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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
A2M_chr12_9062708_9120919 | 9098132 | C | T | intron_variant | MODIFIER | HG04199.hp1 HG04204.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0171a0001c0001t0001g0172 | 2 | 332 | 0.0060 | 0 | c.185 others(8): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/35 | chr12 | TogoVar | ||||||
A2M_chr12_9062708_9120919 | 9098287 | T | C | intron_variant | MODIFIER | HG00639.hp1 HG00738.hp1 HG01070.hp2 others(47): Show |
a0001a0012a0016 | a0001c0001a0001c0003a0001c0021others(2): Show | a0001c0001t0002a0001c0003t0002a0001c0021t0002others(2): Show | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0013others(38): Show | 50 | 332 | 0.1506 | 0 | c.185 others(8): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/35 | chr12 | TogoVar | ||||||
A2M_chr12_9062708_9120919 | 9098306 | C | T | intron_variant | MODIFIER | HG02145.hp2 HG03540.hp2 |
a0001 | a0001c0009 | a0001c0009t0002 | a0001c0009t0002g0082a0001c0009t0002g0083 | 2 | 332 | 0.0060 | 0 | c.185 others(8): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/35 | chr12 | TogoVar | ||||||
A2M_chr12_9062708_9120919 | 9098332 | G | C | intron_variant | MODIFIER | HG02622.hp2 HG02723.hp2 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0143a0001c0001t0002g0144 | 2 | 332 | 0.0060 | 0 | c.185 others(8): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/35 | chr12 | TogoVar | ||||||
A2M_chr12_9062708_9120919 | 9098359 | C | T | intron_variant | MODIFIER | HG02145.hp2 HG03540.hp2 |
a0001 | a0001c0009 | a0001c0009t0002 | a0001c0009t0002g0082a0001c0009t0002g0083 | 2 | 332 | 0.0060 | 0 | c.185 others(8): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/35 | chr12 | TogoVar | ||||||
A2M_chr12_9062708_9120919 | 9098449 | T | A | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
a0001a0002a0003others(8): Show | a0001c0001a0001c0003a0001c0005others(16): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(18): Show | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(195): Show | 241 | 332 | 0.7259 | 0 | c.185 others(8): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/35 | chr12 | TogoVar | ||||||
A2M_chr12_9062708_9120919 | 9098456 | T | G | intron_variant | MODIFIER | HG02145.hp2 HG03540.hp2 |
a0001 | a0001c0009 | a0001c0009t0002 | a0001c0009t0002g0082a0001c0009t0002g0083 | 2 | 332 | 0.0060 | 0 | c.185 others(8): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/35 | chr12 | TogoVar | ||||||
A2M_chr12_9062708_9120919 | 9098597 | A | G | intron_variant | MODIFIER | HG02145.hp2 HG03540.hp2 |
a0001 | a0001c0009 | a0001c0009t0002 | a0001c0009t0002g0082a0001c0009t0002g0083 | 2 | 332 | 0.0060 | 0 | c.185 others(7): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/35 | chr12 | TogoVar | ||||||
A2M_chr12_9062708_9120919 | 9098613 | C | T | synonymous_variant | LOW | HG02145.hp2 HG03540.hp2 |
a0001 | a0001c0009 | a0001c0009t0002 | a0001c0009t0002g0082a0001c0009t0002g0083 | 2 | 332 | 0.0060 | 0 | c.184 others(4): Show |
p.Ala others(6): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/36 | 1915/4610 | 1845/4425 | 615/1474 | chr12 | TogoVar | ||
A2M_chr12_9062708_9120919 | 9098701 | C | T | missense_variant | MODERATE | NA19081.hp1 NA19082.hp2 |
a0006 | a0006c0008 | a0006c0008t0001 | a0006c0008t0001g0217a0006c0008t0001g0229 | 2 | 332 | 0.0060 | 0 | c.175 others(4): Show |
p.Arg others(6): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/36 | 1827/4610 | 1757/4425 | 586/1474 | chr12 | TogoVar | ||
A2M_chr12_9062708_9120919 | 9098811 | T | C | intron_variant | MODIFIER | HG01934.hp1 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0126 | 1 | 332 | 0.0030 | 0 | c.170 others(7): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 14/35 | chr12 | TogoVar | ||||||
A2M_chr12_9062708_9120919 | 9099017 | G | A | intron_variant | MODIFIER | HG01934.hp1 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0126 | 1 | 332 | 0.0030 | 0 | c.170 others(8): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 14/35 | chr12 | TogoVar | ||||||
A2M_chr12_9062708_9120919 | 9099028 | C | T | intron_variant | MODIFIER | HG00639.hp1 HG00738.hp1 HG01070.hp2 others(50): Show |
a0001a0012a0015others(1): Show | a0001c0001a0001c0003a0001c0009others(4): Show | a0001c0001t0002a0001c0003t0002a0001c0009t0002others(4): Show | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0013others(41): Show | 53 | 332 | 0.1596 | 0 | c.170 others(8): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 14/35 | chr12 | TogoVar | ||||||
A2M_chr12_9062708_9120919 | 9099148 | A | C | intron_variant | MODIFIER | HG03516.hp2 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0110 | 1 | 332 | 0.0030 | 0 | c.170 others(8): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 14/35 | chr12 | TogoVar | ||||||
A2M_chr12_9062708_9120919 | 9099527 | G | A | splice_region_variant others(1): Show |
LOW | HG02647.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0037 | 1 | 332 | 0.0030 | 0 | c.155 others(6): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 13/35 | chr12 | TogoVar | ||||||
A2M_chr12_9062708_9120919 | 9099718 | T | C | intron_variant | MODIFIER | NA18990.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0209 | 1 | 332 | 0.0030 | 0 | c.155 others(8): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 13/35 | chr12 | TogoVar | ||||||
A2M_chr12_9062708_9120919 | 9100151 | G | A | intron_variant | MODIFIER | HG01069.hp1 HG01071.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0030 | 2 | 332 | 0.0060 | 0 | c.155 others(8): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 13/35 | chr12 | TogoVar | ||||||
A2M_chr12_9062708_9120919 | 9100160 | G | A | intron_variant | MODIFIER | NA19030.hp2 | a0015 | a0015c0020 | a0015c0020t0002 | a0015c0020t0002g0080 | 1 | 332 | 0.0030 | 0 | c.155 others(8): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 13/35 | chr12 | TogoVar | ||||||
A2M_chr12_9062708_9120919 | 9100182 | C | G | intron_variant | MODIFIER | HG01256.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0052 | 1 | 332 | 0.0030 | 0 | c.155 others(8): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 13/35 | chr12 | TogoVar | ||||||
A2M_chr12_9062708_9120919 | 9100197 | C | A | intron_variant | MODIFIER | HG00423.hp2 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0095 | 1 | 332 | 0.0030 | 0 | c.155 others(8): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 13/35 | chr12 | TogoVar | ||||||
A2M_chr12_9062708_9120919 | 9100212 | A | G | intron_variant | MODIFIER | HG03017.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0259 | 1 | 332 | 0.0030 | 0 | c.155 others(8): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 13/35 | chr12 | TogoVar | ||||||
A2M_chr12_9062708_9120919 | 9100213 | A | C | intron_variant | MODIFIER | HG00423.hp2 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0095 | 1 | 332 | 0.0030 | 0 | c.155 others(8): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 13/35 | chr12 | TogoVar | ||||||
A2M_chr12_9062708_9120919 | 9100511 | T | C | intron_variant | MODIFIER | NA19030.hp2 | a0015 | a0015c0020 | a0015c0020t0002 | a0015c0020t0002g0080 | 1 | 332 | 0.0030 | 0 | c.155 others(8): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 13/35 | chr12 | TogoVar | ||||||
A2M_chr12_9062708_9120919 | 9100530 | C | T | intron_variant | MODIFIER | HG02145.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0050 | 1 | 332 | 0.0030 | 0 | c.155 others(8): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 13/35 | chr12 | TogoVar | ||||||
A2M_chr12_9062708_9120919 | 9100659 | C | A | intron_variant | MODIFIER | HG01169.hp1 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0127 | 1 | 332 | 0.0030 | 0 | c.155 others(8): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 13/35 | chr12 | TogoVar | ||||||
A2M_chr12_9062708_9120919 | 9100720 | G | A | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
a0001a0002a0003others(12): Show | a0001c0001a0001c0003a0001c0005others(23): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(26): Show | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(272): Show | 329 | 332 | 0.9910 | 0 | c.155 others(8): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 13/35 | chr12 | TogoVar | ||||||
A2M_chr12_9062708_9120919 | 9100905 | G | A | intron_variant | MODIFIER | NA19030.hp2 | a0015 | a0015c0020 | a0015c0020t0002 | a0015c0020t0002g0080 | 1 | 332 | 0.0030 | 0 | c.155 others(8): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 13/35 | chr12 | TogoVar | ||||||
A2M_chr12_9062708_9120919 | 9100964 | T | A | intron_variant | MODIFIER | NA18943.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0225 | 1 | 332 | 0.0030 | 0 | c.155 others(8): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 13/35 | chr12 | TogoVar | ||||||
A2M_chr12_9062708_9120919 | 9101116 | G | A | intron_variant | MODIFIER | HG01993.hp2 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0038 | 1 | 332 | 0.0030 | 0 | c.155 others(7): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 13/35 | chr12 | TogoVar | ||||||
A2M_chr12_9062708_9120919 | 9101124 | G | C | intron_variant | MODIFIER | HG02965.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0243 | 1 | 332 | 0.0030 | 0 | c.155 others(7): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 13/35 | chr12 | TogoVar | ||||||
A2M_chr12_9062708_9120919 | 9101298 | C | T | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
a0001a0002a0003others(12): Show | a0001c0001a0001c0003a0001c0005others(22): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(24): Show | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(248): Show | 302 | 332 | 0.9096 | 0 | c.149 others(7): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 12/35 | chr12 | TogoVar | ||||||
A2M_chr12_9062708_9120919 | 9101423 | C | T | intron_variant | MODIFIER | HG01069.hp2 HG02273.hp2 HG02293.hp1 others(4): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0002a0002c0002t0002 | a0001c0001t0002g0104a0001c0001t0002g0106a0002c0002t0002g0103others(4): Show | 7 | 332 | 0.0211 | 0 | c.149 others(7): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 12/35 | chr12 | TogoVar | ||||||
A2M_chr12_9062708_9120919 | 9101539 | G | T | missense_variant | MODERATE | NA18999.hp2 | a0012 | a0012c0014 | a0012c0014t0002 | a0012c0014t0002g0079 | 1 | 332 | 0.0030 | 0 | c.140 others(4): Show |
p.Leu others(6): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 12/36 | 1472/4610 | 1402/4425 | 468/1474 | chr12 | TogoVar | ||
A2M_chr12_9062708_9120919 | 9101557 | C | T | missense_variant | MODERATE | NA19030.hp1 | a0016 | a0016c0013 | a0016c0013t0002 | a0016c0013t0002g0049 | 1 | 332 | 0.0030 | 0 | c.138 others(4): Show |
p.Glu others(6): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 12/36 | 1454/4610 | 1384/4425 | 462/1474 | chr12 | TogoVar | ||
A2M_chr12_9062708_9120919 | 9101602 | T | C | missense_variant | MODERATE | NA18981.hp1 | a0007 | a0007c0027 | a0007c0027t0001 | a0007c0027t0001g0277 | 1 | 332 | 0.0030 | 0 | c.133 others(4): Show |
p.Thr others(6): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 12/36 | 1409/4610 | 1339/4425 | 447/1474 | chr12 | TogoVar | ||
A2M_chr12_9062708_9120919 | 9101630 | C | T | synonymous_variant | LOW | HG02559.hp2 HG02622.hp1 HG02717.hp1 others(4): Show |
a0001 | a0001c0005 | a0001c0005t0002 | a0001c0005t0002g0019a0001c0005t0002g0134a0001c0005t0002g0135others(3): Show | 7 | 332 | 0.0211 | 0 | c.131 others(4): Show |
p.Val others(6): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 12/36 | 1381/4610 | 1311/4425 | 437/1474 | chr12 | TogoVar | ||
A2M_chr12_9062708_9120919 | 9101645 | G | A | synonymous_variant | LOW | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(9): Show |
a0001 | a0001c0003a0001c0021 | a0001c0003t0002a0001c0021t0002 | a0001c0003t0002g0003a0001c0003t0002g0014a0001c0003t0002g0048others(5): Show | 12 | 332 | 0.0361 | 0 | c.129 others(4): Show |
p.Tyr others(6): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 12/36 | 1366/4610 | 1296/4425 | 432/1474 | chr12 | TogoVar | ||
A2M_chr12_9062708_9120919 | 9101789 | T | A | intron_variant | MODIFIER | HG00639.hp1 HG00738.hp1 HG01070.hp2 others(48): Show |
a0001a0012a0016 | a0001c0001a0001c0003a0001c0021others(2): Show | a0001c0001t0002a0001c0003t0002a0001c0021t0002others(2): Show | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0013others(39): Show | 51 | 332 | 0.1536 | 0 | c.126 others(8): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 11/35 | chr12 | TogoVar | ||||||
A2M_chr12_9062708_9120919 | 9101826 | G | C | intron_variant | MODIFIER | HG00639.hp1 HG00738.hp1 HG01070.hp2 others(48): Show |
a0001a0012a0016 | a0001c0001a0001c0003a0001c0021others(2): Show | a0001c0001t0002a0001c0003t0002a0001c0021t0002others(2): Show | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0013others(39): Show | 51 | 332 | 0.1536 | 0 | c.126 others(8): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 11/35 | chr12 | TogoVar | ||||||
A2M_chr12_9062708_9120919 | 9102187 | C | G | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(69): Show |
a0001a0002a0009others(1): Show | a0001c0001a0001c0005a0002c0002others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0005t0002others(4): Show | a0001c0001t0001g0215a0001c0001t0002g0104a0001c0001t0002g0106others(57): Show | 72 | 332 | 0.2169 | 0 | c.126 others(8): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 11/35 | chr12 | TogoVar | ||||||
A2M_chr12_9062708_9120919 | 9102235 | A | T | intron_variant | MODIFIER | HG01993.hp1 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0098 | 1 | 332 | 0.0030 | 0 | c.126 others(8): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 11/35 | chr12 | TogoVar | ||||||
A2M_chr12_9062708_9120919 | 9102254 | C | T | intron_variant | MODIFIER | NA18955.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0168 | 1 | 332 | 0.0030 | 0 | c.126 others(8): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 11/35 | chr12 | TogoVar | ||||||
A2M_chr12_9062708_9120919 | 9102287 | C | A | intron_variant | MODIFIER | HG04228.hp1 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0128 | 1 | 332 | 0.0030 | 0 | c.126 others(8): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 11/35 | chr12 | TogoVar | ||||||
A2M_chr12_9062708_9120919 | 9102417 | C | T | intron_variant | MODIFIER | HG01256.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0167 | 1 | 332 | 0.0030 | 0 | c.126 others(8): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 11/35 | chr12 | TogoVar | ||||||
A2M_chr12_9062708_9120919 | 9102418 | G | A | intron_variant | MODIFIER | HG02735.hp2 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0129 | 1 | 332 | 0.0030 | 0 | c.126 others(8): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 11/35 | chr12 | TogoVar | ||||||
A2M_chr12_9062708_9120919 | 9102438 | T | A | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(143): Show |
a0001a0002a0009others(5): Show | a0001c0001a0001c0003a0001c0005others(12): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(14): Show | a0001c0001t0001g0215a0001c0001t0002g0002a0001c0001t0002g0005others(120): Show | 146 | 332 | 0.4398 | 0 | c.126 others(8): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 11/35 | chr12 | TogoVar | ||||||
A2M_chr12_9062708_9120919 | 9102451 | C | T | intron_variant | MODIFIER | HG03130.hp1 | a0001 | a0001c0022 | a0001c0022t0002 | a0001c0022t0002g0039 | 1 | 332 | 0.0030 | 0 | c.126 others(8): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 11/35 | chr12 | TogoVar | ||||||
A2M_chr12_9062708_9120919 | 9102560 | C | T | intron_variant | MODIFIER | NA19030.hp2 | a0015 | a0015c0020 | a0015c0020t0002 | a0015c0020t0002g0080 | 1 | 332 | 0.0030 | 0 | c.126 others(8): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 11/35 | chr12 | TogoVar | ||||||
A2M_chr12_9062708_9120919 | 9102606 | G | A | intron_variant | MODIFIER | HG02145.hp2 HG03540.hp2 |
a0001 | a0001c0009 | a0001c0009t0002 | a0001c0009t0002g0082a0001c0009t0002g0083 | 2 | 332 | 0.0060 | 0 | c.126 others(8): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 11/35 | chr12 | TogoVar | ||||||
A2M_chr12_9062708_9120919 | 9102643 | T | G | intron_variant | MODIFIER | HG01993.hp2 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0038 | 1 | 332 | 0.0030 | 0 | c.126 others(8): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 11/35 | chr12 | TogoVar |