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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
TMEM132C_chr12_128262170_128712911 | 128469626 | TTG | T | intron_variant | MODIFIER | HG01099.hp2 HG02451.hp1 HG02486.hp2 others(1): Show |
a0003a0004a0010others(1): Show | a0003c0071a0004c0013a0010c0069others(1): Show | a0003c0071t0002a0004c0013t0002a0010c0069t0001others(1): Show | a0003c0071t0002g0079a0004c0013t0002g0065a0010c0069t0001g0021others(1): Show | 4 | 170 | 0.0235 | -2 | c.974 others(21): Show |
TMEM132C | ENSG00000181234.10 | transcript | ENST00000435159.3 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM132C_chr12_128262170_128712911 | 128469662 | GTA | G | intron_variant | MODIFIER | HG01081.hp2 HG02258.hp2 HG04204.hp1 |
a0002a0005 | a0002c0018a0005c0005a0005c0012 | a0002c0018t0002a0005c0005t0002a0005c0012t0004 | a0002c0018t0002g0136a0005c0005t0002g0121a0005c0012t0004g0035 | 3 | 170 | 0.0177 | -2 | c.974 others(21): Show |
TMEM132C | ENSG00000181234.10 | transcript | ENST00000435159.3 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM132C_chr12_128262170_128712911 | 128471391 | CTG | C | intron_variant | MODIFIER | HG01891.hp1 HG02615.hp2 HG02922.hp2 others(2): Show |
a0003a0004a0008others(1): Show | a0003c0016a0004c0008a0008c0028others(2): Show | a0003c0016t0002a0004c0008t0003a0008c0028t0001others(2): Show | a0003c0016t0002g0015a0004c0008t0003g0010a0008c0028t0001g0140others(2): Show | 5 | 170 | 0.0294 | -2 | c.974 others(21): Show |
TMEM132C | ENSG00000181234.10 | transcript | ENST00000435159.3 | protein_coding | 2/8 | chr12 | TogoVar | ||||||
TMEM132C_chr12_128262170_128712911 | 128486862 | CAT | C | intron_variant | MODIFIER | HG02451.hp2 HG02630.hp1 HG02818.hp1 others(3): Show |
a0003a0006a0008others(2): Show | a0003c0073a0003c0084a0006c0024others(3): Show | a0003c0073t0009a0003c0084t0002a0006c0024t0002others(3): Show | a0003c0073t0009g0066a0003c0084t0002g0151a0006c0024t0002g0087others(3): Show | 6 | 170 | 0.0353 | -2 | c.975 others(21): Show |
TMEM132C | ENSG00000181234.10 | transcript | ENST00000435159.3 | protein_coding | 2/8 | chr12 | TogoVar | ||||||
TMEM132C_chr12_128262170_128712911 | 128486876 | AAC | A | intron_variant | MODIFIER | HG00621.hp2 HG01070.hp2 HG01071.hp1 others(26): Show |
a0001a0002a0003others(10): Show | a0001c0001a0001c0019a0002c0004others(18): Show | a0001c0001t0001a0001c0019t0001a0002c0004t0003others(19): Show | a0001c0001t0001g0057a0001c0001t0001g0103a0001c0019t0001g0029others(26): Show | 29 | 170 | 0.1706 | -2 | c.975 others(21): Show |
TMEM132C | ENSG00000181234.10 | transcript | ENST00000435159.3 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM132C_chr12_128262170_128712911 | 128487473 | CGT | C | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(163): Show |
a0001a0002a0003others(30): Show | a0001c0001a0001c0019a0002c0004others(88): Show | a0001c0001t0001a0001c0001t0006a0001c0019t0001others(101): Show | a0001c0001t0001g0027a0001c0001t0001g0036a0001c0001t0001g0043others(163): Show | 166 | 170 | 0.9765 | -2 | c.975 others(21): Show |
TMEM132C | ENSG00000181234.10 | transcript | ENST00000435159.3 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM132C_chr12_128262170_128712911 | 128487603 | GTA | G | intron_variant | MODIFIER | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(72): Show |
a0001a0002a0003others(20): Show | a0001c0001a0001c0019a0002c0004others(48): Show | a0001c0001t0001a0001c0019t0001a0002c0004t0002others(53): Show | a0001c0001t0001g0043a0001c0001t0001g0098a0001c0001t0001g0122others(72): Show | 75 | 170 | 0.4412 | -2 | c.975 others(21): Show |
TMEM132C | ENSG00000181234.10 | transcript | ENST00000435159.3 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM132C_chr12_128262170_128712911 | 128487726 | CAG | C | intron_variant | MODIFIER | HG02615.hp1 HG03540.hp2 |
a0004a0006 | a0004c0007a0006c0025 | a0004c0007t0002a0006c0025t0005 | a0004c0007t0002g0096a0006c0025t0005g0075 | 2 | 170 | 0.0118 | -2 | c.975 others(21): Show |
TMEM132C | ENSG00000181234.10 | transcript | ENST00000435159.3 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM132C_chr12_128262170_128712911 | 128507402 | CTT | C | intron_variant | MODIFIER | HG00140.hp2 HG00558.hp1 HG00609.hp1 others(52): Show |
a0001a0002a0003others(16): Show | a0001c0001a0002c0004a0002c0006others(33): Show | a0001c0001t0001a0001c0001t0006a0002c0004t0002others(36): Show | a0001c0001t0001g0027a0001c0001t0001g0043a0001c0001t0001g0051others(52): Show | 55 | 170 | 0.3235 | -2 | c.975 others(21): Show |
TMEM132C | ENSG00000181234.10 | transcript | ENST00000435159.3 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM132C_chr12_128262170_128712911 | 128518718 | ATG | A | intron_variant | MODIFIER | HG02451.hp2 HG02559.hp2 HG02630.hp1 others(6): Show |
a0003a0006a0008others(4): Show | a0003c0073a0006c0021a0006c0024others(6): Show | a0003c0073t0009a0006c0021t0002a0006c0024t0002others(6): Show | a0003c0073t0009g0066a0006c0021t0002g0002a0006c0024t0002g0087others(6): Show | 9 | 170 | 0.0529 | -2 | c.975 others(21): Show |
TMEM132C | ENSG00000181234.10 | transcript | ENST00000435159.3 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM132C_chr12_128262170_128712911 | 128521307 | GTA | G | intron_variant | MODIFIER | HG00621.hp2 HG01070.hp1 HG01070.hp2 others(14): Show |
a0001a0002a0003others(5): Show | a0001c0001a0002c0004a0002c0006others(13): Show | a0001c0001t0001a0002c0004t0003a0002c0006t0005others(13): Show | a0001c0001t0001g0103a0002c0004t0003g0059a0002c0006t0005g0102others(14): Show | 17 | 170 | 0.1000 | -2 | c.975 others(21): Show |
TMEM132C | ENSG00000181234.10 | transcript | ENST00000435159.3 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM132C_chr12_128262170_128712911 | 128521319 | ATG | A | intron_variant | MODIFIER | HG02809.hp2 HG04228.hp1 |
a0001a0007 | a0001c0001a0007c0017 | a0001c0001t0001a0007c0017t0003 | a0001c0001t0001g0027a0007c0017t0003g0086 | 2 | 170 | 0.0118 | -2 | c.975 others(21): Show |
TMEM132C | ENSG00000181234.10 | transcript | ENST00000435159.3 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM132C_chr12_128262170_128712911 | 128527707 | ATG | A | intron_variant | MODIFIER | HG02145.hp1 HG03195.hp2 |
a0006a0014 | a0006c0021a0014c0068 | a0006c0021t0002a0014c0068t0003 | a0006c0021t0002g0165a0014c0068t0003g0085 | 2 | 170 | 0.0118 | -2 | c.975 others(21): Show |
TMEM132C | ENSG00000181234.10 | transcript | ENST00000435159.3 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM132C_chr12_128262170_128712911 | 128533948 | TAC | T | intron_variant | MODIFIER | HG01243.hp2 HG02145.hp2 HG02257.hp1 others(7): Show |
a0002a0003a0004others(5): Show | a0002c0046a0003c0010a0004c0007others(6): Show | a0002c0046t0002a0003c0010t0003a0004c0007t0002others(6): Show | a0002c0046t0002g0095a0003c0010t0003g0067a0003c0010t0003g0070others(7): Show | 10 | 170 | 0.0588 | -2 | c.975 others(19): Show |
TMEM132C | ENSG00000181234.10 | transcript | ENST00000435159.3 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM132C_chr12_128262170_128712911 | 128535865 | CAA | C | intron_variant | MODIFIER | HG01099.hp2 HG01243.hp1 HG02109.hp1 others(21): Show |
a0002a0003a0004others(10): Show | a0002c0004a0002c0037a0002c0038others(18): Show | a0002c0004t0003a0002c0037t0002a0002c0038t0002others(18): Show | a0002c0004t0003g0052a0002c0037t0002g0022a0002c0038t0002g0014others(21): Show | 24 | 170 | 0.1412 | -2 | c.975 others(19): Show |
TMEM132C | ENSG00000181234.10 | transcript | ENST00000435159.3 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM132C_chr12_128262170_128712911 | 128536749 | TTG | T | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00642.hp2 others(61): Show |
a0001a0002a0003others(19): Show | a0001c0001a0002c0004a0002c0006others(39): Show | a0001c0001t0001a0001c0001t0006a0002c0004t0003others(43): Show | a0001c0001t0001g0051a0001c0001t0001g0114a0001c0001t0001g0117others(61): Show | 64 | 170 | 0.3765 | -2 | c.975 others(19): Show |
TMEM132C | ENSG00000181234.10 | transcript | ENST00000435159.3 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM132C_chr12_128262170_128712911 | 128559096 | AAC | A | intron_variant | MODIFIER | HG00609.hp1 HG01243.hp2 HG01891.hp1 others(17): Show |
a0001a0003a0004others(5): Show | a0001c0001a0003c0010a0003c0016others(15): Show | a0001c0001t0006a0003c0010t0003a0003c0016t0008others(15): Show | a0001c0001t0006g0130a0003c0010t0003g0070a0003c0016t0008g0092others(17): Show | 20 | 170 | 0.1177 | -2 | c.112 others(23): Show |
TMEM132C | ENSG00000181234.10 | transcript | ENST00000435159.3 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM132C_chr12_128262170_128712911 | 128559164 | CAA | C | intron_variant | MODIFIER | HG01243.hp2 HG01891.hp1 HG02145.hp1 others(9): Show |
a0003a0004a0006others(2): Show | a0003c0010a0003c0072a0003c0073others(8): Show | a0003c0010t0003a0003c0072t0007a0003c0073t0009others(8): Show | a0003c0010t0003g0070a0003c0072t0007g0118a0003c0073t0009g0066others(9): Show | 12 | 170 | 0.0706 | -2 | c.112 others(23): Show |
TMEM132C | ENSG00000181234.10 | transcript | ENST00000435159.3 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM132C_chr12_128262170_128712911 | 128567429 | GAC | G | intron_variant | MODIFIER | HG01261.hp2 HG02004.hp1 HG02155.hp1 others(8): Show |
a0001a0002a0004others(4): Show | a0001c0001a0002c0040a0004c0008others(5): Show | a0001c0001t0001a0002c0040t0005a0004c0008t0010others(6): Show | a0001c0001t0001g0114a0002c0040t0005g0097a0004c0008t0010g0006others(8): Show | 11 | 170 | 0.0647 | -2 | c.112 others(23): Show |
TMEM132C | ENSG00000181234.10 | transcript | ENST00000435159.3 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM132C_chr12_128262170_128712911 | 128582414 | CTT | C | intron_variant | MODIFIER | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(30): Show |
a0001a0002a0003others(10): Show | a0001c0001a0002c0006a0002c0052others(15): Show | a0001c0001t0001a0002c0006t0004a0002c0052t0002others(19): Show | a0001c0001t0001g0027a0001c0001t0001g0036a0001c0001t0001g0057others(30): Show | 33 | 170 | 0.1941 | -2 | c.112 others(23): Show |
TMEM132C | ENSG00000181234.10 | transcript | ENST00000435159.3 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM132C_chr12_128262170_128712911 | 128586204 | TTA | T | intron_variant | MODIFIER | HG02257.hp1 HG02258.hp1 HG02486.hp2 others(3): Show |
a0002a0003a0004others(2): Show | a0002c0046a0003c0016a0004c0013others(3): Show | a0002c0046t0002a0003c0016t0002a0004c0013t0002others(3): Show | a0002c0046t0002g0095a0003c0016t0002g0015a0004c0013t0002g0065others(3): Show | 6 | 170 | 0.0353 | -2 | c.112 others(23): Show |
TMEM132C | ENSG00000181234.10 | transcript | ENST00000435159.3 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM132C_chr12_128262170_128712911 | 128603147 | GGA | G | intron_variant | MODIFIER | HG01884.hp1 HG02451.hp2 HG02922.hp2 others(4): Show |
a0003a0006a0008others(1): Show | a0003c0010a0003c0016a0003c0070others(3): Show | a0003c0010t0003a0003c0016t0002a0003c0070t0002others(3): Show | a0003c0010t0003g0164a0003c0016t0002g0015a0003c0070t0002g0083others(4): Show | 7 | 170 | 0.0412 | -2 | c.112 others(23): Show |
TMEM132C | ENSG00000181234.10 | transcript | ENST00000435159.3 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM132C_chr12_128262170_128712911 | 128618353 | CTG | C | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00609.hp1 others(44): Show |
a0001a0002a0003others(17): Show | a0001c0001a0002c0004a0002c0038others(34): Show | a0001c0001t0001a0001c0001t0006a0002c0004t0003others(40): Show | a0001c0001t0001g0051a0001c0001t0006g0130a0002c0004t0003g0052others(44): Show | 47 | 170 | 0.2765 | -2 | c.130 others(21): Show |
TMEM132C | ENSG00000181234.10 | transcript | ENST00000435159.3 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM132C_chr12_128262170_128712911 | 128620232 | CAA | C | intron_variant | MODIFIER | HG02257.hp2 HG02258.hp1 HG02622.hp1 others(4): Show |
a0002a0004a0007others(2): Show | a0002c0045a0004c0013a0007c0017others(3): Show | a0002c0045t0001a0004c0013t0001a0007c0017t0003others(3): Show | a0002c0045t0001g0144a0004c0013t0001g0016a0007c0017t0003g0018others(4): Show | 7 | 170 | 0.0412 | -2 | c.130 others(21): Show |
TMEM132C | ENSG00000181234.10 | transcript | ENST00000435159.3 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM132C_chr12_128262170_128712911 | 128628623 | ACT | A | intron_variant | MODIFIER | HG00639.hp1 HG02145.hp2 HG02257.hp2 others(15): Show |
a0002a0004a0005others(6): Show | a0002c0045a0004c0008a0004c0013others(11): Show | a0002c0045t0001a0004c0008t0013a0004c0013t0001others(12): Show | a0002c0045t0001g0144a0004c0008t0013g0091a0004c0013t0001g0016others(15): Show | 18 | 170 | 0.1059 | -2 | c.130 others(23): Show |
TMEM132C | ENSG00000181234.10 | transcript | ENST00000435159.3 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM132C_chr12_128262170_128712911 | 128636411 | CAT | C | intron_variant | MODIFIER | HG02615.hp1 HG03209.hp1 |
a0006 | a0006c0020a0006c0025 | a0006c0020t0002a0006c0025t0005 | a0006c0020t0002g0150a0006c0025t0005g0075 | 2 | 170 | 0.0118 | -2 | c.130 others(23): Show |
TMEM132C | ENSG00000181234.10 | transcript | ENST00000435159.3 | protein_coding | 4/8 | chr12 | TogoVar | ||||||
TMEM132C_chr12_128262170_128712911 | 128636564 | TTG | T | intron_variant | MODIFIER | HG00642.hp1 HG01071.hp1 HG01071.hp2 others(40): Show |
a0001a0002a0003others(12): Show | a0001c0001a0002c0004a0002c0006others(28): Show | a0001c0001t0001a0002c0004t0003a0002c0006t0004others(31): Show | a0001c0001t0001g0122a0002c0004t0003g0052a0002c0004t0003g0058others(40): Show | 43 | 170 | 0.2529 | -2 | c.130 others(23): Show |
TMEM132C | ENSG00000181234.10 | transcript | ENST00000435159.3 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM132C_chr12_128262170_128712911 | 128647862 | ATG | A | intron_variant | MODIFIER | HG00639.hp1 HG00642.hp1 HG02258.hp2 others(7): Show |
a0002a0005a0006others(4): Show | a0002c0004a0002c0018a0002c0042others(7): Show | a0002c0004t0003a0002c0018t0002a0002c0042t0009others(7): Show | a0002c0004t0003g0058a0002c0018t0002g0136a0002c0042t0009g0004others(7): Show | 10 | 170 | 0.0588 | -2 | c.130 others(23): Show |
TMEM132C | ENSG00000181234.10 | transcript | ENST00000435159.3 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM132C_chr12_128262170_128712911 | 128659780 | GAA | G | intron_variant | MODIFIER | HG01243.hp2 HG01884.hp1 HG02451.hp1 others(4): Show |
a0003a0006a0010others(1): Show | a0003c0009a0003c0010a0006c0053others(3): Show | a0003c0009t0001a0003c0010t0003a0006c0053t0016others(3): Show | a0003c0009t0001g0073a0003c0010t0003g0070a0003c0010t0003g0081others(4): Show | 7 | 170 | 0.0412 | -2 | c.130 others(21): Show |
TMEM132C | ENSG00000181234.10 | transcript | ENST00000435159.3 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM132C_chr12_128262170_128712911 | 128661559 | TAA | T | intron_variant | MODIFIER | HG00558.hp1 HG00642.hp1 HG01071.hp2 others(30): Show |
a0001a0002a0004others(10): Show | a0001c0001a0002c0004a0002c0006others(23): Show | a0001c0001t0001a0002c0004t0003a0002c0006t0005others(24): Show | a0001c0001t0001g0122a0001c0001t0001g0133a0002c0004t0003g0044others(30): Show | 33 | 170 | 0.1941 | -2 | c.130 others(21): Show |
TMEM132C | ENSG00000181234.10 | transcript | ENST00000435159.3 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM132C_chr12_128262170_128712911 | 128665173 | GCA | G | intron_variant | MODIFIER | HG01081.hp1 HG02559.hp1 HG03098.hp2 others(2): Show |
a0002a0004 | a0002c0004a0002c0038a0002c0045others(2): Show | a0002c0004t0002a0002c0038t0002a0002c0045t0001others(2): Show | a0002c0004t0002g0126a0002c0038t0002g0014a0002c0045t0001g0144others(2): Show | 5 | 170 | 0.0294 | -2 | c.130 others(21): Show |
TMEM132C | ENSG00000181234.10 | transcript | ENST00000435159.3 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM132C_chr12_128262170_128712911 | 128665540 | GGC | G | intron_variant | MODIFIER | HG00558.hp1 HG01071.hp2 HG02523.hp2 others(4): Show |
a0001a0002a0007others(3): Show | a0001c0001a0002c0006a0007c0089others(3): Show | a0001c0001t0001a0002c0006t0005a0007c0089t0005others(3): Show | a0001c0001t0001g0122a0001c0001t0001g0133a0002c0006t0005g0102others(4): Show | 7 | 170 | 0.0412 | -2 | c.130 others(21): Show |
TMEM132C | ENSG00000181234.10 | transcript | ENST00000435159.3 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM132C_chr12_128262170_128712911 | 128665554 | GGC | G | intron_variant | MODIFIER | HG01884.hp2 HG02486.hp1 HG02572.hp1 others(18): Show |
a0003a0005a0006others(4): Show | a0003c0010a0003c0016a0003c0071others(14): Show | a0003c0010t0003a0003c0016t0002a0003c0016t0008others(15): Show | a0003c0010t0003g0067a0003c0010t0003g0164a0003c0016t0002g0015others(18): Show | 21 | 170 | 0.1235 | -2 | c.130 others(21): Show |
TMEM132C | ENSG00000181234.10 | transcript | ENST00000435159.3 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM132C_chr12_128262170_128712911 | 128665621 | GCA | G | intron_variant | MODIFIER | HG01081.hp1 HG02004.hp2 HG02109.hp1 others(6): Show |
a0002a0004a0014others(1): Show | a0002c0004a0002c0040a0002c0046others(4): Show | a0002c0004t0002a0002c0004t0003a0002c0040t0005others(5): Show | a0002c0004t0002g0126a0002c0004t0003g0044a0002c0040t0005g0097others(6): Show | 9 | 170 | 0.0529 | -2 | c.130 others(21): Show |
TMEM132C | ENSG00000181234.10 | transcript | ENST00000435159.3 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM132C_chr12_128262170_128712911 | 128665809 | GCA | G | intron_variant | MODIFIER | HG01884.hp2 HG02486.hp1 HG02572.hp1 others(18): Show |
a0003a0005a0006others(4): Show | a0003c0010a0003c0016a0003c0071others(14): Show | a0003c0010t0003a0003c0016t0002a0003c0016t0008others(15): Show | a0003c0010t0003g0067a0003c0010t0003g0164a0003c0016t0002g0015others(18): Show | 21 | 170 | 0.1235 | -2 | c.130 others(21): Show |
TMEM132C | ENSG00000181234.10 | transcript | ENST00000435159.3 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM132C_chr12_128262170_128712911 | 128667208 | CAT | C | intron_variant | MODIFIER | HG02622.hp2 HG02886.hp2 HG03098.hp1 others(4): Show |
a0003a0006a0010others(2): Show | a0003c0070a0006c0020a0006c0024others(3): Show | a0003c0070t0002a0006c0020t0002a0006c0024t0002others(3): Show | a0003c0070t0002g0083a0006c0020t0002g0143a0006c0020t0002g0150others(4): Show | 7 | 170 | 0.0412 | -2 | c.130 others(21): Show |
TMEM132C | ENSG00000181234.10 | transcript | ENST00000435159.3 | protein_coding | 4/8 | chr12 | TogoVar | ||||||
TMEM132C_chr12_128262170_128712911 | 128674693 | TAA | T | intron_variant | MODIFIER | HG02559.hp1 HG03098.hp2 NA18906.hp1 |
a0002a0004 | a0002c0038a0002c0045a0004c0059 | a0002c0038t0002a0002c0045t0001a0004c0059t0002 | a0002c0038t0002g0014a0002c0045t0001g0144a0004c0059t0002g0062 | 3 | 170 | 0.0177 | -2 | c.144 others(21): Show |
TMEM132C | ENSG00000181234.10 | transcript | ENST00000435159.3 | protein_coding | 5/8 | chr12 | TogoVar | ||||||
TMEM132C_chr12_128262170_128712911 | 128681676 | CAG | C | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(91): Show |
a0001a0002a0003others(21): Show | a0001c0001a0001c0019a0002c0004others(54): Show | a0001c0001t0001a0001c0001t0006a0001c0019t0001others(60): Show | a0001c0001t0001g0027a0001c0001t0001g0036a0001c0001t0001g0051others(91): Show | 94 | 170 | 0.5529 | -2 | c.144 others(23): Show |
TMEM132C | ENSG00000181234.10 | transcript | ENST00000435159.3 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM132C_chr12_128262170_128712911 | 128686025 | ATG | A | intron_variant | MODIFIER | HG01243.hp1 HG01891.hp2 HG02145.hp2 others(23): Show |
a0002a0003a0004others(9): Show | a0002c0004a0002c0018a0003c0010others(20): Show | a0002c0004t0003a0002c0018t0002a0003c0010t0003others(20): Show | a0002c0004t0003g0052a0002c0018t0002g0136a0003c0010t0003g0067others(23): Show | 26 | 170 | 0.1529 | -2 | c.145 others(21): Show |
TMEM132C | ENSG00000181234.10 | transcript | ENST00000435159.3 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM132C_chr12_128262170_128712911 | 128686053 | ATG | A | intron_variant | MODIFIER | HG01081.hp2 HG02148.hp1 HG04204.hp1 others(1): Show |
a0003a0005 | a0003c0009a0003c0085a0005c0005others(1): Show | a0003c0009t0004a0003c0085t0004a0005c0005t0002others(1): Show | a0003c0009t0004g0132a0003c0085t0004g0125a0005c0005t0002g0121others(1): Show | 4 | 170 | 0.0235 | -2 | c.145 others(21): Show |
TMEM132C | ENSG00000181234.10 | transcript | ENST00000435159.3 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM132C_chr12_128262170_128712911 | 128686076 | TGC | T | intron_variant | MODIFIER | HG02004.hp2 HG02723.hp1 HG02965.hp2 others(7): Show |
a0002a0003a0005others(2): Show | a0002c0004a0003c0016a0003c0071others(7): Show | a0002c0004t0003a0003c0016t0002a0003c0071t0002others(7): Show | a0002c0004t0003g0044a0003c0016t0002g0015a0003c0071t0002g0079others(7): Show | 10 | 170 | 0.0588 | -2 | c.145 others(21): Show |
TMEM132C | ENSG00000181234.10 | transcript | ENST00000435159.3 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM132C_chr12_128262170_128712911 | 128701899 | CTT | C | intron_variant | MODIFIER | HG00140.hp2 HG00558.hp2 HG00609.hp1 others(43): Show |
a0001a0004a0006others(11): Show | a0001c0001a0001c0019a0004c0013others(19): Show | a0001c0001t0001a0001c0001t0006a0001c0019t0001others(23): Show | a0001c0001t0001g0027a0001c0001t0001g0036a0001c0001t0001g0051others(43): Show | 46 | 170 | 0.2706 | -2 | c.212 others(21): Show |
TMEM132C | ENSG00000181234.10 | transcript | ENST00000435159.3 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM132D_chr12_129066726_129909025 | 129077657 | CAT | C | intron_variant | MODIFIER | HG00099.hp1 HG01167.hp1 HG03710.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0021a0001c0001t0002g0026a0001c0001t0002g0038others(2): Show | 5 | 94 | 0.0532 | -2 | c.211 others(19): Show |
TMEM132D | ENSG00000151952.16 | transcript | ENST00000422113.7 | protein_coding | 8/8 | chr12 | TogoVar | ||||||
TMEM132D_chr12_129066726_129909025 | 129077860 | GAC | G | intron_variant | MODIFIER | HG02280.hp2 HG03225.hp2 HG03579.hp1 |
a0001 | a0001c0001a0001c0002a0001c0013 | a0001c0001t0027a0001c0002t0004a0001c0013t0017 | a0001c0001t0027g0094a0001c0002t0004g0011a0001c0013t0017g0028 | 3 | 94 | 0.0319 | -2 | c.211 others(19): Show |
TMEM132D | ENSG00000151952.16 | transcript | ENST00000422113.7 | protein_coding | 8/8 | chr12 | TogoVar | ||||||
TMEM132D_chr12_129066726_129909025 | 129077880 | GAC | G | intron_variant | MODIFIER | HG00741.hp1 HG01074.hp2 HG01167.hp2 others(20): Show |
a0001a0004 | a0001c0001a0001c0004a0001c0010others(1): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0008others(8): Show | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(20): Show | 23 | 94 | 0.2447 | -2 | c.211 others(19): Show |
TMEM132D | ENSG00000151952.16 | transcript | ENST00000422113.7 | protein_coding | 8/8 | chr12 | TogoVar | ||||||
TMEM132D_chr12_129066726_129909025 | 129086192 | ACG | A | intron_variant | MODIFIER | HG00741.hp1 HG01074.hp2 HG01192.hp1 others(7): Show |
a0001a0009 | a0001c0001a0001c0004a0001c0010others(2): Show | a0001c0001t0003a0001c0001t0022a0001c0004t0001others(5): Show | a0001c0001t0003g0040a0001c0001t0022g0086a0001c0004t0001g0046others(7): Show | 10 | 94 | 0.1064 | -2 | c.144 others(21): Show |
TMEM132D | ENSG00000151952.16 | transcript | ENST00000422113.7 | protein_coding | 5/8 | chr12 | TogoVar | ||||||
TMEM132D_chr12_129066726_129909025 | 129101998 | TTC | T | intron_variant | MODIFIER | HG01884.hp1 HG01891.hp1 HG02809.hp1 others(1): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0006a0001c0002t0004a0002c0003t0001others(1): Show | a0001c0001t0006g0067a0001c0002t0004g0023a0002c0003t0001g0031others(1): Show | 4 | 94 | 0.0426 | -2 | c.144 others(23): Show |
TMEM132D | ENSG00000151952.16 | transcript | ENST00000422113.7 | protein_coding | 5/8 | chr12 | TogoVar | ||||||
TMEM132D_chr12_129066726_129909025 | 129102442 | TAC | T | intron_variant | MODIFIER | HG00408.hp2 HG00741.hp2 HG01975.hp1 others(3): Show |
a0001a0004 | a0001c0002a0001c0006a0001c0007others(1): Show | a0001c0002t0004a0001c0006t0002a0001c0007t0004others(2): Show | a0001c0002t0004g0077a0001c0006t0002g0041a0001c0006t0002g0076others(3): Show | 6 | 94 | 0.0638 | -2 | c.144 others(23): Show |
TMEM132D | ENSG00000151952.16 | transcript | ENST00000422113.7 | protein_coding | 5/8 | chr12 | TogoVar | ||||||
TMEM132D_chr12_129066726_129909025 | 129115444 | TGA | T | intron_variant | MODIFIER | HG03225.hp2 HG03471.hp1 |
a0001 | a0001c0001a0001c0013 | a0001c0001t0006a0001c0013t0017 | a0001c0001t0006g0051a0001c0013t0017g0028 | 2 | 94 | 0.0213 | -2 | c.144 others(23): Show |
TMEM132D | ENSG00000151952.16 | transcript | ENST00000422113.7 | protein_coding | 5/8 | chr12 | TogoVar | ||||||
TMEM132D_chr12_129066726_129909025 | 129116918 | CAA | C | intron_variant | MODIFIER | HG00099.hp1 HG00741.hp1 HG01074.hp2 others(16): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0004others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(12): Show | a0001c0001t0001g0082a0001c0001t0002g0021a0001c0001t0002g0038others(16): Show | 19 | 94 | 0.2021 | -2 | c.144 others(23): Show |
TMEM132D | ENSG00000151952.16 | transcript | ENST00000422113.7 | protein_coding | 5/8 | chr12 | TogoVar |