450 | 0.0178 | -3 | c.*72 others(10): Show |
TMEM151A | ENSG00000179292.5 | transcript | ENST00000327259.5 | protein_coding | 2/2 | 72 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
TMEM151B_chr6_44265450_44284444 | 44277326 | ACTC | A | 3_prime_UTR_variant | MODIFIER | NA18957.hp2 NA18979.hp1 NA19011.hp1 others(1): Show |
a0001a0002 | a0001c0001a0002c0007 | a0001c0001t0013a0002c0007t0013 | a0001c0001t0013g0003 a0002c0007t0013g0005 |
4 | 410 | 0.0098 | -3 | c.*80 others(12): Show |
TMEM151B | ENSG00000178233.18 | transcript | ENST00000451188.7 | protein_coding | 3/3 | 803 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
TMEM154_chr4_152613628_152684997 | 152617581 | ATTT | A | downstream_gene_variant | MODIFIER | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(34): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0005a0001c0001t0017others(8): Show | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0039 others(34): Show |
37 | 300 | 0.1233 | -3 | c.*10 others(16): Show |
TMEM154 | ENSG00000170006.13 | transcript | ENST00000304385.8 | protein_coding | 1046 | chr4 | TogoVar | |||||||
TMEM154_chr4_152613628_152684997 | 152628590 | AAAC | A | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(36): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(10): Show | a0001c0001t0001g0033 a0001c0001t0001g0050 a0001c0001t0001g0063 others(36): Show |
39 | 300 | 0.1300 | -3 | c.537 others(16): Show |
TMEM154 | ENSG00000170006.13 | transcript | ENST00000304385.8 | protein_coding | 6/6 | chr4 | TogoVar | |||||||
TMEM154_chr4_152613628_152684997 | 152631792 | CCTT | C | intron_variant | MODIFIER | HG02572.hp2 HG02615.hp1 HG02896.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0015a0001c0001t0026others(1): Show | a0001c0001t0001g0230 a0001c0001t0001g0285 a0001c0001t0015g0051 others(4): Show |
7 | 300 | 0.0233 | -3 | c.537 others(20): Show |
TMEM154 | ENSG00000170006.13 | transcript | ENST00000304385.8 | protein_coding | 6/6 | chr4 | TogoVar | |||||||
TMEM154_chr4_152613628_152684997 | 152631793 | CTTT | C | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(160): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(32): Show | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0015 others(160): Show |
163 | 300 | 0.5433 | -3 | c.537 others(20): Show |
TMEM154 | ENSG00000170006.13 | transcript | ENST00000304385.8 | protein_coding | 6/6 | chr4 | TogoVar | |||||||
TMEM154_chr4_152613628_152684997 | 152642984 | GTTC | G | intron_variant | MODIFIER | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(17): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0005a0001c0001t0008others(8): Show | a0001c0001t0001g0022 a0001c0001t0001g0126 a0001c0001t0001g0135 others(17): Show |
20 | 300 | 0.0667 | -3 | c.478 others(18): Show |
TMEM154 | ENSG00000170006.13 | transcript | ENST00000304385.8 | protein_coding | 5/6 | chr4 | TogoVar | |||||||
TMEM154_chr4_152613628_152684997 | 152669091 | CTTA | C | intron_variant | MODIFIER | HG01243.hp2 HG02258.hp2 HG02886.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(1): Show | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0228 others(3): Show |
6 | 300 | 0.0200 | -3 | c.64+ others(20): Show |
TMEM154 | ENSG00000170006.13 | transcript | ENST00000304385.8 | protein_coding | 1/6 | chr4 | TogoVar | |||||||
TMEM156_chr4_38961744_39037409 | 38969448 | GCAC | G | intron_variant | MODIFIER | HG03490.hp1 HG03492.hp1 HG03942.hp1 others(3): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0001 | a0001c0001t0001g0013 a0001c0001t0001g0085 a0001c0001t0001g0232 others(3): Show |
6 | 386 | 0.0155 | -3 | c.*38 others(20): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | TogoVar |