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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
TMEM117_chr12_43831081_44394758 | 43885414 | C | CTT | intron_variant | MODIFIER | HG00738.hp2 HG00741.hp2 HG01071.hp1 others(33): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0004 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(33): Show | 36 | 110 | 0.3273 | 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 | 43885419 | C | CTT | 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 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 43885473 | T | TTA | intron_variant | MODIFIER | HG01175.hp1 HG02723.hp1 HG02809.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0004 | a0001c0001t0002g0083a0001c0001t0002g0084a0001c0001t0002g0085others(1): Show | 4 | 110 | 0.0364 | 2 | c.277 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 2/7 | chr12 | TogoVar | ||||||
TMEM117_chr12_43831081_44394758 | 43888546 | T | TTC | intron_variant | MODIFIER | HG01168.hp2 HG01169.hp1 HG01255.hp2 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003 | a0001c0001t0001g0001a0001c0001t0001g0096a0001c0001t0001g0097others(6): Show | 9 | 110 | 0.0818 | 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 | 43891367 | A | ATT | intron_variant | MODIFIER | HG01175.hp1 HG02647.hp1 HG02723.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0004 | a0001c0001t0001g0044a0001c0001t0002g0002a0001c0001t0002g0021others(4): Show | 7 | 110 | 0.0636 | 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 | 43898048 | G | GCA | intron_variant | MODIFIER | HG02559.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003 | a0001c0001t0001g0039a0001c0001t0001g0043a0001c0001t0001g0096others(3): Show | 6 | 110 | 0.0546 | 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 | 43900717 | C | CAA | intron_variant | MODIFIER | HG01175.hp1 HG01175.hp2 HG01255.hp2 others(8): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(1): Show | a0001c0001t0001g0009a0001c0001t0001g0063a0001c0001t0001g0096others(8): Show | 11 | 110 | 0.1000 | 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 | 43906462 | C | CAA | intron_variant | MODIFIER | HG00738.hp1 HG00738.hp2 HG00741.hp2 others(39): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0004 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(39): Show | 42 | 110 | 0.3818 | 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 | T | TTA | intron_variant | MODIFIER | HG03486.hp2 HG03540.hp2 NA18906.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003 | a0001c0001t0001g0081a0001c0001t0002g0015a0001c0001t0003g0016 | 3 | 110 | 0.0273 | 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 | C | CAA | intron_variant | MODIFIER | HG00741.hp1 HG01167.hp1 HG02723.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0002g0025others(2): Show | 5 | 110 | 0.0455 | 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 | 43945173 | G | GAT | intron_variant | MODIFIER | HG00738.hp2 HG01981.hp2 HG02055.hp1 others(19): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(3): Show | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0027others(19): Show | 22 | 110 | 0.2000 | 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 | 43967132 | C | CTT | intron_variant | MODIFIER | HG00741.hp1 HG02258.hp1 HG02486.hp2 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0005 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0046others(7): Show | 10 | 110 | 0.0909 | 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 | C | CGT | intron_variant | MODIFIER | HG01496.hp2 HG02809.hp1 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0004 | a0001c0001t0002g0048a0001c0001t0004g0086 | 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 | 44018725 | C | CTT | intron_variant | MODIFIER | HG02895.hp1 NA18522.hp1 NA18906.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0024a0001c0001t0001g0034a0001c0001t0001g0081others(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 | T | TAC | intron_variant | MODIFIER | HG02622.hp2 HG03098.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003 | a0001c0001t0001g0017a0001c0001t0003g0103 | 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 | 44044709 | G | GTT | intron_variant | MODIFIER | HG02622.hp2 HG02630.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0017a0001c0001t0002g0018 | 2 | 110 | 0.0182 | 2 | c.411 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 3/7 | chr12 | TogoVar | ||||||
TMEM117_chr12_43831081_44394758 | 44047133 | G | GTA | intron_variant | MODIFIER | HG02055.hp2 HG02257.hp1 HG02280.hp1 others(8): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(1): Show | a0001c0001t0001g0030a0001c0001t0001g0096a0001c0001t0001g0097others(8): Show | 11 | 110 | 0.1000 | 2 | c.411 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 44061526 | G | GTT | intron_variant | MODIFIER | HG00738.hp2 HG01167.hp2 HG01168.hp2 others(27): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(1): Show | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(27): Show | 30 | 110 | 0.2727 | 2 | c.411 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 44077797 | C | CAA | intron_variant | MODIFIER | HG00741.hp1 HG01884.hp1 HG01884.hp2 others(17): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(2): Show | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0028others(17): Show | 20 | 110 | 0.1818 | 2 | c.411 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 44083389 | G | GTT | intron_variant | MODIFIER | HG01175.hp1 HG01255.hp2 HG02257.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003 | a0001c0001t0001g0100a0001c0001t0002g0022a0001c0001t0002g0085others(3): Show | 6 | 110 | 0.0546 | 2 | c.411 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 44090839 | G | GTT | intron_variant | MODIFIER | HG02895.hp1 HG03579.hp2 HG06807.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0006 | a0001c0001t0001g0024a0001c0001t0001g0034a0001c0001t0001g0081others(4): Show | 7 | 110 | 0.0636 | 2 | c.411 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 44117344 | G | GTT | intron_variant | MODIFIER | HG01884.hp2 HG02717.hp2 HG03098.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0028a0001c0001t0002g0013a0001c0001t0002g0014others(4): Show | 7 | 110 | 0.0636 | 2 | c.411 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 44139492 | C | CAT | intron_variant | MODIFIER | HG00741.hp1 HG01071.hp2 HG01167.hp2 others(68): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(2): Show | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(68): Show | 71 | 110 | 0.6455 | 2 | c.411 others(19): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 3/7 | chr12 | TogoVar | ||||||
TMEM117_chr12_43831081_44394758 | 44152516 | A | ATT | intron_variant | MODIFIER | HG01884.hp1 HG01884.hp2 HG01981.hp1 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0005 | a0001c0001t0001g0004a0001c0001t0002g0013a0001c0001t0002g0014others(6): Show | 9 | 110 | 0.0818 | 2 | c.510 others(19): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 44152518 | T | TTA | intron_variant | MODIFIER | HG02258.hp2 HG02451.hp1 HG02559.hp2 others(24): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(1): Show | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0028others(24): Show | 27 | 110 | 0.2455 | 2 | c.510 others(19): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 44160292 | T | TAC | intron_variant | MODIFIER | HG01167.hp2 HG01169.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0011a0001c0001t0001g0012 | 2 | 110 | 0.0182 | 2 | c.510 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 44185869 | T | TAC | intron_variant | MODIFIER | HG00738.hp1 HG01255.hp1 HG01496.hp1 others(9): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0007 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0019others(9): Show | 12 | 110 | 0.1091 | 2 | c.511 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 44190884 | C | CAT | intron_variant | MODIFIER | HG02572.hp2 HG02895.hp1 HG06807.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0006 | a0001c0001t0001g0024a0001c0001t0001g0081a0001c0001t0002g0032others(2): Show | 5 | 110 | 0.0455 | 2 | c.511 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 44190962 | T | TTA | intron_variant | MODIFIER | HG01168.hp1 HG02738.hp1 NA18522.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0034a0001c0001t0001g0087a0001c0001t0001g0109 | 3 | 110 | 0.0273 | 2 | c.511 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 44202405 | C | CTG | intron_variant | MODIFIER | HG00741.hp1 HG01071.hp2 HG01168.hp2 others(60): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(2): Show | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(60): Show | 63 | 110 | 0.5727 | 2 | c.511 others(19): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 44208725 | G | GTT | intron_variant | MODIFIER | HG02572.hp2 HG02723.hp2 HG02886.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0034a0001c0001t0001g0053a0001c0001t0001g0081others(4): Show | 7 | 110 | 0.0636 | 2 | c.511 others(19): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 44214138 | A | ATT | intron_variant | MODIFIER | HG02559.hp2 HG02572.hp1 HG02647.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0039a0001c0001t0001g0043a0001c0001t0001g0044others(1): Show | 4 | 110 | 0.0364 | 2 | c.608 others(19): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 44216005 | C | CTT | intron_variant | MODIFIER | HG00741.hp1 HG01884.hp2 HG02055.hp2 others(25): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0027others(25): Show | 28 | 110 | 0.2546 | 2 | c.608 others(19): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 44224470 | A | ATT | intron_variant | MODIFIER | HG01071.hp2 HG01175.hp1 HG01192.hp2 others(18): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(18): Show | 21 | 110 | 0.1909 | 2 | c.608 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 44226501 | A | ATG | intron_variant | MODIFIER | HG00741.hp1 HG02055.hp1 HG02055.hp2 others(8): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0077others(8): Show | 11 | 110 | 0.1000 | 2 | c.608 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 44241397 | T | TAA | intron_variant | MODIFIER | HG00741.hp1 HG02055.hp2 HG02257.hp1 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0030a0001c0001t0002g0020a0001c0001t0002g0022others(5): Show | 8 | 110 | 0.0727 | 2 | c.608 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 44249188 | T | TTG | intron_variant | MODIFIER | HG01884.hp2 HG02717.hp2 HG03130.hp1 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0047 | 3 | 110 | 0.0273 | 2 | c.608 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 44253835 | T | TAC | intron_variant | MODIFIER | HG00738.hp1 HG00738.hp2 HG01167.hp1 others(8): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(1): Show | a0001c0001t0001g0027a0001c0001t0001g0055a0001c0001t0001g0062others(8): Show | 11 | 110 | 0.1000 | 2 | c.608 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 44254011 | C | CAA | intron_variant | MODIFIER | HG01884.hp2 HG02451.hp1 HG02717.hp2 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003 | a0001c0001t0001g0094a0001c0001t0002g0040a0001c0001t0002g0041others(5): Show | 8 | 110 | 0.0727 | 2 | c.608 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 44273373 | C | CAT | intron_variant | MODIFIER | HG01167.hp2 HG01169.hp2 HG02559.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0027others(4): Show | 7 | 110 | 0.0636 | 2 | c.609 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 44276908 | A | ATG | intron_variant | MODIFIER | HG01167.hp2 HG01169.hp2 HG02258.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(2): Show | 5 | 110 | 0.0455 | 2 | c.609 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 44277761 | C | CTT | intron_variant | MODIFIER | HG01071.hp2 HG01192.hp2 HG01261.hp2 others(13): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(13): Show | 16 | 110 | 0.1455 | 2 | c.609 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 44289225 | T | TTG | intron_variant | MODIFIER | HG02572.hp1 HG02647.hp1 HG02809.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(1): Show | 4 | 110 | 0.0364 | 2 | c.609 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 44289550 | C | CTT | intron_variant | MODIFIER | HG02647.hp2 HG03098.hp1 HG03491.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0006 | a0001c0001t0001g0034a0001c0001t0001g0065a0001c0001t0001g0110others(4): Show | 7 | 110 | 0.0636 | 2 | c.609 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 44291374 | G | GTT | intron_variant | MODIFIER | HG01071.hp2 HG01255.hp2 HG01981.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0006a0001c0001t0001g0076a0001c0001t0001g0100others(2): Show | 5 | 110 | 0.0455 | 2 | c.609 others(19): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 44293110 | G | GAT | intron_variant | MODIFIER | HG02486.hp2 HG02622.hp2 HG02630.hp1 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0017a0001c0001t0002g0015a0001c0001t0002g0018others(7): Show | 10 | 110 | 0.0909 | 2 | c.609 others(19): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 44295677 | G | GTT | intron_variant | MODIFIER | HG01261.hp2 HG02055.hp1 HG02895.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001a0001c0001t0001g0024a0001c0001t0001g0028others(2): Show | 5 | 110 | 0.0455 | 2 | c.609 others(19): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 44308619 | C | CTT | intron_variant | MODIFIER | HG01175.hp1 HG01261.hp2 HG02723.hp1 others(8): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0001a0001c0001t0001g0024a0001c0001t0001g0081others(8): Show | 11 | 110 | 0.1000 | 2 | c.768 others(19): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 44311165 | C | CTT | intron_variant | MODIFIER | HG01261.hp2 HG02055.hp1 HG02486.hp2 others(12): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0024others(12): Show | 15 | 110 | 0.1364 | 2 | c.768 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 6/7 | chr12 | TogoVar | ||||||
TMEM117_chr12_43831081_44394758 | 44311797 | G | GTA | intron_variant | MODIFIER | HG01261.hp2 HG02055.hp1 HG02895.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001a0001c0001t0001g0024a0001c0001t0001g0077others(1): Show | 4 | 110 | 0.0364 | 2 | c.768 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar |