Item | Value |
---|---|
geneid | 326625 |
ensemblid | ENSG00000139428.12 |
hgncid | 19331 |
symbol | MMAB |
name | metabolism of cobalamin associated B |
refseq_nuc | NM_052845.4 |
refseq_prot | NP_443077.1 |
ensembl_nuc | ENST00000545712.7 |
ensembl_prot | ENSP00000445920.1 |
mane_status | MANE Select |
chr | chr12 |
start | 109553715 |
end | 109573504 |
strand | - |
ver | v1.2 |
region | chr12:109553715-109573504 |
region5000 | chr12:109548715-109578504 |
regionname0 | MMAB_chr12_109553715_109573504 |
regionname5000 | MMAB_chr12_109548715_109578504 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 250 | 174 | 24 | 26 | 91 | 6 | 26 | 69 | MMAB_chr12_109548715_109578504 | MMAB | MAVCG others(245): Show |
chr12 | 109548715 | 109578504 |
a0002 | 0/0 | 250 | 103 | 33 | 14 | 39 | 7 | 10 | 35 | MMAB_chr12_109548715_109578504 | MMAB | MAVCG others(245): Show |
chr12 | 109548715 | 109578504 |
a0003 | 0/1 | 250 | 87 | 34 | 22 | 21 | 3 | 6 | 16 | MMAB_chr12_109548715_109578504 | MMAB | MAVCG others(245): Show |
chr12 | 109548715 | 109578504 |
a0004 | 0/0 | 250 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | MAVCG others(245): Show |
chr12 | 109548715 | 109578504 |
a0005 | 0/0 | 250 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | MAVCG others(245): Show |
chr12 | 109548715 | 109578504 |
a0006 | 0/0 | 250 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | MAVRG others(245): Show |
chr12 | 109548715 | 109578504 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 750 | 171 | 24 | 26 | 88 | 6 | 26 | MMAB_chr12_109548715_109578504 | MMAB | ATGGC others(745): Show |
chr12 | 109548715 | 109578504 | ||
a0001c0006 | 0/0 | 750 | 2 | 0 | 0 | 2 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | ATGGC others(745): Show |
chr12 | 109548715 | 109578504 | ||
a0001c0009 | 0/0 | 750 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | ATGGC others(745): Show |
chr12 | 109548715 | 109578504 | ||
a0002c0003 | 0/0 | 750 | 86 | 16 | 14 | 39 | 7 | 10 | MMAB_chr12_109548715_109578504 | MMAB | ATGGC others(745): Show |
chr12 | 109548715 | 109578504 | ||
a0002c0004 | 0/0 | 750 | 16 | 16 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | ATGGC others(745): Show |
chr12 | 109548715 | 109578504 | ||
a0002c0010 | 0/0 | 750 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | ATGGC others(745): Show |
chr12 | 109548715 | 109578504 | ||
a0003c0002 | 0/1 | 750 | 86 | 34 | 21 | 21 | 3 | 6 | MMAB_chr12_109548715_109578504 | MMAB | ATGGC others(745): Show |
chr12 | 109548715 | 109578504 | ||
a0003c0008 | 0/0 | 750 | 1 | 0 | 1 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | ATGGC others(745): Show |
chr12 | 109548715 | 109578504 | ||
a0004c0005 | 0/0 | 750 | 2 | 2 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | ATGGC others(745): Show |
chr12 | 109548715 | 109578504 | ||
a0005c0011 | 0/0 | 750 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | ATGGC others(745): Show |
chr12 | 109548715 | 109578504 | ||
a0006c0007 | 0/0 | 750 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | ATGGC others(745): Show |
chr12 | 109548715 | 109578504 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4089 | 57 | 14 | 4 | 30 | 2 | 7 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4084): Show |
chr12 | 109548715 | 109578504 |
a0001c0001t0002 | 1/0 | 4090 | 44 | 1 | 8 | 23 | 3 | 8 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4085): Show |
chr12 | 109548715 | 109578504 |
a0001c0001t0004 | 0/0 | 4090 | 21 | 3 | 7 | 4 | 1 | 6 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4085): Show |
chr12 | 109548715 | 109578504 |
a0001c0001t0006 | 0/0 | 4091 | 17 | 2 | 2 | 10 | 0 | 3 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4086): Show |
chr12 | 109548715 | 109578504 |
a0001c0001t0010 | 0/0 | 4092 | 7 | 0 | 2 | 5 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4087): Show |
chr12 | 109548715 | 109578504 |
a0001c0001t0014 | 0/0 | 4091 | 4 | 0 | 0 | 4 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4086): Show |
chr12 | 109548715 | 109578504 |
a0001c0001t0020 | 0/0 | 4088 | 4 | 0 | 0 | 4 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4083): Show |
chr12 | 109548715 | 109578504 |
a0001c0001t0031 | 0/0 | 4087 | 2 | 2 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4082): Show |
chr12 | 109548715 | 109578504 |
a0001c0001t0033 | 0/0 | 4087 | 2 | 0 | 2 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4082): Show |
chr12 | 109548715 | 109578504 |
a0001c0001t0046 | 0/0 | 4090 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4085): Show |
chr12 | 109548715 | 109578504 |
a0001c0001t0066 | 0/0 | 4092 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4087): Show |
chr12 | 109548715 | 109578504 |
a0001c0001t0067 | 0/0 | 4091 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4086): Show |
chr12 | 109548715 | 109578504 |
a0001c0001t0085 | 0/0 | 4091 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4086): Show |
chr12 | 109548715 | 109578504 |
a0001c0001t0086 | 0/0 | 4091 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4086): Show |
chr12 | 109548715 | 109578504 |
a0001c0001t0087 | 0/0 | 4090 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4085): Show |
chr12 | 109548715 | 109578504 |
a0001c0001t0088 | 0/0 | 4092 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4087): Show |
chr12 | 109548715 | 109578504 |
a0001c0001t0089 | 0/0 | 4089 | 1 | 0 | 0 | 0 | 0 | 1 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4084): Show |
chr12 | 109548715 | 109578504 |
a0001c0001t0090 | 0/0 | 4089 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4084): Show |
chr12 | 109548715 | 109578504 |
a0001c0001t0091 | 0/0 | 4089 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4084): Show |
chr12 | 109548715 | 109578504 |
a0001c0001t0092 | 0/0 | 4090 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4085): Show |
chr12 | 109548715 | 109578504 |
a0001c0001t0097 | 0/0 | 4088 | 1 | 0 | 1 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4083): Show |
chr12 | 109548715 | 109578504 |
a0001c0001t0101 | 0/0 | 4091 | 1 | 0 | 0 | 0 | 0 | 1 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4086): Show |
chr12 | 109548715 | 109578504 |
a0001c0006t0001 | 0/0 | 4089 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4084): Show |
chr12 | 109548715 | 109578504 |
a0001c0006t0004 | 0/0 | 4090 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4085): Show |
chr12 | 109548715 | 109578504 |
a0001c0009t0001 | 0/0 | 4089 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4084): Show |
chr12 | 109548715 | 109578504 |
a0002c0003t0003 | 0/0 | 4094 | 24 | 0 | 5 | 13 | 3 | 3 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4089): Show |
chr12 | 109548715 | 109578504 |
a0002c0003t0005 | 0/0 | 4101 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4096): Show |
chr12 | 109548715 | 109578504 |
a0002c0003t0007 | 0/0 | 4095 | 15 | 2 | 4 | 8 | 0 | 1 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4090): Show |
chr12 | 109548715 | 109578504 |
a0002c0003t0011 | 0/0 | 4093 | 2 | 0 | 0 | 2 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4088): Show |
chr12 | 109548715 | 109578504 |
a0002c0003t0016 | 0/0 | 4077 | 4 | 0 | 1 | 0 | 1 | 2 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4072): Show |
chr12 | 109548715 | 109578504 |
a0002c0003t0019 | 0/0 | 4092 | 3 | 0 | 1 | 1 | 1 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4087): Show |
chr12 | 109548715 | 109578504 |
a0002c0003t0030 | 0/0 | 4097 | 2 | 0 | 0 | 1 | 1 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4092): Show |
chr12 | 109548715 | 109578504 |
a0002c0003t0032 | 0/0 | 4095 | 2 | 0 | 0 | 1 | 0 | 1 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4090): Show |
chr12 | 109548715 | 109578504 |
a0002c0003t0034 | 0/0 | 4097 | 2 | 2 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4092): Show |
chr12 | 109548715 | 109578504 |
a0002c0003t0035 | 0/0 | 4101 | 2 | 0 | 0 | 2 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4096): Show |
chr12 | 109548715 | 109578504 |
a0002c0003t0036 | 0/0 | 4077 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4072): Show |
chr12 | 109548715 | 109578504 |
a0002c0003t0037 | 0/0 | 4104 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4099): Show |
chr12 | 109548715 | 109578504 |
a0002c0003t0038 | 0/0 | 4100 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4095): Show |
chr12 | 109548715 | 109578504 |
a0002c0003t0047 | 0/0 | 4078 | 1 | 0 | 1 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4073): Show |
chr12 | 109548715 | 109578504 |
a0002c0003t0054 | 0/0 | 4090 | 1 | 0 | 1 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4085): Show |
chr12 | 109548715 | 109578504 |
a0002c0003t0056 | 0/0 | 4091 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4086): Show |
chr12 | 109548715 | 109578504 |
a0002c0003t0059 | 0/0 | 4090 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4085): Show |
chr12 | 109548715 | 109578504 |
a0002c0003t0065 | 0/0 | 4092 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4087): Show |
chr12 | 109548715 | 109578504 |
a0002c0003t0068 | 0/0 | 4098 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4093): Show |
chr12 | 109548715 | 109578504 |
a0002c0003t0069 | 0/0 | 4096 | 1 | 0 | 0 | 0 | 0 | 1 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4091): Show |
chr12 | 109548715 | 109578504 |
a0002c0003t0070 | 0/0 | 4096 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4091): Show |
chr12 | 109548715 | 109578504 |
a0002c0003t0071 | 0/0 | 4095 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4090): Show |
chr12 | 109548715 | 109578504 |
a0002c0003t0073 | 0/0 | 4095 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4090): Show |
chr12 | 109548715 | 109578504 |
a0002c0003t0074 | 0/0 | 4103 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4098): Show |
chr12 | 109548715 | 109578504 |
a0002c0003t0075 | 0/0 | 4096 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4091): Show |
chr12 | 109548715 | 109578504 |
a0002c0003t0076 | 0/0 | 4095 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4090): Show |
chr12 | 109548715 | 109578504 |
a0002c0003t0077 | 0/0 | 4104 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4099): Show |
chr12 | 109548715 | 109578504 |
a0002c0003t0078 | 0/0 | 4101 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4096): Show |
chr12 | 109548715 | 109578504 |
a0002c0003t0080 | 0/0 | 4100 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4095): Show |
chr12 | 109548715 | 109578504 |
a0002c0003t0081 | 0/0 | 4097 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4092): Show |
chr12 | 109548715 | 109578504 |
a0002c0003t0082 | 0/0 | 4096 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4091): Show |
chr12 | 109548715 | 109578504 |
a0002c0003t0083 | 0/0 | 4094 | 1 | 0 | 0 | 0 | 1 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4089): Show |
chr12 | 109548715 | 109578504 |
a0002c0003t0084 | 0/0 | 4094 | 1 | 0 | 1 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4089): Show |
chr12 | 109548715 | 109578504 |
a0002c0003t0094 | 0/0 | 4094 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4089): Show |
chr12 | 109548715 | 109578504 |
a0002c0003t0095 | 0/0 | 4094 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4089): Show |
chr12 | 109548715 | 109578504 |
a0002c0003t0096 | 0/0 | 4094 | 1 | 0 | 0 | 0 | 0 | 1 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4089): Show |
chr12 | 109548715 | 109578504 |
a0002c0003t0098 | 0/0 | 4098 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4093): Show |
chr12 | 109548715 | 109578504 |
a0002c0003t0099 | 0/0 | 4102 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4097): Show |
chr12 | 109548715 | 109578504 |
a0002c0003t0100 | 0/0 | 4110 | 1 | 0 | 0 | 0 | 0 | 1 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4105): Show |
chr12 | 109548715 | 109578504 |
a0002c0004t0011 | 0/0 | 4093 | 4 | 4 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4088): Show |
chr12 | 109548715 | 109578504 |
a0002c0004t0018 | 0/0 | 4094 | 4 | 4 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4089): Show |
chr12 | 109548715 | 109578504 |
a0002c0004t0019 | 0/0 | 4092 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4087): Show |
chr12 | 109548715 | 109578504 |
a0002c0004t0025 | 0/0 | 4090 | 2 | 2 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4085): Show |
chr12 | 109548715 | 109578504 |
a0002c0004t0026 | 0/0 | 4089 | 2 | 2 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4084): Show |
chr12 | 109548715 | 109578504 |
a0002c0004t0055 | 0/0 | 4091 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4086): Show |
chr12 | 109548715 | 109578504 |
a0002c0004t0064 | 0/0 | 4093 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4088): Show |
chr12 | 109548715 | 109578504 |
a0002c0004t0079 | 0/0 | 4098 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4093): Show |
chr12 | 109548715 | 109578504 |
a0002c0010t0072 | 0/0 | 4100 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4095): Show |
chr12 | 109548715 | 109578504 |
a0003c0002t0005 | 0/0 | 4101 | 19 | 2 | 2 | 14 | 1 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4096): Show |
chr12 | 109548715 | 109578504 |
a0003c0002t0008 | 0/1 | 4079 | 11 | 4 | 4 | 0 | 0 | 2 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4074): Show |
chr12 | 109548715 | 109578504 |
a0003c0002t0009 | 0/0 | 4102 | 7 | 7 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4097): Show |
chr12 | 109548715 | 109578504 |
a0003c0002t0012 | 0/0 | 4109 | 4 | 0 | 4 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4104): Show |
chr12 | 109548715 | 109578504 |
a0003c0002t0013 | 0/0 | 4075 | 5 | 2 | 2 | 0 | 1 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4070): Show |
chr12 | 109548715 | 109578504 |
a0003c0002t0015 | 0/0 | 4100 | 4 | 4 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4095): Show |
chr12 | 109548715 | 109578504 |
a0003c0002t0017 | 0/0 | 4091 | 4 | 0 | 0 | 4 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4086): Show |
chr12 | 109548715 | 109578504 |
a0003c0002t0021 | 0/0 | 4081 | 3 | 2 | 1 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4076): Show |
chr12 | 109548715 | 109578504 |
a0003c0002t0023 | 0/0 | 4089 | 2 | 0 | 2 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4084): Show |
chr12 | 109548715 | 109578504 |
a0003c0002t0024 | 0/0 | 4075 | 2 | 2 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4070): Show |
chr12 | 109548715 | 109578504 |
a0003c0002t0027 | 0/0 | 4093 | 2 | 0 | 0 | 0 | 0 | 2 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4088): Show |
chr12 | 109548715 | 109578504 |
a0003c0002t0028 | 0/0 | 4077 | 2 | 0 | 2 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4072): Show |
chr12 | 109548715 | 109578504 |
a0003c0002t0029 | 0/0 | 4097 | 2 | 0 | 0 | 2 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4092): Show |
chr12 | 109548715 | 109578504 |
a0003c0002t0039 | 0/0 | 4109 | 1 | 0 | 1 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4104): Show |
chr12 | 109548715 | 109578504 |
a0003c0002t0040 | 0/0 | 4109 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4104): Show |
chr12 | 109548715 | 109578504 |
a0003c0002t0041 | 0/0 | 4108 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4103): Show |
chr12 | 109548715 | 109578504 |
a0003c0002t0042 | 0/0 | 4089 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4084): Show |
chr12 | 109548715 | 109578504 |
a0003c0002t0043 | 0/0 | 4102 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4097): Show |
chr12 | 109548715 | 109578504 |
a0003c0002t0044 | 0/0 | 4101 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4096): Show |
chr12 | 109548715 | 109578504 |
a0003c0002t0045 | 0/0 | 4100 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4095): Show |
chr12 | 109548715 | 109578504 |
a0003c0002t0048 | 0/0 | 4072 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4067): Show |
chr12 | 109548715 | 109578504 |
a0003c0002t0049 | 0/0 | 4079 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4074): Show |
chr12 | 109548715 | 109578504 |
a0003c0002t0050 | 0/0 | 4076 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4071): Show |
chr12 | 109548715 | 109578504 |
a0003c0002t0052 | 0/0 | 4081 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4076): Show |
chr12 | 109548715 | 109578504 |
a0003c0002t0053 | 0/0 | 4081 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4076): Show |
chr12 | 109548715 | 109578504 |
a0003c0002t0057 | 0/0 | 4092 | 1 | 0 | 0 | 0 | 0 | 1 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4087): Show |
chr12 | 109548715 | 109578504 |
a0003c0002t0058 | 0/0 | 4078 | 1 | 0 | 1 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4073): Show |
chr12 | 109548715 | 109578504 |
a0003c0002t0060 | 0/0 | 4080 | 1 | 0 | 0 | 0 | 1 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4075): Show |
chr12 | 109548715 | 109578504 |
a0003c0002t0061 | 0/0 | 4085 | 1 | 0 | 0 | 0 | 0 | 1 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4080): Show |
chr12 | 109548715 | 109578504 |
a0003c0002t0062 | 0/0 | 4094 | 1 | 0 | 1 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4089): Show |
chr12 | 109548715 | 109578504 |
a0003c0002t0063 | 0/0 | 4093 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4088): Show |
chr12 | 109548715 | 109578504 |
a0003c0002t0093 | 0/0 | 4087 | 1 | 0 | 1 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4082): Show |
chr12 | 109548715 | 109578504 |
a0003c0008t0012 | 0/0 | 4109 | 1 | 0 | 1 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4104): Show |
chr12 | 109548715 | 109578504 |
a0004c0005t0022 | 0/0 | 4103 | 2 | 2 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4098): Show |
chr12 | 109548715 | 109578504 |
a0005c0011t0014 | 0/0 | 4091 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4086): Show |
chr12 | 109548715 | 109578504 |
a0006c0007t0051 | 0/0 | 4082 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | AGGTC others(4077): Show |
chr12 | 109548715 | 109578504 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 15 | 0 | 1 | 10 | 0 | 4 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0001g0003 | 0/0 | 15 | 6 | 2 | 5 | 1 | 1 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0001g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0001g0038 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0002g0001 | 0/0 | 23 | 1 | 3 | 15 | 1 | 3 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0002g0023 | 1/0 | 3 | 0 | 2 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0004g0009 | 0/0 | 6 | 1 | 2 | 1 | 1 | 1 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0004g0010 | 0/0 | 5 | 0 | 1 | 1 | 0 | 3 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0004g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0004g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0004g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0004g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0004g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0004g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0004g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0004g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0004g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0006g0007 | 0/0 | 8 | 1 | 2 | 4 | 0 | 1 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0006g0033 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0006g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0006g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0006g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0006g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0006g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0006g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0006g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0010g0021 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0010g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0010g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0010g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0010g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0014g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0014g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0020g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0020g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0020g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0031g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0031g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0033g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0033g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0046g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0066g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0067g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0085g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0086g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0087g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0088g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0089g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0090g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0091g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0092g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0097g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0001t0101g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0006t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0006t0004g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0001c0009t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0003t0003g0005 | 0/0 | 11 | 0 | 1 | 10 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0003t0003g0012 | 0/0 | 4 | 0 | 1 | 1 | 2 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0003t0003g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0003t0003g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0003t0003g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0003t0003g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0003t0003g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0003t0003g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0003t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0003t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0003t0005g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0003t0007g0006 | 0/0 | 8 | 0 | 1 | 6 | 0 | 1 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0003t0007g0017 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0003t0007g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0003t0007g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0003t0007g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0003t0007g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0003t0011g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0003t0011g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0003t0016g0013 | 0/0 | 4 | 0 | 1 | 0 | 1 | 2 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0003t0019g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0003t0019g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0003t0019g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0003t0030g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0003t0030g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0003t0032g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0003t0032g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0003t0034g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0003t0035g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0003t0036g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0003t0037g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0003t0038g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0003t0047g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0003t0054g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0003t0056g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0003t0059g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0003t0065g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0003t0068g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0003t0069g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0003t0070g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0003t0071g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0003t0073g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0003t0074g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0003t0075g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0003t0076g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0003t0077g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0003t0078g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0003t0080g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0003t0081g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0003t0082g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0003t0083g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0003t0084g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0003t0094g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0003t0095g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0003t0096g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0003t0098g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0003t0099g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0003t0100g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0004t0011g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0004t0011g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0004t0018g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0004t0018g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0004t0019g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0004t0025g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0004t0025g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0004t0026g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0004t0055g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0004t0064g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0004t0079g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0002c0010t0072g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0003c0002t0005g0004 | 0/0 | 13 | 0 | 2 | 11 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0003c0002t0005g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0003c0002t0005g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0003c0002t0005g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0003c0002t0005g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0003c0002t0005g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0003c0002t0005g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0003c0002t0008g0008 | 0/1 | 7 | 1 | 3 | 0 | 0 | 2 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0003c0002t0008g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0003c0002t0008g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0003c0002t0008g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0003c0002t0009g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0003c0002t0009g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0003c0002t0009g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0003c0002t0009g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0003c0002t0012g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0003c0002t0012g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0003c0002t0012g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0003c0002t0013g0014 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0003c0002t0013g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0003c0002t0013g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0003c0002t0015g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0003c0002t0015g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0003c0002t0017g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0003c0002t0017g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0003c0002t0017g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0003c0002t0021g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0003c0002t0021g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0003c0002t0021g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0003c0002t0023g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0003c0002t0023g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0003c0002t0024g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0003c0002t0024g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0003c0002t0027g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0003c0002t0027g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0003c0002t0028g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0003c0002t0028g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0003c0002t0029g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0003c0002t0029g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0003c0002t0039g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0003c0002t0040g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0003c0002t0041g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0003c0002t0042g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0003c0002t0043g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0003c0002t0044g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0003c0002t0045g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0003c0002t0048g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0003c0002t0049g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0003c0002t0050g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0003c0002t0052g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0003c0002t0053g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0003c0002t0057g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0003c0002t0058g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0003c0002t0060g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0003c0002t0061g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0003c0002t0062g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0003c0002t0063g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0003c0002t0093g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0003c0008t0012g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0004c0005t0022g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0005c0011t0014g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
a0006c0007t0051g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0003 | c0002 | t0005 | g0077 | EUR | GBR | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG00099 | hp2 | a0002 | c0003 | t0019 | g0109 | EUR | GBR | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG00140 | hp1 | a0002 | c0003 | t0016 | g0013 | EUR | GBR | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG00140 | hp2 | a0002 | c0003 | t0030 | g0113 | EUR | GBR | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG00323 | hp1 | a0002 | c0003 | t0003 | g0112 | EUR | FIN | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0206 | EUR | FIN | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | CHS | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG00423 | hp1 | a0003 | c0002 | t0005 | g0047 | EAS | CHS | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG00423 | hp2 | a0001 | c0001 | t0004 | g0009 | EAS | CHS | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG00597 | hp1 | a0002 | c0003 | t0003 | g0005 | EAS | CHS | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG00597 | hp2 | a0001 | c0001 | t0006 | g0007 | EAS | CHS | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG00609 | hp1 | a0002 | c0003 | t0007 | g0006 | EAS | CHS | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG00609 | hp2 | a0001 | c0001 | t0086 | g0196 | EAS | CHS | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG00621 | hp2 | a0002 | c0003 | t0073 | g0105 | EAS | CHS | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG00639 | hp1 | a0002 | c0003 | t0003 | g0099 | AMR | PUR | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG00639 | hp2 | a0003 | c0002 | t0008 | g0008 | AMR | PUR | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG00642 | hp1 | a0001 | c0001 | t0006 | g0007 | AMR | PUR | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG00642 | hp2 | a0003 | c0002 | t0008 | g0008 | AMR | PUR | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0023 | AMR | PUR | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG00733 | hp2 | a0002 | c0003 | t0019 | g0104 | AMR | PUR | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG00738 | hp1 | a0002 | c0003 | t0007 | g0006 | AMR | PUR | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0023 | AMR | PUR | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG00741 | hp1 | a0001 | c0001 | t0004 | g0039 | AMR | PUR | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG00741 | hp2 | a0001 | c0001 | t0097 | g0168 | AMR | PUR | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0212 | AMR | PUR | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG01070 | hp2 | a0001 | c0001 | t0033 | g0161 | AMR | PUR | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG01071 | hp1 | a0003 | c0002 | t0028 | g0064 | AMR | PUR | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG01071 | hp2 | a0001 | c0001 | t0033 | g0169 | AMR | PUR | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG01081 | hp2 | a0002 | c0003 | t0054 | g0108 | AMR | PUR | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG01099 | hp1 | a0003 | c0002 | t0008 | g0008 | AMR | PUR | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG01099 | hp2 | a0003 | c0002 | t0012 | g0089 | AMR | PUR | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG01106 | hp1 | a0001 | c0001 | t0010 | g0021 | AMR | PUR | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG01106 | hp2 | a0003 | c0002 | t0058 | g0057 | AMR | PUR | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG01109 | hp2 | a0002 | c0003 | t0003 | g0005 | AMR | PUR | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG01168 | hp1 | a0002 | c0003 | t0003 | g0012 | AMR | PUR | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG01168 | hp2 | a0001 | c0001 | t0004 | g0009 | AMR | PUR | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0220 | AMR | PUR | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG01169 | hp2 | a0001 | c0001 | t0004 | g0215 | AMR | PUR | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG01243 | hp1 | a0003 | c0002 | t0013 | g0085 | AMR | PUR | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG01243 | hp2 | a0001 | c0001 | t0004 | g0009 | AMR | PUR | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG01255 | hp1 | a0003 | c0002 | t0062 | g0072 | AMR | CLM | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG01255 | hp2 | a0002 | c0003 | t0003 | g0111 | AMR | CLM | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG01257 | hp1 | a0003 | c0002 | t0023 | g0074 | AMR | CLM | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0216 | AMR | CLM | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG01258 | hp1 | a0003 | c0002 | t0023 | g0070 | AMR | CLM | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG01258 | hp2 | a0003 | c0002 | t0021 | g0055 | AMR | CLM | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG01261 | hp1 | a0001 | c0001 | t0004 | g0010 | AMR | CLM | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG01261 | hp2 | a0001 | c0001 | t0004 | g0039 | AMR | CLM | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG01346 | hp1 | a0002 | c0003 | t0016 | g0013 | AMR | CLM | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG01346 | hp2 | a0003 | c0002 | t0028 | g0058 | AMR | CLM | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG01358 | hp1 | a0001 | c0001 | t0010 | g0185 | AMR | CLM | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG01358 | hp2 | a0002 | c0003 | t0047 | g0218 | AMR | CLM | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG01361 | hp1 | a0002 | c0003 | t0007 | g0017 | AMR | CLM | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG01361 | hp2 | a0003 | c0002 | t0013 | g0014 | AMR | CLM | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG01433 | hp1 | a0003 | c0002 | t0093 | g0045 | AMR | CLM | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG01515 | hp1 | a0002 | c0003 | t0003 | g0012 | EUR | IBS | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0180 | EUR | IBS | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG01516 | hp1 | a0003 | c0002 | t0013 | g0044 | EUR | IBS | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | IBS | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0217 | EUR | IBS | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG01517 | hp2 | a0002 | c0003 | t0003 | g0012 | EUR | IBS | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG01884 | hp1 | a0003 | c0002 | t0015 | g0052 | AFR | ACB | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG01884 | hp2 | a0001 | c0001 | t0031 | g0176 | AFR | ACB | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG01891 | hp1 | a0002 | c0010 | t0072 | g0096 | AFR | ACB | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG01928 | hp2 | a0003 | c0002 | t0005 | g0004 | AMR | PEL | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG01934 | hp1 | a0002 | c0003 | t0003 | g0093 | AMR | PEL | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG01943 | hp1 | a0002 | c0003 | t0084 | g0110 | AMR | PEL | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG01943 | hp2 | a0003 | c0002 | t0008 | g0086 | AMR | PEL | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG01978 | hp1 | a0003 | c0002 | t0012 | g0082 | AMR | PEL | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG01978 | hp2 | a0001 | c0001 | t0004 | g0207 | AMR | PEL | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG01981 | hp1 | a0003 | c0002 | t0012 | g0024 | AMR | PEL | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG01981 | hp2 | a0002 | c0003 | t0007 | g0092 | AMR | PEL | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02004 | hp1 | a0003 | c0008 | t0012 | g0049 | AMR | PEL | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02004 | hp2 | a0003 | c0002 | t0012 | g0024 | AMR | PEL | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02015 | hp1 | a0001 | c0001 | t0085 | g0195 | EAS | KHV | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02015 | hp2 | a0001 | c0001 | t0006 | g0007 | EAS | KHV | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02040 | hp1 | a0001 | c0001 | t0014 | g0022 | EAS | KHV | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02040 | hp2 | a0003 | c0002 | t0005 | g0004 | EAS | KHV | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02056 | hp1 | a0001 | c0001 | t0014 | g0192 | EAS | KHV | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02056 | hp2 | a0003 | c0002 | t0029 | g0073 | EAS | KHV | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02071 | hp1 | a0001 | c0001 | t0092 | g0200 | EAS | KHV | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02071 | hp2 | a0005 | c0011 | t0014 | g0157 | EAS | KHV | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | KHV | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02083 | hp1 | a0003 | c0002 | t0005 | g0004 | EAS | KHV | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02083 | hp2 | a0001 | c0001 | t0010 | g0021 | EAS | KHV | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02132 | hp2 | a0002 | c0003 | t0003 | g0005 | EAS | KHV | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02135 | hp1 | a0001 | c0001 | t0004 | g0170 | EAS | KHV | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02135 | hp2 | a0001 | c0001 | t0006 | g0033 | EAS | KHV | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02145 | hp1 | a0002 | c0003 | t0007 | g0102 | AFR | ACB | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02145 | hp2 | a0001 | c0001 | t0006 | g0033 | AFR | ACB | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02148 | hp1 | a0001 | c0001 | t0006 | g0007 | AMR | PEL | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02148 | hp2 | a0003 | c0002 | t0039 | g0046 | AMR | PEL | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02257 | hp1 | a0003 | c0002 | t0013 | g0014 | AFR | ACB | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02257 | hp2 | a0002 | c0003 | t0074 | g0122 | AFR | ACB | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02258 | hp1 | a0002 | c0003 | t0007 | g0114 | AFR | ACB | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02258 | hp2 | a0002 | c0004 | t0011 | g0120 | AFR | ACB | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02280 | hp1 | a0002 | c0003 | t0077 | g0121 | AFR | ACB | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02280 | hp2 | a0002 | c0003 | t0037 | g0149 | AFR | ACB | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02451 | hp1 | a0002 | c0003 | t0094 | g0143 | AFR | ACB | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02451 | hp2 | a0003 | c0002 | t0008 | g0008 | AFR | ACB | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02572 | hp2 | a0002 | c0004 | t0018 | g0018 | AFR | GWD | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02615 | hp1 | a0003 | c0002 | t0008 | g0025 | AFR | GWD | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02615 | hp2 | a0003 | c0002 | t0050 | g0042 | AFR | GWD | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02622 | hp1 | a0003 | c0002 | t0053 | g0060 | AFR | GWD | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02630 | hp1 | a0002 | c0004 | t0064 | g0117 | AFR | GWD | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02630 | hp2 | a0003 | c0002 | t0008 | g0025 | AFR | GWD | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02647 | hp1 | a0002 | c0004 | t0019 | g0118 | AFR | GWD | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02647 | hp2 | a0003 | c0002 | t0043 | g0075 | AFR | GWD | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02683 | hp2 | a0002 | c0003 | t0016 | g0013 | SAS | PJL | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02698 | hp1 | a0001 | c0001 | t0004 | g0010 | SAS | PJL | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02698 | hp2 | a0002 | c0003 | t0016 | g0013 | SAS | PJL | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02717 | hp1 | a0002 | c0004 | t0026 | g0029 | AFR | GWD | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02717 | hp2 | a0002 | c0004 | t0011 | g0019 | AFR | GWD | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02723 | hp1 | a0003 | c0002 | t0013 | g0014 | AFR | GWD | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02723 | hp2 | a0001 | c0001 | t0004 | g0174 | AFR | GWD | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02735 | hp2 | a0003 | c0002 | t0057 | g0068 | SAS | PJL | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02738 | hp1 | a0001 | c0001 | t0006 | g0164 | SAS | PJL | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02738 | hp2 | a0001 | c0001 | t0006 | g0007 | SAS | PJL | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02818 | hp2 | a0002 | c0004 | t0018 | g0018 | AFR | GWD | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02886 | hp1 | a0002 | c0004 | t0079 | g0119 | AFR | GWD | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02886 | hp2 | a0003 | c0002 | t0042 | g0065 | AFR | GWD | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02896 | hp1 | a0003 | c0002 | t0021 | g0063 | AFR | GWD | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02896 | hp2 | a0003 | c0002 | t0015 | g0015 | AFR | GWD | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02897 | hp1 | a0003 | c0002 | t0044 | g0076 | AFR | GWD | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02897 | hp2 | a0003 | c0002 | t0021 | g0087 | AFR | GWD | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02922 | hp1 | a0002 | c0003 | t0034 | g0031 | AFR | ESN | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | ESN | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02965 | hp1 | a0001 | c0001 | t0031 | g0211 | AFR | ESN | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02970 | hp1 | a0001 | c0001 | t0091 | g0199 | AFR | ESN | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02970 | hp2 | a0003 | c0002 | t0045 | g0051 | AFR | ESN | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02976 | hp1 | a0003 | c0002 | t0005 | g0041 | AFR | ESN | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02976 | hp2 | a0003 | c0002 | t0009 | g0088 | AFR | ESN | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG03017 | hp1 | a0002 | c0003 | t0100 | g0148 | SAS | PJL | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG03041 | hp1 | a0002 | c0003 | t0095 | g0145 | AFR | GWD | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG03041 | hp2 | a0002 | c0004 | t0011 | g0019 | AFR | GWD | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG03098 | hp1 | a0003 | c0002 | t0015 | g0015 | AFR | MSL | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | MSL | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG03130 | hp1 | a0003 | c0002 | t0015 | g0015 | AFR | ESN | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG03130 | hp2 | a0002 | c0004 | t0018 | g0018 | AFR | ESN | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG03139 | hp1 | a0003 | c0002 | t0009 | g0016 | AFR | ESN | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG03139 | hp2 | a0002 | c0004 | t0025 | g0095 | AFR | ESN | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG03195 | hp1 | a0003 | c0002 | t0041 | g0050 | AFR | ESN | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG03195 | hp2 | a0004 | c0005 | t0022 | g0028 | AFR | ESN | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG03209 | hp1 | a0002 | c0003 | t0056 | g0098 | AFR | MSL | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG03225 | hp1 | a0006 | c0007 | t0051 | g0040 | AFR | MSL | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG03225 | hp2 | a0003 | c0002 | t0009 | g0084 | AFR | MSL | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG03239 | hp1 | a0003 | c0002 | t0008 | g0008 | SAS | PJL | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG03453 | hp1 | a0001 | c0001 | t0004 | g0183 | AFR | MSL | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG03453 | hp2 | a0003 | c0002 | t0008 | g0062 | AFR | MSL | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG03486 | hp1 | a0002 | c0004 | t0025 | g0137 | AFR | MSL | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG03486 | hp2 | a0002 | c0004 | t0026 | g0029 | AFR | MSL | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG03490 | hp2 | a0002 | c0003 | t0003 | g0030 | SAS | PJL | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG03491 | hp1 | a0002 | c0003 | t0069 | g0147 | SAS | PJL | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG03492 | hp1 | a0002 | c0003 | t0003 | g0030 | SAS | PJL | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG03492 | hp2 | a0001 | c0001 | t0004 | g0010 | SAS | PJL | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG03516 | hp1 | a0003 | c0002 | t0005 | g0048 | AFR | ESN | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG03516 | hp2 | a0002 | c0004 | t0018 | g0116 | AFR | ESN | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG03540 | hp2 | a0003 | c0002 | t0024 | g0061 | AFR | GWD | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | MSL | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG03654 | hp1 | a0002 | c0003 | t0007 | g0006 | SAS | PJL | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG03654 | hp2 | a0002 | c0003 | t0096 | g0133 | SAS | PJL | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG03669 | hp1 | a0001 | c0001 | t0089 | g0166 | SAS | PJL | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0181 | SAS | PJL | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0165 | SAS | PJL | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG03831 | hp1 | a0001 | c0001 | t0006 | g0177 | SAS | BEB | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG03831 | hp2 | a0003 | c0002 | t0061 | g0054 | SAS | BEB | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0190 | SAS | BEB | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG03927 | hp1 | a0001 | c0001 | t0101 | g0221 | SAS | BEB | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG03927 | hp2 | a0002 | c0003 | t0032 | g0132 | SAS | BEB | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG03942 | hp1 | a0001 | c0001 | t0004 | g0163 | SAS | BEB | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG03942 | hp2 | a0001 | c0001 | t0004 | g0010 | SAS | BEB | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG04115 | hp1 | a0003 | c0002 | t0008 | g0008 | SAS | STU | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG04115 | hp2 | a0003 | c0002 | t0027 | g0071 | SAS | STU | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG04184 | hp1 | a0002 | c0003 | t0003 | g0101 | SAS | BEB | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0179 | SAS | BEB | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG04199 | hp1 | a0001 | c0001 | t0004 | g0009 | SAS | STU | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG04199 | hp2 | a0001 | c0001 | t0004 | g0152 | SAS | STU | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0178 | SAS | STU | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18522 | hp1 | a0002 | c0004 | t0011 | g0019 | AFR | YRI | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18522 | hp2 | a0003 | c0002 | t0052 | g0043 | AFR | YRI | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18612 | hp1 | a0003 | c0002 | t0005 | g0004 | EAS | CHB | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | CHB | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18906 | hp1 | a0003 | c0002 | t0024 | g0056 | AFR | YRI | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18941 | hp1 | a0003 | c0002 | t0017 | g0027 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18942 | hp1 | a0002 | c0003 | t0065 | g0130 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18942 | hp2 | a0003 | c0002 | t0005 | g0004 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18945 | hp2 | a0002 | c0003 | t0081 | g0131 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18946 | hp1 | a0002 | c0003 | t0035 | g0032 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18950 | hp1 | a0002 | c0003 | t0032 | g0127 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18950 | hp2 | a0001 | c0001 | t0088 | g0198 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18951 | hp1 | a0002 | c0003 | t0082 | g0125 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18952 | hp1 | a0003 | c0002 | t0005 | g0004 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18953 | hp1 | a0002 | c0003 | t0035 | g0032 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18953 | hp2 | a0003 | c0002 | t0029 | g0080 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18957 | hp2 | a0002 | c0003 | t0003 | g0135 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18959 | hp1 | a0003 | c0002 | t0017 | g0069 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18960 | hp2 | a0003 | c0002 | t0005 | g0004 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18963 | hp2 | a0003 | c0002 | t0005 | g0004 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18967 | hp1 | a0001 | c0001 | t0010 | g0021 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18967 | hp2 | a0002 | c0003 | t0070 | g0139 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18968 | hp2 | a0002 | c0003 | t0003 | g0005 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18969 | hp1 | a0002 | c0003 | t0007 | g0006 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18969 | hp2 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18970 | hp1 | a0001 | c0001 | t0046 | g0187 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18971 | hp1 | a0001 | c0006 | t0001 | g0151 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18973 | hp1 | a0002 | c0003 | t0007 | g0006 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18973 | hp2 | a0001 | c0001 | t0006 | g0191 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18974 | hp1 | a0001 | c0001 | t0006 | g0209 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18974 | hp2 | a0002 | c0003 | t0007 | g0006 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18977 | hp1 | a0001 | c0001 | t0006 | g0201 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18980 | hp2 | a0003 | c0002 | t0005 | g0004 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18982 | hp1 | a0001 | c0009 | t0001 | g0204 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18984 | hp1 | a0003 | c0002 | t0005 | g0090 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18985 | hp1 | a0001 | c0001 | t0006 | g0007 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18985 | hp2 | a0002 | c0003 | t0007 | g0006 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18986 | hp2 | a0002 | c0003 | t0003 | g0005 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18990 | hp1 | a0003 | c0002 | t0063 | g0079 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18993 | hp1 | a0001 | c0001 | t0004 | g0213 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18993 | hp2 | a0002 | c0003 | t0003 | g0005 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18995 | hp1 | a0003 | c0002 | t0005 | g0004 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18998 | hp1 | a0001 | c0001 | t0020 | g0037 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18998 | hp2 | a0002 | c0003 | t0003 | g0005 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18999 | hp1 | a0003 | c0002 | t0017 | g0078 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA19000 | hp1 | a0003 | c0002 | t0005 | g0081 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA19000 | hp2 | a0002 | c0003 | t0011 | g0094 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA19003 | hp2 | a0002 | c0003 | t0011 | g0126 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA19004 | hp2 | a0003 | c0002 | t0005 | g0004 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA19005 | hp1 | a0001 | c0001 | t0014 | g0022 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA19005 | hp2 | a0001 | c0001 | t0087 | g0197 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA19009 | hp1 | a0003 | c0002 | t0017 | g0027 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA19009 | hp2 | a0002 | c0003 | t0076 | g0106 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA19011 | hp1 | a0002 | c0003 | t0007 | g0006 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA19011 | hp2 | a0001 | c0001 | t0066 | g0194 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA19030 | hp1 | a0001 | c0001 | t0090 | g0154 | AFR | LWK | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA19030 | hp2 | a0003 | c0002 | t0009 | g0016 | AFR | LWK | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA19043 | hp1 | a0004 | c0005 | t0022 | g0028 | AFR | LWK | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA19043 | hp2 | a0002 | c0003 | t0036 | g0219 | AFR | LWK | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA19055 | hp1 | a0002 | c0003 | t0071 | g0144 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA19055 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA19057 | hp1 | a0001 | c0001 | t0020 | g0037 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA19057 | hp2 | a0001 | c0001 | t0020 | g0167 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA19058 | hp1 | a0002 | c0003 | t0007 | g0017 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA19058 | hp2 | a0001 | c0001 | t0020 | g0173 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA19059 | hp1 | a0002 | c0003 | t0003 | g0136 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA19059 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA19060 | hp1 | a0002 | c0003 | t0003 | g0005 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA19062 | hp1 | a0002 | c0003 | t0059 | g0129 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA19062 | hp2 | a0001 | c0001 | t0067 | g0160 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA19064 | hp1 | a0001 | c0001 | t0014 | g0022 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA19064 | hp2 | a0003 | c0002 | t0005 | g0004 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA19066 | hp1 | a0001 | c0001 | t0006 | g0007 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA19066 | hp2 | a0001 | c0001 | t0006 | g0182 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA19067 | hp1 | a0001 | c0006 | t0004 | g0150 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA19067 | hp2 | a0002 | c0003 | t0003 | g0012 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA19074 | hp2 | a0002 | c0003 | t0030 | g0134 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA19075 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA19075 | hp2 | a0002 | c0003 | t0003 | g0005 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA19077 | hp2 | a0001 | c0001 | t0006 | g0208 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA19078 | hp1 | a0001 | c0001 | t0010 | g0159 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA19078 | hp2 | a0002 | c0003 | t0075 | g0100 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA19082 | hp1 | a0001 | c0001 | t0010 | g0214 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA19082 | hp2 | a0002 | c0003 | t0003 | g0005 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA19083 | hp1 | a0002 | c0003 | t0099 | g0140 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA19087 | hp2 | a0002 | c0003 | t0068 | g0138 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA19088 | hp1 | a0001 | c0001 | t0010 | g0205 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA19088 | hp2 | a0002 | c0003 | t0019 | g0128 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA19089 | hp1 | a0002 | c0003 | t0007 | g0097 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA19089 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA19091 | hp1 | a0002 | c0003 | t0003 | g0005 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA19240 | hp2 | a0003 | c0002 | t0009 | g0026 | AFR | YRI | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ASW | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA20129 | hp2 | a0002 | c0003 | t0034 | g0031 | AFR | ASW | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA20752 | hp1 | a0002 | c0003 | t0083 | g0107 | EUR | TSI | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA20752 | hp2 | a0001 | c0001 | t0004 | g0009 | EUR | TSI | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA20805 | hp2 | a0003 | c0002 | t0060 | g0053 | EUR | TSI | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA20905 | hp1 | a0003 | c0002 | t0027 | g0067 | SAS | GIH | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG01123 | hp1 | a0002 | c0003 | t0007 | g0017 | AMR | CLM | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG01123 | hp2 | a0003 | c0002 | t0005 | g0004 | AMR | CLM | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02109 | hp1 | a0003 | c0002 | t0009 | g0026 | AFR | ACB | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02109 | hp2 | a0002 | c0004 | t0055 | g0115 | AFR | ACB | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02486 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | ACB | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02486 | hp2 | a0003 | c0002 | t0049 | g0066 | AFR | ACB | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02559 | hp1 | a0002 | c0003 | t0078 | g0123 | AFR | ACB | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG02559 | hp2 | a0002 | c0003 | t0098 | g0146 | AFR | ACB | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG03471 | hp1 | a0002 | c0003 | t0005 | g0142 | AFR | MSL | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG03471 | hp2 | a0003 | c0002 | t0048 | g0059 | AFR | MSL | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG06807 | hp1 | a0002 | c0003 | t0080 | g0124 | AFR | USA | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
HG06807 | hp2 | a0001 | c0001 | t0006 | g0007 | AFR | USA | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA20300 | hp1 | a0002 | c0003 | t0038 | g0103 | AFR | USA | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA20300 | hp2 | a0003 | c0002 | t0040 | g0083 | AFR | USA | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | LWK | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
NA21309 | hp2 | a0003 | c0002 | t0009 | g0016 | AFR | LWK | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
homoSapiens | chm13v2 | a0003 | c0002 | t0008 | g0008 | REF | REF | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0023 | REF | REF | MMAB_chr12_109548715_109578504 | MMAB | chr12 | 109548715 | 109578504 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | 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 | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:109557065 | A | T | 4 | a0002 a0003 a0004 others(1): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
missense_variant | MODERATE | c.716T>A | p.Met239Lys | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 740/4090 | 716/753 | 239/250 | chr12 | 109557065 | |||
chr12:109561041 | G | A | 1 | a0005 | 1 | HG02071.hp2 | missense_variant&splice_region_variant | MODERATE | c.583C>T | p.Arg195Cys | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 7/9 | 607/4090 | 583/753 | 195/250 | chr12 | 109561041 | |||
chr12:109571660 | G | A | 1 | a0004 | 2 | HG03195.hp2 NA19043.hp1 |
missense_variant | MODERATE | c.185C>T | p.Thr62Met | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 2/9 | 209/4090 | 185/753 | 62/250 | chr12 | 109571660 | |||
chr12:109573425 | C | T | 2 | a0003 a0004 |
88 | HG00099.hp1 HG00423.hp1 HG00639.hp2 others(85): Show |
missense_variant | MODERATE | c.56G>A | p.Arg19His | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 1/9 | 80/4090 | 56/753 | 19/250 | chr12 | 109573425 | |||
chr12:109573471 | A | G | 1 | a0006 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.10T>C | p.Cys4Arg | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 1/9 | 34/4090 | 10/753 | 4/250 | chr12 | 109573471 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | 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 | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:109557049 | C | G | 1 | a0003c0008 | 1 | HG02004.hp1 | synonymous_variant | LOW | c.732G>C | p.Ser244Ser | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 756/4090 | 732/753 | 244/250 | chr12 | 109557049 | |||
chr12:109559116 | G | A | 1 | a0002c0010 | 1 | HG01891.hp1 | synonymous_variant | LOW | c.624C>T | p.Asn208Asn | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 8/9 | 648/4090 | 624/753 | 208/250 | chr12 | 109559116 | |||
chr12:109561495 | C | T | 1 | a0001c0009 | 1 | NA18982.hp1 | synonymous_variant | LOW | c.444G>A | p.Gly148Gly | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 6/9 | 468/4090 | 444/753 | 148/250 | chr12 | 109561495 | |||
chr12:109561814 | C | T | 1 | a0001c0006 | 2 | NA18971.hp1 NA19067.hp1 |
synonymous_variant | LOW | c.387G>A | p.Ala129Ala | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 5/9 | 411/4090 | 387/753 | 129/250 | chr12 | 109561814 | |||
chr12:109568772 | A | G | 1 | a0002c0004 | 16 | HG02109.hp2 HG02258.hp2 HG02572.hp2 others(13): Show |
splice_region_variant&synonymous_variant | LOW | c.288T>C | p.Ile96Ile | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 3/9 | 312/4090 | 288/753 | 96/250 | chr12 | 109568772 | |||
chr12:109573424 | G | T | 3 | a0003c0002 a0003c0008 a0004c0005 |
88 | HG00099.hp1 HG00423.hp1 HG00639.hp2 others(85): Show |
synonymous_variant | LOW | c.57C>A | p.Arg19Arg | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 1/9 | 81/4090 | 57/753 | 19/250 | chr12 | 109573424 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | 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 | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:109553724 | C | G | 1 | a0002c0004t0064 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3304G>C | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 3304 | chr12 | 109553724 | ||||||
chr12:109553733 | G | A | 1 | a0003c0002t0042 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3295C>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 3295 | chr12 | 109553733 | ||||||
chr12:109553744 | T | A | 1 | a0001c0001t0086 | 1 | HG00609.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3284A>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 3284 | chr12 | 109553744 | ||||||
chr12:109553789 | T | G | 1 | a0002c0003t0038 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3239A>C | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 3239 | chr12 | 109553789 | ||||||
chr12:109553850 | G | T | 3 | a0003c0002t0009 a0003c0002t0043 a0003c0002t0044 |
9 | HG02109.hp1 HG02647.hp2 HG02897.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3178C>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 3178 | chr12 | 109553850 | ||||||
chr12:109553880 | C | T | 33 | a0002c0003t0034 a0002c0003t0035 a0002c0003t0068 others(30): Show |
58 | HG00639.hp2 HG00642.hp2 HG01071.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*3148G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 3148 | chr12 | 109553880 | ||||||
chr12:109553953 | C | T | 1 | a0003c0002t0045 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3075G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 3075 | chr12 | 109553953 | ||||||
chr12:109554009 | T | C | 5 | a0002c0003t0056 a0002c0003t0074 a0002c0003t0077 others(2): Show |
5 | HG02257.hp2 HG02280.hp1 HG02559.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3019A>G | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 3019 | chr12 | 109554009 | ||||||
chr12:109554193 | A | G | 31 | a0002c0003t0003 a0002c0003t0007 a0002c0003t0011 others(28): Show |
81 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*2835T>C | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 2835 | chr12 | 109554193 | ||||||
chr12:109554288 | C | T | 1 | a0003c0002t0043 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2740G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 2740 | chr12 | 109554288 | ||||||
chr12:109554322 | T | G | 1 | a0001c0001t0087 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2706A>C | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 2706 | chr12 | 109554322 | ||||||
chr12:109554327 | C | G | 49 | a0002c0003t0003 a0002c0003t0005 a0002c0003t0007 others(46): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*2701G>C | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 2701 | chr12 | 109554327 | ||||||
chr12:109554344 | C | G | 29 | a0002c0003t0003 a0002c0003t0007 a0002c0003t0011 others(26): Show |
79 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*2684G>C | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 2684 | chr12 | 109554344 | ||||||
chr12:109554400 | G | A | 3 | a0003c0002t0009 a0003c0002t0043 a0003c0002t0044 |
9 | HG02109.hp1 HG02647.hp2 HG02897.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2628C>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 2628 | chr12 | 109554400 | ||||||
chr12:109554567 | G | A | 1 | a0002c0003t0036 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2461C>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 2461 | chr12 | 109554567 | ||||||
chr12:109554842 | A | G | 1 | a0002c0003t0083 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2186T>C | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 2186 | chr12 | 109554842 | ||||||
chr12:109554899 | C | G | 1 | a0002c0010t0072 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2129G>C | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 2129 | chr12 | 109554899 | ||||||
chr12:109554939 | A | C | 1 | a0001c0001t0089 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2089T>G | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 2089 | chr12 | 109554939 | ||||||
chr12:109554977 | G | A | 1 | a0003c0002t0039 | 1 | HG02148.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2051C>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 2051 | chr12 | 109554977 | ||||||
chr12:109555076 | A | G | 17 | a0002c0003t0005 a0002c0003t0036 a0002c0003t0037 others(14): Show |
48 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*1952T>C | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 1952 | chr12 | 109555076 | ||||||
chr12:109555115 | C | T | 1 | a0001c0001t0085 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1913G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 1913 | chr12 | 109555115 | ||||||
chr12:109555153 | T | TTA | 27 | a0001c0001t0088 a0002c0003t0003 a0002c0003t0007 others(24): Show |
77 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*1873_*1874dupTA | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 1874 | chr12 | 109555153 | ||||||
chr12:109555153 | T | TTATA | 5 | a0002c0003t0056 a0002c0003t0074 a0002c0003t0077 others(2): Show |
5 | HG02257.hp2 HG02280.hp1 HG02559.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1871_*1874dupTATA | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 1874 | chr12 | 109555153 | ||||||
chr12:109555183 | T | C | 1 | a0002c0003t0084 | 1 | HG01943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1845A>G | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 1845 | chr12 | 109555183 | ||||||
chr12:109555218 | C | T | 17 | a0002c0003t0005 a0002c0003t0036 a0002c0003t0037 others(14): Show |
48 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*1810G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 1810 | chr12 | 109555218 | ||||||
chr12:109555245 | T | A | 1 | a0001c0001t0090 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1783A>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 1783 | chr12 | 109555245 | ||||||
chr12:109555275 | G | GT | 10 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0010 others(7): Show |
52 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*1752dupA | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 1752 | chr12 | 109555275 | ||||||
chr12:109555275 | G | GTTTTT | 7 | a0002c0003t0003 a0002c0003t0030 a0002c0003t0073 others(4): Show |
31 | HG00140.hp2 HG00323.hp1 HG00597.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*1748_*1752dupAAAA others(1): Show |
MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 1752 | chr12 | 109555275 | ||||||
chr12:109555275 | G | GTTTTTT | 8 | a0002c0003t0007 a0002c0003t0034 a0002c0003t0035 others(5): Show |
24 | HG00609.hp1 HG00738.hp1 HG01123.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1747_*1752dupAAAA others(2): Show |
MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 1752 | chr12 | 109555275 | ||||||
chr12:109555275 | G | GTTTTTTT | 13 | a0002c0003t0019 a0002c0003t0059 a0002c0003t0065 others(10): Show |
20 | HG00099.hp2 HG00733.hp2 HG01257.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1746_*1752dupAAAA others(3): Show |
MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 1752 | chr12 | 109555275 | ||||||
chr12:109555275 | G | GTTTTTTT others(1): Show |
10 | a0002c0003t0011 a0002c0003t0032 a0002c0003t0054 others(7): Show |
16 | HG01081.hp2 HG01255.hp1 HG02258.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1745_*1752dupAAAA others(4): Show |
MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 1752 | chr12 | 109555275 | ||||||
chr12:109555275 | G | GTTTTTTT others(2): Show |
5 | a0002c0003t0080 a0002c0004t0018 a0002c0004t0025 others(2): Show |
10 | HG02572.hp2 HG02818.hp2 HG02886.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1744_*1752dupAAAA others(5): Show |
MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 1752 | chr12 | 109555275 | ||||||
chr12:109555275 | G | GTTTTTTT others(3): Show |
3 | a0002c0003t0078 a0002c0004t0055 a0002c0010t0072 |
3 | HG01891.hp1 HG02109.hp2 HG02559.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1743_*1752dupAAAA others(6): Show |
MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 1752 | chr12 | 109555275 | ||||||
chr12:109555275 | G | GTTTTTTT others(4): Show |
1 | a0002c0003t0074 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1742_*1752dupAAAA others(7): Show |
MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 1752 | chr12 | 109555275 | ||||||
chr12:109555275 | G | GTTTTTTT others(6): Show |
1 | a0002c0003t0077 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1740_*1752dupAAAA others(9): Show |
MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 1752 | chr12 | 109555275 | ||||||
chr12:109555275 | G | GTTTTTTT others(8): Show |
1 | a0002c0003t0037 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1738_*1752dupAAAA others(11): Show |
MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 1752 | chr12 | 109555275 | ||||||
chr12:109555275 | GTTTTTT | G | 9 | a0003c0002t0008 a0003c0002t0013 a0003c0002t0021 others(6): Show |
26 | HG00639.hp2 HG00642.hp2 HG01071.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1747_*1752delAAAA others(2): Show |
MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 1747 | chr12 | 109555275 | ||||||
chr12:109555275 | GTTTTTTT others(3): Show |
G | 1 | a0002c0003t0036 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1743_*1752delAAAA others(6): Show |
MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 1743 | chr12 | 109555275 | ||||||
chr12:109555275 | GTTTTTTT others(4): Show |
G | 2 | a0002c0003t0016 a0002c0003t0047 |
5 | HG00140.hp1 HG01346.hp1 HG01358.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1742_*1752delAAAA others(7): Show |
MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 1742 | chr12 | 109555275 | ||||||
chr12:109555283 | T | TGTTTGTT others(6): Show |
1 | a0003c0002t0040 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1744_*1745insCAAA others(9): Show |
MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 1744 | chr12 | 109555283 | ||||||
chr12:109555283 | T | TTTTTGTT others(6): Show |
3 | a0003c0002t0009 a0003c0002t0043 a0003c0002t0044 |
9 | HG02109.hp1 HG02647.hp2 HG02897.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1744_*1745insCAAA others(9): Show |
MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 1744 | chr12 | 109555283 | ||||||
chr12:109555287 | T | G | 1 | a0003c0002t0040 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1741A>C | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 1741 | chr12 | 109555287 | ||||||
chr12:109555287 | T | TGTTTGTT others(6): Show |
10 | a0002c0003t0005 a0002c0003t0038 a0003c0002t0005 others(7): Show |
35 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*1740_*1741insCAAA others(9): Show |
MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 1740 | chr12 | 109555287 | ||||||
chr12:109555291 | T | G | 1 | a0004c0005t0022 | 2 | HG03195.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1737A>C | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 1737 | chr12 | 109555291 | ||||||
chr12:109555299 | T | G | 2 | a0002c0003t0016 a0002c0003t0047 |
5 | HG00140.hp1 HG01346.hp1 HG01358.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1729A>C | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 1729 | chr12 | 109555299 | ||||||
chr12:109555371 | C | T | 3 | a0003c0002t0013 a0003c0002t0050 a0003c0002t0052 |
7 | HG01243.hp1 HG01361.hp2 HG01516.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1657G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 1657 | chr12 | 109555371 | ||||||
chr12:109555449 | A | AT | 6 | a0001c0001t0010 a0001c0001t0014 a0002c0003t0034 others(3): Show |
16 | HG01106.hp1 HG01358.hp1 HG02040.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1578dupA | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 1578 | chr12 | 109555449 | ||||||
chr12:109555449 | AT | A | 28 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0033 others(25): Show |
129 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*1578delA | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 1578 | chr12 | 109555449 | ||||||
chr12:109555449 | ATT | A | 17 | a0001c0001t0020 a0001c0001t0091 a0002c0003t0005 others(14): Show |
45 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*1577_*1578delAA | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 1577 | chr12 | 109555449 | ||||||
chr12:109555449 | ATTT | A | 32 | a0001c0001t0031 a0002c0003t0003 a0002c0003t0007 others(29): Show |
85 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*1576_*1578delAAA | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 1576 | chr12 | 109555449 | ||||||
chr12:109555493 | C | T | 31 | a0002c0003t0003 a0002c0003t0007 a0002c0003t0011 others(28): Show |
81 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*1535G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 1535 | chr12 | 109555493 | ||||||
chr12:109555546 | G | A | 1 | a0001c0001t0092 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1482C>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 1482 | chr12 | 109555546 | ||||||
chr12:109555561 | G | A | 17 | a0002c0003t0005 a0002c0003t0036 a0002c0003t0037 others(14): Show |
48 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*1467C>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 1467 | chr12 | 109555561 | ||||||
chr12:109555594 | G | T | 1 | a0002c0003t0073 | 1 | HG00621.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1434C>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 1434 | chr12 | 109555594 | ||||||
chr12:109555619 | C | T | 7 | a0003c0002t0017 a0003c0002t0023 a0003c0002t0027 others(4): Show |
13 | HG01255.hp1 HG01257.hp1 HG01258.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1409G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 1409 | chr12 | 109555619 | ||||||
chr12:109555798 | C | A | 83 | a0002c0003t0003 a0002c0003t0005 a0002c0003t0007 others(80): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
3_prime_UTR_variant | MODIFIER | c.*1230G>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 1230 | chr12 | 109555798 | ||||||
chr12:109555940 | T | A | 1 | a0003c0002t0042 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1088A>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 1088 | chr12 | 109555940 | ||||||
chr12:109556023 | T | C | 2 | a0002c0003t0016 a0002c0003t0047 |
5 | HG00140.hp1 HG01346.hp1 HG01358.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1005A>G | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 1005 | chr12 | 109556023 | ||||||
chr12:109556137 | G | T | 33 | a0002c0003t0034 a0002c0003t0035 a0002c0003t0068 others(30): Show |
58 | HG00639.hp2 HG00642.hp2 HG01071.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*891C>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 891 | chr12 | 109556137 | ||||||
chr12:109556171 | C | G | 83 | a0002c0003t0003 a0002c0003t0005 a0002c0003t0007 others(80): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
3_prime_UTR_variant | MODIFIER | c.*857G>C | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 857 | chr12 | 109556171 | ||||||
chr12:109556207 | G | A | 1 | a0002c0010t0072 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*821C>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 821 | chr12 | 109556207 | ||||||
chr12:109556307 | A | C | 14 | a0002c0003t0005 a0002c0003t0038 a0003c0002t0005 others(11): Show |
45 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*721T>G | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 721 | chr12 | 109556307 | ||||||
chr12:109556310 | C | G | 1 | a0002c0010t0072 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*718G>C | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 718 | chr12 | 109556310 | ||||||
chr12:109556372 | G | T | 5 | a0003c0002t0008 a0003c0002t0021 a0003c0002t0060 others(2): Show |
16 | HG00639.hp2 HG00642.hp2 HG01099.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*656C>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 656 | chr12 | 109556372 | ||||||
chr12:109556403 | C | G | 33 | a0002c0003t0034 a0002c0003t0035 a0002c0003t0068 others(30): Show |
58 | HG00639.hp2 HG00642.hp2 HG01071.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*625G>C | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 625 | chr12 | 109556403 | ||||||
chr12:109556464 | C | G | 3 | a0003c0002t0009 a0003c0002t0043 a0003c0002t0044 |
9 | HG02109.hp1 HG02647.hp2 HG02897.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*564G>C | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 564 | chr12 | 109556464 | ||||||
chr12:109556640 | G | GCT | 5 | a0001c0001t0066 a0001c0001t0067 a0002c0003t0037 others(2): Show |
6 | HG02280.hp2 HG02886.hp2 HG03195.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*386_*387dupAG | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 387 | chr12 | 109556640 | ||||||
chr12:109556640 | G | GCTCTCTC others(1): Show |
5 | a0003c0002t0012 a0003c0002t0039 a0003c0002t0040 others(2): Show |
8 | HG01099.hp2 HG01978.hp1 HG01981.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*380_*387dupAGAGAG others(2): Show |
MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 387 | chr12 | 109556640 | ||||||
chr12:109556640 | GCT | G | 8 | a0001c0001t0033 a0001c0001t0097 a0002c0003t0032 others(5): Show |
12 | HG00741.hp2 HG01070.hp2 HG01071.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*386_*387delAG | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 386 | chr12 | 109556640 | ||||||
chr12:109556646 | T | A | 2 | a0002c0003t0034 a0002c0003t0098 |
3 | HG02559.hp2 HG02922.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*382A>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 382 | chr12 | 109556646 | ||||||
chr12:109556646 | T | TCACACA | 2 | a0002c0003t0035 a0002c0003t0099 |
3 | NA18946.hp1 NA18953.hp1 NA19083.hp1 |
3_prime_UTR_variant | MODIFIER | c.*381_*382insTGTGTG | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 381 | chr12 | 109556646 | ||||||
chr12:109556646 | T | TCACACAC others(7): Show |
1 | a0002c0003t0100 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*381_*382insTGTGTG others(8): Show |
MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 381 | chr12 | 109556646 | ||||||
chr12:109556646 | TCTCA | T | 12 | a0002c0003t0011 a0002c0003t0019 a0002c0003t0065 others(9): Show |
30 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*378_*381delTGAG | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 378 | chr12 | 109556646 | ||||||
chr12:109556646 | TCTCACA | T | 6 | a0002c0003t0059 a0003c0002t0017 a0003c0002t0027 others(3): Show |
11 | HG01071.hp1 HG01106.hp2 HG01346.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*376_*381delTGTGAG | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 376 | chr12 | 109556646 | ||||||
chr12:109556646 | TCTCACAC others(1): Show |
T | 11 | a0002c0003t0054 a0002c0004t0025 a0002c0004t0026 others(8): Show |
19 | HG01081.hp2 HG01243.hp1 HG01257.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*374_*381delTGTGTG others(2): Show |
MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 374 | chr12 | 109556646 | ||||||
chr12:109556646 | TCTCACAC others(3): Show |
T | 1 | a0003c0002t0049 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*372_*381delTGTGTG others(4): Show |
MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 372 | chr12 | 109556646 | ||||||
chr12:109556646 | TCTCACAC others(5): Show |
T | 1 | a0003c0002t0048 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*370_*381delTGTGTG others(6): Show |
MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 370 | chr12 | 109556646 | ||||||
chr12:109556648 | T | A | 14 | a0002c0003t0034 a0002c0003t0035 a0002c0003t0068 others(11): Show |
16 | HG02451.hp1 HG02559.hp2 HG02886.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*380A>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 380 | chr12 | 109556648 | ||||||
chr12:109556648 | T | TCA | 11 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(8): Show |
36 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*378_*379dupTG | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 379 | chr12 | 109556648 | ||||||
chr12:109556648 | T | TCACA | 7 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(4): Show |
20 | HG02015.hp2 HG02071.hp1 HG02080.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*376_*379dupTGTG | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 379 | chr12 | 109556648 | ||||||
chr12:109556648 | T | TCACACA | 4 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 others(1): Show |
4 | HG01934.hp2 NA19058.hp2 NA19077.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*374_*379dupTGTGTG | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 379 | chr12 | 109556648 | ||||||
chr12:109556648 | T | TCTCTCTC others(11): Show |
1 | a0003c0002t0009 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*379_*380insTGTGTG others(12): Show |
MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 379 | chr12 | 109556648 | ||||||
chr12:109556648 | T | TCTCTCTC others(3): Show |
1 | a0003c0002t0005 | 2 | HG01123.hp2 HG01928.hp2 |
3_prime_UTR_variant | MODIFIER | c.*379_*380insTGAGAG others(4): Show |
MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 379 | chr12 | 109556648 | ||||||
chr12:109556648 | T | TCTCTCTC others(5): Show |
1 | a0003c0002t0005 | 14 | HG00099.hp1 HG00423.hp1 HG02040.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*379_*380insTGTGAG others(6): Show |
MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 379 | chr12 | 109556648 | ||||||
chr12:109556648 | T | TCTCTCTC others(7): Show |
3 | a0002c0003t0005 a0003c0002t0005 a0003c0002t0044 |
4 | HG02897.hp1 HG03471.hp1 NA18980.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*379_*380insTGTGTG others(8): Show |
MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 379 | chr12 | 109556648 | ||||||
chr12:109556648 | T | TCTCTCTC others(9): Show |
1 | a0003c0002t0015 | 4 | HG01884.hp1 HG02896.hp2 HG03098.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*379_*380insTGTGTG others(10): Show |
MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 379 | chr12 | 109556648 | ||||||
chr12:109556648 | T | TCTCTCTC others(11): Show |
2 | a0003c0002t0009 a0003c0002t0045 |
3 | HG02970.hp2 HG03139.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*379_*380insTGTGTG others(12): Show |
MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 379 | chr12 | 109556648 | ||||||
chr12:109556648 | T | TCTCTCTC others(13): Show |
1 | a0003c0002t0009 | 3 | HG02109.hp1 HG02976.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*379_*380insTGTGTG others(14): Show |
MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 379 | chr12 | 109556648 | ||||||
chr12:109556648 | T | TCTCTCTC others(33): Show |
1 | a0003c0002t0043 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*379_*380insTGTGTG others(34): Show |
MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 379 | chr12 | 109556648 | ||||||
chr12:109556648 | T | TCTCTCTC others(37): Show |
1 | a0003c0002t0005 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*379_*380insTGTGTG others(38): Show |
MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 379 | chr12 | 109556648 | ||||||
chr12:109556648 | T | TCTCTCTC others(11): Show |
1 | a0003c0002t0009 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*379_*380insTGTGTG others(12): Show |
MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 379 | chr12 | 109556648 | ||||||
chr12:109556648 | TCA | T | 7 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0091 others(4): Show |
15 | HG00621.hp2 HG01168.hp2 HG01169.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*378_*379delTG | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 378 | chr12 | 109556648 | ||||||
chr12:109556648 | TCACA | T | 8 | a0001c0001t0001 a0001c0001t0031 a0002c0003t0003 others(5): Show |
25 | HG00140.hp2 HG00323.hp1 HG00597.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*376_*379delTGTG | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 376 | chr12 | 109556648 | ||||||
chr12:109556648 | TCACACA | T | 5 | a0001c0001t0001 a0001c0001t0031 a0002c0003t0003 others(2): Show |
9 | HG01255.hp2 HG01884.hp2 HG02056.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*374_*379delTGTGTG | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 374 | chr12 | 109556648 | ||||||
chr12:109556648 | TCACACAC others(1): Show |
T | 6 | a0001c0001t0006 a0002c0003t0003 a0002c0003t0007 others(3): Show |
16 | HG00609.hp1 HG01934.hp1 HG01981.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*372_*379delTGTGTG others(2): Show |
MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 372 | chr12 | 109556648 | ||||||
chr12:109556648 | TCACACAC others(3): Show |
T | 3 | a0001c0001t0004 a0002c0003t0016 a0002c0003t0047 |
6 | HG00140.hp1 HG01346.hp1 HG01358.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*370_*379delTGTGTG others(4): Show |
MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 370 | chr12 | 109556648 | ||||||
chr12:109556650 | A | T | 9 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(6): Show |
13 | HG00741.hp1 HG01261.hp2 HG02280.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*378T>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 378 | chr12 | 109556650 | ||||||
chr12:109556652 | A | T | 4 | a0002c0003t0036 a0002c0003t0037 a0002c0003t0038 others(1): Show |
5 | HG02280.hp2 HG03195.hp2 NA19043.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*376T>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 376 | chr12 | 109556652 | ||||||
chr12:109556654 | A | T | 3 | a0002c0003t0036 a0002c0003t0056 a0004c0005t0022 |
4 | HG03195.hp2 HG03209.hp1 NA19043.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*374T>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 374 | chr12 | 109556654 | ||||||
chr12:109556660 | A | T | 2 | a0002c0003t0016 a0002c0003t0047 |
5 | HG00140.hp1 HG01346.hp1 HG01358.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*368T>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 368 | chr12 | 109556660 | ||||||
chr12:109556662 | A | T | 2 | a0002c0003t0016 a0002c0003t0047 |
5 | HG00140.hp1 HG01346.hp1 HG01358.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*366T>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 366 | chr12 | 109556662 | ||||||
chr12:109556805 | C | T | 1 | a0001c0001t0046 | 1 | NA18970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*223G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 223 | chr12 | 109556805 | ||||||
chr12:109556836 | A | G | 17 | a0002c0003t0005 a0002c0003t0036 a0002c0003t0037 others(14): Show |
48 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*192T>C | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 9/9 | 192 | chr12 | 109556836 | ||||||
chr12:109573489 | C | A | 1 | a0001c0001t0101 | 1 | HG03927.hp1 | 5_prime_UTR_variant | MODIFIER | c.-9G>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 1/9 | 9 | chr12 | 109573489 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:109557228 | G | A | 1 | a0001c0001t0004g0170 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.645-92C>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 8/8 | chr12 | 109557228 | |||||||
chr12:109557239 | C | T | 1 | a0001c0001t0101g0221 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.645-103G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 8/8 | chr12 | 109557239 | |||||||
chr12:109557265 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.645-129C>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 8/8 | chr12 | 109557265 | |||||||
chr12:109557281 | A | C | 3 | a0001c0001t0001g0011 a0001c0001t0004g0213 a0001c0001t0020g0037 |
8 | NA18945.hp1 NA18993.hp1 NA18998.hp1 others(5): Show |
intron_variant | MODIFIER | c.645-145T>G | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 8/8 | chr12 | 109557281 | |||||||
chr12:109557292 | A | G | 131 | a0002c0003t0003g0005 a0002c0003t0003g0012 a0002c0003t0003g0030 others(128): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.645-156T>C | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 8/8 | chr12 | 109557292 | |||||||
chr12:109557352 | C | T | 2 | a0001c0001t0002g0193 a0001c0001t0014g0192 |
2 | HG02056.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.645-216G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 8/8 | chr12 | 109557352 | |||||||
chr12:109557383 | C | T | 24 | a0002c0003t0003g0005 a0002c0003t0003g0012 a0002c0003t0003g0030 others(21): Show |
47 | HG00140.hp2 HG00323.hp1 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.645-247G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 8/8 | chr12 | 109557383 | |||||||
chr12:109557569 | G | A | 1 | a0002c0010t0072g0096 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.645-433C>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 8/8 | chr12 | 109557569 | |||||||
chr12:109557791 | C | T | 1 | a0001c0001t0004g0163 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.645-655G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 8/8 | chr12 | 109557791 | |||||||
chr12:109557845 | C | T | 5 | a0002c0003t0056g0098 a0002c0003t0074g0122 a0002c0003t0077g0121 others(2): Show |
5 | HG02257.hp2 HG02280.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.645-709G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 8/8 | chr12 | 109557845 | |||||||
chr12:109557846 | G | A | 2 | a0001c0001t0006g0201 a0001c0001t0006g0208 |
2 | NA18977.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.645-710C>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 8/8 | chr12 | 109557846 | |||||||
chr12:109557846 | GCCT | G | 11 | a0002c0003t0034g0031 a0002c0003t0035g0032 a0002c0003t0068g0138 others(8): Show |
13 | HG02451.hp1 HG02559.hp2 HG02922.hp1 others(10): Show |
intron_variant | MODIFIER | c.645-713_645-711del others(3): Show |
MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 8/8 | chr12 | 109557846 | |||||||
chr12:109557954 | C | T | 1 | a0001c0001t0006g0191 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.645-818G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 8/8 | chr12 | 109557954 | |||||||
chr12:109557958 | G | A | 2 | a0002c0003t0016g0013 a0002c0003t0047g0218 |
5 | HG00140.hp1 HG01346.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.645-822C>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 8/8 | chr12 | 109557958 | |||||||
chr12:109558052 | C | T | 2 | a0002c0003t0016g0013 a0002c0003t0047g0218 |
5 | HG00140.hp1 HG01346.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.645-916G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 8/8 | chr12 | 109558052 | |||||||
chr12:109558171 | T | C | 26 | a0002c0003t0005g0142 a0002c0003t0038g0103 a0003c0002t0005g0004 others(23): Show |
45 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(42): Show |
intron_variant | MODIFIER | c.644+925A>G | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 8/8 | chr12 | 109558171 | |||||||
chr12:109558176 | C | T | 26 | a0002c0003t0005g0142 a0002c0003t0038g0103 a0003c0002t0005g0004 others(23): Show |
45 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(42): Show |
intron_variant | MODIFIER | c.644+920G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 8/8 | chr12 | 109558176 | |||||||
chr12:109558229 | C | T | 1 | a0002c0010t0072g0096 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.644+867G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 8/8 | chr12 | 109558229 | |||||||
chr12:109558269 | T | C | 29 | a0002c0003t0005g0142 a0002c0003t0038g0103 a0002c0004t0025g0095 others(26): Show |
48 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(45): Show |
intron_variant | MODIFIER | c.644+827A>G | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 8/8 | chr12 | 109558269 | |||||||
chr12:109558312 | C | A | 26 | a0002c0003t0005g0142 a0002c0003t0038g0103 a0003c0002t0005g0004 others(23): Show |
45 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(42): Show |
intron_variant | MODIFIER | c.644+784G>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 8/8 | chr12 | 109558312 | |||||||
chr12:109558322 | G | A | 1 | a0004c0005t0022g0028 | 2 | HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.644+774C>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 8/8 | chr12 | 109558322 | |||||||
chr12:109558446 | G | A | 1 | a0001c0001t0001g0034 | 2 | NA18941.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.644+650C>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 8/8 | chr12 | 109558446 | |||||||
chr12:109558505 | G | C | 3 | a0003c0002t0024g0061 a0003c0002t0048g0059 a0003c0002t0053g0060 |
3 | HG02622.hp1 HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.644+591C>G | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 8/8 | chr12 | 109558505 | |||||||
chr12:109558538 | C | A | 131 | a0002c0003t0003g0005 a0002c0003t0003g0012 a0002c0003t0003g0030 others(128): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.644+558G>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 8/8 | chr12 | 109558538 | |||||||
chr12:109558632 | C | T | 3 | a0002c0004t0025g0095 a0002c0004t0026g0029 a0002c0004t0055g0115 |
4 | HG02109.hp2 HG02717.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.644+464G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 8/8 | chr12 | 109558632 | |||||||
chr12:109558653 | G | A | 11 | a0002c0003t0034g0031 a0002c0003t0035g0032 a0002c0003t0068g0138 others(8): Show |
13 | HG02451.hp1 HG02559.hp2 HG02922.hp1 others(10): Show |
intron_variant | MODIFIER | c.644+443C>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 8/8 | chr12 | 109558653 | |||||||
chr12:109558695 | C | T | 1 | a0002c0003t0019g0128 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.644+401G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 8/8 | chr12 | 109558695 | |||||||
chr12:109558702 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.644+394C>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 8/8 | chr12 | 109558702 | |||||||
chr12:109558824 | A | G | 1 | a0003c0002t0024g0056 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.644+272T>C | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 8/8 | chr12 | 109558824 | |||||||
chr12:109558883 | C | T | 10 | a0003c0002t0009g0016 a0003c0002t0009g0026 a0003c0002t0009g0084 others(7): Show |
15 | HG01884.hp1 HG02109.hp1 HG02647.hp2 others(12): Show |
intron_variant | MODIFIER | c.644+213G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 8/8 | chr12 | 109558883 | |||||||
chr12:109558884 | G | A | 53 | a0001c0001t0031g0211 a0002c0003t0003g0005 a0002c0003t0003g0012 others(50): Show |
81 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.644+212C>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 8/8 | chr12 | 109558884 | |||||||
chr12:109558992 | C | T | 1 | a0001c0001t0002g0212 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.644+104G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 8/8 | chr12 | 109558992 | |||||||
chr12:109559020 | G | GACCGCTG others(1): Show |
12 | a0002c0003t0038g0103 a0003c0002t0005g0004 a0003c0002t0005g0047 others(9): Show |
25 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.644+68_644+75dupGC others(6): Show |
MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 8/8 | chr12 | 109559020 | |||||||
chr12:109559024 | G | A | 1 | a0002c0003t0037g0149 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.644+72C>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 8/8 | chr12 | 109559024 | |||||||
chr12:109559277 | C | T | 1 | a0006c0007t0051g0040 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.585-122G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 7/8 | chr12 | 109559277 | |||||||
chr12:109559282 | G | A | 1 | a0002c0003t0005g0142 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.585-127C>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 7/8 | chr12 | 109559282 | |||||||
chr12:109559329 | C | T | 25 | a0002c0003t0005g0142 a0002c0004t0018g0116 a0003c0002t0005g0004 others(22): Show |
44 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(41): Show |
intron_variant | MODIFIER | c.585-174G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 7/8 | chr12 | 109559329 | |||||||
chr12:109559358 | A | G | 3 | a0002c0003t0036g0219 a0002c0003t0037g0149 a0003c0002t0042g0065 |
3 | HG02280.hp2 HG02886.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.585-203T>C | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 7/8 | chr12 | 109559358 | |||||||
chr12:109559359 | C | T | 49 | a0002c0003t0003g0005 a0002c0003t0003g0030 a0002c0003t0003g0093 others(46): Show |
72 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.585-204G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 7/8 | chr12 | 109559359 | |||||||
chr12:109559417 | C | T | 2 | a0002c0003t0016g0013 a0002c0003t0047g0218 |
5 | HG00140.hp1 HG01346.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.585-262G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 7/8 | chr12 | 109559417 | |||||||
chr12:109559840 | G | C | 130 | a0002c0003t0003g0005 a0002c0003t0003g0012 a0002c0003t0003g0030 others(127): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.585-685C>G | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 7/8 | chr12 | 109559840 | |||||||
chr12:109559894 | G | A | 1 | a0005c0011t0014g0157 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.585-739C>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 7/8 | chr12 | 109559894 | |||||||
chr12:109559933 | GGT | G | 3 | a0003c0002t0024g0061 a0003c0002t0048g0059 a0003c0002t0053g0060 |
3 | HG02622.hp1 HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.585-780_585-779del others(2): Show |
MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 7/8 | chr12 | 109559933 | |||||||
chr12:109559939 | T | C | 1 | a0003c0002t0017g0078 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.585-784A>G | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 7/8 | chr12 | 109559939 | |||||||
chr12:109559985 | G | A | 1 | a0003c0002t0005g0041 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.585-830C>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 7/8 | chr12 | 109559985 | |||||||
chr12:109560023 | G | A | 2 | a0001c0001t0002g0216 a0001c0001t0010g0185 |
2 | HG01257.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.585-868C>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 7/8 | chr12 | 109560023 | |||||||
chr12:109560024 | C | T | 13 | a0003c0002t0013g0014 a0003c0002t0013g0044 a0003c0002t0013g0085 others(10): Show |
15 | HG01071.hp1 HG01106.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.585-869G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 7/8 | chr12 | 109560024 | |||||||
chr12:109560042 | C | T | 54 | a0002c0003t0003g0005 a0002c0003t0003g0012 a0002c0003t0003g0030 others(51): Show |
82 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.585-887G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 7/8 | chr12 | 109560042 | |||||||
chr12:109560168 | G | T | 1 | a0001c0001t0002g0186 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.584+872C>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 7/8 | chr12 | 109560168 | |||||||
chr12:109560173 | G | A | 47 | a0002c0003t0034g0031 a0002c0003t0035g0032 a0002c0003t0068g0138 others(44): Show |
58 | HG00639.hp2 HG00642.hp2 HG01071.hp1 others(55): Show |
intron_variant | MODIFIER | c.584+867C>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 7/8 | chr12 | 109560173 | |||||||
chr12:109560186 | A | G | 1 | a0002c0003t0005g0142 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.584+854T>C | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 7/8 | chr12 | 109560186 | |||||||
chr12:109560292 | A | G | 131 | a0002c0003t0003g0005 a0002c0003t0003g0012 a0002c0003t0003g0030 others(128): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.584+748T>C | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 7/8 | chr12 | 109560292 | |||||||
chr12:109560320 | C | T | 27 | a0002c0003t0005g0142 a0002c0003t0036g0219 a0002c0003t0037g0149 others(24): Show |
46 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(43): Show |
intron_variant | MODIFIER | c.584+720G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 7/8 | chr12 | 109560320 | |||||||
chr12:109560328 | C | T | 2 | a0002c0003t0036g0219 a0002c0003t0037g0149 |
2 | HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.584+712G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 7/8 | chr12 | 109560328 | |||||||
chr12:109560440 | T | C | 5 | a0003c0002t0013g0014 a0003c0002t0013g0044 a0003c0002t0013g0085 others(2): Show |
7 | HG01243.hp1 HG01361.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.584+600A>G | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 7/8 | chr12 | 109560440 | |||||||
chr12:109560468 | G | T | 1 | a0002c0003t0019g0104 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.584+572C>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 7/8 | chr12 | 109560468 | |||||||
chr12:109560479 | G | A | 27 | a0002c0003t0005g0142 a0002c0003t0036g0219 a0002c0003t0037g0149 others(24): Show |
46 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(43): Show |
intron_variant | MODIFIER | c.584+561C>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 7/8 | chr12 | 109560479 | |||||||
chr12:109560719 | G | A | 1 | a0006c0007t0051g0040 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.584+321C>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 7/8 | chr12 | 109560719 | |||||||
chr12:109560786 | T | C | 133 | a0001c0001t0031g0176 a0001c0001t0031g0211 a0002c0003t0003g0005 others(130): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.584+254A>G | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 7/8 | chr12 | 109560786 | |||||||
chr12:109560789 | C | T | 2 | a0002c0003t0016g0013 a0002c0003t0047g0218 |
5 | HG00140.hp1 HG01346.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.584+251G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 7/8 | chr12 | 109560789 | |||||||
chr12:109560982 | C | G | 1 | a0001c0001t0004g0163 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.584+58G>C | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 7/8 | chr12 | 109560982 | |||||||
chr12:109561016 | T | C | 10 | a0003c0002t0008g0008 a0003c0002t0008g0025 a0003c0002t0008g0062 others(7): Show |
16 | HG00639.hp2 HG00642.hp2 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.584+24A>G | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 7/8 | chr12 | 109561016 | |||||||
chr12:109561200 | G | A | 53 | a0002c0003t0003g0005 a0002c0003t0003g0012 a0002c0003t0003g0030 others(50): Show |
81 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.520-96C>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 6/8 | chr12 | 109561200 | |||||||
chr12:109561231 | C | T | 1 | a0002c0003t0036g0219 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.520-127G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 6/8 | chr12 | 109561231 | |||||||
chr12:109561232 | G | A | 54 | a0002c0003t0003g0005 a0002c0003t0003g0012 a0002c0003t0003g0030 others(51): Show |
82 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.520-128C>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 6/8 | chr12 | 109561232 | |||||||
chr12:109561243 | C | T | 13 | a0003c0002t0013g0014 a0003c0002t0013g0044 a0003c0002t0013g0085 others(10): Show |
15 | HG01071.hp1 HG01106.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.520-139G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 6/8 | chr12 | 109561243 | |||||||
chr12:109561263 | G | A | 53 | a0002c0003t0003g0005 a0002c0003t0003g0012 a0002c0003t0003g0030 others(50): Show |
81 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.519+157C>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 6/8 | chr12 | 109561263 | |||||||
chr12:109561322 | G | A | 3 | a0002c0003t0003g0093 a0002c0003t0003g0111 a0002c0003t0007g0092 |
3 | HG01255.hp2 HG01934.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.519+98C>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 6/8 | chr12 | 109561322 | |||||||
chr12:109561590 | C | T | 1 | a0001c0001t0002g0190 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.422-73G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 5/8 | chr12 | 109561590 | |||||||
chr12:109561718 | G | T | 5 | a0003c0002t0013g0014 a0003c0002t0013g0044 a0003c0002t0013g0085 others(2): Show |
7 | HG01243.hp1 HG01361.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.421+62C>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 5/8 | chr12 | 109561718 | |||||||
chr12:109562059 | T | C | 24 | a0003c0002t0008g0008 a0003c0002t0008g0025 a0003c0002t0008g0062 others(21): Show |
32 | HG00639.hp2 HG00642.hp2 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.349-207A>G | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 4/8 | chr12 | 109562059 | |||||||
chr12:109562095 | A | C | 1 | a0003c0002t0017g0069 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.349-243T>G | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 4/8 | chr12 | 109562095 | |||||||
chr12:109562186 | A | G | 7 | a0001c0006t0001g0151 a0001c0006t0004g0150 a0003c0002t0008g0008 others(4): Show |
12 | HG00639.hp2 HG00642.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.349-334T>C | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 4/8 | chr12 | 109562186 | |||||||
chr12:109562226 | C | T | 1 | a0001c0001t0031g0176 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.349-374G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 4/8 | chr12 | 109562226 | |||||||
chr12:109562260 | A | T | 1 | a0001c0001t0002g0189 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.349-408T>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 4/8 | chr12 | 109562260 | |||||||
chr12:109562269 | C | G | 2 | a0002c0003t0016g0013 a0002c0003t0047g0218 |
5 | HG00140.hp1 HG01346.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.349-417G>C | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 4/8 | chr12 | 109562269 | |||||||
chr12:109562388 | C | T | 131 | a0002c0003t0003g0005 a0002c0003t0003g0012 a0002c0003t0003g0030 others(128): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.349-536G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 4/8 | chr12 | 109562388 | |||||||
chr12:109562470 | G | A | 1 | a0003c0008t0012g0049 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.349-618C>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 4/8 | chr12 | 109562470 | |||||||
chr12:109562519 | G | T | 1 | a0003c0002t0005g0077 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.349-667C>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 4/8 | chr12 | 109562519 | |||||||
chr12:109562589 | C | T | 57 | a0001c0001t0002g0189 a0002c0003t0003g0005 a0002c0003t0003g0012 others(54): Show |
85 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.349-737G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 4/8 | chr12 | 109562589 | |||||||
chr12:109562654 | T | A | 1 | a0002c0004t0011g0120 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.349-802A>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 4/8 | chr12 | 109562654 | |||||||
chr12:109562877 | A | G | 5 | a0002c0003t0056g0098 a0002c0003t0074g0122 a0002c0003t0077g0121 others(2): Show |
5 | HG02257.hp2 HG02280.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.349-1025T>C | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 4/8 | chr12 | 109562877 | |||||||
chr12:109562943 | G | A | 53 | a0002c0003t0003g0005 a0002c0003t0003g0012 a0002c0003t0003g0030 others(50): Show |
81 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.349-1091C>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 4/8 | chr12 | 109562943 | |||||||
chr12:109562989 | C | T | 2 | a0002c0003t0036g0219 a0002c0003t0037g0149 |
2 | HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.349-1137G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 4/8 | chr12 | 109562989 | |||||||
chr12:109563217 | A | G | 1 | a0002c0003t0077g0121 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.349-1365T>C | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 4/8 | chr12 | 109563217 | |||||||
chr12:109563250 | C | T | 1 | a0002c0003t0011g0094 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.349-1398G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 4/8 | chr12 | 109563250 | |||||||
chr12:109563390 | A | G | 131 | a0002c0003t0003g0005 a0002c0003t0003g0012 a0002c0003t0003g0030 others(128): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.349-1538T>C | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 4/8 | chr12 | 109563390 | |||||||
chr12:109563409 | C | T | 1 | a0002c0003t0007g0102 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.349-1557G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 4/8 | chr12 | 109563409 | |||||||
chr12:109563410 | G | A | 24 | a0003c0002t0008g0008 a0003c0002t0008g0025 a0003c0002t0008g0062 others(21): Show |
32 | HG00639.hp2 HG00642.hp2 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.349-1558C>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 4/8 | chr12 | 109563410 | |||||||
chr12:109563430 | C | T | 1 | a0002c0003t0003g0101 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.349-1578G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 4/8 | chr12 | 109563430 | |||||||
chr12:109563478 | C | A | 11 | a0003c0002t0005g0004 a0003c0002t0005g0047 a0003c0002t0005g0077 others(8): Show |
24 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.349-1626G>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 4/8 | chr12 | 109563478 | |||||||
chr12:109563582 | C | T | 25 | a0002c0003t0005g0142 a0003c0002t0005g0004 a0003c0002t0005g0041 others(22): Show |
44 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(41): Show |
intron_variant | MODIFIER | c.348+1537G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 4/8 | chr12 | 109563582 | |||||||
chr12:109563784 | A | C | 218 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(215): Show |
362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.348+1335T>G | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 4/8 | chr12 | 109563784 | |||||||
chr12:109563811 | G | A | 53 | a0002c0003t0003g0005 a0002c0003t0003g0012 a0002c0003t0003g0030 others(50): Show |
81 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.348+1308C>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 4/8 | chr12 | 109563811 | |||||||
chr12:109563956 | T | C | 2 | a0002c0003t0036g0219 a0002c0003t0037g0149 |
2 | HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.348+1163A>G | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 4/8 | chr12 | 109563956 | |||||||
chr12:109564064 | C | T | 3 | a0001c0001t0002g0186 a0001c0001t0002g0188 a0001c0001t0046g0187 |
3 | HG00408.hp2 NA18970.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.348+1055G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 4/8 | chr12 | 109564064 | |||||||
chr12:109564074 | G | A | 1 | a0002c0010t0072g0096 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.348+1045C>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 4/8 | chr12 | 109564074 | |||||||
chr12:109564077 | C | T | 2 | a0002c0003t0016g0013 a0002c0003t0047g0218 |
5 | HG00140.hp1 HG01346.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.348+1042G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 4/8 | chr12 | 109564077 | |||||||
chr12:109564153 | C | T | 1 | a0002c0003t0032g0127 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.348+966G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 4/8 | chr12 | 109564153 | |||||||
chr12:109564249 | G | A | 1 | a0001c0001t0006g0208 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.348+870C>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 4/8 | chr12 | 109564249 | |||||||
chr12:109564328 | C | T | 54 | a0002c0003t0003g0005 a0002c0003t0003g0012 a0002c0003t0003g0030 others(51): Show |
82 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.348+791G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 4/8 | chr12 | 109564328 | |||||||
chr12:109564379 | G | GT | 28 | a0001c0001t0001g0184 a0001c0001t0004g0183 a0001c0001t0010g0159 others(25): Show |
39 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.348+739dupA | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 4/8 | chr12 | 109564379 | |||||||
chr12:109564379 | GT | G | 18 | a0001c0001t0001g0162 a0001c0001t0001g0172 a0001c0001t0002g0158 others(15): Show |
18 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.348+739delA | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 4/8 | chr12 | 109564379 | |||||||
chr12:109564557 | A | AT | 7 | a0002c0003t0075g0100 a0003c0002t0013g0014 a0003c0002t0013g0044 others(4): Show |
9 | HG01243.hp1 HG01361.hp2 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.348+561dupA | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 4/8 | chr12 | 109564557 | |||||||
chr12:109564557 | A | T | 26 | a0002c0003t0005g0142 a0002c0003t0016g0013 a0002c0003t0047g0218 others(23): Show |
47 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(44): Show |
intron_variant | MODIFIER | c.348+562T>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 4/8 | chr12 | 109564557 | |||||||
chr12:109564558 | T | TTA | 14 | a0002c0003t0005g0142 a0003c0002t0005g0041 a0003c0002t0005g0048 others(11): Show |
19 | HG01884.hp1 HG02647.hp2 HG02896.hp2 others(16): Show |
intron_variant | MODIFIER | c.348+560_348+561ins others(2): Show |
MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 4/8 | chr12 | 109564558 | |||||||
chr12:109564559 | T | TA | 12 | a0002c0003t0016g0013 a0002c0003t0047g0218 a0003c0002t0005g0004 others(9): Show |
28 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(25): Show |
intron_variant | MODIFIER | c.348+559_348+560ins others(1): Show |
MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 4/8 | chr12 | 109564559 | |||||||
chr12:109564583 | G | C | 2 | a0002c0003t0007g0114 a0002c0003t0030g0113 |
2 | HG00140.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.348+536C>G | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 4/8 | chr12 | 109564583 | |||||||
chr12:109564628 | G | A | 1 | a0003c0002t0005g0048 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.348+491C>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 4/8 | chr12 | 109564628 | |||||||
chr12:109564692 | G | A | 1 | a0003c0002t0042g0065 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.348+427C>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 4/8 | chr12 | 109564692 | |||||||
chr12:109564919 | C | T | 1 | a0002c0003t0094g0143 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.348+200G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 4/8 | chr12 | 109564919 | |||||||
chr12:109564942 | G | A | 24 | a0002c0003t0005g0142 a0003c0002t0005g0004 a0003c0002t0005g0041 others(21): Show |
42 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(39): Show |
intron_variant | MODIFIER | c.348+177C>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 4/8 | chr12 | 109564942 | |||||||
chr12:109564972 | C | T | 92 | a0001c0001t0031g0176 a0001c0001t0031g0211 a0002c0003t0003g0005 others(89): Show |
129 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.348+147G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 4/8 | chr12 | 109564972 | |||||||
chr12:109564989 | G | A | 1 | a0003c0002t0017g0078 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.348+130C>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 4/8 | chr12 | 109564989 | |||||||
chr12:109564995 | G | A | 1 | a0001c0001t0002g0179 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.348+124C>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 4/8 | chr12 | 109564995 | |||||||
chr12:109565014 | A | G | 133 | a0001c0001t0031g0176 a0001c0001t0031g0211 a0002c0003t0003g0005 others(130): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.348+105T>C | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 4/8 | chr12 | 109565014 | |||||||
chr12:109565194 | A | G | 1 | a0001c0001t0006g0182 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.291-18T>C | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 3/8 | chr12 | 109565194 | |||||||
chr12:109565374 | C | T | 1 | a0003c0002t0008g0025 | 2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.291-198G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 3/8 | chr12 | 109565374 | |||||||
chr12:109565375 | G | A | 1 | a0006c0007t0051g0040 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.291-199C>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 3/8 | chr12 | 109565375 | |||||||
chr12:109565438 | G | A | 1 | a0004c0005t0022g0028 | 2 | HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.291-262C>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 3/8 | chr12 | 109565438 | |||||||
chr12:109565594 | G | A | 3 | a0002c0003t0016g0013 a0002c0003t0047g0218 a0003c0002t0042g0065 |
6 | HG00140.hp1 HG01346.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.291-418C>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 3/8 | chr12 | 109565594 | |||||||
chr12:109565697 | T | G | 7 | a0002c0004t0011g0019 a0002c0004t0011g0120 a0002c0004t0018g0018 others(4): Show |
11 | HG02258.hp2 HG02572.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.291-521A>C | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 3/8 | chr12 | 109565697 | |||||||
chr12:109565867 | G | A | 68 | a0002c0003t0003g0005 a0002c0003t0003g0012 a0002c0003t0003g0030 others(65): Show |
98 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.291-691C>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 3/8 | chr12 | 109565867 | |||||||
chr12:109565886 | G | A | 1 | a0003c0002t0049g0066 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.291-710C>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 3/8 | chr12 | 109565886 | |||||||
chr12:109566023 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.291-847C>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 3/8 | chr12 | 109566023 | |||||||
chr12:109566220 | C | T | 11 | a0002c0004t0011g0019 a0002c0004t0011g0120 a0002c0004t0018g0018 others(8): Show |
16 | HG02109.hp2 HG02258.hp2 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.291-1044G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 3/8 | chr12 | 109566220 | |||||||
chr12:109566235 | C | T | 62 | a0001c0001t0031g0176 a0001c0001t0031g0211 a0003c0002t0005g0004 others(59): Show |
90 | HG00099.hp1 HG00423.hp1 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.291-1059G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 3/8 | chr12 | 109566235 | |||||||
chr12:109566263 | G | T | 24 | a0003c0002t0008g0008 a0003c0002t0008g0025 a0003c0002t0008g0062 others(21): Show |
32 | HG00639.hp2 HG00642.hp2 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.291-1087C>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 3/8 | chr12 | 109566263 | |||||||
chr12:109566287 | A | T | 1 | a0003c0002t0013g0085 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.291-1111T>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 3/8 | chr12 | 109566287 | |||||||
chr12:109566499 | C | T | 1 | a0002c0003t0003g0099 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.291-1323G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 3/8 | chr12 | 109566499 | |||||||
chr12:109566643 | C | T | 1 | a0004c0005t0022g0028 | 2 | HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.291-1467G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 3/8 | chr12 | 109566643 | |||||||
chr12:109566736 | G | A | 1 | a0001c0001t0006g0208 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.291-1560C>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 3/8 | chr12 | 109566736 | |||||||
chr12:109566758 | A | G | 1 | a0001c0001t0006g0177 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.291-1582T>C | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 3/8 | chr12 | 109566758 | |||||||
chr12:109566883 | T | G | 1 | a0002c0003t0003g0093 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.291-1707A>C | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 3/8 | chr12 | 109566883 | |||||||
chr12:109566929 | C | G | 4 | a0003c0002t0015g0015 a0003c0002t0015g0052 a0003c0002t0041g0050 others(1): Show |
6 | HG01884.hp1 HG02896.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.291-1753G>C | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 3/8 | chr12 | 109566929 | |||||||
chr12:109566934 | A | G | 11 | a0002c0003t0034g0031 a0002c0003t0035g0032 a0002c0003t0068g0138 others(8): Show |
13 | HG02451.hp1 HG02559.hp2 HG02922.hp1 others(10): Show |
intron_variant | MODIFIER | c.291-1758T>C | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 3/8 | chr12 | 109566934 | |||||||
chr12:109566999 | C | T | 37 | a0002c0003t0003g0005 a0002c0003t0003g0012 a0002c0003t0003g0030 others(34): Show |
60 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.290+1771G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 3/8 | chr12 | 109566999 | |||||||
chr12:109567007 | T | C | 1 | a0002c0003t0037g0149 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.290+1763A>G | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 3/8 | chr12 | 109567007 | |||||||
chr12:109567016 | C | T | 2 | a0001c0001t0031g0176 a0001c0001t0031g0211 |
2 | HG01884.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.290+1754G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 3/8 | chr12 | 109567016 | |||||||
chr12:109567084 | C | T | 11 | a0002c0003t0034g0031 a0002c0003t0035g0032 a0002c0003t0068g0138 others(8): Show |
13 | HG02451.hp1 HG02559.hp2 HG02922.hp1 others(10): Show |
intron_variant | MODIFIER | c.290+1686G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 3/8 | chr12 | 109567084 | |||||||
chr12:109567114 | G | A | 2 | a0001c0001t0031g0176 a0001c0001t0031g0211 |
2 | HG01884.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.290+1656C>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 3/8 | chr12 | 109567114 | |||||||
chr12:109567155 | C | T | 133 | a0001c0001t0031g0176 a0001c0001t0031g0211 a0002c0003t0003g0005 others(130): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.290+1615G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 3/8 | chr12 | 109567155 | |||||||
chr12:109567166 | G | A | 3 | a0003c0002t0017g0027 a0003c0002t0029g0080 a0003c0002t0063g0079 |
4 | NA18941.hp1 NA18953.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.290+1604C>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 3/8 | chr12 | 109567166 | |||||||
chr12:109567192 | G | A | 63 | a0002c0003t0005g0142 a0002c0003t0016g0013 a0002c0003t0047g0218 others(60): Show |
94 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.290+1578C>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 3/8 | chr12 | 109567192 | |||||||
chr12:109567581 | G | GT | 25 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0036 others(22): Show |
45 | HG00558.hp1 HG00558.hp2 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.290+1188dupA | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 3/8 | chr12 | 109567581 | |||||||
chr12:109567597 | G | A | 4 | a0002c0003t0016g0013 a0002c0003t0036g0219 a0002c0003t0037g0149 others(1): Show |
7 | HG00140.hp1 HG01346.hp1 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.290+1173C>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 3/8 | chr12 | 109567597 | |||||||
chr12:109568124 | G | A | 2 | a0002c0003t0036g0219 a0002c0003t0037g0149 |
2 | HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.290+646C>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 3/8 | chr12 | 109568124 | |||||||
chr12:109568127 | A | G | 11 | a0002c0003t0034g0031 a0002c0003t0035g0032 a0002c0003t0068g0138 others(8): Show |
13 | HG02451.hp1 HG02559.hp2 HG02922.hp1 others(10): Show |
intron_variant | MODIFIER | c.290+643T>C | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 3/8 | chr12 | 109568127 | |||||||
chr12:109568519 | A | T | 1 | a0001c0001t0002g0035 | 2 | NA19083.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.290+251T>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 3/8 | chr12 | 109568519 | |||||||
chr12:109568566 | G | A | 11 | a0002c0004t0011g0019 a0002c0004t0011g0120 a0002c0004t0018g0018 others(8): Show |
16 | HG02109.hp2 HG02258.hp2 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.290+204C>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 3/8 | chr12 | 109568566 | |||||||
chr12:109568707 | A | G | 63 | a0001c0001t0031g0176 a0001c0001t0031g0211 a0002c0003t0005g0142 others(60): Show |
91 | HG00099.hp1 HG00423.hp1 HG00639.hp2 others(88): Show |
intron_variant | MODIFIER | c.290+63T>C | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 3/8 | chr12 | 109568707 | |||||||
chr12:109568932 | T | A | 10 | a0003c0002t0005g0004 a0003c0002t0005g0047 a0003c0002t0005g0081 others(7): Show |
23 | HG00423.hp1 HG01099.hp2 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.197-69A>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 2/8 | chr12 | 109568932 | |||||||
chr12:109569009 | G | T | 37 | a0002c0003t0003g0005 a0002c0003t0003g0012 a0002c0003t0003g0030 others(34): Show |
60 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.197-146C>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 2/8 | chr12 | 109569009 | |||||||
chr12:109569237 | G | A | 1 | a0002c0003t0037g0149 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.197-374C>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 2/8 | chr12 | 109569237 | |||||||
chr12:109569268 | A | G | 1 | a0002c0010t0072g0096 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.197-405T>C | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 2/8 | chr12 | 109569268 | |||||||
chr12:109569485 | T | A | 1 | a0006c0007t0051g0040 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.197-622A>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 2/8 | chr12 | 109569485 | |||||||
chr12:109569647 | G | C | 1 | a0003c0002t0009g0084 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.197-784C>G | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 2/8 | chr12 | 109569647 | |||||||
chr12:109569859 | T | C | 2 | a0001c0001t0031g0176 a0001c0001t0031g0211 |
2 | HG01884.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.197-996A>G | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 2/8 | chr12 | 109569859 | |||||||
chr12:109570134 | A | G | 53 | a0002c0003t0003g0005 a0002c0003t0003g0012 a0002c0003t0003g0030 others(50): Show |
81 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.197-1271T>C | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 2/8 | chr12 | 109570134 | |||||||
chr12:109570188 | A | G | 77 | a0001c0001t0031g0176 a0001c0001t0031g0211 a0002c0003t0005g0142 others(74): Show |
110 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.197-1325T>C | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 2/8 | chr12 | 109570188 | |||||||
chr12:109570504 | C | T | 5 | a0003c0002t0005g0041 a0003c0002t0015g0015 a0003c0002t0015g0052 others(2): Show |
7 | HG01884.hp1 HG02896.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.196+1145G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 2/8 | chr12 | 109570504 | |||||||
chr12:109570594 | C | T | 1 | a0004c0005t0022g0028 | 2 | HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.196+1055G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 2/8 | chr12 | 109570594 | |||||||
chr12:109570641 | G | T | 2 | a0002c0003t0016g0013 a0002c0003t0047g0218 |
5 | HG00140.hp1 HG01346.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.196+1008C>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 2/8 | chr12 | 109570641 | |||||||
chr12:109570693 | G | T | 1 | a0002c0003t0032g0127 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.196+956C>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 2/8 | chr12 | 109570693 | |||||||
chr12:109570873 | C | CA | 5 | a0001c0001t0006g0209 a0001c0001t0010g0159 a0001c0001t0101g0221 others(2): Show |
6 | HG03490.hp2 HG03492.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.196+775dupT | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 2/8 | chr12 | 109570873 | |||||||
chr12:109570873 | C | CAAAAAA | 56 | a0002c0003t0005g0142 a0002c0003t0016g0013 a0002c0003t0047g0218 others(53): Show |
85 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.196+770_196+775dup others(6): Show |
MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 2/8 | chr12 | 109570873 | |||||||
chr12:109570873 | C | CAAAAAAA others(3): Show |
1 | a0002c0010t0072g0096 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.196+766_196+775dup others(10): Show |
MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 2/8 | chr12 | 109570873 | |||||||
chr12:109570873 | CA | C | 19 | a0001c0001t0001g0162 a0001c0001t0001g0180 a0001c0001t0033g0161 others(16): Show |
21 | HG01070.hp2 HG01515.hp2 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.196+775delT | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 2/8 | chr12 | 109570873 | |||||||
chr12:109571045 | T | A | 1 | a0002c0010t0072g0096 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.196+604A>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 2/8 | chr12 | 109571045 | |||||||
chr12:109571120 | C | T | 1 | a0006c0007t0051g0040 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.196+529G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 2/8 | chr12 | 109571120 | |||||||
chr12:109571249 | G | T | 53 | a0002c0003t0003g0005 a0002c0003t0003g0012 a0002c0003t0003g0030 others(50): Show |
81 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.196+400C>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 2/8 | chr12 | 109571249 | |||||||
chr12:109571370 | T | G | 2 | a0002c0003t0016g0013 a0002c0003t0047g0218 |
5 | HG00140.hp1 HG01346.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.196+279A>C | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 2/8 | chr12 | 109571370 | |||||||
chr12:109571733 | A | G | 5 | a0003c0002t0013g0014 a0003c0002t0013g0044 a0003c0002t0013g0085 others(2): Show |
7 | HG01243.hp1 HG01361.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.135-23T>C | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 1/8 | chr12 | 109571733 | |||||||
chr12:109571747 | G | GA | 9 | a0002c0003t0011g0094 a0002c0003t0011g0126 a0002c0003t0019g0128 others(6): Show |
9 | HG03654.hp2 HG03927.hp2 NA18942.hp1 others(6): Show |
intron_variant | MODIFIER | c.135-38dupT | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 1/8 | chr12 | 109571747 | |||||||
chr12:109571906 | G | A | 2 | a0001c0001t0031g0176 a0001c0001t0031g0211 |
2 | HG01884.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.135-196C>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 1/8 | chr12 | 109571906 | |||||||
chr12:109571926 | G | T | 1 | a0006c0007t0051g0040 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.135-216C>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 1/8 | chr12 | 109571926 | |||||||
chr12:109571951 | A | G | 61 | a0002c0003t0005g0142 a0003c0002t0005g0004 a0003c0002t0005g0041 others(58): Show |
89 | HG00099.hp1 HG00423.hp1 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.135-241T>C | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 1/8 | chr12 | 109571951 | |||||||
chr12:109572070 | A | C | 2 | a0002c0003t0016g0013 a0002c0003t0047g0218 |
5 | HG00140.hp1 HG01346.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.135-360T>G | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 1/8 | chr12 | 109572070 | |||||||
chr12:109572140 | C | T | 3 | a0001c0001t0002g0178 a0001c0001t0002g0179 a0001c0001t0006g0177 |
3 | HG03831.hp1 HG04184.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.135-430G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 1/8 | chr12 | 109572140 | |||||||
chr12:109572224 | C | T | 1 | a0002c0010t0072g0096 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.135-514G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 1/8 | chr12 | 109572224 | |||||||
chr12:109572243 | A | AT | 2 | a0002c0003t0016g0013 a0002c0003t0047g0218 |
5 | HG00140.hp1 HG01346.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.135-534dupA | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 1/8 | chr12 | 109572243 | |||||||
chr12:109572346 | A | G | 161 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0034 others(158): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.135-636T>C | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 1/8 | chr12 | 109572346 | |||||||
chr12:109572352 | C | T | 1 | a0002c0004t0025g0095 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.135-642G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 1/8 | chr12 | 109572352 | |||||||
chr12:109572369 | C | T | 1 | a0001c0001t0067g0160 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.135-659G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 1/8 | chr12 | 109572369 | |||||||
chr12:109572411 | A | AT | 117 | a0001c0001t0001g0153 a0001c0001t0001g0156 a0001c0001t0002g0155 others(114): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.135-702dupA | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 1/8 | chr12 | 109572411 | |||||||
chr12:109572411 | A | ATT | 14 | a0001c0001t0001g0141 a0002c0003t0003g0093 a0002c0003t0007g0092 others(11): Show |
16 | HG00423.hp1 HG01109.hp1 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.135-703_135-702dup others(2): Show |
MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 1/8 | chr12 | 109572411 | |||||||
chr12:109572411 | AT | A | 9 | a0001c0001t0001g0038 a0001c0001t0001g0210 a0001c0001t0002g0212 others(6): Show |
10 | HG01070.hp1 HG01169.hp2 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.135-702delA | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 1/8 | chr12 | 109572411 | |||||||
chr12:109572411 | ATTTTTTT others(4): Show |
A | 2 | a0002c0003t0016g0013 a0002c0003t0047g0218 |
5 | HG00140.hp1 HG01346.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.135-712_135-702del others(11): Show |
MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 1/8 | chr12 | 109572411 | |||||||
chr12:109572563 | T | C | 1 | a0002c0003t0036g0219 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.134+784A>G | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 1/8 | chr12 | 109572563 | |||||||
chr12:109572626 | G | A | 1 | a0002c0004t0025g0137 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.134+721C>T | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 1/8 | chr12 | 109572626 | |||||||
chr12:109572760 | A | G | 1 | a0001c0001t0002g0220 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.134+587T>C | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 1/8 | chr12 | 109572760 | |||||||
chr12:109573061 | A | G | 115 | a0002c0003t0003g0005 a0002c0003t0003g0012 a0002c0003t0003g0030 others(112): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.134+286T>C | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 1/8 | chr12 | 109573061 | |||||||
chr12:109573144 | T | C | 2 | a0001c0001t0002g0220 a0001c0001t0004g0039 |
3 | HG00741.hp1 HG01169.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.134+203A>G | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 1/8 | chr12 | 109573144 | |||||||
chr12:109573204 | A | C | 1 | a0001c0001t0001g0091 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.134+143T>G | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 1/8 | chr12 | 109573204 | |||||||
chr12:109573293 | C | T | 1 | a0003c0002t0005g0041 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.134+54G>A | MMAB | ENSG00000139428.12 | transcript | ENST00000545712.7 | protein_coding | 1/8 | chr12 | 109573293 |