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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
TMEM114_chr16_8564500_8595511 | 8566897 | GTT | G | downstream_gene_variant | MODIFIER | HG01884.hp2 HG02257.hp2 HG02559.hp2 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(2): Show | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0002g0077others(7): Show | 10 | 416 | 0.0240 | -2 | c.*28 others(13): Show |
TMEM114 | ENSG00000232258.7 | transcript | ENST00000620492.5 | protein_coding | 2602 | chr16 | TogoVar | ||||||
TMEM114_chr16_8564500_8595511 | 8567066 | ATT | A | downstream_gene_variant | MODIFIER | HG00639.hp2 HG00735.hp1 HG01123.hp1 others(33): Show |
a0001a0006 | a0001c0001a0006c0005 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(2): Show | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0027others(31): Show | 36 | 416 | 0.0865 | -2 | c.*27 others(13): Show |
TMEM114 | ENSG00000232258.7 | transcript | ENST00000620492.5 | protein_coding | 2433 | chr16 | TogoVar | ||||||
TMEM114_chr16_8564500_8595511 | 8588286 | CAA | C | intron_variant | MODIFIER | HG00323.hp1 HG01074.hp1 HG01346.hp2 others(13): Show |
a0001a0006 | a0001c0001a0006c0005 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(2): Show | a0001c0001t0001g0010a0001c0001t0001g0074a0001c0001t0002g0061others(8): Show | 16 | 416 | 0.0385 | -2 | c.301 others(17): Show |
TMEM114 | ENSG00000232258.7 | transcript | ENST00000620492.5 | protein_coding | 2/3 | chr16 | TogoVar | ||||||
TMEM114_chr16_8564500_8595511 | 8591192 | CCA | C | upstream_gene_variant | MODIFIER | HG00323.hp1 HG00438.hp2 HG00741.hp1 others(76): Show |
a0001a0006 | a0001c0001a0006c0005 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(4): Show | a0001c0001t0001g0010a0001c0001t0001g0074a0001c0001t0001g0114others(50): Show | 79 | 416 | 0.1899 | -2 | c.-13 others(13): Show |
TMEM114 | ENSG00000232258.7 | transcript | ENST00000620492.5 | protein_coding | 682 | chr16 | TogoVar | ||||||
TMEM115_chr3_50349750_50364521 | 50353228 | CCT | C | downstream_gene_variant | MODIFIER | HG01891.hp2 HG03130.hp2 HG03195.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0005 | a0001c0001t0001g0001a0001c0001t0005g0008 | 4 | 354 | 0.0113 | -2 | c.*21 others(13): Show |
TMEM115 | ENSG00000126062.4 | transcript | ENST00000266025.4 | protein_coding | 1521 | chr3 | TogoVar | ||||||
TMEM115_chr3_50349750_50364521 | 50362635 | TTA | T | upstream_gene_variant | MODIFIER | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(108): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(1): Show | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(4): Show | 111 | 354 | 0.3136 | -2 | c.-35 others(13): Show |
TMEM115 | ENSG00000126062.4 | transcript | ENST00000266025.4 | protein_coding | 3115 | chr3 | TogoVar | ||||||
TMEM115_chr3_50349750_50364521 | 50363466 | CTG | C | upstream_gene_variant | MODIFIER | HG00099.hp1 HG00741.hp1 HG01069.hp2 others(33): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(1): Show | 36 | 354 | 0.1017 | -2 | c.-44 others(13): Show |
TMEM115 | ENSG00000126062.4 | transcript | ENST00000266025.4 | protein_coding | 3946 | chr3 | TogoVar | ||||||
TMEM116_chr12_111926298_112018165 | 111935613 | CGT | C | intron_variant | MODIFIER | HG00544.hp1 HG00733.hp1 HG01071.hp1 others(16): Show |
a0001a0002 | a0001c0001a0002c0002a0002c0010 | a0001c0001t0001a0002c0002t0001a0002c0002t0002others(1): Show | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0024others(16): Show | 19 | 342 | 0.0556 | -2 | c.588 others(19): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 8/10 | chr12 | TogoVar | ||||||
TMEM116_chr12_111926298_112018165 | 111939451 | CAA | C | intron_variant | MODIFIER | HG01169.hp2 HG01943.hp1 HG02071.hp2 others(13): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0001 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0020others(13): Show | 16 | 342 | 0.0468 | -2 | c.316 others(19): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | TogoVar | ||||||
TMEM116_chr12_111926298_112018165 | 111939880 | CTG | C | intron_variant | MODIFIER | HG00140.hp2 HG00733.hp2 HG01106.hp2 others(17): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0001a0002c0002t0002 | a0001c0001t0001g0039a0001c0001t0001g0043a0001c0001t0001g0044others(17): Show | 20 | 342 | 0.0585 | -2 | c.316 others(19): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | TogoVar | ||||||
TMEM116_chr12_111926298_112018165 | 111940523 | GTA | G | intron_variant | MODIFIER | HG00140.hp1 HG01106.hp1 HG01978.hp2 others(30): Show |
a0001a0005a0008 | a0001c0001a0005c0007a0008c0004 | a0001c0001t0001a0005c0007t0001a0008c0004t0001 | a0001c0001t0001g0039a0001c0001t0001g0043a0001c0001t0001g0045others(30): Show | 33 | 342 | 0.0965 | -2 | c.316 others(19): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | TogoVar | ||||||
TMEM116_chr12_111926298_112018165 | 111940544 | TAC | T | intron_variant | MODIFIER | HG02145.hp1 HG02451.hp1 HG02615.hp1 others(11): Show |
a0001a0002a0004 | a0001c0001a0002c0002a0004c0008 | a0001c0001t0001a0002c0002t0001a0002c0002t0002others(1): Show | a0001c0001t0001g0226a0001c0001t0001g0236a0002c0002t0001g0002others(9): Show | 14 | 342 | 0.0409 | -2 | c.316 others(19): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | TogoVar | ||||||
TMEM116_chr12_111926298_112018165 | 111945343 | CAA | C | intron_variant | MODIFIER | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(46): Show |
a0001a0004 | a0001c0001a0004c0008 | a0001c0001t0001a0004c0008t0001 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(45): Show | 49 | 342 | 0.1433 | -2 | c.211 others(19): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | TogoVar | ||||||
TMEM116_chr12_111926298_112018165 | 111958277 | TAA | T | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG01099.hp1 others(65): Show |
a0001a0002a0005others(1): Show | a0001c0001a0002c0002a0002c0010others(2): Show | a0001c0001t0001a0002c0002t0001a0002c0002t0002others(3): Show | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(62): Show | 68 | 342 | 0.1988 | -2 | c.211 others(21): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | TogoVar | ||||||
TMEM116_chr12_111926298_112018165 | 111960491 | CAA | C | intron_variant | MODIFIER | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(67): Show |
a0002a0006a0007 | a0002c0002a0002c0003a0002c0010others(2): Show | a0002c0002t0001a0002c0003t0001a0002c0010t0001others(2): Show | a0002c0002t0001g0003a0002c0002t0001g0241a0002c0002t0001g0244others(65): Show | 70 | 342 | 0.2047 | -2 | c.211 others(21): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | TogoVar | ||||||
TMEM116_chr12_111926298_112018165 | 111963049 | CAT | C | intron_variant | MODIFIER | HG03098.hp1 HG03516.hp1 HG03540.hp2 others(1): Show |
a0001a0004 | a0001c0001a0004c0008 | a0001c0001t0001a0004c0008t0001 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(1): Show | 4 | 342 | 0.0117 | -2 | c.211 others(21): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | TogoVar | ||||||
TMEM116_chr12_111926298_112018165 | 111970586 | GTT | G | intron_variant | MODIFIER | HG01943.hp1 HG02257.hp2 HG02622.hp2 others(10): Show |
a0001a0002a0006 | a0001c0001a0002c0002a0006c0006 | a0001c0001t0001a0002c0002t0001a0006c0006t0001 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(10): Show | 13 | 342 | 0.0380 | -2 | c.210 others(21): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | TogoVar | ||||||
TMEM116_chr12_111926298_112018165 | 111985277 | TAC | T | intron_variant | MODIFIER | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(105): Show |
a0001a0002a0006others(1): Show | a0001c0001a0002c0002a0002c0003others(3): Show | a0001c0001t0003a0002c0002t0001a0002c0002t0002others(4): Show | a0001c0001t0003g0077a0001c0001t0003g0078a0002c0002t0001g0002others(101): Show | 108 | 342 | 0.3158 | -2 | c.210 others(19): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | TogoVar | ||||||
TMEM116_chr12_111926298_112018165 | 111996039 | CAA | C | intron_variant | MODIFIER | HG00597.hp1 HG00735.hp2 HG01071.hp2 others(77): Show |
a0001a0009 | a0001c0001a0009c0011 | a0001c0001t0001a0009c0011t0001 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0016others(74): Show | 80 | 342 | 0.2339 | -2 | c.79- others(17): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | TogoVar | ||||||
TMEM116_chr12_111926298_112018165 | 111997717 | GAA | G | intron_variant | MODIFIER | HG01496.hp2 HG01952.hp1 HG02273.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004 | a0001c0001t0001g0005a0001c0001t0004g0006 | 3 | 342 | 0.0088 | -2 | c.79- others(17): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | TogoVar | ||||||
TMEM117_chr12_43831081_44394758 | 43834523 | ACT | A | upstream_gene_variant | MODIFIER | HG03209.hp2 HG06807.hp2 |
a0001 | a0001c0001 | a0001c0001t0006a0001c0001t0007 | a0001c0001t0006g0080a0001c0001t0007g0079 | 2 | 110 | 0.0182 | -2 | c.-17 others(13): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 1557 | chr12 | TogoVar | ||||||
TMEM117_chr12_43831081_44394758 | 43842721 | AAC | A | intron_variant | MODIFIER | HG00738.hp2 HG01175.hp1 HG01981.hp2 others(10): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(1): Show | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0002g0083others(10): Show | 13 | 110 | 0.1182 | -2 | c.-28 others(19): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 43848642 | AAC | A | intron_variant | MODIFIER | HG01175.hp1 HG01981.hp2 HG02723.hp1 others(2): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0002a0001c0001t0004a0002c0002t0001 | a0001c0001t0002g0083a0001c0001t0002g0084a0001c0001t0002g0085others(2): Show | 5 | 110 | 0.0455 | -2 | c.277 others(19): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 43848648 | CAT | C | intron_variant | MODIFIER | HG00738.hp2 HG02055.hp1 HG02486.hp2 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0002g0088others(5): Show | 8 | 110 | 0.0727 | -2 | c.277 others(19): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 2/7 | chr12 | TogoVar | ||||||
TMEM117_chr12_43831081_44394758 | 43859055 | TCA | T | intron_variant | MODIFIER | HG02486.hp2 HG02630.hp2 HG02896.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0090others(3): Show | 6 | 110 | 0.0546 | -2 | c.277 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 2/7 | chr12 | TogoVar | ||||||
TMEM117_chr12_43831081_44394758 | 43872370 | CTG | C | intron_variant | MODIFIER | HG00738.hp1 HG00738.hp2 HG00741.hp2 others(40): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(1): Show | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(40): Show | 43 | 110 | 0.3909 | -2 | c.277 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 43875220 | AGT | A | intron_variant | MODIFIER | HG01167.hp1 HG01168.hp1 HG01192.hp2 others(24): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(3): Show | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0056others(24): Show | 27 | 110 | 0.2455 | -2 | c.277 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 43877634 | CAA | C | intron_variant | MODIFIER | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(9): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003 | a0001c0001t0001g0001a0001c0001t0001g0096a0001c0001t0001g0097others(9): Show | 12 | 110 | 0.1091 | -2 | c.277 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 43877890 | AAC | A | intron_variant | MODIFIER | HG00738.hp2 HG01981.hp2 HG02559.hp1 others(5): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(3): Show | a0001c0001t0001g0078a0001c0001t0002g0013a0001c0001t0004g0072others(5): Show | 8 | 110 | 0.0727 | -2 | c.277 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 43878063 | GAA | G | intron_variant | MODIFIER | HG00738.hp1 HG00738.hp2 HG00741.hp2 others(46): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(1): Show | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(46): Show | 49 | 110 | 0.4455 | -2 | c.277 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 43897781 | ATT | A | intron_variant | MODIFIER | HG00738.hp1 HG00738.hp2 HG00741.hp2 others(61): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(1): Show | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(61): Show | 64 | 110 | 0.5818 | -2 | c.278 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 43898042 | ACG | A | intron_variant | MODIFIER | HG01192.hp2 HG02559.hp1 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0004 | a0001c0001t0002g0050a0001c0001t0004g0075 | 2 | 110 | 0.0182 | -2 | c.278 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 43898048 | GCA | G | intron_variant | MODIFIER | HG00741.hp1 HG01071.hp2 HG01167.hp2 others(36): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(4): Show | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0011others(36): Show | 39 | 110 | 0.3546 | -2 | c.278 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 43900825 | CAG | C | intron_variant | MODIFIER | HG01192.hp2 HG02723.hp2 HG02886.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0002g0049others(2): Show | 5 | 110 | 0.0455 | -2 | c.278 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 43908539 | GAC | G | intron_variant | MODIFIER | HG01192.hp2 HG02723.hp2 HG02886.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0002g0049others(2): Show | 5 | 110 | 0.0455 | -2 | c.278 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 43912507 | TTA | T | intron_variant | MODIFIER | HG02622.hp2 HG02630.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0017a0001c0001t0002g0018 | 2 | 110 | 0.0182 | -2 | c.278 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 43920549 | CTT | C | intron_variant | MODIFIER | HG01167.hp1 HG01175.hp2 HG02559.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0004 | a0001c0001t0001g0063a0001c0001t0002g0051a0001c0001t0002g0054others(4): Show | 7 | 110 | 0.0636 | -2 | c.278 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 43943176 | CAA | C | intron_variant | MODIFIER | HG02258.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0006 | a0001c0001t0001g0009a0001c0001t0001g0027a0001c0001t0001g0110others(7): Show | 10 | 110 | 0.0909 | -2 | c.278 others(19): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 43944782 | TGA | T | intron_variant | MODIFIER | HG02886.hp1 HG03139.hp2 NA19030.hp1 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0002a0001c0001t0002g0021a0001c0001t0002g0038 | 3 | 110 | 0.0273 | -2 | c.410 others(17): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 43946393 | TTG | T | intron_variant | MODIFIER | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(13): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(1): Show | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(13): Show | 16 | 110 | 0.1455 | -2 | c.410 others(19): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 43950548 | CAA | C | intron_variant | MODIFIER | HG00738.hp1 HG00741.hp2 HG01071.hp1 others(34): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0004 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(34): Show | 37 | 110 | 0.3364 | -2 | c.410 others(19): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 43956500 | CAA | C | intron_variant | MODIFIER | HG00741.hp2 HG01167.hp2 HG01169.hp2 others(13): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(13): Show | 16 | 110 | 0.1455 | -2 | c.410 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 43973920 | TGA | T | intron_variant | MODIFIER | HG02622.hp2 HG02630.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0017a0001c0001t0002g0018 | 2 | 110 | 0.0182 | -2 | c.410 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 43983547 | CGT | C | intron_variant | MODIFIER | HG01071.hp2 HG01168.hp2 HG01169.hp1 others(17): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(2): Show | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(17): Show | 20 | 110 | 0.1818 | -2 | c.410 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 43990916 | TTA | T | intron_variant | MODIFIER | HG02723.hp2 NA19240.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0052a0001c0001t0001g0053 | 2 | 110 | 0.0182 | -2 | c.410 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 43995255 | TTA | T | intron_variant | MODIFIER | HG01175.hp2 HG02572.hp2 HG02622.hp1 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0027a0001c0001t0001g0063a0001c0001t0001g0106others(6): Show | 9 | 110 | 0.0818 | -2 | c.410 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 3/7 | chr12 | TogoVar | ||||||
TMEM117_chr12_43831081_44394758 | 44004234 | CAG | C | intron_variant | MODIFIER | HG02723.hp2 NA19240.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0052a0001c0001t0001g0053 | 2 | 110 | 0.0182 | -2 | c.410 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 3/7 | chr12 | TogoVar | ||||||
TMEM117_chr12_43831081_44394758 | 44017900 | CAG | C | intron_variant | MODIFIER | HG01175.hp2 HG02055.hp2 HG02257.hp1 others(13): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(1): Show | a0001c0001t0001g0009a0001c0001t0001g0030a0001c0001t0001g0063others(13): Show | 16 | 110 | 0.1455 | -2 | c.410 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 44037850 | CCT | C | intron_variant | MODIFIER | HG02451.hp1 HG02896.hp1 NA18906.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003 | a0001c0001t0001g0094a0001c0001t0003g0036a0001c0001t0003g0037others(1): Show | 4 | 110 | 0.0364 | -2 | c.410 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 44042761 | TAC | T | intron_variant | MODIFIER | HG01192.hp1 HG01255.hp2 HG01261.hp2 others(12): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0002c0002t0001 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0019others(12): Show | 15 | 110 | 0.1364 | -2 | c.410 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar |