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 | 44080015 | CAA | C | intron_variant | MODIFIER | HG01169.hp2 HG01884.hp1 HG02258.hp2 others(10): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0005 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0011others(10): Show | 13 | 110 | 0.1182 | -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 | 44086979 | AAT | A | intron_variant | MODIFIER | HG03098.hp1 HG03579.hp2 NA19240.hp2 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0042 | 3 | 110 | 0.0273 | -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 | 44097399 | TAA | T | intron_variant | MODIFIER | HG01071.hp2 HG01167.hp2 HG01168.hp2 others(27): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(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 | 44104526 | CTG | C | intron_variant | MODIFIER | HG01071.hp2 HG01168.hp2 HG01169.hp1 others(20): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(20): Show | 23 | 110 | 0.2091 | -2 | c.411 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 3/7 | chr12 | TogoVar | ||||||
TMEM117_chr12_43831081_44394758 | 44132187 | GTT | G | intron_variant | MODIFIER | HG01071.hp2 HG01168.hp2 HG01169.hp1 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0096others(7): Show | 10 | 110 | 0.0909 | -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 | 44133483 | TTC | T | intron_variant | MODIFIER | HG02895.hp2 HG02897.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | 110 | 0.0182 | -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 | 44150295 | CTG | C | intron_variant | MODIFIER | HG01167.hp2 HG01169.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0011a0001c0001t0001g0012 | 2 | 110 | 0.0182 | -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 | 44152476 | CAT | C | intron_variant | MODIFIER | HG00738.hp2 HG02055.hp1 HG02723.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0002g0083others(1): Show | 4 | 110 | 0.0364 | -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 | 44152536 | CAT | C | intron_variant | MODIFIER | HG01884.hp2 HG02717.hp2 HG03130.hp1 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0047 | 3 | 110 | 0.0273 | -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 | 44168054 | GAC | G | intron_variant | MODIFIER | HG00741.hp1 HG02055.hp2 HG02257.hp1 others(8): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0017a0001c0001t0001g0027a0001c0001t0001g0030others(8): Show | 11 | 110 | 0.1000 | -2 | c.510 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 4/7 | chr12 | TogoVar | ||||||
TMEM117_chr12_43831081_44394758 | 44171013 | CTT | C | intron_variant | MODIFIER | HG01071.hp2 HG01168.hp2 HG01169.hp1 others(21): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(21): Show | 24 | 110 | 0.2182 | -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 | TAC | T | intron_variant | MODIFIER | HG00738.hp2 HG01167.hp2 HG01169.hp2 others(11): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0065others(11): Show | 14 | 110 | 0.1273 | -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 | 44202005 | CTT | C | intron_variant | MODIFIER | HG02723.hp2 HG02886.hp1 HG03139.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0053a0001c0001t0002g0002a0001c0001t0002g0021others(1): Show | 4 | 110 | 0.0364 | -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 | 44203340 | ATC | A | 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(19): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 44208725 | GTT | G | intron_variant | MODIFIER | HG02258.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0106others(2): Show | 5 | 110 | 0.0455 | -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 | ATT | A | intron_variant | MODIFIER | HG00738.hp2 HG01167.hp2 HG02258.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0078others(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 | 44223442 | TTC | T | intron_variant | MODIFIER | HG01071.hp2 HG01168.hp2 HG01169.hp1 others(22): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(22): Show | 25 | 110 | 0.2273 | -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 | 44236171 | CAT | C | intron_variant | MODIFIER | HG01071.hp2 HG01167.hp2 HG01168.hp2 others(60): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(2): Show | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(60): Show | 63 | 110 | 0.5727 | -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 | 44236187 | TAG | T | intron_variant | MODIFIER | HG00741.hp1 HG01884.hp1 HG01981.hp1 others(10): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0034others(10): Show | 13 | 110 | 0.1182 | -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 | 44252085 | TAC | T | intron_variant | MODIFIER | HG02723.hp2 HG02886.hp1 HG02976.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0053a0001c0001t0002g0002a0001c0001t0002g0021others(3): Show | 6 | 110 | 0.0546 | -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 | TAC | T | intron_variant | MODIFIER | HG00741.hp1 HG01261.hp1 HG02055.hp2 others(15): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0017others(15): Show | 18 | 110 | 0.1636 | -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 | 44254649 | GAT | G | intron_variant | MODIFIER | HG01884.hp2 HG01981.hp1 HG02258.hp2 others(10): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0039others(10): Show | 13 | 110 | 0.1182 | -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 | 44261162 | CAG | C | intron_variant | MODIFIER | HG01192.hp2 HG02886.hp2 HG03209.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0015a0001c0001t0002g0049a0001c0001t0002g0050others(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 | 44273373 | CAT | C | intron_variant | MODIFIER | HG02723.hp2 HG02886.hp1 HG02976.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0028a0001c0001t0001g0053a0001c0001t0002g0002others(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 | ATG | A | intron_variant | MODIFIER | HG01884.hp1 HG02738.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0005 | a0001c0001t0001g0004a0001c0001t0005g0005 | 2 | 110 | 0.0182 | -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 | TTG | T | intron_variant | MODIFIER | HG01175.hp1 HG02486.hp2 HG02630.hp2 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0014a0001c0001t0002g0057a0001c0001t0002g0083others(6): Show | 9 | 110 | 0.0818 | -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 | CTT | C | intron_variant | MODIFIER | HG00741.hp1 HG01167.hp1 HG01175.hp1 others(26): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003 | a0001c0001t0001g0106a0001c0001t0002g0014a0001c0001t0002g0020others(26): Show | 29 | 110 | 0.2636 | -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 | 44299128 | ATT | A | intron_variant | MODIFIER | HG02896.hp2 HG02897.hp1 HG03098.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0042a0001c0001t0002g0089a0001c0001t0002g0090others(2): Show | 5 | 110 | 0.0455 | -2 | c.609 others(17): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 44309776 | TAA | T | intron_variant | MODIFIER | HG01175.hp1 HG02486.hp2 HG02622.hp2 others(9): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0017a0001c0001t0002g0015a0001c0001t0002g0018others(9): Show | 12 | 110 | 0.1091 | -2 | c.768 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 44311727 | GTA | G | intron_variant | MODIFIER | HG02451.hp1 HG02486.hp2 HG02622.hp2 others(12): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003 | a0001c0001t0001g0017a0001c0001t0002g0015a0001c0001t0002g0018others(12): Show | 15 | 110 | 0.1364 | -2 | c.768 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 44311757 | GTA | G | intron_variant | MODIFIER | HG01175.hp1 HG01261.hp2 HG02055.hp1 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0001a0001c0001t0001g0024a0001c0001t0001g0077others(6): Show | 9 | 110 | 0.0818 | -2 | c.768 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 44311775 | ATG | A | intron_variant | MODIFIER | HG01261.hp2 HG02055.hp1 HG02559.hp2 others(9): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0001a0001c0001t0001g0024a0001c0001t0001g0028others(9): Show | 12 | 110 | 0.1091 | -2 | c.768 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 44311813 | GTA | G | intron_variant | MODIFIER | HG01167.hp2 HG02622.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0012a0001c0001t0001g0027 | 2 | 110 | 0.0182 | -2 | c.768 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 44311867 | GTA | G | intron_variant | MODIFIER | HG02559.hp2 HG02886.hp1 HG02976.hp1 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0039a0001c0001t0002g0002a0001c0001t0002g0013others(6): Show | 9 | 110 | 0.0818 | -2 | c.768 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 44311907 | ATG | A | intron_variant | MODIFIER | HG00741.hp1 HG01167.hp1 HG01175.hp1 others(34): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0009a0001c0001t0001g0039a0001c0001t0001g0106others(34): Show | 37 | 110 | 0.3364 | -2 | c.768 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 44311913 | GTA | G | intron_variant | MODIFIER | HG01071.hp2 HG01167.hp2 HG01168.hp2 others(15): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0006 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(15): Show | 18 | 110 | 0.1636 | -2 | c.768 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 44330272 | ATG | A | intron_variant | MODIFIER | HG01175.hp1 HG02723.hp1 HG02965.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0057a0001c0001t0002g0083a0001c0001t0002g0084others(2): Show | 5 | 110 | 0.0455 | -2 | c.768 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 44332712 | TAC | T | intron_variant | MODIFIER | HG00741.hp1 HG01071.hp2 HG01167.hp1 others(24): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(24): Show | 27 | 110 | 0.2455 | -2 | c.768 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 44373771 | CTT | C | intron_variant | MODIFIER | HG01168.hp1 HG01261.hp2 HG01496.hp1 others(30): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0002c0002t0001 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(30): Show | 33 | 110 | 0.3000 | -2 | c.769 others(19): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 44374616 | TTG | T | intron_variant | MODIFIER | HG00738.hp2 HG01168.hp2 HG01169.hp2 others(12): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0005 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(12): Show | 15 | 110 | 0.1364 | -2 | c.769 others(19): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 44390199 | GAC | G | downstream_gene_variant | MODIFIER | HG01175.hp1 HG01496.hp2 HG01884.hp2 others(26): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003 | a0001c0001t0001g0009a0001c0001t0002g0015a0001c0001t0002g0018others(26): Show | 29 | 110 | 0.2636 | -2 | c.*15 others(13): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 442 | chr12 | TogoVar | ||||||
TMEM119_chr12_108584851_108603084 | 108585918 | ATT | A | downstream_gene_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(80): Show |
a0001a0002a0004others(2): Show | a0001c0002a0001c0004a0002c0001others(3): Show | a0001c0002t0001a0001c0002t0005a0001c0002t0019others(6): Show | a0001c0002t0001g0002a0001c0002t0001g0013a0001c0002t0001g0022others(17): Show | 83 | 444 | 0.1869 | -2 | c.*56 others(13): Show |
TMEM119 | ENSG00000183160.9 | transcript | ENST00000392806.4 | protein_coding | 3932 | chr12 | TogoVar | ||||||
TMEM119_chr12_108584851_108603084 | 108586536 | ACT | A | downstream_gene_variant | MODIFIER | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(75): Show |
a0001a0009 | a0001c0003a0001c0004a0009c0012 | a0001c0003t0001a0001c0003t0012a0001c0003t0014others(2): Show | a0001c0003t0001g0003a0001c0003t0001g0008a0001c0003t0001g0009others(11): Show | 78 | 444 | 0.1757 | -2 | c.*49 others(13): Show |
TMEM119 | ENSG00000183160.9 | transcript | ENST00000392806.4 | protein_coding | 3314 | chr12 | TogoVar | ||||||
TMEM119_chr12_108584851_108603084 | 108592838 | CAG | C | intron_variant | MODIFIER | NA18960.hp2 NA19057.hp1 NA19082.hp2 |
a0001 | a0001c0003 | a0001c0003t0009 | a0001c0003t0009g0029 | 3 | 444 | 0.0068 | -2 | c.-14 others(17): Show |
TMEM119 | ENSG00000183160.9 | transcript | ENST00000392806.4 | protein_coding | 1/1 | chr12 | TogoVar | ||||||
TMEM119_chr12_108584851_108603084 | 108596429 | AAC | A | intron_variant | MODIFIER | HG01167.hp2 HG02055.hp1 HG02109.hp2 others(5): Show |
a0001 | a0001c0002a0001c0007 | a0001c0002t0005a0001c0007t0003 | a0001c0002t0005g0068a0001c0007t0003g0012 | 8 | 444 | 0.0180 | -2 | c.-15 others(19): Show |
TMEM119 | ENSG00000183160.9 | transcript | ENST00000392806.4 | protein_coding | 1/1 | chr12 | TogoVar | ||||||
TMEM119_chr12_108584851_108603084 | 108601621 | TAC | T | upstream_gene_variant | MODIFIER | HG00323.hp2 HG00423.hp2 HG00741.hp1 others(38): Show |
a0001a0002 | a0001c0002a0001c0003a0001c0006others(1): Show | a0001c0002t0001a0001c0003t0001a0001c0006t0002others(2): Show | a0001c0002t0001g0002a0001c0003t0001g0003a0001c0003t0001g0078others(10): Show | 41 | 444 | 0.0923 | -2 | c.-36 others(13): Show |
TMEM119 | ENSG00000183160.9 | transcript | ENST00000392806.4 | protein_coding | 3538 | chr12 | TogoVar | ||||||
TMEM119_chr12_108584851_108603084 | 108601677 | CAG | C | upstream_gene_variant | MODIFIER | NA19055.hp2 NA19067.hp1 NA19083.hp2 |
a0005 | a0005c0011 | a0005c0011t0004 | a0005c0011t0004g0024 | 3 | 444 | 0.0068 | -2 | c.-37 others(13): Show |
TMEM119 | ENSG00000183160.9 | transcript | ENST00000392806.4 | protein_coding | 3594 | chr12 | TogoVar | ||||||
TMEM11_chr17_21192954_21219161 | 21197001 | ACT | A | downstream_gene_variant | MODIFIER | HG03017.hp1 HG03491.hp1 HG03492.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0025 | 3 | 422 | 0.0071 | -2 | c.*13 others(13): Show |
TMEM11 | ENSG00000178307.10 | transcript | ENST00000317635.6 | protein_coding | 952 | chr17 | TogoVar | ||||||
TMEM11_chr17_21192954_21219161 | 21199145 | CCT | C | intron_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG00609.hp1 others(131): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(44): Show | 134 | 422 | 0.3175 | -2 | c.63- others(15): Show |
TMEM11 | ENSG00000178307.10 | transcript | ENST00000317635.6 | protein_coding | 1/1 | chr17 | TogoVar | ||||||
TMEM11_chr17_21192954_21219161 | 21204122 | TAA | T | intron_variant | MODIFIER | HG01168.hp1 HG01168.hp2 HG01256.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0045a0001c0001t0001g0052a0001c0001t0001g0090others(3): Show | 7 | 422 | 0.0166 | -2 | c.63- others(17): Show |
TMEM11 | ENSG00000178307.10 | transcript | ENST00000317635.6 | protein_coding | 1/1 | chr17 | TogoVar |