regionname | pos | ref | alt | annotation | impact | samples | ahapids | achapids | acthapids | actghapids | ac | an | af | len | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length
|
cds cds pos length
|
aa aa pos length
|
distance | status | chr | external |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
TMEM132D_chr12_129066726_129909025 | 129877628 | CAG | C | intron_variant | MODIFIER | HG00408.hp2 HG01074.hp1 HG01433.hp2 others(9): Show |
a0001a0003a0006others(1): Show | a0001c0001a0001c0004a0001c0007others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(6): Show | a0001c0001t0001g0059a0001c0001t0002g0039a0001c0001t0003g0085others(9): Show | 12 | 94 | 0.1277 | -2 | c.79+ others(19): Show |
TMEM132D | ENSG00000151952.16 | transcript | ENST00000422113.7 | protein_coding | 1/8 | chr12 | TogoVar | ||||||
TMEM132D_chr12_129066726_129909025 | 129899862 | CCA | C | intron_variant | MODIFIER | HG00099.hp2 HG00741.hp2 HG01106.hp2 others(27): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0006others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(18): Show | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(27): Show | 30 | 94 | 0.3192 | -2 | c.79+ others(17): Show |
TMEM132D | ENSG00000151952.16 | transcript | ENST00000422113.7 | protein_coding | 1/8 | chr12 | TogoVar | ||||||
TMEM132E_chr17_34574582_34644318 | 34596066 | ACG | A | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(240): Show |
a0001a0002a0005others(3): Show | a0001c0001a0001c0002a0001c0003others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(88): Show | a0001c0001t0001g0015a0001c0001t0001g0052a0001c0001t0001g0054others(233): Show | 243 | 404 | 0.6015 | -2 | c.67+ others(19): Show |
TMEM132E | ENSG00000181291.8 | transcript | ENST00000631683.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
TMEM132E_chr17_34574582_34644318 | 34596853 | CAA | C | intron_variant | MODIFIER | HG01361.hp1 HG02280.hp1 HG02572.hp2 others(14): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0002a0001c0001t0027a0001c0001t0037others(11): Show | a0001c0001t0002g0022a0001c0001t0002g0145a0001c0001t0027g0198others(14): Show | 17 | 404 | 0.0421 | -2 | c.67+ others(19): Show |
TMEM132E | ENSG00000181291.8 | transcript | ENST00000631683.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
TMEM132E_chr17_34574582_34644318 | 34615517 | ATG | A | intron_variant | MODIFIER | HG01192.hp1 HG02451.hp1 HG03491.hp1 others(9): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0003a0001c0001t0009others(6): Show | a0001c0001t0001g0078a0001c0001t0001g0083a0001c0001t0001g0200others(8): Show | 12 | 404 | 0.0297 | -2 | c.68- others(19): Show |
TMEM132E | ENSG00000181291.8 | transcript | ENST00000631683.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
TMEM132E_chr17_34574582_34644318 | 34618395 | ATT | A | intron_variant | MODIFIER | HG01361.hp1 HG02145.hp1 HG02735.hp2 others(13): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0009others(11): Show | a0001c0001t0002g0022a0001c0001t0003g0294a0001c0001t0009g0257others(13): Show | 16 | 404 | 0.0396 | -2 | c.68- others(17): Show |
TMEM132E | ENSG00000181291.8 | transcript | ENST00000631683.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
TMEM132E_chr17_34574582_34644318 | 34623401 | TCC | T | intron_variant | MODIFIER | HG00558.hp1 HG01070.hp2 HG01516.hp1 others(31): Show |
a0001a0007 | a0001c0001a0001c0003a0007c0016 | a0001c0001t0002a0001c0001t0007a0001c0001t0013others(20): Show | a0001c0001t0002g0029a0001c0001t0002g0046a0001c0001t0002g0064others(30): Show | 34 | 404 | 0.0842 | -2 | c.68- others(17): Show |
TMEM132E | ENSG00000181291.8 | transcript | ENST00000631683.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
TMEM132E_chr17_34574582_34644318 | 34627467 | CGT | C | intron_variant | MODIFIER | HG00408.hp1 HG02809.hp1 HG03017.hp1 others(5): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0002a0001c0002t0001a0001c0002t0003others(5): Show | a0001c0001t0002g0145a0001c0002t0001g0071a0001c0002t0003g0306others(5): Show | 8 | 404 | 0.0198 | -2 | c.998 others(17): Show |
TMEM132E | ENSG00000181291.8 | transcript | ENST00000631683.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
TMEM134_chr11_67456710_67474251 | 67462177 | CAA | C | 3_prime_UTR_variant | MODIFIER | HG01496.hp1 HG01515.hp2 HG02615.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0008a0001c0001t0016 | a0001c0001t0008g0014a0001c0001t0016g0022 | 6 | 352 | 0.0171 | -2 | c.*24 others(13): Show |
TMEM134 | ENSG00000172663.9 | transcript | ENST00000308022.7 | protein_coding | 7/7 | 2435 | chr11 | TogoVar | |||||
TMEM134_chr11_67456710_67474251 | 67474182 | CAA | C | upstream_gene_variant | MODIFIER | HG00609.hp1 HG01070.hp1 HG01074.hp1 others(47): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0003a0001c0001t0008others(4): Show | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0012others(6): Show | 50 | 352 | 0.1421 | -2 | c.-49 others(13): Show |
TMEM134 | ENSG00000172663.9 | transcript | ENST00000308022.7 | protein_coding | 4932 | chr11 | TogoVar | ||||||
TMEM135_chr11_87032934_87333824 | 87036264 | GTT | G | upstream_gene_variant | MODIFIER | HG00544.hp2 HG00673.hp1 HG01099.hp2 others(17): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0003 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(11): Show | a0001c0001t0002g0114a0001c0001t0003g0218a0001c0001t0004g0107others(17): Show | 20 | 274 | 0.0730 | -2 | c.-17 others(13): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 1669 | chr11 | TogoVar | ||||||
TMEM135_chr11_87032934_87333824 | 87038609 | CTT | C | intron_variant | MODIFIER | HG00544.hp2 HG00621.hp2 HG00673.hp1 others(54): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0003c0003others(1): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(22): Show | a0001c0001t0002g0114a0001c0001t0002g0121a0001c0001t0002g0130others(54): Show | 57 | 274 | 0.2080 | -2 | c.141 others(17): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
TMEM135_chr11_87032934_87333824 | 87049490 | AAC | A | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(13): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0003 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(4): Show | a0001c0001t0002g0206a0001c0001t0002g0225a0001c0001t0004g0203others(13): Show | 16 | 274 | 0.0584 | -2 | c.141 others(21): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
TMEM135_chr11_87032934_87333824 | 87053191 | CAA | C | intron_variant | MODIFIER | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(27): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0003 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(12): Show | a0001c0001t0002g0114a0001c0001t0003g0123a0001c0001t0003g0218others(27): Show | 30 | 274 | 0.1095 | -2 | c.142 others(21): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
TMEM135_chr11_87032934_87333824 | 87053292 | AAT | A | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0002a0003c0003others(2): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(44): Show | a0001c0001t0002g0002a0001c0001t0002g0029a0001c0001t0002g0032others(216): Show | 219 | 274 | 0.7993 | -2 | c.142 others(21): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
TMEM135_chr11_87032934_87333824 | 87057815 | GTT | G | intron_variant | MODIFIER | HG01109.hp2 HG02818.hp1 HG02965.hp1 others(2): Show |
a0001a0003 | a0001c0001a0003c0003 | a0001c0001t0003a0001c0001t0052a0003c0003t0041 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(2): Show | 5 | 274 | 0.0183 | -2 | c.142 others(19): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
TMEM135_chr11_87032934_87333824 | 87064262 | CTT | C | intron_variant | MODIFIER | HG00544.hp1 HG01081.hp2 HG01168.hp2 others(30): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0003 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(10): Show | a0001c0001t0002g0228a0001c0001t0002g0229a0001c0001t0004g0143others(30): Show | 33 | 274 | 0.1204 | -2 | c.142 others(19): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
TMEM135_chr11_87032934_87333824 | 87066598 | CAA | C | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(46): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0003 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(14): Show | a0001c0001t0002g0064a0001c0001t0002g0114a0001c0001t0002g0206others(46): Show | 49 | 274 | 0.1788 | -2 | c.142 others(19): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
TMEM135_chr11_87032934_87333824 | 87067164 | AAT | A | intron_variant | MODIFIER | HG02486.hp2 HG02809.hp1 HG03486.hp1 others(1): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0003a0001c0001t0015a0001c0001t0032others(1): Show | a0001c0001t0003g0128a0001c0001t0015g0127a0001c0001t0032g0125others(1): Show | 4 | 274 | 0.0146 | -2 | c.142 others(17): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
TMEM135_chr11_87032934_87333824 | 87068808 | CAA | C | intron_variant | MODIFIER | HG00280.hp2 HG00597.hp2 HG00621.hp2 others(116): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0002a0003c0003others(2): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(26): Show | a0001c0001t0002g0002a0001c0001t0002g0029a0001c0001t0002g0032others(116): Show | 119 | 274 | 0.4343 | -2 | c.269 others(19): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
TMEM135_chr11_87032934_87333824 | 87071674 | ATT | A | intron_variant | MODIFIER | HG00741.hp2 HG01070.hp2 HG01243.hp2 others(19): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0003c0003others(1): Show | a0001c0001t0003a0001c0001t0005a0001c0001t0015others(4): Show | a0001c0001t0003g0015a0001c0001t0003g0213a0001c0001t0005g0007others(19): Show | 22 | 274 | 0.0803 | -2 | c.362 others(15): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
TMEM135_chr11_87032934_87333824 | 87074429 | CTG | C | intron_variant | MODIFIER | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(25): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0003 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(12): Show | a0001c0001t0002g0114a0001c0001t0003g0218a0001c0001t0004g0001others(25): Show | 28 | 274 | 0.1022 | -2 | c.362 others(19): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
TMEM135_chr11_87032934_87333824 | 87075888 | GTC | G | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(179): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0002a0003c0003others(2): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(36): Show | a0001c0001t0002g0002a0001c0001t0002g0029a0001c0001t0002g0032others(179): Show | 182 | 274 | 0.6642 | -2 | c.362 others(19): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
TMEM135_chr11_87032934_87333824 | 87079843 | CTT | C | intron_variant | MODIFIER | HG01099.hp2 HG02486.hp2 HG02809.hp1 others(4): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0003a0001c0001t0015a0001c0001t0020others(3): Show | a0001c0001t0003g0124a0001c0001t0003g0128a0001c0001t0015g0127others(4): Show | 7 | 274 | 0.0256 | -2 | c.362 others(19): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
TMEM135_chr11_87032934_87333824 | 87087290 | CAA | C | intron_variant | MODIFIER | HG00544.hp1 HG00609.hp1 HG01081.hp2 others(29): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0003 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(10): Show | a0001c0001t0002g0228a0001c0001t0002g0229a0001c0001t0004g0143others(29): Show | 32 | 274 | 0.1168 | -2 | c.363 others(19): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
TMEM135_chr11_87032934_87333824 | 87099682 | GTT | G | intron_variant | MODIFIER | HG00741.hp2 HG01070.hp2 HG01243.hp2 others(20): Show |
a0001a0002a0005 | a0001c0001a0002c0002a0005c0006 | a0001c0001t0003a0001c0001t0005a0001c0001t0015others(3): Show | a0001c0001t0003g0015a0001c0001t0005g0007a0001c0001t0005g0008others(20): Show | 23 | 274 | 0.0839 | -2 | c.396 others(19): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
TMEM135_chr11_87032934_87333824 | 87102684 | ATG | A | intron_variant | MODIFIER | HG01891.hp2 HG03453.hp2 NA18522.hp2 |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0006 | a0001c0001t0003g0123a0001c0001t0003g0250a0001c0001t0006g0141 | 3 | 274 | 0.0110 | -2 | c.396 others(21): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
TMEM135_chr11_87032934_87333824 | 87102704 | GTA | G | intron_variant | MODIFIER | NA18959.hp1 NA20129.hp2 homoSapiens_chm13v2.hp1 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0002a0001c0001t0003a0002c0002t0001 | a0001c0001t0002g0032a0001c0001t0003g0124a0002c0002t0001g0087 | 3 | 274 | 0.0110 | -2 | c.396 others(21): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
TMEM135_chr11_87032934_87333824 | 87102714 | GTA | G | intron_variant | MODIFIER | HG01256.hp1 HG01361.hp2 HG01496.hp1 others(4): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0003a0001c0001t0006a0001c0001t0009others(3): Show | a0001c0001t0003g0123a0001c0001t0003g0250a0001c0001t0006g0141others(4): Show | 7 | 274 | 0.0256 | -2 | c.396 others(21): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
TMEM135_chr11_87032934_87333824 | 87102728 | GTA | G | intron_variant | MODIFIER | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(70): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0003 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(17): Show | a0001c0001t0002g0002a0001c0001t0002g0029a0001c0001t0002g0037others(70): Show | 73 | 274 | 0.2664 | -2 | c.396 others(21): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
TMEM135_chr11_87032934_87333824 | 87103492 | TTG | T | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0003c0003others(1): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(29): Show | a0001c0001t0002g0002a0001c0001t0002g0029a0001c0001t0002g0032others(142): Show | 145 | 274 | 0.5292 | -2 | c.396 others(21): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
TMEM135_chr11_87032934_87333824 | 87123581 | TTG | T | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(150): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0002a0003c0003others(2): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(33): Show | a0001c0001t0002g0002a0001c0001t0002g0029a0001c0001t0002g0032others(150): Show | 153 | 274 | 0.5584 | -2 | c.396 others(21): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
TMEM135_chr11_87032934_87333824 | 87128905 | TAC | T | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(149): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0002a0003c0003others(2): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(33): Show | a0001c0001t0002g0002a0001c0001t0002g0029a0001c0001t0002g0032others(149): Show | 152 | 274 | 0.5547 | -2 | c.397 others(21): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
TMEM135_chr11_87032934_87333824 | 87130116 | ATT | A | intron_variant | MODIFIER | HG01109.hp2 HG02818.hp1 HG02965.hp1 others(14): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0003 | a0001c0001t0003a0001c0001t0005a0001c0001t0046others(4): Show | a0001c0001t0003g0124a0001c0001t0003g0263a0001c0001t0003g0264others(14): Show | 17 | 274 | 0.0620 | -2 | c.397 others(21): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
TMEM135_chr11_87032934_87333824 | 87130166 | ATT | A | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00597.hp2 others(113): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0002a0003c0003others(2): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(25): Show | a0001c0001t0002g0002a0001c0001t0002g0029a0001c0001t0002g0032others(113): Show | 116 | 274 | 0.4234 | -2 | c.397 others(21): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
TMEM135_chr11_87032934_87333824 | 87143364 | TTC | T | intron_variant | MODIFIER | HG00544.hp1 HG00609.hp1 HG01070.hp2 others(33): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0003 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(12): Show | a0001c0001t0002g0229a0001c0001t0004g0143a0001c0001t0005g0007others(33): Show | 36 | 274 | 0.1314 | -2 | c.397 others(21): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
TMEM135_chr11_87032934_87333824 | 87157074 | GTT | G | intron_variant | MODIFIER | HG00544.hp1 HG00609.hp1 HG01081.hp2 others(30): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0003 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(12): Show | a0001c0001t0002g0229a0001c0001t0004g0143a0001c0001t0006g0144others(30): Show | 33 | 274 | 0.1204 | -2 | c.397 others(17): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
TMEM135_chr11_87032934_87333824 | 87159593 | GCA | G | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(21): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0003 | a0001c0001t0002a0001c0001t0004a0001c0001t0007others(5): Show | a0001c0001t0002g0064a0001c0001t0002g0206a0001c0001t0002g0225others(21): Show | 24 | 274 | 0.0876 | -2 | c.462 others(19): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
TMEM135_chr11_87032934_87333824 | 87183955 | CAA | C | intron_variant | MODIFIER | HG00544.hp1 HG01243.hp1 HG02129.hp1 others(7): Show |
a0001a0003 | a0001c0001a0003c0003 | a0001c0001t0006a0001c0001t0008a0001c0001t0013others(2): Show | a0001c0001t0006g0216a0001c0001t0006g0231a0001c0001t0006g0232others(7): Show | 10 | 274 | 0.0365 | -2 | c.462 others(21): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
TMEM135_chr11_87032934_87333824 | 87188188 | TAC | T | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(33): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0003 | a0001c0001t0002a0001c0001t0004a0001c0001t0007others(6): Show | a0001c0001t0002g0064a0001c0001t0002g0206a0001c0001t0002g0225others(33): Show | 36 | 274 | 0.1314 | -2 | c.462 others(21): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
TMEM135_chr11_87032934_87333824 | 87195232 | TTC | T | intron_variant | MODIFIER | HG00741.hp2 HG02109.hp2 HG02615.hp1 others(7): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0015a0002c0002t0001 | a0001c0001t0015g0016a0002c0002t0001g0014a0002c0002t0001g0017others(7): Show | 10 | 274 | 0.0365 | -2 | c.462 others(21): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
TMEM135_chr11_87032934_87333824 | 87195389 | CCT | C | intron_variant | MODIFIER | HG01978.hp2 HG03654.hp2 NA19003.hp1 others(1): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0007a0001c0001t0012a0002c0002t0001others(1): Show | a0001c0001t0007g0223a0001c0001t0012g0248a0002c0002t0001g0197others(1): Show | 4 | 274 | 0.0146 | -2 | c.462 others(21): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 5/14 | chr11 | TogoVar | ||||||
TMEM135_chr11_87032934_87333824 | 87203032 | CAA | C | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG01256.hp1 others(19): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0003 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(7): Show | a0001c0001t0002g0064a0001c0001t0002g0206a0001c0001t0002g0225others(19): Show | 22 | 274 | 0.0803 | -2 | c.463 others(21): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
TMEM135_chr11_87032934_87333824 | 87208515 | GAA | G | intron_variant | MODIFIER | HG00544.hp1 HG00609.hp1 HG01081.hp2 others(29): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0003 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(11): Show | a0001c0001t0002g0229a0001c0001t0004g0143a0001c0001t0006g0144others(29): Show | 32 | 274 | 0.1168 | -2 | c.463 others(21): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
TMEM135_chr11_87032934_87333824 | 87223665 | ACG | A | intron_variant | MODIFIER | HG01361.hp1 HG02886.hp1 NA19060.hp1 others(1): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0003 | a0001c0001t0006a0001c0001t0007a0002c0002t0038others(1): Show | a0001c0001t0006g0144a0001c0001t0007g0052a0002c0002t0038g0212others(1): Show | 4 | 274 | 0.0146 | -2 | c.463 others(21): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
TMEM135_chr11_87032934_87333824 | 87223667 | GCA | G | intron_variant | MODIFIER | HG00280.hp2 HG00735.hp1 HG00738.hp2 others(4): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0002a0001c0001t0004a0002c0002t0001others(1): Show | a0001c0001t0002g0032a0001c0001t0004g0211a0002c0002t0001g0024others(4): Show | 7 | 274 | 0.0256 | -2 | c.463 others(21): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
TMEM135_chr11_87032934_87333824 | 87223725 | CTG | C | intron_variant | MODIFIER | HG00544.hp1 HG01081.hp2 HG01978.hp2 others(15): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0007a0001c0001t0008a0001c0001t0012others(5): Show | a0001c0001t0007g0025a0001c0001t0007g0223a0001c0001t0008g0241others(15): Show | 18 | 274 | 0.0657 | -2 | c.463 others(21): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
TMEM135_chr11_87032934_87333824 | 87224759 | GTT | G | intron_variant | MODIFIER | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(34): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0003 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(17): Show | a0001c0001t0002g0114a0001c0001t0004g0001a0001c0001t0004g0107others(34): Show | 37 | 274 | 0.1350 | -2 | c.463 others(21): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
TMEM135_chr11_87032934_87333824 | 87236172 | CTA | C | intron_variant | MODIFIER | HG00544.hp1 HG01081.hp2 HG01978.hp2 others(15): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0007a0001c0001t0008a0001c0001t0012others(5): Show | a0001c0001t0007g0025a0001c0001t0007g0223a0001c0001t0008g0241others(15): Show | 18 | 274 | 0.0657 | -2 | c.463 others(17): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
TMEM135_chr11_87032934_87333824 | 87239451 | CTT | C | intron_variant | MODIFIER | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(21): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0003 | a0001c0001t0002a0001c0001t0004a0001c0001t0020others(9): Show | a0001c0001t0002g0114a0001c0001t0004g0001a0001c0001t0004g0107others(21): Show | 24 | 274 | 0.0876 | -2 | c.509 others(19): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 6/14 | chr11 | TogoVar |