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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
TMEM108_chr3_133033391_133402775 | 133185784 | CTTT | C | intron_variant | MODIFIER | HG00140.hp2 HG01070.hp1 HG01099.hp1 others(39): Show |
a0001a0003a0004 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(14): Show | a0001c0001t0001g0060 a0001c0001t0002g0167 a0001c0001t0002g0196 others(39): Show |
42 | 220 | 0.1909 | -3 | c.-46 others(22): Show |
TMEM108 | ENSG00000144868.14 | transcript | ENST00000321871.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
TMEM108_chr3_133033391_133402775 | 133187883 | CAAA | C | intron_variant | MODIFIER | HG02080.hp1 HG02109.hp1 HG02148.hp1 others(10): Show |
a0001a0002a0006others(1): Show | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0003a0001c0001t0004a0001c0001t0007others(7): Show | a0001c0001t0003g0017 a0001c0001t0004g0106 a0001c0001t0007g0019 others(10): Show |
13 | 220 | 0.0591 | -3 | c.-46 others(22): Show |
TMEM108 | ENSG00000144868.14 | transcript | ENST00000321871.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
TMEM108_chr3_133033391_133402775 | 133197696 | CATG | C | intron_variant | MODIFIER | HG00438.hp2 HG01081.hp1 HG01167.hp1 others(76): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(20): Show | a0001c0001t0001g0039 a0001c0001t0001g0046 a0001c0001t0001g0060 others(76): Show |
79 | 220 | 0.3591 | -3 | c.-46 others(22): Show |
TMEM108 | ENSG00000144868.14 | transcript | ENST00000321871.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
TMEM108_chr3_133033391_133402775 | 133225042 | ATTT | A | intron_variant | MODIFIER | HG01081.hp2 HG02148.hp1 HG02683.hp1 others(3): Show |
a0001a0002a0006 | a0001c0001a0002c0005a0006c0018 | a0001c0001t0001a0002c0005t0003a0006c0018t0003 | a0001c0001t0001g0060 a0001c0001t0001g0176 a0002c0005t0003g0021 others(3): Show |
6 | 220 | 0.0273 | -3 | c.-46 others(20): Show |
TMEM108 | ENSG00000144868.14 | transcript | ENST00000321871.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
TMEM108_chr3_133033391_133402775 | 133227189 | CTTT | C | intron_variant | MODIFIER | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(74): Show |
a0001a0008a0010 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(13): Show | a0001c0001t0001g0045 a0001c0001t0001g0053 a0001c0001t0001g0060 others(74): Show |
77 | 220 | 0.3500 | -3 | c.-46 others(20): Show |
TMEM108 | ENSG00000144868.14 | transcript | ENST00000321871.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
TMEM108_chr3_133033391_133402775 | 133237369 | ATTG | A | intron_variant | MODIFIER | HG00140.hp2 HG01070.hp1 HG01081.hp1 others(20): Show |
a0001a0003a0004 | a0001c0001a0001c0002a0001c0015others(2): Show | a0001c0001t0016a0001c0002t0001a0001c0015t0001others(2): Show | a0001c0001t0016g0099 a0001c0002t0001g0034 a0001c0002t0001g0035 others(20): Show |
23 | 220 | 0.1046 | -3 | c.40+ others(18): Show |
TMEM108 | ENSG00000144868.14 | transcript | ENST00000321871.11 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
TMEM108_chr3_133033391_133402775 | 133241609 | CTTT | C | intron_variant | MODIFIER | HG01884.hp1 HG02080.hp1 HG02615.hp1 others(3): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0001t0007a0001c0001t0024others(1): Show | a0001c0001t0002g0126 a0001c0001t0007g0019 a0001c0001t0007g0110 others(3): Show |
6 | 220 | 0.0273 | -3 | c.40+ others(20): Show |
TMEM108 | ENSG00000144868.14 | transcript | ENST00000321871.11 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
TMEM108_chr3_133033391_133402775 | 133260287 | TAAA | T | intron_variant | MODIFIER | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(55): Show |
a0001a0010 | a0001c0001a0001c0002a0001c0004others(2): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(9): Show | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0013 others(55): Show |
58 | 220 | 0.2636 | -3 | c.40+ others(20): Show |
TMEM108 | ENSG00000144868.14 | transcript | ENST00000321871.11 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
TMEM108_chr3_133033391_133402775 | 133292167 | GTTT | G | intron_variant | MODIFIER | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
a0001a0002a0006others(1): Show | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(20): Show | a0001c0001t0001g0039 a0001c0001t0001g0046 a0001c0001t0001g0060 others(118): Show |
121 | 220 | 0.5500 | -3 | c.40+ others(20): Show |
TMEM108 | ENSG00000144868.14 | transcript | ENST00000321871.11 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
TMEM108_chr3_133033391_133402775 | 133309682 | CTTT | C | intron_variant | MODIFIER | HG00438.hp1 HG01099.hp2 HG01192.hp2 others(20): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0012others(6): Show | a0001c0001t0002g0007 a0001c0001t0002g0024 a0001c0001t0002g0049 others(20): Show |
23 | 220 | 0.1046 | -3 | c.41- others(20): Show |
TMEM108 | ENSG00000144868.14 | transcript | ENST00000321871.11 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
TMEM108_chr3_133033391_133402775 | 133310530 | CTTT | C | intron_variant | MODIFIER | HG00323.hp1 HG01074.hp2 HG01243.hp2 others(39): Show |
a0001a0003a0008others(1): Show | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(16): Show | a0001c0001t0001g0137 a0001c0001t0002g0022 a0001c0001t0002g0030 others(39): Show |
42 | 220 | 0.1909 | -3 | c.41- others(20): Show |
TMEM108 | ENSG00000144868.14 | transcript | ENST00000321871.11 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
TMEM108_chr3_133033391_133402775 | 133354801 | ATTT | A | intron_variant | MODIFIER | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(55): Show |
a0001a0010 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(9): Show | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0013 others(55): Show |
58 | 220 | 0.2636 | -3 | c.41- others(20): Show |
TMEM108 | ENSG00000144868.14 | transcript | ENST00000321871.11 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
TMEM108_chr3_133033391_133402775 | 133371613 | CAAA | C | intron_variant | MODIFIER | HG00140.hp2 HG01070.hp1 HG01081.hp1 others(20): Show |
a0001a0002 | a0001c0002a0001c0015a0002c0005 | a0001c0002t0001a0001c0015t0001a0002c0005t0003 | a0001c0002t0001g0014 a0001c0002t0001g0028 a0001c0002t0001g0034 others(20): Show |
23 | 220 | 0.1046 | -3 | c.41- others(18): Show |
TMEM108 | ENSG00000144868.14 | transcript | ENST00000321871.11 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
TMEM108_chr3_133033391_133402775 | 133394827 | ACTC | A | intron_variant | MODIFIER | HG00140.hp2 HG00438.hp1 HG01070.hp1 others(69): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0004others(4): Show | a0001c0001t0001a0001c0001t0012a0001c0001t0019others(9): Show | a0001c0001t0001g0039 a0001c0001t0012g0012 a0001c0001t0012g0018 others(69): Show |
72 | 220 | 0.3273 | -3 | c.160 others(22): Show |
TMEM108 | ENSG00000144868.14 | transcript | ENST00000321871.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
TMEM109_chr11_60909158_60928443 | 60922875 | CAAG | C | 3_prime_UTR_variant | MODIFIER | HG02615.hp2 HG02622.hp1 HG02818.hp1 others(4): Show |
a0001 | a0001c0002 | a0001c0002t0004 | a0001c0002t0004g0004 | 7 | 362 | 0.0193 | -3 | c.*71 others(12): Show |
TMEM109 | ENSG00000110108.10 | transcript | ENST00000227525.8 | protein_coding | 4/4 | 713 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
TMEM114_chr16_8564500_8595511 | 8566897 | GTTT | G | downstream_gene_variant | MODIFIER | HG02451.hp2 HG02895.hp2 HG02896.hp1 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0005 | a0001c0001t0002g0149 a0001c0001t0002g0173 a0001c0001t0002g0174 others(5): Show |
8 | 416 | 0.0192 | -3 | c.*28 others(14): Show |
TMEM114 | ENSG00000232258.7 | transcript | ENST00000620492.5 | protein_coding | 2602 | chr16 | TogoVar | |||||||
TMEM114_chr16_8564500_8595511 | 8591479 | CCAT | C | upstream_gene_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(276): Show |
a0001a0002a0004others(2): Show | a0001c0001a0001c0007a0002c0002others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(10): Show | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(180): Show |
279 | 416 | 0.6707 | -3 | c.-16 others(14): Show |
TMEM114 | ENSG00000232258.7 | transcript | ENST00000620492.5 | protein_coding | 969 | chr16 | TogoVar | |||||||
TMEM116_chr12_111926298_112018165 | 111929550 | AAGG | A | downstream_gene_variant | MODIFIER | HG01167.hp1 HG02723.hp2 HG02738.hp2 others(11): Show |
a0002a0009 | a0002c0002a0009c0006 | a0002c0002t0001a0009c0006t0001 | a0002c0002t0001g0003 a0002c0002t0001g0241 a0002c0002t0001g0242 others(9): Show |
14 | 342 | 0.0409 | -3 | c.*20 others(14): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1747 | chr12 | TogoVar | |||||||
TMEM116_chr12_111926298_112018165 | 111991217 | CAAA | C | intron_variant | MODIFIER | HG00597.hp2 HG00733.hp1 HG01099.hp2 others(35): Show |
a0002 | a0002c0002 | a0002c0002t0001a0002c0002t0002 | a0002c0002t0001g0130 a0002c0002t0001g0132 a0002c0002t0001g0240 others(35): Show |
38 | 342 | 0.1111 | -3 | c.210 others(18): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | TogoVar | |||||||
TMEM116_chr12_111926298_112018165 | 112010057 | CCCT | C | intron_variant | MODIFIER | HG01943.hp1 HG02717.hp2 HG02809.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(3): Show |
6 | 342 | 0.0175 | -3 | c.-34 others(20): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | TogoVar | |||||||
TMEM117_chr12_43831081_44394758 | 43850732 | CATT | C | intron_variant | MODIFIER | HG00738.hp2 HG02055.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0077 a0001c0001t0001g0078 |
2 | 110 | 0.0182 | -3 | c.277 others(20): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
TMEM117_chr12_43831081_44394758 | 43850860 | GTGA | G | intron_variant | MODIFIER | HG00741.hp1 HG01071.hp2 HG01167.hp2 others(57): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(3): Show | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(57): Show |
60 | 110 | 0.5455 | -3 | c.277 others(20): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
TMEM117_chr12_43831081_44394758 | 43850872 | GTGA | G | intron_variant | MODIFIER | HG00738.hp2 HG01175.hp1 HG01981.hp2 others(10): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(1): Show | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0002g0083 others(10): Show |
13 | 110 | 0.1182 | -3 | c.277 others(20): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
TMEM117_chr12_43831081_44394758 | 43861793 | GAAT | G | intron_variant | MODIFIER | HG02486.hp2 HG02630.hp2 HG02896.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0023 a0001c0001t0002g0088 a0001c0001t0002g0089 others(4): Show |
7 | 110 | 0.0636 | -3 | c.277 others(22): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
TMEM117_chr12_43831081_44394758 | 43877934 | GAAT | G | intron_variant | MODIFIER | HG01168.hp2 HG01169.hp1 HG01255.hp2 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003 | a0001c0001t0001g0001 a0001c0001t0001g0096 a0001c0001t0001g0097 others(6): Show |
9 | 110 | 0.0818 | -3 | c.277 others(22): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
TMEM117_chr12_43831081_44394758 | 43882093 | AAAC | A | intron_variant | MODIFIER | HG02486.hp2 HG02630.hp2 HG02896.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0088 a0001c0001t0002g0089 a0001c0001t0002g0090 others(3): Show |
6 | 110 | 0.0546 | -3 | c.277 others(22): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
TMEM117_chr12_43831081_44394758 | 43886274 | GGAA | G | intron_variant | MODIFIER | HG02818.hp1 HG03130.hp2 HG03540.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0002g0105 |
3 | 110 | 0.0273 | -3 | c.277 others(22): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
TMEM117_chr12_43831081_44394758 | 43919802 | TTTG | T | intron_variant | MODIFIER | HG02451.hp1 HG02896.hp1 NA18906.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003 | a0001c0001t0001g0094 a0001c0001t0003g0036 a0001c0001t0003g0037 others(1): Show |
4 | 110 | 0.0364 | -3 | c.278 others(22): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
TMEM117_chr12_43831081_44394758 | 43946392 | TTTG | T | intron_variant | MODIFIER | HG02280.hp1 HG02451.hp2 HG02622.hp1 others(15): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(1): Show | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0027 others(15): Show |
18 | 110 | 0.1636 | -3 | c.410 others(20): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
TMEM117_chr12_43831081_44394758 | 43961281 | CAAT | C | intron_variant | MODIFIER | HG00738.hp1 HG00741.hp2 HG01071.hp1 others(29): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0004 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(29): Show |
32 | 110 | 0.2909 | -3 | c.410 others(22): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
TMEM117_chr12_43831081_44394758 | 43980397 | CCTT | C | intron_variant | MODIFIER | HG01884.hp1 HG02451.hp1 HG02622.hp2 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0052 others(7): Show |
10 | 110 | 0.0909 | -3 | c.410 others(22): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
TMEM117_chr12_43831081_44394758 | 43984364 | TAAC | T | intron_variant | MODIFIER | HG00738.hp2 HG01167.hp2 HG01168.hp2 others(32): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(3): Show | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(32): Show |
35 | 110 | 0.3182 | -3 | c.410 others(22): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
TMEM117_chr12_43831081_44394758 | 43987180 | AGAC | A | intron_variant | MODIFIER | HG01071.hp1 HG01071.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0006 a0001c0001t0001g0066 |
2 | 110 | 0.0182 | -3 | c.410 others(22): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 3/7 | chr12 | TogoVar | |||||||
TMEM117_chr12_43831081_44394758 | 44067079 | TAAG | T | intron_variant | MODIFIER | HG00741.hp1 HG02258.hp1 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0025 a0001c0001t0002g0026 |
2 | 110 | 0.0182 | -3 | c.411 others(22): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
TMEM117_chr12_43831081_44394758 | 44080015 | CAAA | C | intron_variant | MODIFIER | HG01884.hp2 HG02717.hp2 HG02895.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0024 a0001c0001t0001g0028 a0001c0001t0002g0040 others(2): Show |
5 | 110 | 0.0455 | -3 | c.411 others(22): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
TMEM117_chr12_43831081_44394758 | 44113192 | CCTT | C | intron_variant | MODIFIER | HG02559.hp2 HG02572.hp1 HG02647.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0039 a0001c0001t0001g0043 a0001c0001t0001g0044 others(1): Show |
4 | 110 | 0.0364 | -3 | c.411 others(22): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
TMEM117_chr12_43831081_44394758 | 44151990 | CATT | C | intron_variant | MODIFIER | HG00741.hp1 HG02055.hp2 HG02257.hp1 others(15): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003 | a0001c0001t0001g0017 a0001c0001t0001g0027 a0001c0001t0001g0030 others(15): Show |
18 | 110 | 0.1636 | -3 | c.510 others(20): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
TMEM117_chr12_43831081_44394758 | 44152556 | ATAT | A | intron_variant | MODIFIER | HG02572.hp2 HG02895.hp1 HG06807.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0006 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0081 others(4): Show |
7 | 110 | 0.0636 | -3 | c.510 others(20): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
TMEM117_chr12_43831081_44394758 | 44157368 | ATAT | A | intron_variant | MODIFIER | HG00741.hp1 HG01884.hp2 HG02055.hp2 others(29): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003 | a0001c0001t0001g0017 a0001c0001t0001g0027 a0001c0001t0001g0028 others(29): Show |
32 | 110 | 0.2909 | -3 | c.510 others(22): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
TMEM117_chr12_43831081_44394758 | 44158373 | GACA | G | intron_variant | MODIFIER | HG02895.hp2 HG02897.hp2 HG03098.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0003g0016 others(1): Show |
4 | 110 | 0.0364 | -3 | c.510 others(22): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
TMEM117_chr12_43831081_44394758 | 44158713 | TAAC | T | intron_variant | MODIFIER | HG02723.hp2 HG02886.hp1 HG02976.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0053 a0001c0001t0002g0002 a0001c0001t0002g0021 others(3): Show |
6 | 110 | 0.0546 | -3 | c.510 others(22): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
TMEM117_chr12_43831081_44394758 | 44159826 | GATA | G | intron_variant | MODIFIER | HG01884.hp1 HG02738.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0005 | a0001c0001t0001g0004 a0001c0001t0005g0005 |
2 | 110 | 0.0182 | -3 | c.510 others(22): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
TMEM117_chr12_43831081_44394758 | 44168485 | ATCT | A | intron_variant | MODIFIER | HG00741.hp1 HG02055.hp2 HG02257.hp1 others(15): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003 | a0001c0001t0001g0017 a0001c0001t0001g0027 a0001c0001t0001g0030 others(15): Show |
18 | 110 | 0.1636 | -3 | c.510 others(22): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
TMEM117_chr12_43831081_44394758 | 44190939 | ATAG | A | intron_variant | MODIFIER | HG02559.hp2 HG02572.hp1 HG02647.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0039 a0001c0001t0001g0043 a0001c0001t0001g0044 others(1): Show |
4 | 110 | 0.0364 | -3 | c.511 others(22): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
TMEM117_chr12_43831081_44394758 | 44201331 | TGAA | T | intron_variant | MODIFIER | HG02717.hp1 HG02818.hp2 HG03041.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0003 a0001c0001t0001g0055 a0001c0001t0001g0061 others(2): Show |
5 | 110 | 0.0455 | -3 | c.511 others(20): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 4/7 | chr12 | TogoVar | |||||||
TMEM117_chr12_43831081_44394758 | 44208725 | GTTT | G | intron_variant | MODIFIER | HG02451.hp1 HG02896.hp1 NA18906.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003 | a0001c0001t0001g0094 a0001c0001t0003g0036 a0001c0001t0003g0037 others(1): Show |
4 | 110 | 0.0364 | -3 | c.511 others(20): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
TMEM117_chr12_43831081_44394758 | 44214137 | AATT | A | intron_variant | MODIFIER | HG01071.hp2 HG01168.hp2 HG01169.hp1 others(11): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(11): Show |
14 | 110 | 0.1273 | -3 | c.608 others(20): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 5/7 | chr12 | TogoVar | |||||||
TMEM117_chr12_43831081_44394758 | 44219300 | TTTG | T | intron_variant | MODIFIER | HG00741.hp1 HG02055.hp2 HG02257.hp1 others(8): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0017 a0001c0001t0001g0027 a0001c0001t0001g0030 others(8): Show |
11 | 110 | 0.1000 | -3 | c.608 others(20): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
TMEM117_chr12_43831081_44394758 | 44289224 | TTTG | T | intron_variant | MODIFIER | HG03540.hp2 NA19030.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0003 a0001c0001t0002g0015 |
2 | 110 | 0.0182 | -3 | c.609 others(22): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
TMEM117_chr12_43831081_44394758 | 44289550 | CTTT | C | intron_variant | MODIFIER | HG01071.hp2 HG01167.hp2 HG01168.hp2 others(11): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0011 others(11): Show |
14 | 110 | 0.1273 | -3 | c.609 others(22): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar |