Item | Value |
---|---|
geneid | 10827 |
ensemblid | ENSG00000055147.19 |
hgncid | 1333 |
symbol | FAM114A2 |
name | family with sequence similarity 114 member A2 |
refseq_nuc | NM_018691.4 |
refseq_prot | NP_061161.2 |
ensembl_nuc | ENST00000351797.9 |
ensembl_prot | ENSP00000341597.4 |
mane_status | MANE Select |
chr | chr5 |
start | 153990148 |
end | 154038910 |
strand | - |
ver | v1.2 |
region | chr5:153990148-154038910 |
region5000 | chr5:153985148-154043910 |
regionname0 | FAM114A2_chr5_153990148_154038910 |
regionname5000 | FAM114A2_chr5_153985148_154043910 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 505 | 220 | 51 | 34 | 102 | 5 | 28 | 71 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | MSDKD others(500): Show |
chr5 | 153985148 | 154043910 |
a0002 | 1/1 | 505 | 104 | 28 | 24 | 33 | 5 | 12 | 26 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | MSDKD others(500): Show |
chr5 | 153985148 | 154043910 |
a0003 | 0/0 | 505 | 8 | 0 | 4 | 0 | 2 | 2 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | MSDKD others(500): Show |
chr5 | 153985148 | 154043910 |
a0004 | 0/0 | 505 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | MSDKD others(500): Show |
chr5 | 153985148 | 154043910 |
a0005 | 0/0 | 505 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | MSDKD others(500): Show |
chr5 | 153985148 | 154043910 |
a0006 | 0/0 | 505 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | MSDKD others(500): Show |
chr5 | 153985148 | 154043910 |
a0007 | 0/0 | 505 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | MSDKD others(500): Show |
chr5 | 153985148 | 154043910 |
a0008 | 0/0 | 505 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | MSDKD others(500): Show |
chr5 | 153985148 | 154043910 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1515 | 215 | 49 | 34 | 99 | 5 | 28 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | ATGTC others(1510): Show |
chr5 | 153985148 | 154043910 | ||
a0001c0006 | 0/0 | 1515 | 2 | 0 | 0 | 2 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | ATGTC others(1510): Show |
chr5 | 153985148 | 154043910 | ||
a0001c0007 | 0/0 | 1515 | 2 | 2 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | ATGTC others(1510): Show |
chr5 | 153985148 | 154043910 | ||
a0001c0009 | 0/0 | 1515 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | ATGTC others(1510): Show |
chr5 | 153985148 | 154043910 | ||
a0002c0002 | 1/1 | 1515 | 75 | 15 | 17 | 29 | 1 | 11 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | ATGTC others(1510): Show |
chr5 | 153985148 | 154043910 | ||
a0002c0003 | 0/0 | 1515 | 29 | 13 | 7 | 4 | 4 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | ATGTC others(1510): Show |
chr5 | 153985148 | 154043910 | ||
a0003c0004 | 0/0 | 1515 | 8 | 0 | 4 | 0 | 2 | 2 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | ATGTC others(1510): Show |
chr5 | 153985148 | 154043910 | ||
a0004c0005 | 0/0 | 1515 | 7 | 7 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | ATGTC others(1510): Show |
chr5 | 153985148 | 154043910 | ||
a0005c0008 | 0/0 | 1515 | 2 | 2 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | ATGTC others(1510): Show |
chr5 | 153985148 | 154043910 | ||
a0006c0010 | 0/0 | 1515 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | ATGTC others(1510): Show |
chr5 | 153985148 | 154043910 | ||
a0007c0011 | 0/0 | 1515 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | ATGTC others(1510): Show |
chr5 | 153985148 | 154043910 | ||
a0008c0012 | 0/0 | 1515 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | ATGTC others(1510): Show |
chr5 | 153985148 | 154043910 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4412 | 87 | 13 | 13 | 55 | 1 | 5 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | AGTAG others(4407): Show |
chr5 | 153985148 | 154043910 |
a0001c0001t0002 | 0/0 | 4413 | 40 | 8 | 10 | 12 | 2 | 8 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | AGTAG others(4408): Show |
chr5 | 153985148 | 154043910 |
a0001c0001t0005 | 0/0 | 4413 | 22 | 7 | 6 | 2 | 2 | 5 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | AGTAG others(4408): Show |
chr5 | 153985148 | 154043910 |
a0001c0001t0006 | 0/0 | 4413 | 19 | 0 | 0 | 19 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | AGTAG others(4408): Show |
chr5 | 153985148 | 154043910 |
a0001c0001t0011 | 0/0 | 4417 | 7 | 6 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | AGTAG others(4412): Show |
chr5 | 153985148 | 154043910 |
a0001c0001t0012 | 0/0 | 4417 | 6 | 2 | 1 | 0 | 0 | 3 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | AGTAG others(4412): Show |
chr5 | 153985148 | 154043910 |
a0001c0001t0014 | 0/0 | 4413 | 4 | 0 | 0 | 0 | 0 | 4 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | AGTAG others(4408): Show |
chr5 | 153985148 | 154043910 |
a0001c0001t0015 | 0/0 | 4411 | 6 | 1 | 0 | 5 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | AGTAG others(4406): Show |
chr5 | 153985148 | 154043910 |
a0001c0001t0017 | 0/0 | 4414 | 3 | 0 | 2 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | AGTAG others(4409): Show |
chr5 | 153985148 | 154043910 |
a0001c0001t0018 | 0/0 | 4411 | 4 | 4 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | AGTAG others(4406): Show |
chr5 | 153985148 | 154043910 |
a0001c0001t0020 | 0/0 | 4411 | 2 | 2 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | AGTAG others(4406): Show |
chr5 | 153985148 | 154043910 |
a0001c0001t0022 | 0/0 | 4414 | 2 | 0 | 0 | 2 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | AGTAG others(4409): Show |
chr5 | 153985148 | 154043910 |
a0001c0001t0023 | 0/0 | 4414 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | AGTAG others(4409): Show |
chr5 | 153985148 | 154043910 |
a0001c0001t0024 | 0/0 | 4412 | 2 | 0 | 0 | 0 | 0 | 2 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | AGTAG others(4407): Show |
chr5 | 153985148 | 154043910 |
a0001c0001t0025 | 0/0 | 4412 | 2 | 2 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | AGTAG others(4407): Show |
chr5 | 153985148 | 154043910 |
a0001c0001t0026 | 0/0 | 4413 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | AGTAG others(4408): Show |
chr5 | 153985148 | 154043910 |
a0001c0001t0034 | 0/0 | 4412 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | AGTAG others(4407): Show |
chr5 | 153985148 | 154043910 |
a0001c0001t0035 | 0/0 | 4413 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | AGTAG others(4408): Show |
chr5 | 153985148 | 154043910 |
a0001c0001t0036 | 0/0 | 4412 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | AGTAG others(4407): Show |
chr5 | 153985148 | 154043910 |
a0001c0001t0037 | 0/0 | 4415 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | AGTAG others(4410): Show |
chr5 | 153985148 | 154043910 |
a0001c0001t0038 | 0/0 | 4412 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | AGTAG others(4407): Show |
chr5 | 153985148 | 154043910 |
a0001c0001t0039 | 0/0 | 4414 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | AGTAG others(4409): Show |
chr5 | 153985148 | 154043910 |
a0001c0001t0040 | 0/0 | 4412 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | AGTAG others(4407): Show |
chr5 | 153985148 | 154043910 |
a0001c0006t0006 | 0/0 | 4413 | 2 | 0 | 0 | 2 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | AGTAG others(4408): Show |
chr5 | 153985148 | 154043910 |
a0001c0007t0014 | 0/0 | 4413 | 2 | 2 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | AGTAG others(4408): Show |
chr5 | 153985148 | 154043910 |
a0001c0009t0001 | 0/0 | 4412 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | AGTAG others(4407): Show |
chr5 | 153985148 | 154043910 |
a0002c0002t0003 | 0/0 | 4414 | 32 | 0 | 3 | 26 | 0 | 3 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | AGTAG others(4409): Show |
chr5 | 153985148 | 154043910 |
a0002c0002t0004 | 0/0 | 4414 | 7 | 6 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | AGTAG others(4409): Show |
chr5 | 153985148 | 154043910 |
a0002c0002t0007 | 0/0 | 4414 | 13 | 5 | 3 | 0 | 0 | 5 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | AGTAG others(4409): Show |
chr5 | 153985148 | 154043910 |
a0002c0002t0008 | 1/1 | 4414 | 10 | 1 | 7 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | AGTAG others(4409): Show |
chr5 | 153985148 | 154043910 |
a0002c0002t0010 | 0/0 | 4413 | 7 | 3 | 1 | 0 | 1 | 2 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | AGTAG others(4408): Show |
chr5 | 153985148 | 154043910 |
a0002c0002t0027 | 0/0 | 4415 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | AGTAG others(4410): Show |
chr5 | 153985148 | 154043910 |
a0002c0002t0028 | 0/0 | 4413 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | AGTAG others(4408): Show |
chr5 | 153985148 | 154043910 |
a0002c0002t0029 | 0/0 | 4413 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | AGTAG others(4408): Show |
chr5 | 153985148 | 154043910 |
a0002c0002t0030 | 0/0 | 4416 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | AGTAG others(4411): Show |
chr5 | 153985148 | 154043910 |
a0002c0002t0031 | 0/0 | 4415 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | AGTAG others(4410): Show |
chr5 | 153985148 | 154043910 |
a0002c0002t0033 | 0/0 | 4413 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | AGTAG others(4408): Show |
chr5 | 153985148 | 154043910 |
a0002c0003t0004 | 0/0 | 4414 | 16 | 7 | 4 | 3 | 2 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | AGTAG others(4409): Show |
chr5 | 153985148 | 154043910 |
a0002c0003t0013 | 0/0 | 4414 | 6 | 5 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | AGTAG others(4409): Show |
chr5 | 153985148 | 154043910 |
a0002c0003t0016 | 0/0 | 4414 | 4 | 0 | 1 | 0 | 2 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | AGTAG others(4409): Show |
chr5 | 153985148 | 154043910 |
a0002c0003t0019 | 0/0 | 4415 | 2 | 1 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | AGTAG others(4410): Show |
chr5 | 153985148 | 154043910 |
a0002c0003t0032 | 0/0 | 4413 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | AGTAG others(4408): Show |
chr5 | 153985148 | 154043910 |
a0003c0004t0001 | 0/0 | 4412 | 1 | 0 | 0 | 0 | 1 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | AGTAG others(4407): Show |
chr5 | 153985148 | 154043910 |
a0003c0004t0002 | 0/0 | 4413 | 5 | 0 | 4 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | AGTAG others(4408): Show |
chr5 | 153985148 | 154043910 |
a0003c0004t0017 | 0/0 | 4414 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | AGTAG others(4409): Show |
chr5 | 153985148 | 154043910 |
a0003c0004t0023 | 0/0 | 4414 | 1 | 0 | 0 | 0 | 1 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | AGTAG others(4409): Show |
chr5 | 153985148 | 154043910 |
a0004c0005t0009 | 0/0 | 4417 | 7 | 7 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | AGTAG others(4412): Show |
chr5 | 153985148 | 154043910 |
a0005c0008t0021 | 0/0 | 4414 | 2 | 2 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | AGTAG others(4409): Show |
chr5 | 153985148 | 154043910 |
a0006c0010t0001 | 0/0 | 4412 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | AGTAG others(4407): Show |
chr5 | 153985148 | 154043910 |
a0007c0011t0004 | 0/0 | 4414 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | AGTAG others(4409): Show |
chr5 | 153985148 | 154043910 |
a0008c0012t0001 | 0/0 | 4412 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | AGTAG others(4407): Show |
chr5 | 153985148 | 154043910 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 10 | 0 | 4 | 4 | 0 | 2 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0003 | 0/0 | 9 | 1 | 1 | 7 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0007 | 0/0 | 6 | 2 | 1 | 3 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0002g0006 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0002g0014 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0002g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0002g0032 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0002g0036 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0005g0012 | 0/0 | 4 | 0 | 1 | 0 | 1 | 2 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0005g0033 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0005g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0005g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0005g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0005g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0005g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0005g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0005g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0005g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0005g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0005g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0005g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0005g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0005g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0005g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0005g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0005g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0006g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0006g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0006g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0006g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0006g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0006g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0006g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0006g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0006g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0006g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0006g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0006g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0006g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0006g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0011g0009 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0011g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0011g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0012g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0012g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0012g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0012g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0012g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0014g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0014g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0014g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0014g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0015g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0015g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0015g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0015g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0015g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0015g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0017g0031 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0017g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0018g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0018g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0018g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0020g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0020g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0022g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0022g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0023g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0024g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0024g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0025g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0025g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0026g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0034g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0035g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0036g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0037g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0038g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0039g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0040g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0006t0006g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0006t0006g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0007t0014g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0009t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0003g0002 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0003g0005 | 0/0 | 7 | 0 | 3 | 4 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0003g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0003g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0003g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0003g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0003g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0004g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0004g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0004g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0004g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0004g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0004g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0007g0004 | 0/0 | 8 | 2 | 2 | 0 | 0 | 4 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0007g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0007g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0007g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0007g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0007g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0008g0008 | 1/1 | 5 | 0 | 3 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0008g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0008g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0008g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0008g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0010g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0010g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0010g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0010g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0010g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0010g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0010g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0027g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0028g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0029g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0030g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0031g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0033g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0003t0004g0015 | 0/0 | 3 | 1 | 0 | 0 | 2 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0003t0004g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0003t0004g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0003t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0003t0004g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0003t0004g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0003t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0003t0004g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0003t0004g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0003t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0003t0004g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0003t0004g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0003t0013g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0003t0013g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0003t0013g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0003t0013g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0003t0013g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0003t0016g0024 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0003t0016g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0003t0016g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0003t0019g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0003t0019g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0003t0032g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0003c0004t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0003c0004t0002g0017 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0003c0004t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0003c0004t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0003c0004t0017g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0003c0004t0023g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0004c0005t0009g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0004c0005t0009g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0004c0005t0009g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0004c0005t0009g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0004c0005t0009g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0004c0005t0009g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0004c0005t0009g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0005c0008t0021g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0005c0008t0021g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0006c0010t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0007c0011t0004g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0008c0012t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0005 | g0012 | EUR | GBR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG00099 | hp2 | a0003 | c0004 | t0023 | g0165 | EUR | GBR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG00140 | hp1 | a0001 | c0001 | t0005 | g0033 | EUR | GBR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG00140 | hp2 | a0002 | c0002 | t0010 | g0089 | EUR | GBR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0154 | EUR | FIN | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG00323 | hp2 | a0003 | c0004 | t0001 | g0161 | EUR | FIN | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | CHS | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | CHS | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG00438 | hp1 | a0001 | c0001 | t0022 | g0132 | EAS | CHS | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG00438 | hp2 | a0001 | c0001 | t0006 | g0119 | EAS | CHS | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | CHS | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG00597 | hp1 | a0001 | c0001 | t0015 | g0187 | EAS | CHS | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG00597 | hp2 | a0001 | c0001 | t0015 | g0226 | EAS | CHS | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | CHS | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | CHS | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG00621 | hp2 | a0001 | c0009 | t0001 | g0188 | EAS | CHS | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG00639 | hp1 | a0002 | c0002 | t0033 | g0095 | AMR | PUR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG00639 | hp2 | a0001 | c0001 | t0017 | g0031 | AMR | PUR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG00735 | hp1 | a0002 | c0002 | t0004 | g0056 | AMR | PUR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG00738 | hp1 | a0001 | c0001 | t0039 | g0208 | AMR | PUR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG00738 | hp2 | a0002 | c0002 | t0008 | g0059 | AMR | PUR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01069 | hp1 | a0002 | c0002 | t0008 | g0008 | AMR | PUR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01069 | hp2 | a0002 | c0003 | t0004 | g0023 | AMR | PUR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01070 | hp1 | a0002 | c0002 | t0008 | g0021 | AMR | PUR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01071 | hp1 | a0002 | c0003 | t0004 | g0023 | AMR | PUR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01071 | hp2 | a0002 | c0002 | t0008 | g0008 | AMR | PUR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01074 | hp1 | a0003 | c0004 | t0002 | g0017 | AMR | PUR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01081 | hp1 | a0003 | c0004 | t0002 | g0017 | AMR | PUR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01081 | hp2 | a0002 | c0002 | t0031 | g0067 | AMR | PUR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01099 | hp1 | a0001 | c0001 | t0017 | g0145 | AMR | PUR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0166 | AMR | PUR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01106 | hp1 | a0002 | c0002 | t0007 | g0004 | AMR | PUR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01167 | hp2 | a0002 | c0003 | t0032 | g0096 | AMR | PUR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01168 | hp1 | a0001 | c0001 | t0005 | g0012 | AMR | PUR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01168 | hp2 | a0002 | c0002 | t0008 | g0021 | AMR | PUR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01169 | hp1 | a0002 | c0003 | t0013 | g0097 | AMR | PUR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01169 | hp2 | a0002 | c0002 | t0008 | g0008 | AMR | PUR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01192 | hp1 | a0001 | c0001 | t0012 | g0102 | AMR | PUR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01255 | hp1 | a0002 | c0002 | t0010 | g0088 | AMR | CLM | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | CLM | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01256 | hp1 | a0002 | c0003 | t0016 | g0081 | AMR | CLM | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | CLM | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01257 | hp1 | a0001 | c0001 | t0005 | g0148 | AMR | CLM | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01257 | hp2 | a0002 | c0002 | t0003 | g0005 | AMR | CLM | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01258 | hp1 | a0001 | c0001 | t0005 | g0180 | AMR | CLM | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | CLM | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | CLM | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01261 | hp2 | a0002 | c0002 | t0007 | g0004 | AMR | CLM | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01358 | hp1 | a0002 | c0002 | t0007 | g0099 | AMR | CLM | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01361 | hp1 | a0002 | c0003 | t0004 | g0025 | AMR | CLM | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01361 | hp2 | a0001 | c0001 | t0005 | g0033 | AMR | CLM | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01433 | hp1 | a0002 | c0003 | t0004 | g0025 | AMR | CLM | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0163 | EUR | IBS | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01515 | hp2 | a0002 | c0003 | t0016 | g0024 | EUR | IBS | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0233 | EUR | IBS | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01516 | hp2 | a0002 | c0003 | t0004 | g0015 | EUR | IBS | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01517 | hp1 | a0002 | c0003 | t0004 | g0015 | EUR | IBS | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01517 | hp2 | a0002 | c0003 | t0016 | g0024 | EUR | IBS | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01884 | hp1 | a0001 | c0001 | t0005 | g0231 | AFR | ACB | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01884 | hp2 | a0001 | c0001 | t0011 | g0242 | AFR | ACB | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0237 | AFR | ACB | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01891 | hp2 | a0001 | c0001 | t0012 | g0101 | AFR | ACB | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01928 | hp1 | a0001 | c0001 | t0005 | g0146 | AMR | PEL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01928 | hp2 | a0002 | c0002 | t0003 | g0005 | AMR | PEL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01934 | hp1 | a0001 | c0001 | t0005 | g0175 | AMR | PEL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01934 | hp2 | a0003 | c0004 | t0002 | g0194 | AMR | PEL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0198 | AMR | PEL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PEL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0167 | AMR | PEL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | PEL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01981 | hp2 | a0001 | c0001 | t0011 | g0009 | AMR | PEL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02015 | hp1 | a0001 | c0001 | t0005 | g0157 | EAS | KHV | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02015 | hp2 | a0002 | c0002 | t0003 | g0002 | EAS | KHV | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02027 | hp1 | a0002 | c0003 | t0004 | g0079 | EAS | KHV | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02040 | hp2 | a0001 | c0001 | t0034 | g0239 | EAS | KHV | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02055 | hp1 | a0002 | c0003 | t0004 | g0072 | AFR | ACB | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0193 | AFR | ACB | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02071 | hp1 | a0001 | c0001 | t0006 | g0113 | EAS | KHV | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02074 | hp1 | a0002 | c0002 | t0003 | g0005 | EAS | KHV | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02083 | hp2 | a0002 | c0002 | t0003 | g0049 | EAS | KHV | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02132 | hp2 | a0001 | c0006 | t0006 | g0115 | EAS | KHV | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02135 | hp2 | a0002 | c0002 | t0003 | g0045 | EAS | KHV | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02145 | hp1 | a0001 | c0001 | t0037 | g0147 | AFR | ACB | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02145 | hp2 | a0005 | c0008 | t0021 | g0133 | AFR | ACB | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0224 | AMR | PEL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0197 | AMR | PEL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02155 | hp1 | a0001 | c0001 | t0006 | g0011 | EAS | CDX | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | CDX | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | CDX | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02165 | hp2 | a0002 | c0002 | t0003 | g0020 | EAS | CDX | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02257 | hp1 | a0002 | c0003 | t0004 | g0078 | AFR | ACB | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02258 | hp1 | a0002 | c0003 | t0013 | g0071 | AFR | ACB | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02258 | hp2 | a0001 | c0001 | t0020 | g0124 | AFR | ACB | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02280 | hp1 | a0002 | c0003 | t0004 | g0015 | AFR | ACB | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02280 | hp2 | a0004 | c0005 | t0009 | g0105 | AFR | ACB | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PEL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02293 | hp2 | a0002 | c0002 | t0008 | g0061 | AMR | PEL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02300 | hp2 | a0002 | c0002 | t0003 | g0005 | AMR | PEL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02572 | hp2 | a0002 | c0003 | t0013 | g0022 | AFR | GWD | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0234 | SAS | PJL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02602 | hp2 | a0002 | c0002 | t0007 | g0004 | SAS | PJL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02615 | hp1 | a0001 | c0001 | t0018 | g0029 | AFR | GWD | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02615 | hp2 | a0002 | c0002 | t0004 | g0084 | AFR | GWD | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02622 | hp1 | a0002 | c0002 | t0010 | g0087 | AFR | GWD | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02622 | hp2 | a0006 | c0010 | t0001 | g0185 | AFR | GWD | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02630 | hp1 | a0004 | c0005 | t0009 | g0104 | AFR | GWD | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0191 | AFR | GWD | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02647 | hp2 | a0001 | c0001 | t0035 | g0192 | AFR | GWD | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02683 | hp1 | a0001 | c0001 | t0014 | g0190 | SAS | PJL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02683 | hp2 | a0001 | c0001 | t0012 | g0103 | SAS | PJL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02698 | hp1 | a0001 | c0001 | t0012 | g0026 | SAS | PJL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02698 | hp2 | a0001 | c0001 | t0005 | g0012 | SAS | PJL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02717 | hp1 | a0002 | c0002 | t0007 | g0065 | AFR | GWD | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02717 | hp2 | a0001 | c0001 | t0011 | g0009 | AFR | GWD | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02723 | hp1 | a0002 | c0003 | t0004 | g0083 | AFR | GWD | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0032 | SAS | PJL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0036 | SAS | PJL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02738 | hp1 | a0001 | c0001 | t0005 | g0177 | SAS | PJL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02738 | hp2 | a0002 | c0002 | t0007 | g0069 | SAS | PJL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02809 | hp1 | a0001 | c0001 | t0011 | g0009 | AFR | GWD | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02809 | hp2 | a0001 | c0001 | t0018 | g0126 | AFR | GWD | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02818 | hp2 | a0002 | c0002 | t0004 | g0058 | AFR | GWD | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02886 | hp1 | a0001 | c0001 | t0020 | g0125 | AFR | GWD | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02886 | hp2 | a0005 | c0008 | t0021 | g0171 | AFR | GWD | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02895 | hp1 | a0001 | c0007 | t0014 | g0039 | AFR | GWD | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02895 | hp2 | a0002 | c0002 | t0004 | g0091 | AFR | GWD | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02896 | hp1 | a0001 | c0001 | t0018 | g0127 | AFR | GWD | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02896 | hp2 | a0002 | c0002 | t0010 | g0085 | AFR | GWD | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02897 | hp1 | a0002 | c0002 | t0010 | g0086 | AFR | GWD | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02897 | hp2 | a0001 | c0007 | t0014 | g0039 | AFR | GWD | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02922 | hp2 | a0004 | c0005 | t0009 | g0107 | AFR | ESN | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ESN | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02970 | hp1 | a0001 | c0001 | t0011 | g0243 | AFR | ESN | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02976 | hp1 | a0002 | c0003 | t0019 | g0073 | AFR | ESN | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02976 | hp2 | a0001 | c0001 | t0005 | g0138 | AFR | ESN | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03041 | hp2 | a0001 | c0001 | t0023 | g0130 | AFR | GWD | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03098 | hp1 | a0004 | c0005 | t0009 | g0042 | AFR | MSL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03098 | hp2 | a0002 | c0003 | t0013 | g0076 | AFR | MSL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03130 | hp1 | a0002 | c0002 | t0007 | g0004 | AFR | ESN | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03130 | hp2 | a0002 | c0002 | t0004 | g0090 | AFR | ESN | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03139 | hp1 | a0001 | c0001 | t0011 | g0009 | AFR | ESN | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0241 | AFR | ESN | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03195 | hp2 | a0001 | c0001 | t0011 | g0009 | AFR | ESN | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03225 | hp1 | a0001 | c0001 | t0025 | g0128 | AFR | MSL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03225 | hp2 | a0002 | c0003 | t0013 | g0022 | AFR | MSL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03239 | hp1 | a0002 | c0002 | t0007 | g0004 | SAS | PJL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03239 | hp2 | a0003 | c0004 | t0002 | g0017 | SAS | PJL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03453 | hp1 | a0002 | c0003 | t0013 | g0075 | AFR | MSL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03453 | hp2 | a0001 | c0001 | t0012 | g0100 | AFR | MSL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03486 | hp1 | a0002 | c0003 | t0004 | g0080 | AFR | MSL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03486 | hp2 | a0007 | c0011 | t0004 | g0098 | AFR | MSL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03490 | hp1 | a0002 | c0002 | t0010 | g0094 | SAS | PJL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03490 | hp2 | a0002 | c0002 | t0007 | g0004 | SAS | PJL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0236 | SAS | PJL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03491 | hp2 | a0001 | c0001 | t0024 | g0203 | SAS | PJL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0235 | SAS | PJL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03492 | hp2 | a0002 | c0002 | t0007 | g0004 | SAS | PJL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03516 | hp1 | a0002 | c0002 | t0007 | g0004 | AFR | ESN | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03516 | hp2 | a0002 | c0003 | t0004 | g0070 | AFR | ESN | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03540 | hp1 | a0001 | c0001 | t0005 | g0173 | AFR | GWD | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03540 | hp2 | a0002 | c0002 | t0007 | g0064 | AFR | GWD | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03579 | hp1 | a0002 | c0003 | t0004 | g0077 | AFR | MSL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | MSL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03654 | hp1 | a0003 | c0004 | t0017 | g0164 | SAS | PJL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03654 | hp2 | a0001 | c0001 | t0005 | g0178 | SAS | PJL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03688 | hp1 | a0002 | c0002 | t0030 | g0068 | SAS | STU | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03688 | hp2 | a0001 | c0001 | t0005 | g0212 | SAS | STU | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03704 | hp1 | a0001 | c0001 | t0014 | g0135 | SAS | PJL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03704 | hp2 | a0001 | c0001 | t0024 | g0221 | SAS | PJL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03710 | hp1 | a0001 | c0001 | t0005 | g0012 | SAS | PJL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03710 | hp2 | a0001 | c0001 | t0014 | g0136 | SAS | PJL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03831 | hp1 | a0002 | c0003 | t0016 | g0082 | SAS | BEB | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03831 | hp2 | a0002 | c0002 | t0003 | g0055 | SAS | BEB | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03834 | hp1 | a0002 | c0002 | t0003 | g0054 | SAS | BEB | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | BEB | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | BEB | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03942 | hp2 | a0001 | c0001 | t0014 | g0170 | SAS | BEB | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG04184 | hp2 | a0001 | c0001 | t0012 | g0026 | SAS | BEB | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG04199 | hp1 | a0002 | c0002 | t0010 | g0092 | SAS | STU | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | STU | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0129 | SAS | STU | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG04228 | hp1 | a0002 | c0002 | t0003 | g0050 | SAS | STU | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0030 | SAS | STU | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18522 | hp1 | a0001 | c0001 | t0005 | g0137 | AFR | YRI | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0162 | AFR | YRI | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | CHB | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18747 | hp2 | a0002 | c0003 | t0004 | g0074 | EAS | CHB | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18906 | hp1 | a0001 | c0001 | t0015 | g0156 | AFR | YRI | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0169 | AFR | YRI | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18939 | hp1 | a0002 | c0002 | t0028 | g0047 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18939 | hp2 | a0001 | c0001 | t0015 | g0155 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18941 | hp2 | a0002 | c0002 | t0003 | g0052 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18942 | hp1 | a0002 | c0002 | t0003 | g0010 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18946 | hp2 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18947 | hp1 | a0002 | c0002 | t0003 | g0046 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18947 | hp2 | a0001 | c0001 | t0005 | g0150 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18950 | hp2 | a0008 | c0012 | t0001 | g0232 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18952 | hp1 | a0001 | c0001 | t0006 | g0028 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18952 | hp2 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18953 | hp1 | a0002 | c0002 | t0003 | g0005 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18953 | hp2 | a0001 | c0001 | t0006 | g0123 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18954 | hp1 | a0001 | c0001 | t0006 | g0027 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18954 | hp2 | a0002 | c0002 | t0003 | g0010 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18961 | hp1 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18963 | hp1 | a0001 | c0001 | t0006 | g0011 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18963 | hp2 | a0001 | c0001 | t0015 | g0151 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18965 | hp1 | a0002 | c0003 | t0019 | g0062 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18965 | hp2 | a0001 | c0001 | t0022 | g0134 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18966 | hp1 | a0001 | c0001 | t0006 | g0120 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18966 | hp2 | a0002 | c0003 | t0004 | g0063 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18967 | hp1 | a0001 | c0001 | t0006 | g0114 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18968 | hp1 | a0002 | c0002 | t0003 | g0010 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18968 | hp2 | a0001 | c0001 | t0006 | g0110 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18969 | hp2 | a0002 | c0002 | t0029 | g0044 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18970 | hp2 | a0001 | c0001 | t0006 | g0121 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18972 | hp1 | a0001 | c0001 | t0006 | g0011 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18973 | hp2 | a0001 | c0001 | t0006 | g0111 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18974 | hp2 | a0001 | c0001 | t0036 | g0143 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18975 | hp2 | a0002 | c0002 | t0003 | g0005 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18977 | hp1 | a0001 | c0001 | t0006 | g0117 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18978 | hp1 | a0001 | c0006 | t0006 | g0118 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18980 | hp1 | a0001 | c0001 | t0015 | g0238 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18982 | hp1 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18983 | hp2 | a0001 | c0001 | t0006 | g0027 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18984 | hp2 | a0001 | c0001 | t0038 | g0215 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18987 | hp2 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19000 | hp2 | a0001 | c0001 | t0006 | g0011 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19005 | hp2 | a0002 | c0002 | t0003 | g0043 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19007 | hp1 | a0002 | c0002 | t0003 | g0048 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19011 | hp1 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19030 | hp1 | a0002 | c0002 | t0004 | g0093 | AFR | LWK | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0142 | AFR | LWK | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19043 | hp1 | a0001 | c0001 | t0026 | g0040 | AFR | LWK | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19043 | hp2 | a0001 | c0001 | t0018 | g0029 | AFR | LWK | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19057 | hp1 | a0002 | c0002 | t0003 | g0010 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19057 | hp2 | a0001 | c0001 | t0040 | g0116 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19058 | hp2 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19070 | hp1 | a0002 | c0002 | t0003 | g0020 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19078 | hp2 | a0002 | c0002 | t0003 | g0053 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19079 | hp2 | a0002 | c0002 | t0027 | g0051 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19080 | hp1 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19081 | hp2 | a0001 | c0001 | t0006 | g0028 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19083 | hp1 | a0002 | c0002 | t0003 | g0005 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19084 | hp2 | a0001 | c0001 | t0006 | g0112 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19090 | hp1 | a0001 | c0001 | t0006 | g0122 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA20129 | hp1 | a0001 | c0001 | t0005 | g0139 | AFR | ASW | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA20129 | hp2 | a0004 | c0005 | t0009 | g0041 | AFR | ASW | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0030 | SAS | GIH | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA20905 | hp2 | a0001 | c0001 | t0017 | g0031 | SAS | GIH | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01123 | hp1 | a0003 | c0004 | t0002 | g0195 | AMR | CLM | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02109 | hp1 | a0001 | c0001 | t0005 | g0141 | AFR | ACB | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02109 | hp2 | a0004 | c0005 | t0009 | g0108 | AFR | ACB | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02486 | hp1 | a0001 | c0001 | t0025 | g0201 | AFR | ACB | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02486 | hp2 | a0002 | c0002 | t0007 | g0066 | AFR | ACB | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02559 | hp1 | a0002 | c0002 | t0008 | g0060 | AFR | ACB | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02559 | hp2 | a0002 | c0002 | t0004 | g0057 | AFR | ACB | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | MSL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03471 | hp2 | a0004 | c0005 | t0009 | g0106 | AFR | MSL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA20300 | hp1 | a0001 | c0001 | t0005 | g0200 | AFR | USA | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | USA | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
homoSapiens | chm13v2 | a0002 | c0002 | t0008 | g0008 | REF | REF | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
homoSapiens | grch38p0 | a0002 | c0002 | t0008 | g0008 | REF | REF | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:153993004 | T | C | 1 | a0004 | 7 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(4): Show |
missense_variant | MODERATE | c.1490A>G | p.Gln497Arg | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 1558/4414 | 1490/1518 | 497/505 | chr5 | 153993004 | |||
chr5:153993010 | T | G | 1 | a0007 | 1 | HG03486.hp2 | missense_variant | MODERATE | c.1484A>C | p.Glu495Ala | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 1552/4414 | 1484/1518 | 495/505 | chr5 | 153993010 | |||
chr5:154002251 | T | C | 1 | a0006 | 1 | HG02622.hp2 | missense_variant&splice_region_variant | MODERATE | c.1256A>G | p.Gln419Arg | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/14 | 1324/4414 | 1256/1518 | 419/505 | chr5 | 154002251 | |||
chr5:154002288 | C | T | 1 | a0003 | 8 | HG00099.hp2 HG00323.hp2 HG01074.hp1 others(5): Show |
missense_variant | MODERATE | c.1219G>A | p.Glu407Lys | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/14 | 1287/4414 | 1219/1518 | 407/505 | chr5 | 154002288 | |||
chr5:154027304 | T | C | 1 | a0005 | 2 | HG02145.hp2 HG02886.hp2 |
missense_variant | MODERATE | c.661A>G | p.Ile221Val | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 7/14 | 729/4414 | 661/1518 | 221/505 | chr5 | 154027304 | |||
chr5:154033830 | C | T | 6 | a0001 a0003 a0004 others(3): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
missense_variant | MODERATE | c.364G>A | p.Gly122Ser | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/14 | 432/4414 | 364/1518 | 122/505 | chr5 | 154033830 | |||
chr5:154034373 | T | C | 1 | a0008 | 1 | NA18950.hp2 | missense_variant | MODERATE | c.215A>G | p.Asn72Ser | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 3/14 | 283/4414 | 215/1518 | 72/505 | chr5 | 154034373 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:153993012 | A | G | 1 | a0001c0009 | 1 | HG00621.hp2 | synonymous_variant | LOW | c.1482T>C | p.His494His | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 1550/4414 | 1482/1518 | 494/505 | chr5 | 153993012 | |||
chr5:154002313 | T | A | 1 | a0001c0006 | 2 | HG02132.hp2 NA18978.hp1 |
synonymous_variant | LOW | c.1194A>T | p.Ala398Ala | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/14 | 1262/4414 | 1194/1518 | 398/505 | chr5 | 154002313 | |||
chr5:154002889 | C | T | 1 | a0008c0012 | 1 | NA18950.hp2 | synonymous_variant | LOW | c.1074G>A | p.Ser358Ser | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 10/14 | 1142/4414 | 1074/1518 | 358/505 | chr5 | 154002889 | |||
chr5:154002958 | G | A | 1 | a0002c0003 | 29 | HG01069.hp2 HG01071.hp1 HG01167.hp2 others(26): Show |
synonymous_variant | LOW | c.1005C>T | p.Thr335Thr | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 10/14 | 1073/4414 | 1005/1518 | 335/505 | chr5 | 154002958 | |||
chr5:154026403 | T | C | 1 | a0001c0007 | 2 | HG02895.hp1 HG02897.hp2 |
synonymous_variant | LOW | c.909A>G | p.Lys303Lys | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/14 | 977/4414 | 909/1518 | 303/505 | chr5 | 154026403 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:153990428 | T | C | 1 | a0001c0001t0038 | 1 | NA18984.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2548A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 2548 | chr5 | 153990428 | ||||||
chr5:153990499 | T | TA | 1 | a0004c0005t0009 | 7 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2476dupT | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 2476 | chr5 | 153990499 | ||||||
chr5:153990499 | TA | T | 12 | a0001c0001t0005 a0001c0001t0014 a0001c0001t0017 others(9): Show |
45 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*2476delT | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 2476 | chr5 | 153990499 | ||||||
chr5:153990499 | TAA | T | 15 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0015 others(12): Show |
150 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(147): Show |
3_prime_UTR_variant | MODIFIER | c.*2475_*2476delTT | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 2475 | chr5 | 153990499 | ||||||
chr5:153990739 | A | G | 1 | a0002c0003t0016 | 4 | HG01256.hp1 HG01515.hp2 HG01517.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2237T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 2237 | chr5 | 153990739 | ||||||
chr5:153990753 | G | T | 1 | a0005c0008t0021 | 2 | HG02145.hp2 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2223C>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 2223 | chr5 | 153990753 | ||||||
chr5:153990831 | A | C | 50 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(47): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
3_prime_UTR_variant | MODIFIER | c.*2145T>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 2145 | chr5 | 153990831 | ||||||
chr5:153990872 | T | C | 3 | a0001c0001t0011 a0001c0001t0012 a0004c0005t0009 |
20 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2104A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 2104 | chr5 | 153990872 | ||||||
chr5:153991006 | T | C | 31 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(28): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
3_prime_UTR_variant | MODIFIER | c.*1970A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 1970 | chr5 | 153991006 | ||||||
chr5:153991389 | C | T | 2 | a0002c0003t0013 a0002c0003t0032 |
7 | HG01167.hp2 HG01169.hp1 HG02258.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1587G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 1587 | chr5 | 153991389 | ||||||
chr5:153991433 | T | C | 1 | a0002c0002t0033 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1543A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 1543 | chr5 | 153991433 | ||||||
chr5:153991646 | G | A | 47 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(44): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
3_prime_UTR_variant | MODIFIER | c.*1330C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 1330 | chr5 | 153991646 | ||||||
chr5:153991681 | T | G | 1 | a0001c0001t0024 | 2 | HG03491.hp2 HG03704.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1295A>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 1295 | chr5 | 153991681 | ||||||
chr5:153991692 | A | AT | 9 | a0001c0001t0002 a0001c0001t0017 a0001c0001t0022 others(6): Show |
56 | HG00438.hp1 HG00609.hp1 HG00639.hp2 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*1283dupA | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 1283 | chr5 | 153991692 | ||||||
chr5:153991692 | A | ATT | 5 | a0001c0001t0023 a0001c0001t0037 a0002c0002t0030 others(2): Show |
11 | HG00099.hp2 HG02109.hp2 HG02145.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1282_*1283dupAA | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 1283 | chr5 | 153991692 | ||||||
chr5:153991692 | A | ATTT | 2 | a0001c0001t0011 a0001c0001t0012 |
13 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1281_*1283dupAAA | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 1283 | chr5 | 153991692 | ||||||
chr5:153991692 | AT | A | 8 | a0001c0001t0006 a0001c0001t0015 a0001c0001t0025 others(5): Show |
39 | HG00140.hp2 HG00438.hp2 HG00597.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*1283delA | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 1283 | chr5 | 153991692 | ||||||
chr5:153991692 | ATT | A | 3 | a0001c0001t0018 a0001c0001t0020 a0001c0001t0040 |
7 | HG02258.hp2 HG02615.hp1 HG02809.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1282_*1283delAA | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 1282 | chr5 | 153991692 | ||||||
chr5:153991762 | A | T | 1 | a0001c0001t0036 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1214T>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 1214 | chr5 | 153991762 | ||||||
chr5:153991828 | C | T | 1 | a0001c0001t0035 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1148G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 1148 | chr5 | 153991828 | ||||||
chr5:153991845 | C | T | 31 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(28): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
3_prime_UTR_variant | MODIFIER | c.*1131G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 1131 | chr5 | 153991845 | ||||||
chr5:153991903 | C | T | 34 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(31): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
3_prime_UTR_variant | MODIFIER | c.*1073G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 1073 | chr5 | 153991903 | ||||||
chr5:153992132 | C | G | 1 | a0001c0001t0034 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*844G>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 844 | chr5 | 153992132 | ||||||
chr5:153992200 | C | G | 3 | a0001c0001t0014 a0001c0001t0022 a0001c0007t0014 |
8 | HG00438.hp1 HG02683.hp1 HG02895.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*776G>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 776 | chr5 | 153992200 | ||||||
chr5:153992320 | G | T | 1 | a0005c0008t0021 | 2 | HG02145.hp2 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*656C>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 656 | chr5 | 153992320 | ||||||
chr5:153992529 | A | T | 4 | a0002c0002t0003 a0002c0002t0027 a0002c0002t0028 others(1): Show |
35 | HG01257.hp2 HG01928.hp2 HG02015.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*447T>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 447 | chr5 | 153992529 | ||||||
chr5:153992616 | T | C | 3 | a0001c0001t0006 a0001c0001t0040 a0001c0006t0006 |
22 | HG00438.hp2 HG02071.hp1 HG02132.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*360A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 360 | chr5 | 153992616 | ||||||
chr5:153992657 | C | T | 1 | a0001c0001t0020 | 2 | HG02258.hp2 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*319G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 319 | chr5 | 153992657 | ||||||
chr5:153992965 | G | A | 31 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(28): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
3_prime_UTR_variant | MODIFIER | c.*11C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 11 | chr5 | 153992965 | ||||||
chr5:154038885 | A | T | 1 | a0001c0001t0026 | 1 | NA19043.hp1 | 5_prime_UTR_variant | MODIFIER | c.-43T>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/14 | 3932 | chr5 | 154038885 | ||||||
chr5:154038887 | G | A | 1 | a0001c0001t0011 | 7 | HG01884.hp2 HG01981.hp2 HG02717.hp2 others(4): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-45C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/14 | chr5 | 154038887 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:153993183 | G | A | 174 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(171): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.1384-73C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 13/13 | chr5 | 153993183 | |||||||
chr5:153993187 | A | T | 1 | a0001c0001t0026g0040 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1384-77T>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 13/13 | chr5 | 153993187 | |||||||
chr5:153993193 | T | C | 17 | a0001c0001t0006g0011 a0001c0001t0006g0027 a0001c0001t0006g0028 others(14): Show |
22 | HG00438.hp2 HG02071.hp1 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.1384-83A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 13/13 | chr5 | 153993193 | |||||||
chr5:153993202 | G | A | 1 | a0002c0002t0004g0084 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1384-92C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 13/13 | chr5 | 153993202 | |||||||
chr5:153993317 | ATGTCAGC others(13): Show |
A | 4 | a0001c0001t0001g0140 a0001c0001t0005g0137 a0001c0001t0005g0141 others(1): Show |
4 | HG02109.hp1 HG02965.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1384-227_1384-208d others(22): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 13/13 | chr5 | 153993317 | |||||||
chr5:153993475 | T | C | 6 | a0004c0005t0009g0041 a0004c0005t0009g0042 a0004c0005t0009g0104 others(3): Show |
6 | HG02109.hp2 HG02630.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1384-365A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 13/13 | chr5 | 153993475 | |||||||
chr5:153993785 | C | G | 172 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(169): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.1384-675G>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 13/13 | chr5 | 153993785 | |||||||
chr5:153993786 | C | A | 2 | a0005c0008t0021g0133 a0005c0008t0021g0171 |
2 | HG02145.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1384-676G>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 13/13 | chr5 | 153993786 | |||||||
chr5:153993786 | CA | C | 7 | a0001c0001t0011g0009 a0001c0001t0011g0242 a0001c0001t0011g0243 others(4): Show |
12 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.1384-677delT | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 13/13 | chr5 | 153993786 | |||||||
chr5:153993823 | A | G | 1 | a0001c0001t0012g0100 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1384-713T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 13/13 | chr5 | 153993823 | |||||||
chr5:153994058 | A | G | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(154): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.1383+861T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 13/13 | chr5 | 153994058 | |||||||
chr5:153994464 | A | T | 4 | a0002c0002t0004g0084 a0002c0002t0010g0085 a0002c0002t0010g0086 others(1): Show |
4 | HG02615.hp2 HG02622.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1383+455T>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 13/13 | chr5 | 153994464 | |||||||
chr5:153994538 | T | C | 15 | a0001c0001t0011g0009 a0001c0001t0011g0242 a0001c0001t0011g0243 others(12): Show |
20 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.1383+381A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 13/13 | chr5 | 153994538 | |||||||
chr5:153994810 | T | C | 2 | a0001c0001t0005g0200 a0001c0001t0025g0201 |
2 | HG02486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1383+109A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 13/13 | chr5 | 153994810 | |||||||
chr5:153994836 | A | T | 1 | a0001c0001t0001g0152 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1383+83T>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 13/13 | chr5 | 153994836 | |||||||
chr5:153995047 | A | AAC | 3 | a0001c0001t0011g0009 a0001c0001t0011g0242 a0001c0001t0011g0243 |
7 | HG01884.hp2 HG01981.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1330-77_1330-76dup others(2): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153995047 | |||||||
chr5:153995068 | A | G | 1 | a0002c0002t0008g0060 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1330-96T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153995068 | |||||||
chr5:153995222 | A | G | 135 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(132): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.1330-250T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153995222 | |||||||
chr5:153995279 | T | C | 1 | a0001c0001t0005g0200 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1330-307A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153995279 | |||||||
chr5:153995332 | A | G | 174 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(171): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.1330-360T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153995332 | |||||||
chr5:153995338 | C | T | 174 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(171): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.1330-366G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153995338 | |||||||
chr5:153995475 | A | G | 17 | a0001c0001t0006g0011 a0001c0001t0006g0027 a0001c0001t0006g0028 others(14): Show |
22 | HG00438.hp2 HG02071.hp1 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.1330-503T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153995475 | |||||||
chr5:153995550 | A | T | 1 | a0002c0002t0004g0093 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1330-578T>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153995550 | |||||||
chr5:153995723 | T | C | 1 | a0001c0001t0001g0179 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1330-751A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153995723 | |||||||
chr5:153995814 | C | T | 3 | a0001c0001t0018g0126 a0001c0001t0018g0127 a0001c0001t0025g0128 |
3 | HG02809.hp2 HG02896.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1330-842G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153995814 | |||||||
chr5:153995837 | C | T | 1 | a0001c0001t0005g0146 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1330-865G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153995837 | |||||||
chr5:153996012 | A | G | 230 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(227): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.1330-1040T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153996012 | |||||||
chr5:153996021 | T | G | 1 | a0001c0001t0006g0120 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1330-1049A>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153996021 | |||||||
chr5:153996210 | T | C | 1 | a0001c0001t0018g0127 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1330-1238A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153996210 | |||||||
chr5:153996334 | C | T | 2 | a0002c0002t0004g0090 a0002c0002t0004g0091 |
2 | HG02895.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1330-1362G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153996334 | |||||||
chr5:153996406 | G | T | 8 | a0001c0001t0011g0009 a0001c0001t0011g0242 a0001c0001t0011g0243 others(5): Show |
13 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.1329+1397C>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153996406 | |||||||
chr5:153996455 | A | C | 2 | a0005c0008t0021g0133 a0005c0008t0021g0171 |
2 | HG02145.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1329+1348T>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153996455 | |||||||
chr5:153996484 | C | T | 1 | a0001c0001t0012g0101 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1329+1319G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153996484 | |||||||
chr5:153996569 | TA | T | 19 | a0001c0001t0001g0037 a0001c0001t0001g0152 a0001c0001t0001g0153 others(16): Show |
25 | HG00735.hp1 HG01884.hp2 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.1329+1233delT | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153996569 | |||||||
chr5:153996569 | TAA | T | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(154): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.1329+1232_1329+123 others(6): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153996569 | |||||||
chr5:153996594 | C | A | 1 | a0001c0001t0018g0029 | 2 | HG02615.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1329+1209G>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153996594 | |||||||
chr5:153996613 | AAAC | A | 17 | a0002c0002t0003g0002 a0002c0002t0003g0005 a0002c0002t0003g0010 others(14): Show |
35 | HG01257.hp2 HG01928.hp2 HG02015.hp2 others(32): Show |
intron_variant | MODIFIER | c.1329+1187_1329+118 others(7): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153996613 | |||||||
chr5:153996636 | G | A | 136 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(133): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.1329+1167C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153996636 | |||||||
chr5:153996754 | TG | T | 159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(156): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.1329+1048delC | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153996754 | |||||||
chr5:153996967 | A | C | 8 | a0001c0001t0011g0009 a0001c0001t0011g0242 a0001c0001t0011g0243 others(5): Show |
13 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.1329+836T>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153996967 | |||||||
chr5:153996991 | T | TA | 8 | a0002c0002t0004g0058 a0002c0002t0004g0084 a0002c0002t0004g0090 others(5): Show |
8 | HG02615.hp2 HG02717.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1329+811dupT | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153996991 | |||||||
chr5:153996991 | TA | T | 99 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(96): Show |
141 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.1329+811delT | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153996991 | |||||||
chr5:153996991 | TAA | T | 74 | a0001c0001t0001g0131 a0001c0001t0001g0154 a0001c0001t0001g0158 others(71): Show |
98 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.1329+810_1329+811d others(4): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153996991 | |||||||
chr5:153997007 | A | G | 1 | a0002c0002t0003g0052 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1329+796T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153997007 | |||||||
chr5:153997012 | A | T | 174 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(171): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.1329+791T>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153997012 | |||||||
chr5:153997553 | A | G | 211 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(208): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.1329+250T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153997553 | |||||||
chr5:153997672 | G | A | 7 | a0004c0005t0009g0041 a0004c0005t0009g0042 a0004c0005t0009g0104 others(4): Show |
7 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1329+131C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153997672 | |||||||
chr5:153997754 | C | T | 1 | a0001c0001t0015g0238 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1329+49G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153997754 | |||||||
chr5:153997778 | T | C | 15 | a0001c0001t0011g0009 a0001c0001t0011g0242 a0001c0001t0011g0243 others(12): Show |
20 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.1329+25A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153997778 | |||||||
chr5:153997788 | G | C | 1 | a0003c0004t0023g0165 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1329+15C>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153997788 | |||||||
chr5:153997917 | T | A | 3 | a0002c0002t0004g0090 a0002c0002t0004g0091 a0002c0002t0004g0093 |
3 | HG02895.hp2 HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1257-42A>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 153997917 | |||||||
chr5:153998017 | C | T | 1 | a0002c0002t0003g0050 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1257-142G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 153998017 | |||||||
chr5:153998031 | T | C | 1 | a0001c0001t0023g0130 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1257-156A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 153998031 | |||||||
chr5:153998038 | A | G | 172 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(169): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.1257-163T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 153998038 | |||||||
chr5:153998097 | T | A | 2 | a0001c0001t0020g0124 a0001c0001t0020g0125 |
2 | HG02258.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1257-222A>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 153998097 | |||||||
chr5:153998116 | A | G | 17 | a0001c0001t0006g0011 a0001c0001t0006g0027 a0001c0001t0006g0028 others(14): Show |
22 | HG00438.hp2 HG02071.hp1 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.1257-241T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 153998116 | |||||||
chr5:153998123 | T | A | 2 | a0002c0003t0004g0074 a0002c0003t0004g0079 |
2 | HG02027.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.1257-248A>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 153998123 | |||||||
chr5:153998425 | C | A | 1 | a0001c0001t0001g0220 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1257-550G>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 153998425 | |||||||
chr5:153998476 | T | G | 1 | a0001c0001t0001g0222 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1257-601A>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 153998476 | |||||||
chr5:153998539 | G | A | 1 | a0001c0007t0014g0039 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1257-664C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 153998539 | |||||||
chr5:153998846 | G | A | 15 | a0001c0001t0011g0009 a0001c0001t0011g0242 a0001c0001t0011g0243 others(12): Show |
20 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.1257-971C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 153998846 | |||||||
chr5:153998858 | G | A | 1 | a0002c0002t0010g0092 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1257-983C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 153998858 | |||||||
chr5:153999055 | G | C | 3 | a0001c0001t0001g0018 a0001c0001t0001g0037 a0001c0001t0002g0225 |
6 | HG00408.hp1 HG02040.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.1257-1180C>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 153999055 | |||||||
chr5:153999077 | T | C | 4 | a0001c0001t0001g0140 a0001c0001t0005g0137 a0001c0001t0005g0141 others(1): Show |
4 | HG02109.hp1 HG02965.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1257-1202A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 153999077 | |||||||
chr5:153999327 | G | C | 11 | a0001c0001t0002g0014 a0001c0001t0002g0030 a0001c0001t0002g0129 others(8): Show |
15 | HG01255.hp2 HG01256.hp2 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1257-1452C>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 153999327 | |||||||
chr5:153999453 | T | C | 2 | a0001c0001t0020g0124 a0001c0001t0020g0125 |
2 | HG02258.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1257-1578A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 153999453 | |||||||
chr5:153999491 | T | C | 1 | a0001c0001t0026g0040 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1257-1616A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 153999491 | |||||||
chr5:153999533 | C | T | 159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(156): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.1257-1658G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 153999533 | |||||||
chr5:153999666 | T | A | 1 | a0001c0001t0005g0177 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1257-1791A>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 153999666 | |||||||
chr5:153999686 | T | C | 1 | a0001c0001t0015g0155 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1257-1811A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 153999686 | |||||||
chr5:153999718 | A | G | 4 | a0001c0001t0018g0029 a0001c0001t0018g0126 a0001c0001t0018g0127 others(1): Show |
5 | HG02615.hp1 HG02809.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1257-1843T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 153999718 | |||||||
chr5:153999871 | T | C | 4 | a0002c0002t0003g0010 a0002c0002t0003g0048 a0002c0002t0027g0051 others(1): Show |
7 | NA18939.hp1 NA18942.hp1 NA18954.hp2 others(4): Show |
intron_variant | MODIFIER | c.1257-1996A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 153999871 | |||||||
chr5:153999925 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1257-2050C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 153999925 | |||||||
chr5:153999925 | G | GTGTGTGT others(11): Show |
3 | a0001c0001t0012g0026 a0001c0001t0012g0102 a0001c0001t0012g0103 |
4 | HG01192.hp1 HG02683.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.1257-2068_1257-205 others(22): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 153999925 | |||||||
chr5:153999972 | T | C | 15 | a0001c0001t0011g0009 a0001c0001t0011g0242 a0001c0001t0011g0243 others(12): Show |
20 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.1257-2097A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 153999972 | |||||||
chr5:154000024 | A | T | 1 | a0007c0011t0004g0098 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1257-2149T>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 154000024 | |||||||
chr5:154000045 | A | T | 1 | a0001c0001t0012g0100 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1257-2170T>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 154000045 | |||||||
chr5:154000069 | G | A | 15 | a0001c0001t0011g0009 a0001c0001t0011g0242 a0001c0001t0011g0243 others(12): Show |
20 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.1256+2182C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 154000069 | |||||||
chr5:154000462 | C | CAT | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(154): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.1256+1787_1256+178 others(6): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 154000462 | |||||||
chr5:154000506 | G | A | 8 | a0002c0002t0004g0090 a0002c0002t0004g0091 a0002c0002t0004g0093 others(5): Show |
8 | HG00140.hp2 HG00639.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.1256+1745C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 154000506 | |||||||
chr5:154000562 | C | T | 2 | a0001c0001t0020g0124 a0001c0001t0020g0125 |
2 | HG02258.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1256+1689G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 154000562 | |||||||
chr5:154000817 | A | G | 1 | a0002c0003t0004g0077 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1256+1434T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 154000817 | |||||||
chr5:154001720 | A | G | 174 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(171): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.1256+531T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 154001720 | |||||||
chr5:154002060 | G | T | 1 | a0002c0002t0010g0088 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1256+191C>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 154002060 | |||||||
chr5:154002110 | A | C | 7 | a0004c0005t0009g0041 a0004c0005t0009g0042 a0004c0005t0009g0104 others(4): Show |
7 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1256+141T>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 154002110 | |||||||
chr5:154002151 | C | T | 15 | a0001c0001t0011g0009 a0001c0001t0011g0242 a0001c0001t0011g0243 others(12): Show |
20 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.1256+100G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 154002151 | |||||||
chr5:154002438 | G | A | 17 | a0001c0001t0006g0011 a0001c0001t0006g0027 a0001c0001t0006g0028 others(14): Show |
22 | HG00438.hp2 HG02071.hp1 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.1117-48C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 10/13 | chr5 | 154002438 | |||||||
chr5:154002512 | GTCT | G | 159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(156): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.1117-125_1117-123d others(5): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 10/13 | chr5 | 154002512 | |||||||
chr5:154002564 | T | C | 159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(156): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.1117-174A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 10/13 | chr5 | 154002564 | |||||||
chr5:154002650 | A | G | 2 | a0001c0001t0020g0124 a0001c0001t0020g0125 |
2 | HG02258.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1116+197T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 10/13 | chr5 | 154002650 | |||||||
chr5:154002658 | C | T | 12 | a0002c0002t0004g0084 a0002c0002t0004g0090 a0002c0002t0004g0091 others(9): Show |
12 | HG00140.hp2 HG00639.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.1116+189G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 10/13 | chr5 | 154002658 | |||||||
chr5:154002659 | G | A | 1 | a0001c0001t0025g0201 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1116+188C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 10/13 | chr5 | 154002659 | |||||||
chr5:154002660 | C | T | 1 | a0001c0001t0005g0175 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1116+187G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 10/13 | chr5 | 154002660 | |||||||
chr5:154002738 | C | T | 15 | a0001c0001t0011g0009 a0001c0001t0011g0242 a0001c0001t0011g0243 others(12): Show |
20 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.1116+109G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 10/13 | chr5 | 154002738 | |||||||
chr5:154002786 | T | C | 1 | a0002c0003t0016g0024 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1116+61A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 10/13 | chr5 | 154002786 | |||||||
chr5:154003042 | A | G | 6 | a0003c0004t0001g0161 a0003c0004t0002g0017 a0003c0004t0002g0194 others(3): Show |
8 | HG00099.hp2 HG00323.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.994-73T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154003042 | |||||||
chr5:154003134 | T | C | 1 | a0001c0001t0001g0214 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.994-165A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154003134 | |||||||
chr5:154003177 | G | GC | 5 | a0001c0001t0001g0176 a0001c0001t0002g0197 a0001c0001t0002g0224 others(2): Show |
5 | HG01934.hp1 HG02148.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.994-209_994-208ins others(1): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154003177 | |||||||
chr5:154003177 | G | GT | 5 | a0001c0001t0006g0114 a0001c0001t0012g0026 a0001c0001t0012g0101 others(2): Show |
6 | HG01192.hp1 HG01891.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.994-209dupA | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154003177 | |||||||
chr5:154003177 | G | GTT | 4 | a0001c0001t0011g0009 a0001c0001t0011g0242 a0001c0001t0011g0243 others(1): Show |
8 | HG01884.hp2 HG01981.hp2 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.994-209_994-208ins others(2): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154003177 | |||||||
chr5:154003178 | T | C | 128 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(125): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.994-209A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154003178 | |||||||
chr5:154003178 | TA | T | 7 | a0004c0005t0009g0041 a0004c0005t0009g0042 a0004c0005t0009g0104 others(4): Show |
7 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.994-210delT | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154003178 | |||||||
chr5:154003179 | A | C | 2 | a0001c0001t0002g0234 a0001c0001t0005g0200 |
2 | HG02602.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.994-210T>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154003179 | |||||||
chr5:154003179 | A | T | 165 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(162): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.994-210T>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154003179 | |||||||
chr5:154003228 | G | T | 1 | a0001c0001t0002g0167 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.994-259C>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154003228 | |||||||
chr5:154003367 | C | T | 1 | a0002c0002t0008g0059 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.994-398G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154003367 | |||||||
chr5:154003471 | G | A | 5 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0182 others(2): Show |
5 | HG02257.hp2 HG02572.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.994-502C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154003471 | |||||||
chr5:154003489 | T | C | 17 | a0002c0002t0003g0002 a0002c0002t0003g0005 a0002c0002t0003g0010 others(14): Show |
35 | HG01257.hp2 HG01928.hp2 HG02015.hp2 others(32): Show |
intron_variant | MODIFIER | c.994-520A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154003489 | |||||||
chr5:154003575 | C | T | 1 | a0004c0005t0009g0104 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.994-606G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154003575 | |||||||
chr5:154003607 | C | T | 7 | a0001c0001t0011g0009 a0001c0001t0011g0242 a0001c0001t0011g0243 others(4): Show |
12 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.994-638G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154003607 | |||||||
chr5:154003819 | T | A | 2 | a0002c0003t0004g0023 a0002c0003t0004g0070 |
3 | HG01069.hp2 HG01071.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.994-850A>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154003819 | |||||||
chr5:154003832 | A | G | 1 | a0001c0001t0001g0228 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.994-863T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154003832 | |||||||
chr5:154003911 | T | C | 4 | a0001c0001t0018g0029 a0001c0001t0018g0126 a0001c0001t0018g0127 others(1): Show |
5 | HG02615.hp1 HG02809.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.994-942A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154003911 | |||||||
chr5:154004184 | A | G | 1 | a0001c0007t0014g0039 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.994-1215T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154004184 | |||||||
chr5:154004204 | T | C | 1 | a0001c0001t0001g0229 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.994-1235A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154004204 | |||||||
chr5:154004215 | A | T | 1 | a0002c0002t0003g0045 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.994-1246T>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154004215 | |||||||
chr5:154004470 | C | T | 1 | a0002c0003t0013g0071 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.994-1501G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154004470 | |||||||
chr5:154004567 | A | AC | 230 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(227): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.994-1599dupG | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154004567 | |||||||
chr5:154004732 | TCCTC | T | 159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(156): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.994-1767_994-1764d others(6): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154004732 | |||||||
chr5:154004885 | T | C | 1 | a0001c0001t0002g0168 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.994-1916A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154004885 | |||||||
chr5:154004912 | G | C | 7 | a0004c0005t0009g0041 a0004c0005t0009g0042 a0004c0005t0009g0104 others(4): Show |
7 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.994-1943C>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154004912 | |||||||
chr5:154005348 | C | G | 1 | a0001c0001t0026g0040 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.994-2379G>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154005348 | |||||||
chr5:154005443 | A | C | 1 | a0001c0001t0026g0040 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.994-2474T>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154005443 | |||||||
chr5:154005612 | G | C | 7 | a0001c0001t0001g0038 a0001c0001t0001g0214 a0001c0001t0001g0216 others(4): Show |
8 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(5): Show |
intron_variant | MODIFIER | c.994-2643C>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154005612 | |||||||
chr5:154005673 | C | T | 174 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(171): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.994-2704G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154005673 | |||||||
chr5:154005762 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.994-2793G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154005762 | |||||||
chr5:154005866 | G | A | 1 | a0001c0001t0012g0100 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.994-2897C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154005866 | |||||||
chr5:154006092 | C | T | 1 | a0001c0007t0014g0039 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.994-3123G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154006092 | |||||||
chr5:154006179 | T | C | 1 | a0001c0001t0012g0100 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.994-3210A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154006179 | |||||||
chr5:154006187 | T | A | 174 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(171): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.994-3218A>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154006187 | |||||||
chr5:154006192 | T | A | 1 | a0001c0001t0023g0130 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.994-3223A>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154006192 | |||||||
chr5:154006203 | C | A | 7 | a0001c0001t0011g0009 a0001c0001t0011g0242 a0001c0001t0011g0243 others(4): Show |
12 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.994-3234G>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154006203 | |||||||
chr5:154006326 | T | C | 1 | a0002c0002t0004g0091 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.994-3357A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154006326 | |||||||
chr5:154006422 | C | G | 3 | a0001c0001t0018g0126 a0001c0001t0018g0127 a0001c0001t0025g0128 |
3 | HG02809.hp2 HG02896.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.994-3453G>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154006422 | |||||||
chr5:154006444 | A | G | 6 | a0004c0005t0009g0041 a0004c0005t0009g0042 a0004c0005t0009g0104 others(3): Show |
6 | HG02109.hp2 HG02630.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.994-3475T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154006444 | |||||||
chr5:154006451 | T | C | 7 | a0004c0005t0009g0041 a0004c0005t0009g0042 a0004c0005t0009g0104 others(4): Show |
7 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.994-3482A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154006451 | |||||||
chr5:154006543 | A | G | 174 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(171): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.994-3574T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154006543 | |||||||
chr5:154006589 | A | G | 4 | a0001c0001t0012g0026 a0001c0001t0012g0101 a0001c0001t0012g0102 others(1): Show |
5 | HG01192.hp1 HG01891.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.994-3620T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154006589 | |||||||
chr5:154006597 | G | A | 2 | a0001c0001t0020g0124 a0001c0001t0020g0125 |
2 | HG02258.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.994-3628C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154006597 | |||||||
chr5:154006641 | A | G | 3 | a0002c0002t0004g0090 a0002c0002t0004g0091 a0002c0002t0004g0093 |
3 | HG02895.hp2 HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.994-3672T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154006641 | |||||||
chr5:154006751 | A | C | 1 | a0001c0001t0001g0158 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.994-3782T>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154006751 | |||||||
chr5:154006765 | G | A | 17 | a0001c0001t0006g0011 a0001c0001t0006g0027 a0001c0001t0006g0028 others(14): Show |
22 | HG00438.hp2 HG02071.hp1 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.994-3796C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154006765 | |||||||
chr5:154006773 | TA | T | 7 | a0004c0005t0009g0041 a0004c0005t0009g0042 a0004c0005t0009g0104 others(4): Show |
7 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.994-3805delT | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154006773 | |||||||
chr5:154006796 | AT | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(151): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.994-3828delA | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154006796 | |||||||
chr5:154006796 | ATT | A | 20 | a0001c0001t0001g0174 a0001c0001t0005g0148 a0001c0001t0005g0173 others(17): Show |
26 | HG01192.hp1 HG01257.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.994-3829_994-3828d others(4): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154006796 | |||||||
chr5:154007031 | A | G | 174 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(171): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.994-4062T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154007031 | |||||||
chr5:154007075 | G | C | 1 | a0001c0001t0026g0040 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.994-4106C>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154007075 | |||||||
chr5:154007131 | T | C | 1 | a0003c0004t0002g0195 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.993+4110A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154007131 | |||||||
chr5:154007336 | A | G | 1 | a0002c0002t0004g0058 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.993+3905T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154007336 | |||||||
chr5:154007428 | C | T | 1 | a0001c0001t0018g0029 | 2 | HG02615.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.993+3813G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154007428 | |||||||
chr5:154007536 | C | G | 2 | a0001c0001t0020g0124 a0001c0001t0020g0125 |
2 | HG02258.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.993+3705G>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154007536 | |||||||
chr5:154007568 | C | T | 1 | a0001c0001t0005g0200 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.993+3673G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154007568 | |||||||
chr5:154007824 | C | A | 1 | a0001c0007t0014g0039 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.993+3417G>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154007824 | |||||||
chr5:154007839 | A | G | 174 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(171): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.993+3402T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154007839 | |||||||
chr5:154008245 | A | T | 2 | a0001c0001t0002g0235 a0001c0001t0002g0236 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.993+2996T>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154008245 | |||||||
chr5:154008319 | G | A | 2 | a0001c0001t0020g0124 a0001c0001t0020g0125 |
2 | HG02258.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.993+2922C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154008319 | |||||||
chr5:154008330 | G | C | 174 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(171): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.993+2911C>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154008330 | |||||||
chr5:154008356 | C | A | 159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(156): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.993+2885G>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154008356 | |||||||
chr5:154008398 | T | C | 1 | a0001c0001t0038g0215 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.993+2843A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154008398 | |||||||
chr5:154008522 | C | T | 2 | a0002c0002t0003g0020 a0002c0002t0003g0049 |
3 | HG02083.hp2 HG02165.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.993+2719G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154008522 | |||||||
chr5:154008562 | T | A | 1 | a0004c0005t0009g0107 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.993+2679A>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154008562 | |||||||
chr5:154008646 | T | C | 1 | a0002c0002t0008g0061 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.993+2595A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154008646 | |||||||
chr5:154008658 | ACAG | A | 15 | a0001c0001t0011g0009 a0001c0001t0011g0242 a0001c0001t0011g0243 others(12): Show |
20 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.993+2580_993+2582d others(5): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154008658 | |||||||
chr5:154008674 | A | ATG | 9 | a0001c0001t0001g0144 a0002c0002t0004g0090 a0002c0002t0004g0091 others(6): Show |
9 | HG00140.hp2 HG00639.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.993+2565_993+2566d others(4): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154008674 | |||||||
chr5:154008881 | T | C | 17 | a0001c0001t0006g0011 a0001c0001t0006g0027 a0001c0001t0006g0028 others(14): Show |
22 | HG00438.hp2 HG02071.hp1 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.993+2360A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154008881 | |||||||
chr5:154008964 | T | A | 2 | a0001c0001t0014g0136 a0001c0001t0014g0170 |
2 | HG03710.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.993+2277A>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154008964 | |||||||
chr5:154009081 | G | C | 1 | a0004c0005t0009g0105 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.993+2160C>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154009081 | |||||||
chr5:154009278 | C | A | 1 | a0002c0002t0030g0068 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.993+1963G>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154009278 | |||||||
chr5:154009352 | G | A | 174 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(171): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.993+1889C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154009352 | |||||||
chr5:154009602 | T | C | 1 | a0002c0002t0007g0065 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.993+1639A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154009602 | |||||||
chr5:154009916 | G | T | 1 | a0001c0001t0001g0210 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.993+1325C>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154009916 | |||||||
chr5:154009933 | A | G | 1 | a0001c0001t0005g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.993+1308T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154009933 | |||||||
chr5:154010044 | G | A | 159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(156): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.993+1197C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154010044 | |||||||
chr5:154010171 | A | G | 1 | a0001c0001t0026g0040 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.993+1070T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154010171 | |||||||
chr5:154010205 | T | C | 7 | a0001c0001t0011g0009 a0001c0001t0011g0242 a0001c0001t0011g0243 others(4): Show |
12 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.993+1036A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154010205 | |||||||
chr5:154010221 | G | A | 174 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(171): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.993+1020C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154010221 | |||||||
chr5:154010389 | G | C | 1 | a0002c0002t0003g0048 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.993+852C>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154010389 | |||||||
chr5:154010434 | T | C | 1 | a0002c0002t0003g0052 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.993+807A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154010434 | |||||||
chr5:154010569 | T | G | 17 | a0001c0001t0006g0011 a0001c0001t0006g0027 a0001c0001t0006g0028 others(14): Show |
22 | HG00438.hp2 HG02071.hp1 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.993+672A>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154010569 | |||||||
chr5:154010636 | G | A | 4 | a0002c0002t0004g0084 a0002c0002t0010g0085 a0002c0002t0010g0086 others(1): Show |
4 | HG02615.hp2 HG02622.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.993+605C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154010636 | |||||||
chr5:154010663 | A | T | 1 | a0002c0002t0004g0084 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.993+578T>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154010663 | |||||||
chr5:154010761 | G | C | 15 | a0001c0001t0011g0009 a0001c0001t0011g0242 a0001c0001t0011g0243 others(12): Show |
20 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.993+480C>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154010761 | |||||||
chr5:154010794 | C | T | 159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(156): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.993+447G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154010794 | |||||||
chr5:154010856 | G | A | 135 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(132): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.993+385C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154010856 | |||||||
chr5:154010889 | T | A | 37 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(34): Show |
53 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.993+352A>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154010889 | |||||||
chr5:154010979 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.993+262C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154010979 | |||||||
chr5:154011010 | T | A | 1 | a0001c0001t0006g0113 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.993+231A>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154011010 | |||||||
chr5:154011115 | T | C | 1 | a0001c0001t0005g0200 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.993+126A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154011115 | |||||||
chr5:154011153 | C | G | 4 | a0001c0001t0012g0026 a0001c0001t0012g0101 a0001c0001t0012g0102 others(1): Show |
5 | HG01192.hp1 HG01891.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.993+88G>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154011153 | |||||||
chr5:154011155 | C | A | 15 | a0001c0001t0011g0009 a0001c0001t0011g0242 a0001c0001t0011g0243 others(12): Show |
20 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.993+86G>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154011155 | |||||||
chr5:154011212 | A | G | 1 | a0001c0007t0014g0039 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.993+29T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154011212 | |||||||
chr5:154011367 | G | A | 1 | a0001c0001t0006g0111 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.914-47C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154011367 | |||||||
chr5:154011621 | C | G | 2 | a0001c0001t0002g0166 a0001c0001t0002g0191 |
2 | HG01099.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.914-301G>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154011621 | |||||||
chr5:154011715 | TAAGC | T | 6 | a0002c0003t0013g0022 a0002c0003t0013g0071 a0002c0003t0013g0075 others(3): Show |
7 | HG01167.hp2 HG01169.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.914-399_914-396del others(4): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154011715 | |||||||
chr5:154011749 | G | A | 2 | a0002c0002t0007g0064 a0002c0002t0007g0065 |
2 | HG02717.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.914-429C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154011749 | |||||||
chr5:154011888 | G | A | 2 | a0001c0001t0006g0110 a0001c0001t0006g0111 |
2 | NA18968.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.914-568C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154011888 | |||||||
chr5:154011952 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.914-632C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154011952 | |||||||
chr5:154012058 | G | A | 159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(156): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.914-738C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154012058 | |||||||
chr5:154012069 | T | C | 159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(156): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.914-749A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154012069 | |||||||
chr5:154012118 | A | T | 1 | a0001c0001t0002g0196 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.914-798T>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154012118 | |||||||
chr5:154012122 | A | G | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | NA18960.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.914-802T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154012122 | |||||||
chr5:154012149 | A | G | 174 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(171): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.914-829T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154012149 | |||||||
chr5:154012218 | G | A | 4 | a0001c0001t0001g0204 a0001c0001t0001g0217 a0001c0001t0001g0218 others(1): Show |
4 | HG00423.hp2 HG02071.hp2 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.914-898C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154012218 | |||||||
chr5:154012555 | T | A | 1 | a0001c0001t0011g0242 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.914-1235A>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154012555 | |||||||
chr5:154012976 | T | C | 1 | a0001c0001t0002g0219 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.914-1656A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154012976 | |||||||
chr5:154013039 | TTA | T | 7 | a0004c0005t0009g0041 a0004c0005t0009g0042 a0004c0005t0009g0104 others(4): Show |
7 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.914-1721_914-1720d others(4): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154013039 | |||||||
chr5:154013084 | C | T | 2 | a0005c0008t0021g0133 a0005c0008t0021g0171 |
2 | HG02145.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.914-1764G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154013084 | |||||||
chr5:154013094 | G | A | 2 | a0001c0001t0002g0235 a0001c0001t0002g0236 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.914-1774C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154013094 | |||||||
chr5:154013903 | C | T | 1 | a0001c0001t0002g0162 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.914-2583G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154013903 | |||||||
chr5:154014009 | T | C | 1 | a0002c0002t0004g0058 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.914-2689A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154014009 | |||||||
chr5:154014024 | A | T | 1 | a0002c0002t0007g0065 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.914-2704T>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154014024 | |||||||
chr5:154014034 | C | T | 15 | a0001c0001t0011g0009 a0001c0001t0011g0242 a0001c0001t0011g0243 others(12): Show |
20 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.914-2714G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154014034 | |||||||
chr5:154014076 | A | G | 19 | a0002c0002t0003g0002 a0002c0002t0003g0005 a0002c0002t0003g0010 others(16): Show |
37 | HG00735.hp1 HG01257.hp2 HG01928.hp2 others(34): Show |
intron_variant | MODIFIER | c.914-2756T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154014076 | |||||||
chr5:154014359 | G | A | 159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(156): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.914-3039C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154014359 | |||||||
chr5:154014363 | A | G | 7 | a0004c0005t0009g0041 a0004c0005t0009g0042 a0004c0005t0009g0104 others(4): Show |
7 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.914-3043T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154014363 | |||||||
chr5:154014385 | A | G | 17 | a0001c0001t0006g0011 a0001c0001t0006g0027 a0001c0001t0006g0028 others(14): Show |
22 | HG00438.hp2 HG02071.hp1 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.914-3065T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154014385 | |||||||
chr5:154014604 | G | A | 136 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(133): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.914-3284C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154014604 | |||||||
chr5:154014648 | C | G | 1 | a0001c0001t0001g0209 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.914-3328G>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154014648 | |||||||
chr5:154014769 | C | T | 15 | a0001c0001t0011g0009 a0001c0001t0011g0242 a0001c0001t0011g0243 others(12): Show |
20 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.914-3449G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154014769 | |||||||
chr5:154014989 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.914-3669G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154014989 | |||||||
chr5:154015003 | G | T | 1 | a0001c0001t0026g0040 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.914-3683C>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154015003 | |||||||
chr5:154015053 | A | T | 1 | a0001c0001t0026g0040 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.914-3733T>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154015053 | |||||||
chr5:154015154 | A | G | 17 | a0001c0001t0006g0011 a0001c0001t0006g0027 a0001c0001t0006g0028 others(14): Show |
22 | HG00438.hp2 HG02071.hp1 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.914-3834T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154015154 | |||||||
chr5:154015196 | A | T | 6 | a0004c0005t0009g0041 a0004c0005t0009g0042 a0004c0005t0009g0104 others(3): Show |
6 | HG02109.hp2 HG02630.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.914-3876T>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154015196 | |||||||
chr5:154015295 | C | T | 1 | a0002c0002t0003g0048 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.914-3975G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154015295 | |||||||
chr5:154015405 | G | A | 1 | a0004c0005t0009g0107 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.914-4085C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154015405 | |||||||
chr5:154015698 | T | C | 6 | a0003c0004t0001g0161 a0003c0004t0002g0017 a0003c0004t0002g0194 others(3): Show |
8 | HG00099.hp2 HG00323.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.914-4378A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154015698 | |||||||
chr5:154015837 | G | A | 1 | a0003c0004t0001g0161 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.914-4517C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154015837 | |||||||
chr5:154015912 | T | C | 159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(156): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.914-4592A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154015912 | |||||||
chr5:154016002 | T | C | 6 | a0001c0001t0001g0140 a0001c0001t0005g0137 a0001c0001t0005g0138 others(3): Show |
6 | HG02109.hp1 HG02965.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.914-4682A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154016002 | |||||||
chr5:154016002 | T | G | 15 | a0001c0001t0011g0009 a0001c0001t0011g0242 a0001c0001t0011g0243 others(12): Show |
20 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.914-4682A>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154016002 | |||||||
chr5:154016127 | T | C | 174 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(171): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.914-4807A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154016127 | |||||||
chr5:154016221 | GCCT | G | 8 | a0001c0001t0011g0009 a0001c0001t0011g0242 a0001c0001t0011g0243 others(5): Show |
13 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.914-4904_914-4902d others(5): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154016221 | |||||||
chr5:154016239 | G | A | 3 | a0001c0001t0001g0016 a0001c0001t0001g0181 a0001c0001t0036g0143 |
5 | NA18948.hp2 NA18961.hp2 NA18972.hp2 others(2): Show |
intron_variant | MODIFIER | c.914-4919C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154016239 | |||||||
chr5:154016340 | GA | G | 7 | a0001c0001t0006g0027 a0001c0001t0006g0114 a0001c0001t0006g0119 others(4): Show |
8 | HG00438.hp2 HG02132.hp2 NA18953.hp2 others(5): Show |
intron_variant | MODIFIER | c.914-5021delT | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154016340 | |||||||
chr5:154016343 | A | G | 7 | a0001c0001t0006g0027 a0001c0001t0006g0114 a0001c0001t0006g0119 others(4): Show |
8 | HG00438.hp2 HG02132.hp2 NA18953.hp2 others(5): Show |
intron_variant | MODIFIER | c.914-5023T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154016343 | |||||||
chr5:154016360 | T | G | 174 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(171): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.914-5040A>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154016360 | |||||||
chr5:154016554 | C | A | 17 | a0001c0001t0006g0011 a0001c0001t0006g0027 a0001c0001t0006g0028 others(14): Show |
22 | HG00438.hp2 HG02071.hp1 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.914-5234G>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154016554 | |||||||
chr5:154016678 | T | G | 1 | a0001c0001t0005g0150 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.914-5358A>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154016678 | |||||||
chr5:154016710 | A | T | 1 | a0002c0002t0004g0058 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.914-5390T>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154016710 | |||||||
chr5:154016814 | G | A | 1 | a0001c0001t0015g0151 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.914-5494C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154016814 | |||||||
chr5:154016972 | G | C | 7 | a0004c0005t0009g0041 a0004c0005t0009g0042 a0004c0005t0009g0104 others(4): Show |
7 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.914-5652C>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154016972 | |||||||
chr5:154017155 | G | T | 31 | a0001c0001t0001g0131 a0001c0001t0001g0199 a0001c0001t0002g0006 others(28): Show |
44 | HG00099.hp2 HG00323.hp2 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.914-5835C>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154017155 | |||||||
chr5:154017214 | A | G | 174 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(171): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.914-5894T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154017214 | |||||||
chr5:154017346 | G | A | 1 | a0002c0003t0004g0080 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.914-6026C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154017346 | |||||||
chr5:154017373 | C | T | 23 | a0002c0003t0004g0015 a0002c0003t0004g0023 a0002c0003t0004g0025 others(20): Show |
29 | HG01069.hp2 HG01071.hp1 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.914-6053G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154017373 | |||||||
chr5:154017497 | G | A | 1 | a0001c0001t0025g0201 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.914-6177C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154017497 | |||||||
chr5:154017503 | C | CT | 159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(156): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.914-6184dupA | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154017503 | |||||||
chr5:154017518 | G | A | 1 | a0001c0007t0014g0039 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.914-6198C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154017518 | |||||||
chr5:154017592 | C | T | 6 | a0001c0001t0001g0140 a0001c0001t0005g0137 a0001c0001t0005g0138 others(3): Show |
6 | HG02109.hp1 HG02965.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.914-6272G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154017592 | |||||||
chr5:154017600 | A | G | 1 | a0001c0001t0001g0230 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.914-6280T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154017600 | |||||||
chr5:154017658 | T | C | 8 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0182 others(5): Show |
8 | HG02257.hp2 HG02258.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.914-6338A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154017658 | |||||||
chr5:154017669 | C | T | 6 | a0003c0004t0001g0161 a0003c0004t0002g0017 a0003c0004t0002g0194 others(3): Show |
8 | HG00099.hp2 HG00323.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.914-6349G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154017669 | |||||||
chr5:154017687 | T | C | 3 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0039g0208 |
3 | HG00738.hp1 HG01070.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.914-6367A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154017687 | |||||||
chr5:154017688 | A | G | 7 | a0001c0001t0011g0009 a0001c0001t0011g0242 a0001c0001t0011g0243 others(4): Show |
12 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.914-6368T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154017688 | |||||||
chr5:154017703 | C | T | 2 | a0002c0002t0010g0089 a0002c0002t0033g0095 |
2 | HG00140.hp2 HG00639.hp1 |
intron_variant | MODIFIER | c.914-6383G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154017703 | |||||||
chr5:154017711 | A | G | 1 | a0001c0001t0001g0223 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.914-6391T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154017711 | |||||||
chr5:154017758 | G | A | 3 | a0001c0001t0011g0009 a0001c0001t0011g0242 a0001c0001t0011g0243 |
7 | HG01884.hp2 HG01981.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.914-6438C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154017758 | |||||||
chr5:154017941 | C | T | 1 | a0002c0002t0004g0056 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.914-6621G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154017941 | |||||||
chr5:154017991 | G | A | 1 | a0005c0008t0021g0133 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.914-6671C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154017991 | |||||||
chr5:154018114 | C | T | 174 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(171): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.914-6794G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154018114 | |||||||
chr5:154018289 | C | G | 1 | a0002c0002t0028g0047 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.914-6969G>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154018289 | |||||||
chr5:154018349 | G | C | 6 | a0004c0005t0009g0041 a0004c0005t0009g0042 a0004c0005t0009g0104 others(3): Show |
6 | HG02109.hp2 HG02630.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.914-7029C>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154018349 | |||||||
chr5:154018610 | A | G | 2 | a0002c0002t0004g0058 a0007c0011t0004g0098 |
2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.914-7290T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154018610 | |||||||
chr5:154018804 | A | T | 4 | a0001c0001t0018g0029 a0001c0001t0018g0126 a0001c0001t0018g0127 others(1): Show |
5 | HG02615.hp1 HG02809.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.914-7484T>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154018804 | |||||||
chr5:154018880 | C | T | 17 | a0001c0001t0006g0011 a0001c0001t0006g0027 a0001c0001t0006g0028 others(14): Show |
22 | HG00438.hp2 HG02071.hp1 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.913+7519G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154018880 | |||||||
chr5:154019000 | A | T | 2 | a0001c0001t0020g0124 a0001c0001t0020g0125 |
2 | HG02258.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.913+7399T>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154019000 | |||||||
chr5:154019071 | A | C | 2 | a0002c0002t0030g0068 a0002c0002t0031g0067 |
2 | HG01081.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.913+7328T>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154019071 | |||||||
chr5:154019349 | G | T | 1 | a0001c0001t0001g0154 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.913+7050C>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154019349 | |||||||
chr5:154019359 | A | G | 23 | a0002c0003t0004g0015 a0002c0003t0004g0023 a0002c0003t0004g0025 others(20): Show |
29 | HG01069.hp2 HG01071.hp1 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.913+7040T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154019359 | |||||||
chr5:154019502 | C | A | 1 | a0001c0001t0005g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.913+6897G>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154019502 | |||||||
chr5:154019696 | T | C | 1 | a0001c0001t0012g0100 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.913+6703A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154019696 | |||||||
chr5:154019783 | A | C | 2 | a0001c0001t0005g0138 a0001c0001t0005g0139 |
2 | HG02976.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.913+6616T>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154019783 | |||||||
chr5:154019786 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.913+6613C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154019786 | |||||||
chr5:154019836 | A | G | 4 | a0001c0001t0018g0029 a0001c0001t0018g0126 a0001c0001t0018g0127 others(1): Show |
5 | HG02615.hp1 HG02809.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.913+6563T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154019836 | |||||||
chr5:154020162 | C | T | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(154): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.913+6237G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154020162 | |||||||
chr5:154020326 | C | CA | 156 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(153): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.913+6072dupT | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154020326 | |||||||
chr5:154020440 | C | T | 1 | a0001c0001t0018g0029 | 2 | HG02615.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.913+5959G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154020440 | |||||||
chr5:154020486 | T | A | 3 | a0001c0001t0018g0126 a0001c0001t0018g0127 a0001c0001t0025g0128 |
3 | HG02809.hp2 HG02896.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.913+5913A>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154020486 | |||||||
chr5:154020583 | A | G | 1 | a0001c0001t0005g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.913+5816T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154020583 | |||||||
chr5:154020757 | A | G | 1 | a0001c0001t0005g0137 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.913+5642T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154020757 | |||||||
chr5:154020867 | C | A | 135 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(132): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.913+5532G>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154020867 | |||||||
chr5:154020915 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.913+5484C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154020915 | |||||||
chr5:154020932 | A | G | 135 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(132): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.913+5467T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154020932 | |||||||
chr5:154021261 | G | A | 9 | a0001c0001t0001g0186 a0001c0001t0015g0155 a0001c0001t0015g0187 others(6): Show |
9 | HG00423.hp1 HG00597.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.913+5138C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154021261 | |||||||
chr5:154021306 | GC | G | 17 | a0001c0001t0006g0011 a0001c0001t0006g0027 a0001c0001t0006g0028 others(14): Show |
22 | HG00438.hp2 HG02071.hp1 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.913+5092delG | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154021306 | |||||||
chr5:154021448 | G | A | 1 | a0001c0001t0012g0100 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.913+4951C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154021448 | |||||||
chr5:154021567 | A | T | 23 | a0002c0003t0004g0015 a0002c0003t0004g0023 a0002c0003t0004g0025 others(20): Show |
29 | HG01069.hp2 HG01071.hp1 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.913+4832T>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154021567 | |||||||
chr5:154021571 | G | A | 3 | a0002c0003t0016g0024 a0002c0003t0016g0081 a0002c0003t0016g0082 |
4 | HG01256.hp1 HG01515.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.913+4828C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154021571 | |||||||
chr5:154021636 | C | T | 159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(156): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.913+4763G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154021636 | |||||||
chr5:154021691 | A | G | 2 | a0001c0001t0002g0162 a0001c0001t0035g0192 |
2 | HG02647.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.913+4708T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154021691 | |||||||
chr5:154021728 | T | G | 1 | a0001c0001t0012g0103 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.913+4671A>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154021728 | |||||||
chr5:154021855 | A | C | 5 | a0002c0002t0003g0005 a0002c0002t0003g0043 a0002c0002t0003g0052 others(2): Show |
11 | HG01257.hp2 HG01928.hp2 HG02074.hp1 others(8): Show |
intron_variant | MODIFIER | c.913+4544T>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154021855 | |||||||
chr5:154022129 | A | C | 92 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(89): Show |
132 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.913+4270T>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154022129 | |||||||
chr5:154022272 | A | G | 159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(156): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.913+4127T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154022272 | |||||||
chr5:154022400 | G | T | 1 | a0001c0001t0001g0189 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.913+3999C>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154022400 | |||||||
chr5:154022467 | T | C | 1 | a0001c0001t0012g0100 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.913+3932A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154022467 | |||||||
chr5:154022476 | G | T | 1 | a0001c0001t0025g0201 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.913+3923C>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154022476 | |||||||
chr5:154022490 | T | C | 174 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(171): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.913+3909A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154022490 | |||||||
chr5:154022495 | C | T | 2 | a0002c0002t0004g0058 a0007c0011t0004g0098 |
2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.913+3904G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154022495 | |||||||
chr5:154022719 | A | T | 1 | a0002c0002t0003g0046 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.913+3680T>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154022719 | |||||||
chr5:154022823 | G | A | 2 | a0001c0001t0001g0013 a0001c0001t0015g0156 |
5 | HG02630.hp2 HG02922.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.913+3576C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154022823 | |||||||
chr5:154022933 | A | G | 1 | a0001c0001t0001g0222 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.913+3466T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154022933 | |||||||
chr5:154022975 | T | C | 12 | a0002c0002t0004g0084 a0002c0002t0004g0090 a0002c0002t0004g0091 others(9): Show |
12 | HG00140.hp2 HG00639.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.913+3424A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154022975 | |||||||
chr5:154023125 | T | C | 17 | a0001c0001t0006g0011 a0001c0001t0006g0027 a0001c0001t0006g0028 others(14): Show |
22 | HG00438.hp2 HG02071.hp1 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.913+3274A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154023125 | |||||||
chr5:154023143 | A | G | 174 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(171): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.913+3256T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154023143 | |||||||
chr5:154023223 | C | A | 23 | a0002c0003t0004g0015 a0002c0003t0004g0023 a0002c0003t0004g0025 others(20): Show |
29 | HG01069.hp2 HG01071.hp1 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.913+3176G>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154023223 | |||||||
chr5:154023324 | G | T | 8 | a0001c0001t0011g0009 a0001c0001t0011g0242 a0001c0001t0011g0243 others(5): Show |
13 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.913+3075C>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154023324 | |||||||
chr5:154023390 | C | T | 1 | a0001c0001t0026g0040 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.913+3009G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154023390 | |||||||
chr5:154023463 | T | C | 1 | a0001c0001t0012g0100 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.913+2936A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154023463 | |||||||
chr5:154023510 | A | C | 7 | a0001c0001t0011g0009 a0001c0001t0011g0242 a0001c0001t0011g0243 others(4): Show |
12 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.913+2889T>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154023510 | |||||||
chr5:154023670 | T | C | 84 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(81): Show |
124 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.913+2729A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154023670 | |||||||
chr5:154023863 | C | T | 3 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0039g0208 |
3 | HG00738.hp1 HG01070.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.913+2536G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154023863 | |||||||
chr5:154023864 | T | G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(100): Show |
144 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.913+2535A>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154023864 | |||||||
chr5:154023992 | G | T | 1 | a0002c0002t0007g0065 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.913+2407C>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154023992 | |||||||
chr5:154024055 | A | G | 174 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(171): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.913+2344T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154024055 | |||||||
chr5:154024085 | C | T | 12 | a0002c0002t0004g0084 a0002c0002t0004g0090 a0002c0002t0004g0091 others(9): Show |
12 | HG00140.hp2 HG00639.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.913+2314G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154024085 | |||||||
chr5:154024108 | T | A | 1 | a0001c0001t0005g0157 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.913+2291A>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154024108 | |||||||
chr5:154024327 | A | C | 1 | a0001c0001t0001g0205 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.913+2072T>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154024327 | |||||||
chr5:154024394 | A | T | 1 | a0001c0001t0002g0163 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.913+2005T>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154024394 | |||||||
chr5:154024467 | A | G | 12 | a0002c0002t0004g0084 a0002c0002t0004g0090 a0002c0002t0004g0091 others(9): Show |
12 | HG00140.hp2 HG00639.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.913+1932T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154024467 | |||||||
chr5:154024620 | A | G | 1 | a0001c0001t0001g0172 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.913+1779T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154024620 | |||||||
chr5:154024634 | C | A | 4 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(1): Show |
4 | HG00621.hp2 NA18960.hp2 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.913+1765G>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154024634 | |||||||
chr5:154024658 | C | T | 1 | a0002c0003t0013g0075 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.913+1741G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154024658 | |||||||
chr5:154024673 | A | G | 1 | a0001c0001t0026g0040 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.913+1726T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154024673 | |||||||
chr5:154024842 | C | G | 1 | a0001c0001t0001g0204 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.913+1557G>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154024842 | |||||||
chr5:154025011 | A | C | 1 | a0001c0001t0026g0040 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.913+1388T>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154025011 | |||||||
chr5:154025139 | C | T | 1 | a0002c0002t0007g0065 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.913+1260G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154025139 | |||||||
chr5:154025141 | C | CA | 17 | a0001c0001t0006g0011 a0001c0001t0006g0027 a0001c0001t0006g0028 others(14): Show |
22 | HG00438.hp2 HG02071.hp1 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.913+1257dupT | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154025141 | |||||||
chr5:154025291 | C | CT | 160 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(157): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.913+1107dupA | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154025291 | |||||||
chr5:154025331 | A | G | 15 | a0001c0001t0011g0009 a0001c0001t0011g0242 a0001c0001t0011g0243 others(12): Show |
20 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.913+1068T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154025331 | |||||||
chr5:154025428 | G | GA | 27 | a0001c0001t0001g0131 a0001c0001t0001g0199 a0001c0001t0001g0240 others(24): Show |
39 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.913+970dupT | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154025428 | |||||||
chr5:154025502 | C | CTCATAGA others(200): Show |
1 | a0001c0001t0001g0189 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.913+896_913+897ins others(207): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154025502 | |||||||
chr5:154025525 | C | T | 174 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(171): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.913+874G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154025525 | |||||||
chr5:154025582 | A | T | 1 | a0001c0001t0002g0241 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.913+817T>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154025582 | |||||||
chr5:154025744 | C | A | 1 | a0002c0002t0003g0053 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.913+655G>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154025744 | |||||||
chr5:154025854 | T | G | 100 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(97): Show |
141 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.913+545A>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154025854 | |||||||
chr5:154026024 | G | A | 15 | a0001c0001t0011g0009 a0001c0001t0011g0242 a0001c0001t0011g0243 others(12): Show |
20 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.913+375C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154026024 | |||||||
chr5:154026094 | T | C | 174 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(171): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.913+305A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154026094 | |||||||
chr5:154026266 | T | A | 7 | a0004c0005t0009g0041 a0004c0005t0009g0042 a0004c0005t0009g0104 others(4): Show |
7 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.913+133A>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154026266 | |||||||
chr5:154026360 | C | T | 7 | a0001c0001t0014g0135 a0001c0001t0014g0136 a0001c0001t0014g0170 others(4): Show |
8 | HG00438.hp1 HG02683.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.913+39G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154026360 | |||||||
chr5:154026588 | G | A | 1 | a0001c0001t0026g0040 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.790-66C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 7/13 | chr5 | 154026588 | |||||||
chr5:154026750 | CAGTGTTT | C | 17 | a0001c0001t0006g0011 a0001c0001t0006g0027 a0001c0001t0006g0028 others(14): Show |
22 | HG00438.hp2 HG02071.hp1 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.790-235_790-229del others(7): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 7/13 | chr5 | 154026750 | |||||||
chr5:154026793 | T | C | 5 | a0002c0003t0004g0072 a0002c0003t0004g0077 a0002c0003t0004g0078 others(2): Show |
5 | HG02055.hp1 HG02257.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.790-271A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 7/13 | chr5 | 154026793 | |||||||
chr5:154026829 | C | A | 159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(156): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.790-307G>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 7/13 | chr5 | 154026829 | |||||||
chr5:154026830 | A | C | 159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(156): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.790-308T>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 7/13 | chr5 | 154026830 | |||||||
chr5:154026881 | T | TA | 165 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(162): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.789+294dupT | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 7/13 | chr5 | 154026881 | |||||||
chr5:154026881 | T | TAAA | 5 | a0002c0002t0003g0005 a0002c0002t0003g0043 a0002c0002t0003g0052 others(2): Show |
11 | HG01257.hp2 HG01928.hp2 HG02074.hp1 others(8): Show |
intron_variant | MODIFIER | c.789+292_789+294dup others(3): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 7/13 | chr5 | 154026881 | |||||||
chr5:154026924 | T | C | 1 | a0001c0007t0014g0039 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.789+252A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 7/13 | chr5 | 154026924 | |||||||
chr5:154026932 | T | G | 1 | a0001c0001t0002g0169 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.789+244A>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 7/13 | chr5 | 154026932 | |||||||
chr5:154027010 | A | C | 2 | a0002c0002t0010g0088 a0002c0002t0010g0094 |
2 | HG01255.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.789+166T>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 7/13 | chr5 | 154027010 | |||||||
chr5:154027016 | A | T | 159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(156): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.789+160T>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 7/13 | chr5 | 154027016 | |||||||
chr5:154027084 | C | T | 173 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(170): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.789+92G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 7/13 | chr5 | 154027084 | |||||||
chr5:154027381 | A | C | 1 | a0001c0001t0034g0239 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.631-47T>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 6/13 | chr5 | 154027381 | |||||||
chr5:154027401 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.631-67C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 6/13 | chr5 | 154027401 | |||||||
chr5:154027427 | G | C | 174 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(171): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.631-93C>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 6/13 | chr5 | 154027427 | |||||||
chr5:154027649 | C | T | 1 | a0001c0001t0026g0040 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.631-315G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 6/13 | chr5 | 154027649 | |||||||
chr5:154027689 | C | T | 1 | a0001c0001t0002g0191 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.631-355G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 6/13 | chr5 | 154027689 | |||||||
chr5:154027690 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.631-356C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 6/13 | chr5 | 154027690 | |||||||
chr5:154027718 | C | T | 7 | a0004c0005t0009g0041 a0004c0005t0009g0042 a0004c0005t0009g0104 others(4): Show |
7 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.631-384G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 6/13 | chr5 | 154027718 | |||||||
chr5:154027777 | A | G | 1 | a0003c0004t0001g0161 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.630+372T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 6/13 | chr5 | 154027777 | |||||||
chr5:154027837 | A | G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(100): Show |
144 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.630+312T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 6/13 | chr5 | 154027837 | |||||||
chr5:154027968 | G | C | 2 | a0001c0001t0020g0124 a0001c0001t0020g0125 |
2 | HG02258.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.630+181C>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 6/13 | chr5 | 154027968 | |||||||
chr5:154028612 | C | T | 1 | a0001c0001t0026g0040 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.496-329G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 5/13 | chr5 | 154028612 | |||||||
chr5:154028764 | A | G | 1 | a0002c0002t0004g0093 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.496-481T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 5/13 | chr5 | 154028764 | |||||||
chr5:154028827 | G | A | 2 | a0001c0001t0001g0131 a0001c0001t0001g0199 |
2 | HG03834.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.496-544C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 5/13 | chr5 | 154028827 | |||||||
chr5:154028871 | C | G | 1 | a0001c0001t0001g0202 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.496-588G>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 5/13 | chr5 | 154028871 | |||||||
chr5:154028969 | T | C | 15 | a0001c0001t0011g0009 a0001c0001t0011g0242 a0001c0001t0011g0243 others(12): Show |
20 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.495+520A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 5/13 | chr5 | 154028969 | |||||||
chr5:154028983 | G | C | 1 | a0002c0002t0007g0065 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.495+506C>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 5/13 | chr5 | 154028983 | |||||||
chr5:154029112 | C | T | 2 | a0005c0008t0021g0133 a0005c0008t0021g0171 |
2 | HG02145.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.495+377G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 5/13 | chr5 | 154029112 | |||||||
chr5:154029423 | G | C | 1 | a0002c0002t0003g0054 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.495+66C>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 5/13 | chr5 | 154029423 | |||||||
chr5:154029592 | A | C | 17 | a0001c0001t0006g0011 a0001c0001t0006g0027 a0001c0001t0006g0028 others(14): Show |
22 | HG00438.hp2 HG02071.hp1 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.404-12T>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154029592 | |||||||
chr5:154029635 | C | T | 17 | a0001c0001t0006g0011 a0001c0001t0006g0027 a0001c0001t0006g0028 others(14): Show |
22 | HG00438.hp2 HG02071.hp1 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.404-55G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154029635 | |||||||
chr5:154029995 | T | C | 15 | a0001c0001t0011g0009 a0001c0001t0011g0242 a0001c0001t0011g0243 others(12): Show |
20 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.404-415A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154029995 | |||||||
chr5:154030107 | A | G | 15 | a0001c0001t0011g0009 a0001c0001t0011g0242 a0001c0001t0011g0243 others(12): Show |
20 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.404-527T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154030107 | |||||||
chr5:154030232 | G | A | 1 | a0001c0001t0018g0029 | 2 | HG02615.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.404-652C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154030232 | |||||||
chr5:154030383 | C | T | 15 | a0001c0001t0011g0009 a0001c0001t0011g0242 a0001c0001t0011g0243 others(12): Show |
20 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.404-803G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154030383 | |||||||
chr5:154030460 | G | A | 159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(156): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.404-880C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154030460 | |||||||
chr5:154030461 | T | C | 32 | a0001c0001t0001g0131 a0001c0001t0001g0199 a0001c0001t0002g0006 others(29): Show |
45 | HG00099.hp2 HG00323.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.404-881A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154030461 | |||||||
chr5:154030616 | G | T | 2 | a0001c0001t0005g0200 a0001c0001t0025g0201 |
2 | HG02486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.404-1036C>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154030616 | |||||||
chr5:154030628 | C | A | 1 | a0002c0002t0003g0055 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.404-1048G>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154030628 | |||||||
chr5:154030628 | C | T | 1 | a0002c0002t0007g0066 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.404-1048G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154030628 | |||||||
chr5:154030629 | G | A | 1 | a0001c0001t0005g0200 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.404-1049C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154030629 | |||||||
chr5:154030660 | C | T | 159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(156): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.404-1080G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154030660 | |||||||
chr5:154030714 | C | A | 1 | a0001c0001t0014g0170 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.404-1134G>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154030714 | |||||||
chr5:154030803 | C | A | 10 | a0002c0003t0004g0015 a0002c0003t0004g0025 a0002c0003t0004g0063 others(7): Show |
14 | HG01256.hp1 HG01361.hp1 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.404-1223G>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154030803 | |||||||
chr5:154030855 | G | A | 7 | a0004c0005t0009g0041 a0004c0005t0009g0042 a0004c0005t0009g0104 others(4): Show |
7 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.404-1275C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154030855 | |||||||
chr5:154030862 | TGA | T | 3 | a0001c0001t0006g0112 a0001c0001t0006g0113 a0001c0001t0006g0117 |
3 | HG02071.hp1 NA18977.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.404-1284_404-1283d others(4): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154030862 | |||||||
chr5:154030937 | G | A | 1 | a0001c0001t0026g0040 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.404-1357C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154030937 | |||||||
chr5:154030944 | C | G | 15 | a0001c0001t0011g0009 a0001c0001t0011g0242 a0001c0001t0011g0243 others(12): Show |
20 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.404-1364G>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154030944 | |||||||
chr5:154030995 | T | C | 3 | a0002c0003t0016g0024 a0002c0003t0016g0081 a0002c0003t0016g0082 |
4 | HG01256.hp1 HG01515.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.404-1415A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154030995 | |||||||
chr5:154031080 | G | T | 1 | a0001c0001t0022g0132 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.404-1500C>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154031080 | |||||||
chr5:154031312 | C | CA | 20 | a0002c0002t0003g0002 a0002c0002t0003g0005 a0002c0002t0003g0010 others(17): Show |
38 | HG00735.hp1 HG01257.hp2 HG01928.hp2 others(35): Show |
intron_variant | MODIFIER | c.404-1733dupT | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154031312 | |||||||
chr5:154031312 | C | CAAAAAAA others(2): Show |
3 | a0001c0001t0011g0009 a0001c0001t0011g0242 a0001c0001t0012g0100 |
7 | HG01884.hp2 HG01981.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.404-1741_404-1733d others(11): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154031312 | |||||||
chr5:154031312 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0011g0243 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.404-1742_404-1733d others(12): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154031312 | |||||||
chr5:154031312 | C | CAAAAAAA others(4): Show |
6 | a0001c0001t0001g0131 a0004c0005t0009g0041 a0004c0005t0009g0104 others(3): Show |
6 | HG02280.hp2 HG02630.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.404-1743_404-1733d others(13): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154031312 | |||||||
chr5:154031312 | C | CAAAAAAA others(5): Show |
87 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(84): Show |
129 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.404-1744_404-1733d others(14): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154031312 | |||||||
chr5:154031312 | C | CAAAAAAA others(6): Show |
68 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0037 others(65): Show |
81 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.404-1745_404-1733d others(15): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154031312 | |||||||
chr5:154031312 | C | CAAAAAAA others(7): Show |
20 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0202 others(17): Show |
25 | HG00639.hp1 HG01123.hp2 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.404-1746_404-1733d others(16): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154031312 | |||||||
chr5:154031312 | C | CAAAAAAA others(8): Show |
3 | a0002c0003t0004g0025 a0002c0003t0004g0063 a0002c0003t0016g0082 |
4 | HG01361.hp1 HG01433.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.404-1747_404-1733d others(17): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154031312 | |||||||
chr5:154031312 | C | CAAAAAAA others(11): Show |
7 | a0001c0001t0006g0027 a0001c0001t0006g0028 a0001c0001t0006g0112 others(4): Show |
9 | HG02071.hp1 HG02132.hp2 NA18952.hp1 others(6): Show |
intron_variant | MODIFIER | c.404-1733_404-1732i others(20): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154031312 | |||||||
chr5:154031312 | C | CAAAAAAA others(12): Show |
6 | a0001c0001t0006g0011 a0001c0001t0006g0117 a0001c0001t0006g0119 others(3): Show |
9 | HG00438.hp2 HG02155.hp1 NA18963.hp1 others(6): Show |
intron_variant | MODIFIER | c.404-1733_404-1732i others(21): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154031312 | |||||||
chr5:154031312 | C | CAAAAAAA others(13): Show |
2 | a0001c0001t0006g0122 a0001c0001t0006g0123 |
2 | NA18953.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.404-1733_404-1732i others(22): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154031312 | |||||||
chr5:154031330 | C | T | 1 | a0001c0001t0023g0130 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.404-1750G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154031330 | |||||||
chr5:154031374 | G | A | 135 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(132): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.404-1794C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154031374 | |||||||
chr5:154031500 | A | T | 1 | a0001c0001t0012g0100 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.404-1920T>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154031500 | |||||||
chr5:154031861 | A | G | 8 | a0001c0001t0011g0009 a0001c0001t0011g0242 a0001c0001t0011g0243 others(5): Show |
13 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.403+1930T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154031861 | |||||||
chr5:154031865 | T | G | 1 | a0001c0001t0023g0130 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.403+1926A>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154031865 | |||||||
chr5:154031980 | C | T | 4 | a0002c0002t0004g0084 a0002c0002t0010g0085 a0002c0002t0010g0086 others(1): Show |
4 | HG02615.hp2 HG02622.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.403+1811G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154031980 | |||||||
chr5:154032363 | T | C | 1 | a0001c0001t0026g0040 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.403+1428A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154032363 | |||||||
chr5:154032413 | G | A | 8 | a0002c0002t0004g0090 a0002c0002t0004g0091 a0002c0002t0004g0093 others(5): Show |
8 | HG00140.hp2 HG00639.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.403+1378C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154032413 | |||||||
chr5:154032418 | A | G | 4 | a0002c0002t0004g0084 a0002c0002t0010g0085 a0002c0002t0010g0086 others(1): Show |
4 | HG02615.hp2 HG02622.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.403+1373T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154032418 | |||||||
chr5:154032421 | T | C | 2 | a0001c0001t0020g0124 a0001c0001t0020g0125 |
2 | HG02258.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.403+1370A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154032421 | |||||||
chr5:154032521 | T | C | 1 | a0001c0001t0018g0029 | 2 | HG02615.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.403+1270A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154032521 | |||||||
chr5:154032524 | T | C | 1 | a0002c0003t0004g0083 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.403+1267A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154032524 | |||||||
chr5:154032625 | C | G | 174 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(171): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.403+1166G>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154032625 | |||||||
chr5:154032921 | G | A | 19 | a0002c0002t0003g0002 a0002c0002t0003g0005 a0002c0002t0003g0010 others(16): Show |
37 | HG00735.hp1 HG01257.hp2 HG01928.hp2 others(34): Show |
intron_variant | MODIFIER | c.403+870C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154032921 | |||||||
chr5:154032969 | G | A | 188 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(185): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.403+822C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154032969 | |||||||
chr5:154033285 | G | A | 159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(156): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.403+506C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154033285 | |||||||
chr5:154033363 | G | A | 1 | a0001c0001t0001g0230 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.403+428C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154033363 | |||||||
chr5:154033522 | T | C | 37 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(34): Show |
53 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.403+269A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154033522 | |||||||
chr5:154033688 | G | A | 2 | a0002c0003t0013g0097 a0002c0003t0032g0096 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.403+103C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154033688 | |||||||
chr5:154033706 | T | A | 1 | a0001c0001t0005g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.403+85A>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154033706 | |||||||
chr5:154034982 | G | GC | 15 | a0001c0001t0011g0009 a0001c0001t0011g0242 a0001c0001t0011g0243 others(12): Show |
20 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-14-16dupG | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154034982 | |||||||
chr5:154034985 | C | CA | 158 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(155): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.-14-19dupT | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154034985 | |||||||
chr5:154034986 | A | C | 1 | a0004c0005t0009g0104 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-14-19T>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154034986 | |||||||
chr5:154035074 | G | A | 1 | a0002c0002t0004g0056 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-14-107C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154035074 | |||||||
chr5:154035212 | C | T | 15 | a0001c0001t0011g0009 a0001c0001t0011g0242 a0001c0001t0011g0243 others(12): Show |
20 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-14-245G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154035212 | |||||||
chr5:154035273 | C | T | 2 | a0002c0002t0007g0064 a0002c0002t0007g0065 |
2 | HG02717.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-14-306G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154035273 | |||||||
chr5:154035539 | T | G | 1 | a0007c0011t0004g0098 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-14-572A>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154035539 | |||||||
chr5:154035676 | A | T | 1 | a0002c0002t0003g0045 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-14-709T>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154035676 | |||||||
chr5:154035759 | T | A | 17 | a0001c0001t0006g0011 a0001c0001t0006g0027 a0001c0001t0006g0028 others(14): Show |
22 | HG00438.hp2 HG02071.hp1 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.-14-792A>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154035759 | |||||||
chr5:154035915 | T | A | 15 | a0001c0001t0011g0009 a0001c0001t0011g0242 a0001c0001t0011g0243 others(12): Show |
20 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-14-948A>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154035915 | |||||||
chr5:154035922 | T | C | 174 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(171): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.-14-955A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154035922 | |||||||
chr5:154036045 | G | T | 2 | a0002c0003t0004g0063 a0002c0003t0019g0062 |
2 | NA18965.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.-14-1078C>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154036045 | |||||||
chr5:154036137 | T | C | 155 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(152): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.-14-1170A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154036137 | |||||||
chr5:154036269 | T | A | 5 | a0001c0001t0002g0233 a0001c0001t0002g0234 a0001c0001t0002g0235 others(2): Show |
5 | HG01516.hp1 HG01891.hp1 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14-1302A>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154036269 | |||||||
chr5:154036283 | T | A | 238 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(235): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.-14-1316A>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154036283 | |||||||
chr5:154036469 | C | T | 2 | a0001c0001t0002g0030 a0001c0001t0002g0129 |
3 | HG04204.hp1 HG04228.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-14-1502G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154036469 | |||||||
chr5:154036533 | T | C | 1 | a0001c0001t0018g0029 | 2 | HG02615.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-14-1566A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154036533 | |||||||
chr5:154036572 | G | A | 155 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(152): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.-14-1605C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154036572 | |||||||
chr5:154036668 | G | GA | 8 | a0001c0001t0011g0009 a0001c0001t0011g0242 a0001c0001t0011g0243 others(5): Show |
14 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.-14-1702dupT | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154036668 | |||||||
chr5:154036806 | G | A | 170 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(167): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.-14-1839C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154036806 | |||||||
chr5:154036859 | T | TA | 15 | a0001c0001t0011g0009 a0001c0001t0011g0242 a0001c0001t0011g0243 others(12): Show |
20 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-14-1893dupT | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154036859 | |||||||
chr5:154037079 | G | A | 1 | a0002c0002t0004g0057 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-15+1778C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154037079 | |||||||
chr5:154037248 | A | G | 2 | a0001c0001t0020g0124 a0001c0001t0020g0125 |
2 | HG02258.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-15+1609T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154037248 | |||||||
chr5:154037428 | T | C | 1 | a0001c0001t0015g0238 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-15+1429A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154037428 | |||||||
chr5:154037448 | C | T | 17 | a0001c0001t0006g0011 a0001c0001t0006g0027 a0001c0001t0006g0028 others(14): Show |
22 | HG00438.hp2 HG02071.hp1 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.-15+1409G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154037448 | |||||||
chr5:154037617 | C | A | 1 | a0002c0002t0007g0099 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-15+1240G>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154037617 | |||||||
chr5:154037742 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-15+1115G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154037742 | |||||||
chr5:154037780 | G | A | 1 | a0001c0001t0034g0239 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-15+1077C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154037780 | |||||||
chr5:154037814 | A | G | 1 | a0002c0002t0004g0058 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-15+1043T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154037814 | |||||||
chr5:154037868 | C | T | 8 | a0001c0001t0011g0009 a0001c0001t0011g0242 a0001c0001t0011g0243 others(5): Show |
13 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.-15+989G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154037868 | |||||||
chr5:154038049 | A | G | 19 | a0002c0002t0003g0002 a0002c0002t0003g0005 a0002c0002t0003g0010 others(16): Show |
37 | HG00735.hp1 HG01257.hp2 HG01928.hp2 others(34): Show |
intron_variant | MODIFIER | c.-15+808T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154038049 | |||||||
chr5:154038085 | A | G | 2 | a0002c0002t0003g0043 a0002c0002t0029g0044 |
2 | NA18969.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.-15+772T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154038085 | |||||||
chr5:154038161 | T | C | 174 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(171): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.-15+696A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154038161 | |||||||
chr5:154038245 | C | T | 1 | a0002c0002t0003g0002 | 4 | NA18946.hp2 NA18982.hp1 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+612G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154038245 | |||||||
chr5:154038255 | T | C | 15 | a0001c0001t0011g0009 a0001c0001t0011g0242 a0001c0001t0011g0243 others(12): Show |
20 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-15+602A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154038255 | |||||||
chr5:154038399 | T | G | 159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(156): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.-15+458A>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154038399 | |||||||
chr5:154038546 | T | C | 1 | a0001c0001t0001g0240 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-15+311A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154038546 | |||||||
chr5:154038685 | ATTCCTCA others(15): Show |
A | 1 | a0001c0001t0002g0241 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-15+150_-15+171del others(22): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154038685 | |||||||
chr5:154038828 | C | T | 2 | a0004c0005t0009g0041 a0004c0005t0009g0042 |
2 | HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-15+29G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154038828 |