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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
APOB_chr2_20996429_21049073 | 21006574 | G | C | missense_variant | MODERATE | NA20805.hp1 | a0066 | a0066c0058 | a0066c0058t0001 | a0066c0058t0001g0073 | 1 | 350 | 0.0029 | 0 | c.102 others(5): Show |
p.Gln others(7): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 10422/14121 | 10294/13692 | 3432/4563 | chr2 | TogoVar | ||
APOB_chr2_20996429_21049073 | 21006931 | G | T | missense_variant | MODERATE | HG01109.hp2 | a0054 | a0054c0082 | a0054c0082t0001 | a0054c0082t0001g0169 | 1 | 350 | 0.0029 | 0 | c.993 others(4): Show |
p.Leu others(7): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 10065/14121 | 9937/13692 | 3313/4563 | chr2 | TogoVar | ||
APOB_chr2_20996429_21049073 | 21006988 | A | G | missense_variant | MODERATE | HG01255.hp1 HG01496.hp2 HG01891.hp1 others(8): Show |
a0011a0015a0076 | a0011c0013a0015c0022a0015c0069others(1): Show | a0011c0013t0001a0015c0022t0001a0015c0069t0001others(1): Show | a0011c0013t0001g0025a0011c0013t0001g0026a0011c0013t0001g0102others(5): Show | 11 | 350 | 0.0314 | 0 | c.988 others(4): Show |
p.Ser others(7): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 10008/14121 | 9880/13692 | 3294/4563 | chr2 | TogoVar | ||
APOB_chr2_20996429_21049073 | 21007033 | T | C | missense_variant | MODERATE | HG01433.hp1 HG02630.hp1 NA18522.hp1 others(1): Show |
a0019a0065 | a0019c0023a0065c0053 | a0019c0023t0001a0065c0053t0001 | a0019c0023t0001g0108a0019c0023t0001g0145a0019c0023t0001g0146others(1): Show | 4 | 350 | 0.0114 | 0 | c.983 others(4): Show |
p.Ser others(7): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 9963/14121 | 9835/13692 | 3279/4563 | chr2 | TogoVar | ||
APOB_chr2_20996429_21049073 | 21007377 | G | A | missense_variant | MODERATE | NA19084.hp1 | a0050 | a0050c0091 | a0050c0091t0001 | a0050c0091t0001g0221 | 1 | 350 | 0.0029 | 0 | c.949 others(4): Show |
p.Thr others(7): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 9619/14121 | 9491/13692 | 3164/4563 | chr2 | TogoVar | ||
APOB_chr2_20996429_21049073 | 21007728 | G | C | missense_variant | MODERATE | HG01934.hp1 HG02647.hp2 |
a0033 | a0033c0025 | a0033c0025t0001 | a0033c0025t0001g0018 | 2 | 350 | 0.0057 | 0 | c.914 others(4): Show |
p.Thr others(7): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 9268/14121 | 9140/13692 | 3047/4563 | chr2 | TogoVar | ||
APOB_chr2_20996429_21049073 | 21008406 | G | A | missense_variant | MODERATE | HG00323.hp1 HG00741.hp1 |
a0053a0071 | a0053c0084a0071c0060 | a0053c0084t0001a0071c0060t0001 | a0053c0084t0001g0176a0071c0060t0001g0095 | 2 | 350 | 0.0057 | 0 | c.846 others(4): Show |
p.Pro others(7): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 8590/14121 | 8462/13692 | 2821/4563 | chr2 | TogoVar | ||
APOB_chr2_20996429_21049073 | 21008515 | T | G | missense_variant | MODERATE | HG02083.hp1 NA18612.hp2 NA18942.hp1 others(8): Show |
a0008a0050 | a0008c0010a0008c0027a0050c0091 | a0008c0010t0001a0008c0027t0001a0050c0091t0001 | a0008c0010t0001g0006a0008c0010t0001g0064a0008c0010t0001g0069others(2): Show | 11 | 350 | 0.0314 | 0 | c.835 others(4): Show |
p.Asn others(7): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 8481/14121 | 8353/13692 | 2785/4563 | chr2 | TogoVar | ||
APOB_chr2_20996429_21049073 | 21008652 | G | A | missense_variant | MODERATE | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(118): Show |
a0001a0008a0009others(18): Show | a0001c0001a0001c0014a0001c0036others(29): Show | a0001c0001t0001a0001c0014t0001a0001c0036t0001others(30): Show | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(72): Show | 121 | 350 | 0.3457 | 0 | c.821 others(4): Show |
p.Pro others(7): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 8344/14121 | 8216/13692 | 2739/4563 | chr2 | TogoVar | ||
APOB_chr2_20996429_21049073 | 21009172 | C | T | missense_variant | MODERATE | HG01106.hp2 HG01192.hp2 |
a0024 | a0024c0039 | a0024c0039t0001 | a0024c0039t0001g0036 | 2 | 350 | 0.0057 | 0 | c.769 others(4): Show |
p.Glu others(7): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 7824/14121 | 7696/13692 | 2566/4563 | chr2 | TogoVar | ||
APOB_chr2_20996429_21049073 | 21009253 | C | T | missense_variant | MODERATE | HG00280.hp2 | a0049 | a0049c0081 | a0049c0081t0001 | a0049c0081t0001g0167 | 1 | 350 | 0.0029 | 0 | c.761 others(4): Show |
p.Val others(7): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 7743/14121 | 7615/13692 | 2539/4563 | chr2 | TogoVar | ||
APOB_chr2_20996429_21049073 | 21009291 | A | G | missense_variant | MODERATE | HG02145.hp2 | a0062 | a0062c0102 | a0062c0102t0001 | a0062c0102t0001g0227 | 1 | 350 | 0.0029 | 0 | c.757 others(4): Show |
p.Met others(7): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 7705/14121 | 7577/13692 | 2526/4563 | chr2 | TogoVar | ||
APOB_chr2_20996429_21049073 | 21009396 | A | G | missense_variant | MODERATE | HG01978.hp2 | a0044 | a0044c0070 | a0044c0070t0001 | a0044c0070t0001g0148 | 1 | 350 | 0.0029 | 0 | c.747 others(4): Show |
p.Leu others(7): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 7600/14121 | 7472/13692 | 2491/4563 | chr2 | TogoVar | ||
APOB_chr2_20996429_21049073 | 21009501 | G | T | missense_variant | MODERATE | HG01255.hp1 HG01496.hp2 HG01891.hp1 others(8): Show |
a0011a0015a0076 | a0011c0013a0015c0022a0015c0069others(1): Show | a0011c0013t0001a0015c0022t0001a0015c0069t0001others(1): Show | a0011c0013t0001g0025a0011c0013t0001g0026a0011c0013t0001g0102others(5): Show | 11 | 350 | 0.0314 | 0 | c.736 others(4): Show |
p.Ala others(7): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 7495/14121 | 7367/13692 | 2456/4563 | chr2 | TogoVar | ||
APOB_chr2_20996429_21049073 | 21009626 | T | G | missense_variant | MODERATE | HG03209.hp2 NA19043.hp1 |
a0042a0060 | a0042c0074a0060c0065 | a0042c0074t0001a0060c0065t0004 | a0042c0074t0001g0131a0060c0065t0004g0236 | 2 | 350 | 0.0057 | 0 | c.724 others(4): Show |
p.Glu others(7): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 7370/14121 | 7242/13692 | 2414/4563 | chr2 | TogoVar | ||
APOB_chr2_20996429_21049073 | 21009828 | C | T | missense_variant | MODERATE | HG00408.hp2 | a0048 | a0048c0080 | a0048c0080t0001 | a0048c0080t0001g0184 | 1 | 350 | 0.0029 | 0 | c.704 others(4): Show |
p.Arg others(7): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 7168/14121 | 7040/13692 | 2347/4563 | chr2 | TogoVar | ||
APOB_chr2_20996429_21049073 | 21009927 | A | G | missense_variant | MODERATE | HG03041.hp1 | a0077 | a0077c0046 | a0077c0046t0002 | a0077c0046t0002g0066 | 1 | 350 | 0.0029 | 0 | c.694 others(4): Show |
p.Leu others(7): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 7069/14121 | 6941/13692 | 2314/4563 | chr2 | TogoVar | ||
APOB_chr2_20996429_21049073 | 21009931 | T | C | missense_variant | MODERATE | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(343): Show |
a0001a0002a0003others(73): Show | a0001c0001a0001c0014a0001c0036others(98): Show | a0001c0001t0001a0001c0014t0001a0001c0036t0001others(102): Show | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(230): Show | 346 | 350 | 0.9886 | 0 | c.693 others(4): Show |
p.Ile others(7): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 7065/14121 | 6937/13692 | 2313/4563 | chr2 | TogoVar | ||
APOB_chr2_20996429_21049073 | 21009973 | C | G | missense_variant | MODERATE | HG02055.hp2 HG03041.hp1 HG03471.hp1 others(1): Show |
a0045a0061a0069others(1): Show | a0045c0067a0061c0099a0069c0052others(1): Show | a0045c0067t0002a0061c0099t0002a0069c0052t0002others(1): Show | a0045c0067t0002g0125a0061c0099t0002g0234a0069c0052t0002g0077others(1): Show | 4 | 350 | 0.0114 | 0 | c.689 others(4): Show |
p.Asp others(7): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 7023/14121 | 6895/13692 | 2299/4563 | chr2 | TogoVar | ||
APOB_chr2_20996429_21049073 | 21011100 | T | C | missense_variant | MODERATE | HG04228.hp2 homoSapiens_chm13v2.hp1 |
a0025 | a0025c0037 | a0025c0037t0001 | a0025c0037t0001g0113a0025c0037t0001g0143 | 2 | 350 | 0.0057 | 0 | c.576 others(4): Show |
p.His others(7): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 5896/14121 | 5768/13692 | 1923/4563 | chr2 | TogoVar | ||
APOB_chr2_20996429_21049073 | 21011127 | T | C | missense_variant | MODERATE | HG01361.hp1 HG01975.hp1 |
a0031 | a0031c0030 | a0031c0030t0001 | a0031c0030t0001g0022 | 2 | 350 | 0.0057 | 0 | c.574 others(4): Show |
p.Asn others(7): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 5869/14121 | 5741/13692 | 1914/4563 | chr2 | TogoVar | ||
APOB_chr2_20996429_21049073 | 21011409 | T | G | missense_variant | MODERATE | HG01256.hp2 HG01258.hp2 |
a0026 | a0026c0038 | a0026c0038t0001 | a0026c0038t0001g0040 | 2 | 350 | 0.0057 | 0 | c.545 others(4): Show |
p.Lys others(7): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 5587/14121 | 5459/13692 | 1820/4563 | chr2 | TogoVar | ||
APOB_chr2_20996429_21049073 | 21012493 | T | C | missense_variant | MODERATE | HG02572.hp2 HG02809.hp1 |
a0027 | a0027c0033 | a0027c0033t0001 | a0027c0033t0001g0136a0027c0033t0001g0174 | 2 | 350 | 0.0057 | 0 | c.437 others(4): Show |
p.Ser others(7): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 4503/14121 | 4375/13692 | 1459/4563 | chr2 | TogoVar | ||
APOB_chr2_20996429_21049073 | 21013213 | C | T | missense_variant | MODERATE | HG02523.hp2 | a0047 | a0047c0079 | a0047c0079t0001 | a0047c0079t0001g0196 | 1 | 350 | 0.0029 | 0 | c.416 others(4): Show |
p.Arg others(7): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 25/29 | 4291/14121 | 4163/13692 | 1388/4563 | chr2 | TogoVar | ||
APOB_chr2_20996429_21049073 | 21014578 | G | T | missense_variant | MODERATE | HG02647.hp1 | a0063 | a0063c0103 | a0063c0103t0004 | a0063c0103t0004g0237 | 1 | 350 | 0.0029 | 0 | c.371 others(4): Show |
p.Leu others(7): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 24/29 | 3840/14121 | 3712/13692 | 1238/4563 | chr2 | TogoVar | ||
APOB_chr2_20996429_21049073 | 21015135 | G | T | missense_variant | MODERATE | HG01884.hp2 HG01891.hp2 HG02145.hp2 others(8): Show |
a0027a0028a0029others(5): Show | a0027c0033a0028c0041a0029c0042others(5): Show | a0027c0033t0001a0028c0041t0001a0029c0042t0001others(5): Show | a0027c0033t0001g0136a0027c0033t0001g0174a0028c0041t0001g0226others(8): Show | 11 | 350 | 0.0314 | 0 | c.363 others(4): Show |
p.Leu others(7): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 23/29 | 3762/14121 | 3634/13692 | 1212/4563 | chr2 | TogoVar | ||
APOB_chr2_20996429_21049073 | 21015451 | G | A | missense_variant | MODERATE | HG00738.hp2 | a0056 | a0056c0096 | a0056c0096t0001 | a0056c0096t0001g0173 | 1 | 350 | 0.0029 | 0 | c.342 others(4): Show |
p.Pro others(7): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 22/29 | 3555/14121 | 3427/13692 | 1143/4563 | chr2 | TogoVar | ||
APOB_chr2_20996429_21049073 | 21015453 | G | A | missense_variant | MODERATE | NA18969.hp1 | a0046 | a0046c0093 | a0046c0093t0001 | a0046c0093t0001g0161 | 1 | 350 | 0.0029 | 0 | c.342 others(4): Show |
p.Ser others(7): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 22/29 | 3553/14121 | 3425/13692 | 1142/4563 | chr2 | TogoVar | ||
APOB_chr2_20996429_21049073 | 21015496 | G | A | missense_variant | MODERATE | NA19240.hp1 | a0039 | a0039c0073 | a0039c0073t0001 | a0039c0073t0001g0117 | 1 | 350 | 0.0029 | 0 | c.338 others(4): Show |
p.Arg others(7): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 22/29 | 3510/14121 | 3382/13692 | 1128/4563 | chr2 | TogoVar | ||
APOB_chr2_20996429_21049073 | 21019061 | C | T | missense_variant | MODERATE | NA19074.hp2 | a0057 | a0057c0078 | a0057c0078t0001 | a0057c0078t0001g0182 | 1 | 350 | 0.0029 | 0 | c.305 others(4): Show |
p.Ala others(7): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/29 | 3180/14121 | 3052/13692 | 1018/4563 | chr2 | TogoVar | ||
APOB_chr2_20996429_21049073 | 21019859 | G | A | missense_variant | MODERATE | NA19000.hp1 | a0058 | a0058c0094 | a0058c0094t0001 | a0058c0094t0001g0212 | 1 | 350 | 0.0029 | 0 | c.286 others(4): Show |
p.Pro others(6): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 19/29 | 2991/14121 | 2863/13692 | 955/4563 | chr2 | TogoVar | ||
APOB_chr2_20996429_21049073 | 21024971 | G | T | missense_variant | MODERATE | NA18971.hp1 | a0070 | a0070c0051 | a0070c0051t0001 | a0070c0051t0001g0080 | 1 | 350 | 0.0029 | 0 | c.239 others(4): Show |
p.Leu others(6): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 16/29 | 2526/14121 | 2398/13692 | 800/4563 | chr2 | TogoVar | ||
APOB_chr2_20996429_21049073 | 21026810 | G | T | missense_variant | MODERATE | HG01884.hp2 HG02109.hp1 HG02145.hp2 others(9): Show |
a0010a0028a0036others(2): Show | a0010c0011a0028c0041a0036c0064others(2): Show | a0010c0011t0001a0028c0041t0001a0036c0064t0001others(2): Show | a0010c0011t0001g0016a0010c0011t0001g0046a0010c0011t0001g0047others(5): Show | 12 | 350 | 0.0343 | 0 | c.222 others(4): Show |
p.Thr others(6): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 15/29 | 2350/14121 | 2222/13692 | 741/4563 | chr2 | TogoVar | ||
APOB_chr2_20996429_21049073 | 21026844 | C | T | missense_variant | MODERATE | HG01261.hp2 HG01433.hp2 |
a0022 | a0022c0032 | a0022c0032t0001 | a0022c0032t0001g0028 | 2 | 350 | 0.0057 | 0 | c.218 others(4): Show |
p.Val others(6): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 15/29 | 2316/14121 | 2188/13692 | 730/4563 | chr2 | TogoVar | ||
APOB_chr2_20996429_21049073 | 21027842 | C | G | missense_variant | MODERATE | HG01978.hp1 | a0059 | a0059c0077 | a0059c0077t0001 | a0059c0077t0001g0159 | 1 | 350 | 0.0029 | 0 | c.205 others(4): Show |
p.Ala others(6): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 14/29 | 2181/14121 | 2053/13692 | 685/4563 | chr2 | TogoVar | ||
APOB_chr2_20996429_21049073 | 21028042 | G | A | missense_variant | MODERATE | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(184): Show |
a0001a0004a0006others(36): Show | a0001c0001a0001c0014a0001c0036others(51): Show | a0001c0001t0001a0001c0014t0001a0001c0036t0001others(52): Show | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(121): Show | 187 | 350 | 0.5343 | 0 | c.185 others(4): Show |
p.Ala others(6): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 14/29 | 1981/14121 | 1853/13692 | 618/4563 | chr2 | TogoVar | ||
APOB_chr2_20996429_21049073 | 21029662 | G | A | missense_variant | MODERATE | HG00544.hp2 HG00558.hp2 HG00621.hp2 others(23): Show |
a0004a0073a0079 | a0004c0003a0004c0097a0004c0098others(2): Show | a0004c0003t0001a0004c0003t0005a0004c0097t0001others(3): Show | a0004c0003t0001g0005a0004c0003t0001g0015a0004c0003t0001g0042others(13): Show | 26 | 350 | 0.0743 | 0 | c.159 others(4): Show |
p.Arg others(6): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 12/29 | 1722/14121 | 1594/13692 | 532/4563 | chr2 | TogoVar | ||
APOB_chr2_20996429_21049073 | 21032483 | A | G | missense_variant | MODERATE | NA19043.hp1 | a0060 | a0060c0065 | a0060c0065t0004 | a0060c0065t0004g0236 | 1 | 350 | 0.0029 | 0 | c.122 others(4): Show |
p.Ile others(6): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 10/29 | 1351/14121 | 1223/13692 | 408/4563 | chr2 | TogoVar | ||
APOB_chr2_20996429_21049073 | 21037186 | T | C | missense_variant | MODERATE | HG02055.hp2 | a0061 | a0061c0099 | a0061c0099t0002 | a0061c0099t0002g0234 | 1 | 350 | 0.0029 | 0 | c.607 others(3): Show |
p.Ile others(6): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 6/29 | 735/14121 | 607/13692 | 203/4563 | chr2 | TogoVar | ||
APOB_chr2_20996429_21049073 | 21037187 | T | A | missense_variant | MODERATE | HG06807.hp2 | a0038 | a0038c0100 | a0038c0100t0001 | a0038c0100t0001g0211 | 1 | 350 | 0.0029 | 0 | c.606 others(3): Show |
p.Glu others(6): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 6/29 | 734/14121 | 606/13692 | 202/4563 | chr2 | TogoVar | ||
APOB_chr2_20996429_21049073 | 21037212 | G | A | missense_variant | MODERATE | HG02129.hp1 HG02135.hp1 NA19011.hp2 others(2): Show |
a0013 | a0013c0015 | a0013c0015t0001 | a0013c0015t0001g0013a0013c0015t0001g0156a0013c0015t0001g0157 | 5 | 350 | 0.0143 | 0 | c.581 others(3): Show |
p.Thr others(6): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 6/29 | 709/14121 | 581/13692 | 194/4563 | chr2 | TogoVar | ||
APOB_chr2_20996429_21049073 | 21038061 | G | A | missense_variant | MODERATE | HG02257.hp1 | a0037 | a0037c0104 | a0037c0104t0001 | a0037c0104t0001g0150 | 1 | 350 | 0.0029 | 0 | c.434 others(3): Show |
p.Pro others(6): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 5/29 | 562/14121 | 434/13692 | 145/4563 | chr2 | TogoVar | ||
APOB_chr2_20996429_21049073 | 21038062 | G | A | missense_variant | MODERATE | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(13): Show |
a0010a0028a0029others(5): Show | a0010c0011a0028c0041a0029c0042others(5): Show | a0010c0011t0001a0028c0041t0001a0029c0042t0001others(5): Show | a0010c0011t0001g0016a0010c0011t0001g0046a0010c0011t0001g0047others(9): Show | 16 | 350 | 0.0457 | 0 | c.433 others(3): Show |
p.Pro others(6): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 5/29 | 561/14121 | 433/13692 | 145/4563 | chr2 | TogoVar | ||
APOB_chr2_20996429_21049073 | 21041014 | A | G | missense_variant | MODERATE | HG03579.hp1 | a0036 | a0036c0064 | a0036c0064t0001 | a0036c0064t0001g0225 | 1 | 350 | 0.0029 | 0 | c.307 others(3): Show |
p.Tyr others(6): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 4/29 | 435/14121 | 307/13692 | 103/4563 | chr2 | TogoVar | ||
APOB_chr2_20996429_21049073 | 21041028 | G | A | missense_variant | MODERATE | HG00280.hp1 HG00323.hp2 HG00733.hp1 others(50): Show |
a0003a0012a0017others(12): Show | a0003c0002a0003c0029a0003c0054others(15): Show | a0003c0002t0001a0003c0029t0001a0003c0054t0001others(16): Show | a0003c0002t0001g0004a0003c0002t0001g0011a0003c0002t0001g0012others(34): Show | 53 | 350 | 0.1514 | 0 | c.293 others(3): Show |
p.Thr others(5): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 4/29 | 421/14121 | 293/13692 | 98/4563 | chr2 | TogoVar | ||
APOB_chr2_20996429_21049073 | 21041038 | T | C | missense_variant | MODERATE | NA19066.hp2 | a0064 | a0064c0062 | a0064c0062t0001 | a0064c0062t0001g0098 | 1 | 350 | 0.0029 | 0 | c.283 others(3): Show |
p.Ser others(5): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 4/29 | 411/14121 | 283/13692 | 95/4563 | chr2 | TogoVar | ||
APOB_chr2_20996429_21049073 | 21041083 | C | G | missense_variant others(1): Show |
MODERATE | NA18948.hp2 | a0035 | a0035c0063 | a0035c0063t0001 | a0035c0063t0001g0135 | 1 | 350 | 0.0029 | 0 | c.238 others(3): Show |
p.Val others(5): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 4/29 | 366/14121 | 238/13692 | 80/4563 | chr2 | TogoVar | ||
APOB_chr2_20996429_21049073 | 21042384 | T | C | missense_variant | MODERATE | HG02300.hp2 | a0034 | a0034c0105 | a0034c0105t0001 | a0034c0105t0001g0223 | 1 | 350 | 0.0029 | 0 | c.214 others(3): Show |
p.Ser others(5): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 3/29 | 342/14121 | 214/13692 | 72/4563 | chr2 | TogoVar | ||
APOC1_chr19_44909608_44924346 | 44914939 | C | G | missense_variant | MODERATE | HG00735.hp2 HG01433.hp2 |
a0003 | a0003c0003 | a0003c0003t0001 | a0003c0003t0001g0009a0003c0003t0001g0140 | 2 | 436 | 0.0046 | 0 | c.48C others(2): Show |
p.Ile others(5): Show |
APOC1 | ENSG00000130208.10 | transcript | ENST00000592535.6 | protein_coding | 2/4 | 194/514 | 48/252 | 16/83 | chr19 | TogoVar | ||
APOC1_chr19_44909608_44924346 | 44919189 | A | T | missense_variant | MODERATE | HG01069.hp2 HG01257.hp1 |
a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0005a0002c0002t0001g0008 | 2 | 436 | 0.0046 | 0 | c.211 others(3): Show |
p.Thr others(5): Show |
APOC1 | ENSG00000130208.10 | transcript | ENST00000592535.6 | protein_coding | 4/4 | 357/514 | 211/252 | 71/83 | chr19 | TogoVar |