Item | Value |
---|---|
geneid | 123876 |
ensemblid | ENSG00000183747.12 |
hgncid | 32017 |
symbol | ACSM2A |
name | acyl-CoA synthetase medium chain family member 2A |
refseq_nuc | NM_001308172.2 |
refseq_prot | NP_001295101.1 |
ensembl_nuc | ENST00000573854.6 |
ensembl_prot | ENSP00000459451.1 |
mane_status | MANE Select |
chr | chr16 |
start | 20451521 |
end | 20487669 |
strand | + |
ver | v1.2 |
region | chr16:20451521-20487669 |
region5000 | chr16:20446521-20492669 |
regionname0 | ACSM2A_chr16_20451521_20487669 |
regionname5000 | ACSM2A_chr16_20446521_20492669 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 577 | 110 | 19 | 50 | 20 | 8 | 13 | 14 | ACSM2A_chr16_20446521_20492669 | ACSM2A | MHWLR others(572): Show |
chr16 | 20446521 | 20492669 |
a0002 | 0/0 | 577 | 90 | 0 | 8 | 68 | 4 | 10 | 57 | ACSM2A_chr16_20446521_20492669 | ACSM2A | MHWLQ others(572): Show |
chr16 | 20446521 | 20492669 |
a0003 | 0/1 | 577 | 71 | 44 | 5 | 13 | 1 | 7 | 12 | ACSM2A_chr16_20446521_20492669 | ACSM2A | MHWLR others(572): Show |
chr16 | 20446521 | 20492669 |
a0004 | 0/0 | 577 | 51 | 8 | 6 | 31 | 1 | 5 | 24 | ACSM2A_chr16_20446521_20492669 | ACSM2A | MHWLR others(572): Show |
chr16 | 20446521 | 20492669 |
a0005 | 1/0 | 577 | 34 | 1 | 4 | 22 | 2 | 4 | 13 | ACSM2A_chr16_20446521_20492669 | ACSM2A | MHWLR others(572): Show |
chr16 | 20446521 | 20492669 |
a0006 | 0/0 | 114 | 34 | 0 | 0 | 33 | 0 | 1 | 29 | ACSM2A_chr16_20446521_20492669 | ACSM2A | MHWLR others(109): Show |
chr16 | 20446521 | 20492669 |
a0007 | 0/0 | 577 | 12 | 9 | 3 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | MHWLR others(572): Show |
chr16 | 20446521 | 20492669 |
a0008 | 0/0 | 577 | 8 | 2 | 3 | 3 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | MHWLR others(572): Show |
chr16 | 20446521 | 20492669 |
a0009 | 0/0 | 577 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | MHWLR others(572): Show |
chr16 | 20446521 | 20492669 |
a0010 | 0/0 | 577 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | MHWLR others(572): Show |
chr16 | 20446521 | 20492669 |
a0011 | 0/0 | 577 | 4 | 0 | 0 | 0 | 0 | 4 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | MHWLR others(572): Show |
chr16 | 20446521 | 20492669 |
a0012 | 0/0 | 577 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ACSM2A_chr16_20446521_20492669 | ACSM2A | MHWLQ others(572): Show |
chr16 | 20446521 | 20492669 |
a0013 | 0/0 | 577 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | MHWLR others(572): Show |
chr16 | 20446521 | 20492669 |
a0014 | 0/0 | 577 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | MHWLR others(572): Show |
chr16 | 20446521 | 20492669 |
a0015 | 0/0 | 577 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | MHWLR others(572): Show |
chr16 | 20446521 | 20492669 |
a0016 | 0/0 | 577 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | MHWLR others(572): Show |
chr16 | 20446521 | 20492669 |
a0017 | 0/0 | 577 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | MHWLQ others(572): Show |
chr16 | 20446521 | 20492669 |
a0018 | 0/0 | 577 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | MHWLR others(572): Show |
chr16 | 20446521 | 20492669 |
a0019 | 0/0 | 577 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | MHWLQ others(572): Show |
chr16 | 20446521 | 20492669 |
a0020 | 0/0 | 577 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | MHWLR others(572): Show |
chr16 | 20446521 | 20492669 |
a0021 | 0/0 | 69 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | MHWLQ others(64): Show |
chr16 | 20446521 | 20492669 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1731 | 107 | 17 | 49 | 20 | 8 | 13 | ACSM2A_chr16_20446521_20492669 | ACSM2A | ATGCA others(1726): Show |
chr16 | 20446521 | 20492669 | ||
a0001c0017 | 0/0 | 1731 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | ATGCA others(1726): Show |
chr16 | 20446521 | 20492669 | ||
a0001c0018 | 0/0 | 1731 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | ATGCA others(1726): Show |
chr16 | 20446521 | 20492669 | ||
a0002c0002 | 0/0 | 1731 | 89 | 0 | 8 | 67 | 4 | 10 | ACSM2A_chr16_20446521_20492669 | ACSM2A | ATGCA others(1726): Show |
chr16 | 20446521 | 20492669 | ||
a0002c0022 | 0/0 | 1731 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | ATGCA others(1726): Show |
chr16 | 20446521 | 20492669 | ||
a0003c0003 | 0/1 | 1731 | 61 | 35 | 5 | 13 | 1 | 6 | ACSM2A_chr16_20446521_20492669 | ACSM2A | ATGCA others(1726): Show |
chr16 | 20446521 | 20492669 | ||
a0003c0010 | 0/0 | 1731 | 6 | 6 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | ATGCA others(1726): Show |
chr16 | 20446521 | 20492669 | ||
a0003c0015 | 0/0 | 1731 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | ATGCA others(1726): Show |
chr16 | 20446521 | 20492669 | ||
a0003c0023 | 0/0 | 1731 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | ATGCA others(1726): Show |
chr16 | 20446521 | 20492669 | ||
a0003c0026 | 0/0 | 1731 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | ATGCA others(1726): Show |
chr16 | 20446521 | 20492669 | ||
a0004c0004 | 0/0 | 1731 | 49 | 6 | 6 | 31 | 1 | 5 | ACSM2A_chr16_20446521_20492669 | ACSM2A | ATGCA others(1726): Show |
chr16 | 20446521 | 20492669 | ||
a0004c0014 | 0/0 | 1731 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | ATGCA others(1726): Show |
chr16 | 20446521 | 20492669 | ||
a0005c0005 | 1/0 | 1731 | 34 | 1 | 4 | 22 | 2 | 4 | ACSM2A_chr16_20446521_20492669 | ACSM2A | ATGCA others(1726): Show |
chr16 | 20446521 | 20492669 | ||
a0006c0006 | 0/0 | 1731 | 32 | 0 | 0 | 31 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | ATGCA others(1726): Show |
chr16 | 20446521 | 20492669 | ||
a0006c0016 | 0/0 | 1731 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | ATGCA others(1726): Show |
chr16 | 20446521 | 20492669 | ||
a0007c0007 | 0/0 | 1731 | 12 | 9 | 3 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | ATGCA others(1726): Show |
chr16 | 20446521 | 20492669 | ||
a0008c0008 | 0/0 | 1731 | 8 | 2 | 3 | 3 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | ATGCA others(1726): Show |
chr16 | 20446521 | 20492669 | ||
a0009c0009 | 0/0 | 1731 | 7 | 7 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | ATGCA others(1726): Show |
chr16 | 20446521 | 20492669 | ||
a0010c0011 | 0/0 | 1731 | 4 | 4 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | ATGCA others(1726): Show |
chr16 | 20446521 | 20492669 | ||
a0011c0012 | 0/0 | 1731 | 4 | 0 | 0 | 0 | 0 | 4 | ACSM2A_chr16_20446521_20492669 | ACSM2A | ATGCA others(1726): Show |
chr16 | 20446521 | 20492669 | ||
a0012c0013 | 0/0 | 1731 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | ATGCA others(1726): Show |
chr16 | 20446521 | 20492669 | ||
a0013c0030 | 0/0 | 1731 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | ATGCA others(1726): Show |
chr16 | 20446521 | 20492669 | ||
a0014c0027 | 0/0 | 1731 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | ATGCA others(1726): Show |
chr16 | 20446521 | 20492669 | ||
a0015c0028 | 0/0 | 1731 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | ATGCA others(1726): Show |
chr16 | 20446521 | 20492669 | ||
a0016c0025 | 0/0 | 1731 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | ATGCA others(1726): Show |
chr16 | 20446521 | 20492669 | ||
a0017c0019 | 0/0 | 1731 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | ATGCA others(1726): Show |
chr16 | 20446521 | 20492669 | ||
a0018c0024 | 0/0 | 1731 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | ATGCA others(1726): Show |
chr16 | 20446521 | 20492669 | ||
a0019c0021 | 0/0 | 1731 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | ATGCA others(1726): Show |
chr16 | 20446521 | 20492669 | ||
a0020c0029 | 0/0 | 1731 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | ATGCA others(1726): Show |
chr16 | 20446521 | 20492669 | ||
a0021c0020 | 0/0 | 1731 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | ATGCA others(1726): Show |
chr16 | 20446521 | 20492669 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2894 | 91 | 10 | 45 | 17 | 7 | 12 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0001c0001t0004 | 0/0 | 2894 | 6 | 0 | 4 | 0 | 1 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0001c0001t0006 | 0/0 | 2894 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0001c0001t0010 | 0/0 | 2894 | 5 | 5 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0001c0001t0024 | 0/0 | 2894 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0001c0001t0025 | 0/0 | 2894 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0001c0001t0026 | 0/0 | 2894 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0001c0001t0027 | 0/0 | 2894 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0001c0017t0001 | 0/0 | 2894 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0001c0018t0001 | 0/0 | 2894 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0002c0002t0002 | 0/0 | 2894 | 9 | 0 | 2 | 6 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0002c0002t0003 | 0/0 | 2894 | 63 | 0 | 4 | 48 | 4 | 7 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0002c0002t0007 | 0/0 | 2894 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0002c0002t0008 | 0/0 | 2894 | 7 | 0 | 0 | 7 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0002c0002t0009 | 0/0 | 2894 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0002c0002t0014 | 0/0 | 2894 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0002c0002t0015 | 0/0 | 2894 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0002c0002t0017 | 0/0 | 2894 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0002c0002t0018 | 0/0 | 2894 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0002c0002t0021 | 0/0 | 2894 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0002c0002t0022 | 0/0 | 2894 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0002c0022t0003 | 0/0 | 2894 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0003c0003t0002 | 0/0 | 2894 | 33 | 19 | 1 | 10 | 0 | 3 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0003c0003t0003 | 0/1 | 2894 | 9 | 0 | 4 | 1 | 1 | 2 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0003c0003t0005 | 0/0 | 2894 | 11 | 11 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0003c0003t0007 | 0/0 | 2894 | 5 | 5 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0003c0003t0009 | 0/0 | 2894 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0003c0003t0012 | 0/0 | 2894 | 2 | 0 | 0 | 1 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0003c0010t0001 | 0/0 | 2894 | 4 | 4 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0003c0010t0006 | 0/0 | 2894 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0003c0015t0001 | 0/0 | 2894 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0003c0023t0002 | 0/0 | 2894 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0003c0026t0007 | 0/0 | 2894 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0004c0004t0002 | 0/0 | 2894 | 47 | 4 | 6 | 31 | 1 | 5 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0004c0004t0013 | 0/0 | 2894 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0004c0014t0001 | 0/0 | 2894 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0005c0005t0001 | 0/0 | 2894 | 18 | 1 | 3 | 12 | 0 | 2 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0005c0005t0004 | 1/0 | 2894 | 11 | 0 | 0 | 9 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0005c0005t0016 | 0/0 | 2894 | 2 | 0 | 0 | 0 | 2 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0005c0005t0029 | 0/0 | 2894 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0005c0005t0030 | 0/0 | 2894 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0005c0005t0032 | 0/0 | 2894 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0006c0006t0002 | 0/0 | 2894 | 21 | 0 | 0 | 20 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0006c0006t0003 | 0/0 | 2894 | 7 | 0 | 0 | 7 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0006c0006t0009 | 0/0 | 2894 | 3 | 0 | 0 | 3 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0006c0006t0019 | 0/0 | 2894 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0006c0016t0002 | 0/0 | 2894 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0007c0007t0001 | 0/0 | 2894 | 7 | 4 | 3 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0007c0007t0011 | 0/0 | 2894 | 3 | 3 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0007c0007t0023 | 0/0 | 2894 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0007c0007t0028 | 0/0 | 2894 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0008c0008t0001 | 0/0 | 2894 | 8 | 2 | 3 | 3 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0009c0009t0001 | 0/0 | 2894 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0009c0009t0006 | 0/0 | 2894 | 6 | 6 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0010c0011t0005 | 0/0 | 2894 | 3 | 3 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0010c0011t0007 | 0/0 | 2894 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0011c0012t0001 | 0/0 | 2894 | 4 | 0 | 0 | 0 | 0 | 4 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0012c0013t0002 | 0/0 | 2894 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0013c0030t0031 | 0/0 | 2894 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0014c0027t0020 | 0/0 | 2894 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0015c0028t0001 | 0/0 | 2894 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0016c0025t0005 | 0/0 | 2894 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0017c0019t0003 | 0/0 | 2894 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0018c0024t0002 | 0/0 | 2894 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0019c0021t0002 | 0/0 | 2894 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0020c0029t0001 | 0/0 | 2894 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
a0021c0020t0003 | 0/0 | 2894 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | AATGA others(2889): Show |
chr16 | 20446521 | 20492669 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0003 | 0/0 | 5 | 1 | 1 | 0 | 1 | 2 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0004 | 0/0 | 5 | 1 | 4 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0005 | 0/0 | 5 | 0 | 3 | 0 | 2 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0004g0024 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0004g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0004g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0004g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0004g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0006g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0010g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0010g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0010g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0010g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0010g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0024g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0025g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0026g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0027g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0017t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0017t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0018t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0002g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0006 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0031 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0007g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0008g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0008g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0008g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0008g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0008g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0009g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0014g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0015g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0015g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0017g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0018g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0021g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0022g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0022t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0002g0037 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0002g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0002g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0002g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0002g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0002g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0002g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0002g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0002g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0002g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0002g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0002g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0002g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0003g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0003g0182 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0003g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0003g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0003g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0003g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0003g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0003g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0005g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0005g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0005g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0005g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0005g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0005g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0005g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0005g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0005g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0007g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0007g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0007g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0009g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0012g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0012g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0010t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0010t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0010t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0010t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0010t0006g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0010t0006g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0015t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0015t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0023t0002g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0026t0007g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0002 | 0/0 | 6 | 0 | 0 | 5 | 1 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0013g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0013g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0014t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0014t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0005c0005t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0005c0005t0001g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0005c0005t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0005c0005t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0005c0005t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0005c0005t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0005c0005t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0005c0005t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0005c0005t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0005c0005t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0005c0005t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0005c0005t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0005c0005t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0005c0005t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0005c0005t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0005c0005t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0005c0005t0004g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0005c0005t0004g0043 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0005c0005t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0005c0005t0004g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0005c0005t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0005c0005t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0005c0005t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0005c0005t0004g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0005c0005t0004g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0005c0005t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0005c0005t0016g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0005c0005t0016g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0005c0005t0029g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0005c0005t0030g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0005c0005t0032g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0006c0006t0002g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0006c0006t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0006c0006t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0006c0006t0002g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0006c0006t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0006c0006t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0006c0006t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0006c0006t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0006c0006t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0006c0006t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0006c0006t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0006c0006t0002g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0006c0006t0002g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0006c0006t0002g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0006c0006t0002g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0006c0006t0002g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0006c0006t0002g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0006c0006t0002g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0006c0006t0002g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0006c0006t0003g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0006c0006t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0006c0006t0003g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0006c0006t0003g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0006c0006t0003g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0006c0006t0009g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0006c0006t0009g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0006c0006t0009g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0006c0006t0019g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0006c0016t0002g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0006c0016t0002g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0007c0007t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0007c0007t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0007c0007t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0007c0007t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0007c0007t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0007c0007t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0007c0007t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0007c0007t0011g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0007c0007t0011g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0007c0007t0023g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0007c0007t0028g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0008c0008t0001g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0008c0008t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0008c0008t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0008c0008t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0008c0008t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0008c0008t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0008c0008t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0009c0009t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0009c0009t0006g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0009c0009t0006g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0009c0009t0006g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0009c0009t0006g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0009c0009t0006g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0010c0011t0005g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0010c0011t0005g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0010c0011t0005g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0010c0011t0007g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0011c0012t0001g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0011c0012t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0011c0012t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0012c0013t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0012c0013t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0013c0030t0031g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0014c0027t0020g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0015c0028t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0016c0025t0005g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0017c0019t0003g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0018c0024t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0019c0021t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0020c0029t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0021c0020t0003g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0005 | c0005 | t0016 | g0125 | EUR | GBR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0052 | EUR | GBR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00140 | hp2 | a0004 | c0004 | t0002 | g0002 | EUR | GBR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0108 | EUR | FIN | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00280 | hp2 | a0002 | c0002 | t0003 | g0229 | EUR | FIN | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00323 | hp1 | a0005 | c0005 | t0016 | g0126 | EUR | FIN | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0103 | EUR | FIN | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00408 | hp1 | a0004 | c0004 | t0002 | g0002 | EAS | CHS | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00408 | hp2 | a0002 | c0002 | t0003 | g0202 | EAS | CHS | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00423 | hp1 | a0005 | c0005 | t0001 | g0122 | EAS | CHS | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | CHS | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00438 | hp1 | a0002 | c0002 | t0003 | g0012 | EAS | CHS | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00438 | hp2 | a0005 | c0005 | t0001 | g0020 | EAS | CHS | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00544 | hp2 | a0005 | c0005 | t0004 | g0068 | EAS | CHS | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00558 | hp1 | a0001 | c0001 | t0027 | g0141 | EAS | CHS | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00558 | hp2 | a0004 | c0004 | t0002 | g0312 | EAS | CHS | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00609 | hp1 | a0008 | c0008 | t0001 | g0140 | EAS | CHS | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00609 | hp2 | a0002 | c0002 | t0002 | g0209 | EAS | CHS | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00621 | hp1 | a0004 | c0004 | t0002 | g0304 | EAS | CHS | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00621 | hp2 | a0005 | c0005 | t0001 | g0045 | EAS | CHS | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00639 | hp1 | a0001 | c0001 | t0004 | g0110 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00673 | hp1 | a0002 | c0002 | t0015 | g0012 | EAS | CHS | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00673 | hp2 | a0006 | c0006 | t0002 | g0015 | EAS | CHS | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00733 | hp1 | a0002 | c0002 | t0017 | g0225 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00733 | hp2 | a0001 | c0001 | t0004 | g0116 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00735 | hp1 | a0005 | c0005 | t0032 | g0118 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00738 | hp1 | a0002 | c0002 | t0018 | g0186 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00741 | hp1 | a0003 | c0003 | t0003 | g0239 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00741 | hp2 | a0008 | c0008 | t0001 | g0176 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01070 | hp1 | a0003 | c0003 | t0003 | g0039 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01071 | hp2 | a0003 | c0003 | t0003 | g0336 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01074 | hp1 | a0004 | c0004 | t0002 | g0283 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01074 | hp2 | a0002 | c0002 | t0003 | g0230 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01081 | hp1 | a0002 | c0002 | t0003 | g0232 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01081 | hp2 | a0004 | c0004 | t0002 | g0282 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01099 | hp2 | a0008 | c0008 | t0001 | g0019 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01109 | hp2 | a0007 | c0007 | t0001 | g0063 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01168 | hp1 | a0008 | c0008 | t0001 | g0041 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01175 | hp1 | a0005 | c0005 | t0001 | g0127 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01175 | hp2 | a0005 | c0005 | t0001 | g0026 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01243 | hp2 | a0002 | c0002 | t0002 | g0224 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | CLM | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01256 | hp1 | a0004 | c0004 | t0002 | g0356 | AMR | CLM | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01258 | hp1 | a0003 | c0003 | t0002 | g0298 | AMR | CLM | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01346 | hp1 | a0001 | c0018 | t0001 | g0046 | AMR | CLM | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01358 | hp1 | a0005 | c0005 | t0001 | g0069 | AMR | CLM | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01358 | hp2 | a0002 | c0002 | t0002 | g0364 | AMR | CLM | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01361 | hp1 | a0003 | c0003 | t0003 | g0238 | AMR | CLM | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01361 | hp2 | a0001 | c0001 | t0004 | g0111 | AMR | CLM | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01496 | hp1 | a0007 | c0007 | t0001 | g0095 | AMR | CLM | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01515 | hp2 | a0002 | c0002 | t0003 | g0165 | EUR | IBS | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01516 | hp1 | a0002 | c0002 | t0003 | g0031 | EUR | IBS | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01516 | hp2 | a0001 | c0001 | t0004 | g0024 | EUR | IBS | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01517 | hp1 | a0002 | c0002 | t0003 | g0031 | EUR | IBS | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01884 | hp1 | a0003 | c0003 | t0005 | g0034 | AFR | ACB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01891 | hp1 | a0003 | c0003 | t0002 | g0354 | AFR | ACB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01928 | hp2 | a0013 | c0030 | t0031 | g0109 | AMR | PEL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01934 | hp1 | a0007 | c0007 | t0001 | g0087 | AMR | PEL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01978 | hp1 | a0004 | c0004 | t0002 | g0292 | AMR | PEL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01993 | hp2 | a0001 | c0001 | t0004 | g0024 | AMR | PEL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02015 | hp1 | a0005 | c0005 | t0001 | g0121 | EAS | KHV | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02015 | hp2 | a0003 | c0003 | t0009 | g0297 | EAS | KHV | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02027 | hp1 | a0005 | c0005 | t0030 | g0098 | EAS | KHV | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02027 | hp2 | a0002 | c0002 | t0003 | g0191 | EAS | KHV | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02055 | hp1 | a0001 | c0001 | t0006 | g0091 | AFR | ACB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02055 | hp2 | a0008 | c0008 | t0001 | g0134 | AFR | ACB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02056 | hp2 | a0004 | c0004 | t0002 | g0276 | EAS | KHV | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02071 | hp1 | a0006 | c0006 | t0009 | g0341 | EAS | KHV | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02071 | hp2 | a0002 | c0002 | t0003 | g0008 | EAS | KHV | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02080 | hp1 | a0002 | c0002 | t0014 | g0029 | EAS | KHV | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02080 | hp2 | a0004 | c0004 | t0002 | g0303 | EAS | KHV | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02083 | hp1 | a0005 | c0005 | t0001 | g0075 | EAS | KHV | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02083 | hp2 | a0006 | c0006 | t0003 | g0039 | EAS | KHV | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02129 | hp1 | a0006 | c0016 | t0002 | g0345 | EAS | KHV | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02129 | hp2 | a0004 | c0004 | t0002 | g0275 | EAS | KHV | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02132 | hp1 | a0005 | c0005 | t0001 | g0076 | EAS | KHV | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02132 | hp2 | a0004 | c0004 | t0002 | g0002 | EAS | KHV | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02135 | hp1 | a0002 | c0002 | t0014 | g0029 | EAS | KHV | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02145 | hp1 | a0003 | c0015 | t0001 | g0138 | AFR | ACB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02145 | hp2 | a0010 | c0011 | t0005 | g0260 | AFR | ACB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02148 | hp1 | a0004 | c0004 | t0002 | g0287 | AMR | PEL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02148 | hp2 | a0004 | c0004 | t0002 | g0299 | AMR | PEL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02165 | hp1 | a0002 | c0002 | t0003 | g0207 | EAS | CDX | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CDX | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02257 | hp1 | a0003 | c0003 | t0002 | g0258 | AFR | ACB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02257 | hp2 | a0003 | c0003 | t0005 | g0362 | AFR | ACB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02258 | hp1 | a0009 | c0009 | t0006 | g0153 | AFR | ACB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02258 | hp2 | a0003 | c0003 | t0002 | g0324 | AFR | ACB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02280 | hp1 | a0003 | c0003 | t0002 | g0274 | AFR | ACB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02280 | hp2 | a0003 | c0003 | t0002 | g0038 | AFR | ACB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02451 | hp1 | a0007 | c0007 | t0001 | g0094 | AFR | ACB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02451 | hp2 | a0003 | c0003 | t0002 | g0263 | AFR | ACB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02572 | hp1 | a0003 | c0003 | t0002 | g0269 | AFR | GWD | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02572 | hp2 | a0003 | c0003 | t0002 | g0325 | AFR | GWD | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02602 | hp1 | a0003 | c0003 | t0003 | g0188 | SAS | PJL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02615 | hp1 | a0001 | c0001 | t0010 | g0050 | AFR | GWD | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02615 | hp2 | a0003 | c0003 | t0005 | g0272 | AFR | GWD | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02622 | hp1 | a0003 | c0023 | t0002 | g0326 | AFR | GWD | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02622 | hp2 | a0001 | c0001 | t0010 | g0049 | AFR | GWD | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02630 | hp1 | a0003 | c0003 | t0007 | g0257 | AFR | GWD | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02630 | hp2 | a0004 | c0004 | t0002 | g0285 | AFR | GWD | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02647 | hp1 | a0003 | c0003 | t0005 | g0035 | AFR | GWD | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02647 | hp2 | a0003 | c0003 | t0002 | g0270 | AFR | GWD | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02698 | hp1 | a0003 | c0003 | t0002 | g0311 | SAS | PJL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02698 | hp2 | a0003 | c0003 | t0002 | g0037 | SAS | PJL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02717 | hp1 | a0003 | c0010 | t0006 | g0151 | AFR | GWD | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02717 | hp2 | a0001 | c0017 | t0001 | g0079 | AFR | GWD | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02723 | hp1 | a0007 | c0007 | t0001 | g0086 | AFR | GWD | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02723 | hp2 | a0003 | c0003 | t0002 | g0038 | AFR | GWD | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02735 | hp1 | a0005 | c0005 | t0001 | g0124 | SAS | PJL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02735 | hp2 | a0002 | c0002 | t0003 | g0184 | SAS | PJL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02738 | hp1 | a0004 | c0004 | t0002 | g0310 | SAS | PJL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02809 | hp2 | a0001 | c0001 | t0010 | g0051 | AFR | GWD | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02818 | hp1 | a0003 | c0003 | t0002 | g0327 | AFR | GWD | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02818 | hp2 | a0009 | c0009 | t0006 | g0027 | AFR | GWD | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02886 | hp1 | a0003 | c0010 | t0001 | g0147 | AFR | GWD | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02895 | hp1 | a0008 | c0008 | t0001 | g0019 | AFR | GWD | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02895 | hp2 | a0003 | c0003 | t0005 | g0035 | AFR | GWD | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02896 | hp1 | a0003 | c0010 | t0001 | g0150 | AFR | GWD | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02896 | hp2 | a0001 | c0001 | t0010 | g0048 | AFR | GWD | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02897 | hp1 | a0001 | c0001 | t0010 | g0047 | AFR | GWD | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02897 | hp2 | a0003 | c0003 | t0005 | g0273 | AFR | GWD | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02922 | hp1 | a0003 | c0003 | t0002 | g0355 | AFR | ESN | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02922 | hp2 | a0003 | c0003 | t0005 | g0034 | AFR | ESN | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02965 | hp1 | a0003 | c0003 | t0007 | g0013 | AFR | ESN | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02965 | hp2 | a0007 | c0007 | t0011 | g0084 | AFR | ESN | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02970 | hp1 | a0003 | c0003 | t0007 | g0235 | AFR | ESN | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02970 | hp2 | a0004 | c0004 | t0002 | g0265 | AFR | ESN | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ESN | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02976 | hp2 | a0003 | c0003 | t0002 | g0340 | AFR | ESN | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03041 | hp1 | a0004 | c0014 | t0001 | g0145 | AFR | GWD | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03041 | hp2 | a0009 | c0009 | t0006 | g0142 | AFR | GWD | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03098 | hp1 | a0004 | c0004 | t0002 | g0266 | AFR | MSL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03098 | hp2 | a0007 | c0007 | t0001 | g0096 | AFR | MSL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03130 | hp1 | a0007 | c0007 | t0023 | g0083 | AFR | ESN | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03130 | hp2 | a0010 | c0011 | t0005 | g0262 | AFR | ESN | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03139 | hp1 | a0007 | c0007 | t0028 | g0085 | AFR | ESN | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03139 | hp2 | a0003 | c0003 | t0005 | g0163 | AFR | ESN | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03195 | hp1 | a0007 | c0007 | t0001 | g0007 | AFR | ESN | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03195 | hp2 | a0003 | c0010 | t0001 | g0149 | AFR | ESN | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03209 | hp1 | a0004 | c0014 | t0001 | g0148 | AFR | MSL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03209 | hp2 | a0003 | c0003 | t0005 | g0164 | AFR | MSL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03225 | hp1 | a0014 | c0027 | t0020 | g0267 | AFR | MSL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03225 | hp2 | a0003 | c0003 | t0007 | g0013 | AFR | MSL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03453 | hp1 | a0003 | c0003 | t0002 | g0359 | AFR | MSL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03453 | hp2 | a0003 | c0010 | t0001 | g0146 | AFR | MSL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03486 | hp1 | a0003 | c0003 | t0002 | g0040 | AFR | MSL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03486 | hp2 | a0009 | c0009 | t0006 | g0154 | AFR | MSL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03490 | hp1 | a0011 | c0012 | t0001 | g0017 | SAS | PJL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03490 | hp2 | a0003 | c0003 | t0002 | g0037 | SAS | PJL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03491 | hp1 | a0015 | c0028 | t0001 | g0078 | SAS | PJL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03491 | hp2 | a0002 | c0002 | t0003 | g0243 | SAS | PJL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03492 | hp1 | a0011 | c0012 | t0001 | g0017 | SAS | PJL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03492 | hp2 | a0002 | c0002 | t0003 | g0006 | SAS | PJL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03516 | hp1 | a0007 | c0007 | t0011 | g0007 | AFR | ESN | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03516 | hp2 | a0001 | c0001 | t0026 | g0062 | AFR | ESN | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03540 | hp1 | a0016 | c0025 | t0005 | g0277 | AFR | GWD | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03540 | hp2 | a0003 | c0003 | t0002 | g0342 | AFR | GWD | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | MSL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03579 | hp2 | a0003 | c0003 | t0005 | g0244 | AFR | MSL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03654 | hp1 | a0002 | c0002 | t0003 | g0192 | SAS | PJL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03654 | hp2 | a0001 | c0001 | t0004 | g0112 | SAS | PJL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03669 | hp2 | a0004 | c0004 | t0002 | g0309 | SAS | PJL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03688 | hp1 | a0005 | c0005 | t0001 | g0057 | SAS | STU | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03688 | hp2 | a0005 | c0005 | t0004 | g0099 | SAS | STU | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03704 | hp2 | a0003 | c0026 | t0007 | g0158 | SAS | PJL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03710 | hp1 | a0002 | c0002 | t0003 | g0199 | SAS | PJL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03831 | hp1 | a0003 | c0003 | t0012 | g0161 | SAS | BEB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03831 | hp2 | a0006 | c0006 | t0002 | g0323 | SAS | BEB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | BEB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | BEB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03927 | hp1 | a0011 | c0012 | t0001 | g0054 | SAS | BEB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03927 | hp2 | a0002 | c0002 | t0007 | g0227 | SAS | BEB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | BEB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03942 | hp2 | a0017 | c0019 | t0003 | g0012 | SAS | BEB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | STU | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG04115 | hp2 | a0002 | c0002 | t0021 | g0222 | SAS | STU | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG04184 | hp1 | a0011 | c0012 | t0001 | g0055 | SAS | BEB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG04184 | hp2 | a0004 | c0004 | t0002 | g0284 | SAS | BEB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG04199 | hp1 | a0003 | c0003 | t0003 | g0240 | SAS | STU | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG04199 | hp2 | a0002 | c0002 | t0003 | g0234 | SAS | STU | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | STU | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG04204 | hp2 | a0004 | c0004 | t0002 | g0302 | SAS | STU | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG04228 | hp1 | a0004 | c0004 | t0002 | g0301 | SAS | STU | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG04228 | hp2 | a0002 | c0002 | t0003 | g0187 | SAS | STU | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18522 | hp1 | a0003 | c0010 | t0006 | g0152 | AFR | YRI | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18522 | hp2 | a0001 | c0017 | t0001 | g0080 | AFR | YRI | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18612 | hp1 | a0008 | c0008 | t0001 | g0173 | EAS | CHB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18612 | hp2 | a0005 | c0005 | t0001 | g0072 | EAS | CHB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18747 | hp1 | a0002 | c0002 | t0003 | g0246 | EAS | CHB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18747 | hp2 | a0002 | c0002 | t0003 | g0189 | EAS | CHB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18940 | hp2 | a0002 | c0002 | t0008 | g0195 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18941 | hp1 | a0003 | c0003 | t0002 | g0160 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18941 | hp2 | a0002 | c0002 | t0003 | g0231 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18942 | hp1 | a0002 | c0002 | t0003 | g0008 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18942 | hp2 | a0006 | c0006 | t0002 | g0332 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18943 | hp1 | a0005 | c0005 | t0001 | g0074 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18943 | hp2 | a0003 | c0003 | t0002 | g0306 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18945 | hp1 | a0004 | c0004 | t0002 | g0036 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18945 | hp2 | a0002 | c0002 | t0002 | g0241 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18946 | hp1 | a0006 | c0006 | t0002 | g0338 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18946 | hp2 | a0005 | c0005 | t0001 | g0132 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18948 | hp1 | a0002 | c0002 | t0003 | g0006 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18948 | hp2 | a0002 | c0002 | t0008 | g0011 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18949 | hp1 | a0004 | c0004 | t0002 | g0002 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18949 | hp2 | a0006 | c0006 | t0002 | g0333 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18950 | hp1 | a0002 | c0002 | t0003 | g0213 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18950 | hp2 | a0004 | c0004 | t0002 | g0319 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18951 | hp1 | a0003 | c0003 | t0002 | g0159 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18951 | hp2 | a0002 | c0002 | t0003 | g0206 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18952 | hp1 | a0002 | c0002 | t0003 | g0218 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18953 | hp1 | a0006 | c0006 | t0003 | g0014 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18953 | hp2 | a0002 | c0002 | t0003 | g0196 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18954 | hp1 | a0006 | c0006 | t0002 | g0339 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18954 | hp2 | a0002 | c0002 | t0003 | g0006 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18956 | hp1 | a0006 | c0006 | t0002 | g0351 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18956 | hp2 | a0002 | c0002 | t0003 | g0008 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18957 | hp1 | a0004 | c0004 | t0002 | g0002 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18957 | hp2 | a0006 | c0006 | t0003 | g0014 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18959 | hp1 | a0006 | c0006 | t0002 | g0015 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18959 | hp2 | a0002 | c0002 | t0003 | g0033 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18960 | hp1 | a0004 | c0004 | t0002 | g0305 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18960 | hp2 | a0002 | c0002 | t0003 | g0183 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18961 | hp1 | a0004 | c0004 | t0002 | g0315 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18961 | hp2 | a0006 | c0006 | t0009 | g0358 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18962 | hp2 | a0002 | c0002 | t0003 | g0030 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18964 | hp1 | a0005 | c0005 | t0004 | g0044 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18964 | hp2 | a0002 | c0002 | t0003 | g0204 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18965 | hp1 | a0002 | c0002 | t0003 | g0251 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18965 | hp2 | a0005 | c0005 | t0001 | g0131 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18966 | hp1 | a0002 | c0002 | t0003 | g0223 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18966 | hp2 | a0005 | c0005 | t0004 | g0070 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18967 | hp2 | a0002 | c0002 | t0008 | g0193 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18968 | hp1 | a0006 | c0006 | t0002 | g0256 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18968 | hp2 | a0002 | c0002 | t0002 | g0210 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18969 | hp1 | a0001 | c0001 | t0024 | g0157 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18969 | hp2 | a0012 | c0013 | t0002 | g0219 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18970 | hp1 | a0002 | c0002 | t0003 | g0032 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18970 | hp2 | a0005 | c0005 | t0004 | g0123 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18971 | hp1 | a0003 | c0003 | t0002 | g0316 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18971 | hp2 | a0003 | c0003 | t0002 | g0293 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18972 | hp1 | a0004 | c0004 | t0002 | g0288 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18972 | hp2 | a0002 | c0002 | t0003 | g0253 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18974 | hp1 | a0002 | c0002 | t0008 | g0011 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18974 | hp2 | a0006 | c0006 | t0002 | g0352 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18975 | hp2 | a0003 | c0003 | t0003 | g0290 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18978 | hp1 | a0006 | c0006 | t0002 | g0015 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18978 | hp2 | a0006 | c0006 | t0002 | g0328 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18979 | hp1 | a0002 | c0002 | t0003 | g0200 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18979 | hp2 | a0006 | c0006 | t0002 | g0335 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18982 | hp1 | a0005 | c0005 | t0004 | g0021 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18987 | hp1 | a0002 | c0002 | t0003 | g0214 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18987 | hp2 | a0004 | c0004 | t0002 | g0322 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18988 | hp1 | a0002 | c0002 | t0003 | g0033 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18988 | hp2 | a0004 | c0004 | t0002 | g0279 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18989 | hp1 | a0002 | c0002 | t0003 | g0220 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18989 | hp2 | a0004 | c0004 | t0002 | g0291 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18990 | hp1 | a0004 | c0004 | t0002 | g0286 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18990 | hp2 | a0002 | c0002 | t0003 | g0208 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18991 | hp2 | a0005 | c0005 | t0004 | g0021 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18992 | hp1 | a0004 | c0004 | t0002 | g0320 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18992 | hp2 | a0002 | c0002 | t0003 | g0254 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18994 | hp1 | a0002 | c0002 | t0003 | g0032 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18994 | hp2 | a0006 | c0006 | t0002 | g0331 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18995 | hp1 | a0004 | c0004 | t0002 | g0313 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18995 | hp2 | a0002 | c0002 | t0002 | g0211 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18997 | hp1 | a0005 | c0005 | t0004 | g0119 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18997 | hp2 | a0006 | c0006 | t0003 | g0337 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18998 | hp1 | a0002 | c0022 | t0003 | g0215 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18998 | hp2 | a0003 | c0003 | t0002 | g0281 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18999 | hp1 | a0003 | c0003 | t0002 | g0294 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18999 | hp2 | a0006 | c0016 | t0002 | g0343 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19000 | hp1 | a0006 | c0006 | t0002 | g0353 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19000 | hp2 | a0005 | c0005 | t0004 | g0073 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19002 | hp1 | a0002 | c0002 | t0003 | g0248 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19002 | hp2 | a0002 | c0002 | t0003 | g0197 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19004 | hp2 | a0002 | c0002 | t0015 | g0242 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19006 | hp1 | a0002 | c0002 | t0003 | g0361 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19006 | hp2 | a0006 | c0006 | t0003 | g0357 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19007 | hp1 | a0005 | c0005 | t0001 | g0020 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19007 | hp2 | a0006 | c0006 | t0002 | g0350 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19010 | hp1 | a0002 | c0002 | t0003 | g0205 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19010 | hp2 | a0006 | c0006 | t0009 | g0330 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19011 | hp1 | a0002 | c0002 | t0003 | g0233 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19011 | hp2 | a0002 | c0002 | t0003 | g0180 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19012 | hp1 | a0004 | c0004 | t0002 | g0036 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19012 | hp2 | a0004 | c0004 | t0002 | g0314 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19030 | hp1 | a0009 | c0009 | t0006 | g0027 | AFR | LWK | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19030 | hp2 | a0007 | c0007 | t0011 | g0007 | AFR | LWK | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19043 | hp1 | a0003 | c0003 | t0002 | g0268 | AFR | LWK | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19043 | hp2 | a0010 | c0011 | t0007 | g0261 | AFR | LWK | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19054 | hp1 | a0006 | c0006 | t0002 | g0040 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19054 | hp2 | a0012 | c0013 | t0002 | g0226 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19056 | hp1 | a0006 | c0006 | t0003 | g0014 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19056 | hp2 | a0002 | c0002 | t0008 | g0194 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19058 | hp1 | a0005 | c0005 | t0004 | g0071 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19058 | hp2 | a0003 | c0003 | t0002 | g0296 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19060 | hp1 | a0003 | c0003 | t0002 | g0295 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19062 | hp1 | a0018 | c0024 | t0002 | g0300 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19062 | hp2 | a0004 | c0004 | t0002 | g0280 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19064 | hp1 | a0004 | c0004 | t0002 | g0360 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19064 | hp2 | a0003 | c0003 | t0012 | g0162 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19065 | hp1 | a0004 | c0004 | t0002 | g0002 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19065 | hp2 | a0002 | c0002 | t0003 | g0252 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19066 | hp1 | a0002 | c0002 | t0003 | g0247 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19066 | hp2 | a0004 | c0004 | t0002 | g0307 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19067 | hp1 | a0002 | c0002 | t0003 | g0221 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19067 | hp2 | a0006 | c0006 | t0002 | g0349 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19068 | hp1 | a0006 | c0006 | t0003 | g0344 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19068 | hp2 | a0002 | c0002 | t0003 | g0030 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19070 | hp1 | a0002 | c0002 | t0003 | g0006 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19070 | hp2 | a0005 | c0005 | t0001 | g0120 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19072 | hp1 | a0003 | c0003 | t0002 | g0317 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19072 | hp2 | a0002 | c0002 | t0003 | g0250 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19075 | hp1 | a0019 | c0021 | t0002 | g0198 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19075 | hp2 | a0002 | c0002 | t0003 | g0203 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19076 | hp1 | a0002 | c0002 | t0008 | g0011 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19076 | hp2 | a0002 | c0002 | t0002 | g0212 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19079 | hp1 | a0002 | c0002 | t0022 | g0181 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19080 | hp1 | a0006 | c0006 | t0002 | g0346 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19080 | hp2 | a0002 | c0002 | t0003 | g0217 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19082 | hp1 | a0006 | c0006 | t0002 | g0348 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19082 | hp2 | a0004 | c0004 | t0002 | g0318 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19083 | hp1 | a0002 | c0002 | t0008 | g0179 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19083 | hp2 | a0002 | c0002 | t0009 | g0245 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19084 | hp1 | a0020 | c0029 | t0001 | g0067 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19086 | hp1 | a0002 | c0002 | t0002 | g0190 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19086 | hp2 | a0006 | c0006 | t0019 | g0329 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19087 | hp1 | a0004 | c0004 | t0002 | g0308 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19087 | hp2 | a0021 | c0020 | t0003 | g0006 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19088 | hp1 | a0004 | c0004 | t0002 | g0289 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19088 | hp2 | a0004 | c0004 | t0002 | g0278 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19089 | hp1 | a0002 | c0002 | t0003 | g0008 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19089 | hp2 | a0001 | c0001 | t0025 | g0058 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19090 | hp1 | a0004 | c0004 | t0002 | g0321 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19090 | hp2 | a0008 | c0008 | t0001 | g0169 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19091 | hp1 | a0002 | c0002 | t0003 | g0249 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19091 | hp2 | a0006 | c0006 | t0002 | g0347 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19240 | hp1 | a0003 | c0003 | t0002 | g0236 | AFR | YRI | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19240 | hp2 | a0003 | c0003 | t0007 | g0013 | AFR | YRI | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ASW | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA20129 | hp2 | a0004 | c0004 | t0002 | g0255 | AFR | ASW | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA20752 | hp1 | a0003 | c0003 | t0003 | g0237 | EUR | TSI | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0166 | EUR | TSI | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA20905 | hp1 | a0002 | c0002 | t0002 | g0185 | SAS | GIH | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA20905 | hp2 | a0005 | c0005 | t0029 | g0077 | SAS | GIH | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01123 | hp1 | a0002 | c0002 | t0003 | g0228 | AMR | CLM | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01123 | hp2 | a0002 | c0002 | t0003 | g0201 | AMR | CLM | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02109 | hp1 | a0003 | c0003 | t0005 | g0271 | AFR | ACB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02109 | hp2 | a0009 | c0009 | t0006 | g0144 | AFR | ACB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02486 | hp2 | a0003 | c0015 | t0001 | g0139 | AFR | ACB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02559 | hp1 | a0004 | c0004 | t0013 | g0264 | AFR | ACB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02559 | hp2 | a0003 | c0003 | t0002 | g0334 | AFR | ACB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG06807 | hp1 | a0005 | c0005 | t0001 | g0026 | AFR | USA | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG06807 | hp2 | a0009 | c0009 | t0001 | g0155 | AFR | USA | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18955 | hp2 | a0002 | c0002 | t0003 | g0216 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA20300 | hp1 | a0010 | c0011 | t0005 | g0259 | AFR | USA | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA20300 | hp2 | a0004 | c0004 | t0013 | g0363 | AFR | USA | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | LWK | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
homoSapiens | chm13v2 | a0003 | c0003 | t0003 | g0182 | REF | REF | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
homoSapiens | grch38p0 | a0005 | c0005 | t0004 | g0043 | REF | REF | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:20460128 | G | A | 5 | a0002 a0012 a0017 others(2): Show |
95 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(92): Show |
missense_variant | MODERATE | c.14G>A | p.Arg5Gln | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/14 | 183/2894 | 14/1734 | 5/577 | chr16 | 20460128 | |||
chr16:20460139 | G | A | 1 | a0017 | 1 | HG03942.hp2 | missense_variant | MODERATE | c.25G>A | p.Gly9Arg | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/14 | 194/2894 | 25/1734 | 9/577 | chr16 | 20460139 | |||
chr16:20460165 | G | C | 1 | a0009 | 7 | HG02109.hp2 HG02258.hp1 HG02818.hp2 others(4): Show |
missense_variant | MODERATE | c.51G>C | p.Gln17His | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/14 | 220/2894 | 51/1734 | 17/577 | chr16 | 20460165 | |||
chr16:20465530 | T | C | 12 | a0002 a0003 a0004 others(9): Show |
263 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(260): Show |
missense_variant | MODERATE | c.191T>C | p.Leu64Pro | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/14 | 360/2894 | 191/1734 | 64/577 | chr16 | 20465530 | |||
chr16:20465549 | G | A | 1 | a0021 | 1 | NA19087.hp2 | stop_gained | HIGH | c.210G>A | p.Trp70* | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/14 | 379/2894 | 210/1734 | 70/577 | chr16 | 20465549 | |||
chr16:20465571 | G | A | 1 | a0011 | 4 | HG03490.hp1 HG03492.hp1 HG03927.hp1 others(1): Show |
missense_variant | MODERATE | c.232G>A | p.Glu78Lys | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/14 | 401/2894 | 232/1734 | 78/577 | chr16 | 20465571 | |||
chr16:20465652 | C | T | 1 | a0010 | 4 | HG02145.hp2 HG03130.hp2 NA19043.hp2 others(1): Show |
missense_variant | MODERATE | c.313C>T | p.Arg105Cys | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/14 | 482/2894 | 313/1734 | 105/577 | chr16 | 20465652 | |||
chr16:20465673 | G | A | 1 | a0019 | 1 | NA19075.hp1 | missense_variant | MODERATE | c.334G>A | p.Val112Met | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/14 | 503/2894 | 334/1734 | 112/577 | chr16 | 20465673 | |||
chr16:20465682 | C | T | 1 | a0006 | 34 | HG00673.hp2 HG02071.hp1 HG02083.hp2 others(31): Show |
stop_gained | HIGH | c.343C>T | p.Arg115* | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/14 | 512/2894 | 343/1734 | 115/577 | chr16 | 20465682 | |||
chr16:20469575 | T | A | 1 | a0018 | 1 | NA19062.hp1 | missense_variant | MODERATE | c.452T>A | p.Met151Lys | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/14 | 621/2894 | 452/1734 | 151/577 | chr16 | 20469575 | |||
chr16:20471605 | G | C | 1 | a0015 | 1 | HG03491.hp1 | missense_variant | MODERATE | c.810G>C | p.Leu270Phe | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/14 | 979/2894 | 810/1734 | 270/577 | chr16 | 20471605 | |||
chr16:20471606 | T | G | 1 | a0016 | 1 | HG03540.hp1 | missense_variant | MODERATE | c.811T>G | p.Cys271Gly | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/14 | 980/2894 | 811/1734 | 271/577 | chr16 | 20471606 | |||
chr16:20480604 | G | A | 1 | a0007 | 12 | HG01109.hp2 HG01496.hp1 HG01934.hp1 others(9): Show |
missense_variant | MODERATE | c.1313G>A | p.Arg438Gln | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 11/14 | 1482/2894 | 1313/1734 | 438/577 | chr16 | 20480604 | |||
chr16:20480678 | A | G | 18 | a0001 a0002 a0003 others(15): Show |
396 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(393): Show |
missense_variant | MODERATE | c.1387A>G | p.Asn463Asp | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 11/14 | 1556/2894 | 1387/1734 | 463/577 | chr16 | 20480678 | |||
chr16:20483076 | G | A | 1 | a0013 | 1 | HG01928.hp2 | missense_variant | MODERATE | c.1528G>A | p.Val510Ile | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/14 | 1697/2894 | 1528/1734 | 510/577 | chr16 | 20483076 | |||
chr16:20483086 | C | T | 6 | a0004 a0006 a0008 others(3): Show |
65 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(62): Show |
missense_variant | MODERATE | c.1538C>T | p.Ser513Leu | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/14 | 1707/2894 | 1538/1734 | 513/577 | chr16 | 20483086 | |||
chr16:20486625 | G | A | 1 | a0013 | 1 | HG01928.hp2 | missense_variant | MODERATE | c.1681G>A | p.Ala561Thr | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 1850/2894 | 1681/1734 | 561/577 | chr16 | 20486625 | |||
chr16:20486674 | A | G | 1 | a0014 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.1730A>G | p.Gln577Arg | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 1899/2894 | 1730/1734 | 577/577 | chr16 | 20486674 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:20460120 | T | C | 1 | a0001c0018 | 1 | HG01346.hp1 | synonymous_variant | LOW | c.6T>C | p.His2His | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/14 | 175/2894 | 6/1734 | 2/577 | chr16 | 20460120 | |||
chr16:20460273 | C | T | 1 | a0002c0022 | 1 | NA18998.hp1 | synonymous_variant | LOW | c.159C>T | p.His53His | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/14 | 328/2894 | 159/1734 | 53/577 | chr16 | 20460273 | |||
chr16:20465567 | G | A | 1 | a0003c0023 | 1 | HG02622.hp1 | synonymous_variant | LOW | c.228G>A | p.Gly76Gly | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/14 | 397/2894 | 228/1734 | 76/577 | chr16 | 20465567 | |||
chr16:20475403 | C | T | 1 | a0003c0015 | 2 | HG02145.hp1 HG02486.hp2 |
synonymous_variant | LOW | c.936C>T | p.Pro312Pro | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 7/14 | 1105/2894 | 936/1734 | 312/577 | chr16 | 20475403 | |||
chr16:20475711 | C | T | 1 | a0001c0017 | 2 | HG02717.hp2 NA18522.hp2 |
synonymous_variant | LOW | c.1036C>T | p.Leu346Leu | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 8/14 | 1205/2894 | 1036/1734 | 346/577 | chr16 | 20475711 | |||
chr16:20477374 | A | G | 16 | a0002c0002 a0002c0022 a0003c0003 others(13): Show |
247 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(244): Show |
synonymous_variant | LOW | c.1104A>G | p.Leu368Leu | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 9/14 | 1273/2894 | 1104/1734 | 368/577 | chr16 | 20477374 | |||
chr16:20480885 | G | A | 1 | a0003c0026 | 1 | HG03704.hp2 | synonymous_variant | LOW | c.1473G>A | p.Thr491Thr | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/14 | 1642/2894 | 1473/1734 | 491/577 | chr16 | 20480885 | |||
chr16:20483078 | C | A | 1 | a0013c0030 | 1 | HG01928.hp2 | synonymous_variant | LOW | c.1530C>A | p.Val510Val | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/14 | 1699/2894 | 1530/1734 | 510/577 | chr16 | 20483078 | |||
chr16:20483096 | G | A | 1 | a0013c0030 | 1 | HG01928.hp2 | synonymous_variant | LOW | c.1548G>A | p.Leu516Leu | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/14 | 1717/2894 | 1548/1734 | 516/577 | chr16 | 20483096 | |||
chr16:20486630 | G | A | 1 | a0013c0030 | 1 | HG01928.hp2 | synonymous_variant | LOW | c.1686G>A | p.Lys562Lys | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 1855/2894 | 1686/1734 | 562/577 | chr16 | 20486630 | |||
chr16:20486675 | G | A | 1 | a0014c0027 | 1 | HG03225.hp1 | synonymous_variant | LOW | c.1731G>A | p.Gln577Gln | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 1900/2894 | 1731/1734 | 577/577 | chr16 | 20486675 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:20451602 | G | A | 36 | a0002c0002t0002 a0002c0002t0003 a0002c0002t0007 others(33): Show |
247 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(244): Show |
5_prime_UTR_variant | MODIFIER | c.-88G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/14 | 8513 | chr16 | 20451602 | ||||||
chr16:20451631 | G | A | 1 | a0002c0002t0017 | 1 | HG00733.hp1 | 5_prime_UTR_variant | MODIFIER | c.-59G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/14 | 8484 | chr16 | 20451631 | ||||||
chr16:20451641 | C | T | 2 | a0005c0005t0016 a0005c0005t0032 |
3 | HG00099.hp1 HG00323.hp1 HG00735.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-49C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/14 | chr16 | 20451641 | |||||||
chr16:20451653 | T | C | 1 | a0002c0002t0018 | 1 | HG00738.hp1 | 5_prime_UTR_variant | MODIFIER | c.-37T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/14 | 8462 | chr16 | 20451653 | ||||||
chr16:20486680 | A | G | 1 | a0013c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 2 | chr16 | 20486680 | ||||||
chr16:20486682 | A | G | 1 | a0013c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 4 | chr16 | 20486682 | ||||||
chr16:20486687 | A | G | 1 | a0013c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 9 | chr16 | 20486687 | ||||||
chr16:20486709 | C | T | 3 | a0003c0003t0005 a0010c0011t0005 a0016c0025t0005 |
15 | HG01884.hp1 HG02109.hp1 HG02145.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*31C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 31 | chr16 | 20486709 | ||||||
chr16:20486738 | C | A | 1 | a0007c0007t0023 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*60C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 60 | chr16 | 20486738 | ||||||
chr16:20486749 | C | A | 2 | a0001c0001t0024 a0013c0030t0031 |
2 | HG01928.hp2 NA18969.hp1 |
3_prime_UTR_variant | MODIFIER | c.*71C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 71 | chr16 | 20486749 | ||||||
chr16:20486757 | T | G | 50 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0024 others(47): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
3_prime_UTR_variant | MODIFIER | c.*79T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 79 | chr16 | 20486757 | ||||||
chr16:20486775 | G | A | 1 | a0013c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*97G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 97 | chr16 | 20486775 | ||||||
chr16:20486782 | A | G | 2 | a0002c0002t0021 a0005c0005t0029 |
2 | HG04115.hp2 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*104A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 104 | chr16 | 20486782 | ||||||
chr16:20486788 | A | G | 1 | a0013c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*110A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 110 | chr16 | 20486788 | ||||||
chr16:20486805 | T | C | 1 | a0013c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*127T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 127 | chr16 | 20486805 | ||||||
chr16:20486824 | T | A | 1 | a0013c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*146T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 146 | chr16 | 20486824 | ||||||
chr16:20486829 | C | T | 1 | a0013c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*151C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 151 | chr16 | 20486829 | ||||||
chr16:20486839 | G | A | 1 | a0013c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*161G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 161 | chr16 | 20486839 | ||||||
chr16:20486846 | G | T | 1 | a0013c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*168G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 168 | chr16 | 20486846 | ||||||
chr16:20486897 | A | G | 1 | a0013c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*219A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 219 | chr16 | 20486897 | ||||||
chr16:20486938 | G | A | 1 | a0013c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*260G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 260 | chr16 | 20486938 | ||||||
chr16:20486970 | A | G | 1 | a0013c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*292A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 292 | chr16 | 20486970 | ||||||
chr16:20486971 | A | G | 1 | a0013c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*293A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 293 | chr16 | 20486971 | ||||||
chr16:20486976 | G | A | 1 | a0001c0001t0025 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*298G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 298 | chr16 | 20486976 | ||||||
chr16:20486977 | A | C | 1 | a0013c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*299A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 299 | chr16 | 20486977 | ||||||
chr16:20487006 | G | A | 1 | a0013c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*328G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 328 | chr16 | 20487006 | ||||||
chr16:20487012 | A | C | 1 | a0014c0027t0020 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*334A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 334 | chr16 | 20487012 | ||||||
chr16:20487026 | G | T | 2 | a0004c0004t0013 a0014c0027t0020 |
3 | HG02559.hp1 HG03225.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*348G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 348 | chr16 | 20487026 | ||||||
chr16:20487061 | A | T | 2 | a0002c0002t0015 a0005c0005t0030 |
3 | HG00673.hp1 HG02027.hp1 NA19004.hp2 |
3_prime_UTR_variant | MODIFIER | c.*383A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 383 | chr16 | 20487061 | ||||||
chr16:20487069 | A | T | 1 | a0014c0027t0020 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*391A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 391 | chr16 | 20487069 | ||||||
chr16:20487078 | C | A | 50 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0024 others(47): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
3_prime_UTR_variant | MODIFIER | c.*400C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 400 | chr16 | 20487078 | ||||||
chr16:20487131 | C | G | 1 | a0001c0001t0010 | 5 | HG02615.hp1 HG02622.hp2 HG02809.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*453C>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 453 | chr16 | 20487131 | ||||||
chr16:20487180 | T | G | 1 | a0014c0027t0020 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*502T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 502 | chr16 | 20487180 | ||||||
chr16:20487182 | G | T | 9 | a0001c0001t0006 a0002c0002t0007 a0003c0003t0007 others(6): Show |
20 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*504G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 504 | chr16 | 20487182 | ||||||
chr16:20487222 | A | C | 2 | a0003c0003t0012 a0013c0030t0031 |
3 | HG01928.hp2 HG03831.hp1 NA19064.hp2 |
3_prime_UTR_variant | MODIFIER | c.*544A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 544 | chr16 | 20487222 | ||||||
chr16:20487241 | A | G | 1 | a0013c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*563A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 563 | chr16 | 20487241 | ||||||
chr16:20487249 | A | G | 1 | a0013c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*571A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 571 | chr16 | 20487249 | ||||||
chr16:20487268 | T | C | 1 | a0013c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*590T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 590 | chr16 | 20487268 | ||||||
chr16:20487278 | T | C | 1 | a0002c0002t0008 | 7 | NA18940.hp2 NA18948.hp2 NA18967.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*600T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 600 | chr16 | 20487278 | ||||||
chr16:20487295 | G | C | 3 | a0002c0002t0009 a0003c0003t0009 a0006c0006t0009 |
5 | HG02015.hp2 HG02071.hp1 NA18961.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*617G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 617 | chr16 | 20487295 | ||||||
chr16:20487334 | C | A | 1 | a0013c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*656C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 656 | chr16 | 20487334 | ||||||
chr16:20487335 | C | A | 1 | a0013c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*657C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 657 | chr16 | 20487335 | ||||||
chr16:20487340 | C | T | 1 | a0013c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*662C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 662 | chr16 | 20487340 | ||||||
chr16:20487343 | C | T | 1 | a0013c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*665C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 665 | chr16 | 20487343 | ||||||
chr16:20487349 | A | T | 1 | a0013c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*671A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 671 | chr16 | 20487349 | ||||||
chr16:20487353 | C | A | 1 | a0006c0006t0019 | 1 | NA19086.hp2 | 3_prime_UTR_variant | MODIFIER | c.*675C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 675 | chr16 | 20487353 | ||||||
chr16:20487358 | A | G | 1 | a0013c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*680A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 680 | chr16 | 20487358 | ||||||
chr16:20487394 | T | C | 1 | a0013c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*716T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 716 | chr16 | 20487394 | ||||||
chr16:20487414 | A | G | 1 | a0013c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*736A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 736 | chr16 | 20487414 | ||||||
chr16:20487415 | C | T | 1 | a0007c0007t0028 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*737C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 737 | chr16 | 20487415 | ||||||
chr16:20487423 | C | T | 1 | a0013c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*745C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 745 | chr16 | 20487423 | ||||||
chr16:20487434 | G | A | 1 | a0013c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*756G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 756 | chr16 | 20487434 | ||||||
chr16:20487458 | C | T | 2 | a0001c0001t0027 a0013c0030t0031 |
2 | HG00558.hp1 HG01928.hp2 |
3_prime_UTR_variant | MODIFIER | c.*780C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 780 | chr16 | 20487458 | ||||||
chr16:20487494 | A | G | 1 | a0013c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*816A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 816 | chr16 | 20487494 | ||||||
chr16:20487502 | T | C | 1 | a0013c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*824T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 824 | chr16 | 20487502 | ||||||
chr16:20487503 | G | A | 1 | a0013c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*825G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 825 | chr16 | 20487503 | ||||||
chr16:20487519 | G | A | 1 | a0013c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*841G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 841 | chr16 | 20487519 | ||||||
chr16:20487519 | G | T | 1 | a0002c0002t0014 | 2 | HG02080.hp1 HG02135.hp1 |
3_prime_UTR_variant | MODIFIER | c.*841G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 841 | chr16 | 20487519 | ||||||
chr16:20487574 | C | A | 2 | a0001c0001t0026 a0013c0030t0031 |
2 | HG01928.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*896C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 896 | chr16 | 20487574 | ||||||
chr16:20487580 | C | T | 1 | a0002c0002t0022 | 1 | NA19079.hp1 | 3_prime_UTR_variant | MODIFIER | c.*902C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 902 | chr16 | 20487580 | ||||||
chr16:20487607 | T | C | 2 | a0007c0007t0011 a0013c0030t0031 |
4 | HG01928.hp2 HG02965.hp2 HG03516.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*929T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 929 | chr16 | 20487607 | ||||||
chr16:20487620 | A | G | 1 | a0013c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*942A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 942 | chr16 | 20487620 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:20451741 | CT | C | 2 | a0001c0001t0001g0016 a0008c0008t0001g0041 |
3 | HG01168.hp1 HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-9+64delT | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20451741 | ||||||
chr16:20451776 | C | T | 1 | a0002c0002t0002g0364 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-9+95C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20451776 | |||||||
chr16:20451781 | C | T | 2 | a0003c0003t0005g0362 a0004c0004t0013g0363 |
2 | HG02257.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-9+100C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20451781 | |||||||
chr16:20451864 | C | G | 234 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0028 others(231): Show |
272 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(269): Show |
intron_variant | MODIFIER | c.-9+183C>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20451864 | |||||||
chr16:20451888 | C | T | 2 | a0001c0001t0001g0156 a0001c0001t0024g0157 |
2 | NA18955.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.-9+207C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20451888 | |||||||
chr16:20451918 | G | T | 1 | a0002c0002t0003g0361 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-9+237G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20451918 | |||||||
chr16:20451919 | G | T | 120 | a0003c0003t0002g0037 a0003c0003t0002g0038 a0003c0003t0002g0040 others(117): Show |
134 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(131): Show |
intron_variant | MODIFIER | c.-9+238G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20451919 | |||||||
chr16:20451920 | G | A | 1 | a0003c0026t0007g0158 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-9+239G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20451920 | |||||||
chr16:20451956 | T | C | 1 | a0001c0001t0001g0042 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-9+275T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20451956 | |||||||
chr16:20451974 | G | A | 7 | a0003c0003t0002g0159 a0003c0003t0002g0160 a0003c0003t0005g0163 others(4): Show |
7 | HG03139.hp2 HG03209.hp2 HG03704.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9+293G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20451974 | |||||||
chr16:20452032 | T | G | 1 | a0002c0002t0003g0361 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-9+351T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20452032 | |||||||
chr16:20452081 | A | G | 368 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(365): Show |
433 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(430): Show |
intron_variant | MODIFIER | c.-9+400A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20452081 | |||||||
chr16:20452111 | A | G | 210 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(207): Show |
239 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.-9+430A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20452111 | |||||||
chr16:20452113 | T | C | 4 | a0003c0003t0002g0159 a0003c0003t0002g0160 a0003c0003t0012g0161 others(1): Show |
4 | HG03831.hp1 NA18941.hp1 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+432T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20452113 | |||||||
chr16:20452132 | T | A | 1 | a0004c0004t0002g0255 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-9+451T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20452132 | |||||||
chr16:20452259 | A | C | 5 | a0002c0002t0003g0032 a0002c0002t0003g0033 a0002c0002t0003g0253 others(2): Show |
7 | NA18959.hp2 NA18970.hp1 NA18972.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9+578A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20452259 | |||||||
chr16:20452368 | A | C | 233 | a0001c0001t0001g0143 a0002c0002t0002g0185 a0002c0002t0002g0190 others(230): Show |
263 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.-9+687A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20452368 | |||||||
chr16:20452423 | G | C | 1 | a0006c0006t0002g0256 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-9+742G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20452423 | |||||||
chr16:20452482 | A | T | 1 | a0002c0002t0003g0361 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-9+801A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20452482 | |||||||
chr16:20452483 | T | A | 1 | a0002c0002t0003g0361 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-9+802T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20452483 | |||||||
chr16:20452484 | A | T | 1 | a0002c0002t0003g0361 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-9+803A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20452484 | |||||||
chr16:20452487 | CTGTATAT others(13): Show |
C | 1 | a0002c0002t0003g0180 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-9+823_-9+842delGT others(18): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20452487 | ||||||
chr16:20452511 | A | G | 45 | a0003c0003t0002g0038 a0003c0003t0002g0040 a0003c0003t0002g0324 others(42): Show |
50 | HG00673.hp2 HG01070.hp1 HG01071.hp2 others(47): Show |
intron_variant | MODIFIER | c.-9+830A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20452511 | |||||||
chr16:20452562 | G | A | 219 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(216): Show |
248 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.-9+881G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20452562 | |||||||
chr16:20452567 | T | C | 2 | a0003c0003t0002g0258 a0003c0003t0007g0257 |
2 | HG02257.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.-9+886T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20452567 | |||||||
chr16:20452583 | A | T | 211 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(208): Show |
240 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.-9+902A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20452583 | |||||||
chr16:20452623 | C | T | 1 | a0002c0002t0003g0361 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-9+942C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20452623 | |||||||
chr16:20452625 | A | C | 1 | a0002c0002t0003g0361 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-9+944A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20452625 | |||||||
chr16:20452626 | T | A | 1 | a0002c0002t0003g0361 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-9+945T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20452626 | |||||||
chr16:20452699 | A | G | 1 | a0004c0004t0002g0322 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-9+1018A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20452699 | |||||||
chr16:20452710 | A | G | 2 | a0003c0003t0005g0163 a0003c0003t0005g0164 |
2 | HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-9+1029A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20452710 | |||||||
chr16:20452715 | T | A | 4 | a0010c0011t0005g0259 a0010c0011t0005g0260 a0010c0011t0005g0262 others(1): Show |
4 | HG02145.hp2 HG03130.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9+1034T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20452715 | |||||||
chr16:20452745 | T | C | 218 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(215): Show |
247 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.-9+1064T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20452745 | |||||||
chr16:20452746 | G | A | 218 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(215): Show |
247 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.-9+1065G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20452746 | |||||||
chr16:20452794 | G | A | 2 | a0003c0003t0005g0163 a0003c0003t0005g0164 |
2 | HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-9+1113G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20452794 | |||||||
chr16:20452917 | C | G | 49 | a0003c0003t0002g0037 a0003c0003t0002g0281 a0003c0003t0002g0293 others(46): Show |
56 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.-9+1236C>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20452917 | |||||||
chr16:20453012 | G | A | 1 | a0005c0005t0004g0044 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-9+1331G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20453012 | |||||||
chr16:20453026 | A | C | 2 | a0001c0001t0027g0141 a0008c0008t0001g0140 |
2 | HG00558.hp1 HG00609.hp1 |
intron_variant | MODIFIER | c.-9+1345A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20453026 | |||||||
chr16:20453028 | C | A | 2 | a0001c0001t0027g0141 a0008c0008t0001g0140 |
2 | HG00558.hp1 HG00609.hp1 |
intron_variant | MODIFIER | c.-9+1347C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20453028 | |||||||
chr16:20453028 | C | G | 218 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(215): Show |
247 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.-9+1347C>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20453028 | |||||||
chr16:20453029 | G | A | 1 | a0005c0005t0001g0045 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-9+1348G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20453029 | |||||||
chr16:20453092 | C | T | 2 | a0003c0015t0001g0138 a0003c0015t0001g0139 |
2 | HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-9+1411C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20453092 | |||||||
chr16:20453235 | T | C | 1 | a0002c0002t0022g0181 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-9+1554T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20453235 | |||||||
chr16:20453323 | T | C | 1 | a0001c0018t0001g0046 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-9+1642T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20453323 | |||||||
chr16:20453420 | C | T | 2 | a0001c0001t0001g0137 a0016c0025t0005g0277 |
2 | HG01433.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-9+1739C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20453420 | |||||||
chr16:20453453 | A | C | 51 | a0003c0003t0002g0037 a0003c0003t0002g0281 a0003c0003t0002g0293 others(48): Show |
58 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.-9+1772A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20453453 | |||||||
chr16:20453514 | G | A | 6 | a0001c0001t0001g0143 a0001c0001t0010g0047 a0001c0001t0010g0048 others(3): Show |
6 | HG01884.hp2 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9+1833G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20453514 | |||||||
chr16:20453577 | T | C | 211 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(208): Show |
240 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.-9+1896T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20453577 | |||||||
chr16:20453654 | G | T | 1 | a0002c0002t0003g0361 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-9+1973G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20453654 | |||||||
chr16:20453675 | T | C | 1 | a0003c0003t0002g0263 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-9+1994T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20453675 | |||||||
chr16:20453740 | G | A | 2 | a0009c0009t0006g0027 a0009c0009t0006g0144 |
3 | HG02109.hp2 HG02818.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-9+2059G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20453740 | |||||||
chr16:20453768 | A | G | 1 | a0004c0004t0002g0321 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-9+2087A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20453768 | |||||||
chr16:20453796 | T | G | 220 | a0001c0001t0001g0052 a0001c0001t0001g0166 a0002c0002t0002g0185 others(217): Show |
249 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.-9+2115T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20453796 | |||||||
chr16:20453834 | C | T | 2 | a0002c0002t0003g0252 a0016c0025t0005g0277 |
2 | HG03540.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.-9+2153C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20453834 | |||||||
chr16:20453842 | C | T | 6 | a0009c0009t0001g0155 a0009c0009t0006g0027 a0009c0009t0006g0142 others(3): Show |
7 | HG02109.hp2 HG02258.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9+2161C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20453842 | |||||||
chr16:20453896 | G | T | 7 | a0003c0003t0002g0159 a0003c0003t0002g0160 a0003c0003t0005g0163 others(4): Show |
7 | HG03139.hp2 HG03209.hp2 HG03704.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9+2215G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20453896 | |||||||
chr16:20453933 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-9+2252C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20453933 | |||||||
chr16:20453937 | G | C | 2 | a0003c0003t0005g0163 a0003c0003t0005g0164 |
2 | HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-9+2256G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20453937 | |||||||
chr16:20453992 | C | T | 7 | a0003c0003t0002g0159 a0003c0003t0002g0160 a0003c0003t0005g0163 others(4): Show |
7 | HG03139.hp2 HG03209.hp2 HG03704.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9+2311C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20453992 | |||||||
chr16:20453995 | C | T | 1 | a0003c0003t0002g0359 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-9+2314C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20453995 | |||||||
chr16:20454074 | C | T | 1 | a0016c0025t0005g0277 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-9+2393C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20454074 | |||||||
chr16:20454075 | A | G | 234 | a0001c0001t0001g0135 a0002c0002t0002g0185 a0002c0002t0002g0190 others(231): Show |
265 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.-9+2394A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20454075 | |||||||
chr16:20454109 | A | T | 14 | a0003c0010t0001g0146 a0003c0010t0001g0147 a0003c0010t0001g0149 others(11): Show |
15 | HG02109.hp2 HG02258.hp1 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.-9+2428A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20454109 | |||||||
chr16:20454126 | G | T | 7 | a0003c0003t0002g0159 a0003c0003t0002g0160 a0003c0003t0005g0163 others(4): Show |
7 | HG03139.hp2 HG03209.hp2 HG03704.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9+2445G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20454126 | |||||||
chr16:20454129 | C | T | 1 | a0009c0009t0001g0155 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-9+2448C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20454129 | |||||||
chr16:20454164 | A | G | 6 | a0002c0002t0003g0247 a0002c0002t0003g0248 a0002c0002t0003g0249 others(3): Show |
6 | NA18965.hp1 NA19002.hp1 NA19065.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9+2483A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20454164 | |||||||
chr16:20454227 | C | G | 1 | a0008c0008t0001g0134 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-9+2546C>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20454227 | |||||||
chr16:20454228 | G | A | 2 | a0002c0002t0003g0183 a0002c0002t0003g0184 |
2 | HG02735.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.-9+2547G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20454228 | |||||||
chr16:20454272 | G | A | 1 | a0006c0006t0002g0323 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-9+2591G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20454272 | |||||||
chr16:20454360 | T | A | 1 | a0016c0025t0005g0277 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-9+2679T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20454360 | |||||||
chr16:20454406 | A | T | 6 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(3): Show |
6 | HG01934.hp2 HG01943.hp2 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9+2725A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20454406 | |||||||
chr16:20454418 | A | T | 1 | a0002c0002t0003g0361 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-9+2737A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20454418 | |||||||
chr16:20454438 | C | T | 92 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(89): Show |
107 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.-9+2757C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20454438 | |||||||
chr16:20454645 | A | G | 1 | a0005c0005t0001g0127 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-9+2964A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20454645 | |||||||
chr16:20454659 | A | G | 1 | a0009c0009t0001g0155 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-9+2978A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20454659 | |||||||
chr16:20454744 | A | C | 1 | a0002c0002t0003g0361 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-9+3063A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20454744 | |||||||
chr16:20454745 | C | A | 1 | a0002c0002t0003g0361 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-9+3064C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20454745 | |||||||
chr16:20454765 | C | A | 14 | a0003c0010t0001g0146 a0003c0010t0001g0147 a0003c0010t0001g0149 others(11): Show |
15 | HG02109.hp2 HG02258.hp1 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.-9+3084C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20454765 | |||||||
chr16:20454769 | A | C | 15 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(12): Show |
15 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(12): Show |
intron_variant | MODIFIER | c.-9+3088A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20454769 | |||||||
chr16:20454840 | C | G | 2 | a0003c0015t0001g0138 a0003c0015t0001g0139 |
2 | HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-9+3159C>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20454840 | |||||||
chr16:20454853 | A | C | 211 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(208): Show |
240 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.-9+3172A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20454853 | |||||||
chr16:20454866 | A | C | 14 | a0003c0010t0001g0146 a0003c0010t0001g0147 a0003c0010t0001g0149 others(11): Show |
15 | HG02109.hp2 HG02258.hp1 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.-9+3185A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20454866 | |||||||
chr16:20454900 | G | GA | 208 | a0001c0001t0001g0028 a0001c0001t0001g0167 a0002c0002t0002g0185 others(205): Show |
238 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.-9+3230dupA | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20454900 | ||||||
chr16:20454900 | GA | G | 7 | a0003c0026t0007g0158 a0009c0009t0001g0155 a0009c0009t0006g0027 others(4): Show |
8 | HG02109.hp2 HG02258.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.-9+3230delA | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20454900 | ||||||
chr16:20454956 | C | T | 7 | a0003c0003t0002g0159 a0003c0003t0002g0160 a0003c0003t0005g0163 others(4): Show |
7 | HG03139.hp2 HG03209.hp2 HG03704.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9+3275C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20454956 | |||||||
chr16:20455006 | T | A | 1 | a0001c0001t0001g0053 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-9+3325T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20455006 | |||||||
chr16:20455068 | A | AT | 232 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(229): Show |
262 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(259): Show |
intron_variant | MODIFIER | c.-9+3391dupT | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20455068 | ||||||
chr16:20455100 | GA | G | 212 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(209): Show |
242 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(239): Show |
intron_variant | MODIFIER | c.-9+3429delA | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20455100 | ||||||
chr16:20455144 | A | G | 211 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(208): Show |
240 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.-9+3463A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20455144 | |||||||
chr16:20455152 | A | T | 1 | a0002c0002t0009g0245 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-9+3471A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20455152 | |||||||
chr16:20455165 | T | A | 6 | a0003c0003t0002g0038 a0003c0003t0002g0324 a0003c0003t0002g0325 others(3): Show |
7 | HG02258.hp2 HG02280.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9+3484T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20455165 | |||||||
chr16:20455165 | T | G | 49 | a0003c0003t0002g0040 a0003c0003t0002g0258 a0003c0003t0002g0268 others(46): Show |
53 | HG00673.hp2 HG01070.hp1 HG01071.hp2 others(50): Show |
intron_variant | MODIFIER | c.-9+3484T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20455165 | |||||||
chr16:20455178 | C | A | 6 | a0003c0003t0002g0159 a0003c0003t0002g0160 a0003c0003t0005g0163 others(3): Show |
6 | HG03139.hp2 HG03209.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9+3497C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20455178 | |||||||
chr16:20455198 | C | A | 235 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(232): Show |
265 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.-9+3517C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20455198 | |||||||
chr16:20455251 | A | G | 218 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(215): Show |
247 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.-9+3570A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20455251 | |||||||
chr16:20455394 | G | A | 51 | a0003c0003t0002g0037 a0003c0003t0002g0281 a0003c0003t0002g0293 others(48): Show |
58 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.-9+3713G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20455394 | |||||||
chr16:20455418 | A | T | 155 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(152): Show |
177 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.-9+3737A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20455418 | |||||||
chr16:20455486 | C | T | 1 | a0003c0003t0002g0258 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-9+3805C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20455486 | |||||||
chr16:20455664 | A | T | 6 | a0003c0003t0002g0159 a0003c0003t0002g0160 a0003c0003t0005g0163 others(3): Show |
6 | HG03139.hp2 HG03209.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9+3983A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20455664 | |||||||
chr16:20455685 | A | C | 1 | a0006c0006t0003g0357 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-9+4004A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20455685 | |||||||
chr16:20455736 | T | TA | 65 | a0003c0003t0002g0038 a0003c0003t0002g0040 a0003c0003t0002g0268 others(62): Show |
71 | HG00673.hp2 HG01070.hp1 HG01071.hp2 others(68): Show |
intron_variant | MODIFIER | c.-9+4065dupA | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20455736 | ||||||
chr16:20455823 | C | T | 1 | a0003c0003t0005g0244 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-9+4142C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20455823 | |||||||
chr16:20455980 | T | A | 6 | a0002c0002t0002g0185 a0002c0002t0018g0186 a0003c0026t0007g0158 others(3): Show |
7 | HG00738.hp1 HG03490.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.-8-4127T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20455980 | |||||||
chr16:20456009 | C | T | 4 | a0010c0011t0005g0259 a0010c0011t0005g0260 a0010c0011t0005g0262 others(1): Show |
4 | HG02145.hp2 HG03130.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-4098C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20456009 | |||||||
chr16:20456247 | A | T | 1 | a0002c0002t0003g0165 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-8-3860A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20456247 | |||||||
chr16:20456287 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-8-3820G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20456287 | |||||||
chr16:20456338 | A | G | 2 | a0003c0003t0002g0263 a0003c0003t0002g0274 |
2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-8-3769A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20456338 | |||||||
chr16:20456427 | G | C | 4 | a0003c0003t0002g0281 a0004c0004t0002g0278 a0004c0004t0002g0279 others(1): Show |
4 | NA18988.hp2 NA18998.hp2 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-3680G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20456427 | |||||||
chr16:20456462 | G | A | 219 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(216): Show |
248 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.-8-3645G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20456462 | |||||||
chr16:20456512 | G | A | 1 | a0016c0025t0005g0277 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-8-3595G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20456512 | |||||||
chr16:20456560 | A | C | 2 | a0001c0001t0001g0028 a0001c0001t0001g0167 |
3 | HG01069.hp2 HG01071.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.-8-3547A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20456560 | |||||||
chr16:20456607 | T | C | 3 | a0002c0002t0003g0187 a0003c0003t0005g0163 a0003c0003t0005g0164 |
3 | HG03139.hp2 HG03209.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-8-3500T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20456607 | |||||||
chr16:20456664 | T | A | 218 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(215): Show |
247 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.-8-3443T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20456664 | |||||||
chr16:20456860 | C | G | 1 | a0003c0003t0002g0317 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-8-3247C>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20456860 | |||||||
chr16:20456877 | T | C | 218 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(215): Show |
247 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.-8-3230T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20456877 | |||||||
chr16:20456903 | A | G | 1 | a0004c0004t0002g0356 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-8-3204A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20456903 | |||||||
chr16:20456911 | C | CA | 60 | a0001c0001t0001g0018 a0001c0001t0001g0059 a0001c0001t0001g0137 others(57): Show |
66 | HG00673.hp2 HG00738.hp2 HG01070.hp1 others(63): Show |
intron_variant | MODIFIER | c.-8-3183dupA | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20456911 | ||||||
chr16:20456911 | CA | C | 46 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(43): Show |
66 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.-8-3183delA | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20456911 | ||||||
chr16:20456980 | C | T | 4 | a0001c0001t0001g0018 a0001c0001t0001g0059 a0001c0001t0001g0137 others(1): Show |
5 | HG00738.hp2 HG01261.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-3127C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20456980 | |||||||
chr16:20457051 | G | A | 1 | a0003c0026t0007g0158 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-8-3056G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20457051 | |||||||
chr16:20457069 | C | T | 1 | a0016c0025t0005g0277 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-8-3038C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20457069 | |||||||
chr16:20457185 | C | T | 14 | a0003c0010t0001g0146 a0003c0010t0001g0147 a0003c0010t0001g0149 others(11): Show |
15 | HG02109.hp2 HG02258.hp1 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.-8-2922C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20457185 | |||||||
chr16:20457186 | G | C | 2 | a0003c0003t0002g0263 a0003c0003t0002g0274 |
2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-8-2921G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20457186 | |||||||
chr16:20457202 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-8-2905T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20457202 | |||||||
chr16:20457266 | C | T | 1 | a0005c0005t0004g0044 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-8-2841C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20457266 | |||||||
chr16:20457309 | T | G | 1 | a0002c0002t0003g0189 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-8-2798T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20457309 | |||||||
chr16:20457424 | C | T | 1 | a0003c0003t0002g0354 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-8-2683C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20457424 | |||||||
chr16:20457486 | C | T | 155 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(152): Show |
177 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.-8-2621C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20457486 | |||||||
chr16:20457509 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-8-2598C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20457509 | |||||||
chr16:20457552 | A | T | 2 | a0002c0002t0003g0183 a0002c0002t0003g0184 |
2 | HG02735.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.-8-2555A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20457552 | |||||||
chr16:20457566 | A | C | 2 | a0002c0002t0015g0242 a0003c0003t0002g0327 |
2 | HG02818.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.-8-2541A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20457566 | |||||||
chr16:20457626 | T | C | 45 | a0003c0003t0002g0038 a0003c0003t0002g0040 a0003c0003t0002g0324 others(42): Show |
50 | HG00673.hp2 HG01070.hp1 HG01071.hp2 others(47): Show |
intron_variant | MODIFIER | c.-8-2481T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20457626 | |||||||
chr16:20457666 | T | C | 1 | a0016c0025t0005g0277 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-8-2441T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20457666 | |||||||
chr16:20457690 | T | C | 1 | a0002c0002t0002g0190 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-8-2417T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20457690 | |||||||
chr16:20457702 | C | A | 1 | a0001c0001t0001g0061 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-8-2405C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20457702 | |||||||
chr16:20457882 | G | C | 211 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(208): Show |
240 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.-8-2225G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20457882 | |||||||
chr16:20457898 | A | G | 1 | a0003c0003t0002g0316 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-8-2209A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20457898 | |||||||
chr16:20458025 | A | G | 1 | a0002c0002t0002g0241 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-8-2082A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458025 | |||||||
chr16:20458104 | C | T | 3 | a0001c0001t0001g0061 a0001c0001t0001g0101 a0001c0001t0001g0102 |
3 | HG01891.hp2 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-8-2003C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458104 | |||||||
chr16:20458196 | G | A | 4 | a0003c0003t0002g0159 a0003c0003t0002g0160 a0003c0003t0012g0161 others(1): Show |
4 | HG03831.hp1 NA18941.hp1 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-1911G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458196 | |||||||
chr16:20458283 | T | G | 9 | a0003c0003t0002g0263 a0003c0003t0002g0274 a0003c0003t0005g0034 others(6): Show |
11 | HG01884.hp1 HG02109.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.-8-1824T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458283 | |||||||
chr16:20458445 | C | CA | 218 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(215): Show |
247 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.-8-1662_-8-1661ins others(1): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458445 | |||||||
chr16:20458485 | T | C | 51 | a0003c0003t0002g0037 a0003c0003t0002g0281 a0003c0003t0002g0293 others(48): Show |
58 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.-8-1622T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458485 | |||||||
chr16:20458661 | A | T | 2 | a0005c0005t0016g0125 a0005c0005t0016g0126 |
2 | HG00099.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.-8-1446A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458661 | |||||||
chr16:20458694 | CTA | C | 7 | a0006c0006t0002g0256 a0006c0006t0002g0348 a0006c0006t0002g0349 others(4): Show |
7 | NA18956.hp1 NA18968.hp1 NA18974.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8-1403_-8-1402del others(2): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20458694 | ||||||
chr16:20458723 | G | A | 4 | a0010c0011t0005g0259 a0010c0011t0005g0260 a0010c0011t0005g0262 others(1): Show |
4 | HG02145.hp2 HG03130.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-1384G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458723 | |||||||
chr16:20458809 | A | T | 1 | a0009c0009t0006g0142 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-8-1298A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458809 | |||||||
chr16:20458840 | G | T | 211 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(208): Show |
240 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.-8-1267G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458840 | |||||||
chr16:20458892 | T | TTATATAT others(17): Show |
1 | a0005c0005t0001g0127 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-8-1203_-8-1180dup others(24): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20458892 | ||||||
chr16:20458896 | A | ATATATAT others(3): Show |
1 | a0003c0003t0005g0163 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-8-1204_-8-1203ins others(10): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20458896 | ||||||
chr16:20458897 | TATATATG others(1): Show |
T | 5 | a0009c0009t0001g0155 a0009c0009t0006g0027 a0009c0009t0006g0142 others(2): Show |
6 | HG02109.hp2 HG02258.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8-1203_-8-1196del others(8): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20458897 | ||||||
chr16:20458897 | TATATATG others(29): Show |
T | 158 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(155): Show |
180 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(177): Show |
intron_variant | MODIFIER | c.-8-1203_-8-1168del others(36): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20458897 | ||||||
chr16:20458899 | TATATGCA others(27): Show |
T | 2 | a0003c0003t0003g0240 a0004c0004t0013g0363 |
2 | HG04199.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-8-1203_-8-1170del others(34): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20458899 | ||||||
chr16:20458901 | TATGC | T | 8 | a0003c0010t0001g0146 a0003c0010t0001g0147 a0003c0010t0001g0149 others(5): Show |
8 | HG02717.hp1 HG02886.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-8-1203_-8-1200del others(4): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20458901 | ||||||
chr16:20458903 | TGCATATA others(2): Show |
T | 10 | a0003c0003t0002g0037 a0004c0004t0002g0002 a0004c0004t0002g0279 others(7): Show |
11 | HG00621.hp1 HG02148.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.-8-1203_-8-1195del others(9): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458903 | |||||||
chr16:20458903 | TGCATATA others(4): Show |
T | 38 | a0003c0003t0002g0281 a0003c0003t0002g0293 a0003c0003t0002g0294 others(35): Show |
43 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.-8-1203_-8-1193del others(11): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458903 | |||||||
chr16:20458903 | TGCATATA others(6): Show |
T | 2 | a0004c0004t0002g0314 a0004c0004t0002g0315 |
2 | NA18961.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.-8-1203_-8-1191del others(13): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458903 | |||||||
chr16:20458904 | G | A | 3 | a0003c0003t0005g0163 a0003c0003t0005g0164 a0008c0008t0001g0134 |
3 | HG02055.hp2 HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-8-1203G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458904 | |||||||
chr16:20458904 | G | GTATATAT others(23): Show |
1 | a0003c0026t0007g0158 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-8-1203_-8-1202ins others(30): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458904 | |||||||
chr16:20458905 | C | CAT | 22 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(19): Show |
37 | HG00099.hp2 HG00735.hp2 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.-8-1176_-8-1175dup others(2): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20458905 | ||||||
chr16:20458905 | C | CATAT | 3 | a0001c0001t0001g0174 a0001c0001t0006g0091 a0011c0012t0001g0055 |
3 | HG01433.hp1 HG02055.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-8-1178_-8-1175dup others(4): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20458905 | ||||||
chr16:20458905 | C | CATATAT | 4 | a0001c0001t0001g0042 a0001c0001t0001g0089 a0001c0001t0027g0141 others(1): Show |
4 | HG00558.hp1 HG00609.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-1180_-8-1175dup others(6): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20458905 | ||||||
chr16:20458905 | C | CATATATA others(1): Show |
5 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0090 others(2): Show |
8 | HG01168.hp2 HG01169.hp1 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.-8-1182_-8-1175dup others(8): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20458905 | ||||||
chr16:20458905 | C | CATATATA others(3): Show |
1 | a0001c0001t0001g0066 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-8-1184_-8-1175dup others(10): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20458905 | ||||||
chr16:20458905 | C | CATATATA others(5): Show |
4 | a0001c0001t0001g0007 a0001c0001t0001g0065 a0001c0001t0001g0082 others(1): Show |
4 | HG01993.hp1 HG02602.hp2 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-1186_-8-1175dup others(12): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20458905 | ||||||
chr16:20458905 | C | CATATATA others(9): Show |
2 | a0001c0001t0001g0156 a0001c0001t0024g0157 |
2 | NA18955.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.-8-1190_-8-1175dup others(16): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20458905 | ||||||
chr16:20458905 | C | T | 8 | a0003c0003t0002g0159 a0003c0003t0002g0160 a0003c0003t0005g0163 others(5): Show |
8 | HG02055.hp2 HG03139.hp2 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.-8-1202C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458905 | |||||||
chr16:20458905 | CAT | C | 20 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0025 others(17): Show |
22 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.-8-1176_-8-1175del others(2): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20458905 | ||||||
chr16:20458906 | A | G | 1 | a0008c0008t0001g0134 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-8-1201A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458906 | |||||||
chr16:20458907 | T | C | 1 | a0008c0008t0001g0134 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-8-1200T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458907 | |||||||
chr16:20458909 | T | TATATATA others(3): Show |
2 | a0003c0003t0012g0161 a0003c0003t0012g0162 |
2 | HG03831.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.-8-1189_-8-1188ins others(10): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20458909 | ||||||
chr16:20458910 | A | G | 8 | a0003c0010t0001g0146 a0003c0010t0001g0147 a0003c0010t0001g0149 others(5): Show |
8 | HG02717.hp1 HG02886.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-8-1197A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458910 | |||||||
chr16:20458911 | T | A | 2 | a0004c0004t0002g0285 a0004c0004t0002g0292 |
2 | HG01978.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.-8-1196T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458911 | |||||||
chr16:20458912 | A | G | 2 | a0004c0004t0002g0285 a0004c0004t0002g0292 |
2 | HG01978.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.-8-1195A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458912 | |||||||
chr16:20458913 | T | A | 10 | a0003c0003t0002g0037 a0004c0004t0002g0002 a0004c0004t0002g0279 others(7): Show |
11 | HG00621.hp1 HG02148.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.-8-1194T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458913 | |||||||
chr16:20458914 | A | G | 18 | a0003c0003t0002g0037 a0004c0004t0002g0002 a0004c0004t0002g0279 others(15): Show |
20 | HG00621.hp1 HG01978.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.-8-1193A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458914 | |||||||
chr16:20458915 | T | A | 38 | a0003c0003t0002g0281 a0003c0003t0002g0293 a0003c0003t0002g0294 others(35): Show |
43 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.-8-1192T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458915 | |||||||
chr16:20458916 | A | G | 47 | a0003c0003t0002g0037 a0003c0003t0002g0281 a0003c0003t0002g0293 others(44): Show |
54 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.-8-1191A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458916 | |||||||
chr16:20458917 | T | A | 2 | a0004c0004t0002g0314 a0004c0004t0002g0315 |
2 | NA18961.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.-8-1190T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458917 | |||||||
chr16:20458918 | A | G | 40 | a0003c0003t0002g0281 a0003c0003t0002g0293 a0003c0003t0002g0294 others(37): Show |
45 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.-8-1189A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458918 | |||||||
chr16:20458920 | A | G | 2 | a0004c0004t0002g0314 a0004c0004t0002g0315 |
2 | NA18961.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.-8-1187A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458920 | |||||||
chr16:20458921 | T | C | 8 | a0003c0010t0001g0146 a0003c0010t0001g0147 a0003c0010t0001g0149 others(5): Show |
8 | HG02717.hp1 HG02886.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-8-1186T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458921 | |||||||
chr16:20458925 | T | C | 6 | a0009c0009t0001g0155 a0009c0009t0006g0027 a0009c0009t0006g0142 others(3): Show |
7 | HG02109.hp2 HG02258.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8-1182T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458925 | |||||||
chr16:20458931 | T | C | 1 | a0005c0005t0004g0119 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-8-1176T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458931 | |||||||
chr16:20458932 | A | ATG | 3 | a0007c0007t0001g0086 a0007c0007t0001g0087 a0007c0007t0001g0096 |
3 | HG01934.hp1 HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-8-1175_-8-1174ins others(2): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458932 | |||||||
chr16:20458932 | A | G | 2 | a0007c0007t0023g0083 a0007c0007t0028g0085 |
2 | HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-8-1175A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458932 | |||||||
chr16:20458933 | C | T | 72 | a0003c0003t0002g0037 a0003c0003t0002g0159 a0003c0003t0002g0160 others(69): Show |
80 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.-8-1174C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458933 | |||||||
chr16:20458935 | T | C | 2 | a0001c0001t0026g0062 a0008c0008t0001g0019 |
3 | HG01099.hp2 HG02895.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-8-1172T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458935 | |||||||
chr16:20458986 | G | T | 2 | a0004c0004t0002g0314 a0004c0004t0002g0315 |
2 | NA18961.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.-8-1121G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458986 | |||||||
chr16:20459141 | T | C | 1 | a0004c0004t0002g0283 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-8-966T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20459141 | |||||||
chr16:20459163 | G | C | 2 | a0003c0003t0005g0163 a0003c0003t0005g0164 |
2 | HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-8-944G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20459163 | |||||||
chr16:20459231 | T | A | 1 | a0016c0025t0005g0277 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-8-876T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20459231 | |||||||
chr16:20459322 | T | A | 1 | a0004c0004t0002g0255 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-8-785T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20459322 | |||||||
chr16:20459402 | T | A | 2 | a0006c0006t0002g0328 a0006c0006t0019g0329 |
2 | NA18978.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.-8-705T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20459402 | |||||||
chr16:20459403 | T | A | 1 | a0003c0026t0007g0158 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-8-704T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20459403 | |||||||
chr16:20459406 | A | G | 1 | a0001c0001t0001g0100 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-8-701A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20459406 | |||||||
chr16:20459479 | A | G | 1 | a0004c0004t0002g0313 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-8-628A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20459479 | |||||||
chr16:20459768 | T | C | 232 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(229): Show |
262 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(259): Show |
intron_variant | MODIFIER | c.-8-339T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20459768 | |||||||
chr16:20459853 | G | A | 1 | a0003c0003t0005g0271 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-8-254G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20459853 | |||||||
chr16:20459855 | G | A | 82 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(79): Show |
95 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.-8-252G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20459855 | |||||||
chr16:20459870 | T | A | 41 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(38): Show |
61 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.-8-237T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20459870 | |||||||
chr16:20459887 | G | T | 9 | a0003c0003t0002g0263 a0003c0003t0002g0274 a0003c0003t0005g0034 others(6): Show |
11 | HG01884.hp1 HG02109.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.-8-220G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20459887 | |||||||
chr16:20459898 | G | C | 1 | a0011c0012t0001g0017 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-8-209G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20459898 | |||||||
chr16:20459963 | T | A | 1 | a0004c0004t0002g0282 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-8-144T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20459963 | |||||||
chr16:20459984 | C | A | 1 | a0007c0007t0001g0063 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-8-123C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20459984 | |||||||
chr16:20460042 | T | C | 218 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(215): Show |
247 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.-8-65T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20460042 | |||||||
chr16:20460057 | G | C | 14 | a0003c0010t0001g0146 a0003c0010t0001g0147 a0003c0010t0001g0149 others(11): Show |
15 | HG02109.hp2 HG02258.hp1 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.-8-50G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20460057 | |||||||
chr16:20460059 | G | A | 2 | a0001c0001t0010g0047 a0001c0001t0010g0048 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-8-48G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20460059 | |||||||
chr16:20460105 | A | G | 1 | a0001c0001t0001g0178 | 1 | NA18962.hp1 | splice_acceptor_variant&intron_variant | HIGH | c.-8-2A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20460105 | |||||||
chr16:20460304 | A | C | 1 | a0004c0004t0002g0312 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.177+13A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20460304 | |||||||
chr16:20460412 | G | A | 1 | a0016c0025t0005g0277 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.177+121G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20460412 | |||||||
chr16:20460424 | G | A | 3 | a0005c0005t0016g0125 a0005c0005t0016g0126 a0005c0005t0032g0118 |
3 | HG00099.hp1 HG00323.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.177+133G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20460424 | |||||||
chr16:20460543 | A | G | 1 | a0005c0005t0004g0099 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.177+252A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20460543 | |||||||
chr16:20460609 | G | A | 1 | a0002c0002t0003g0191 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.177+318G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20460609 | |||||||
chr16:20460663 | C | T | 217 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(214): Show |
246 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.177+372C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20460663 | |||||||
chr16:20460728 | A | T | 1 | a0005c0005t0030g0098 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.177+437A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20460728 | |||||||
chr16:20460812 | A | G | 218 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(215): Show |
247 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.177+521A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20460812 | |||||||
chr16:20460813 | C | T | 1 | a0003c0003t0002g0311 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.177+522C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20460813 | |||||||
chr16:20461154 | G | A | 232 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(229): Show |
262 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(259): Show |
intron_variant | MODIFIER | c.177+863G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20461154 | |||||||
chr16:20461260 | C | G | 1 | a0001c0001t0001g0097 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.177+969C>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20461260 | |||||||
chr16:20461430 | A | G | 4 | a0010c0011t0005g0259 a0010c0011t0005g0260 a0010c0011t0005g0262 others(1): Show |
4 | HG02145.hp2 HG03130.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.177+1139A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20461430 | |||||||
chr16:20461436 | C | T | 1 | a0006c0006t0002g0347 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.177+1145C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20461436 | |||||||
chr16:20461486 | A | C | 1 | a0003c0026t0007g0158 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.177+1195A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20461486 | |||||||
chr16:20461488 | T | C | 1 | a0003c0026t0007g0158 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.177+1197T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20461488 | |||||||
chr16:20461491 | C | A | 1 | a0003c0026t0007g0158 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.177+1200C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20461491 | |||||||
chr16:20461539 | G | A | 1 | a0006c0006t0002g0347 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.177+1248G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20461539 | |||||||
chr16:20461541 | A | G | 232 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(229): Show |
262 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(259): Show |
intron_variant | MODIFIER | c.177+1250A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20461541 | |||||||
chr16:20461723 | A | G | 1 | a0007c0007t0001g0096 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.177+1432A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20461723 | |||||||
chr16:20461951 | C | G | 14 | a0003c0010t0001g0146 a0003c0010t0001g0147 a0003c0010t0001g0149 others(11): Show |
15 | HG02109.hp2 HG02258.hp1 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.177+1660C>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20461951 | |||||||
chr16:20461954 | A | G | 234 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(231): Show |
264 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.177+1663A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20461954 | |||||||
chr16:20462137 | A | G | 2 | a0004c0004t0002g0309 a0004c0004t0002g0310 |
2 | HG02738.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.177+1846A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20462137 | |||||||
chr16:20462140 | G | C | 6 | a0009c0009t0001g0155 a0009c0009t0006g0027 a0009c0009t0006g0142 others(3): Show |
7 | HG02109.hp2 HG02258.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.177+1849G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20462140 | |||||||
chr16:20462156 | G | A | 4 | a0001c0001t0001g0064 a0003c0003t0007g0013 a0003c0003t0007g0235 others(1): Show |
6 | HG02965.hp1 HG02970.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.177+1865G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20462156 | |||||||
chr16:20462272 | A | G | 50 | a0003c0003t0002g0037 a0003c0003t0002g0281 a0003c0003t0002g0293 others(47): Show |
57 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.177+1981A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20462272 | |||||||
chr16:20462274 | A | G | 232 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(229): Show |
262 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(259): Show |
intron_variant | MODIFIER | c.177+1983A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20462274 | |||||||
chr16:20462442 | C | T | 1 | a0002c0002t0003g0187 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.177+2151C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20462442 | |||||||
chr16:20462470 | T | G | 1 | a0002c0002t0003g0192 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.177+2179T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20462470 | |||||||
chr16:20462471 | C | T | 1 | a0002c0002t0003g0192 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.177+2180C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20462471 | |||||||
chr16:20462581 | G | A | 232 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(229): Show |
262 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(259): Show |
intron_variant | MODIFIER | c.177+2290G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20462581 | |||||||
chr16:20462637 | C | A | 2 | a0003c0003t0005g0163 a0003c0003t0005g0164 |
2 | HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.177+2346C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20462637 | |||||||
chr16:20462713 | A | G | 1 | a0003c0026t0007g0158 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.177+2422A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20462713 | |||||||
chr16:20462796 | C | G | 2 | a0003c0003t0002g0258 a0003c0003t0007g0257 |
2 | HG02257.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.177+2505C>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20462796 | |||||||
chr16:20462821 | T | A | 2 | a0003c0015t0001g0138 a0003c0015t0001g0139 |
2 | HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.177+2530T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20462821 | |||||||
chr16:20462828 | C | CA | 8 | a0003c0010t0001g0146 a0003c0010t0001g0147 a0003c0010t0001g0149 others(5): Show |
8 | HG02717.hp1 HG02886.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.177+2545dupA | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 20462828 | ||||||
chr16:20462982 | C | CA | 4 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0010g0047 others(1): Show |
4 | HG01175.hp1 HG02897.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.178-2528dupA | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 20462982 | ||||||
chr16:20462998 | A | C | 235 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(232): Show |
265 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.178-2519A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20462998 | |||||||
chr16:20462998 | A | T | 1 | a0005c0005t0001g0127 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.178-2519A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20462998 | |||||||
chr16:20463008 | C | G | 1 | a0001c0001t0001g0061 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.178-2509C>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20463008 | |||||||
chr16:20463031 | A | G | 6 | a0009c0009t0001g0155 a0009c0009t0006g0027 a0009c0009t0006g0142 others(3): Show |
7 | HG02109.hp2 HG02258.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.178-2486A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20463031 | |||||||
chr16:20463061 | A | T | 2 | a0003c0015t0001g0138 a0003c0015t0001g0139 |
2 | HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.178-2456A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20463061 | |||||||
chr16:20463098 | G | T | 218 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(215): Show |
247 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.178-2419G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20463098 | |||||||
chr16:20463109 | A | T | 1 | a0003c0010t0006g0152 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-2408A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20463109 | |||||||
chr16:20463115 | C | T | 326 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(323): Show |
387 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(384): Show |
intron_variant | MODIFIER | c.178-2402C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20463115 | |||||||
chr16:20463125 | A | G | 1 | a0003c0026t0007g0158 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.178-2392A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20463125 | |||||||
chr16:20463137 | C | T | 1 | a0002c0002t0003g0165 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.178-2380C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20463137 | |||||||
chr16:20463138 | G | A | 1 | a0002c0002t0003g0191 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.178-2379G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20463138 | |||||||
chr16:20463169 | C | T | 1 | a0003c0026t0007g0158 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.178-2348C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20463169 | |||||||
chr16:20463181 | T | C | 6 | a0002c0002t0003g0196 a0002c0002t0008g0011 a0002c0002t0008g0179 others(3): Show |
8 | NA18940.hp2 NA18948.hp2 NA18953.hp2 others(5): Show |
intron_variant | MODIFIER | c.178-2336T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20463181 | |||||||
chr16:20463190 | C | T | 1 | a0002c0002t0003g0234 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.178-2327C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20463190 | |||||||
chr16:20463206 | A | C | 2 | a0007c0007t0001g0094 a0007c0007t0001g0095 |
2 | HG01496.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.178-2311A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20463206 | |||||||
chr16:20463231 | T | C | 5 | a0003c0003t0005g0034 a0003c0003t0005g0035 a0003c0003t0005g0271 others(2): Show |
7 | HG01884.hp1 HG02109.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.178-2286T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20463231 | |||||||
chr16:20463264 | A | C | 14 | a0003c0010t0001g0146 a0003c0010t0001g0147 a0003c0010t0001g0149 others(11): Show |
15 | HG02109.hp2 HG02258.hp1 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.178-2253A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20463264 | |||||||
chr16:20463270 | A | G | 2 | a0003c0003t0002g0269 a0003c0003t0002g0270 |
2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.178-2247A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20463270 | |||||||
chr16:20463345 | G | T | 1 | a0002c0002t0003g0233 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.178-2172G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20463345 | |||||||
chr16:20463360 | T | C | 234 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(231): Show |
264 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.178-2157T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20463360 | |||||||
chr16:20463462 | C | A | 1 | a0002c0002t0003g0197 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.178-2055C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20463462 | |||||||
chr16:20463479 | G | A | 6 | a0009c0009t0001g0155 a0009c0009t0006g0027 a0009c0009t0006g0142 others(3): Show |
7 | HG02109.hp2 HG02258.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.178-2038G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20463479 | |||||||
chr16:20463647 | A | T | 6 | a0003c0003t0002g0159 a0003c0003t0002g0160 a0003c0003t0005g0163 others(3): Show |
6 | HG03139.hp2 HG03209.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.178-1870A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20463647 | |||||||
chr16:20463697 | G | A | 1 | a0020c0029t0001g0067 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.178-1820G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20463697 | |||||||
chr16:20463728 | A | G | 2 | a0003c0015t0001g0138 a0003c0015t0001g0139 |
2 | HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.178-1789A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20463728 | |||||||
chr16:20463767 | G | A | 1 | a0008c0008t0001g0134 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.178-1750G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20463767 | |||||||
chr16:20463885 | T | C | 1 | a0004c0004t0002g0285 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.178-1632T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20463885 | |||||||
chr16:20463906 | C | T | 1 | a0006c0006t0002g0346 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.178-1611C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20463906 | |||||||
chr16:20463932 | C | T | 90 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(87): Show |
105 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.178-1585C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20463932 | |||||||
chr16:20463956 | C | G | 224 | a0001c0001t0001g0143 a0001c0001t0010g0047 a0001c0001t0010g0048 others(221): Show |
253 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.178-1561C>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20463956 | |||||||
chr16:20463983 | C | T | 1 | a0002c0002t0003g0232 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.178-1534C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20463983 | |||||||
chr16:20464091 | G | C | 5 | a0001c0001t0027g0141 a0003c0003t0005g0163 a0003c0003t0005g0164 others(2): Show |
5 | HG00558.hp1 HG00609.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.178-1426G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20464091 | |||||||
chr16:20464120 | A | G | 3 | a0001c0001t0001g0016 a0001c0001t0001g0092 a0001c0001t0001g0093 |
4 | HG01168.hp2 HG01169.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.178-1397A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20464120 | |||||||
chr16:20464147 | G | T | 1 | a0008c0008t0001g0041 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.178-1370G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20464147 | |||||||
chr16:20464201 | G | A | 1 | a0006c0006t0002g0348 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.178-1316G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20464201 | |||||||
chr16:20464228 | G | T | 51 | a0003c0003t0002g0037 a0003c0003t0002g0281 a0003c0003t0002g0293 others(48): Show |
58 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.178-1289G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20464228 | |||||||
chr16:20464245 | T | A | 218 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(215): Show |
247 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.178-1272T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20464245 | |||||||
chr16:20464357 | C | T | 51 | a0003c0003t0002g0037 a0003c0003t0002g0281 a0003c0003t0002g0293 others(48): Show |
58 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.178-1160C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20464357 | |||||||
chr16:20464412 | T | C | 234 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(231): Show |
264 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.178-1105T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20464412 | |||||||
chr16:20464436 | C | T | 1 | a0005c0005t0029g0077 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.178-1081C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20464436 | |||||||
chr16:20464499 | T | C | 1 | a0003c0003t0002g0236 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.178-1018T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20464499 | |||||||
chr16:20464562 | ATCTTATG others(449): Show |
A | 1 | a0004c0004t0002g0282 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.178-953_178-498del | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 20464562 | ||||||
chr16:20464607 | C | T | 2 | a0002c0002t0002g0185 a0002c0002t0018g0186 |
2 | HG00738.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.178-910C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20464607 | |||||||
chr16:20464622 | C | G | 1 | a0006c0006t0002g0015 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.178-895C>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20464622 | |||||||
chr16:20464735 | A | T | 6 | a0009c0009t0001g0155 a0009c0009t0006g0027 a0009c0009t0006g0142 others(3): Show |
7 | HG02109.hp2 HG02258.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.178-782A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20464735 | |||||||
chr16:20464749 | G | A | 2 | a0002c0002t0003g0183 a0002c0002t0003g0184 |
2 | HG02735.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.178-768G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20464749 | |||||||
chr16:20464796 | G | A | 1 | a0004c0004t0002g0307 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.178-721G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20464796 | |||||||
chr16:20464811 | G | A | 1 | a0003c0003t0002g0334 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.178-706G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20464811 | |||||||
chr16:20464988 | A | T | 1 | a0003c0003t0003g0238 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.178-529A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20464988 | |||||||
chr16:20465016 | G | T | 217 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(214): Show |
246 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.178-501G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20465016 | |||||||
chr16:20465019 | T | G | 1 | a0004c0004t0002g0282 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.178-498T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20465019 | |||||||
chr16:20465020 | T | G | 1 | a0004c0004t0002g0282 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.178-497T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20465020 | |||||||
chr16:20465021 | T | G | 1 | a0004c0004t0002g0282 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.178-496T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20465021 | |||||||
chr16:20465155 | A | G | 212 | a0001c0001t0006g0091 a0002c0002t0002g0185 a0002c0002t0002g0190 others(209): Show |
241 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.178-362A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20465155 | |||||||
chr16:20465164 | C | T | 1 | a0003c0003t0005g0164 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.178-353C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20465164 | |||||||
chr16:20465250 | T | C | 1 | a0003c0003t0002g0324 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.178-267T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20465250 | |||||||
chr16:20465364 | G | C | 91 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(88): Show |
106 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.178-153G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20465364 | |||||||
chr16:20465372 | A | G | 91 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(88): Show |
106 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.178-145A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20465372 | |||||||
chr16:20465373 | A | G | 218 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(215): Show |
247 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.178-144A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20465373 | |||||||
chr16:20465408 | G | A | 1 | a0005c0005t0001g0057 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.178-109G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20465408 | |||||||
chr16:20465469 | T | A | 2 | a0003c0003t0005g0163 a0003c0003t0005g0164 |
2 | HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.178-48T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20465469 | |||||||
chr16:20465491 | G | A | 1 | a0019c0021t0002g0198 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.178-26G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20465491 | |||||||
chr16:20465502 | C | T | 1 | a0019c0021t0002g0198 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.178-15C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20465502 | |||||||
chr16:20465514 | C | T | 1 | a0002c0002t0003g0231 | 1 | NA18941.hp2 | splice_region_variant&intron_variant | LOW | c.178-3C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20465514 | |||||||
chr16:20465779 | G | A | 1 | a0005c0005t0004g0068 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.388+52G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20465779 | |||||||
chr16:20465781 | T | G | 1 | a0004c0004t0002g0285 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.388+54T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20465781 | |||||||
chr16:20465821 | T | G | 1 | a0019c0021t0002g0198 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.388+94T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20465821 | |||||||
chr16:20465841 | G | C | 232 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(229): Show |
262 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(259): Show |
intron_variant | MODIFIER | c.388+114G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20465841 | |||||||
chr16:20465843 | A | C | 232 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(229): Show |
262 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(259): Show |
intron_variant | MODIFIER | c.388+116A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20465843 | |||||||
chr16:20465860 | A | T | 1 | a0019c0021t0002g0198 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.388+133A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20465860 | |||||||
chr16:20465868 | A | G | 1 | a0019c0021t0002g0198 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.388+141A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20465868 | |||||||
chr16:20466023 | T | G | 1 | a0019c0021t0002g0198 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.388+296T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20466023 | |||||||
chr16:20466052 | A | C | 1 | a0019c0021t0002g0198 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.388+325A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20466052 | |||||||
chr16:20466065 | C | T | 1 | a0019c0021t0002g0198 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.388+338C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20466065 | |||||||
chr16:20466097 | A | C | 8 | a0002c0002t0002g0185 a0002c0002t0003g0031 a0002c0002t0003g0228 others(5): Show |
9 | HG00280.hp2 HG00738.hp1 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.388+370A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20466097 | |||||||
chr16:20466134 | G | GCTATGCC others(12): Show |
8 | a0002c0002t0002g0185 a0002c0002t0003g0031 a0002c0002t0003g0228 others(5): Show |
9 | HG00280.hp2 HG00738.hp1 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.388+407_388+408ins others(19): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20466134 | |||||||
chr16:20466152 | G | T | 331 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(328): Show |
392 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(389): Show |
intron_variant | MODIFIER | c.388+425G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20466152 | |||||||
chr16:20466160 | A | G | 8 | a0002c0002t0002g0185 a0002c0002t0003g0031 a0002c0002t0003g0228 others(5): Show |
9 | HG00280.hp2 HG00738.hp1 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.388+433A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20466160 | |||||||
chr16:20466176 | T | A | 1 | a0003c0026t0007g0158 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.388+449T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20466176 | |||||||
chr16:20466186 | A | G | 1 | a0019c0021t0002g0198 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.388+459A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20466186 | |||||||
chr16:20466244 | AG | A | 3 | a0001c0001t0001g0022 a0001c0001t0001g0056 a0001c0001t0001g0064 |
4 | HG00735.hp2 HG01109.hp1 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.388+518delG | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20466244 | |||||||
chr16:20466267 | G | A | 1 | a0019c0021t0002g0198 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.388+540G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20466267 | |||||||
chr16:20466268 | A | G | 1 | a0019c0021t0002g0198 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.388+541A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20466268 | |||||||
chr16:20466410 | A | C | 1 | a0003c0026t0007g0158 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.388+683A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20466410 | |||||||
chr16:20466475 | T | C | 217 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(214): Show |
246 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.388+748T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20466475 | |||||||
chr16:20466476 | G | A | 215 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(212): Show |
244 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(241): Show |
intron_variant | MODIFIER | c.388+749G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20466476 | |||||||
chr16:20466538 | A | G | 217 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(214): Show |
246 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.388+811A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20466538 | |||||||
chr16:20466589 | T | A | 232 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(229): Show |
262 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(259): Show |
intron_variant | MODIFIER | c.388+862T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20466589 | |||||||
chr16:20466697 | A | G | 1 | a0019c0021t0002g0198 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.388+970A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20466697 | |||||||
chr16:20466789 | A | T | 1 | a0016c0025t0005g0277 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.388+1062A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20466789 | |||||||
chr16:20466820 | A | C | 2 | a0009c0009t0006g0142 a0009c0009t0006g0153 |
2 | HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.388+1093A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20466820 | |||||||
chr16:20466837 | T | A | 1 | a0006c0006t0002g0346 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.388+1110T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20466837 | |||||||
chr16:20467008 | C | G | 1 | a0003c0026t0007g0158 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.388+1281C>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20467008 | |||||||
chr16:20467109 | A | G | 2 | a0003c0015t0001g0138 a0003c0015t0001g0139 |
2 | HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.388+1382A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20467109 | |||||||
chr16:20467114 | T | A | 12 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0023 others(9): Show |
21 | HG00280.hp1 HG00639.hp2 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.388+1387T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20467114 | |||||||
chr16:20467124 | G | T | 1 | a0003c0026t0007g0158 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.388+1397G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20467124 | |||||||
chr16:20467162 | A | G | 1 | a0003c0026t0007g0158 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.388+1435A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20467162 | |||||||
chr16:20467260 | C | T | 232 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(229): Show |
262 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(259): Show |
intron_variant | MODIFIER | c.388+1533C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20467260 | |||||||
chr16:20467280 | T | A | 218 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(215): Show |
247 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.388+1553T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20467280 | |||||||
chr16:20467331 | GATTGAGT others(20): Show |
G | 45 | a0003c0003t0002g0038 a0003c0003t0002g0040 a0003c0003t0002g0324 others(42): Show |
50 | HG00673.hp2 HG01070.hp1 HG01071.hp2 others(47): Show |
intron_variant | MODIFIER | c.388+1633_388+1659d others(29): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr16 | 20467331 | ||||||
chr16:20467402 | C | A | 288 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(285): Show |
328 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(325): Show |
intron_variant | MODIFIER | c.388+1675C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20467402 | |||||||
chr16:20467410 | T | C | 1 | a0015c0028t0001g0078 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.388+1683T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20467410 | |||||||
chr16:20467494 | C | T | 7 | a0003c0003t0002g0159 a0003c0003t0002g0160 a0003c0003t0005g0163 others(4): Show |
7 | HG03139.hp2 HG03209.hp2 HG03704.hp2 others(4): Show |
intron_variant | MODIFIER | c.388+1767C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20467494 | |||||||
chr16:20467561 | G | T | 2 | a0003c0003t0002g0258 a0003c0003t0007g0257 |
2 | HG02257.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.388+1834G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20467561 | |||||||
chr16:20467613 | G | T | 2 | a0003c0003t0012g0161 a0003c0003t0012g0162 |
2 | HG03831.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.388+1886G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20467613 | |||||||
chr16:20467648 | C | T | 4 | a0003c0003t0002g0159 a0003c0003t0002g0160 a0003c0003t0012g0161 others(1): Show |
4 | HG03831.hp1 NA18941.hp1 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.389-1864C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20467648 | |||||||
chr16:20468021 | A | G | 1 | a0001c0001t0001g0102 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.389-1491A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20468021 | |||||||
chr16:20468028 | C | T | 2 | a0003c0003t0002g0263 a0003c0003t0002g0274 |
2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.389-1484C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20468028 | |||||||
chr16:20468067 | C | T | 232 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(229): Show |
262 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(259): Show |
intron_variant | MODIFIER | c.389-1445C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20468067 | |||||||
chr16:20468286 | G | T | 1 | a0006c0016t0002g0345 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.389-1226G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20468286 | |||||||
chr16:20468418 | G | T | 1 | a0006c0006t0002g0353 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.389-1094G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20468418 | |||||||
chr16:20468462 | C | A | 1 | a0004c0004t0002g0287 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.389-1050C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20468462 | |||||||
chr16:20468691 | T | A | 232 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(229): Show |
262 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(259): Show |
intron_variant | MODIFIER | c.389-821T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20468691 | |||||||
chr16:20468721 | C | T | 9 | a0003c0003t0002g0263 a0003c0003t0002g0274 a0003c0003t0005g0034 others(6): Show |
11 | HG01884.hp1 HG02109.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.389-791C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20468721 | |||||||
chr16:20468978 | A | G | 1 | a0003c0003t0005g0272 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.389-534A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20468978 | |||||||
chr16:20469024 | G | C | 55 | a0003c0003t0002g0038 a0003c0003t0002g0040 a0003c0003t0002g0258 others(52): Show |
60 | HG00673.hp2 HG01070.hp1 HG01071.hp2 others(57): Show |
intron_variant | MODIFIER | c.389-488G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20469024 | |||||||
chr16:20469122 | A | T | 146 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(143): Show |
166 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.389-390A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20469122 | |||||||
chr16:20469205 | AT | A | 56 | a0001c0001t0001g0104 a0003c0003t0002g0038 a0003c0003t0002g0040 others(53): Show |
61 | HG00673.hp2 HG01070.hp1 HG01071.hp2 others(58): Show |
intron_variant | MODIFIER | c.389-299delT | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr16 | 20469205 | ||||||
chr16:20469287 | C | A | 3 | a0001c0001t0001g0081 a0001c0017t0001g0079 a0001c0017t0001g0080 |
3 | HG02486.hp1 HG02717.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.389-225C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20469287 | |||||||
chr16:20469357 | T | A | 160 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(157): Show |
182 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.389-155T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20469357 | |||||||
chr16:20469496 | T | C | 217 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(214): Show |
246 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.389-16T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20469496 | |||||||
chr16:20469786 | C | T | 4 | a0010c0011t0005g0259 a0010c0011t0005g0260 a0010c0011t0005g0262 others(1): Show |
4 | HG02145.hp2 HG03130.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.596+67C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/13 | chr16 | 20469786 | |||||||
chr16:20469870 | GTA | G | 135 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(132): Show |
158 | HG00280.hp2 HG00609.hp2 HG00673.hp2 others(155): Show |
intron_variant | MODIFIER | c.596+153_596+154del others(2): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr16 | 20469870 | ||||||
chr16:20469870 | GTAT | G | 49 | a0002c0002t0003g0183 a0003c0003t0002g0037 a0003c0003t0002g0258 others(46): Show |
56 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.596+153_596+155del others(3): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr16 | 20469870 | ||||||
chr16:20469871 | TA | T | 32 | a0002c0002t0003g0012 a0002c0002t0003g0165 a0002c0002t0003g0191 others(29): Show |
32 | HG00408.hp2 HG00438.hp1 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.596+153delA | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/13 | chr16 | 20469871 | |||||||
chr16:20469872 | A | AT | 8 | a0001c0001t0001g0018 a0001c0001t0001g0117 a0001c0001t0004g0024 others(5): Show |
9 | HG00621.hp2 HG01261.hp2 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.596+177dupT | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr16 | 20469872 | ||||||
chr16:20469872 | A | T | 15 | a0002c0002t0008g0193 a0003c0003t0002g0268 a0003c0003t0002g0269 others(12): Show |
15 | HG00741.hp1 HG01361.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.596+153A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/13 | chr16 | 20469872 | |||||||
chr16:20469872 | AT | A | 46 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(43): Show |
51 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.596+177delT | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr16 | 20469872 | ||||||
chr16:20469872 | ATT | A | 14 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(11): Show |
15 | HG01168.hp2 HG01169.hp1 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.596+176_596+177del others(2): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr16 | 20469872 | ||||||
chr16:20469883 | T | G | 1 | a0006c0006t0002g0348 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.596+164T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/13 | chr16 | 20469883 | |||||||
chr16:20469884 | T | G | 43 | a0003c0003t0002g0038 a0003c0003t0002g0040 a0003c0003t0002g0324 others(40): Show |
48 | HG00673.hp2 HG01070.hp1 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.596+165T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/13 | chr16 | 20469884 | |||||||
chr16:20469885 | T | G | 2 | a0006c0006t0002g0331 a0006c0006t0009g0330 |
2 | NA18994.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.596+166T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/13 | chr16 | 20469885 | |||||||
chr16:20470077 | C | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0059 |
3 | HG00738.hp2 HG01261.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.596+358C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/13 | chr16 | 20470077 | |||||||
chr16:20470093 | C | G | 219 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(216): Show |
248 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.596+374C>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/13 | chr16 | 20470093 | |||||||
chr16:20470150 | T | C | 1 | a0008c0008t0001g0134 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.596+431T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/13 | chr16 | 20470150 | |||||||
chr16:20470175 | A | G | 1 | a0008c0008t0001g0134 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.596+456A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/13 | chr16 | 20470175 | |||||||
chr16:20470180 | A | G | 1 | a0003c0003t0003g0239 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.596+461A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/13 | chr16 | 20470180 | |||||||
chr16:20470248 | C | T | 1 | a0001c0001t0001g0090 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.596+529C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/13 | chr16 | 20470248 | |||||||
chr16:20470294 | C | G | 5 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0056 others(2): Show |
10 | HG00099.hp2 HG00735.hp2 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.596+575C>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/13 | chr16 | 20470294 | |||||||
chr16:20470334 | T | C | 1 | a0003c0026t0007g0158 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.596+615T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/13 | chr16 | 20470334 | |||||||
chr16:20470350 | A | T | 218 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(215): Show |
247 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.596+631A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/13 | chr16 | 20470350 | |||||||
chr16:20470413 | T | C | 14 | a0003c0010t0001g0146 a0003c0010t0001g0147 a0003c0010t0001g0149 others(11): Show |
15 | HG02109.hp2 HG02258.hp1 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.597-660T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/13 | chr16 | 20470413 | |||||||
chr16:20470555 | C | T | 2 | a0003c0003t0002g0258 a0003c0003t0007g0257 |
2 | HG02257.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.597-518C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/13 | chr16 | 20470555 | |||||||
chr16:20470630 | T | A | 1 | a0004c0004t0002g0285 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.597-443T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/13 | chr16 | 20470630 | |||||||
chr16:20470639 | A | G | 2 | a0001c0001t0001g0177 a0003c0003t0002g0324 |
2 | HG02135.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.597-434A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/13 | chr16 | 20470639 | |||||||
chr16:20470664 | T | C | 1 | a0005c0005t0001g0026 | 2 | HG01175.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.597-409T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/13 | chr16 | 20470664 | |||||||
chr16:20470685 | G | A | 1 | a0003c0026t0007g0158 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.597-388G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/13 | chr16 | 20470685 | |||||||
chr16:20470706 | A | G | 4 | a0003c0003t0002g0159 a0003c0003t0002g0160 a0003c0003t0012g0161 others(1): Show |
4 | HG03831.hp1 NA18941.hp1 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.597-367A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/13 | chr16 | 20470706 | |||||||
chr16:20470744 | T | C | 8 | a0001c0001t0001g0168 a0001c0001t0001g0170 a0001c0001t0001g0171 others(5): Show |
8 | HG00423.hp2 HG00544.hp1 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.597-329T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/13 | chr16 | 20470744 | |||||||
chr16:20470831 | C | G | 7 | a0003c0003t0005g0034 a0003c0003t0005g0035 a0003c0003t0005g0271 others(4): Show |
9 | HG01884.hp1 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.597-242C>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/13 | chr16 | 20470831 | |||||||
chr16:20471002 | A | G | 1 | a0001c0001t0001g0133 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.597-71A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/13 | chr16 | 20471002 | |||||||
chr16:20471046 | A | G | 232 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(229): Show |
262 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(259): Show |
intron_variant | MODIFIER | c.597-27A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/13 | chr16 | 20471046 | |||||||
chr16:20471301 | G | T | 234 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(231): Show |
264 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.740+85G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 5/13 | chr16 | 20471301 | |||||||
chr16:20471367 | CT | C | 4 | a0010c0011t0005g0259 a0010c0011t0005g0260 a0010c0011t0005g0262 others(1): Show |
4 | HG02145.hp2 HG03130.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.740+155delT | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 20471367 | ||||||
chr16:20471416 | C | A | 2 | a0003c0015t0001g0138 a0003c0015t0001g0139 |
2 | HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.741-120C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 5/13 | chr16 | 20471416 | |||||||
chr16:20471429 | A | G | 232 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(229): Show |
262 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(259): Show |
intron_variant | MODIFIER | c.741-107A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 5/13 | chr16 | 20471429 | |||||||
chr16:20471440 | C | T | 1 | a0005c0005t0001g0132 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.741-96C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 5/13 | chr16 | 20471440 | |||||||
chr16:20471452 | C | T | 6 | a0003c0003t0002g0159 a0003c0003t0002g0160 a0003c0003t0005g0163 others(3): Show |
6 | HG03139.hp2 HG03209.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.741-84C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 5/13 | chr16 | 20471452 | |||||||
chr16:20471468 | C | A | 52 | a0003c0003t0002g0037 a0003c0003t0002g0281 a0003c0003t0002g0293 others(49): Show |
59 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.741-68C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 5/13 | chr16 | 20471468 | |||||||
chr16:20471482 | G | A | 3 | a0002c0002t0003g0247 a0002c0002t0003g0248 a0002c0002t0003g0251 |
3 | NA18965.hp1 NA19002.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.741-54G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 5/13 | chr16 | 20471482 | |||||||
chr16:20471701 | T | A | 4 | a0003c0003t0003g0290 a0004c0004t0002g0287 a0004c0004t0002g0289 others(1): Show |
4 | HG02148.hp1 NA18960.hp1 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.894+12T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20471701 | |||||||
chr16:20471754 | A | T | 2 | a0003c0015t0001g0138 a0003c0015t0001g0139 |
2 | HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.894+65A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20471754 | |||||||
chr16:20471778 | A | G | 9 | a0003c0003t0002g0263 a0003c0003t0002g0274 a0003c0003t0005g0034 others(6): Show |
11 | HG01884.hp1 HG02109.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.894+89A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20471778 | |||||||
chr16:20471966 | G | C | 1 | a0001c0018t0001g0046 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.894+277G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20471966 | |||||||
chr16:20472007 | G | A | 1 | a0010c0011t0005g0259 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.894+318G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20472007 | |||||||
chr16:20472041 | G | A | 2 | a0003c0003t0002g0269 a0003c0003t0002g0270 |
2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.894+352G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20472041 | |||||||
chr16:20472407 | T | C | 8 | a0003c0010t0001g0146 a0003c0010t0001g0147 a0003c0010t0001g0149 others(5): Show |
8 | HG02717.hp1 HG02886.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.894+718T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20472407 | |||||||
chr16:20472467 | C | T | 2 | a0001c0001t0027g0141 a0008c0008t0001g0140 |
2 | HG00558.hp1 HG00609.hp1 |
intron_variant | MODIFIER | c.894+778C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20472467 | |||||||
chr16:20472639 | G | A | 211 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(208): Show |
238 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.894+950G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20472639 | |||||||
chr16:20472640 | C | T | 7 | a0003c0003t0005g0034 a0003c0003t0005g0035 a0003c0003t0005g0271 others(4): Show |
9 | HG01884.hp1 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.894+951C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20472640 | |||||||
chr16:20472663 | A | C | 7 | a0003c0003t0005g0034 a0003c0003t0005g0035 a0003c0003t0005g0271 others(4): Show |
9 | HG01884.hp1 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.894+974A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20472663 | |||||||
chr16:20472667 | A | G | 7 | a0003c0003t0005g0034 a0003c0003t0005g0035 a0003c0003t0005g0271 others(4): Show |
9 | HG01884.hp1 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.894+978A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20472667 | |||||||
chr16:20472673 | T | C | 1 | a0001c0001t0001g0061 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.894+984T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20472673 | |||||||
chr16:20472675 | C | T | 7 | a0003c0003t0005g0034 a0003c0003t0005g0035 a0003c0003t0005g0271 others(4): Show |
9 | HG01884.hp1 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.894+986C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20472675 | |||||||
chr16:20472706 | TG | T | 7 | a0003c0003t0005g0034 a0003c0003t0005g0035 a0003c0003t0005g0271 others(4): Show |
9 | HG01884.hp1 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.894+1019delG | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr16 | 20472706 | ||||||
chr16:20472709 | A | C | 7 | a0003c0003t0005g0034 a0003c0003t0005g0035 a0003c0003t0005g0271 others(4): Show |
9 | HG01884.hp1 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.894+1020A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20472709 | |||||||
chr16:20472726 | G | A | 7 | a0003c0003t0005g0034 a0003c0003t0005g0035 a0003c0003t0005g0271 others(4): Show |
9 | HG01884.hp1 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.894+1037G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20472726 | |||||||
chr16:20472728 | C | A | 7 | a0003c0003t0005g0034 a0003c0003t0005g0035 a0003c0003t0005g0271 others(4): Show |
9 | HG01884.hp1 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.894+1039C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20472728 | |||||||
chr16:20472730 | A | C | 7 | a0003c0003t0005g0034 a0003c0003t0005g0035 a0003c0003t0005g0271 others(4): Show |
9 | HG01884.hp1 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.894+1041A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20472730 | |||||||
chr16:20472738 | G | A | 7 | a0003c0003t0005g0034 a0003c0003t0005g0035 a0003c0003t0005g0271 others(4): Show |
9 | HG01884.hp1 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.894+1049G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20472738 | |||||||
chr16:20472748 | G | T | 7 | a0003c0003t0005g0034 a0003c0003t0005g0035 a0003c0003t0005g0271 others(4): Show |
9 | HG01884.hp1 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.894+1059G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20472748 | |||||||
chr16:20472794 | C | T | 3 | a0002c0002t0003g0030 a0002c0002t0003g0197 a0002c0002t0003g0233 |
4 | NA18962.hp2 NA19002.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.894+1105C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20472794 | |||||||
chr16:20472848 | A | G | 1 | a0003c0003t0002g0324 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.894+1159A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20472848 | |||||||
chr16:20472849 | T | C | 2 | a0003c0003t0002g0269 a0003c0003t0002g0270 |
2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.894+1160T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20472849 | |||||||
chr16:20472898 | T | C | 1 | a0004c0004t0002g0305 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.894+1209T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20472898 | |||||||
chr16:20473068 | C | T | 218 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(215): Show |
247 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.894+1379C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20473068 | |||||||
chr16:20473322 | T | A | 1 | a0001c0001t0001g0105 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.894+1633T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20473322 | |||||||
chr16:20473495 | G | A | 1 | a0002c0002t0003g0203 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.894+1806G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20473495 | |||||||
chr16:20473548 | G | T | 159 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(156): Show |
181 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(178): Show |
intron_variant | MODIFIER | c.895-1814G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20473548 | |||||||
chr16:20473665 | A | G | 1 | a0001c0001t0001g0089 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.895-1697A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20473665 | |||||||
chr16:20473678 | G | A | 1 | a0004c0004t0002g0291 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.895-1684G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20473678 | |||||||
chr16:20473755 | T | C | 218 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(215): Show |
247 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.895-1607T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20473755 | |||||||
chr16:20473818 | A | T | 2 | a0002c0002t0003g0202 a0012c0013t0002g0226 |
2 | HG00408.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.895-1544A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20473818 | |||||||
chr16:20473849 | G | A | 235 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(232): Show |
265 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.895-1513G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20473849 | |||||||
chr16:20473857 | T | A | 218 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(215): Show |
247 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.895-1505T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20473857 | |||||||
chr16:20473895 | A | G | 10 | a0002c0002t0002g0185 a0002c0002t0002g0224 a0002c0002t0003g0031 others(7): Show |
11 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.895-1467A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20473895 | |||||||
chr16:20473914 | C | T | 241 | a0001c0001t0001g0143 a0001c0001t0010g0047 a0001c0001t0010g0048 others(238): Show |
271 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(268): Show |
intron_variant | MODIFIER | c.895-1448C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20473914 | |||||||
chr16:20473919 | A | C | 241 | a0001c0001t0001g0143 a0001c0001t0010g0047 a0001c0001t0010g0048 others(238): Show |
271 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(268): Show |
intron_variant | MODIFIER | c.895-1443A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20473919 | |||||||
chr16:20473931 | T | C | 241 | a0001c0001t0001g0143 a0001c0001t0010g0047 a0001c0001t0010g0048 others(238): Show |
271 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(268): Show |
intron_variant | MODIFIER | c.895-1431T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20473931 | |||||||
chr16:20473935 | G | A | 159 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(156): Show |
181 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(178): Show |
intron_variant | MODIFIER | c.895-1427G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20473935 | |||||||
chr16:20474064 | A | G | 218 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(215): Show |
247 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.895-1298A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20474064 | |||||||
chr16:20474092 | T | C | 1 | a0004c0004t0002g0285 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.895-1270T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20474092 | |||||||
chr16:20474144 | C | T | 14 | a0003c0010t0001g0146 a0003c0010t0001g0147 a0003c0010t0001g0149 others(11): Show |
15 | HG02109.hp2 HG02258.hp1 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.895-1218C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20474144 | |||||||
chr16:20474158 | A | C | 232 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(229): Show |
262 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(259): Show |
intron_variant | MODIFIER | c.895-1204A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20474158 | |||||||
chr16:20474225 | T | C | 1 | a0006c0006t0002g0347 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.895-1137T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20474225 | |||||||
chr16:20474266 | T | C | 6 | a0009c0009t0001g0155 a0009c0009t0006g0027 a0009c0009t0006g0142 others(3): Show |
7 | HG02109.hp2 HG02258.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.895-1096T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20474266 | |||||||
chr16:20474282 | G | A | 6 | a0001c0001t0001g0018 a0001c0001t0001g0059 a0001c0001t0001g0137 others(3): Show |
7 | HG00738.hp2 HG01261.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.895-1080G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20474282 | |||||||
chr16:20474318 | G | A | 2 | a0003c0003t0002g0258 a0003c0003t0007g0257 |
2 | HG02257.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.895-1044G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20474318 | |||||||
chr16:20474324 | T | A | 1 | a0004c0014t0001g0145 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.895-1038T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20474324 | |||||||
chr16:20474341 | C | A | 232 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(229): Show |
262 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(259): Show |
intron_variant | MODIFIER | c.895-1021C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20474341 | |||||||
chr16:20474377 | T | C | 3 | a0005c0005t0016g0125 a0005c0005t0016g0126 a0005c0005t0032g0118 |
3 | HG00099.hp1 HG00323.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.895-985T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20474377 | |||||||
chr16:20474473 | C | T | 7 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0028 others(4): Show |
16 | HG00741.hp2 HG01069.hp2 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.895-889C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20474473 | |||||||
chr16:20474655 | C | T | 4 | a0010c0011t0005g0259 a0010c0011t0005g0260 a0010c0011t0005g0262 others(1): Show |
4 | HG02145.hp2 HG03130.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.895-707C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20474655 | |||||||
chr16:20474718 | C | G | 1 | a0016c0025t0005g0277 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.895-644C>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20474718 | |||||||
chr16:20474893 | A | G | 2 | a0004c0004t0002g0291 a0004c0004t0002g0304 |
2 | HG00621.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.895-469A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20474893 | |||||||
chr16:20474917 | T | C | 2 | a0002c0002t0003g0228 a0002c0002t0003g0229 |
2 | HG00280.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.895-445T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20474917 | |||||||
chr16:20475043 | G | A | 52 | a0003c0003t0002g0037 a0003c0003t0002g0281 a0003c0003t0002g0293 others(49): Show |
59 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.895-319G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20475043 | |||||||
chr16:20475044 | G | T | 4 | a0001c0001t0001g0018 a0001c0001t0001g0059 a0001c0001t0001g0137 others(1): Show |
5 | HG00738.hp2 HG01261.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.895-318G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20475044 | |||||||
chr16:20475046 | G | C | 4 | a0001c0001t0001g0018 a0001c0001t0001g0059 a0001c0001t0001g0137 others(1): Show |
5 | HG00738.hp2 HG01261.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.895-316G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20475046 | |||||||
chr16:20475047 | A | C | 4 | a0001c0001t0001g0018 a0001c0001t0001g0059 a0001c0001t0001g0137 others(1): Show |
5 | HG00738.hp2 HG01261.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.895-315A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20475047 | |||||||
chr16:20475048 | T | C | 4 | a0001c0001t0001g0018 a0001c0001t0001g0059 a0001c0001t0001g0137 others(1): Show |
5 | HG00738.hp2 HG01261.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.895-314T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20475048 | |||||||
chr16:20475049 | C | T | 4 | a0001c0001t0001g0018 a0001c0001t0001g0059 a0001c0001t0001g0137 others(1): Show |
5 | HG00738.hp2 HG01261.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.895-313C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20475049 | |||||||
chr16:20475051 | A | AG | 4 | a0001c0001t0001g0018 a0001c0001t0001g0059 a0001c0001t0001g0137 others(1): Show |
5 | HG00738.hp2 HG01261.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.895-311_895-310ins others(1): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20475051 | |||||||
chr16:20475070 | C | T | 1 | a0011c0012t0001g0055 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.895-292C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20475070 | |||||||
chr16:20475317 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.895-45C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20475317 | |||||||
chr16:20475530 | C | T | 1 | a0004c0004t0002g0303 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.974+89C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 7/13 | chr16 | 20475530 | |||||||
chr16:20475583 | C | A | 1 | a0003c0003t0003g0188 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.975-67C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 7/13 | chr16 | 20475583 | |||||||
chr16:20475591 | G | T | 52 | a0003c0003t0002g0037 a0003c0003t0002g0281 a0003c0003t0002g0293 others(49): Show |
59 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.975-59G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 7/13 | chr16 | 20475591 | |||||||
chr16:20475792 | A | T | 3 | a0001c0001t0001g0061 a0001c0001t0001g0101 a0001c0001t0001g0102 |
3 | HG01891.hp2 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1098+19A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 8/13 | chr16 | 20475792 | |||||||
chr16:20475803 | T | G | 217 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(214): Show |
246 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.1098+30T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 8/13 | chr16 | 20475803 | |||||||
chr16:20475875 | C | T | 1 | a0004c0004t0002g0305 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1098+102C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 8/13 | chr16 | 20475875 | |||||||
chr16:20475891 | A | G | 2 | a0003c0015t0001g0138 a0003c0015t0001g0139 |
2 | HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1098+118A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 8/13 | chr16 | 20475891 | |||||||
chr16:20475893 | C | T | 14 | a0003c0010t0001g0146 a0003c0010t0001g0147 a0003c0010t0001g0149 others(11): Show |
15 | HG02109.hp2 HG02258.hp1 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.1098+120C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 8/13 | chr16 | 20475893 | |||||||
chr16:20475930 | C | A | 2 | a0002c0002t0003g0204 a0006c0006t0002g0332 |
2 | NA18942.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.1098+157C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 8/13 | chr16 | 20475930 | |||||||
chr16:20476001 | A | C | 5 | a0003c0003t0002g0159 a0003c0003t0002g0160 a0003c0003t0005g0035 others(2): Show |
6 | HG01168.hp1 HG02647.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1098+228A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 8/13 | chr16 | 20476001 | |||||||
chr16:20476068 | C | G | 17 | a0003c0003t0007g0013 a0003c0003t0007g0235 a0003c0010t0001g0146 others(14): Show |
20 | HG02055.hp2 HG02109.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.1098+295C>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 8/13 | chr16 | 20476068 | |||||||
chr16:20476182 | A | G | 232 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(229): Show |
262 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(259): Show |
intron_variant | MODIFIER | c.1098+409A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 8/13 | chr16 | 20476182 | |||||||
chr16:20476243 | A | G | 2 | a0001c0001t0001g0101 a0001c0001t0001g0102 |
2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1098+470A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 8/13 | chr16 | 20476243 | |||||||
chr16:20476405 | C | T | 1 | a0003c0003t0003g0188 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1098+632C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 8/13 | chr16 | 20476405 | |||||||
chr16:20476477 | C | T | 14 | a0003c0010t0001g0146 a0003c0010t0001g0147 a0003c0010t0001g0149 others(11): Show |
15 | HG02109.hp2 HG02258.hp1 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.1098+704C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 8/13 | chr16 | 20476477 | |||||||
chr16:20476540 | T | C | 1 | a0002c0002t0003g0234 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1098+767T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 8/13 | chr16 | 20476540 | |||||||
chr16:20476700 | G | A | 1 | a0003c0026t0007g0158 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1099-669G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 8/13 | chr16 | 20476700 | |||||||
chr16:20476700 | G | T | 1 | a0003c0003t0005g0271 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1099-669G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 8/13 | chr16 | 20476700 | |||||||
chr16:20476785 | C | A | 157 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(154): Show |
179 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(176): Show |
intron_variant | MODIFIER | c.1099-584C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 8/13 | chr16 | 20476785 | |||||||
chr16:20476793 | T | C | 1 | a0004c0004t0002g0292 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1099-576T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 8/13 | chr16 | 20476793 | |||||||
chr16:20476997 | T | C | 1 | a0016c0025t0005g0277 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1099-372T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 8/13 | chr16 | 20476997 | |||||||
chr16:20477047 | C | T | 231 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(228): Show |
261 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(258): Show |
intron_variant | MODIFIER | c.1099-322C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 8/13 | chr16 | 20477047 | |||||||
chr16:20477125 | G | A | 8 | a0003c0010t0001g0146 a0003c0010t0001g0147 a0003c0010t0001g0149 others(5): Show |
8 | HG02717.hp1 HG02886.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1099-244G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 8/13 | chr16 | 20477125 | |||||||
chr16:20477198 | G | T | 1 | a0005c0005t0001g0076 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1099-171G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 8/13 | chr16 | 20477198 | |||||||
chr16:20477289 | T | C | 1 | a0001c0001t0001g0106 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1099-80T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 8/13 | chr16 | 20477289 | |||||||
chr16:20477473 | G | A | 2 | a0003c0003t0003g0237 a0003c0003t0003g0239 |
2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1179+24G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 9/13 | chr16 | 20477473 | |||||||
chr16:20477481 | T | A | 103 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(100): Show |
134 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.1179+32T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 9/13 | chr16 | 20477481 | |||||||
chr16:20477577 | A | G | 14 | a0003c0010t0001g0146 a0003c0010t0001g0147 a0003c0010t0001g0149 others(11): Show |
15 | HG02109.hp2 HG02258.hp1 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.1179+128A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 9/13 | chr16 | 20477577 | |||||||
chr16:20477639 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1179+190T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 9/13 | chr16 | 20477639 | |||||||
chr16:20477708 | T | C | 1 | a0003c0003t0002g0325 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1179+259T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 9/13 | chr16 | 20477708 | |||||||
chr16:20477812 | C | T | 14 | a0003c0010t0001g0146 a0003c0010t0001g0147 a0003c0010t0001g0149 others(11): Show |
15 | HG02109.hp2 HG02258.hp1 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.1179+363C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 9/13 | chr16 | 20477812 | |||||||
chr16:20477880 | T | C | 232 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(229): Show |
262 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(259): Show |
intron_variant | MODIFIER | c.1179+431T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 9/13 | chr16 | 20477880 | |||||||
chr16:20477943 | C | T | 1 | a0006c0006t0003g0344 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1179+494C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 9/13 | chr16 | 20477943 | |||||||
chr16:20477957 | C | T | 14 | a0003c0010t0001g0146 a0003c0010t0001g0147 a0003c0010t0001g0149 others(11): Show |
15 | HG02109.hp2 HG02258.hp1 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.1179+508C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 9/13 | chr16 | 20477957 | |||||||
chr16:20478047 | T | G | 6 | a0006c0006t0002g0332 a0006c0006t0002g0333 a0006c0006t0002g0349 others(3): Show |
8 | NA18942.hp2 NA18949.hp2 NA18953.hp1 others(5): Show |
intron_variant | MODIFIER | c.1180-529T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 9/13 | chr16 | 20478047 | |||||||
chr16:20478195 | C | A | 232 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(229): Show |
262 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(259): Show |
intron_variant | MODIFIER | c.1180-381C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 9/13 | chr16 | 20478195 | |||||||
chr16:20478252 | G | C | 218 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(215): Show |
247 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.1180-324G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 9/13 | chr16 | 20478252 | |||||||
chr16:20478280 | G | A | 11 | a0003c0003t0002g0293 a0003c0003t0002g0294 a0003c0003t0002g0295 others(8): Show |
12 | NA18943.hp2 NA18945.hp1 NA18971.hp1 others(9): Show |
intron_variant | MODIFIER | c.1180-296G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 9/13 | chr16 | 20478280 | |||||||
chr16:20478332 | G | A | 54 | a0003c0003t0002g0038 a0003c0003t0002g0040 a0003c0003t0002g0258 others(51): Show |
59 | HG00673.hp2 HG01070.hp1 HG01071.hp2 others(56): Show |
intron_variant | MODIFIER | c.1180-244G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 9/13 | chr16 | 20478332 | |||||||
chr16:20478409 | C | T | 1 | a0001c0001t0025g0058 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1180-167C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 9/13 | chr16 | 20478409 | |||||||
chr16:20478546 | A | C | 52 | a0003c0003t0002g0037 a0003c0003t0002g0281 a0003c0003t0002g0293 others(49): Show |
59 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.1180-30A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 9/13 | chr16 | 20478546 | |||||||
chr16:20478546 | A | G | 1 | a0003c0003t0002g0296 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1180-30A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 9/13 | chr16 | 20478546 | |||||||
chr16:20478693 | C | T | 2 | a0003c0003t0005g0163 a0003c0003t0005g0164 |
2 | HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1281+16C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20478693 | |||||||
chr16:20478733 | G | A | 6 | a0009c0009t0001g0155 a0009c0009t0006g0027 a0009c0009t0006g0142 others(3): Show |
7 | HG02109.hp2 HG02258.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1281+56G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20478733 | |||||||
chr16:20478746 | A | C | 66 | a0003c0003t0002g0037 a0003c0003t0002g0281 a0003c0003t0002g0293 others(63): Show |
74 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.1281+69A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20478746 | |||||||
chr16:20478793 | C | G | 2 | a0002c0002t0003g0246 a0003c0003t0002g0236 |
2 | NA18747.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1281+116C>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20478793 | |||||||
chr16:20478954 | T | C | 1 | a0002c0002t0008g0195 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1281+277T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20478954 | |||||||
chr16:20479026 | C | A | 1 | a0004c0004t0002g0320 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1281+349C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20479026 | |||||||
chr16:20479035 | A | G | 3 | a0003c0003t0002g0037 a0004c0004t0002g0301 a0004c0004t0002g0302 |
4 | HG02698.hp2 HG03490.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.1281+358A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20479035 | |||||||
chr16:20479049 | G | T | 2 | a0006c0006t0002g0332 a0006c0006t0002g0333 |
2 | NA18942.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.1281+372G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20479049 | |||||||
chr16:20479291 | C | T | 217 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(214): Show |
246 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.1281+614C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20479291 | |||||||
chr16:20479305 | A | T | 1 | a0004c0004t0002g0310 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1281+628A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20479305 | |||||||
chr16:20479336 | T | C | 231 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(228): Show |
261 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(258): Show |
intron_variant | MODIFIER | c.1281+659T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20479336 | |||||||
chr16:20479389 | A | C | 1 | a0004c0004t0002g0307 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1281+712A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20479389 | |||||||
chr16:20479400 | A | C | 14 | a0003c0010t0001g0146 a0003c0010t0001g0147 a0003c0010t0001g0149 others(11): Show |
15 | HG02109.hp2 HG02258.hp1 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.1281+723A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20479400 | |||||||
chr16:20479406 | G | A | 2 | a0001c0001t0001g0065 a0001c0001t0001g0082 |
2 | NA19060.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1281+729G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20479406 | |||||||
chr16:20479417 | C | T | 2 | a0009c0009t0006g0142 a0009c0009t0006g0153 |
2 | HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1281+740C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20479417 | |||||||
chr16:20479447 | T | A | 2 | a0002c0002t0003g0202 a0012c0013t0002g0226 |
2 | HG00408.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.1281+770T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20479447 | |||||||
chr16:20479575 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1281+898T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20479575 | |||||||
chr16:20479661 | G | A | 14 | a0003c0010t0001g0146 a0003c0010t0001g0147 a0003c0010t0001g0149 others(11): Show |
15 | HG02109.hp2 HG02258.hp1 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.1282-912G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20479661 | |||||||
chr16:20479675 | T | A | 158 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(155): Show |
180 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(177): Show |
intron_variant | MODIFIER | c.1282-898T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20479675 | |||||||
chr16:20479730 | A | C | 1 | a0004c0004t0002g0291 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1282-843A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20479730 | |||||||
chr16:20479736 | C | T | 231 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(228): Show |
261 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(258): Show |
intron_variant | MODIFIER | c.1282-837C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20479736 | |||||||
chr16:20479772 | A | C | 1 | a0001c0001t0001g0143 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1282-801A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20479772 | |||||||
chr16:20479890 | C | A | 1 | a0002c0002t0003g0205 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1282-683C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20479890 | |||||||
chr16:20479906 | G | A | 2 | a0002c0002t0003g0199 a0004c0004t0002g0291 |
2 | HG03710.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.1282-667G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20479906 | |||||||
chr16:20480035 | C | A | 1 | a0002c0002t0003g0206 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1282-538C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20480035 | |||||||
chr16:20480099 | C | T | 1 | a0003c0003t0002g0236 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1282-474C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20480099 | |||||||
chr16:20480201 | T | G | 1 | a0003c0010t0001g0146 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1282-372T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20480201 | |||||||
chr16:20480235 | A | G | 1 | a0005c0005t0001g0131 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1282-338A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20480235 | |||||||
chr16:20480244 | G | A | 158 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(155): Show |
180 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(177): Show |
intron_variant | MODIFIER | c.1282-329G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20480244 | |||||||
chr16:20480285 | T | C | 1 | a0003c0026t0007g0158 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1282-288T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20480285 | |||||||
chr16:20480375 | A | G | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1282-198A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20480375 | |||||||
chr16:20480397 | G | A | 1 | a0001c0001t0004g0110 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1282-176G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20480397 | |||||||
chr16:20480572 | G | T | 1 | a0004c0004t0002g0280 | 1 | NA19062.hp2 | splice_acceptor_variant&intron_variant | HIGH | c.1282-1G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20480572 | |||||||
chr16:20480761 | C | G | 1 | a0018c0024t0002g0300 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1409+61C>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 11/13 | chr16 | 20480761 | |||||||
chr16:20480765 | T | C | 2 | a0003c0015t0001g0138 a0003c0015t0001g0139 |
2 | HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1410-57T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 11/13 | chr16 | 20480765 | |||||||
chr16:20480928 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG01891.hp2 | splice_region_variant&intron_variant | LOW | c.1509+7G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20480928 | |||||||
chr16:20480954 | C | G | 6 | a0009c0009t0001g0155 a0009c0009t0006g0027 a0009c0009t0006g0142 others(3): Show |
7 | HG02109.hp2 HG02258.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1509+33C>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20480954 | |||||||
chr16:20480977 | G | A | 1 | a0015c0028t0001g0078 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1509+56G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20480977 | |||||||
chr16:20480982 | A | T | 233 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(230): Show |
263 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.1509+61A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20480982 | |||||||
chr16:20480985 | G | A | 233 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(230): Show |
263 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.1509+64G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20480985 | |||||||
chr16:20480994 | C | T | 235 | a0002c0002t0002g0185 a0002c0002t0002g0190 a0002c0002t0002g0209 others(232): Show |
265 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.1509+73C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20480994 | |||||||
chr16:20481065 | C | T | 53 | a0002c0002t0008g0194 a0003c0003t0002g0037 a0003c0003t0002g0281 others(50): Show |
60 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.1509+144C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481065 | |||||||
chr16:20481069 | C | T | 1 | a0001c0001t0004g0116 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1509+148C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481069 | |||||||
chr16:20481077 | C | T | 2 | a0005c0005t0001g0074 a0005c0005t0001g0075 |
2 | HG02083.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.1509+156C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481077 | |||||||
chr16:20481097 | C | T | 1 | a0002c0002t0008g0194 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1509+176C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481097 | |||||||
chr16:20481098 | C | T | 1 | a0002c0002t0008g0194 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1509+177C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481098 | |||||||
chr16:20481125 | A | T | 1 | a0004c0004t0002g0280 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1509+204A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481125 | |||||||
chr16:20481174 | A | C | 12 | a0001c0001t0001g0143 a0001c0001t0006g0091 a0002c0002t0008g0194 others(9): Show |
13 | HG01884.hp2 HG01934.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1509+253A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481174 | |||||||
chr16:20481199 | C | T | 2 | a0002c0002t0008g0194 a0003c0003t0002g0268 |
2 | NA19043.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.1509+278C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481199 | |||||||
chr16:20481250 | A | G | 1 | a0002c0002t0008g0194 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1509+329A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481250 | |||||||
chr16:20481257 | G | A | 1 | a0002c0002t0008g0194 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1509+336G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481257 | |||||||
chr16:20481266 | C | T | 1 | a0002c0002t0008g0194 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1509+345C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481266 | |||||||
chr16:20481269 | A | G | 1 | a0002c0002t0014g0029 | 2 | HG02080.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.1509+348A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481269 | |||||||
chr16:20481278 | G | T | 6 | a0002c0002t0008g0194 a0003c0003t0002g0159 a0003c0003t0002g0160 others(3): Show |
6 | HG03831.hp1 NA18522.hp1 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.1509+357G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481278 | |||||||
chr16:20481331 | G | A | 9 | a0002c0002t0003g0203 a0002c0002t0003g0208 a0002c0002t0008g0194 others(6): Show |
9 | HG02559.hp1 HG02970.hp2 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.1509+410G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481331 | |||||||
chr16:20481333 | G | T | 1 | a0004c0004t0002g0280 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1509+412G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481333 | |||||||
chr16:20481386 | T | C | 7 | a0002c0002t0003g0203 a0002c0002t0003g0208 a0003c0003t0002g0159 others(4): Show |
7 | HG02630.hp2 HG03831.hp1 NA18941.hp1 others(4): Show |
intron_variant | MODIFIER | c.1509+465T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481386 | |||||||
chr16:20481387 | G | A | 7 | a0002c0002t0003g0203 a0002c0002t0003g0208 a0003c0003t0002g0159 others(4): Show |
7 | HG02630.hp2 HG03831.hp1 NA18941.hp1 others(4): Show |
intron_variant | MODIFIER | c.1509+466G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481387 | |||||||
chr16:20481388 | T | C | 1 | a0003c0003t0002g0311 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1509+467T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481388 | |||||||
chr16:20481398 | A | G | 9 | a0002c0002t0003g0203 a0002c0002t0003g0208 a0003c0003t0002g0159 others(6): Show |
9 | HG02258.hp1 HG02630.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.1509+477A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481398 | |||||||
chr16:20481424 | T | G | 1 | a0011c0012t0001g0054 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1509+503T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481424 | |||||||
chr16:20481452 | C | G | 212 | a0001c0001t0001g0061 a0001c0001t0001g0081 a0001c0001t0001g0088 others(209): Show |
239 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.1509+531C>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481452 | |||||||
chr16:20481458 | T | C | 7 | a0001c0001t0006g0091 a0009c0009t0001g0155 a0009c0009t0006g0027 others(4): Show |
8 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1509+537T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481458 | |||||||
chr16:20481474 | A | AG | 66 | a0001c0001t0006g0091 a0003c0003t0002g0263 a0003c0003t0002g0268 others(63): Show |
73 | HG00140.hp2 HG00408.hp1 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.1509+553_1509+554i others(3): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481474 | |||||||
chr16:20481486 | G | A | 67 | a0001c0001t0006g0091 a0003c0003t0002g0268 a0003c0003t0002g0281 others(64): Show |
74 | HG00140.hp2 HG00408.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.1509+565G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481486 | |||||||
chr16:20481500 | G | A | 168 | a0001c0001t0001g0052 a0001c0001t0001g0060 a0001c0001t0001g0168 others(165): Show |
188 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.1509+579G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481500 | |||||||
chr16:20481507 | T | A | 179 | a0001c0001t0001g0052 a0001c0001t0001g0060 a0001c0001t0001g0168 others(176): Show |
201 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.1509+586T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481507 | |||||||
chr16:20481518 | C | T | 68 | a0001c0001t0001g0016 a0001c0001t0001g0066 a0001c0001t0001g0081 others(65): Show |
77 | HG00673.hp2 HG01168.hp2 HG01169.hp1 others(74): Show |
intron_variant | MODIFIER | c.1509+597C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481518 | |||||||
chr16:20481590 | G | A | 7 | a0003c0003t0005g0034 a0003c0003t0005g0035 a0003c0003t0005g0271 others(4): Show |
9 | HG01884.hp1 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1509+669G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481590 | |||||||
chr16:20481618 | G | T | 30 | a0001c0001t0001g0016 a0001c0001t0001g0081 a0002c0002t0003g0201 others(27): Show |
32 | HG00741.hp1 HG01123.hp2 HG01168.hp1 others(29): Show |
intron_variant | MODIFIER | c.1509+697G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481618 | |||||||
chr16:20481621 | G | A | 30 | a0001c0001t0001g0016 a0001c0001t0001g0081 a0002c0002t0003g0201 others(27): Show |
32 | HG00741.hp1 HG01123.hp2 HG01168.hp1 others(29): Show |
intron_variant | MODIFIER | c.1509+700G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481621 | |||||||
chr16:20481629 | T | TTAGA | 4 | a0003c0003t0003g0188 a0003c0003t0003g0238 a0003c0003t0003g0239 others(1): Show |
4 | HG00741.hp1 HG01361.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.1509+711_1509+712i others(6): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr16 | 20481629 | ||||||
chr16:20481633 | C | A | 4 | a0003c0003t0003g0188 a0003c0003t0003g0238 a0003c0003t0003g0239 others(1): Show |
4 | HG00741.hp1 HG01361.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.1509+712C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481633 | |||||||
chr16:20481640 | A | G | 2 | a0002c0002t0003g0220 a0002c0002t0003g0221 |
2 | NA18989.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.1509+719A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481640 | |||||||
chr16:20481642 | G | A | 3 | a0003c0003t0003g0188 a0003c0003t0003g0238 a0003c0003t0003g0239 |
3 | HG00741.hp1 HG01361.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.1509+721G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481642 | |||||||
chr16:20481660 | A | C | 11 | a0001c0001t0006g0091 a0001c0001t0026g0062 a0003c0003t0002g0263 others(8): Show |
11 | HG02055.hp1 HG02258.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1509+739A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481660 | |||||||
chr16:20481674 | A | G | 97 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0156 others(94): Show |
106 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.1509+753A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481674 | |||||||
chr16:20481685 | C | T | 1 | a0003c0003t0002g0327 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1509+764C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481685 | |||||||
chr16:20481773 | A | C | 1 | a0014c0027t0020g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1509+852A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481773 | |||||||
chr16:20481774 | C | A | 1 | a0014c0027t0020g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1509+853C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481774 | |||||||
chr16:20481829 | G | T | 2 | a0004c0004t0002g0266 a0008c0008t0001g0134 |
2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1509+908G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481829 | |||||||
chr16:20481859 | A | T | 1 | a0002c0002t0003g0223 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1509+938A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481859 | |||||||
chr16:20481876 | T | G | 286 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(283): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.1509+955T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481876 | |||||||
chr16:20481902 | C | T | 181 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(178): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.1509+981C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481902 | |||||||
chr16:20481976 | A | C | 1 | a0014c0027t0020g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1509+1055A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481976 | |||||||
chr16:20481997 | T | C | 270 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(267): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.1510-1061T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481997 | |||||||
chr16:20482053 | T | G | 2 | a0002c0002t0007g0227 a0003c0026t0007g0158 |
2 | HG03704.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1510-1005T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482053 | |||||||
chr16:20482071 | T | G | 2 | a0002c0002t0007g0227 a0003c0026t0007g0158 |
2 | HG03704.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1510-987T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482071 | |||||||
chr16:20482084 | G | A | 2 | a0006c0006t0002g0256 a0013c0030t0031g0109 |
2 | HG01928.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.1510-974G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482084 | |||||||
chr16:20482091 | T | C | 16 | a0001c0001t0006g0091 a0003c0003t0002g0355 a0003c0003t0007g0257 others(13): Show |
17 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.1510-967T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482091 | |||||||
chr16:20482093 | C | A | 8 | a0003c0003t0005g0034 a0003c0003t0005g0035 a0003c0003t0005g0164 others(5): Show |
10 | HG01884.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1510-965C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482093 | |||||||
chr16:20482095 | C | T | 16 | a0001c0001t0006g0091 a0003c0003t0002g0355 a0003c0003t0007g0257 others(13): Show |
17 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.1510-963C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482095 | |||||||
chr16:20482100 | A | C | 1 | a0001c0001t0001g0115 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1510-958A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482100 | |||||||
chr16:20482122 | G | A | 5 | a0002c0002t0007g0227 a0003c0003t0007g0013 a0003c0003t0007g0235 others(2): Show |
7 | HG02055.hp2 HG02965.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1510-936G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482122 | |||||||
chr16:20482130 | G | C | 3 | a0002c0002t0007g0227 a0003c0026t0007g0158 a0008c0008t0001g0134 |
3 | HG02055.hp2 HG03704.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1510-928G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482130 | |||||||
chr16:20482134 | C | CA | 23 | a0001c0001t0001g0082 a0001c0001t0001g0101 a0001c0001t0006g0091 others(20): Show |
24 | HG00408.hp2 HG02055.hp1 HG02056.hp2 others(21): Show |
intron_variant | MODIFIER | c.1510-903dupA | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr16 | 20482134 | ||||||
chr16:20482134 | CA | C | 21 | a0001c0001t0001g0059 a0001c0001t0001g0106 a0002c0002t0003g0243 others(18): Show |
23 | HG00738.hp2 HG01884.hp1 HG01981.hp1 others(20): Show |
intron_variant | MODIFIER | c.1510-903delA | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr16 | 20482134 | ||||||
chr16:20482134 | CAA | C | 44 | a0001c0001t0001g0081 a0001c0001t0026g0062 a0002c0002t0002g0190 others(41): Show |
49 | HG00673.hp2 HG01258.hp1 HG01891.hp1 others(46): Show |
intron_variant | MODIFIER | c.1510-904_1510-903d others(4): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr16 | 20482134 | ||||||
chr16:20482152 | A | G | 2 | a0003c0003t0007g0013 a0003c0003t0007g0235 |
4 | HG02965.hp1 HG02970.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1510-906A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482152 | |||||||
chr16:20482164 | A | G | 272 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(269): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.1510-894A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482164 | |||||||
chr16:20482169 | A | C | 1 | a0014c0027t0020g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1510-889A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482169 | |||||||
chr16:20482170 | G | GA | 6 | a0003c0003t0002g0258 a0003c0003t0002g0334 a0003c0003t0002g0355 others(3): Show |
6 | HG02257.hp1 HG02559.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1510-881dupA | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr16 | 20482170 | ||||||
chr16:20482271 | G | A | 3 | a0004c0004t0002g0279 a0007c0007t0001g0094 a0016c0025t0005g0277 |
3 | HG02451.hp1 HG03540.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.1510-787G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482271 | |||||||
chr16:20482289 | G | T | 1 | a0004c0004t0002g0279 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1510-769G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482289 | |||||||
chr16:20482295 | C | T | 1 | a0004c0004t0002g0279 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1510-763C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482295 | |||||||
chr16:20482305 | A | C | 1 | a0009c0009t0001g0155 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1510-753A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482305 | |||||||
chr16:20482340 | G | C | 1 | a0003c0003t0005g0163 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1510-718G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482340 | |||||||
chr16:20482356 | G | A | 1 | a0003c0003t0005g0163 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1510-702G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482356 | |||||||
chr16:20482388 | T | A | 1 | a0004c0004t0002g0280 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1510-670T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482388 | |||||||
chr16:20482399 | G | C | 1 | a0014c0027t0020g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1510-659G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482399 | |||||||
chr16:20482400 | C | G | 19 | a0001c0001t0006g0091 a0002c0002t0007g0227 a0003c0003t0007g0013 others(16): Show |
22 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.1510-658C>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482400 | |||||||
chr16:20482470 | G | A | 1 | a0002c0002t0003g0246 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1510-588G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482470 | |||||||
chr16:20482594 | T | A | 60 | a0003c0003t0007g0013 a0003c0003t0007g0235 a0004c0004t0002g0002 others(57): Show |
69 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.1510-464T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482594 | |||||||
chr16:20482610 | T | C | 2 | a0004c0004t0002g0307 a0008c0008t0001g0169 |
2 | NA19066.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1510-448T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482610 | |||||||
chr16:20482665 | C | T | 2 | a0002c0002t0007g0227 a0003c0026t0007g0158 |
2 | HG03704.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1510-393C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482665 | |||||||
chr16:20482710 | C | T | 3 | a0005c0005t0004g0021 a0005c0005t0004g0044 a0005c0005t0004g0073 |
4 | NA18964.hp1 NA18982.hp1 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.1510-348C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482710 | |||||||
chr16:20482790 | C | T | 1 | a0001c0017t0001g0080 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1510-268C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482790 | |||||||
chr16:20482791 | T | A | 1 | a0014c0027t0020g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1510-267T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482791 | |||||||
chr16:20482815 | T | C | 1 | a0002c0002t0003g0201 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1510-243T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482815 | |||||||
chr16:20482823 | T | C | 4 | a0003c0003t0005g0163 a0010c0011t0005g0259 a0010c0011t0005g0260 others(1): Show |
4 | HG02145.hp2 HG03130.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1510-235T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482823 | |||||||
chr16:20482861 | T | C | 1 | a0002c0002t0003g0361 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1510-197T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482861 | |||||||
chr16:20482946 | G | C | 1 | a0004c0004t0002g0322 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1510-112G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482946 | |||||||
chr16:20482957 | G | T | 1 | a0002c0002t0002g0185 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1510-101G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482957 | |||||||
chr16:20482974 | G | C | 2 | a0003c0003t0007g0013 a0003c0003t0007g0235 |
4 | HG02965.hp1 HG02970.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1510-84G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482974 | |||||||
chr16:20483014 | T | C | 47 | a0001c0001t0001g0081 a0001c0001t0001g0113 a0001c0001t0026g0062 others(44): Show |
50 | HG00673.hp2 HG01258.hp1 HG01891.hp1 others(47): Show |
intron_variant | MODIFIER | c.1510-44T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20483014 | |||||||
chr16:20483257 | G | C | 18 | a0001c0001t0006g0091 a0002c0002t0007g0227 a0003c0003t0007g0013 others(15): Show |
21 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.1629+80G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483257 | |||||||
chr16:20483263 | T | C | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+86T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483263 | |||||||
chr16:20483265 | C | T | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+88C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483265 | |||||||
chr16:20483287 | T | TG | 19 | a0001c0001t0006g0091 a0002c0002t0007g0227 a0003c0003t0007g0013 others(16): Show |
22 | HG01928.hp2 HG02055.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1629+112dupG | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr16 | 20483287 | ||||||
chr16:20483291 | T | C | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+114T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483291 | |||||||
chr16:20483294 | G | A | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+117G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483294 | |||||||
chr16:20483296 | G | A | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+119G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483296 | |||||||
chr16:20483300 | C | T | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+123C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483300 | |||||||
chr16:20483301 | A | G | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+124A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483301 | |||||||
chr16:20483305 | C | G | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+128C>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483305 | |||||||
chr16:20483308 | G | A | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+131G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483308 | |||||||
chr16:20483313 | T | C | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+136T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483313 | |||||||
chr16:20483330 | G | A | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+153G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483330 | |||||||
chr16:20483335 | T | C | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+158T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483335 | |||||||
chr16:20483336 | G | A | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+159G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483336 | |||||||
chr16:20483342 | G | A | 1 | a0002c0002t0003g0199 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1629+165G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483342 | |||||||
chr16:20483358 | T | G | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+181T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483358 | |||||||
chr16:20483372 | T | C | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+195T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483372 | |||||||
chr16:20483385 | C | A | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+208C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483385 | |||||||
chr16:20483391 | GA | G | 129 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(126): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.1629+217delA | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr16 | 20483391 | ||||||
chr16:20483399 | A | G | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+222A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483399 | |||||||
chr16:20483427 | C | T | 19 | a0001c0001t0006g0091 a0002c0002t0007g0227 a0003c0003t0007g0013 others(16): Show |
22 | HG01928.hp2 HG02055.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1629+250C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483427 | |||||||
chr16:20483485 | A | G | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+308A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483485 | |||||||
chr16:20483488 | T | C | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+311T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483488 | |||||||
chr16:20483503 | G | T | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+326G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483503 | |||||||
chr16:20483512 | G | A | 1 | a0002c0002t0002g0185 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1629+335G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483512 | |||||||
chr16:20483524 | T | C | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+347T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483524 | |||||||
chr16:20483525 | G | A | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+348G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483525 | |||||||
chr16:20483538 | G | C | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+361G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483538 | |||||||
chr16:20483544 | C | T | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+367C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483544 | |||||||
chr16:20483546 | G | A | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+369G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483546 | |||||||
chr16:20483562 | T | C | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+385T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483562 | |||||||
chr16:20483569 | C | CA | 14 | a0001c0001t0010g0051 a0002c0002t0003g0183 a0002c0002t0003g0214 others(11): Show |
16 | HG00673.hp2 HG01074.hp2 HG02071.hp1 others(13): Show |
intron_variant | MODIFIER | c.1629+425dupA | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr16 | 20483569 | ||||||
chr16:20483569 | C | CAA | 43 | a0001c0001t0004g0112 a0001c0001t0010g0047 a0001c0001t0010g0048 others(40): Show |
50 | HG00280.hp2 HG00408.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.1629+424_1629+425d others(4): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr16 | 20483569 | ||||||
chr16:20483569 | C | CAAA | 51 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0052 others(48): Show |
65 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.1629+423_1629+425d others(5): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr16 | 20483569 | ||||||
chr16:20483569 | C | CAAAA | 54 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(51): Show |
65 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.1629+422_1629+425d others(6): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr16 | 20483569 | ||||||
chr16:20483569 | C | CAAAAA | 42 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0018 others(39): Show |
57 | HG00423.hp1 HG00558.hp1 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.1629+421_1629+425d others(7): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr16 | 20483569 | ||||||
chr16:20483569 | C | CAAAAAA | 13 | a0001c0001t0001g0010 a0001c0001t0001g0042 a0001c0001t0001g0092 others(10): Show |
16 | HG00423.hp2 HG00438.hp2 HG00621.hp2 others(13): Show |
intron_variant | MODIFIER | c.1629+420_1629+425d others(8): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr16 | 20483569 | ||||||
chr16:20483569 | C | CAAAAAAA | 11 | a0001c0001t0001g0060 a0001c0001t0001g0064 a0001c0001t0001g0137 others(8): Show |
11 | HG00544.hp1 HG00609.hp2 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.1629+419_1629+425d others(9): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr16 | 20483569 | ||||||
chr16:20483569 | CA | C | 19 | a0001c0001t0001g0113 a0001c0001t0004g0110 a0002c0002t0002g0190 others(16): Show |
20 | HG00639.hp1 HG02056.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.1629+425delA | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr16 | 20483569 | ||||||
chr16:20483569 | CAA | C | 20 | a0003c0003t0002g0340 a0004c0004t0002g0255 a0004c0004t0002g0266 others(17): Show |
20 | HG01978.hp1 HG02129.hp2 HG02148.hp2 others(17): Show |
intron_variant | MODIFIER | c.1629+424_1629+425d others(4): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr16 | 20483569 | ||||||
chr16:20483569 | CAAA | C | 36 | a0002c0002t0007g0227 a0004c0004t0002g0002 a0004c0004t0002g0036 others(33): Show |
43 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.1629+423_1629+425d others(5): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr16 | 20483569 | ||||||
chr16:20483569 | CAAAAAAA | C | 11 | a0001c0001t0006g0091 a0003c0003t0007g0257 a0003c0010t0006g0151 others(8): Show |
12 | HG02055.hp1 HG02258.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.1629+419_1629+425d others(9): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr16 | 20483569 | ||||||
chr16:20483569 | CAAAAAAA others(5): Show |
C | 5 | a0001c0001t0001g0061 a0001c0017t0001g0079 a0001c0017t0001g0080 others(2): Show |
5 | HG01891.hp2 HG02717.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1629+414_1629+425d others(14): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr16 | 20483569 | ||||||
chr16:20483569 | CAAAAAAA others(7): Show |
C | 8 | a0003c0003t0005g0034 a0003c0003t0005g0035 a0003c0003t0005g0164 others(5): Show |
10 | HG01884.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1629+412_1629+425d others(16): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr16 | 20483569 | ||||||
chr16:20483569 | CAAAAAAA others(10): Show |
C | 4 | a0003c0003t0005g0163 a0010c0011t0005g0259 a0010c0011t0005g0260 others(1): Show |
4 | HG02145.hp2 HG03130.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1629+409_1629+425d others(19): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr16 | 20483569 | ||||||
chr16:20483577 | A | AAAACCAA others(14): Show |
1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+403_1629+404i others(23): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr16 | 20483577 | ||||||
chr16:20483589 | A | C | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+412A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483589 | |||||||
chr16:20483600 | A | C | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+423A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483600 | |||||||
chr16:20483603 | G | C | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+426G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483603 | |||||||
chr16:20483608 | T | C | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+431T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483608 | |||||||
chr16:20483614 | A | C | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+437A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483614 | |||||||
chr16:20483650 | C | G | 3 | a0003c0003t0002g0263 a0003c0003t0002g0274 a0007c0007t0001g0094 |
3 | HG02280.hp1 HG02451.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1629+473C>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483650 | |||||||
chr16:20483686 | T | C | 2 | a0002c0002t0003g0249 a0013c0030t0031g0109 |
2 | HG01928.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1629+509T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483686 | |||||||
chr16:20483701 | A | G | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+524A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483701 | |||||||
chr16:20483715 | T | C | 1 | a0001c0001t0001g0101 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1629+538T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483715 | |||||||
chr16:20483849 | A | T | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+672A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483849 | |||||||
chr16:20483856 | G | A | 3 | a0003c0003t0007g0013 a0003c0003t0007g0235 a0013c0030t0031g0109 |
5 | HG01928.hp2 HG02965.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1629+679G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483856 | |||||||
chr16:20483857 | G | A | 3 | a0003c0003t0007g0013 a0003c0003t0007g0235 a0013c0030t0031g0109 |
5 | HG01928.hp2 HG02965.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1629+680G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483857 | |||||||
chr16:20483884 | G | A | 1 | a0014c0027t0020g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1629+707G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483884 | |||||||
chr16:20483906 | G | A | 61 | a0002c0002t0007g0227 a0003c0003t0007g0013 a0003c0003t0007g0235 others(58): Show |
70 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.1629+729G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483906 | |||||||
chr16:20483906 | G | T | 143 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(140): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.1629+729G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483906 | |||||||
chr16:20483907 | T | A | 1 | a0014c0027t0020g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1629+730T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483907 | |||||||
chr16:20483910 | C | A | 62 | a0002c0002t0007g0227 a0003c0003t0007g0013 a0003c0003t0007g0235 others(59): Show |
71 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.1629+733C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483910 | |||||||
chr16:20483948 | T | C | 20 | a0001c0001t0006g0091 a0002c0002t0007g0227 a0003c0003t0007g0013 others(17): Show |
23 | HG01928.hp2 HG02055.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1629+771T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483948 | |||||||
chr16:20483983 | A | G | 129 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(126): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.1629+806A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483983 | |||||||
chr16:20484033 | T | C | 1 | a0002c0002t0003g0232 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1629+856T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20484033 | |||||||
chr16:20484091 | C | G | 18 | a0001c0001t0006g0091 a0002c0002t0007g0227 a0003c0003t0007g0013 others(15): Show |
21 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.1629+914C>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20484091 | |||||||
chr16:20484140 | A | T | 1 | a0004c0004t0002g0280 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1629+963A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20484140 | |||||||
chr16:20484202 | G | C | 13 | a0001c0001t0001g0143 a0001c0001t0006g0091 a0003c0003t0007g0257 others(10): Show |
14 | HG01884.hp2 HG01928.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.1629+1025G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20484202 | |||||||
chr16:20484216 | C | T | 1 | a0003c0003t0003g0239 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1629+1039C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20484216 | |||||||
chr16:20484218 | T | G | 1 | a0001c0001t0001g0108 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1629+1041T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20484218 | |||||||
chr16:20484230 | G | T | 2 | a0003c0003t0007g0013 a0003c0003t0007g0235 |
4 | HG02965.hp1 HG02970.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1629+1053G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20484230 | |||||||
chr16:20484239 | C | T | 5 | a0001c0001t0001g0061 a0001c0017t0001g0079 a0001c0017t0001g0080 others(2): Show |
5 | HG01891.hp2 HG02717.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1629+1062C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20484239 | |||||||
chr16:20484341 | G | A | 1 | a0001c0001t0001g0128 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1629+1164G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20484341 | |||||||
chr16:20484413 | C | T | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+1236C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20484413 | |||||||
chr16:20484504 | C | G | 13 | a0003c0003t0005g0034 a0003c0003t0005g0035 a0003c0003t0005g0163 others(10): Show |
15 | HG01884.hp1 HG01928.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1629+1327C>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20484504 | |||||||
chr16:20484514 | T | C | 1 | a0005c0005t0004g0070 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1629+1337T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20484514 | |||||||
chr16:20484555 | C | T | 2 | a0003c0003t0012g0161 a0003c0003t0012g0162 |
2 | HG03831.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.1629+1378C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20484555 | |||||||
chr16:20484723 | GT | G | 14 | a0001c0001t0006g0091 a0003c0003t0007g0257 a0003c0003t0012g0161 others(11): Show |
15 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.1629+1548delT | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr16 | 20484723 | ||||||
chr16:20484761 | T | C | 1 | a0004c0004t0002g0285 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1629+1584T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20484761 | |||||||
chr16:20484764 | A | C | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+1587A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20484764 | |||||||
chr16:20484785 | A | G | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+1608A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20484785 | |||||||
chr16:20484824 | C | A | 3 | a0003c0003t0002g0281 a0003c0003t0002g0294 a0003c0003t0002g0316 |
3 | NA18971.hp1 NA18998.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.1629+1647C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20484824 | |||||||
chr16:20484838 | C | T | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+1661C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20484838 | |||||||
chr16:20484854 | T | C | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+1677T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20484854 | |||||||
chr16:20484857 | T | C | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+1680T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20484857 | |||||||
chr16:20484859 | T | G | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+1682T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20484859 | |||||||
chr16:20484860 | T | G | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+1683T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20484860 | |||||||
chr16:20484868 | C | T | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+1691C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20484868 | |||||||
chr16:20484869 | A | G | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+1692A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20484869 | |||||||
chr16:20484874 | G | A | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+1697G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20484874 | |||||||
chr16:20484906 | C | T | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-1668C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20484906 | |||||||
chr16:20484951 | A | G | 77 | a0001c0001t0006g0091 a0002c0002t0007g0227 a0003c0003t0007g0013 others(74): Show |
87 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.1630-1623A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20484951 | |||||||
chr16:20484960 | C | T | 2 | a0004c0004t0002g0292 a0004c0004t0002g0299 |
2 | HG01978.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.1630-1614C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20484960 | |||||||
chr16:20484988 | T | C | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-1586T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20484988 | |||||||
chr16:20484998 | G | A | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-1576G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20484998 | |||||||
chr16:20485012 | G | C | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-1562G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485012 | |||||||
chr16:20485019 | A | G | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-1555A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485019 | |||||||
chr16:20485032 | A | T | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-1542A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485032 | |||||||
chr16:20485069 | TGTTACCC others(130): Show |
T | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-1503_1630-136 others(4): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr16 | 20485069 | ||||||
chr16:20485210 | T | C | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-1364T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485210 | |||||||
chr16:20485211 | G | A | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-1363G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485211 | |||||||
chr16:20485238 | G | T | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-1336G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485238 | |||||||
chr16:20485258 | C | T | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-1316C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485258 | |||||||
chr16:20485343 | G | A | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-1231G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485343 | |||||||
chr16:20485357 | T | C | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-1217T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485357 | |||||||
chr16:20485369 | C | T | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-1205C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485369 | |||||||
chr16:20485413 | G | A | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-1161G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485413 | |||||||
chr16:20485485 | C | T | 14 | a0001c0001t0006g0091 a0003c0003t0007g0257 a0003c0003t0012g0161 others(11): Show |
15 | HG01928.hp2 HG02055.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1630-1089C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485485 | |||||||
chr16:20485490 | C | T | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-1084C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485490 | |||||||
chr16:20485507 | T | G | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-1067T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485507 | |||||||
chr16:20485523 | T | A | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-1051T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485523 | |||||||
chr16:20485549 | T | G | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-1025T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485549 | |||||||
chr16:20485591 | G | C | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-983G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485591 | |||||||
chr16:20485601 | G | T | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-973G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485601 | |||||||
chr16:20485610 | T | A | 1 | a0014c0027t0020g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1630-964T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485610 | |||||||
chr16:20485614 | T | C | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-960T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485614 | |||||||
chr16:20485616 | A | G | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-958A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485616 | |||||||
chr16:20485638 | T | G | 1 | a0014c0027t0020g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1630-936T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485638 | |||||||
chr16:20485645 | C | T | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-929C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485645 | |||||||
chr16:20485646 | A | G | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-928A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485646 | |||||||
chr16:20485648 | G | C | 1 | a0001c0001t0001g0107 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1630-926G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485648 | |||||||
chr16:20485668 | C | G | 4 | a0008c0008t0001g0173 a0012c0013t0002g0219 a0013c0030t0031g0109 others(1): Show |
4 | HG01928.hp2 NA18612.hp1 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.1630-906C>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485668 | |||||||
chr16:20485670 | T | A | 1 | a0001c0001t0001g0114 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1630-904T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485670 | |||||||
chr16:20485691 | C | T | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-883C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485691 | |||||||
chr16:20485703 | A | C | 5 | a0003c0003t0005g0163 a0010c0011t0005g0259 a0010c0011t0005g0260 others(2): Show |
5 | HG01928.hp2 HG02145.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1630-871A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485703 | |||||||
chr16:20485804 | G | C | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-770G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485804 | |||||||
chr16:20485805 | G | T | 17 | a0001c0001t0006g0091 a0002c0002t0007g0227 a0003c0003t0007g0013 others(14): Show |
20 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.1630-769G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485805 | |||||||
chr16:20485823 | A | G | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-751A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485823 | |||||||
chr16:20485833 | A | G | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-741A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485833 | |||||||
chr16:20485835 | C | A | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-739C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485835 | |||||||
chr16:20485836 | A | G | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-738A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485836 | |||||||
chr16:20485843 | C | T | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-731C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485843 | |||||||
chr16:20485849 | G | C | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-725G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485849 | |||||||
chr16:20485866 | T | C | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-708T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485866 | |||||||
chr16:20485890 | A | G | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-684A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485890 | |||||||
chr16:20485895 | C | T | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-679C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485895 | |||||||
chr16:20485897 | C | T | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-677C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485897 | |||||||
chr16:20485925 | A | T | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-649A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485925 | |||||||
chr16:20485951 | A | G | 51 | a0001c0001t0001g0081 a0001c0001t0001g0113 a0001c0001t0026g0062 others(48): Show |
54 | HG00673.hp2 HG01258.hp1 HG01891.hp1 others(51): Show |
intron_variant | MODIFIER | c.1630-623A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485951 | |||||||
chr16:20485969 | T | G | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-605T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485969 | |||||||
chr16:20485992 | T | A | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-582T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485992 | |||||||
chr16:20485998 | G | A | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-576G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485998 | |||||||
chr16:20486057 | T | A | 50 | a0001c0001t0001g0081 a0001c0001t0001g0113 a0001c0001t0026g0062 others(47): Show |
53 | HG00673.hp2 HG01258.hp1 HG01891.hp1 others(50): Show |
intron_variant | MODIFIER | c.1630-517T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20486057 | |||||||
chr16:20486066 | G | C | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-508G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20486066 | |||||||
chr16:20486089 | C | T | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-485C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20486089 | |||||||
chr16:20486111 | A | T | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-463A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20486111 | |||||||
chr16:20486134 | G | A | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-440G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20486134 | |||||||
chr16:20486138 | G | A | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-436G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20486138 | |||||||
chr16:20486150 | T | A | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-424T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20486150 | |||||||
chr16:20486164 | T | G | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-410T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20486164 | |||||||
chr16:20486190 | A | G | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-384A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20486190 | |||||||
chr16:20486223 | T | G | 1 | a0002c0002t0003g0200 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1630-351T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20486223 | |||||||
chr16:20486251 | T | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(127): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.1630-323T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20486251 | |||||||
chr16:20486268 | T | C | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-306T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20486268 | |||||||
chr16:20486294 | A | T | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-280A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20486294 | |||||||
chr16:20486323 | C | T | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-251C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20486323 | |||||||
chr16:20486350 | T | C | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-224T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20486350 | |||||||
chr16:20486355 | T | C | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-219T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20486355 | |||||||
chr16:20486366 | G | A | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-208G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20486366 | |||||||
chr16:20486377 | A | C | 1 | a0014c0027t0020g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1630-197A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20486377 | |||||||
chr16:20486378 | G | T | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-196G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20486378 | |||||||
chr16:20486414 | C | G | 2 | a0003c0003t0007g0013 a0003c0003t0007g0235 |
4 | HG02965.hp1 HG02970.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1630-160C>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20486414 | |||||||
chr16:20486430 | T | C | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-144T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20486430 | |||||||
chr16:20486453 | G | C | 129 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(126): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.1630-121G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20486453 | |||||||
chr16:20486457 | A | G | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-117A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20486457 | |||||||
chr16:20486461 | G | A | 1 | a0013c0030t0031g0109 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-113G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20486461 | |||||||
chr16:20486533 | G | A | 3 | a0002c0002t0007g0227 a0003c0026t0007g0158 a0013c0030t0031g0109 |
3 | HG01928.hp2 HG03704.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1630-41G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20486533 |