Item | Value |
---|---|
geneid | 348158 |
ensemblid | ENSG00000066813.14 |
hgncid | 30931 |
symbol | ACSM2B |
name | acyl-CoA synthetase medium chain family member 2B |
refseq_nuc | NM_001105069.2 |
refseq_prot | NP_001098539.1 |
ensembl_nuc | ENST00000329697.10 |
ensembl_prot | ENSP00000327453.6 |
mane_status | MANE Select |
chr | chr16 |
start | 20536226 |
end | 20576367 |
strand | - |
ver | v1.2 |
region | chr16:20536226-20576367 |
region5000 | chr16:20531226-20581367 |
regionname0 | ACSM2B_chr16_20536226_20576367 |
regionname5000 | ACSM2B_chr16_20531226_20581367 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 577 | 253 | 25 | 59 | 124 | 12 | 32 | 95 | ACSM2B_chr16_20531226_20581367 | ACSM2B | MHWLR others(572): Show |
chr16 | 20531226 | 20581367 |
a0002 | 0/0 | 577 | 53 | 14 | 4 | 30 | 0 | 5 | 27 | ACSM2B_chr16_20531226_20581367 | ACSM2B | MHWLR others(572): Show |
chr16 | 20531226 | 20581367 |
a0003 | 0/0 | 577 | 22 | 18 | 1 | 0 | 0 | 3 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | MHWLR others(572): Show |
chr16 | 20531226 | 20581367 |
a0004 | 0/0 | 577 | 19 | 17 | 2 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | MHWLR others(572): Show |
chr16 | 20531226 | 20581367 |
a0005 | 1/0 | 577 | 11 | 6 | 2 | 0 | 0 | 2 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | MHWLR others(572): Show |
chr16 | 20531226 | 20581367 |
a0006 | 0/0 | 577 | 10 | 10 | 0 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | MHWLR others(572): Show |
chr16 | 20531226 | 20581367 |
a0007 | 0/0 | 577 | 4 | 0 | 0 | 4 | 0 | 0 | 3 | ACSM2B_chr16_20531226_20581367 | ACSM2B | MHWLR others(572): Show |
chr16 | 20531226 | 20581367 |
a0008 | 0/0 | 577 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | MHWLR others(572): Show |
chr16 | 20531226 | 20581367 |
a0009 | 0/0 | 577 | 3 | 0 | 0 | 0 | 0 | 3 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | MHWLR others(572): Show |
chr16 | 20531226 | 20581367 |
a0010 | 0/0 | 577 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | MHWLR others(572): Show |
chr16 | 20531226 | 20581367 |
a0011 | 0/0 | 577 | 2 | 0 | 0 | 1 | 0 | 1 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | MHWLR others(572): Show |
chr16 | 20531226 | 20581367 |
a0012 | 0/0 | 577 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | MHWLR others(572): Show |
chr16 | 20531226 | 20581367 |
a0013 | 0/0 | 577 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | MHWLR others(572): Show |
chr16 | 20531226 | 20581367 |
a0014 | 0/0 | 577 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | MHWLR others(572): Show |
chr16 | 20531226 | 20581367 |
a0015 | 0/0 | 577 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | MHWLR others(572): Show |
chr16 | 20531226 | 20581367 |
a0016 | 0/0 | 577 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | MHWLR others(572): Show |
chr16 | 20531226 | 20581367 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1731 | 99 | 0 | 10 | 80 | 4 | 5 | ACSM2B_chr16_20531226_20581367 | ACSM2B | ATGCA others(1726): Show |
chr16 | 20531226 | 20581367 | ||
a0001c0002 | 0/1 | 1731 | 97 | 19 | 40 | 10 | 7 | 20 | ACSM2B_chr16_20531226_20581367 | ACSM2B | ATGCA others(1726): Show |
chr16 | 20531226 | 20581367 | ||
a0001c0004 | 0/0 | 1731 | 35 | 0 | 7 | 26 | 0 | 2 | ACSM2B_chr16_20531226_20581367 | ACSM2B | ATGCA others(1726): Show |
chr16 | 20531226 | 20581367 | ||
a0001c0006 | 0/0 | 1731 | 13 | 1 | 1 | 8 | 1 | 2 | ACSM2B_chr16_20531226_20581367 | ACSM2B | ATGCA others(1726): Show |
chr16 | 20531226 | 20581367 | ||
a0001c0012 | 0/0 | 1731 | 5 | 4 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | ATGCA others(1726): Show |
chr16 | 20531226 | 20581367 | ||
a0001c0017 | 0/0 | 1731 | 3 | 0 | 0 | 0 | 0 | 3 | ACSM2B_chr16_20531226_20581367 | ACSM2B | ATGCA others(1726): Show |
chr16 | 20531226 | 20581367 | ||
a0001c0027 | 0/0 | 1731 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | ATGCA others(1726): Show |
chr16 | 20531226 | 20581367 | ||
a0002c0003 | 0/0 | 1731 | 37 | 13 | 3 | 19 | 0 | 2 | ACSM2B_chr16_20531226_20581367 | ACSM2B | ATGCA others(1726): Show |
chr16 | 20531226 | 20581367 | ||
a0002c0009 | 0/0 | 1731 | 9 | 0 | 0 | 7 | 0 | 2 | ACSM2B_chr16_20531226_20581367 | ACSM2B | ATGCA others(1726): Show |
chr16 | 20531226 | 20581367 | ||
a0002c0018 | 0/0 | 1731 | 3 | 1 | 0 | 1 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | ATGCA others(1726): Show |
chr16 | 20531226 | 20581367 | ||
a0002c0019 | 0/0 | 1731 | 3 | 0 | 0 | 3 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | ATGCA others(1726): Show |
chr16 | 20531226 | 20581367 | ||
a0002c0029 | 0/0 | 1731 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | ATGCA others(1726): Show |
chr16 | 20531226 | 20581367 | ||
a0003c0007 | 0/0 | 1731 | 11 | 9 | 1 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | ATGCA others(1726): Show |
chr16 | 20531226 | 20581367 | ||
a0003c0008 | 0/0 | 1731 | 9 | 8 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | ATGCA others(1726): Show |
chr16 | 20531226 | 20581367 | ||
a0003c0025 | 0/0 | 1731 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | ATGCA others(1726): Show |
chr16 | 20531226 | 20581367 | ||
a0003c0033 | 0/0 | 1731 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | ATGCA others(1726): Show |
chr16 | 20531226 | 20581367 | ||
a0004c0005 | 0/0 | 1731 | 19 | 17 | 2 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | ATGCA others(1726): Show |
chr16 | 20531226 | 20581367 | ||
a0005c0011 | 1/0 | 1731 | 7 | 3 | 2 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | ATGCA others(1726): Show |
chr16 | 20531226 | 20581367 | ||
a0005c0016 | 0/0 | 1731 | 3 | 2 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | ATGCA others(1726): Show |
chr16 | 20531226 | 20581367 | ||
a0005c0024 | 0/0 | 1731 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | ATGCA others(1726): Show |
chr16 | 20531226 | 20581367 | ||
a0006c0010 | 0/0 | 1731 | 8 | 8 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | ATGCA others(1726): Show |
chr16 | 20531226 | 20581367 | ||
a0006c0020 | 0/0 | 1731 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | ATGCA others(1726): Show |
chr16 | 20531226 | 20581367 | ||
a0007c0014 | 0/0 | 1731 | 4 | 0 | 0 | 4 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | ATGCA others(1726): Show |
chr16 | 20531226 | 20581367 | ||
a0008c0013 | 0/0 | 1731 | 4 | 4 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | ATGCA others(1726): Show |
chr16 | 20531226 | 20581367 | ||
a0009c0015 | 0/0 | 1731 | 3 | 0 | 0 | 0 | 0 | 3 | ACSM2B_chr16_20531226_20581367 | ACSM2B | ATGCA others(1726): Show |
chr16 | 20531226 | 20581367 | ||
a0010c0022 | 0/0 | 1731 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | ATGCA others(1726): Show |
chr16 | 20531226 | 20581367 | ||
a0010c0023 | 0/0 | 1731 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | ATGCA others(1726): Show |
chr16 | 20531226 | 20581367 | ||
a0011c0021 | 0/0 | 1731 | 2 | 0 | 0 | 1 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | ATGCA others(1726): Show |
chr16 | 20531226 | 20581367 | ||
a0012c0032 | 0/0 | 1731 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | ATGCA others(1726): Show |
chr16 | 20531226 | 20581367 | ||
a0013c0026 | 0/0 | 1731 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | ATGCA others(1726): Show |
chr16 | 20531226 | 20581367 | ||
a0014c0028 | 0/0 | 1731 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | ATGCA others(1726): Show |
chr16 | 20531226 | 20581367 | ||
a0015c0030 | 0/0 | 1731 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | ATGCA others(1726): Show |
chr16 | 20531226 | 20581367 | ||
a0016c0031 | 0/0 | 1731 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | ATGCA others(1726): Show |
chr16 | 20531226 | 20581367 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2935 | 63 | 0 | 7 | 48 | 4 | 4 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2930): Show |
chr16 | 20531226 | 20581367 |
a0001c0001t0003 | 0/0 | 2935 | 27 | 0 | 3 | 24 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2930): Show |
chr16 | 20531226 | 20581367 |
a0001c0001t0008 | 0/0 | 2935 | 3 | 0 | 0 | 3 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2930): Show |
chr16 | 20531226 | 20581367 |
a0001c0001t0012 | 0/0 | 2935 | 4 | 0 | 0 | 4 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2930): Show |
chr16 | 20531226 | 20581367 |
a0001c0001t0018 | 0/0 | 2935 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2930): Show |
chr16 | 20531226 | 20581367 |
a0001c0001t0023 | 0/0 | 2935 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2930): Show |
chr16 | 20531226 | 20581367 |
a0001c0002t0002 | 0/0 | 2935 | 36 | 7 | 20 | 1 | 0 | 8 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2930): Show |
chr16 | 20531226 | 20581367 |
a0001c0002t0003 | 0/0 | 2935 | 9 | 8 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2930): Show |
chr16 | 20531226 | 20581367 |
a0001c0002t0004 | 0/0 | 2935 | 42 | 3 | 15 | 8 | 6 | 10 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2930): Show |
chr16 | 20531226 | 20581367 |
a0001c0002t0007 | 0/1 | 2935 | 7 | 1 | 2 | 1 | 1 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2930): Show |
chr16 | 20531226 | 20581367 |
a0001c0002t0021 | 0/0 | 2935 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2930): Show |
chr16 | 20531226 | 20581367 |
a0001c0002t0022 | 0/0 | 2935 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2930): Show |
chr16 | 20531226 | 20581367 |
a0001c0002t0024 | 0/0 | 2935 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2930): Show |
chr16 | 20531226 | 20581367 |
a0001c0004t0002 | 0/0 | 2935 | 21 | 0 | 7 | 12 | 0 | 2 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2930): Show |
chr16 | 20531226 | 20581367 |
a0001c0004t0004 | 0/0 | 2935 | 7 | 0 | 0 | 7 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2930): Show |
chr16 | 20531226 | 20581367 |
a0001c0004t0007 | 0/0 | 2935 | 7 | 0 | 0 | 7 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2930): Show |
chr16 | 20531226 | 20581367 |
a0001c0006t0001 | 0/0 | 2935 | 8 | 0 | 1 | 4 | 1 | 2 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2930): Show |
chr16 | 20531226 | 20581367 |
a0001c0006t0003 | 0/0 | 2935 | 4 | 0 | 0 | 4 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2930): Show |
chr16 | 20531226 | 20581367 |
a0001c0006t0011 | 0/0 | 2935 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2930): Show |
chr16 | 20531226 | 20581367 |
a0001c0012t0002 | 0/0 | 2935 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2930): Show |
chr16 | 20531226 | 20581367 |
a0001c0012t0007 | 0/0 | 2935 | 4 | 4 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2930): Show |
chr16 | 20531226 | 20581367 |
a0001c0017t0004 | 0/0 | 2935 | 3 | 0 | 0 | 0 | 0 | 3 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2930): Show |
chr16 | 20531226 | 20581367 |
a0001c0027t0003 | 0/0 | 2935 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2930): Show |
chr16 | 20531226 | 20581367 |
a0002c0003t0005 | 0/0 | 2935 | 28 | 6 | 2 | 19 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2930): Show |
chr16 | 20531226 | 20581367 |
a0002c0003t0010 | 0/0 | 2935 | 5 | 4 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2930): Show |
chr16 | 20531226 | 20581367 |
a0002c0003t0013 | 0/0 | 2935 | 4 | 3 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2930): Show |
chr16 | 20531226 | 20581367 |
a0002c0009t0009 | 0/0 | 2935 | 9 | 0 | 0 | 7 | 0 | 2 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2930): Show |
chr16 | 20531226 | 20581367 |
a0002c0018t0005 | 0/0 | 2935 | 2 | 0 | 0 | 1 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2930): Show |
chr16 | 20531226 | 20581367 |
a0002c0018t0010 | 0/0 | 2935 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2930): Show |
chr16 | 20531226 | 20581367 |
a0002c0019t0006 | 0/0 | 2935 | 3 | 0 | 0 | 3 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2930): Show |
chr16 | 20531226 | 20581367 |
a0002c0029t0010 | 0/0 | 2935 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2930): Show |
chr16 | 20531226 | 20581367 |
a0003c0007t0003 | 0/0 | 2935 | 3 | 3 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2930): Show |
chr16 | 20531226 | 20581367 |
a0003c0007t0004 | 0/0 | 2935 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2930): Show |
chr16 | 20531226 | 20581367 |
a0003c0007t0007 | 0/0 | 2935 | 3 | 2 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2930): Show |
chr16 | 20531226 | 20581367 |
a0003c0007t0014 | 0/0 | 2935 | 4 | 4 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2930): Show |
chr16 | 20531226 | 20581367 |
a0003c0008t0001 | 0/0 | 2935 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2930): Show |
chr16 | 20531226 | 20581367 |
a0003c0008t0003 | 0/0 | 2935 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2930): Show |
chr16 | 20531226 | 20581367 |
a0003c0008t0011 | 0/0 | 2935 | 4 | 4 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2930): Show |
chr16 | 20531226 | 20581367 |
a0003c0008t0015 | 0/0 | 2931 | 3 | 3 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2926): Show |
chr16 | 20531226 | 20581367 |
a0003c0025t0003 | 0/0 | 2935 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2930): Show |
chr16 | 20531226 | 20581367 |
a0003c0033t0003 | 0/0 | 2935 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2930): Show |
chr16 | 20531226 | 20581367 |
a0004c0005t0006 | 0/0 | 2935 | 19 | 17 | 2 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2930): Show |
chr16 | 20531226 | 20581367 |
a0005c0011t0001 | 1/0 | 2935 | 1 | 0 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2930): Show |
chr16 | 20531226 | 20581367 |
a0005c0011t0008 | 0/0 | 2935 | 3 | 0 | 2 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2930): Show |
chr16 | 20531226 | 20581367 |
a0005c0011t0019 | 0/0 | 2935 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2930): Show |
chr16 | 20531226 | 20581367 |
a0005c0011t0026 | 0/0 | 2935 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2930): Show |
chr16 | 20531226 | 20581367 |
a0005c0016t0016 | 0/0 | 2935 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2930): Show |
chr16 | 20531226 | 20581367 |
a0005c0016t0028 | 0/0 | 2935 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2930): Show |
chr16 | 20531226 | 20581367 |
a0005c0016t0029 | 0/0 | 2923 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2918): Show |
chr16 | 20531226 | 20581367 |
a0005c0024t0016 | 0/0 | 2935 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2930): Show |
chr16 | 20531226 | 20581367 |
a0006c0010t0003 | 0/0 | 2935 | 6 | 6 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2930): Show |
chr16 | 20531226 | 20581367 |
a0006c0010t0017 | 0/0 | 2935 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2930): Show |
chr16 | 20531226 | 20581367 |
a0006c0020t0003 | 0/0 | 2935 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2930): Show |
chr16 | 20531226 | 20581367 |
a0006c0020t0020 | 0/0 | 2935 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2930): Show |
chr16 | 20531226 | 20581367 |
a0007c0014t0001 | 0/0 | 2935 | 4 | 0 | 0 | 4 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2930): Show |
chr16 | 20531226 | 20581367 |
a0008c0013t0002 | 0/0 | 2935 | 4 | 4 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2930): Show |
chr16 | 20531226 | 20581367 |
a0009c0015t0008 | 0/0 | 2935 | 3 | 0 | 0 | 0 | 0 | 3 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2930): Show |
chr16 | 20531226 | 20581367 |
a0010c0022t0008 | 0/0 | 2935 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2930): Show |
chr16 | 20531226 | 20581367 |
a0010c0023t0027 | 0/0 | 2935 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2930): Show |
chr16 | 20531226 | 20581367 |
a0011c0021t0001 | 0/0 | 2935 | 2 | 0 | 0 | 1 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2930): Show |
chr16 | 20531226 | 20581367 |
a0012c0032t0025 | 0/0 | 2935 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2930): Show |
chr16 | 20531226 | 20581367 |
a0013c0026t0002 | 0/0 | 2935 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2930): Show |
chr16 | 20531226 | 20581367 |
a0014c0028t0003 | 0/0 | 2935 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2930): Show |
chr16 | 20531226 | 20581367 |
a0015c0030t0018 | 0/0 | 2935 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2930): Show |
chr16 | 20531226 | 20581367 |
a0016c0031t0016 | 0/0 | 2935 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | AATGA others(2930): Show |
chr16 | 20531226 | 20581367 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0002 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0003g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0003g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0003g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0003g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0003g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0008g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0008g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0008g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0012g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0012g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0018g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0023g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0008 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0003g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0003g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0003g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0003g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0003g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0003 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0034 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0035 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0007g0031 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0007g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0007g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0007g0223 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0007g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0007g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0021g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0022g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0024g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0004t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0004t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0004t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0004t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0004t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0004t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0004t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0004t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0004t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0004t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0004t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0004t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0004t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0004t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0004t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0004t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0004t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0004t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0004t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0004t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0004t0004g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0004t0004g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0004t0004g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0004t0004g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0004t0004g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0004t0007g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0004t0007g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0004t0007g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0004t0007g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0004t0007g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0006t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0006t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0006t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0006t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0006t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0006t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0006t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0006t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0006t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0006t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0006t0003g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0006t0003g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0006t0011g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0012t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0012t0007g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0012t0007g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0012t0007g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0017t0004g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0017t0004g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0027t0003g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0005g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0005g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0005g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0005g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0005g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0005g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0005g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0005g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0005g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0005g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0005g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0005g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0005g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0005g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0005g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0005g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0005g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0005g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0005g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0005g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0005g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0005g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0005g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0005g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0005g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0005g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0010g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0010g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0010g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0013g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0013g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0013g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0013g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0009t0009g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0009t0009g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0009t0009g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0009t0009g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0009t0009g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0009t0009g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0009t0009g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0009t0009g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0018t0005g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0018t0005g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0018t0010g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0019t0006g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0019t0006g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0019t0006g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0029t0010g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0003c0007t0003g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0003c0007t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0003c0007t0004g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0003c0007t0007g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0003c0007t0007g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0003c0007t0007g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0003c0007t0014g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0003c0007t0014g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0003c0007t0014g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0003c0007t0014g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0003c0008t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0003c0008t0003g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0003c0008t0011g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0003c0008t0011g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0003c0008t0011g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0003c0008t0011g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0003c0008t0015g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0003c0008t0015g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0003c0025t0003g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0003c0033t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0004c0005t0006g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0004c0005t0006g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0004c0005t0006g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0004c0005t0006g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0004c0005t0006g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0004c0005t0006g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0004c0005t0006g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0004c0005t0006g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0004c0005t0006g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0004c0005t0006g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0004c0005t0006g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0004c0005t0006g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0004c0005t0006g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0004c0005t0006g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0004c0005t0006g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0004c0005t0006g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0004c0005t0006g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0004c0005t0006g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0004c0005t0006g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0005c0011t0001g0244 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0005c0011t0008g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0005c0011t0008g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0005c0011t0008g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0005c0011t0019g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0005c0011t0026g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0005c0016t0016g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0005c0016t0028g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0005c0016t0029g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0005c0024t0016g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0006c0010t0003g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0006c0010t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0006c0010t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0006c0010t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0006c0010t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0006c0010t0017g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0006c0010t0017g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0006c0020t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0006c0020t0020g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0007c0014t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0007c0014t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0007c0014t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0007c0014t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0008c0013t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0008c0013t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0008c0013t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0008c0013t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0009c0015t0008g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0009c0015t0008g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0010c0022t0008g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0010c0023t0027g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0011c0021t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0011c0021t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0012c0032t0025g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0013c0026t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0014c0028t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0015c0030t0018g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0016c0031t0016g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0001 | c0002 | t0004 | g0269 | EUR | FIN | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG00323 | hp1 | a0001 | c0002 | t0004 | g0260 | EUR | FIN | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG00323 | hp2 | a0001 | c0002 | t0004 | g0296 | EUR | FIN | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG00423 | hp1 | a0012 | c0032 | t0025 | g0330 | EAS | CHS | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG00423 | hp2 | a0001 | c0004 | t0007 | g0024 | EAS | CHS | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG00438 | hp1 | a0001 | c0001 | t0003 | g0179 | EAS | CHS | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG00438 | hp2 | a0001 | c0006 | t0001 | g0279 | EAS | CHS | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | CHS | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG00558 | hp2 | a0001 | c0002 | t0002 | g0306 | EAS | CHS | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG00597 | hp1 | a0001 | c0001 | t0003 | g0153 | EAS | CHS | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG00597 | hp2 | a0001 | c0004 | t0002 | g0149 | EAS | CHS | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG00609 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | CHS | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG00609 | hp2 | a0001 | c0006 | t0003 | g0305 | EAS | CHS | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0152 | EAS | CHS | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG00621 | hp2 | a0001 | c0004 | t0004 | g0025 | EAS | CHS | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG00639 | hp1 | a0001 | c0002 | t0004 | g0301 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG00639 | hp2 | a0001 | c0002 | t0007 | g0031 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG00642 | hp1 | a0001 | c0002 | t0004 | g0294 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG00642 | hp2 | a0001 | c0002 | t0021 | g0262 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG00673 | hp1 | a0002 | c0003 | t0005 | g0049 | EAS | CHS | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG00673 | hp2 | a0001 | c0004 | t0002 | g0016 | EAS | CHS | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG00733 | hp1 | a0001 | c0006 | t0001 | g0289 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG00735 | hp1 | a0001 | c0002 | t0002 | g0231 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG00735 | hp2 | a0001 | c0004 | t0002 | g0169 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG00738 | hp2 | a0001 | c0002 | t0002 | g0030 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG00741 | hp1 | a0001 | c0001 | t0003 | g0193 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG00741 | hp2 | a0003 | c0007 | t0007 | g0248 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01069 | hp1 | a0001 | c0002 | t0002 | g0008 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01069 | hp2 | a0001 | c0002 | t0004 | g0003 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01070 | hp2 | a0001 | c0002 | t0002 | g0245 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01071 | hp1 | a0001 | c0002 | t0002 | g0008 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01074 | hp1 | a0001 | c0004 | t0002 | g0143 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01074 | hp2 | a0001 | c0012 | t0002 | g0230 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01081 | hp2 | a0001 | c0002 | t0003 | g0255 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01099 | hp1 | a0001 | c0002 | t0002 | g0229 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01099 | hp2 | a0004 | c0005 | t0006 | g0095 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01109 | hp1 | a0001 | c0002 | t0002 | g0237 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01109 | hp2 | a0001 | c0002 | t0002 | g0233 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01167 | hp1 | a0001 | c0002 | t0002 | g0251 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01167 | hp2 | a0001 | c0002 | t0004 | g0259 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01168 | hp1 | a0005 | c0011 | t0008 | g0320 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01168 | hp2 | a0001 | c0004 | t0002 | g0154 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01169 | hp1 | a0005 | c0011 | t0008 | g0321 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01169 | hp2 | a0001 | c0002 | t0002 | g0252 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01175 | hp1 | a0001 | c0002 | t0004 | g0278 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01175 | hp2 | a0001 | c0002 | t0004 | g0271 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01192 | hp1 | a0001 | c0002 | t0002 | g0008 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01192 | hp2 | a0001 | c0002 | t0002 | g0250 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01256 | hp1 | a0002 | c0029 | t0010 | g0076 | AMR | CLM | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01256 | hp2 | a0001 | c0004 | t0002 | g0130 | AMR | CLM | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01257 | hp1 | a0002 | c0003 | t0005 | g0074 | AMR | CLM | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01257 | hp2 | a0001 | c0001 | t0003 | g0174 | AMR | CLM | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01261 | hp1 | a0001 | c0002 | t0002 | g0030 | AMR | CLM | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01261 | hp2 | a0001 | c0002 | t0002 | g0243 | AMR | CLM | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01346 | hp1 | a0001 | c0002 | t0004 | g0003 | AMR | CLM | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01346 | hp2 | a0001 | c0002 | t0002 | g0295 | AMR | CLM | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01361 | hp1 | a0001 | c0002 | t0007 | g0240 | AMR | CLM | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01496 | hp1 | a0001 | c0002 | t0004 | g0219 | AMR | CLM | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01496 | hp2 | a0001 | c0002 | t0002 | g0241 | AMR | CLM | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01515 | hp1 | a0001 | c0002 | t0004 | g0035 | EUR | IBS | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0136 | EUR | IBS | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01516 | hp1 | a0001 | c0006 | t0001 | g0282 | EUR | IBS | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | IBS | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | IBS | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01517 | hp2 | a0001 | c0002 | t0004 | g0035 | EUR | IBS | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01884 | hp1 | a0004 | c0005 | t0006 | g0094 | AFR | ACB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01884 | hp2 | a0006 | c0010 | t0017 | g0045 | AFR | ACB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01891 | hp1 | a0005 | c0011 | t0019 | g0041 | AFR | ACB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01891 | hp2 | a0002 | c0003 | t0005 | g0064 | AFR | ACB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01934 | hp1 | a0001 | c0002 | t0004 | g0314 | AMR | PEL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01934 | hp2 | a0004 | c0005 | t0006 | g0101 | AMR | PEL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01943 | hp1 | a0002 | c0003 | t0013 | g0075 | AMR | PEL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01943 | hp2 | a0001 | c0004 | t0002 | g0148 | AMR | PEL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01952 | hp1 | a0001 | c0004 | t0002 | g0156 | AMR | PEL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01952 | hp2 | a0001 | c0002 | t0004 | g0267 | AMR | PEL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01975 | hp1 | a0001 | c0002 | t0002 | g0032 | AMR | PEL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01975 | hp2 | a0002 | c0003 | t0005 | g0059 | AMR | PEL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01981 | hp1 | a0001 | c0002 | t0024 | g0265 | AMR | PEL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01981 | hp2 | a0001 | c0002 | t0004 | g0266 | AMR | PEL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02004 | hp1 | a0001 | c0002 | t0002 | g0246 | AMR | PEL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02004 | hp2 | a0001 | c0002 | t0004 | g0264 | AMR | PEL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02015 | hp2 | a0001 | c0002 | t0004 | g0288 | EAS | KHV | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02027 | hp1 | a0001 | c0004 | t0002 | g0016 | EAS | KHV | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02040 | hp1 | a0002 | c0003 | t0005 | g0058 | EAS | KHV | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02055 | hp1 | a0003 | c0033 | t0003 | g0168 | AFR | ACB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02055 | hp2 | a0003 | c0007 | t0007 | g0313 | AFR | ACB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02056 | hp1 | a0001 | c0006 | t0003 | g0304 | EAS | KHV | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02056 | hp2 | a0001 | c0001 | t0003 | g0127 | EAS | KHV | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02074 | hp1 | a0007 | c0014 | t0001 | g0198 | EAS | KHV | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02074 | hp2 | a0002 | c0009 | t0009 | g0082 | EAS | KHV | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | KHV | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02080 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | KHV | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02083 | hp2 | a0001 | c0002 | t0004 | g0038 | EAS | KHV | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02132 | hp1 | a0001 | c0002 | t0004 | g0276 | EAS | KHV | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0144 | EAS | KHV | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02145 | hp1 | a0002 | c0003 | t0013 | g0055 | AFR | ACB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02145 | hp2 | a0003 | c0008 | t0011 | g0312 | AFR | ACB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02148 | hp1 | a0001 | c0001 | t0003 | g0164 | AMR | PEL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02148 | hp2 | a0001 | c0004 | t0002 | g0155 | AMR | PEL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02155 | hp1 | a0001 | c0001 | t0008 | g0328 | EAS | CDX | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02155 | hp2 | a0001 | c0004 | t0007 | g0024 | EAS | CDX | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02257 | hp1 | a0008 | c0013 | t0002 | g0111 | AFR | ACB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02257 | hp2 | a0003 | c0008 | t0011 | g0307 | AFR | ACB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02258 | hp1 | a0004 | c0005 | t0006 | g0104 | AFR | ACB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02258 | hp2 | a0003 | c0007 | t0014 | g0331 | AFR | ACB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02280 | hp1 | a0006 | c0010 | t0003 | g0119 | AFR | ACB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02280 | hp2 | a0001 | c0002 | t0003 | g0256 | AFR | ACB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02293 | hp1 | a0001 | c0002 | t0002 | g0247 | AMR | PEL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02293 | hp2 | a0001 | c0002 | t0004 | g0273 | AMR | PEL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02300 | hp1 | a0001 | c0002 | t0004 | g0003 | AMR | PEL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02300 | hp2 | a0001 | c0002 | t0002 | g0032 | AMR | PEL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02451 | hp1 | a0005 | c0016 | t0016 | g0317 | AFR | ACB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02451 | hp2 | a0001 | c0002 | t0003 | g0254 | AFR | ACB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02572 | hp1 | a0001 | c0002 | t0003 | g0013 | AFR | GWD | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02572 | hp2 | a0004 | c0005 | t0006 | g0107 | AFR | GWD | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02602 | hp1 | a0001 | c0002 | t0007 | g0220 | SAS | PJL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02602 | hp2 | a0001 | c0004 | t0002 | g0145 | SAS | PJL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02615 | hp1 | a0003 | c0008 | t0015 | g0309 | AFR | GWD | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02615 | hp2 | a0006 | c0010 | t0003 | g0120 | AFR | GWD | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02622 | hp1 | a0003 | c0007 | t0003 | g0239 | AFR | GWD | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02622 | hp2 | a0004 | c0005 | t0006 | g0103 | AFR | GWD | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02630 | hp1 | a0010 | c0022 | t0008 | g0316 | AFR | GWD | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02630 | hp2 | a0010 | c0023 | t0027 | g0323 | AFR | GWD | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02647 | hp1 | a0001 | c0002 | t0003 | g0013 | AFR | GWD | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02647 | hp2 | a0006 | c0010 | t0003 | g0122 | AFR | GWD | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02683 | hp1 | a0001 | c0002 | t0002 | g0249 | SAS | PJL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02683 | hp2 | a0001 | c0002 | t0004 | g0258 | SAS | PJL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02698 | hp1 | a0001 | c0004 | t0002 | g0139 | SAS | PJL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02698 | hp2 | a0001 | c0017 | t0004 | g0033 | SAS | PJL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02717 | hp1 | a0013 | c0026 | t0002 | g0117 | AFR | GWD | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02717 | hp2 | a0003 | c0007 | t0014 | g0332 | AFR | GWD | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02723 | hp1 | a0004 | c0005 | t0006 | g0091 | AFR | GWD | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02723 | hp2 | a0004 | c0005 | t0006 | g0098 | AFR | GWD | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02735 | hp2 | a0001 | c0002 | t0004 | g0280 | SAS | PJL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02738 | hp1 | a0001 | c0002 | t0002 | g0235 | SAS | PJL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02738 | hp2 | a0005 | c0011 | t0008 | g0322 | SAS | PJL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02809 | hp1 | a0003 | c0008 | t0001 | g0310 | AFR | GWD | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02809 | hp2 | a0002 | c0003 | t0005 | g0089 | AFR | GWD | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02818 | hp1 | a0004 | c0005 | t0006 | g0100 | AFR | GWD | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02818 | hp2 | a0001 | c0027 | t0003 | g0275 | AFR | GWD | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02886 | hp1 | a0002 | c0003 | t0005 | g0087 | AFR | GWD | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02886 | hp2 | a0008 | c0013 | t0002 | g0113 | AFR | GWD | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02895 | hp1 | a0006 | c0010 | t0003 | g0012 | AFR | GWD | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02895 | hp2 | a0001 | c0002 | t0003 | g0116 | AFR | GWD | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02896 | hp1 | a0003 | c0008 | t0015 | g0039 | AFR | GWD | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02896 | hp2 | a0008 | c0013 | t0002 | g0112 | AFR | GWD | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02897 | hp1 | a0003 | c0008 | t0015 | g0039 | AFR | GWD | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02897 | hp2 | a0006 | c0010 | t0003 | g0012 | AFR | GWD | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02922 | hp1 | a0005 | c0024 | t0016 | g0325 | AFR | ESN | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02922 | hp2 | a0006 | c0010 | t0017 | g0044 | AFR | ESN | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02965 | hp1 | a0001 | c0012 | t0007 | g0028 | AFR | ESN | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02965 | hp2 | a0001 | c0002 | t0002 | g0029 | AFR | ESN | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02970 | hp1 | a0001 | c0012 | t0007 | g0222 | AFR | ESN | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02970 | hp2 | a0002 | c0018 | t0010 | g0046 | AFR | ESN | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02976 | hp1 | a0004 | c0005 | t0006 | g0108 | AFR | ESN | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02976 | hp2 | a0002 | c0003 | t0005 | g0050 | AFR | ESN | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03017 | hp1 | a0001 | c0002 | t0004 | g0297 | SAS | PJL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03017 | hp2 | a0003 | c0007 | t0004 | g0303 | SAS | PJL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03098 | hp1 | a0014 | c0028 | t0003 | g0123 | AFR | MSL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03098 | hp2 | a0004 | c0005 | t0006 | g0105 | AFR | MSL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03130 | hp1 | a0003 | c0008 | t0011 | g0311 | AFR | ESN | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03130 | hp2 | a0003 | c0007 | t0014 | g0334 | AFR | ESN | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03139 | hp1 | a0003 | c0008 | t0011 | g0308 | AFR | ESN | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03139 | hp2 | a0004 | c0005 | t0006 | g0099 | AFR | ESN | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03195 | hp1 | a0002 | c0003 | t0005 | g0052 | AFR | ESN | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03195 | hp2 | a0001 | c0002 | t0002 | g0238 | AFR | ESN | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03209 | hp1 | a0006 | c0020 | t0003 | g0110 | AFR | MSL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03209 | hp2 | a0004 | c0005 | t0006 | g0096 | AFR | MSL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03225 | hp1 | a0001 | c0012 | t0007 | g0028 | AFR | MSL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03225 | hp2 | a0002 | c0003 | t0010 | g0005 | AFR | MSL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03239 | hp1 | a0001 | c0002 | t0002 | g0228 | SAS | PJL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03239 | hp2 | a0001 | c0002 | t0004 | g0268 | SAS | PJL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03453 | hp1 | a0008 | c0013 | t0002 | g0114 | AFR | MSL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03453 | hp2 | a0002 | c0003 | t0013 | g0054 | AFR | MSL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03486 | hp1 | a0001 | c0006 | t0011 | g0115 | AFR | MSL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03486 | hp2 | a0002 | c0003 | t0005 | g0061 | AFR | MSL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03490 | hp1 | a0001 | c0017 | t0004 | g0033 | SAS | PJL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03490 | hp2 | a0009 | c0015 | t0008 | g0040 | SAS | PJL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03491 | hp1 | a0002 | c0009 | t0009 | g0011 | SAS | PJL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03491 | hp2 | a0002 | c0003 | t0010 | g0086 | SAS | PJL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03492 | hp1 | a0002 | c0009 | t0009 | g0011 | SAS | PJL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03492 | hp2 | a0009 | c0015 | t0008 | g0040 | SAS | PJL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03516 | hp1 | a0003 | c0007 | t0007 | g0274 | AFR | ESN | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03516 | hp2 | a0001 | c0002 | t0002 | g0029 | AFR | ESN | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03540 | hp1 | a0004 | c0005 | t0006 | g0097 | AFR | GWD | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03540 | hp2 | a0005 | c0011 | t0026 | g0318 | AFR | GWD | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03579 | hp1 | a0006 | c0020 | t0020 | g0042 | AFR | MSL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03579 | hp2 | a0001 | c0002 | t0002 | g0242 | AFR | MSL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03654 | hp2 | a0001 | c0002 | t0004 | g0034 | SAS | PJL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03669 | hp1 | a0001 | c0002 | t0002 | g0221 | SAS | PJL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03669 | hp2 | a0001 | c0002 | t0002 | g0284 | SAS | PJL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03688 | hp1 | a0001 | c0002 | t0004 | g0226 | SAS | STU | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03688 | hp2 | a0001 | c0006 | t0001 | g0285 | SAS | STU | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03704 | hp1 | a0003 | c0025 | t0003 | g0124 | SAS | PJL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03704 | hp2 | a0001 | c0002 | t0004 | g0298 | SAS | PJL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03710 | hp1 | a0001 | c0006 | t0001 | g0292 | SAS | PJL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03710 | hp2 | a0002 | c0018 | t0005 | g0056 | SAS | PJL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03831 | hp1 | a0011 | c0021 | t0001 | g0188 | SAS | BEB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03831 | hp2 | a0002 | c0003 | t0005 | g0067 | SAS | BEB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03834 | hp1 | a0001 | c0002 | t0004 | g0283 | SAS | BEB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03834 | hp2 | a0001 | c0017 | t0004 | g0261 | SAS | BEB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03927 | hp1 | a0003 | c0008 | t0003 | g0125 | SAS | BEB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03927 | hp2 | a0009 | c0015 | t0008 | g0319 | SAS | BEB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03942 | hp1 | a0001 | c0001 | t0023 | g0202 | SAS | BEB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03942 | hp2 | a0001 | c0002 | t0002 | g0232 | SAS | BEB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG04115 | hp1 | a0001 | c0002 | t0004 | g0291 | SAS | STU | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG04115 | hp2 | a0001 | c0002 | t0022 | g0302 | SAS | STU | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | STU | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG04199 | hp2 | a0005 | c0016 | t0029 | g0315 | SAS | STU | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | STU | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG04228 | hp2 | a0001 | c0002 | t0002 | g0281 | SAS | STU | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18522 | hp1 | a0001 | c0002 | t0002 | g0118 | AFR | YRI | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18522 | hp2 | a0003 | c0007 | t0014 | g0333 | AFR | YRI | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18612 | hp1 | a0001 | c0004 | t0004 | g0025 | EAS | CHB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18612 | hp2 | a0001 | c0001 | t0008 | g0326 | EAS | CHB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18906 | hp1 | a0005 | c0016 | t0028 | g0324 | AFR | YRI | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18906 | hp2 | a0004 | c0005 | t0006 | g0102 | AFR | YRI | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18939 | hp1 | a0002 | c0003 | t0005 | g0090 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18939 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18942 | hp1 | a0002 | c0003 | t0005 | g0009 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18943 | hp1 | a0001 | c0004 | t0007 | g0216 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18943 | hp2 | a0001 | c0002 | t0004 | g0038 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18945 | hp1 | a0001 | c0002 | t0004 | g0037 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18946 | hp1 | a0001 | c0004 | t0004 | g0214 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18946 | hp2 | a0002 | c0003 | t0005 | g0009 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18947 | hp1 | a0015 | c0030 | t0018 | g0146 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18948 | hp1 | a0002 | c0009 | t0009 | g0081 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18951 | hp1 | a0001 | c0004 | t0004 | g0197 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18953 | hp1 | a0001 | c0001 | t0012 | g0043 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18953 | hp2 | a0007 | c0014 | t0001 | g0160 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18954 | hp1 | a0002 | c0003 | t0005 | g0060 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18956 | hp2 | a0002 | c0003 | t0005 | g0065 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18957 | hp1 | a0001 | c0001 | t0012 | g0004 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18957 | hp2 | a0001 | c0004 | t0007 | g0200 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18959 | hp1 | a0002 | c0003 | t0005 | g0051 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18959 | hp2 | a0002 | c0009 | t0009 | g0078 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18960 | hp2 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18961 | hp1 | a0001 | c0006 | t0003 | g0224 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18961 | hp2 | a0001 | c0004 | t0007 | g0201 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18964 | hp2 | a0001 | c0002 | t0004 | g0290 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18966 | hp1 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18966 | hp2 | a0001 | c0004 | t0002 | g0140 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18967 | hp1 | a0001 | c0004 | t0004 | g0023 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18967 | hp2 | a0002 | c0009 | t0009 | g0079 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18968 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18968 | hp2 | a0002 | c0003 | t0005 | g0070 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18972 | hp1 | a0001 | c0001 | t0003 | g0147 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18973 | hp1 | a0001 | c0001 | t0003 | g0162 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18973 | hp2 | a0001 | c0004 | t0002 | g0134 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18974 | hp1 | a0002 | c0003 | t0005 | g0010 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18974 | hp2 | a0002 | c0009 | t0009 | g0057 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18975 | hp1 | a0001 | c0004 | t0002 | g0182 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18977 | hp1 | a0001 | c0006 | t0003 | g0225 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18978 | hp1 | a0002 | c0003 | t0005 | g0068 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18978 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18982 | hp1 | a0001 | c0004 | t0002 | g0181 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18982 | hp2 | a0001 | c0002 | t0004 | g0263 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18988 | hp1 | a0002 | c0019 | t0006 | g0083 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18989 | hp2 | a0001 | c0001 | t0003 | g0211 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18990 | hp1 | a0001 | c0001 | t0003 | g0142 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18990 | hp2 | a0001 | c0006 | t0001 | g0300 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18992 | hp1 | a0001 | c0004 | t0002 | g0131 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18994 | hp1 | a0002 | c0003 | t0005 | g0071 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18997 | hp1 | a0007 | c0014 | t0001 | g0173 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19001 | hp1 | a0001 | c0004 | t0002 | g0129 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19004 | hp1 | a0001 | c0004 | t0004 | g0023 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19004 | hp2 | a0001 | c0004 | t0002 | g0187 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19005 | hp1 | a0002 | c0003 | t0005 | g0053 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19005 | hp2 | a0001 | c0001 | t0018 | g0132 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19006 | hp1 | a0001 | c0001 | t0012 | g0004 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19007 | hp1 | a0001 | c0004 | t0007 | g0017 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19007 | hp2 | a0001 | c0006 | t0001 | g0286 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19009 | hp1 | a0001 | c0004 | t0004 | g0171 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19010 | hp1 | a0002 | c0003 | t0005 | g0048 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19012 | hp1 | a0001 | c0002 | t0004 | g0037 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19012 | hp2 | a0001 | c0001 | t0003 | g0133 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19030 | hp1 | a0001 | c0002 | t0003 | g0036 | AFR | LWK | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19030 | hp2 | a0001 | c0002 | t0002 | g0236 | AFR | LWK | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19043 | hp1 | a0001 | c0002 | t0007 | g0109 | AFR | LWK | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19043 | hp2 | a0004 | c0005 | t0006 | g0093 | AFR | LWK | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19054 | hp1 | a0002 | c0003 | t0005 | g0062 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19054 | hp2 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19056 | hp1 | a0002 | c0009 | t0009 | g0080 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19056 | hp2 | a0001 | c0001 | t0012 | g0004 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19062 | hp1 | a0001 | c0004 | t0002 | g0141 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19062 | hp2 | a0002 | c0019 | t0006 | g0092 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19064 | hp1 | a0011 | c0021 | t0001 | g0189 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19064 | hp2 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19065 | hp2 | a0001 | c0001 | t0003 | g0137 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19067 | hp1 | a0001 | c0004 | t0007 | g0017 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19070 | hp1 | a0002 | c0003 | t0005 | g0010 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19072 | hp2 | a0002 | c0003 | t0005 | g0066 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19074 | hp1 | a0007 | c0014 | t0001 | g0204 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19077 | hp1 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19077 | hp2 | a0002 | c0003 | t0005 | g0069 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19079 | hp2 | a0016 | c0031 | t0016 | g0329 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19081 | hp1 | a0002 | c0018 | t0005 | g0073 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19081 | hp2 | a0001 | c0006 | t0001 | g0299 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19083 | hp1 | a0002 | c0009 | t0009 | g0077 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19083 | hp2 | a0001 | c0002 | t0007 | g0287 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19084 | hp1 | a0001 | c0001 | t0008 | g0327 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19084 | hp2 | a0001 | c0004 | t0002 | g0180 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19088 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19088 | hp2 | a0002 | c0019 | t0006 | g0072 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19090 | hp1 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19091 | hp2 | a0002 | c0003 | t0005 | g0063 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19240 | hp1 | a0005 | c0011 | t0019 | g0041 | AFR | YRI | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19240 | hp2 | a0001 | c0012 | t0007 | g0277 | AFR | YRI | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA20129 | hp1 | a0004 | c0005 | t0006 | g0085 | AFR | ASW | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA20129 | hp2 | a0001 | c0002 | t0004 | g0003 | AFR | ASW | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA20752 | hp1 | a0001 | c0002 | t0004 | g0270 | EUR | TSI | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA20752 | hp2 | a0001 | c0002 | t0007 | g0031 | EUR | TSI | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA20905 | hp1 | a0001 | c0002 | t0002 | g0227 | SAS | GIH | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA20905 | hp2 | a0001 | c0002 | t0004 | g0293 | SAS | GIH | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01123 | hp2 | a0001 | c0002 | t0004 | g0272 | AMR | CLM | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02109 | hp1 | a0006 | c0010 | t0003 | g0121 | AFR | ACB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02109 | hp2 | a0001 | c0002 | t0003 | g0036 | AFR | ACB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02486 | hp1 | a0002 | c0003 | t0013 | g0084 | AFR | ACB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02486 | hp2 | a0003 | c0007 | t0003 | g0014 | AFR | ACB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02559 | hp1 | a0002 | c0003 | t0010 | g0088 | AFR | ACB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02559 | hp2 | a0002 | c0003 | t0010 | g0005 | AFR | ACB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03471 | hp1 | a0003 | c0007 | t0003 | g0014 | AFR | MSL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03471 | hp2 | a0004 | c0005 | t0006 | g0106 | AFR | MSL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG06807 | hp1 | a0004 | c0005 | t0006 | g0047 | AFR | USA | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG06807 | hp2 | a0001 | c0002 | t0004 | g0257 | AFR | USA | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA20300 | hp1 | a0002 | c0003 | t0010 | g0005 | AFR | USA | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA20300 | hp2 | a0001 | c0002 | t0003 | g0253 | AFR | USA | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA21309 | hp1 | a0001 | c0002 | t0002 | g0234 | AFR | LWK | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA21309 | hp2 | a0001 | c0002 | t0004 | g0034 | AFR | LWK | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
homoSapiens | chm13v2 | a0001 | c0002 | t0007 | g0223 | REF | REF | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
homoSapiens | grch38p0 | a0005 | c0011 | t0001 | g0244 | REF | REF | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:20537269 | G | C | 1 | a0013 | 1 | HG02717.hp1 | missense_variant | MODERATE | c.1723C>G | p.Arg575Gly | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 14/14 | 1892/2935 | 1723/1734 | 575/577 | chr16 | 20537269 | |||
chr16:20540654 | C | G | 1 | a0011 | 2 | HG03831.hp1 NA19064.hp1 |
missense_variant&splice_region_variant | MODERATE | c.1629G>C | p.Lys543Asn | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/14 | 1798/2935 | 1629/1734 | 543/577 | chr16 | 20540654 | |||
chr16:20540692 | C | A | 1 | a0016 | 1 | NA19079.hp2 | missense_variant | MODERATE | c.1591G>T | p.Val531Leu | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/14 | 1760/2935 | 1591/1734 | 531/577 | chr16 | 20540692 | |||
chr16:20540766 | T | C | 1 | a0012 | 1 | HG00423.hp1 | missense_variant | MODERATE | c.1517A>G | p.Lys506Arg | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/14 | 1686/2935 | 1517/1734 | 506/577 | chr16 | 20540766 | |||
chr16:20542973 | T | C | 1 | a0008 | 4 | HG02257.hp1 HG02886.hp2 HG02896.hp2 others(1): Show |
missense_variant | MODERATE | c.1450A>G | p.Lys484Glu | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/14 | 1619/2935 | 1450/1734 | 484/577 | chr16 | 20542973 | |||
chr16:20543238 | T | A | 1 | a0007 | 4 | HG02074.hp1 NA18953.hp2 NA18997.hp1 others(1): Show |
missense_variant | MODERATE | c.1306A>T | p.Asn436Tyr | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 11/14 | 1475/2935 | 1306/1734 | 436/577 | chr16 | 20543238 | |||
chr16:20543260 | T | G | 6 | a0003 a0004 a0006 others(3): Show |
58 | HG00741.hp2 HG01099.hp2 HG01884.hp1 others(55): Show |
missense_variant&splice_region_variant | MODERATE | c.1284A>C | p.Glu428Asp | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 11/14 | 1453/2935 | 1284/1734 | 428/577 | chr16 | 20543260 | |||
chr16:20545228 | G | A | 1 | a0014 | 1 | HG03098.hp1 | missense_variant | MODERATE | c.1210C>T | p.Pro404Ser | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/14 | 1379/2935 | 1210/1734 | 404/577 | chr16 | 20545228 | |||
chr16:20548455 | T | C | 2 | a0006 a0008 |
14 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(11): Show |
missense_variant | MODERATE | c.913A>G | p.Ile305Val | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 7/14 | 1082/2935 | 913/1734 | 305/577 | chr16 | 20548455 | |||
chr16:20552206 | T | C | 2 | a0002 a0004 |
72 | HG00673.hp1 HG01099.hp2 HG01256.hp1 others(69): Show |
missense_variant | MODERATE | c.832A>G | p.Thr278Ala | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/14 | 1001/2935 | 832/1734 | 278/577 | chr16 | 20552206 | |||
chr16:20559267 | A | T | 1 | a0015 | 1 | NA18947.hp1 | missense_variant | MODERATE | c.358T>A | p.Trp120Arg | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/14 | 527/2935 | 358/1734 | 120/577 | chr16 | 20559267 | |||
chr16:20559339 | T | C | 14 | a0001 a0002 a0003 others(11): Show |
374 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(371): Show |
missense_variant | MODERATE | c.286A>G | p.Ile96Val | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/14 | 455/2935 | 286/1734 | 96/577 | chr16 | 20559339 | |||
chr16:20559434 | A | G | 1 | a0009 | 3 | HG03490.hp2 HG03492.hp2 HG03927.hp2 |
missense_variant | MODERATE | c.191T>C | p.Leu64Pro | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/14 | 360/2935 | 191/1734 | 64/577 | chr16 | 20559434 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:20540717 | C | T | 1 | a0002c0029 | 1 | HG01256.hp1 | synonymous_variant | LOW | c.1566G>A | p.Gln522Gln | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/14 | 1735/2935 | 1566/1734 | 522/577 | chr16 | 20540717 | |||
chr16:20540744 | C | T | 1 | a0001c0012 | 5 | HG01074.hp2 HG02965.hp1 HG02970.hp1 others(2): Show |
synonymous_variant | LOW | c.1539G>A | p.Ser513Ser | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/14 | 1708/2935 | 1539/1734 | 513/577 | chr16 | 20540744 | |||
chr16:20540753 | G | T | 20 | a0001c0002 a0001c0004 a0001c0012 others(17): Show |
233 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(230): Show |
synonymous_variant | LOW | c.1530C>A | p.Ile510Ile | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/14 | 1699/2935 | 1530/1734 | 510/577 | chr16 | 20540753 | |||
chr16:20542926 | G | A | 4 | a0002c0003 a0002c0009 a0002c0019 others(1): Show |
50 | HG00673.hp1 HG01256.hp1 HG01257.hp1 others(47): Show |
synonymous_variant | LOW | c.1497C>T | p.Pro499Pro | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/14 | 1666/2935 | 1497/1734 | 499/577 | chr16 | 20542926 | |||
chr16:20542983 | A | G | 1 | a0003c0033 | 1 | HG02055.hp1 | synonymous_variant | LOW | c.1440T>C | p.Asn480Asn | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/14 | 1609/2935 | 1440/1734 | 480/577 | chr16 | 20542983 | |||
chr16:20543215 | G | A | 1 | a0001c0027 | 1 | HG02818.hp2 | synonymous_variant | LOW | c.1329C>T | p.Leu443Leu | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 11/14 | 1498/2935 | 1329/1734 | 443/577 | chr16 | 20543215 | |||
chr16:20546409 | G | A | 1 | a0005c0024 | 1 | HG02922.hp1 | synonymous_variant | LOW | c.1164C>T | p.Ser388Ser | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 9/14 | 1333/2935 | 1164/1734 | 388/577 | chr16 | 20546409 | |||
chr16:20546469 | T | C | 1 | a0014c0028 | 1 | HG03098.hp1 | synonymous_variant | LOW | c.1104A>G | p.Leu368Leu | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 9/14 | 1273/2935 | 1104/1734 | 368/577 | chr16 | 20546469 | |||
chr16:20548432 | A | G | 2 | a0001c0017 a0006c0010 |
11 | HG01884.hp2 HG02109.hp1 HG02280.hp1 others(8): Show |
synonymous_variant | LOW | c.936T>C | p.Pro312Pro | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 7/14 | 1105/2935 | 936/1734 | 312/577 | chr16 | 20548432 | |||
chr16:20555301 | G | A | 1 | a0002c0019 | 3 | NA18988.hp1 NA19062.hp2 NA19088.hp2 |
synonymous_variant | LOW | c.564C>T | p.Cys188Cys | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 4/14 | 733/2935 | 564/1734 | 188/577 | chr16 | 20555301 | |||
chr16:20559274 | A | T | 1 | a0003c0025 | 1 | HG03704.hp1 | synonymous_variant | LOW | c.351T>A | p.Pro117Pro | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/14 | 520/2935 | 351/1734 | 117/577 | chr16 | 20559274 | |||
chr16:20564726 | C | A | 8 | a0001c0001 a0001c0004 a0003c0033 others(5): Show |
144 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(141): Show |
synonymous_variant | LOW | c.120G>T | p.Val40Val | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/14 | 289/2935 | 120/1734 | 40/577 | chr16 | 20564726 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:20536326 | T | G | 1 | a0001c0002t0021 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*932A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 14/14 | 932 | chr16 | 20536326 | ||||||
chr16:20536472 | G | A | 19 | a0001c0002t0002 a0001c0002t0004 a0001c0002t0021 others(16): Show |
133 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*786C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 14/14 | 786 | chr16 | 20536472 | ||||||
chr16:20536516 | C | T | 1 | a0010c0023t0027 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*742G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 14/14 | 742 | chr16 | 20536516 | ||||||
chr16:20536640 | C | G | 1 | a0005c0011t0026 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*618G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 14/14 | 618 | chr16 | 20536640 | ||||||
chr16:20536686 | C | T | 2 | a0001c0001t0018 a0015c0030t0018 |
2 | NA18947.hp1 NA19005.hp2 |
3_prime_UTR_variant | MODIFIER | c.*572G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 14/14 | 572 | chr16 | 20536686 | ||||||
chr16:20536753 | C | A | 2 | a0001c0006t0011 a0003c0008t0011 |
5 | HG02145.hp2 HG02257.hp2 HG03130.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*505G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 14/14 | 505 | chr16 | 20536753 | ||||||
chr16:20536768 | CCTTTCTC others(5): Show |
C | 1 | a0005c0016t0029 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*478_*489delAGAGGG others(6): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 14/14 | 478 | chr16 | 20536768 | ||||||
chr16:20536791 | CTCTT | C | 1 | a0003c0008t0015 | 3 | HG02615.hp1 HG02896.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*463_*466delAAGA | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 14/14 | 463 | chr16 | 20536791 | ||||||
chr16:20536804 | G | A | 1 | a0001c0001t0023 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*454C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 14/14 | 454 | chr16 | 20536804 | ||||||
chr16:20536838 | C | T | 1 | a0001c0002t0022 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*420G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 14/14 | 420 | chr16 | 20536838 | ||||||
chr16:20536929 | C | T | 8 | a0001c0002t0004 a0001c0002t0021 a0001c0002t0024 others(5): Show |
60 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*329G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 14/14 | 329 | chr16 | 20536929 | ||||||
chr16:20536958 | G | A | 8 | a0001c0002t0007 a0001c0004t0007 a0001c0012t0007 others(5): Show |
52 | HG00423.hp2 HG00639.hp2 HG00673.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*300C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 14/14 | 300 | chr16 | 20536958 | ||||||
chr16:20537012 | C | T | 54 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0018 others(51): Show |
289 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(286): Show |
3_prime_UTR_variant | MODIFIER | c.*246G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 14/14 | 246 | chr16 | 20537012 | ||||||
chr16:20537112 | T | G | 2 | a0001c0006t0011 a0003c0008t0011 |
5 | HG02145.hp2 HG02257.hp2 HG03130.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*146A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 14/14 | 146 | chr16 | 20537112 | ||||||
chr16:20537114 | T | C | 1 | a0001c0002t0024 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*144A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 14/14 | 144 | chr16 | 20537114 | ||||||
chr16:20576235 | G | A | 1 | a0003c0007t0014 | 4 | HG02258.hp2 HG02717.hp2 HG03130.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-37C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/14 | 11390 | chr16 | 20576235 | ||||||
chr16:20576246 | C | T | 9 | a0002c0003t0005 a0002c0003t0010 a0002c0003t0013 others(6): Show |
72 | HG00673.hp1 HG01099.hp2 HG01256.hp1 others(69): Show |
5_prime_UTR_variant | MODIFIER | c.-48G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/14 | 11401 | chr16 | 20576246 | ||||||
chr16:20576286 | C | T | 1 | a0006c0010t0017 | 2 | HG01884.hp2 HG02922.hp2 |
5_prime_UTR_variant | MODIFIER | c.-88G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/14 | 11441 | chr16 | 20576286 | ||||||
chr16:20576338 | A | G | 1 | a0001c0001t0012 | 4 | NA18953.hp1 NA18957.hp1 NA19006.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-140T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/14 | 11493 | chr16 | 20576338 | ||||||
chr16:20576344 | G | A | 14 | a0001c0001t0008 a0003c0007t0014 a0005c0011t0008 others(11): Show |
24 | HG00423.hp1 HG01168.hp1 HG01169.hp1 others(21): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-146C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/14 | chr16 | 20576344 | |||||||
chr16:20576347 | A | G | 1 | a0006c0020t0020 | 1 | HG03579.hp1 | 5_prime_UTR_variant | MODIFIER | c.-149T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/14 | 11502 | chr16 | 20576347 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:20537475 | T | C | 2 | a0002c0003t0005g0061 a0005c0016t0028g0324 |
2 | HG03486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1630-113A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20537475 | |||||||
chr16:20537502 | A | G | 5 | a0001c0006t0011g0115 a0003c0008t0011g0307 a0003c0008t0011g0308 others(2): Show |
5 | HG02145.hp2 HG02257.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1630-140T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20537502 | |||||||
chr16:20537532 | G | C | 2 | a0002c0003t0010g0088 a0005c0024t0016g0325 |
2 | HG02559.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1630-170C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20537532 | |||||||
chr16:20537562 | G | C | 3 | a0001c0002t0002g0118 a0005c0016t0016g0317 a0013c0026t0002g0117 |
3 | HG02451.hp1 HG02717.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1630-200C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20537562 | |||||||
chr16:20537572 | C | T | 1 | a0001c0001t0001g0210 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1630-210G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20537572 | |||||||
chr16:20537684 | C | T | 26 | a0001c0002t0003g0013 a0001c0002t0003g0116 a0001c0002t0003g0255 others(23): Show |
28 | HG01081.hp2 HG01099.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.1630-322G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20537684 | |||||||
chr16:20537771 | C | A | 1 | a0005c0011t0026g0318 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1630-409G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20537771 | |||||||
chr16:20537785 | C | T | 205 | a0001c0002t0002g0008 a0001c0002t0002g0029 a0001c0002t0002g0030 others(202): Show |
233 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(230): Show |
intron_variant | MODIFIER | c.1630-423G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20537785 | |||||||
chr16:20537808 | T | G | 40 | a0001c0001t0003g0007 a0001c0001t0003g0015 a0001c0001t0003g0020 others(37): Show |
45 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.1630-446A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20537808 | |||||||
chr16:20537827 | G | C | 1 | a0002c0009t0009g0081 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1630-465C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20537827 | |||||||
chr16:20537853 | T | A | 1 | a0010c0023t0027g0323 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1630-491A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20537853 | |||||||
chr16:20537884 | A | G | 1 | a0001c0002t0022g0302 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1630-522T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20537884 | |||||||
chr16:20537949 | TA | T | 3 | a0001c0012t0007g0028 a0001c0012t0007g0222 a0001c0012t0007g0277 |
4 | HG02965.hp1 HG02970.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1630-588delT | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20537949 | |||||||
chr16:20537950 | A | C | 44 | a0001c0001t0003g0007 a0001c0001t0003g0015 a0001c0001t0003g0020 others(41): Show |
49 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.1630-588T>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20537950 | |||||||
chr16:20537987 | G | A | 36 | a0001c0002t0003g0013 a0001c0002t0003g0036 a0001c0002t0003g0116 others(33): Show |
39 | HG01081.hp2 HG01099.hp2 HG01884.hp1 others(36): Show |
intron_variant | MODIFIER | c.1630-625C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20537987 | |||||||
chr16:20538067 | C | T | 5 | a0001c0006t0011g0115 a0003c0008t0011g0307 a0003c0008t0011g0308 others(2): Show |
5 | HG02145.hp2 HG02257.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1630-705G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20538067 | |||||||
chr16:20538102 | T | C | 2 | a0001c0004t0007g0216 a0002c0018t0005g0073 |
2 | NA18943.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1630-740A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20538102 | |||||||
chr16:20538141 | G | C | 1 | a0001c0004t0002g0129 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1630-779C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20538141 | |||||||
chr16:20538183 | G | A | 256 | a0001c0001t0003g0007 a0001c0001t0003g0015 a0001c0001t0003g0020 others(253): Show |
289 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(286): Show |
intron_variant | MODIFIER | c.1630-821C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20538183 | |||||||
chr16:20538266 | A | G | 1 | a0001c0001t0001g0178 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1630-904T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20538266 | |||||||
chr16:20538266 | A | T | 2 | a0001c0002t0003g0116 a0004c0005t0006g0095 |
2 | HG01099.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1630-904T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20538266 | |||||||
chr16:20538272 | T | C | 5 | a0001c0006t0011g0115 a0003c0008t0011g0307 a0003c0008t0011g0308 others(2): Show |
5 | HG02145.hp2 HG02257.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1630-910A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20538272 | |||||||
chr16:20538300 | G | A | 205 | a0001c0002t0002g0008 a0001c0002t0002g0029 a0001c0002t0002g0030 others(202): Show |
233 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(230): Show |
intron_variant | MODIFIER | c.1630-938C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20538300 | |||||||
chr16:20538455 | G | A | 205 | a0001c0002t0002g0008 a0001c0002t0002g0029 a0001c0002t0002g0030 others(202): Show |
233 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(230): Show |
intron_variant | MODIFIER | c.1630-1093C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20538455 | |||||||
chr16:20538458 | C | A | 1 | a0002c0009t0009g0011 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1630-1096G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20538458 | |||||||
chr16:20538580 | G | T | 7 | a0001c0002t0003g0036 a0001c0027t0003g0275 a0003c0007t0014g0331 others(4): Show |
8 | HG02055.hp1 HG02109.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1630-1218C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20538580 | |||||||
chr16:20538582 | G | T | 1 | a0001c0006t0001g0286 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1630-1220C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20538582 | |||||||
chr16:20538588 | G | A | 51 | a0001c0001t0003g0007 a0001c0001t0003g0015 a0001c0001t0003g0020 others(48): Show |
56 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.1630-1226C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20538588 | |||||||
chr16:20538695 | C | T | 3 | a0001c0002t0004g0034 a0001c0002t0004g0268 a0001c0002t0004g0272 |
4 | HG01123.hp2 HG03239.hp2 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.1630-1333G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20538695 | |||||||
chr16:20538726 | T | C | 1 | a0003c0007t0007g0313 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1630-1364A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20538726 | |||||||
chr16:20538734 | C | T | 205 | a0001c0002t0002g0008 a0001c0002t0002g0029 a0001c0002t0002g0030 others(202): Show |
233 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(230): Show |
intron_variant | MODIFIER | c.1630-1372G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20538734 | |||||||
chr16:20538778 | G | A | 115 | a0001c0002t0002g0008 a0001c0002t0002g0029 a0001c0002t0002g0030 others(112): Show |
133 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.1630-1416C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20538778 | |||||||
chr16:20538808 | A | G | 1 | a0002c0003t0005g0069 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1630-1446T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20538808 | |||||||
chr16:20538933 | C | T | 1 | a0001c0004t0002g0143 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1630-1571G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20538933 | |||||||
chr16:20539019 | T | C | 1 | a0004c0005t0006g0100 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1629+1635A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20539019 | |||||||
chr16:20539025 | C | T | 5 | a0001c0006t0011g0115 a0003c0008t0011g0307 a0003c0008t0011g0308 others(2): Show |
5 | HG02145.hp2 HG02257.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1629+1629G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20539025 | |||||||
chr16:20539042 | C | G | 169 | a0001c0002t0002g0008 a0001c0002t0002g0029 a0001c0002t0002g0030 others(166): Show |
194 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.1629+1612G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20539042 | |||||||
chr16:20539162 | C | T | 1 | a0002c0009t0009g0078 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1629+1492G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20539162 | |||||||
chr16:20539288 | ACCTATGA others(7): Show |
A | 7 | a0006c0010t0003g0012 a0006c0010t0003g0119 a0006c0010t0003g0120 others(4): Show |
8 | HG01884.hp2 HG02109.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1629+1352_1629+136 others(18): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20539288 | |||||||
chr16:20539291 | T | A | 3 | a0002c0003t0005g0052 a0002c0003t0005g0087 a0002c0003t0005g0089 |
3 | HG02809.hp2 HG02886.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1629+1363A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20539291 | |||||||
chr16:20539291 | T | C | 2 | a0001c0004t0002g0129 a0001c0004t0002g0131 |
2 | NA18992.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.1629+1363A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20539291 | |||||||
chr16:20539301 | AG | A | 162 | a0001c0002t0002g0008 a0001c0002t0002g0029 a0001c0002t0002g0030 others(159): Show |
186 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.1629+1352delC | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20539301 | |||||||
chr16:20539302 | G | C | 80 | a0001c0001t0003g0007 a0001c0001t0003g0015 a0001c0001t0003g0020 others(77): Show |
88 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.1629+1352C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20539302 | |||||||
chr16:20539305 | T | C | 169 | a0001c0002t0002g0008 a0001c0002t0002g0029 a0001c0002t0002g0030 others(166): Show |
194 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.1629+1349A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20539305 | |||||||
chr16:20539393 | G | A | 205 | a0001c0002t0002g0008 a0001c0002t0002g0029 a0001c0002t0002g0030 others(202): Show |
233 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(230): Show |
intron_variant | MODIFIER | c.1629+1261C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20539393 | |||||||
chr16:20539399 | A | AT | 255 | a0001c0001t0003g0007 a0001c0001t0003g0015 a0001c0001t0003g0020 others(252): Show |
288 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(285): Show |
intron_variant | MODIFIER | c.1629+1254dupA | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20539399 | |||||||
chr16:20539399 | A | T | 1 | a0001c0002t0004g0271 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1629+1255T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20539399 | |||||||
chr16:20539567 | G | A | 1 | a0005c0011t0019g0041 | 2 | HG01891.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1629+1087C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20539567 | |||||||
chr16:20539604 | G | C | 5 | a0001c0006t0011g0115 a0003c0008t0011g0307 a0003c0008t0011g0308 others(2): Show |
5 | HG02145.hp2 HG02257.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1629+1050C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20539604 | |||||||
chr16:20539721 | G | A | 1 | a0003c0007t0014g0332 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1629+933C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20539721 | |||||||
chr16:20539823 | C | T | 116 | a0001c0001t0001g0175 a0001c0002t0002g0008 a0001c0002t0002g0029 others(113): Show |
134 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.1629+831G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20539823 | |||||||
chr16:20539900 | C | A | 44 | a0001c0001t0003g0007 a0001c0001t0003g0015 a0001c0001t0003g0020 others(41): Show |
49 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.1629+754G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20539900 | |||||||
chr16:20539929 | T | C | 5 | a0001c0006t0011g0115 a0003c0008t0011g0307 a0003c0008t0011g0308 others(2): Show |
5 | HG02145.hp2 HG02257.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1629+725A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20539929 | |||||||
chr16:20539957 | A | T | 51 | a0001c0001t0003g0007 a0001c0001t0003g0015 a0001c0001t0003g0020 others(48): Show |
56 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.1629+697T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20539957 | |||||||
chr16:20540014 | T | A | 44 | a0001c0001t0003g0007 a0001c0001t0003g0015 a0001c0001t0003g0020 others(41): Show |
49 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.1629+640A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20540014 | |||||||
chr16:20540109 | A | G | 5 | a0001c0006t0011g0115 a0003c0008t0011g0307 a0003c0008t0011g0308 others(2): Show |
5 | HG02145.hp2 HG02257.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1629+545T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20540109 | |||||||
chr16:20540176 | A | G | 1 | a0001c0002t0022g0302 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1629+478T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20540176 | |||||||
chr16:20540209 | A | C | 1 | a0001c0006t0011g0115 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1629+445T>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20540209 | |||||||
chr16:20540213 | G | T | 2 | a0003c0008t0011g0311 a0003c0008t0011g0312 |
2 | HG02145.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1629+441C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20540213 | |||||||
chr16:20540213 | GTTTTTTT others(6): Show |
G | 1 | a0001c0001t0012g0004 | 3 | NA18957.hp1 NA19006.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.1629+428_1629+440d others(15): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20540213 | |||||||
chr16:20540224 | G | GT | 57 | a0001c0001t0001g0026 a0001c0002t0002g0029 a0001c0002t0002g0236 others(54): Show |
64 | HG00423.hp2 HG00639.hp2 HG00673.hp1 others(61): Show |
intron_variant | MODIFIER | c.1629+429dupA | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20540224 | |||||||
chr16:20540224 | GT | G | 52 | a0001c0001t0003g0007 a0001c0001t0003g0015 a0001c0001t0003g0020 others(49): Show |
58 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.1629+429delA | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20540224 | |||||||
chr16:20540226 | T | G | 44 | a0001c0001t0003g0007 a0001c0001t0003g0015 a0001c0001t0003g0020 others(41): Show |
49 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.1629+428A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20540226 | |||||||
chr16:20540231 | T | G | 1 | a0001c0002t0022g0302 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1629+423A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20540231 | |||||||
chr16:20540233 | T | G | 12 | a0001c0002t0003g0036 a0001c0002t0003g0253 a0001c0002t0003g0254 others(9): Show |
13 | HG02055.hp1 HG02109.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1629+421A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20540233 | |||||||
chr16:20540233 | T | TG | 60 | a0001c0002t0002g0008 a0001c0002t0002g0030 a0001c0002t0002g0032 others(57): Show |
67 | HG00558.hp2 HG00597.hp2 HG00673.hp2 others(64): Show |
intron_variant | MODIFIER | c.1629+420_1629+421i others(3): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20540233 | |||||||
chr16:20540233 | T | TTG | 53 | a0001c0002t0002g0118 a0001c0002t0004g0003 a0001c0002t0004g0034 others(50): Show |
63 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.1629+420_1629+421i others(4): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20540233 | |||||||
chr16:20540246 | T | G | 1 | a0001c0004t0004g0214 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1629+408A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20540246 | |||||||
chr16:20540250 | G | GT | 60 | a0001c0001t0003g0176 a0001c0002t0002g0118 a0001c0002t0002g0236 others(57): Show |
70 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.1629+403dupA | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20540250 | |||||||
chr16:20540250 | G | T | 1 | a0001c0001t0012g0043 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1629+404C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20540250 | |||||||
chr16:20540284 | T | C | 1 | a0001c0001t0001g0158 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1629+370A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20540284 | |||||||
chr16:20540286 | A | G | 1 | a0001c0001t0001g0158 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1629+368T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20540286 | |||||||
chr16:20540292 | G | C | 1 | a0001c0001t0001g0158 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1629+362C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20540292 | |||||||
chr16:20540324 | C | T | 1 | a0001c0002t0021g0262 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1629+330G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20540324 | |||||||
chr16:20540327 | A | C | 1 | a0005c0011t0026g0318 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1629+327T>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20540327 | |||||||
chr16:20540383 | C | T | 46 | a0001c0001t0003g0007 a0001c0001t0003g0015 a0001c0001t0003g0020 others(43): Show |
51 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.1629+271G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20540383 | |||||||
chr16:20540386 | G | A | 25 | a0001c0002t0004g0037 a0001c0002t0004g0038 a0001c0002t0004g0226 others(22): Show |
29 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(26): Show |
intron_variant | MODIFIER | c.1629+268C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20540386 | |||||||
chr16:20540463 | G | C | 1 | a0001c0002t0004g0258 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1629+191C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20540463 | |||||||
chr16:20540502 | C | T | 1 | a0003c0008t0011g0308 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1629+152G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20540502 | |||||||
chr16:20540519 | A | G | 1 | a0003c0007t0007g0313 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1629+135T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20540519 | |||||||
chr16:20540533 | A | G | 260 | a0001c0001t0003g0007 a0001c0001t0003g0015 a0001c0001t0003g0020 others(257): Show |
295 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(292): Show |
intron_variant | MODIFIER | c.1629+121T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20540533 | |||||||
chr16:20540637 | G | C | 2 | a0001c0004t0002g0129 a0001c0004t0002g0131 |
2 | NA18992.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.1629+17C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20540637 | |||||||
chr16:20540782 | T | C | 24 | a0001c0002t0003g0013 a0001c0002t0003g0116 a0001c0002t0003g0255 others(21): Show |
26 | HG01081.hp2 HG01099.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.1510-9A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20540782 | |||||||
chr16:20540800 | T | G | 1 | a0005c0011t0026g0318 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1510-27A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20540800 | |||||||
chr16:20540862 | C | T | 43 | a0001c0001t0003g0007 a0001c0001t0003g0015 a0001c0001t0003g0020 others(40): Show |
48 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.1510-89G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20540862 | |||||||
chr16:20541012 | C | T | 2 | a0006c0020t0003g0110 a0006c0020t0020g0042 |
2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1510-239G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541012 | |||||||
chr16:20541018 | C | T | 1 | a0001c0001t0001g0026 | 2 | NA19001.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1510-245G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541018 | |||||||
chr16:20541071 | G | A | 3 | a0001c0002t0003g0253 a0001c0002t0003g0254 a0001c0002t0003g0256 |
3 | HG02280.hp2 HG02451.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1510-298C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541071 | |||||||
chr16:20541127 | G | A | 205 | a0001c0002t0002g0008 a0001c0002t0002g0029 a0001c0002t0002g0030 others(202): Show |
233 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(230): Show |
intron_variant | MODIFIER | c.1510-354C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541127 | |||||||
chr16:20541140 | G | A | 2 | a0003c0008t0003g0125 a0003c0025t0003g0124 |
2 | HG03704.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1510-367C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541140 | |||||||
chr16:20541144 | A | G | 45 | a0001c0002t0007g0031 a0001c0002t0007g0220 a0001c0002t0007g0240 others(42): Show |
51 | HG00423.hp2 HG00639.hp2 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.1510-371T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541144 | |||||||
chr16:20541172 | T | G | 205 | a0001c0002t0002g0008 a0001c0002t0002g0029 a0001c0002t0002g0030 others(202): Show |
233 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(230): Show |
intron_variant | MODIFIER | c.1510-399A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541172 | |||||||
chr16:20541221 | G | A | 1 | a0004c0005t0006g0047 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1510-448C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541221 | |||||||
chr16:20541240 | A | C | 24 | a0001c0002t0003g0013 a0001c0002t0003g0116 a0001c0002t0003g0255 others(21): Show |
26 | HG01081.hp2 HG01099.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.1510-467T>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541240 | |||||||
chr16:20541244 | T | A | 24 | a0001c0002t0003g0013 a0001c0002t0003g0116 a0001c0002t0003g0255 others(21): Show |
26 | HG01081.hp2 HG01099.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.1510-471A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541244 | |||||||
chr16:20541314 | G | T | 42 | a0001c0001t0003g0007 a0001c0001t0003g0015 a0001c0001t0003g0020 others(39): Show |
47 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.1510-541C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541314 | |||||||
chr16:20541350 | A | G | 2 | a0001c0002t0002g0030 a0001c0002t0002g0306 |
3 | HG00558.hp2 HG00738.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.1510-577T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541350 | |||||||
chr16:20541444 | G | A | 1 | a0003c0008t0011g0308 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1510-671C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541444 | |||||||
chr16:20541470 | C | A | 15 | a0001c0002t0003g0013 a0003c0007t0003g0014 a0003c0007t0003g0239 others(12): Show |
17 | HG01934.hp2 HG02258.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.1510-697G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541470 | |||||||
chr16:20541475 | T | C | 5 | a0001c0006t0011g0115 a0003c0008t0011g0307 a0003c0008t0011g0308 others(2): Show |
5 | HG02145.hp2 HG02257.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1510-702A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541475 | |||||||
chr16:20541479 | C | T | 5 | a0001c0006t0011g0115 a0003c0008t0011g0307 a0003c0008t0011g0308 others(2): Show |
5 | HG02145.hp2 HG02257.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1510-706G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541479 | |||||||
chr16:20541526 | G | T | 1 | a0001c0002t0007g0287 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1510-753C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541526 | |||||||
chr16:20541546 | C | G | 5 | a0001c0006t0011g0115 a0003c0008t0011g0307 a0003c0008t0011g0308 others(2): Show |
5 | HG02145.hp2 HG02257.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1510-773G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541546 | |||||||
chr16:20541560 | T | C | 1 | a0001c0002t0004g0283 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1510-787A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541560 | |||||||
chr16:20541572 | A | T | 1 | a0001c0001t0001g0191 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1510-799T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541572 | |||||||
chr16:20541674 | T | A | 1 | a0003c0025t0003g0124 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1510-901A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541674 | |||||||
chr16:20541674 | T | C | 5 | a0003c0008t0003g0125 a0005c0011t0026g0318 a0006c0020t0003g0110 others(2): Show |
5 | HG02630.hp2 HG03209.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510-901A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541674 | |||||||
chr16:20541675 | T | C | 1 | a0001c0002t0002g0241 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1510-902A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541675 | |||||||
chr16:20541676 | TC | T | 6 | a0003c0008t0003g0125 a0003c0025t0003g0124 a0005c0011t0026g0318 others(3): Show |
6 | HG02630.hp2 HG03209.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.1510-904delG | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541676 | |||||||
chr16:20541677 | C | T | 1 | a0001c0002t0002g0241 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1510-904G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541677 | |||||||
chr16:20541678 | T | C | 1 | a0001c0012t0007g0028 | 2 | HG02965.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1510-905A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541678 | |||||||
chr16:20541679 | T | C | 1 | a0001c0002t0002g0241 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1510-906A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541679 | |||||||
chr16:20541679 | TTC | T | 89 | a0001c0002t0002g0029 a0001c0002t0003g0013 a0001c0002t0003g0036 others(86): Show |
100 | HG00423.hp2 HG00639.hp2 HG00673.hp1 others(97): Show |
intron_variant | MODIFIER | c.1510-908_1510-907d others(4): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541679 | |||||||
chr16:20541680 | TC | T | 110 | a0001c0002t0002g0008 a0001c0002t0002g0029 a0001c0002t0002g0030 others(107): Show |
122 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.1510-908delG | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541680 | |||||||
chr16:20541681 | C | T | 11 | a0001c0002t0002g0030 a0001c0002t0002g0241 a0001c0002t0002g0284 others(8): Show |
11 | HG00323.hp2 HG00738.hp2 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.1510-908G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541681 | |||||||
chr16:20541681 | CT | C | 36 | a0001c0001t0001g0019 a0001c0001t0003g0007 a0001c0001t0003g0015 others(33): Show |
41 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.1510-909delA | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541681 | |||||||
chr16:20541684 | T | C | 1 | a0001c0004t0002g0182 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1510-911A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541684 | |||||||
chr16:20541684 | T | TC | 5 | a0003c0008t0003g0125 a0005c0011t0026g0318 a0006c0020t0003g0110 others(2): Show |
5 | HG02630.hp2 HG03209.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510-912_1510-911i others(3): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541684 | |||||||
chr16:20541685 | T | C | 3 | a0001c0001t0001g0215 a0001c0002t0003g0255 a0003c0025t0003g0124 |
3 | HG01081.hp2 HG03704.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.1510-912A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541685 | |||||||
chr16:20541713 | C | T | 254 | a0001c0001t0001g0022 a0001c0001t0001g0195 a0001c0001t0003g0007 others(251): Show |
288 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(285): Show |
intron_variant | MODIFIER | c.1510-940G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541713 | |||||||
chr16:20541717 | C | T | 2 | a0001c0001t0001g0159 a0001c0001t0001g0209 |
2 | NA19002.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1510-944G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541717 | |||||||
chr16:20541740 | A | G | 7 | a0001c0001t0001g0212 a0001c0002t0002g0241 a0001c0002t0002g0281 others(4): Show |
7 | HG01496.hp2 HG02015.hp2 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1510-967T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541740 | |||||||
chr16:20541744 | G | A | 7 | a0001c0001t0001g0212 a0001c0002t0002g0241 a0001c0002t0002g0281 others(4): Show |
7 | HG01168.hp2 HG01496.hp2 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1510-971C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541744 | |||||||
chr16:20541745 | C | T | 2 | a0006c0020t0003g0110 a0006c0020t0020g0042 |
2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1510-972G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541745 | |||||||
chr16:20541764 | A | C | 210 | a0001c0001t0001g0199 a0001c0002t0002g0008 a0001c0002t0002g0029 others(207): Show |
236 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(233): Show |
intron_variant | MODIFIER | c.1510-991T>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541764 | |||||||
chr16:20541838 | G | A | 6 | a0001c0001t0001g0161 a0001c0001t0001g0186 a0001c0001t0001g0190 others(3): Show |
6 | HG03209.hp1 NA18942.hp2 NA19010.hp2 others(3): Show |
intron_variant | MODIFIER | c.1510-1065C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541838 | |||||||
chr16:20541884 | T | C | 1 | a0004c0005t0006g0095 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1509+1030A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541884 | |||||||
chr16:20541933 | A | G | 4 | a0001c0001t0001g0006 a0001c0001t0001g0191 a0001c0001t0001g0195 others(1): Show |
6 | HG02080.hp1 HG02717.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.1509+981T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541933 | |||||||
chr16:20541959 | C | A | 3 | a0003c0008t0003g0125 a0003c0025t0003g0124 a0010c0023t0027g0323 |
3 | HG02630.hp2 HG03704.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1509+955G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541959 | |||||||
chr16:20542006 | C | A | 141 | a0001c0002t0002g0008 a0001c0002t0002g0029 a0001c0002t0002g0030 others(138): Show |
160 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.1509+908G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542006 | |||||||
chr16:20542026 | G | A | 1 | a0001c0002t0022g0302 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1509+888C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542026 | |||||||
chr16:20542150 | G | A | 8 | a0003c0007t0003g0014 a0003c0007t0003g0239 a0004c0005t0006g0097 others(5): Show |
9 | HG02486.hp2 HG02572.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1509+764C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542150 | |||||||
chr16:20542161 | T | C | 118 | a0001c0001t0001g0022 a0001c0001t0001g0172 a0001c0001t0001g0199 others(115): Show |
136 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(133): Show |
intron_variant | MODIFIER | c.1509+753A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542161 | |||||||
chr16:20542175 | T | G | 7 | a0001c0002t0002g0237 a0003c0007t0014g0331 a0003c0007t0014g0333 others(4): Show |
7 | HG01109.hp1 HG02258.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1509+739A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542175 | |||||||
chr16:20542193 | C | T | 4 | a0001c0006t0011g0115 a0003c0007t0014g0332 a0003c0007t0014g0334 others(1): Show |
4 | HG02055.hp1 HG02717.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1509+721G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542193 | |||||||
chr16:20542201 | T | TTCTA | 18 | a0001c0002t0002g0241 a0001c0002t0003g0013 a0001c0006t0011g0115 others(15): Show |
20 | HG01496.hp2 HG01934.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.1509+712_1509+713i others(6): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542201 | |||||||
chr16:20542202 | G | T | 19 | a0001c0002t0002g0241 a0001c0002t0003g0013 a0001c0006t0011g0115 others(16): Show |
21 | HG01496.hp2 HG01934.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.1509+712C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542202 | |||||||
chr16:20542214 | C | T | 29 | a0001c0002t0002g0284 a0001c0002t0003g0253 a0001c0002t0003g0256 others(26): Show |
31 | HG01168.hp1 HG01168.hp2 HG01169.hp1 others(28): Show |
intron_variant | MODIFIER | c.1509+700G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542214 | |||||||
chr16:20542217 | C | A | 29 | a0001c0002t0002g0284 a0001c0002t0003g0253 a0001c0002t0003g0256 others(26): Show |
31 | HG01168.hp1 HG01168.hp2 HG01169.hp1 others(28): Show |
intron_variant | MODIFIER | c.1509+697G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542217 | |||||||
chr16:20542255 | C | T | 1 | a0003c0008t0011g0307 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1509+659G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542255 | |||||||
chr16:20542286 | T | C | 3 | a0008c0013t0002g0113 a0008c0013t0002g0114 a0010c0023t0027g0323 |
3 | HG02630.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1509+628A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542286 | |||||||
chr16:20542317 | G | A | 138 | a0001c0001t0001g0199 a0001c0001t0003g0179 a0001c0001t0003g0183 others(135): Show |
158 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.1509+597C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542317 | |||||||
chr16:20542328 | T | A | 186 | a0001c0001t0001g0199 a0001c0001t0001g0205 a0001c0001t0003g0179 others(183): Show |
211 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.1509+586A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542328 | |||||||
chr16:20542335 | T | C | 203 | a0001c0001t0001g0199 a0001c0001t0001g0205 a0001c0001t0003g0179 others(200): Show |
231 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(228): Show |
intron_variant | MODIFIER | c.1509+579A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542335 | |||||||
chr16:20542345 | AAC | A | 5 | a0003c0007t0014g0331 a0003c0007t0014g0332 a0003c0007t0014g0333 others(2): Show |
5 | HG02055.hp1 HG02258.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1509+567_1509+568d others(4): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542345 | |||||||
chr16:20542369 | C | T | 1 | a0001c0006t0011g0115 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1509+545G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542369 | |||||||
chr16:20542383 | G | C | 127 | a0001c0001t0001g0161 a0001c0001t0001g0190 a0001c0001t0001g0191 others(124): Show |
146 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.1509+531C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542383 | |||||||
chr16:20542389 | A | G | 1 | a0001c0002t0004g0294 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1509+525T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542389 | |||||||
chr16:20542428 | A | G | 1 | a0005c0011t0008g0322 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1509+486T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542428 | |||||||
chr16:20542437 | C | T | 1 | a0014c0028t0003g0123 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1509+477G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542437 | |||||||
chr16:20542450 | C | A | 1 | a0003c0007t0014g0331 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1509+464G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542450 | |||||||
chr16:20542504 | T | C | 14 | a0001c0001t0001g0203 a0001c0001t0003g0179 a0003c0007t0007g0274 others(11): Show |
15 | HG00438.hp1 HG02040.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.1509+410A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542504 | |||||||
chr16:20542533 | G | A | 96 | a0001c0001t0003g0183 a0001c0002t0002g0008 a0001c0002t0002g0030 others(93): Show |
113 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.1509+381C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542533 | |||||||
chr16:20542557 | A | C | 4 | a0001c0001t0003g0007 a0001c0001t0003g0162 a0001c0001t0003g0179 others(1): Show |
6 | HG00438.hp1 HG00609.hp1 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.1509+357T>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542557 | |||||||
chr16:20542568 | T | C | 2 | a0006c0020t0003g0110 a0006c0020t0020g0042 |
2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1509+346A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542568 | |||||||
chr16:20542569 | A | G | 4 | a0001c0001t0003g0007 a0001c0001t0003g0162 a0001c0001t0003g0179 others(1): Show |
6 | HG00438.hp1 HG00609.hp1 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.1509+345T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542569 | |||||||
chr16:20542578 | T | C | 1 | a0004c0005t0006g0047 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1509+336A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542578 | |||||||
chr16:20542585 | T | C | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(171): Show |
203 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.1509+329A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542585 | |||||||
chr16:20542661 | G | T | 1 | a0001c0006t0003g0304 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1509+253C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542661 | |||||||
chr16:20542683 | C | T | 5 | a0003c0008t0001g0310 a0003c0008t0011g0311 a0003c0008t0011g0312 others(2): Show |
6 | HG02145.hp2 HG02615.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1509+231G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542683 | |||||||
chr16:20542737 | A | G | 3 | a0001c0002t0003g0036 a0001c0027t0003g0275 a0002c0018t0005g0073 |
4 | HG02109.hp2 HG02818.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1509+177T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542737 | |||||||
chr16:20542738 | A | G | 3 | a0001c0002t0003g0036 a0001c0027t0003g0275 a0002c0018t0005g0073 |
4 | HG02109.hp2 HG02818.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1509+176T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542738 | |||||||
chr16:20542759 | C | T | 7 | a0006c0010t0003g0012 a0006c0010t0003g0119 a0006c0010t0003g0120 others(4): Show |
8 | HG01884.hp2 HG02109.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1509+155G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542759 | |||||||
chr16:20542770 | A | G | 1 | a0002c0018t0005g0073 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1509+144T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542770 | |||||||
chr16:20542812 | G | A | 1 | a0001c0004t0002g0130 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1509+102C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542812 | |||||||
chr16:20542881 | C | G | 8 | a0001c0002t0002g0030 a0001c0002t0004g0283 a0006c0020t0003g0110 others(5): Show |
9 | HG00738.hp2 HG01261.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1509+33G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542881 | |||||||
chr16:20543051 | C | T | 1 | a0003c0033t0003g0168 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1410-38G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 11/13 | chr16 | 20543051 | |||||||
chr16:20543070 | G | A | 15 | a0001c0001t0001g0207 a0003c0033t0003g0168 a0006c0010t0003g0012 others(12): Show |
16 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1410-57C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 11/13 | chr16 | 20543070 | |||||||
chr16:20543291 | G | A | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(104): Show |
131 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.1282-29C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20543291 | |||||||
chr16:20543438 | T | C | 7 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0165 others(4): Show |
11 | HG00280.hp2 HG00733.hp2 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.1282-176A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20543438 | |||||||
chr16:20543689 | C | T | 1 | a0010c0023t0027g0323 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1282-427G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20543689 | |||||||
chr16:20543735 | C | G | 31 | a0003c0007t0003g0014 a0003c0007t0003g0239 a0003c0007t0007g0274 others(28): Show |
32 | HG01099.hp2 HG01884.hp1 HG01934.hp2 others(29): Show |
intron_variant | MODIFIER | c.1282-473G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20543735 | |||||||
chr16:20543752 | A | G | 1 | a0011c0021t0001g0188 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1282-490T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20543752 | |||||||
chr16:20543765 | T | C | 9 | a0002c0003t0005g0065 a0003c0007t0007g0274 a0003c0007t0014g0331 others(6): Show |
9 | HG02258.hp2 HG02717.hp2 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.1282-503A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20543765 | |||||||
chr16:20543782 | C | G | 8 | a0003c0007t0007g0274 a0003c0007t0014g0331 a0003c0007t0014g0332 others(5): Show |
8 | HG02258.hp2 HG02717.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.1282-520G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20543782 | |||||||
chr16:20543818 | A | T | 23 | a0003c0007t0003g0014 a0003c0007t0003g0239 a0004c0005t0006g0047 others(20): Show |
24 | HG01099.hp2 HG01884.hp1 HG01934.hp2 others(21): Show |
intron_variant | MODIFIER | c.1282-556T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20543818 | |||||||
chr16:20543882 | A | G | 8 | a0003c0007t0007g0274 a0003c0007t0014g0331 a0003c0007t0014g0332 others(5): Show |
8 | HG02258.hp2 HG02717.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.1282-620T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20543882 | |||||||
chr16:20543937 | T | A | 62 | a0002c0003t0005g0009 a0002c0003t0005g0010 a0002c0003t0005g0048 others(59): Show |
68 | HG00673.hp1 HG01256.hp1 HG01257.hp1 others(65): Show |
intron_variant | MODIFIER | c.1282-675A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20543937 | |||||||
chr16:20544071 | G | T | 2 | a0002c0003t0010g0005 a0002c0018t0010g0046 |
4 | HG02559.hp2 HG02970.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1282-809C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20544071 | |||||||
chr16:20544098 | A | G | 3 | a0001c0001t0001g0018 a0002c0019t0006g0072 a0002c0019t0006g0083 |
4 | NA18988.hp1 NA18989.hp1 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.1282-836T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20544098 | |||||||
chr16:20544116 | C | T | 1 | a0014c0028t0003g0123 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1282-854G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20544116 | |||||||
chr16:20544152 | T | C | 49 | a0002c0003t0005g0009 a0002c0003t0005g0010 a0002c0003t0005g0048 others(46): Show |
54 | HG00673.hp1 HG01256.hp1 HG01257.hp1 others(51): Show |
intron_variant | MODIFIER | c.1282-890A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20544152 | |||||||
chr16:20544268 | C | A | 39 | a0003c0007t0003g0014 a0003c0007t0003g0239 a0003c0007t0007g0274 others(36): Show |
41 | HG01099.hp2 HG01884.hp1 HG01934.hp2 others(38): Show |
intron_variant | MODIFIER | c.1281+889G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20544268 | |||||||
chr16:20544380 | C | G | 2 | a0003c0008t0011g0307 a0003c0008t0011g0308 |
2 | HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1281+777G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20544380 | |||||||
chr16:20544387 | T | A | 31 | a0003c0007t0003g0014 a0003c0007t0003g0239 a0003c0007t0007g0313 others(28): Show |
33 | HG01099.hp2 HG01884.hp1 HG01934.hp2 others(30): Show |
intron_variant | MODIFIER | c.1281+770A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20544387 | |||||||
chr16:20544434 | G | T | 49 | a0001c0002t0004g0258 a0002c0003t0005g0009 a0002c0003t0005g0010 others(46): Show |
54 | HG00673.hp1 HG01256.hp1 HG01257.hp1 others(51): Show |
intron_variant | MODIFIER | c.1281+723C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20544434 | |||||||
chr16:20544560 | G | A | 2 | a0006c0020t0003g0110 a0006c0020t0020g0042 |
2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1281+597C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20544560 | |||||||
chr16:20544579 | A | G | 4 | a0008c0013t0002g0111 a0008c0013t0002g0112 a0008c0013t0002g0113 others(1): Show |
4 | HG02257.hp1 HG02886.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1281+578T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20544579 | |||||||
chr16:20544597 | T | G | 1 | a0004c0005t0006g0095 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1281+560A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20544597 | |||||||
chr16:20544655 | T | C | 3 | a0003c0008t0003g0125 a0003c0025t0003g0124 a0014c0028t0003g0123 |
3 | HG03098.hp1 HG03704.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1281+502A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20544655 | |||||||
chr16:20544761 | C | T | 7 | a0006c0010t0003g0012 a0006c0010t0003g0119 a0006c0010t0003g0120 others(4): Show |
8 | HG01884.hp2 HG02109.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1281+396G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20544761 | |||||||
chr16:20544763 | A | C | 7 | a0006c0010t0003g0012 a0006c0010t0003g0119 a0006c0010t0003g0120 others(4): Show |
8 | HG01884.hp2 HG02109.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1281+394T>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20544763 | |||||||
chr16:20544764 | C | T | 7 | a0006c0010t0003g0012 a0006c0010t0003g0119 a0006c0010t0003g0120 others(4): Show |
8 | HG01884.hp2 HG02109.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1281+393G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20544764 | |||||||
chr16:20544804 | T | G | 2 | a0006c0020t0003g0110 a0006c0020t0020g0042 |
2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1281+353A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20544804 | |||||||
chr16:20544982 | C | A | 1 | a0001c0001t0001g0203 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1281+175G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20544982 | |||||||
chr16:20545010 | T | G | 1 | a0001c0006t0001g0289 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1281+147A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20545010 | |||||||
chr16:20545041 | C | G | 2 | a0006c0020t0003g0110 a0006c0020t0020g0042 |
2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1281+116G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20545041 | |||||||
chr16:20545054 | T | C | 2 | a0006c0020t0003g0110 a0006c0020t0020g0042 |
2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1281+103A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20545054 | |||||||
chr16:20545055 | A | G | 1 | a0001c0001t0001g0006 | 3 | NA18948.hp2 NA18964.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1281+102T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20545055 | |||||||
chr16:20545060 | A | G | 2 | a0006c0020t0003g0110 a0006c0020t0020g0042 |
2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1281+97T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20545060 | |||||||
chr16:20545101 | C | T | 8 | a0003c0007t0007g0313 a0003c0008t0001g0310 a0003c0008t0011g0307 others(5): Show |
9 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1281+56G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20545101 | |||||||
chr16:20545378 | G | A | 1 | a0002c0018t0005g0056 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1180-120C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 9/13 | chr16 | 20545378 | |||||||
chr16:20545383 | C | A | 1 | a0001c0001t0001g0161 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1180-125G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 9/13 | chr16 | 20545383 | |||||||
chr16:20545431 | C | G | 2 | a0003c0008t0003g0125 a0003c0025t0003g0124 |
2 | HG03704.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1180-173G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 9/13 | chr16 | 20545431 | |||||||
chr16:20545528 | C | T | 1 | a0001c0002t0004g0260 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1180-270G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 9/13 | chr16 | 20545528 | |||||||
chr16:20545582 | C | G | 8 | a0003c0007t0007g0274 a0003c0007t0014g0331 a0003c0007t0014g0332 others(5): Show |
8 | HG02258.hp2 HG02717.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.1180-324G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 9/13 | chr16 | 20545582 | |||||||
chr16:20545612 | AG | A | 3 | a0001c0001t0001g0135 a0001c0004t0002g0139 a0001c0004t0002g0145 |
3 | HG02602.hp2 HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1180-355delC | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 9/13 | chr16 | 20545612 | |||||||
chr16:20545699 | T | C | 2 | a0001c0002t0007g0109 a0005c0024t0016g0325 |
2 | HG02922.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1180-441A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 9/13 | chr16 | 20545699 | |||||||
chr16:20545705 | T | A | 11 | a0006c0010t0003g0012 a0006c0010t0003g0119 a0006c0010t0003g0120 others(8): Show |
12 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1180-447A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 9/13 | chr16 | 20545705 | |||||||
chr16:20545714 | A | T | 22 | a0003c0007t0003g0014 a0003c0007t0003g0239 a0004c0005t0006g0047 others(19): Show |
23 | HG01099.hp2 HG01884.hp1 HG01934.hp2 others(20): Show |
intron_variant | MODIFIER | c.1180-456T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 9/13 | chr16 | 20545714 | |||||||
chr16:20545756 | G | T | 1 | a0001c0006t0001g0299 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1180-498C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 9/13 | chr16 | 20545756 | |||||||
chr16:20545789 | C | A | 8 | a0003c0007t0007g0313 a0003c0008t0001g0310 a0003c0008t0011g0307 others(5): Show |
9 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1180-531G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 9/13 | chr16 | 20545789 | |||||||
chr16:20545911 | T | C | 2 | a0005c0011t0026g0318 a0005c0016t0016g0317 |
2 | HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1179+483A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 9/13 | chr16 | 20545911 | |||||||
chr16:20545940 | C | T | 1 | a0005c0016t0029g0315 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1179+454G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 9/13 | chr16 | 20545940 | |||||||
chr16:20545955 | C | T | 8 | a0003c0007t0007g0313 a0003c0008t0001g0310 a0003c0008t0011g0307 others(5): Show |
9 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1179+439G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 9/13 | chr16 | 20545955 | |||||||
chr16:20545985 | T | A | 23 | a0003c0007t0003g0014 a0003c0007t0003g0239 a0004c0005t0006g0047 others(20): Show |
24 | HG01099.hp2 HG01884.hp1 HG01934.hp2 others(21): Show |
intron_variant | MODIFIER | c.1179+409A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 9/13 | chr16 | 20545985 | |||||||
chr16:20546053 | G | C | 1 | a0014c0028t0003g0123 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1179+341C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 9/13 | chr16 | 20546053 | |||||||
chr16:20546211 | T | C | 31 | a0003c0007t0003g0014 a0003c0007t0003g0239 a0003c0007t0007g0313 others(28): Show |
33 | HG01099.hp2 HG01884.hp1 HG01934.hp2 others(30): Show |
intron_variant | MODIFIER | c.1179+183A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 9/13 | chr16 | 20546211 | |||||||
chr16:20546298 | T | G | 62 | a0002c0003t0005g0009 a0002c0003t0005g0010 a0002c0003t0005g0048 others(59): Show |
68 | HG00673.hp1 HG01256.hp1 HG01257.hp1 others(65): Show |
intron_variant | MODIFIER | c.1179+96A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 9/13 | chr16 | 20546298 | |||||||
chr16:20546312 | A | T | 48 | a0002c0003t0005g0009 a0002c0003t0005g0010 a0002c0003t0005g0048 others(45): Show |
53 | HG00673.hp1 HG01256.hp1 HG01257.hp1 others(50): Show |
intron_variant | MODIFIER | c.1179+82T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 9/13 | chr16 | 20546312 | |||||||
chr16:20546339 | T | C | 8 | a0003c0007t0007g0313 a0003c0008t0001g0310 a0003c0008t0011g0307 others(5): Show |
9 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1179+55A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 9/13 | chr16 | 20546339 | |||||||
chr16:20546362 | A | T | 2 | a0002c0003t0005g0052 a0003c0008t0015g0309 |
2 | HG02615.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1179+32T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 9/13 | chr16 | 20546362 | |||||||
chr16:20546366 | T | C | 115 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(112): Show |
139 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.1179+28A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 9/13 | chr16 | 20546366 | |||||||
chr16:20546511 | A | G | 1 | a0001c0006t0003g0305 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1099-37T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20546511 | |||||||
chr16:20546553 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1099-79G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20546553 | |||||||
chr16:20546613 | C | T | 20 | a0003c0007t0003g0014 a0004c0005t0006g0047 a0004c0005t0006g0085 others(17): Show |
21 | HG01099.hp2 HG01884.hp1 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.1099-139G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20546613 | |||||||
chr16:20546638 | T | C | 6 | a0001c0004t0002g0130 a0002c0003t0005g0061 a0003c0008t0011g0307 others(3): Show |
6 | HG01256.hp2 HG02257.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1099-164A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20546638 | |||||||
chr16:20546652 | G | T | 1 | a0014c0028t0003g0123 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1099-178C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20546652 | |||||||
chr16:20546654 | C | T | 4 | a0001c0002t0002g0306 a0001c0004t0002g0130 a0003c0008t0011g0307 others(1): Show |
4 | HG00558.hp2 HG01256.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.1099-180G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20546654 | |||||||
chr16:20546657 | A | G | 4 | a0001c0002t0002g0306 a0001c0004t0002g0130 a0003c0008t0011g0307 others(1): Show |
4 | HG00558.hp2 HG01256.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.1099-183T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20546657 | |||||||
chr16:20546668 | T | A | 50 | a0001c0006t0001g0286 a0002c0003t0005g0009 a0002c0003t0005g0010 others(47): Show |
55 | HG00673.hp1 HG01256.hp1 HG01257.hp1 others(52): Show |
intron_variant | MODIFIER | c.1099-194A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20546668 | |||||||
chr16:20546743 | G | A | 4 | a0001c0002t0002g0241 a0001c0002t0004g0278 a0001c0006t0001g0282 others(1): Show |
4 | HG00733.hp1 HG01175.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.1099-269C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20546743 | |||||||
chr16:20546744 | T | C | 4 | a0001c0002t0002g0241 a0001c0002t0004g0278 a0001c0006t0001g0282 others(1): Show |
4 | HG00733.hp1 HG01175.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.1099-270A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20546744 | |||||||
chr16:20546761 | G | A | 3 | a0001c0002t0004g0278 a0001c0006t0001g0282 a0001c0006t0001g0289 |
3 | HG00733.hp1 HG01175.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.1099-287C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20546761 | |||||||
chr16:20546763 | T | A | 2 | a0006c0020t0003g0110 a0006c0020t0020g0042 |
2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1099-289A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20546763 | |||||||
chr16:20546783 | G | T | 3 | a0001c0002t0004g0278 a0001c0006t0001g0282 a0001c0006t0001g0289 |
3 | HG00733.hp1 HG01175.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.1099-309C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20546783 | |||||||
chr16:20546825 | A | C | 1 | a0004c0005t0006g0091 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1099-351T>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20546825 | |||||||
chr16:20546879 | G | A | 2 | a0001c0017t0004g0033 a0001c0017t0004g0261 |
3 | HG02698.hp2 HG03490.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1099-405C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20546879 | |||||||
chr16:20546907 | G | A | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(108): Show |
134 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.1099-433C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20546907 | |||||||
chr16:20546912 | A | G | 1 | a0003c0007t0003g0014 | 2 | HG02486.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1099-438T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20546912 | |||||||
chr16:20546978 | G | A | 1 | a0001c0002t0007g0109 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1099-504C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20546978 | |||||||
chr16:20546991 | C | T | 1 | a0003c0033t0003g0168 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1099-517G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20546991 | |||||||
chr16:20547013 | C | T | 3 | a0001c0002t0003g0013 a0003c0007t0003g0014 a0014c0028t0003g0123 |
5 | HG02486.hp2 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1099-539G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20547013 | |||||||
chr16:20547032 | C | A | 4 | a0001c0002t0002g0118 a0001c0002t0003g0116 a0001c0006t0011g0115 others(1): Show |
4 | HG02717.hp1 HG02895.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1099-558G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20547032 | |||||||
chr16:20547042 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1099-568C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20547042 | |||||||
chr16:20547119 | A | G | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(120): Show |
150 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.1099-645T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20547119 | |||||||
chr16:20547187 | G | A | 2 | a0002c0003t0010g0005 a0002c0018t0010g0046 |
4 | HG02559.hp2 HG02970.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1099-713C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20547187 | |||||||
chr16:20547238 | T | C | 1 | a0001c0001t0001g0218 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1099-764A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20547238 | |||||||
chr16:20547246 | T | C | 1 | a0001c0001t0003g0183 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1099-772A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20547246 | |||||||
chr16:20547277 | C | T | 2 | a0001c0001t0001g0206 a0001c0001t0001g0207 |
2 | NA18950.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1098+785G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20547277 | |||||||
chr16:20547445 | T | G | 2 | a0001c0002t0002g0029 a0001c0002t0002g0236 |
3 | HG02965.hp2 HG03516.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1098+617A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20547445 | |||||||
chr16:20547535 | A | G | 3 | a0004c0005t0006g0099 a0004c0005t0006g0101 a0004c0005t0006g0105 |
3 | HG01934.hp2 HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1098+527T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20547535 | |||||||
chr16:20547612 | C | T | 2 | a0006c0020t0003g0110 a0006c0020t0020g0042 |
2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1098+450G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20547612 | |||||||
chr16:20547742 | G | C | 17 | a0001c0001t0003g0007 a0001c0001t0003g0162 a0001c0001t0003g0179 others(14): Show |
21 | HG00438.hp1 HG00609.hp1 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.1098+320C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20547742 | |||||||
chr16:20547767 | C | G | 1 | a0007c0014t0001g0173 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1098+295G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20547767 | |||||||
chr16:20547941 | G | C | 7 | a0006c0010t0003g0012 a0006c0010t0003g0119 a0006c0010t0003g0120 others(4): Show |
8 | HG01884.hp2 HG02109.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1098+121C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20547941 | |||||||
chr16:20548017 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1098+45C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20548017 | |||||||
chr16:20548022 | A | G | 2 | a0001c0001t0001g0027 a0001c0004t0007g0216 |
3 | NA18943.hp1 NA19002.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.1098+40T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20548022 | |||||||
chr16:20548032 | A | C | 1 | a0001c0002t0002g0281 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1098+30T>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20548032 | |||||||
chr16:20548243 | G | C | 1 | a0002c0003t0005g0071 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.975-58C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 7/13 | chr16 | 20548243 | |||||||
chr16:20548244 | C | A | 1 | a0001c0001t0003g0133 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.975-59G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 7/13 | chr16 | 20548244 | |||||||
chr16:20548252 | T | G | 7 | a0001c0001t0001g0185 a0001c0001t0003g0133 a0001c0002t0003g0013 others(4): Show |
9 | HG02486.hp2 HG02572.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.975-67A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 7/13 | chr16 | 20548252 | |||||||
chr16:20548307 | G | A | 5 | a0001c0002t0003g0013 a0003c0007t0003g0014 a0003c0008t0003g0125 others(2): Show |
7 | HG02486.hp2 HG02572.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.974+87C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 7/13 | chr16 | 20548307 | |||||||
chr16:20548349 | G | A | 5 | a0004c0005t0006g0097 a0004c0005t0006g0098 a0004c0005t0006g0102 others(2): Show |
5 | HG02622.hp2 HG02723.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.974+45C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 7/13 | chr16 | 20548349 | |||||||
chr16:20548548 | A | G | 1 | a0003c0025t0003g0124 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.895-75T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20548548 | |||||||
chr16:20548715 | T | C | 26 | a0001c0002t0003g0255 a0001c0002t0004g0003 a0001c0002t0004g0034 others(23): Show |
32 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.895-242A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20548715 | |||||||
chr16:20548722 | C | A | 1 | a0001c0002t0004g0294 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.895-249G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20548722 | |||||||
chr16:20548765 | A | G | 81 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(78): Show |
105 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.895-292T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20548765 | |||||||
chr16:20548781 | G | C | 12 | a0003c0007t0007g0313 a0003c0007t0014g0331 a0003c0007t0014g0332 others(9): Show |
13 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.895-308C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20548781 | |||||||
chr16:20548786 | T | G | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(118): Show |
148 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.895-313A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20548786 | |||||||
chr16:20548803 | C | T | 13 | a0006c0010t0003g0012 a0006c0010t0003g0119 a0006c0010t0003g0120 others(10): Show |
14 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.895-330G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20548803 | |||||||
chr16:20548885 | T | A | 65 | a0002c0003t0005g0009 a0002c0003t0005g0010 a0002c0003t0005g0048 others(62): Show |
68 | HG00673.hp1 HG01099.hp2 HG01256.hp1 others(65): Show |
intron_variant | MODIFIER | c.895-412A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20548885 | |||||||
chr16:20548986 | A | G | 1 | a0001c0001t0001g0218 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.895-513T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20548986 | |||||||
chr16:20549055 | T | C | 84 | a0001c0002t0003g0013 a0002c0003t0005g0009 a0002c0003t0005g0010 others(81): Show |
92 | HG00673.hp1 HG01099.hp2 HG01256.hp1 others(89): Show |
intron_variant | MODIFIER | c.895-582A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20549055 | |||||||
chr16:20549091 | A | G | 3 | a0001c0002t0003g0013 a0003c0007t0003g0014 a0014c0028t0003g0123 |
5 | HG02486.hp2 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.895-618T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20549091 | |||||||
chr16:20549286 | T | C | 1 | a0001c0001t0001g0215 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.895-813A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20549286 | |||||||
chr16:20549402 | T | G | 1 | a0001c0012t0007g0222 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.895-929A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20549402 | |||||||
chr16:20549427 | C | T | 3 | a0001c0002t0003g0013 a0003c0007t0003g0014 a0014c0028t0003g0123 |
5 | HG02486.hp2 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.895-954G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20549427 | |||||||
chr16:20549431 | T | C | 3 | a0002c0003t0013g0054 a0002c0003t0013g0055 a0002c0003t0013g0084 |
3 | HG02145.hp1 HG02486.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.895-958A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20549431 | |||||||
chr16:20549691 | G | A | 2 | a0001c0001t0012g0004 a0001c0001t0012g0043 |
4 | NA18953.hp1 NA18957.hp1 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.895-1218C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20549691 | |||||||
chr16:20549712 | C | T | 1 | a0001c0001t0003g0164 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.895-1239G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20549712 | |||||||
chr16:20549764 | T | C | 1 | a0001c0001t0001g0186 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.895-1291A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20549764 | |||||||
chr16:20549771 | T | C | 1 | a0001c0001t0003g0127 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.895-1298A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20549771 | |||||||
chr16:20549824 | TA | T | 3 | a0001c0002t0003g0013 a0003c0007t0003g0014 a0014c0028t0003g0123 |
5 | HG02486.hp2 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.895-1352delT | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20549824 | |||||||
chr16:20549836 | T | G | 1 | a0001c0001t0003g0127 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.895-1363A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20549836 | |||||||
chr16:20549868 | G | T | 205 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(202): Show |
240 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(237): Show |
intron_variant | MODIFIER | c.895-1395C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20549868 | |||||||
chr16:20549998 | A | AT | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(118): Show |
148 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.895-1526dupA | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20549998 | |||||||
chr16:20550007 | T | A | 36 | a0002c0003t0005g0009 a0002c0003t0005g0010 a0002c0003t0005g0048 others(33): Show |
39 | HG00673.hp1 HG01256.hp1 HG01257.hp1 others(36): Show |
intron_variant | MODIFIER | c.895-1534A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20550007 | |||||||
chr16:20550166 | C | A | 67 | a0002c0003t0005g0009 a0002c0003t0005g0010 a0002c0003t0005g0048 others(64): Show |
72 | HG00673.hp1 HG01099.hp2 HG01256.hp1 others(69): Show |
intron_variant | MODIFIER | c.895-1693G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20550166 | |||||||
chr16:20550268 | A | G | 1 | a0003c0008t0011g0307 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.895-1795T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20550268 | |||||||
chr16:20550284 | T | C | 79 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(76): Show |
103 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.895-1811A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20550284 | |||||||
chr16:20550295 | C | T | 1 | a0001c0001t0001g0172 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.895-1822G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20550295 | |||||||
chr16:20550451 | T | A | 2 | a0003c0008t0003g0125 a0003c0025t0003g0124 |
2 | HG03704.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.894+1693A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20550451 | |||||||
chr16:20550474 | G | T | 1 | a0001c0002t0004g0278 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.894+1670C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20550474 | |||||||
chr16:20550500 | T | G | 13 | a0006c0010t0003g0012 a0006c0010t0003g0119 a0006c0010t0003g0120 others(10): Show |
14 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.894+1644A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20550500 | |||||||
chr16:20550561 | C | T | 12 | a0003c0007t0007g0313 a0003c0007t0014g0331 a0003c0007t0014g0332 others(9): Show |
13 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.894+1583G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20550561 | |||||||
chr16:20550625 | G | A | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(215): Show |
254 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(251): Show |
intron_variant | MODIFIER | c.894+1519C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20550625 | |||||||
chr16:20550664 | G | A | 2 | a0003c0008t0003g0125 a0003c0025t0003g0124 |
2 | HG03704.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.894+1480C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20550664 | |||||||
chr16:20550689 | G | A | 1 | a0001c0001t0003g0127 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.894+1455C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20550689 | |||||||
chr16:20550756 | C | T | 1 | a0001c0001t0001g0213 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.894+1388G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20550756 | |||||||
chr16:20550820 | A | G | 1 | a0003c0008t0011g0308 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.894+1324T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20550820 | |||||||
chr16:20550842 | G | C | 1 | a0001c0002t0004g0276 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.894+1302C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20550842 | |||||||
chr16:20551055 | A | G | 1 | a0001c0002t0004g0038 | 2 | HG02083.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.894+1089T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20551055 | |||||||
chr16:20551165 | A | G | 1 | a0001c0002t0003g0254 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.894+979T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20551165 | |||||||
chr16:20551166 | C | T | 5 | a0001c0002t0003g0013 a0003c0007t0003g0014 a0003c0008t0003g0125 others(2): Show |
7 | HG02486.hp2 HG02572.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.894+978G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20551166 | |||||||
chr16:20551267 | G | T | 4 | a0002c0003t0005g0052 a0002c0003t0005g0087 a0002c0003t0005g0089 others(1): Show |
4 | HG02559.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.894+877C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20551267 | |||||||
chr16:20551276 | G | C | 1 | a0001c0001t0001g0001 | 6 | NA18970.hp1 NA18972.hp2 NA18988.hp2 others(3): Show |
intron_variant | MODIFIER | c.894+868C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20551276 | |||||||
chr16:20551337 | T | C | 200 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(197): Show |
233 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(230): Show |
intron_variant | MODIFIER | c.894+807A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20551337 | |||||||
chr16:20551353 | T | C | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(214): Show |
253 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(250): Show |
intron_variant | MODIFIER | c.894+791A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20551353 | |||||||
chr16:20551409 | T | A | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(196): Show |
232 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(229): Show |
intron_variant | MODIFIER | c.894+735A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20551409 | |||||||
chr16:20551415 | T | C | 101 | a0001c0002t0002g0008 a0001c0002t0002g0029 a0001c0002t0002g0030 others(98): Show |
117 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.894+729A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20551415 | |||||||
chr16:20551424 | T | G | 100 | a0001c0002t0002g0008 a0001c0002t0002g0029 a0001c0002t0002g0030 others(97): Show |
116 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.894+720A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20551424 | |||||||
chr16:20551529 | T | C | 1 | a0001c0001t0003g0152 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.894+615A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20551529 | |||||||
chr16:20551532 | T | C | 3 | a0001c0002t0003g0013 a0003c0007t0003g0014 a0014c0028t0003g0123 |
5 | HG02486.hp2 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+612A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20551532 | |||||||
chr16:20551768 | AAC | A | 3 | a0001c0002t0003g0013 a0003c0007t0003g0014 a0014c0028t0003g0123 |
5 | HG02486.hp2 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+374_894+375del others(2): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20551768 | |||||||
chr16:20551793 | G | A | 2 | a0011c0021t0001g0188 a0011c0021t0001g0189 |
2 | HG03831.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.894+351C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20551793 | |||||||
chr16:20551799 | G | A | 5 | a0001c0001t0001g0161 a0001c0001t0001g0190 a0001c0001t0001g0194 others(2): Show |
5 | NA18942.hp2 NA19063.hp1 NA19079.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+345C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20551799 | |||||||
chr16:20551837 | G | A | 13 | a0006c0010t0003g0012 a0006c0010t0003g0119 a0006c0010t0003g0120 others(10): Show |
14 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.894+307C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20551837 | |||||||
chr16:20551871 | T | C | 4 | a0003c0007t0014g0331 a0003c0007t0014g0332 a0003c0007t0014g0333 others(1): Show |
4 | HG02258.hp2 HG02717.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.894+273A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20551871 | |||||||
chr16:20551878 | G | C | 4 | a0008c0013t0002g0111 a0008c0013t0002g0112 a0008c0013t0002g0113 others(1): Show |
4 | HG02257.hp1 HG02886.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.894+266C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20551878 | |||||||
chr16:20551931 | A | G | 79 | a0002c0003t0005g0009 a0002c0003t0005g0010 a0002c0003t0005g0048 others(76): Show |
85 | HG00673.hp1 HG01099.hp2 HG01256.hp1 others(82): Show |
intron_variant | MODIFIER | c.894+213T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20551931 | |||||||
chr16:20551946 | A | G | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(77): Show |
104 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.894+198T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20551946 | |||||||
chr16:20551958 | G | C | 4 | a0001c0017t0004g0033 a0002c0003t0013g0054 a0002c0003t0013g0055 others(1): Show |
5 | HG02145.hp1 HG02486.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.894+186C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20551958 | |||||||
chr16:20551974 | C | A | 1 | a0001c0001t0001g0191 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.894+170G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20551974 | |||||||
chr16:20552010 | G | C | 1 | a0001c0001t0001g0213 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.894+134C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20552010 | |||||||
chr16:20552020 | C | T | 1 | a0001c0002t0007g0240 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.894+124G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20552020 | |||||||
chr16:20552341 | G | A | 17 | a0001c0002t0002g0118 a0001c0002t0003g0116 a0001c0006t0011g0115 others(14): Show |
18 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.741-44C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20552341 | |||||||
chr16:20552351 | C | T | 2 | a0006c0020t0003g0110 a0006c0020t0020g0042 |
2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.741-54G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20552351 | |||||||
chr16:20552364 | G | C | 17 | a0001c0002t0002g0118 a0001c0002t0003g0116 a0001c0006t0011g0115 others(14): Show |
18 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.741-67C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20552364 | |||||||
chr16:20552404 | C | T | 1 | a0001c0002t0002g0229 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.741-107G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20552404 | |||||||
chr16:20552405 | G | A | 70 | a0001c0002t0007g0109 a0002c0003t0005g0009 a0002c0003t0005g0010 others(67): Show |
75 | HG00673.hp1 HG01099.hp2 HG01256.hp1 others(72): Show |
intron_variant | MODIFIER | c.741-108C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20552405 | |||||||
chr16:20552430 | C | A | 79 | a0002c0003t0005g0009 a0002c0003t0005g0010 a0002c0003t0005g0048 others(76): Show |
85 | HG00673.hp1 HG01099.hp2 HG01256.hp1 others(82): Show |
intron_variant | MODIFIER | c.741-133G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20552430 | |||||||
chr16:20552437 | T | C | 5 | a0001c0002t0003g0013 a0003c0007t0003g0014 a0003c0008t0003g0125 others(2): Show |
7 | HG02486.hp2 HG02572.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.741-140A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20552437 | |||||||
chr16:20552440 | A | T | 5 | a0001c0002t0003g0013 a0003c0007t0003g0014 a0003c0008t0003g0125 others(2): Show |
7 | HG02486.hp2 HG02572.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.741-143T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20552440 | |||||||
chr16:20552447 | G | A | 1 | a0001c0002t0003g0013 | 2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.741-150C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20552447 | |||||||
chr16:20552457 | G | A | 5 | a0001c0002t0004g0037 a0001c0002t0004g0263 a0001c0002t0004g0290 others(2): Show |
6 | HG00438.hp2 NA18945.hp1 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.741-160C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20552457 | |||||||
chr16:20552474 | G | A | 5 | a0001c0002t0003g0013 a0003c0007t0003g0014 a0003c0008t0003g0125 others(2): Show |
7 | HG02486.hp2 HG02572.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.741-177C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20552474 | |||||||
chr16:20552488 | C | A | 2 | a0006c0020t0003g0110 a0006c0020t0020g0042 |
2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.741-191G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20552488 | |||||||
chr16:20552488 | C | T | 5 | a0001c0002t0003g0013 a0003c0007t0003g0014 a0003c0008t0003g0125 others(2): Show |
7 | HG02486.hp2 HG02572.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.741-191G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20552488 | |||||||
chr16:20552491 | T | C | 5 | a0001c0002t0003g0013 a0003c0007t0003g0014 a0003c0008t0003g0125 others(2): Show |
7 | HG02486.hp2 HG02572.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.741-194A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20552491 | |||||||
chr16:20552492 | G | A | 5 | a0001c0002t0003g0013 a0003c0007t0003g0014 a0003c0008t0003g0125 others(2): Show |
7 | HG02486.hp2 HG02572.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.741-195C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20552492 | |||||||
chr16:20552494 | T | C | 5 | a0001c0002t0003g0013 a0003c0007t0003g0014 a0003c0008t0003g0125 others(2): Show |
7 | HG02486.hp2 HG02572.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.741-197A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20552494 | |||||||
chr16:20552506 | G | A | 17 | a0001c0002t0002g0118 a0001c0002t0003g0116 a0001c0006t0011g0115 others(14): Show |
18 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.741-209C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20552506 | |||||||
chr16:20552510 | G | A | 5 | a0001c0002t0003g0013 a0003c0007t0003g0014 a0003c0008t0003g0125 others(2): Show |
7 | HG02486.hp2 HG02572.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.741-213C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20552510 | |||||||
chr16:20552525 | A | G | 5 | a0001c0002t0003g0013 a0003c0007t0003g0014 a0003c0008t0003g0125 others(2): Show |
7 | HG02486.hp2 HG02572.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.741-228T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20552525 | |||||||
chr16:20552541 | T | C | 12 | a0003c0007t0007g0313 a0003c0007t0014g0331 a0003c0007t0014g0332 others(9): Show |
13 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.741-244A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20552541 | |||||||
chr16:20552636 | G | A | 65 | a0002c0003t0005g0009 a0002c0003t0005g0010 a0002c0003t0005g0048 others(62): Show |
68 | HG00673.hp1 HG01099.hp2 HG01256.hp1 others(65): Show |
intron_variant | MODIFIER | c.741-339C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20552636 | |||||||
chr16:20552637 | A | G | 321 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(318): Show |
373 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(370): Show |
intron_variant | MODIFIER | c.741-340T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20552637 | |||||||
chr16:20552683 | T | C | 3 | a0001c0002t0007g0109 a0005c0024t0016g0325 a0010c0022t0008g0316 |
3 | HG02630.hp1 HG02922.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.741-386A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20552683 | |||||||
chr16:20552851 | C | T | 1 | a0001c0006t0003g0304 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.741-554G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20552851 | |||||||
chr16:20552859 | G | A | 1 | a0001c0002t0002g0235 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.741-562C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20552859 | |||||||
chr16:20552978 | C | T | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(215): Show |
254 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(251): Show |
intron_variant | MODIFIER | c.741-681G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20552978 | |||||||
chr16:20552981 | C | T | 4 | a0002c0003t0005g0051 a0002c0003t0005g0053 a0002c0003t0005g0062 others(1): Show |
4 | NA18959.hp1 NA19005.hp1 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.741-684G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20552981 | |||||||
chr16:20553065 | A | G | 3 | a0005c0011t0008g0320 a0005c0011t0008g0321 a0005c0011t0008g0322 |
3 | HG01168.hp1 HG01169.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.740+712T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20553065 | |||||||
chr16:20553068 | G | T | 25 | a0001c0002t0003g0255 a0001c0002t0004g0003 a0001c0002t0004g0034 others(22): Show |
31 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.740+709C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20553068 | |||||||
chr16:20553118 | T | C | 79 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(76): Show |
103 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.740+659A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20553118 | |||||||
chr16:20553171 | T | C | 96 | a0001c0002t0002g0118 a0001c0002t0003g0116 a0001c0006t0011g0115 others(93): Show |
103 | HG00673.hp1 HG01099.hp2 HG01256.hp1 others(100): Show |
intron_variant | MODIFIER | c.740+606A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20553171 | |||||||
chr16:20553347 | G | A | 1 | a0001c0002t0004g0280 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.740+430C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20553347 | |||||||
chr16:20553407 | A | G | 12 | a0003c0007t0007g0313 a0003c0007t0014g0331 a0003c0007t0014g0332 others(9): Show |
13 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.740+370T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20553407 | |||||||
chr16:20553420 | A | C | 1 | a0001c0002t0004g0257 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.740+357T>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20553420 | |||||||
chr16:20553523 | A | G | 1 | a0001c0002t0003g0256 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.740+254T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20553523 | |||||||
chr16:20553608 | G | T | 1 | a0002c0003t0010g0086 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.740+169C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20553608 | |||||||
chr16:20553617 | T | C | 2 | a0005c0011t0026g0318 a0005c0016t0016g0317 |
2 | HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.740+160A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20553617 | |||||||
chr16:20553681 | A | G | 2 | a0003c0008t0003g0125 a0003c0025t0003g0124 |
2 | HG03704.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.740+96T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20553681 | |||||||
chr16:20553698 | A | G | 1 | a0001c0004t0002g0130 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.740+79T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20553698 | |||||||
chr16:20553753 | G | C | 4 | a0001c0001t0001g0027 a0001c0001t0001g0192 a0001c0001t0001g0217 others(1): Show |
5 | NA18943.hp1 NA19002.hp1 NA19072.hp1 others(2): Show |
intron_variant | MODIFIER | c.740+24C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20553753 | |||||||
chr16:20554002 | A | T | 2 | a0006c0020t0003g0110 a0006c0020t0020g0042 |
2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.597-82T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 4/13 | chr16 | 20554002 | |||||||
chr16:20554017 | G | A | 1 | a0001c0002t0002g0241 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.597-97C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 4/13 | chr16 | 20554017 | |||||||
chr16:20554072 | A | C | 17 | a0001c0002t0002g0118 a0001c0002t0003g0116 a0001c0006t0011g0115 others(14): Show |
18 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.597-152T>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 4/13 | chr16 | 20554072 | |||||||
chr16:20554074 | C | T | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(210): Show |
247 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(244): Show |
intron_variant | MODIFIER | c.597-154G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 4/13 | chr16 | 20554074 | |||||||
chr16:20554263 | G | A | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(215): Show |
254 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(251): Show |
intron_variant | MODIFIER | c.597-343C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 4/13 | chr16 | 20554263 | |||||||
chr16:20554298 | C | T | 1 | a0007c0014t0001g0198 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.597-378G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 4/13 | chr16 | 20554298 | |||||||
chr16:20554344 | T | A | 1 | a0014c0028t0003g0123 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.597-424A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 4/13 | chr16 | 20554344 | |||||||
chr16:20554406 | A | T | 1 | a0001c0002t0002g0229 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.597-486T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 4/13 | chr16 | 20554406 | |||||||
chr16:20554416 | T | C | 1 | a0001c0002t0004g0263 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.597-496A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 4/13 | chr16 | 20554416 | |||||||
chr16:20554485 | G | T | 2 | a0002c0003t0010g0005 a0002c0018t0010g0046 |
4 | HG02559.hp2 HG02970.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.597-565C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 4/13 | chr16 | 20554485 | |||||||
chr16:20554493 | G | A | 37 | a0001c0001t0001g0126 a0001c0001t0001g0135 a0001c0001t0001g0136 others(34): Show |
40 | HG00558.hp1 HG00597.hp1 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.597-573C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 4/13 | chr16 | 20554493 | |||||||
chr16:20554528 | A | T | 65 | a0002c0003t0005g0009 a0002c0003t0005g0010 a0002c0003t0005g0048 others(62): Show |
68 | HG00673.hp1 HG01099.hp2 HG01256.hp1 others(65): Show |
intron_variant | MODIFIER | c.597-608T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 4/13 | chr16 | 20554528 | |||||||
chr16:20554572 | G | A | 1 | a0002c0003t0005g0048 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.597-652C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 4/13 | chr16 | 20554572 | |||||||
chr16:20554736 | G | C | 1 | a0008c0013t0002g0114 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.596+533C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 4/13 | chr16 | 20554736 | |||||||
chr16:20554776 | T | G | 2 | a0006c0020t0003g0110 a0006c0020t0020g0042 |
2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.596+493A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 4/13 | chr16 | 20554776 | |||||||
chr16:20554895 | T | C | 1 | a0003c0007t0007g0313 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.596+374A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 4/13 | chr16 | 20554895 | |||||||
chr16:20554911 | C | G | 6 | a0001c0002t0002g0029 a0001c0002t0002g0236 a0001c0002t0002g0237 others(3): Show |
7 | HG01109.hp1 HG01496.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.596+358G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 4/13 | chr16 | 20554911 | |||||||
chr16:20554932 | C | T | 1 | a0001c0004t0002g0155 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.596+337G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 4/13 | chr16 | 20554932 | |||||||
chr16:20554965 | C | G | 96 | a0001c0002t0002g0118 a0001c0002t0003g0116 a0001c0006t0011g0115 others(93): Show |
103 | HG00673.hp1 HG01099.hp2 HG01256.hp1 others(100): Show |
intron_variant | MODIFIER | c.596+304G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 4/13 | chr16 | 20554965 | |||||||
chr16:20555010 | G | A | 2 | a0003c0008t0003g0125 a0003c0025t0003g0124 |
2 | HG03704.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.596+259C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 4/13 | chr16 | 20555010 | |||||||
chr16:20555024 | T | TA | 3 | a0001c0001t0001g0135 a0001c0004t0002g0139 a0001c0004t0002g0145 |
3 | HG02602.hp2 HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.596+244dupT | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 4/13 | chr16 | 20555024 | |||||||
chr16:20555107 | G | GA | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(213): Show |
252 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(249): Show |
intron_variant | MODIFIER | c.596+161dupT | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 4/13 | chr16 | 20555107 | |||||||
chr16:20555156 | T | G | 1 | a0003c0025t0003g0124 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.596+113A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 4/13 | chr16 | 20555156 | |||||||
chr16:20555246 | G | C | 8 | a0001c0002t0002g0118 a0001c0002t0003g0116 a0001c0006t0011g0115 others(5): Show |
8 | HG02257.hp1 HG02717.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.596+23C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 4/13 | chr16 | 20555246 | |||||||
chr16:20555671 | G | A | 1 | a0001c0001t0003g0193 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.389-195C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20555671 | |||||||
chr16:20555798 | C | T | 12 | a0003c0007t0007g0313 a0003c0007t0014g0331 a0003c0007t0014g0332 others(9): Show |
13 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.389-322G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20555798 | |||||||
chr16:20555875 | A | C | 1 | a0001c0001t0001g0218 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.389-399T>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20555875 | |||||||
chr16:20555955 | T | A | 2 | a0004c0005t0006g0104 a0004c0005t0006g0108 |
2 | HG02258.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.389-479A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20555955 | |||||||
chr16:20556016 | T | C | 101 | a0001c0002t0002g0008 a0001c0002t0002g0029 a0001c0002t0002g0030 others(98): Show |
117 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.389-540A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20556016 | |||||||
chr16:20556088 | AT | A | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(215): Show |
254 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(251): Show |
intron_variant | MODIFIER | c.389-613delA | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20556088 | |||||||
chr16:20556160 | G | A | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(114): Show |
144 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.389-684C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20556160 | |||||||
chr16:20556356 | C | T | 1 | a0014c0028t0003g0123 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.389-880G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20556356 | |||||||
chr16:20556381 | T | C | 1 | a0001c0001t0001g0194 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.389-905A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20556381 | |||||||
chr16:20556422 | C | T | 1 | a0001c0004t0004g0171 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.389-946G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20556422 | |||||||
chr16:20556444 | A | G | 1 | a0004c0005t0006g0085 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.389-968T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20556444 | |||||||
chr16:20556524 | C | T | 1 | a0001c0004t0004g0197 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.389-1048G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20556524 | |||||||
chr16:20556567 | A | G | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(114): Show |
144 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.389-1091T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20556567 | |||||||
chr16:20556721 | T | C | 1 | a0001c0002t0007g0109 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.389-1245A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20556721 | |||||||
chr16:20556780 | A | G | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(114): Show |
144 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.389-1304T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20556780 | |||||||
chr16:20556938 | A | G | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(114): Show |
144 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.389-1462T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20556938 | |||||||
chr16:20557017 | G | A | 3 | a0001c0002t0003g0013 a0003c0007t0003g0014 a0014c0028t0003g0123 |
5 | HG02486.hp2 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.389-1541C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20557017 | |||||||
chr16:20557180 | C | G | 1 | a0001c0002t0004g0280 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.389-1704G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20557180 | |||||||
chr16:20557194 | C | A | 126 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(123): Show |
153 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.389-1718G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20557194 | |||||||
chr16:20557199 | A | T | 2 | a0006c0020t0003g0110 a0006c0020t0020g0042 |
2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.389-1723T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20557199 | |||||||
chr16:20557216 | CT | C | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(114): Show |
144 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.389-1741delA | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20557216 | |||||||
chr16:20557240 | C | G | 1 | a0001c0001t0001g0163 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.389-1764G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20557240 | |||||||
chr16:20557268 | G | C | 1 | a0003c0007t0014g0331 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.389-1792C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20557268 | |||||||
chr16:20557271 | A | C | 1 | a0007c0014t0001g0204 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.389-1795T>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20557271 | |||||||
chr16:20557290 | A | G | 1 | a0001c0002t0002g0246 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.389-1814T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20557290 | |||||||
chr16:20557404 | T | G | 1 | a0001c0002t0004g0297 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.388+1833A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20557404 | |||||||
chr16:20557405 | TC | T | 67 | a0002c0003t0005g0009 a0002c0003t0005g0010 a0002c0003t0005g0048 others(64): Show |
72 | HG00673.hp1 HG01099.hp2 HG01256.hp1 others(69): Show |
intron_variant | MODIFIER | c.388+1831delG | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20557405 | |||||||
chr16:20557408 | C | A | 46 | a0002c0003t0005g0009 a0002c0003t0005g0010 a0002c0003t0005g0048 others(43): Show |
49 | HG00673.hp1 HG01256.hp1 HG01257.hp1 others(46): Show |
intron_variant | MODIFIER | c.388+1829G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20557408 | |||||||
chr16:20557434 | ATCTCCAT others(1): Show |
A | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(114): Show |
144 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.388+1795_388+1802d others(10): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20557434 | |||||||
chr16:20557443 | T | G | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(114): Show |
144 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.388+1794A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20557443 | |||||||
chr16:20557486 | T | C | 1 | a0001c0001t0008g0327 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.388+1751A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20557486 | |||||||
chr16:20557521 | C | T | 319 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(316): Show |
371 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(368): Show |
intron_variant | MODIFIER | c.388+1716G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20557521 | |||||||
chr16:20557546 | C | G | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(77): Show |
104 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.388+1691G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20557546 | |||||||
chr16:20557686 | T | A | 15 | a0001c0002t0002g0118 a0001c0002t0003g0116 a0001c0006t0011g0115 others(12): Show |
16 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.388+1551A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20557686 | |||||||
chr16:20557713 | C | T | 7 | a0006c0010t0003g0012 a0006c0010t0003g0119 a0006c0010t0003g0120 others(4): Show |
8 | HG01884.hp2 HG02109.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.388+1524G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20557713 | |||||||
chr16:20557783 | T | A | 2 | a0002c0003t0010g0005 a0002c0018t0010g0046 |
4 | HG02559.hp2 HG02970.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.388+1454A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20557783 | |||||||
chr16:20557800 | T | C | 1 | a0001c0002t0004g0270 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.388+1437A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20557800 | |||||||
chr16:20557803 | C | T | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(114): Show |
144 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.388+1434G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20557803 | |||||||
chr16:20557821 | C | G | 15 | a0001c0002t0002g0118 a0001c0002t0003g0116 a0001c0006t0011g0115 others(12): Show |
16 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.388+1416G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20557821 | |||||||
chr16:20557833 | T | A | 1 | a0004c0005t0006g0107 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.388+1404A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20557833 | |||||||
chr16:20557972 | A | T | 1 | a0001c0004t0002g0148 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.388+1265T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20557972 | |||||||
chr16:20558059 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.388+1178G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20558059 | |||||||
chr16:20558124 | C | T | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(114): Show |
144 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.388+1113G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20558124 | |||||||
chr16:20558125 | G | A | 1 | a0002c0003t0005g0059 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.388+1112C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20558125 | |||||||
chr16:20558233 | A | G | 2 | a0003c0008t0003g0125 a0003c0025t0003g0124 |
2 | HG03704.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.388+1004T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20558233 | |||||||
chr16:20558335 | C | A | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(114): Show |
144 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.388+902G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20558335 | |||||||
chr16:20558336 | C | T | 3 | a0001c0001t0001g0167 a0001c0001t0001g0196 a0001c0001t0001g0208 |
3 | NA18945.hp2 NA18947.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.388+901G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20558336 | |||||||
chr16:20558343 | C | T | 125 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(122): Show |
152 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.388+894G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20558343 | |||||||
chr16:20558351 | C | T | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(114): Show |
144 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.388+886G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20558351 | |||||||
chr16:20558352 | T | A | 1 | a0014c0028t0003g0123 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.388+885A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20558352 | |||||||
chr16:20558354 | C | G | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(114): Show |
144 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.388+883G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20558354 | |||||||
chr16:20558691 | A | G | 17 | a0001c0002t0002g0118 a0001c0002t0003g0116 a0001c0006t0011g0115 others(14): Show |
18 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.388+546T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20558691 | |||||||
chr16:20558714 | A | G | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(114): Show |
144 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.388+523T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20558714 | |||||||
chr16:20558743 | G | A | 1 | a0001c0001t0003g0211 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.388+494C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20558743 | |||||||
chr16:20558794 | T | C | 1 | a0006c0020t0020g0042 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.388+443A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20558794 | |||||||
chr16:20558896 | T | A | 3 | a0001c0002t0003g0036 a0001c0027t0003g0275 a0003c0007t0007g0274 |
4 | HG02109.hp2 HG02818.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.388+341A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20558896 | |||||||
chr16:20558902 | A | G | 1 | a0001c0001t0001g0163 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.388+335T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20558902 | |||||||
chr16:20559045 | T | C | 1 | a0001c0002t0007g0109 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.388+192A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20559045 | |||||||
chr16:20559143 | C | A | 2 | a0006c0020t0003g0110 a0006c0020t0020g0042 |
2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.388+94G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20559143 | |||||||
chr16:20559144 | A | G | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(212): Show |
251 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(248): Show |
intron_variant | MODIFIER | c.388+93T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20559144 | |||||||
chr16:20559453 | G | T | 15 | a0001c0002t0002g0118 a0001c0002t0003g0116 a0001c0006t0011g0115 others(12): Show |
16 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(13): Show |
splice_region_variant&intron_variant | LOW | c.178-6C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20559453 | |||||||
chr16:20559462 | A | G | 3 | a0004c0005t0006g0101 a0009c0015t0008g0040 a0009c0015t0008g0319 |
4 | HG01934.hp2 HG03490.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.178-15T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20559462 | |||||||
chr16:20559473 | T | C | 2 | a0009c0015t0008g0040 a0009c0015t0008g0319 |
3 | HG03490.hp2 HG03492.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.178-26A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20559473 | |||||||
chr16:20559515 | C | T | 2 | a0001c0002t0002g0029 a0001c0002t0002g0236 |
3 | HG02965.hp2 HG03516.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.178-68G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20559515 | |||||||
chr16:20559530 | C | T | 14 | a0003c0007t0007g0313 a0003c0007t0014g0331 a0003c0007t0014g0332 others(11): Show |
16 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.178-83G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20559530 | |||||||
chr16:20559540 | G | A | 1 | a0006c0010t0003g0012 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.178-93C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20559540 | |||||||
chr16:20559574 | A | T | 14 | a0003c0007t0007g0313 a0003c0007t0014g0331 a0003c0007t0014g0332 others(11): Show |
16 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.178-127T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20559574 | |||||||
chr16:20559580 | A | G | 14 | a0003c0007t0007g0313 a0003c0007t0014g0331 a0003c0007t0014g0332 others(11): Show |
16 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.178-133T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20559580 | |||||||
chr16:20559584 | T | C | 3 | a0001c0002t0003g0013 a0003c0007t0003g0014 a0014c0028t0003g0123 |
5 | HG02486.hp2 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.178-137A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20559584 | |||||||
chr16:20559592 | C | T | 14 | a0003c0007t0007g0313 a0003c0007t0014g0331 a0003c0007t0014g0332 others(11): Show |
16 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.178-145G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20559592 | |||||||
chr16:20559600 | G | C | 14 | a0003c0007t0007g0313 a0003c0007t0014g0331 a0003c0007t0014g0332 others(11): Show |
16 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.178-153C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20559600 | |||||||
chr16:20559625 | A | G | 14 | a0003c0007t0007g0313 a0003c0007t0014g0331 a0003c0007t0014g0332 others(11): Show |
16 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.178-178T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20559625 | |||||||
chr16:20559639 | T | C | 100 | a0001c0002t0002g0008 a0001c0002t0002g0029 a0001c0002t0002g0030 others(97): Show |
116 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.178-192A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20559639 | |||||||
chr16:20559721 | AT | A | 84 | a0001c0002t0002g0118 a0001c0002t0003g0116 a0001c0006t0011g0115 others(81): Show |
90 | HG00673.hp1 HG01099.hp2 HG01256.hp1 others(87): Show |
intron_variant | MODIFIER | c.178-275delA | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20559721 | |||||||
chr16:20559742 | G | A | 14 | a0003c0007t0007g0313 a0003c0007t0014g0331 a0003c0007t0014g0332 others(11): Show |
16 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.178-295C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20559742 | |||||||
chr16:20559743 | T | A | 14 | a0003c0007t0007g0313 a0003c0007t0014g0331 a0003c0007t0014g0332 others(11): Show |
16 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.178-296A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20559743 | |||||||
chr16:20559783 | T | TTTTA | 14 | a0003c0007t0007g0313 a0003c0007t0014g0331 a0003c0007t0014g0332 others(11): Show |
16 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.178-340_178-337dup others(4): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20559783 | |||||||
chr16:20559796 | A | G | 14 | a0003c0007t0007g0313 a0003c0007t0014g0331 a0003c0007t0014g0332 others(11): Show |
16 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.178-349T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20559796 | |||||||
chr16:20559805 | T | C | 13 | a0003c0007t0007g0313 a0003c0007t0014g0331 a0003c0007t0014g0332 others(10): Show |
14 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.178-358A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20559805 | |||||||
chr16:20559812 | A | G | 17 | a0001c0002t0002g0118 a0001c0002t0003g0116 a0001c0006t0011g0115 others(14): Show |
18 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.178-365T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20559812 | |||||||
chr16:20559823 | T | C | 14 | a0003c0007t0007g0313 a0003c0007t0014g0331 a0003c0007t0014g0332 others(11): Show |
16 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.178-376A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20559823 | |||||||
chr16:20559836 | T | A | 14 | a0003c0007t0007g0313 a0003c0007t0014g0331 a0003c0007t0014g0332 others(11): Show |
16 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.178-389A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20559836 | |||||||
chr16:20559841 | T | A | 1 | a0001c0002t0004g0266 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.178-394A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20559841 | |||||||
chr16:20559848 | C | G | 2 | a0002c0003t0010g0005 a0002c0018t0010g0046 |
4 | HG02559.hp2 HG02970.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.178-401G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20559848 | |||||||
chr16:20559894 | T | C | 14 | a0003c0007t0007g0313 a0003c0007t0014g0331 a0003c0007t0014g0332 others(11): Show |
16 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.178-447A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20559894 | |||||||
chr16:20559921 | T | G | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(128): Show |
160 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.178-474A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20559921 | |||||||
chr16:20559944 | C | A | 14 | a0003c0007t0007g0313 a0003c0007t0014g0331 a0003c0007t0014g0332 others(11): Show |
16 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.178-497G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20559944 | |||||||
chr16:20559950 | TCACTTTA others(1819): Show |
T | 2 | a0009c0015t0008g0040 a0009c0015t0008g0319 |
3 | HG03490.hp2 HG03492.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.178-2329_178-504de others(1): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20559950 | |||||||
chr16:20559973 | T | G | 12 | a0003c0007t0007g0313 a0003c0007t0014g0331 a0003c0007t0014g0332 others(9): Show |
13 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.178-526A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20559973 | |||||||
chr16:20559986 | C | T | 12 | a0003c0007t0007g0313 a0003c0007t0014g0331 a0003c0007t0014g0332 others(9): Show |
13 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.178-539G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20559986 | |||||||
chr16:20560006 | G | A | 12 | a0003c0007t0007g0313 a0003c0007t0014g0331 a0003c0007t0014g0332 others(9): Show |
13 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.178-559C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20560006 | |||||||
chr16:20560031 | G | A | 12 | a0003c0007t0007g0313 a0003c0007t0014g0331 a0003c0007t0014g0332 others(9): Show |
13 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.178-584C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20560031 | |||||||
chr16:20560114 | GA | G | 12 | a0003c0007t0007g0313 a0003c0007t0014g0331 a0003c0007t0014g0332 others(9): Show |
13 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.178-668delT | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20560114 | |||||||
chr16:20560129 | C | A | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(77): Show |
104 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.178-682G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20560129 | |||||||
chr16:20560135 | C | T | 17 | a0001c0002t0003g0013 a0003c0007t0003g0014 a0003c0007t0007g0313 others(14): Show |
20 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.178-688G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20560135 | |||||||
chr16:20560150 | C | T | 15 | a0001c0002t0002g0118 a0001c0002t0003g0116 a0001c0006t0011g0115 others(12): Show |
16 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.178-703G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20560150 | |||||||
chr16:20560165 | T | C | 12 | a0003c0007t0007g0313 a0003c0007t0014g0331 a0003c0007t0014g0332 others(9): Show |
13 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.178-718A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20560165 | |||||||
chr16:20560181 | A | T | 12 | a0003c0007t0007g0313 a0003c0007t0014g0331 a0003c0007t0014g0332 others(9): Show |
13 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.178-734T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20560181 | |||||||
chr16:20560213 | T | G | 12 | a0003c0007t0007g0313 a0003c0007t0014g0331 a0003c0007t0014g0332 others(9): Show |
13 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.178-766A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20560213 | |||||||
chr16:20560319 | A | G | 12 | a0003c0007t0007g0313 a0003c0007t0014g0331 a0003c0007t0014g0332 others(9): Show |
13 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.178-872T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20560319 | |||||||
chr16:20560479 | T | G | 5 | a0001c0002t0003g0013 a0003c0007t0003g0014 a0003c0008t0003g0125 others(2): Show |
7 | HG02486.hp2 HG02572.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.178-1032A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20560479 | |||||||
chr16:20560572 | T | C | 2 | a0002c0003t0010g0005 a0002c0018t0010g0046 |
4 | HG02559.hp2 HG02970.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.178-1125A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20560572 | |||||||
chr16:20560586 | T | G | 1 | a0001c0002t0004g0271 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.178-1139A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20560586 | |||||||
chr16:20560650 | T | C | 6 | a0003c0008t0003g0125 a0004c0005t0006g0085 a0004c0005t0006g0091 others(3): Show |
6 | HG01884.hp1 HG02723.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.178-1203A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20560650 | |||||||
chr16:20560783 | G | A | 2 | a0003c0008t0003g0125 a0003c0025t0003g0124 |
2 | HG03704.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.178-1336C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20560783 | |||||||
chr16:20560848 | G | T | 12 | a0003c0007t0007g0313 a0003c0007t0014g0331 a0003c0007t0014g0332 others(9): Show |
13 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.178-1401C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20560848 | |||||||
chr16:20560899 | G | A | 1 | a0008c0013t0002g0113 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.178-1452C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20560899 | |||||||
chr16:20560924 | A | C | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(114): Show |
144 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.178-1477T>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20560924 | |||||||
chr16:20560927 | A | G | 1 | a0001c0002t0007g0109 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.178-1480T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20560927 | |||||||
chr16:20561054 | C | T | 2 | a0001c0004t0002g0134 a0001c0004t0002g0140 |
2 | NA18966.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.178-1607G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20561054 | |||||||
chr16:20561102 | T | C | 96 | a0001c0002t0002g0118 a0001c0002t0003g0116 a0001c0006t0011g0115 others(93): Show |
103 | HG00673.hp1 HG01099.hp2 HG01256.hp1 others(100): Show |
intron_variant | MODIFIER | c.178-1655A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20561102 | |||||||
chr16:20561143 | C | G | 100 | a0001c0002t0002g0008 a0001c0002t0002g0029 a0001c0002t0002g0030 others(97): Show |
116 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.178-1696G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20561143 | |||||||
chr16:20561170 | C | A | 2 | a0005c0024t0016g0325 a0010c0022t0008g0316 |
2 | HG02630.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.178-1723G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20561170 | |||||||
chr16:20561170 | C | G | 1 | a0001c0006t0003g0305 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.178-1723G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20561170 | |||||||
chr16:20561230 | C | T | 1 | a0001c0001t0008g0328 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.178-1783G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20561230 | |||||||
chr16:20561241 | T | C | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(215): Show |
254 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(251): Show |
intron_variant | MODIFIER | c.178-1794A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20561241 | |||||||
chr16:20561369 | C | T | 67 | a0002c0003t0005g0009 a0002c0003t0005g0010 a0002c0003t0005g0048 others(64): Show |
72 | HG00673.hp1 HG01099.hp2 HG01256.hp1 others(69): Show |
intron_variant | MODIFIER | c.178-1922G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20561369 | |||||||
chr16:20561385 | G | A | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(114): Show |
144 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.178-1938C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20561385 | |||||||
chr16:20561387 | G | T | 1 | a0001c0002t0007g0031 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.178-1940C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20561387 | |||||||
chr16:20561526 | G | T | 19 | a0004c0005t0006g0047 a0004c0005t0006g0085 a0004c0005t0006g0091 others(16): Show |
19 | HG01099.hp2 HG01884.hp1 HG01934.hp2 others(16): Show |
intron_variant | MODIFIER | c.178-2079C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20561526 | |||||||
chr16:20561528 | C | T | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(113): Show |
143 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.178-2081G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20561528 | |||||||
chr16:20561643 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.178-2196G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20561643 | |||||||
chr16:20561684 | C | CT | 4 | a0001c0001t0003g0183 a0001c0002t0003g0013 a0003c0007t0003g0014 others(1): Show |
6 | HG02486.hp2 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.178-2238dupA | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20561684 | |||||||
chr16:20561684 | CT | C | 38 | a0001c0001t0001g0126 a0001c0001t0001g0135 a0001c0001t0001g0136 others(35): Show |
41 | HG00558.hp1 HG00597.hp1 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.178-2238delA | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20561684 | |||||||
chr16:20561811 | C | A | 64 | a0001c0002t0002g0281 a0001c0002t0002g0284 a0001c0002t0002g0295 others(61): Show |
73 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.178-2364G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20561811 | |||||||
chr16:20561821 | A | G | 2 | a0009c0015t0008g0040 a0009c0015t0008g0319 |
3 | HG03490.hp2 HG03492.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.178-2374T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20561821 | |||||||
chr16:20561843 | G | A | 3 | a0001c0001t0001g0161 a0009c0015t0008g0040 a0009c0015t0008g0319 |
4 | HG03490.hp2 HG03492.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.178-2396C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20561843 | |||||||
chr16:20561860 | C | A | 7 | a0001c0001t0001g0150 a0001c0001t0003g0151 a0001c0001t0003g0152 others(4): Show |
9 | HG00597.hp1 HG00621.hp1 HG03490.hp2 others(6): Show |
intron_variant | MODIFIER | c.178-2413G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20561860 | |||||||
chr16:20561866 | C | T | 2 | a0002c0003t0010g0005 a0002c0018t0010g0046 |
4 | HG02559.hp2 HG02970.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.178-2419G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20561866 | |||||||
chr16:20561905 | T | C | 1 | a0016c0031t0016g0329 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.178-2458A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20561905 | |||||||
chr16:20561949 | T | A | 18 | a0001c0001t0001g0126 a0001c0001t0001g0135 a0001c0001t0001g0136 others(15): Show |
19 | HG00597.hp2 HG00673.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.178-2502A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20561949 | |||||||
chr16:20561960 | A | G | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(114): Show |
144 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.178-2513T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20561960 | |||||||
chr16:20561968 | G | GT | 315 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(312): Show |
367 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(364): Show |
intron_variant | MODIFIER | c.178-2522dupA | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20561968 | |||||||
chr16:20561968 | G | T | 1 | a0001c0006t0003g0304 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.178-2521C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20561968 | |||||||
chr16:20561979 | C | CTTGCCAT others(3): Show |
2 | a0009c0015t0008g0040 a0009c0015t0008g0319 |
3 | HG03490.hp2 HG03492.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.178-2542_178-2533d others(12): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20561979 | |||||||
chr16:20562090 | T | A | 1 | a0001c0002t0003g0013 | 2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.177+2579A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20562090 | |||||||
chr16:20562095 | A | T | 2 | a0006c0020t0003g0110 a0006c0020t0020g0042 |
2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.177+2574T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20562095 | |||||||
chr16:20562098 | T | C | 1 | a0012c0032t0025g0330 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.177+2571A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20562098 | |||||||
chr16:20562137 | A | T | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(114): Show |
144 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.177+2532T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20562137 | |||||||
chr16:20562138 | C | A | 12 | a0003c0007t0007g0313 a0003c0007t0014g0331 a0003c0007t0014g0332 others(9): Show |
13 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.177+2531G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20562138 | |||||||
chr16:20562185 | A | G | 2 | a0002c0003t0010g0005 a0002c0018t0010g0046 |
4 | HG02559.hp2 HG02970.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.177+2484T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20562185 | |||||||
chr16:20562249 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.177+2420C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20562249 | |||||||
chr16:20562253 | C | T | 7 | a0006c0010t0003g0012 a0006c0010t0003g0119 a0006c0010t0003g0120 others(4): Show |
8 | HG01884.hp2 HG02109.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.177+2416G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20562253 | |||||||
chr16:20562325 | T | C | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(114): Show |
144 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.177+2344A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20562325 | |||||||
chr16:20562392 | C | A | 2 | a0002c0003t0010g0005 a0002c0018t0010g0046 |
4 | HG02559.hp2 HG02970.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.177+2277G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20562392 | |||||||
chr16:20562536 | T | C | 14 | a0002c0003t0010g0005 a0002c0018t0010g0046 a0003c0007t0007g0313 others(11): Show |
17 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.177+2133A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20562536 | |||||||
chr16:20562548 | A | C | 12 | a0003c0007t0007g0313 a0003c0007t0014g0331 a0003c0007t0014g0332 others(9): Show |
13 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.177+2121T>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20562548 | |||||||
chr16:20562584 | G | T | 1 | a0006c0010t0017g0044 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.177+2085C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20562584 | |||||||
chr16:20562784 | G | A | 1 | a0001c0001t0001g0212 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.177+1885C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20562784 | |||||||
chr16:20562866 | C | A | 2 | a0001c0012t0007g0028 a0001c0012t0007g0222 |
3 | HG02965.hp1 HG02970.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.177+1803G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20562866 | |||||||
chr16:20562878 | C | G | 1 | a0001c0002t0004g0314 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.177+1791G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20562878 | |||||||
chr16:20562915 | G | A | 1 | a0001c0002t0007g0109 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.177+1754C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20562915 | |||||||
chr16:20562960 | C | A | 6 | a0001c0001t0001g0136 a0001c0004t0002g0130 a0001c0004t0002g0143 others(3): Show |
6 | HG01074.hp1 HG01168.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.177+1709G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20562960 | |||||||
chr16:20563063 | C | G | 67 | a0002c0003t0005g0009 a0002c0003t0005g0010 a0002c0003t0005g0048 others(64): Show |
72 | HG00673.hp1 HG01099.hp2 HG01256.hp1 others(69): Show |
intron_variant | MODIFIER | c.177+1606G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20563063 | |||||||
chr16:20563103 | C | T | 17 | a0001c0002t0002g0118 a0001c0002t0003g0116 a0001c0006t0011g0115 others(14): Show |
18 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.177+1566G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20563103 | |||||||
chr16:20563143 | A | G | 1 | a0005c0016t0029g0315 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.177+1526T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20563143 | |||||||
chr16:20563144 | A | T | 5 | a0001c0002t0003g0013 a0003c0007t0003g0014 a0003c0008t0003g0125 others(2): Show |
7 | HG02486.hp2 HG02572.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.177+1525T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20563144 | |||||||
chr16:20563220 | C | A | 2 | a0003c0008t0003g0125 a0003c0025t0003g0124 |
2 | HG03704.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.177+1449G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20563220 | |||||||
chr16:20563429 | A | G | 1 | a0001c0006t0003g0224 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.177+1240T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20563429 | |||||||
chr16:20563587 | A | T | 1 | a0001c0004t0002g0130 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.177+1082T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20563587 | |||||||
chr16:20563592 | TA | T | 15 | a0001c0002t0002g0118 a0001c0002t0003g0116 a0001c0006t0011g0115 others(12): Show |
16 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.177+1076delT | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20563592 | |||||||
chr16:20563680 | G | T | 98 | a0001c0002t0002g0008 a0001c0002t0002g0029 a0001c0002t0002g0030 others(95): Show |
113 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.177+989C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20563680 | |||||||
chr16:20563729 | C | A | 100 | a0001c0002t0002g0008 a0001c0002t0002g0029 a0001c0002t0002g0030 others(97): Show |
116 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.177+940G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20563729 | |||||||
chr16:20563740 | T | C | 67 | a0002c0003t0005g0009 a0002c0003t0005g0010 a0002c0003t0005g0048 others(64): Show |
72 | HG00673.hp1 HG01099.hp2 HG01256.hp1 others(69): Show |
intron_variant | MODIFIER | c.177+929A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20563740 | |||||||
chr16:20563771 | G | A | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(113): Show |
143 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.177+898C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20563771 | |||||||
chr16:20563805 | T | C | 4 | a0001c0002t0003g0253 a0001c0002t0003g0254 a0001c0002t0003g0256 others(1): Show |
4 | HG02280.hp2 HG02451.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.177+864A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20563805 | |||||||
chr16:20563985 | G | A | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(114): Show |
144 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.177+684C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20563985 | |||||||
chr16:20564108 | C | T | 12 | a0003c0007t0007g0313 a0003c0007t0014g0331 a0003c0007t0014g0332 others(9): Show |
13 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.177+561G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20564108 | |||||||
chr16:20564148 | C | T | 4 | a0001c0001t0001g0126 a0001c0004t0002g0129 a0001c0004t0002g0131 others(1): Show |
4 | NA18992.hp1 NA19001.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.177+521G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20564148 | |||||||
chr16:20564151 | T | A | 1 | a0001c0002t0007g0220 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.177+518A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20564151 | |||||||
chr16:20564274 | A | G | 4 | a0001c0001t0001g0126 a0001c0004t0002g0129 a0001c0004t0002g0131 others(1): Show |
4 | NA18992.hp1 NA19001.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.177+395T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20564274 | |||||||
chr16:20564297 | G | A | 2 | a0001c0012t0007g0028 a0001c0012t0007g0222 |
3 | HG02965.hp1 HG02970.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.177+372C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20564297 | |||||||
chr16:20564305 | G | T | 65 | a0002c0003t0005g0009 a0002c0003t0005g0010 a0002c0003t0005g0048 others(62): Show |
68 | HG00673.hp1 HG01099.hp2 HG01256.hp1 others(65): Show |
intron_variant | MODIFIER | c.177+364C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20564305 | |||||||
chr16:20564340 | C | T | 11 | a0003c0007t0014g0331 a0003c0007t0014g0332 a0003c0007t0014g0333 others(8): Show |
12 | HG02145.hp2 HG02257.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.177+329G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20564340 | |||||||
chr16:20564432 | G | C | 1 | a0001c0002t0004g0266 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.177+237C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20564432 | |||||||
chr16:20564918 | G | A | 1 | a0001c0002t0004g0314 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-8-65C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20564918 | |||||||
chr16:20564945 | T | C | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(114): Show |
144 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.-8-92A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20564945 | |||||||
chr16:20564997 | T | A | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(210): Show |
247 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(244): Show |
intron_variant | MODIFIER | c.-8-144A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20564997 | |||||||
chr16:20565039 | G | T | 2 | a0005c0011t0019g0041 a0005c0016t0028g0324 |
3 | HG01891.hp1 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-8-186C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20565039 | |||||||
chr16:20565106 | C | T | 1 | a0001c0002t0002g0229 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-8-253G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20565106 | |||||||
chr16:20565147 | G | A | 1 | a0001c0001t0001g0163 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-8-294C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20565147 | |||||||
chr16:20565221 | T | C | 2 | a0003c0008t0011g0307 a0003c0008t0011g0308 |
2 | HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-8-368A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20565221 | |||||||
chr16:20565231 | A | T | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(229): Show |
270 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(267): Show |
intron_variant | MODIFIER | c.-8-378T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20565231 | |||||||
chr16:20565361 | C | G | 2 | a0001c0001t0012g0004 a0001c0001t0012g0043 |
4 | NA18953.hp1 NA18957.hp1 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-508G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20565361 | |||||||
chr16:20565424 | T | A | 46 | a0002c0003t0005g0009 a0002c0003t0005g0010 a0002c0003t0005g0048 others(43): Show |
49 | HG00673.hp1 HG01256.hp1 HG01257.hp1 others(46): Show |
intron_variant | MODIFIER | c.-8-571A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20565424 | |||||||
chr16:20565563 | G | A | 3 | a0003c0008t0001g0310 a0003c0008t0015g0039 a0003c0008t0015g0309 |
4 | HG02615.hp1 HG02809.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-710C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20565563 | |||||||
chr16:20565580 | T | G | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(114): Show |
144 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.-8-727A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20565580 | |||||||
chr16:20565608 | G | C | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(114): Show |
144 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.-8-755C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20565608 | |||||||
chr16:20565783 | A | G | 1 | a0001c0002t0002g0242 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-8-930T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20565783 | |||||||
chr16:20565954 | G | A | 2 | a0003c0008t0003g0125 a0003c0025t0003g0124 |
2 | HG03704.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-8-1101C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20565954 | |||||||
chr16:20565990 | C | T | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(114): Show |
144 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.-8-1137G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20565990 | |||||||
chr16:20566043 | T | C | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(200): Show |
238 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(235): Show |
intron_variant | MODIFIER | c.-8-1190A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566043 | |||||||
chr16:20566105 | C | A | 2 | a0005c0011t0026g0318 a0005c0016t0016g0317 |
2 | HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-8-1252G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566105 | |||||||
chr16:20566105 | C | T | 1 | a0006c0020t0003g0110 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-8-1252G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566105 | |||||||
chr16:20566112 | A | G | 1 | a0003c0025t0003g0124 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-8-1259T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566112 | |||||||
chr16:20566115 | T | TA | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(209): Show |
246 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(243): Show |
intron_variant | MODIFIER | c.-8-1263dupT | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566115 | |||||||
chr16:20566130 | T | A | 1 | a0001c0001t0003g0147 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-8-1277A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566130 | |||||||
chr16:20566131 | A | T | 1 | a0001c0001t0003g0147 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-8-1278T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566131 | |||||||
chr16:20566173 | G | A | 5 | a0001c0002t0003g0013 a0003c0007t0003g0014 a0003c0008t0003g0125 others(2): Show |
7 | HG02486.hp2 HG02572.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-8-1320C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566173 | |||||||
chr16:20566212 | C | G | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(229): Show |
270 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(267): Show |
intron_variant | MODIFIER | c.-8-1359G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566212 | |||||||
chr16:20566247 | T | TTA | 29 | a0001c0002t0002g0281 a0001c0002t0002g0284 a0001c0002t0004g0257 others(26): Show |
30 | HG00323.hp2 HG00609.hp2 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.-8-1396_-8-1395dup others(2): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566247 | |||||||
chr16:20566247 | T | TTATA | 20 | a0001c0002t0002g0241 a0001c0002t0002g0242 a0001c0002t0002g0251 others(17): Show |
23 | HG00280.hp1 HG01167.hp1 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.-8-1398_-8-1395dup others(4): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566247 | |||||||
chr16:20566247 | T | TTATATA | 21 | a0001c0002t0002g0008 a0001c0002t0002g0032 a0001c0002t0002g0232 others(18): Show |
25 | HG00639.hp1 HG00642.hp1 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.-8-1400_-8-1395dup others(6): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566247 | |||||||
chr16:20566247 | T | TTATATAT others(1): Show |
3 | a0001c0002t0002g0252 a0001c0002t0003g0253 a0005c0011t0008g0321 |
3 | HG01169.hp1 HG01169.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-8-1402_-8-1395dup others(8): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566247 | |||||||
chr16:20566247 | T | TTTATATA others(6): Show |
1 | a0002c0018t0005g0073 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-8-1395_-8-1394ins others(13): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566247 | |||||||
chr16:20566247 | T | TTTTATA | 5 | a0002c0003t0005g0050 a0002c0003t0005g0053 a0002c0003t0005g0059 others(2): Show |
5 | HG01891.hp2 HG01975.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-1395_-8-1394ins others(6): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566247 | |||||||
chr16:20566247 | T | TTTTATAT others(1): Show |
14 | a0002c0003t0005g0009 a0002c0003t0005g0051 a0002c0003t0005g0052 others(11): Show |
15 | HG01257.hp1 HG02809.hp2 HG03195.hp1 others(12): Show |
intron_variant | MODIFIER | c.-8-1395_-8-1394ins others(8): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566247 | |||||||
chr16:20566247 | T | TTTTATAT others(3): Show |
15 | a0002c0003t0005g0049 a0002c0003t0005g0058 a0002c0003t0005g0063 others(12): Show |
16 | HG00673.hp1 HG01943.hp1 HG02040.hp1 others(13): Show |
intron_variant | MODIFIER | c.-8-1395_-8-1394ins others(10): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566247 | |||||||
chr16:20566247 | T | TTTTATAT others(5): Show |
6 | a0002c0003t0005g0010 a0002c0003t0005g0061 a0002c0003t0010g0088 others(3): Show |
7 | HG01256.hp1 HG02559.hp1 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8-1395_-8-1394ins others(12): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566247 | |||||||
chr16:20566247 | T | TTTTATAT others(7): Show |
2 | a0002c0003t0010g0086 a0002c0003t0013g0084 |
2 | HG02486.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.-8-1395_-8-1394ins others(14): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566247 | |||||||
chr16:20566247 | TTA | T | 26 | a0001c0002t0002g0233 a0001c0002t0002g0234 a0001c0002t0002g0235 others(23): Show |
28 | HG00323.hp1 HG00639.hp2 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.-8-1396_-8-1395del others(2): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566247 | |||||||
chr16:20566247 | TTATA | T | 23 | a0001c0002t0002g0030 a0001c0002t0002g0118 a0001c0002t0002g0237 others(20): Show |
26 | HG00738.hp2 HG01109.hp1 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.-8-1398_-8-1395del others(4): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566247 | |||||||
chr16:20566247 | TTATATA | T | 15 | a0001c0001t0001g0203 a0001c0002t0002g0029 a0001c0002t0002g0236 others(12): Show |
18 | HG00558.hp2 HG00597.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.-8-1400_-8-1395del others(6): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566247 | |||||||
chr16:20566247 | TTATATAT others(1): Show |
T | 25 | a0001c0001t0001g0126 a0001c0001t0001g0150 a0001c0001t0001g0166 others(22): Show |
30 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.-8-1402_-8-1395del others(8): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566247 | |||||||
chr16:20566247 | TTATATAT others(3): Show |
T | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(84): Show |
108 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.-8-1404_-8-1395del others(10): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566247 | |||||||
chr16:20566247 | TTATATAT others(5): Show |
T | 5 | a0001c0001t0001g0167 a0001c0001t0003g0020 a0001c0004t0002g0140 others(2): Show |
6 | HG02055.hp1 HG03209.hp1 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8-1406_-8-1395del others(12): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566247 | |||||||
chr16:20566247 | TTATATAT others(7): Show |
T | 1 | a0006c0020t0020g0042 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-8-1408_-8-1395del others(14): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566247 | |||||||
chr16:20566247 | TTATATAT others(9): Show |
T | 4 | a0001c0002t0003g0036 a0001c0027t0003g0275 a0003c0007t0007g0274 others(1): Show |
5 | HG02109.hp2 HG02630.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-1410_-8-1395del others(16): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566247 | |||||||
chr16:20566251 | A | T | 4 | a0006c0010t0003g0012 a0006c0010t0003g0120 a0006c0010t0003g0121 others(1): Show |
5 | HG02109.hp1 HG02615.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-1398T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566251 | |||||||
chr16:20566253 | A | T | 6 | a0001c0002t0002g0118 a0001c0002t0003g0116 a0001c0006t0011g0115 others(3): Show |
6 | HG01884.hp2 HG02717.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8-1400T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566253 | |||||||
chr16:20566255 | A | T | 4 | a0008c0013t0002g0111 a0008c0013t0002g0112 a0008c0013t0002g0113 others(1): Show |
4 | HG02257.hp1 HG02886.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-1402T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566255 | |||||||
chr16:20566257 | A | T | 1 | a0006c0010t0003g0119 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-8-1404T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566257 | |||||||
chr16:20566286 | G | T | 1 | a0002c0003t0010g0086 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-8-1433C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566286 | |||||||
chr16:20566388 | A | C | 1 | a0001c0001t0001g0166 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-8-1535T>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566388 | |||||||
chr16:20566395 | G | A | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(210): Show |
247 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(244): Show |
intron_variant | MODIFIER | c.-8-1542C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566395 | |||||||
chr16:20566404 | T | C | 1 | a0001c0001t0001g0163 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-8-1551A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566404 | |||||||
chr16:20566422 | T | A | 1 | a0001c0001t0003g0147 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-8-1569A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566422 | |||||||
chr16:20566423 | A | T | 1 | a0001c0001t0003g0147 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-8-1570T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566423 | |||||||
chr16:20566424 | T | A | 1 | a0001c0001t0003g0147 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-8-1571A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566424 | |||||||
chr16:20566425 | T | C | 1 | a0001c0004t0007g0201 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-8-1572A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566425 | |||||||
chr16:20566461 | T | C | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(114): Show |
144 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.-8-1608A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566461 | |||||||
chr16:20566534 | ATACTATA others(4): Show |
A | 1 | a0007c0014t0001g0160 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-8-1692_-8-1682del others(11): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566534 | |||||||
chr16:20566544 | A | C | 12 | a0003c0007t0007g0313 a0003c0007t0014g0331 a0003c0007t0014g0332 others(9): Show |
13 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-8-1691T>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566544 | |||||||
chr16:20566545 | C | G | 1 | a0001c0002t0004g0301 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-8-1692G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566545 | |||||||
chr16:20566615 | A | G | 4 | a0002c0003t0005g0051 a0002c0003t0005g0053 a0002c0003t0005g0062 others(1): Show |
4 | NA18959.hp1 NA19005.hp1 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-1762T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566615 | |||||||
chr16:20566634 | G | A | 1 | a0001c0002t0004g0272 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-8-1781C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566634 | |||||||
chr16:20566634 | G | C | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(115): Show |
145 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.-8-1781C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566634 | |||||||
chr16:20566635 | T | C | 3 | a0001c0001t0023g0202 a0003c0008t0011g0307 a0003c0008t0011g0308 |
3 | HG02257.hp2 HG03139.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-8-1782A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566635 | |||||||
chr16:20566640 | A | AC | 16 | a0001c0002t0002g0118 a0001c0002t0003g0116 a0001c0006t0011g0115 others(13): Show |
17 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.-8-1788_-8-1787ins others(1): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566640 | |||||||
chr16:20566640 | ATATAC | A | 3 | a0001c0004t0002g0129 a0002c0003t0005g0089 a0003c0008t0011g0307 |
3 | HG02257.hp2 HG02809.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.-8-1792_-8-1788del others(5): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566640 | |||||||
chr16:20566644 | A | AGTATATA others(92): Show |
1 | a0001c0001t0001g0203 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-8-1792_-8-1791ins others(99): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566644 | |||||||
chr16:20566644 | AC | A | 16 | a0001c0002t0002g0118 a0001c0002t0003g0116 a0001c0006t0011g0115 others(13): Show |
17 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.-8-1792delG | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566644 | |||||||
chr16:20566645 | C | A | 3 | a0001c0001t0001g0203 a0001c0001t0003g0147 a0001c0002t0007g0109 |
3 | HG02040.hp2 NA18972.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-8-1792G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566645 | |||||||
chr16:20566645 | C | CTATA | 102 | a0001c0001t0001g0026 a0001c0001t0001g0163 a0001c0001t0001g0208 others(99): Show |
113 | HG00597.hp1 HG00673.hp1 HG01099.hp2 others(110): Show |
intron_variant | MODIFIER | c.-8-1796_-8-1793dup others(4): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566645 | |||||||
chr16:20566645 | C | CTATATAT others(24): Show |
1 | a0001c0001t0003g0015 | 2 | HG00558.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.-8-1793_-8-1792ins others(31): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566645 | |||||||
chr16:20566645 | C | CTATATAT others(83): Show |
1 | a0001c0001t0008g0326 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-8-1793_-8-1792ins others(90): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566645 | |||||||
chr16:20566645 | C | CTATATAT others(101): Show |
1 | a0001c0004t0004g0214 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-8-1793_-8-1792ins others(108): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566645 | |||||||
chr16:20566645 | C | CTATATAT others(40): Show |
15 | a0001c0001t0003g0127 a0001c0001t0003g0142 a0001c0001t0003g0144 others(12): Show |
17 | HG00597.hp2 HG00673.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.-8-1793_-8-1792ins others(47): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566645 | |||||||
chr16:20566645 | C | CTATATAT others(83): Show |
14 | a0001c0001t0001g0126 a0001c0001t0001g0135 a0001c0001t0001g0136 others(11): Show |
14 | HG01515.hp2 HG01952.hp1 HG02698.hp1 others(11): Show |
intron_variant | MODIFIER | c.-8-1793_-8-1792ins others(90): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566645 | |||||||
chr16:20566645 | C | CTATATAT others(74): Show |
1 | a0001c0001t0018g0132 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-8-1793_-8-1792ins others(81): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566645 | |||||||
chr16:20566645 | C | CTATATAT others(40): Show |
1 | a0005c0016t0016g0317 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-8-1793_-8-1792ins others(47): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566645 | |||||||
chr16:20566645 | C | CTATATAT others(121): Show |
1 | a0005c0011t0008g0322 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-8-1793_-8-1792ins others(128): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566645 | |||||||
chr16:20566645 | C | CTATATAT others(26): Show |
1 | a0001c0001t0001g0213 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-8-1793_-8-1792ins others(33): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566645 | |||||||
chr16:20566645 | C | CTATATAT others(103): Show |
1 | a0001c0004t0004g0171 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-8-1793_-8-1792ins others(110): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566645 | |||||||
chr16:20566645 | C | CTATATAT others(150): Show |
4 | a0001c0001t0001g0027 a0001c0001t0001g0192 a0001c0001t0001g0217 others(1): Show |
5 | NA18943.hp1 NA19002.hp1 NA19072.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-1793_-8-1792ins others(157): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566645 | |||||||
chr16:20566645 | C | CTATATAT others(69): Show |
4 | a0001c0001t0001g0167 a0001c0001t0001g0191 a0001c0001t0001g0196 others(1): Show |
4 | HG02080.hp1 NA18945.hp2 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-1793_-8-1792ins others(76): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566645 | |||||||
chr16:20566645 | C | CTATATAT others(103): Show |
54 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0018 others(51): Show |
70 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.-8-1793_-8-1792ins others(110): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566645 | |||||||
chr16:20566645 | C | CTATATAT others(137): Show |
3 | a0001c0001t0001g0001 a0001c0001t0001g0172 a0001c0004t0002g0187 |
8 | NA18956.hp1 NA18970.hp1 NA18972.hp2 others(5): Show |
intron_variant | MODIFIER | c.-8-1793_-8-1792ins others(144): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566645 | |||||||
chr16:20566645 | C | CTATATAT others(94): Show |
1 | a0001c0001t0001g0165 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-8-1793_-8-1792ins others(101): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566645 | |||||||
chr16:20566645 | C | CTATATAT others(103): Show |
4 | a0001c0001t0001g0021 a0001c0001t0001g0157 a0001c0001t0001g0158 others(1): Show |
4 | NA18951.hp2 NA18960.hp1 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-1793_-8-1792ins others(110): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566645 | |||||||
chr16:20566645 | C | CTATATAT others(83): Show |
1 | a0001c0001t0003g0152 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-8-1793_-8-1792ins others(90): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566645 | |||||||
chr16:20566650 | C | G | 2 | a0006c0020t0003g0110 a0006c0020t0020g0042 |
2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-8-1797G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566650 | |||||||
chr16:20566656 | A | ATAC | 68 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(65): Show |
90 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.-8-1804_-8-1803ins others(3): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566656 | |||||||
chr16:20566658 | A | AC | 2 | a0001c0001t0001g0019 a0001c0001t0001g0165 |
3 | HG01361.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-8-1806_-8-1805ins others(1): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566658 | |||||||
chr16:20566658 | A | ACTATATA others(1): Show |
4 | a0001c0002t0003g0013 a0003c0007t0003g0014 a0014c0028t0003g0123 others(1): Show |
6 | HG02486.hp2 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8-1806_-8-1805ins others(8): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566658 | |||||||
chr16:20566658 | A | AG | 45 | a0002c0003t0005g0009 a0002c0003t0005g0010 a0002c0003t0005g0048 others(42): Show |
48 | HG00673.hp1 HG01256.hp1 HG01257.hp1 others(45): Show |
intron_variant | MODIFIER | c.-8-1806_-8-1805ins others(1): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566658 | |||||||
chr16:20566658 | A | AGTATATA others(98): Show |
1 | a0003c0008t0003g0125 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-8-1806_-8-1805ins others(105): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566658 | |||||||
chr16:20566658 | A | AGTATATA others(100): Show |
1 | a0003c0025t0003g0124 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-8-1806_-8-1805ins others(107): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566658 | |||||||
chr16:20566658 | AT | A | 103 | a0001c0001t0001g0126 a0001c0001t0001g0135 a0001c0001t0001g0136 others(100): Show |
112 | HG00558.hp1 HG00597.hp1 HG00597.hp2 others(109): Show |
intron_variant | MODIFIER | c.-8-1806delA | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566658 | |||||||
chr16:20566659 | T | A | 6 | a0001c0002t0003g0013 a0003c0007t0003g0014 a0003c0008t0003g0125 others(3): Show |
8 | HG02486.hp2 HG02572.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.-8-1806A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566659 | |||||||
chr16:20566659 | T | TA | 7 | a0001c0001t0001g0026 a0001c0001t0001g0163 a0001c0001t0001g0208 others(4): Show |
8 | NA18950.hp1 NA18977.hp2 NA18989.hp2 others(5): Show |
intron_variant | MODIFIER | c.-8-1807_-8-1806ins others(1): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566659 | |||||||
chr16:20566660 | G | A | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(113): Show |
142 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.-8-1807C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566660 | |||||||
chr16:20566660 | G | C | 73 | a0001c0001t0001g0026 a0001c0001t0001g0126 a0001c0001t0001g0135 others(70): Show |
79 | HG00558.hp1 HG00597.hp1 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.-8-1807C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566660 | |||||||
chr16:20566669 | G | C | 89 | a0001c0001t0001g0026 a0001c0001t0001g0208 a0001c0001t0001g0209 others(86): Show |
97 | HG00597.hp1 HG00673.hp1 HG01168.hp1 others(94): Show |
intron_variant | MODIFIER | c.-8-1816C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566669 | |||||||
chr16:20566669 | G | T | 2 | a0002c0003t0010g0005 a0002c0018t0010g0046 |
4 | HG02559.hp2 HG02970.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-1816C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566669 | |||||||
chr16:20566670 | T | A | 2 | a0002c0003t0010g0005 a0002c0018t0010g0046 |
4 | HG02559.hp2 HG02970.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-1817A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566670 | |||||||
chr16:20566671 | A | C | 2 | a0002c0003t0010g0005 a0002c0018t0010g0046 |
4 | HG02559.hp2 HG02970.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-1818T>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566671 | |||||||
chr16:20566672 | TATAC | T | 9 | a0001c0002t0003g0116 a0001c0006t0011g0115 a0006c0010t0003g0119 others(6): Show |
9 | HG01884.hp2 HG02109.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.-8-1823_-8-1820del others(4): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566672 | |||||||
chr16:20566673 | A | ATATAC | 46 | a0001c0001t0003g0153 a0001c0002t0002g0118 a0002c0003t0005g0009 others(43): Show |
51 | HG00597.hp1 HG00673.hp1 HG01168.hp1 others(48): Show |
intron_variant | MODIFIER | c.-8-1821_-8-1820ins others(5): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566673 | |||||||
chr16:20566673 | A | ATATACTA others(156): Show |
1 | a0001c0002t0007g0109 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-8-1821_-8-1820ins others(163): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566673 | |||||||
chr16:20566673 | A | ATATACTA others(127): Show |
1 | a0002c0003t0013g0084 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-8-1821_-8-1820ins others(134): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566673 | |||||||
chr16:20566673 | A | ATATACTA others(129): Show |
9 | a0002c0003t0010g0086 a0002c0009t0009g0011 a0002c0009t0009g0077 others(6): Show |
10 | HG02074.hp2 HG03491.hp1 HG03491.hp2 others(7): Show |
intron_variant | MODIFIER | c.-8-1821_-8-1820ins others(136): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566673 | |||||||
chr16:20566673 | A | ATATACTA others(158): Show |
1 | a0002c0009t0009g0078 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-8-1821_-8-1820ins others(165): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566673 | |||||||
chr16:20566673 | A | ATATAG | 6 | a0003c0008t0011g0308 a0005c0011t0026g0318 a0008c0013t0002g0111 others(3): Show |
6 | HG02257.hp1 HG02886.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8-1821_-8-1820ins others(5): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566673 | |||||||
chr16:20566673 | A | ATATAGTA others(144): Show |
3 | a0003c0007t0014g0331 a0003c0007t0014g0333 a0003c0007t0014g0334 |
3 | HG02258.hp2 HG03130.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-8-1821_-8-1820ins others(151): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566673 | |||||||
chr16:20566673 | A | ATATAGTA others(171): Show |
3 | a0003c0008t0001g0310 a0003c0008t0015g0039 a0003c0008t0015g0309 |
4 | HG02615.hp1 HG02809.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-1821_-8-1820ins others(178): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566673 | |||||||
chr16:20566673 | A | ATATAGTA others(146): Show |
1 | a0003c0007t0014g0332 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-8-1821_-8-1820ins others(153): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566673 | |||||||
chr16:20566673 | A | ATATATAC others(127): Show |
5 | a0004c0005t0006g0085 a0004c0005t0006g0091 a0004c0005t0006g0093 others(2): Show |
5 | HG01099.hp2 HG02723.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-1821_-8-1820ins others(134): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566673 | |||||||
chr16:20566673 | A | ATATATAC others(410): Show |
1 | a0004c0005t0006g0094 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-8-1821_-8-1820ins others(417): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566673 | |||||||
chr16:20566673 | A | ATATATAC others(105): Show |
1 | a0004c0005t0006g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-8-1821_-8-1820ins others(112): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566673 | |||||||
chr16:20566674 | TAC | T | 8 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0004t0002g0129 others(5): Show |
10 | HG02145.hp2 HG02257.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-8-1823_-8-1822del others(2): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566674 | |||||||
chr16:20566676 | C | CTAT | 6 | a0001c0001t0001g0163 a0002c0003t0005g0061 a0003c0007t0007g0248 others(3): Show |
6 | HG00741.hp2 HG02451.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8-1824_-8-1823ins others(3): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566676 | |||||||
chr16:20566676 | C | CTATATAT others(12): Show |
1 | a0015c0030t0018g0146 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-8-1824_-8-1823ins others(19): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566676 | |||||||
chr16:20566676 | C | CTATATAT others(240): Show |
1 | a0006c0020t0003g0110 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-8-1824_-8-1823ins others(247): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566676 | |||||||
chr16:20566676 | C | CTATATAT others(267): Show |
1 | a0006c0020t0020g0042 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-8-1824_-8-1823ins others(274): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566676 | |||||||
chr16:20566676 | C | T | 192 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(189): Show |
226 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(223): Show |
intron_variant | MODIFIER | c.-8-1823G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566676 | |||||||
chr16:20566676 | CATAT | C | 15 | a0001c0001t0003g0127 a0001c0001t0003g0142 a0001c0001t0003g0144 others(12): Show |
17 | HG00597.hp2 HG00673.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.-8-1827_-8-1824del others(4): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566676 | |||||||
chr16:20566678 | T | C | 1 | a0001c0002t0002g0295 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-8-1825A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566678 | |||||||
chr16:20566679 | A | ACTATATA others(67): Show |
12 | a0004c0005t0006g0047 a0004c0005t0006g0098 a0004c0005t0006g0099 others(9): Show |
12 | HG01934.hp2 HG02258.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.-8-1827_-8-1826ins others(74): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566679 | |||||||
chr16:20566680 | T | C | 20 | a0001c0001t0001g0026 a0001c0001t0001g0208 a0001c0001t0001g0209 others(17): Show |
23 | HG01099.hp2 HG01884.hp1 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.-8-1827A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566680 | |||||||
chr16:20566680 | T | G | 2 | a0003c0008t0011g0311 a0003c0008t0011g0312 |
2 | HG02145.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-8-1827A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566680 | |||||||
chr16:20566680 | T | TC | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(83): Show |
110 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.-8-1828_-8-1827ins others(1): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566680 | |||||||
chr16:20566681 | A | ACTATATG others(4): Show |
1 | a0005c0016t0016g0317 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-8-1829_-8-1828ins others(11): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566681 | |||||||
chr16:20566681 | A | T | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(114): Show |
146 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.-8-1828T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566681 | |||||||
chr16:20566681 | AG | A | 12 | a0004c0005t0006g0047 a0004c0005t0006g0098 a0004c0005t0006g0099 others(9): Show |
12 | HG01934.hp2 HG02258.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.-8-1829delC | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566681 | |||||||
chr16:20566682 | G | A | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(104): Show |
134 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.-8-1829C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566682 | |||||||
chr16:20566682 | G | C | 10 | a0001c0001t0001g0163 a0001c0002t0003g0116 a0001c0006t0011g0115 others(7): Show |
10 | HG01884.hp2 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.-8-1829C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566682 | |||||||
chr16:20566682 | G | GTA | 14 | a0002c0003t0010g0086 a0002c0003t0013g0084 a0002c0009t0009g0011 others(11): Show |
15 | HG02055.hp2 HG02074.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.-8-1831_-8-1830dup others(2): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566682 | |||||||
chr16:20566682 | G | GTATATAC others(45): Show |
4 | a0005c0016t0029g0315 a0009c0015t0008g0040 a0009c0015t0008g0319 others(1): Show |
5 | HG02630.hp2 HG03490.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-1830_-8-1829ins others(52): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566682 | |||||||
chr16:20566682 | G | GTATATAC others(115): Show |
8 | a0001c0002t0002g0008 a0001c0002t0002g0032 a0001c0002t0002g0246 others(5): Show |
11 | HG01069.hp1 HG01071.hp1 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.-8-1830_-8-1829ins others(122): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566682 | |||||||
chr16:20566682 | G | GTATATAC others(140): Show |
1 | a0001c0002t0002g0245 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-8-1830_-8-1829ins others(147): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566682 | |||||||
chr16:20566682 | G | GTATATAT others(4): Show |
2 | a0003c0008t0011g0308 a0006c0010t0003g0012 |
3 | HG02895.hp1 HG02897.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-8-1830_-8-1829ins others(11): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566682 | |||||||
chr16:20566682 | G | GTATATAT others(99): Show |
1 | a0003c0007t0007g0248 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-8-1830_-8-1829ins others(106): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566682 | |||||||
chr16:20566682 | G | GTATATAT others(79): Show |
2 | a0002c0003t0005g0052 a0002c0003t0010g0088 |
2 | HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-8-1830_-8-1829ins others(86): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566682 | |||||||
chr16:20566682 | G | GTATATAT others(106): Show |
2 | a0002c0003t0013g0054 a0002c0003t0013g0055 |
2 | HG02145.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-8-1830_-8-1829ins others(113): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566682 | |||||||
chr16:20566682 | G | GTATATAT others(140): Show |
3 | a0002c0003t0005g0074 a0002c0003t0013g0075 a0002c0029t0010g0076 |
3 | HG01256.hp1 HG01257.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.-8-1830_-8-1829ins others(147): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566682 | |||||||
chr16:20566682 | G | GTATATAT others(108): Show |
20 | a0002c0003t0005g0009 a0002c0003t0005g0010 a0002c0003t0005g0049 others(17): Show |
22 | HG00673.hp1 HG01891.hp2 HG02886.hp1 others(19): Show |
intron_variant | MODIFIER | c.-8-1830_-8-1829ins others(115): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566682 | |||||||
chr16:20566682 | G | GTATATAT others(137): Show |
3 | a0002c0003t0005g0051 a0002c0003t0005g0059 a0002c0003t0005g0060 |
3 | HG01975.hp2 NA18954.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.-8-1830_-8-1829ins others(144): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566682 | |||||||
chr16:20566682 | G | GTATATAT others(166): Show |
3 | a0002c0003t0005g0058 a0002c0009t0009g0057 a0002c0018t0005g0056 |
3 | HG02040.hp1 HG03710.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.-8-1830_-8-1829ins others(173): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566682 | |||||||
chr16:20566682 | G | GTATATAT others(119): Show |
1 | a0002c0003t0005g0048 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-8-1830_-8-1829ins others(126): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566682 | |||||||
chr16:20566689 | C | A | 1 | a0001c0001t0001g0163 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-8-1836G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566689 | |||||||
chr16:20566689 | C | G | 2 | a0003c0008t0011g0307 a0003c0008t0011g0308 |
2 | HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-8-1836G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566689 | |||||||
chr16:20566689 | C | T | 9 | a0001c0002t0003g0116 a0001c0006t0011g0115 a0006c0010t0003g0119 others(6): Show |
9 | HG01884.hp2 HG02109.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.-8-1836G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566689 | |||||||
chr16:20566690 | T | A | 9 | a0001c0002t0003g0116 a0001c0006t0011g0115 a0006c0010t0003g0119 others(6): Show |
9 | HG01884.hp2 HG02109.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.-8-1837A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566690 | |||||||
chr16:20566691 | A | G | 9 | a0001c0002t0003g0116 a0001c0006t0011g0115 a0006c0010t0003g0119 others(6): Show |
9 | HG01884.hp2 HG02109.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.-8-1838T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566691 | |||||||
chr16:20566697 | AGT | A | 29 | a0001c0001t0001g0213 a0001c0001t0003g0127 a0001c0001t0003g0142 others(26): Show |
31 | HG00597.hp1 HG00597.hp2 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.-8-1846_-8-1845del others(2): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566697 | |||||||
chr16:20566698 | G | A | 2 | a0002c0003t0010g0005 a0002c0018t0010g0046 |
4 | HG02559.hp2 HG02970.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-1845C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566698 | |||||||
chr16:20566698 | G | C | 104 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(101): Show |
130 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.-8-1845C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566698 | |||||||
chr16:20566698 | GTA | G | 15 | a0001c0002t0004g0298 a0001c0002t0022g0302 a0001c0006t0001g0299 others(12): Show |
15 | HG00741.hp2 HG01099.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.-8-1847_-8-1846del others(2): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566698 | |||||||
chr16:20566700 | A | ATATAC | 4 | a0001c0004t0002g0129 a0002c0003t0010g0005 a0002c0018t0010g0046 others(1): Show |
7 | HG02559.hp2 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(5): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | |||||||
chr16:20566700 | A | ATATATAC | 16 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0212 others(13): Show |
17 | HG02074.hp2 HG02486.hp1 HG03130.hp2 others(14): Show |
intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(7): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | |||||||
chr16:20566700 | A | ATATATAC others(25): Show |
4 | a0008c0013t0002g0111 a0008c0013t0002g0112 a0008c0013t0002g0113 others(1): Show |
4 | HG02257.hp1 HG02886.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(32): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | |||||||
chr16:20566700 | A | ATATATAC others(27): Show |
2 | a0003c0008t0003g0125 a0003c0025t0003g0124 |
2 | HG03704.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(34): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | |||||||
chr16:20566700 | A | ATATATAC others(16): Show |
1 | a0004c0005t0006g0098 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(23): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | |||||||
chr16:20566700 | A | ATATATAC others(18): Show |
42 | a0002c0003t0005g0009 a0002c0003t0005g0010 a0002c0003t0005g0048 others(39): Show |
44 | HG00673.hp1 HG01256.hp1 HG01257.hp1 others(41): Show |
intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(25): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | |||||||
chr16:20566700 | A | ATATATAC others(43): Show |
2 | a0002c0003t0005g0087 a0002c0003t0010g0088 |
2 | HG02559.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(50): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | |||||||
chr16:20566700 | A | ATATATAC others(88): Show |
3 | a0001c0002t0004g0226 a0001c0002t0004g0293 a0001c0006t0001g0292 |
3 | HG03688.hp1 HG03710.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(95): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | |||||||
chr16:20566700 | A | ATATATAC others(113): Show |
2 | a0001c0012t0007g0028 a0001c0012t0007g0222 |
3 | HG02965.hp1 HG02970.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(120): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | |||||||
chr16:20566700 | A | ATATATAC others(138): Show |
1 | a0001c0002t0002g0233 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(145): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | |||||||
chr16:20566700 | A | ATATATAG | 7 | a0001c0001t0001g0026 a0003c0007t0014g0331 a0003c0007t0014g0332 others(4): Show |
9 | HG02258.hp2 HG02615.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(7): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | |||||||
chr16:20566700 | A | ATATATAG others(109): Show |
1 | a0001c0006t0003g0304 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(116): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | |||||||
chr16:20566700 | A | ATATATAG others(185): Show |
1 | a0001c0002t0004g0263 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(192): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | |||||||
chr16:20566700 | A | ATATATAG others(151): Show |
3 | a0001c0002t0003g0253 a0001c0002t0003g0254 a0001c0002t0004g0290 |
3 | HG02451.hp2 NA18964.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(158): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | |||||||
chr16:20566700 | A | ATATATAG others(50): Show |
1 | a0001c0001t0001g0208 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(57): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | |||||||
chr16:20566700 | A | ATATATAG others(147): Show |
2 | a0005c0024t0016g0325 a0010c0022t0008g0316 |
2 | HG02630.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(154): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | |||||||
chr16:20566700 | A | ATATATAG others(210): Show |
1 | a0005c0011t0026g0318 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(217): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | |||||||
chr16:20566700 | A | ATATATAG others(113): Show |
1 | a0001c0002t0004g0273 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(120): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | |||||||
chr16:20566700 | A | ATATATAG others(95): Show |
1 | a0005c0016t0029g0315 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(102): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | |||||||
chr16:20566700 | A | ATATATAG others(79): Show |
2 | a0005c0016t0016g0317 a0010c0023t0027g0323 |
2 | HG02451.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(86): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | |||||||
chr16:20566700 | A | ATATATAG others(133): Show |
2 | a0005c0011t0019g0041 a0005c0016t0028g0324 |
3 | HG01891.hp1 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(140): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | |||||||
chr16:20566700 | A | ATATATAG others(153): Show |
2 | a0003c0008t0011g0311 a0003c0008t0011g0312 |
2 | HG02145.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(160): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | |||||||
chr16:20566700 | A | ATATATAG others(134): Show |
1 | a0001c0002t0002g0228 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(141): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | |||||||
chr16:20566700 | A | ATATATAG others(113): Show |
12 | a0001c0002t0002g0029 a0001c0002t0002g0030 a0001c0002t0002g0236 others(9): Show |
15 | HG00558.hp2 HG00639.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(120): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | |||||||
chr16:20566700 | A | ATATATAG others(70): Show |
1 | a0001c0002t0002g0295 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(77): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | |||||||
chr16:20566700 | A | ATATATAG others(104): Show |
1 | a0001c0002t0002g0243 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(111): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | |||||||
chr16:20566700 | A | ATATATAG others(113): Show |
25 | a0001c0002t0002g0227 a0001c0002t0002g0234 a0001c0002t0002g0235 others(22): Show |
27 | HG00323.hp2 HG00438.hp2 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(120): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | |||||||
chr16:20566700 | A | ATATATAG others(138): Show |
7 | a0001c0002t0002g0229 a0001c0002t0002g0231 a0001c0002t0002g0232 others(4): Show |
7 | HG00735.hp1 HG01074.hp2 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(145): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | |||||||
chr16:20566700 | A | ATATATAG others(172): Show |
1 | a0001c0002t0002g0221 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(179): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | |||||||
chr16:20566700 | A | ATATATAG others(160): Show |
1 | a0001c0002t0004g0038 | 2 | HG02083.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(167): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | |||||||
chr16:20566700 | A | ATATATAG others(122): Show |
1 | a0001c0002t0004g0264 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(129): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | |||||||
chr16:20566700 | A | ATATATAG others(104): Show |
1 | a0001c0002t0003g0255 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(111): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | |||||||
chr16:20566700 | A | ATATATAG others(113): Show |
16 | a0001c0002t0004g0003 a0001c0002t0004g0034 a0001c0002t0004g0219 others(13): Show |
21 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(120): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | |||||||
chr16:20566700 | A | ATATATAG others(138): Show |
1 | a0001c0002t0021g0262 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(145): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | |||||||
chr16:20566700 | A | ATATATAG others(138): Show |
2 | a0001c0002t0004g0259 a0001c0002t0004g0297 |
2 | HG01167.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(145): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | |||||||
chr16:20566700 | A | ATATATAG others(113): Show |
1 | a0001c0017t0004g0261 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(120): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | |||||||
chr16:20566700 | A | ATATATAG others(104): Show |
1 | a0001c0002t0004g0291 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(111): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | |||||||
chr16:20566700 | A | ATATATAG others(144): Show |
1 | a0001c0002t0004g0294 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(151): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | |||||||
chr16:20566700 | A | ATATATAG others(171): Show |
1 | a0001c0002t0004g0035 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(178): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | |||||||
chr16:20566700 | A | ATATATAG others(60): Show |
1 | a0001c0001t0003g0147 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(67): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | |||||||
chr16:20566700 | A | ATATATAT others(3): Show |
1 | a0001c0001t0001g0163 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(10): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | |||||||
chr16:20566700 | A | C | 29 | a0001c0001t0001g0213 a0001c0001t0003g0127 a0001c0001t0003g0142 others(26): Show |
31 | HG00597.hp1 HG00597.hp2 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.-8-1847T>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | |||||||
chr16:20566702 | A | ATATACTA others(68): Show |
1 | a0001c0002t0002g0118 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-8-1850_-8-1849ins others(75): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566702 | |||||||
chr16:20566703 | T | A | 1 | a0004c0005t0006g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-8-1850A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566703 | |||||||
chr16:20566703 | T | TATAGTAT others(104): Show |
2 | a0009c0015t0008g0040 a0009c0015t0008g0319 |
3 | HG03490.hp2 HG03492.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-8-1851_-8-1850ins others(111): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566703 | |||||||
chr16:20566703 | T | TATAGTAT others(36): Show |
1 | a0005c0011t0008g0322 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-8-1851_-8-1850ins others(43): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566703 | |||||||
chr16:20566703 | T | TATAGTAT others(158): Show |
2 | a0005c0011t0008g0320 a0005c0011t0008g0321 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-8-1851_-8-1850ins others(165): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566703 | |||||||
chr16:20566707 | T | C | 90 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(87): Show |
114 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.-8-1854A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566707 | |||||||
chr16:20566709 | G | C | 45 | a0001c0001t0001g0163 a0001c0001t0001g0208 a0001c0001t0003g0127 others(42): Show |
52 | HG00597.hp2 HG00673.hp2 HG01074.hp1 others(49): Show |
intron_variant | MODIFIER | c.-8-1856C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566709 | |||||||
chr16:20566712 | T | C | 1 | a0004c0005t0006g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-8-1859A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566712 | |||||||
chr16:20566716 | T | C | 56 | a0001c0001t0003g0153 a0001c0002t0002g0118 a0001c0002t0004g0259 others(53): Show |
59 | HG00597.hp1 HG00673.hp1 HG01167.hp2 others(56): Show |
intron_variant | MODIFIER | c.-8-1863A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566716 | |||||||
chr16:20566716 | T | TACTATAT others(79): Show |
14 | a0001c0002t0003g0116 a0001c0006t0011g0115 a0006c0010t0003g0012 others(11): Show |
15 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-8-1864_-8-1863ins others(86): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566716 | |||||||
chr16:20566716 | T | TAGTATAT others(2): Show |
7 | a0002c0003t0010g0086 a0004c0005t0006g0085 a0004c0005t0006g0091 others(4): Show |
7 | HG01099.hp2 HG01884.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-8-1872_-8-1864dup others(9): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566716 | |||||||
chr16:20566717 | A | ACT | 4 | a0002c0003t0005g0087 a0002c0003t0010g0088 a0006c0020t0003g0110 others(1): Show |
4 | HG02559.hp1 HG02886.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-1865_-8-1864ins others(2): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566717 | |||||||
chr16:20566717 | A | T | 4 | a0001c0001t0003g0153 a0001c0002t0004g0259 a0001c0002t0004g0296 others(1): Show |
4 | HG00323.hp2 HG00597.hp1 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-1864T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566717 | |||||||
chr16:20566718 | G | A | 7 | a0001c0002t0004g0259 a0001c0002t0004g0296 a0001c0002t0004g0297 others(4): Show |
7 | HG00323.hp2 HG01167.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-8-1865C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566718 | |||||||
chr16:20566718 | G | C | 4 | a0001c0001t0001g0163 a0001c0001t0001g0208 a0001c0001t0003g0147 others(1): Show |
4 | HG02809.hp2 NA18972.hp1 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-1865C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566718 | |||||||
chr16:20566718 | G | GTA | 15 | a0001c0002t0003g0255 a0002c0003t0005g0052 a0003c0007t0007g0313 others(12): Show |
16 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.-8-1867_-8-1866dup others(2): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566718 | |||||||
chr16:20566718 | G | GTATATAC others(18): Show |
1 | a0001c0002t0004g0314 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-8-1890_-8-1866dup others(25): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566718 | |||||||
chr16:20566718 | G | GTATATAT others(304): Show |
1 | a0001c0002t0003g0013 | 2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-8-1866_-8-1865ins others(311): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566718 | |||||||
chr16:20566718 | G | GTATATAT others(304): Show |
1 | a0003c0007t0003g0014 | 2 | HG02486.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-8-1866_-8-1865ins others(311): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566718 | |||||||
chr16:20566718 | G | GTATATAT others(304): Show |
1 | a0014c0028t0003g0123 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-8-1866_-8-1865ins others(311): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566718 | |||||||
chr16:20566718 | G | GTATATAT others(31): Show |
2 | a0001c0006t0001g0299 a0001c0006t0001g0300 |
2 | NA18990.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.-8-1866_-8-1865ins others(38): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566718 | |||||||
chr16:20566718 | G | GTATATAT others(56): Show |
1 | a0001c0002t0022g0302 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-8-1866_-8-1865ins others(63): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566718 | |||||||
chr16:20566718 | G | GTATATAT others(165): Show |
1 | a0001c0002t0004g0298 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-8-1866_-8-1865ins others(172): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566718 | |||||||
chr16:20566722 | A | G | 1 | a0001c0004t0004g0214 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-8-1869T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566722 | |||||||
chr16:20566723 | T | TATAC | 3 | a0001c0001t0001g0163 a0001c0001t0001g0208 a0001c0001t0003g0147 |
3 | NA18972.hp1 NA18977.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.-8-1871_-8-1870ins others(4): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566723 | |||||||
chr16:20566723 | T | TATATATC others(27): Show |
16 | a0001c0001t0003g0127 a0001c0001t0003g0142 a0001c0001t0003g0144 others(13): Show |
18 | HG00597.hp2 HG00673.hp2 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.-8-1871_-8-1870ins others(34): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566723 | |||||||
chr16:20566725 | C | CTATATAT others(4): Show |
2 | a0001c0001t0001g0206 a0001c0001t0001g0207 |
2 | NA18950.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.-8-1873_-8-1872ins others(11): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566725 | |||||||
chr16:20566725 | C | G | 22 | a0001c0001t0001g0163 a0001c0001t0001g0208 a0001c0001t0003g0127 others(19): Show |
24 | HG00597.hp2 HG00673.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.-8-1872G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566725 | |||||||
chr16:20566725 | C | T | 1 | a0003c0008t0011g0307 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-8-1872G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566725 | |||||||
chr16:20566726 | T | A | 1 | a0003c0008t0011g0307 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-8-1873A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566726 | |||||||
chr16:20566727 | A | G | 2 | a0001c0004t0002g0129 a0003c0008t0011g0307 |
2 | HG02257.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.-8-1874T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566727 | |||||||
chr16:20566732 | T | C | 1 | a0001c0002t0003g0255 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-8-1879A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566732 | |||||||
chr16:20566733 | A | ATT | 2 | a0003c0007t0003g0014 a0014c0028t0003g0123 |
3 | HG02486.hp2 HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-8-1881_-8-1880ins others(2): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566733 | |||||||
chr16:20566733 | A | T | 1 | a0001c0002t0003g0255 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-8-1880T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566733 | |||||||
chr16:20566734 | G | A | 7 | a0001c0002t0003g0255 a0001c0004t0002g0129 a0002c0003t0005g0089 others(4): Show |
10 | HG01081.hp2 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-8-1881C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566734 | |||||||
chr16:20566734 | G | C | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(92): Show |
120 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.-8-1881C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566734 | |||||||
chr16:20566734 | G | GTA | 68 | a0001c0002t0002g0118 a0001c0002t0003g0013 a0001c0002t0003g0116 others(65): Show |
73 | HG00673.hp1 HG01256.hp1 HG01257.hp1 others(70): Show |
intron_variant | MODIFIER | c.-8-1883_-8-1882dup others(2): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566734 | |||||||
chr16:20566734 | G | GTATA | 3 | a0003c0008t0001g0310 a0003c0008t0015g0039 a0003c0008t0015g0309 |
4 | HG02615.hp1 HG02809.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-1885_-8-1882dup others(4): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566734 | |||||||
chr16:20566734 | G | GTATATAC others(56): Show |
1 | a0002c0003t0005g0052 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-8-1882_-8-1881ins others(63): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566734 | |||||||
chr16:20566734 | G | GTATATAC others(95): Show |
2 | a0001c0006t0001g0299 a0001c0006t0001g0300 |
2 | NA18990.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.-8-1882_-8-1881ins others(102): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566734 | |||||||
chr16:20566734 | G | GTATATAT others(164): Show |
1 | a0003c0008t0011g0308 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-8-1882_-8-1881ins others(171): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566734 | |||||||
chr16:20566734 | G | GTATATAT others(137): Show |
1 | a0003c0007t0007g0313 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-8-1882_-8-1881ins others(144): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566734 | |||||||
chr16:20566735 | TATATA | T | 88 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(85): Show |
112 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.-8-1887_-8-1883del others(5): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566735 | |||||||
chr16:20566740 | A | ATACTATA others(70): Show |
1 | a0001c0001t0003g0153 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-8-1888_-8-1887ins others(77): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566740 | |||||||
chr16:20566740 | A | ATACTATA others(76): Show |
1 | a0001c0001t0001g0213 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-8-1888_-8-1887ins others(83): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566740 | |||||||
chr16:20566740 | A | ATAGTATA others(110): Show |
5 | a0001c0001t0001g0026 a0001c0001t0001g0209 a0001c0001t0001g0210 others(2): Show |
6 | NA18950.hp1 NA18989.hp2 NA19001.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8-1888_-8-1887ins others(117): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566740 | |||||||
chr16:20566741 | C | G | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(92): Show |
120 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.-8-1888G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566741 | |||||||
chr16:20566750 | C | CTATATAT others(2): Show |
14 | a0001c0002t0007g0109 a0005c0011t0008g0320 a0005c0011t0008g0321 others(11): Show |
16 | HG01168.hp1 HG01169.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.-8-1906_-8-1898dup others(9): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566750 | |||||||
chr16:20566750 | C | CTGTATAT others(4): Show |
21 | a0001c0001t0001g0163 a0001c0001t0001g0206 a0001c0001t0001g0207 others(18): Show |
23 | HG00597.hp2 HG00673.hp2 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.-8-1898_-8-1897ins others(11): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566750 | |||||||
chr16:20566750 | C | G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(100): Show |
130 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.-8-1897G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566750 | |||||||
chr16:20566758 | A | AGTATATA others(9): Show |
1 | a0001c0004t0002g0129 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-8-1906_-8-1905ins others(16): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566758 | |||||||
chr16:20566759 | G | C | 5 | a0002c0003t0005g0052 a0003c0007t0007g0313 a0003c0008t0011g0307 others(2): Show |
5 | HG02055.hp2 HG02257.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-1906C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566759 | |||||||
chr16:20566759 | G | GTATATAC others(158): Show |
1 | a0002c0003t0005g0089 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-8-1907_-8-1906ins others(165): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566759 | |||||||
chr16:20566759 | G | GTATATAT others(2): Show |
88 | a0001c0002t0002g0118 a0001c0002t0003g0116 a0001c0006t0011g0115 others(85): Show |
93 | HG00673.hp1 HG01099.hp2 HG01256.hp1 others(90): Show |
intron_variant | MODIFIER | c.-8-1907_-8-1906ins others(9): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566759 | |||||||
chr16:20566759 | G | GTATATAT others(180): Show |
2 | a0002c0003t0010g0005 a0002c0018t0010g0046 |
4 | HG02559.hp2 HG02970.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-1907_-8-1906ins others(187): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566759 | |||||||
chr16:20566759 | G | T | 3 | a0001c0002t0003g0013 a0003c0007t0003g0014 a0014c0028t0003g0123 |
5 | HG02486.hp2 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-1906C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566759 | |||||||
chr16:20566920 | A | T | 1 | a0002c0003t0005g0051 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-8-2067T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566920 | |||||||
chr16:20566937 | A | T | 29 | a0001c0002t0002g0118 a0001c0002t0003g0116 a0001c0006t0011g0115 others(26): Show |
31 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(28): Show |
intron_variant | MODIFIER | c.-8-2084T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566937 | |||||||
chr16:20566952 | ATATATAT | A | 16 | a0001c0002t0002g0118 a0001c0002t0003g0116 a0001c0002t0007g0109 others(13): Show |
17 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.-8-2106_-8-2100del others(7): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566952 | |||||||
chr16:20567070 | T | C | 234 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(231): Show |
273 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(270): Show |
intron_variant | MODIFIER | c.-8-2217A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20567070 | |||||||
chr16:20567249 | T | G | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(114): Show |
144 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.-8-2396A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20567249 | |||||||
chr16:20567346 | AATATATT | A | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(215): Show |
254 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(251): Show |
intron_variant | MODIFIER | c.-8-2500_-8-2494del others(7): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20567346 | |||||||
chr16:20567381 | TATA | T | 12 | a0003c0007t0007g0313 a0003c0007t0014g0331 a0003c0007t0014g0332 others(9): Show |
13 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-8-2531_-8-2529del others(3): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20567381 | |||||||
chr16:20567396 | A | G | 1 | a0010c0023t0027g0323 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-8-2543T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20567396 | |||||||
chr16:20567405 | T | C | 2 | a0003c0008t0003g0125 a0003c0025t0003g0124 |
2 | HG03704.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-8-2552A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20567405 | |||||||
chr16:20567416 | T | C | 1 | a0001c0004t0004g0214 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-8-2563A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20567416 | |||||||
chr16:20567463 | TATA | T | 3 | a0001c0002t0007g0031 a0001c0002t0007g0240 a0003c0007t0007g0248 |
4 | HG00639.hp2 HG00741.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-2613_-8-2611del others(3): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20567463 | |||||||
chr16:20567493 | A | AATATATA others(4): Show |
230 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(227): Show |
268 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(265): Show |
intron_variant | MODIFIER | c.-8-2651_-8-2641dup others(11): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20567493 | |||||||
chr16:20567510 | A | T | 1 | a0001c0001t0003g0147 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-8-2657T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20567510 | |||||||
chr16:20567512 | T | A | 1 | a0001c0001t0003g0147 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-8-2659A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20567512 | |||||||
chr16:20567520 | A | AAAGTAAT others(6): Show |
1 | a0001c0001t0003g0147 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-8-2668_-8-2667ins others(13): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20567520 | |||||||
chr16:20567522 | A | G | 1 | a0008c0013t0002g0111 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-8-2669T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20567522 | |||||||
chr16:20567531 | A | C | 1 | a0001c0001t0001g0163 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-8-2678T>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20567531 | |||||||
chr16:20567619 | G | A | 1 | a0001c0002t0007g0109 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-8-2766C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20567619 | |||||||
chr16:20567642 | A | C | 12 | a0003c0007t0007g0313 a0003c0007t0014g0331 a0003c0007t0014g0332 others(9): Show |
13 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-8-2789T>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20567642 | |||||||
chr16:20567645 | C | G | 96 | a0001c0002t0002g0118 a0001c0002t0003g0116 a0001c0006t0011g0115 others(93): Show |
103 | HG00673.hp1 HG01099.hp2 HG01256.hp1 others(100): Show |
intron_variant | MODIFIER | c.-8-2792G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20567645 | |||||||
chr16:20567669 | C | G | 1 | a0001c0002t0004g0260 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-8-2816G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20567669 | |||||||
chr16:20567669 | C | T | 8 | a0001c0002t0002g0118 a0001c0002t0003g0116 a0001c0006t0011g0115 others(5): Show |
8 | HG02257.hp1 HG02717.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.-8-2816G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20567669 | |||||||
chr16:20567684 | A | G | 1 | a0001c0002t0003g0256 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-8-2831T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20567684 | |||||||
chr16:20567698 | A | C | 12 | a0003c0007t0007g0313 a0003c0007t0014g0331 a0003c0007t0014g0332 others(9): Show |
13 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-8-2845T>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20567698 | |||||||
chr16:20567731 | G | C | 1 | a0001c0002t0004g0301 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-8-2878C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20567731 | |||||||
chr16:20567808 | T | C | 1 | a0006c0020t0020g0042 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-8-2955A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20567808 | |||||||
chr16:20567823 | T | C | 1 | a0001c0002t0002g0249 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-8-2970A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20567823 | |||||||
chr16:20567973 | T | C | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(77): Show |
104 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.-8-3120A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20567973 | |||||||
chr16:20568083 | A | G | 1 | a0001c0001t0001g0018 | 2 | NA18989.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.-8-3230T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20568083 | |||||||
chr16:20568286 | T | C | 1 | a0004c0005t0006g0108 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-8-3433A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20568286 | |||||||
chr16:20568335 | TATATA | T | 36 | a0001c0001t0001g0126 a0001c0001t0001g0135 a0001c0001t0001g0136 others(33): Show |
39 | HG00558.hp1 HG00597.hp1 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.-8-3487_-8-3483del others(5): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20568335 | |||||||
chr16:20568341 | A | T | 1 | a0001c0001t0003g0147 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-8-3488T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20568341 | |||||||
chr16:20568342 | T | C | 1 | a0001c0001t0003g0147 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-8-3489A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20568342 | |||||||
chr16:20568344 | T | C | 1 | a0003c0008t0011g0312 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-8-3491A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20568344 | |||||||
chr16:20568350 | A | T | 67 | a0002c0003t0005g0009 a0002c0003t0005g0010 a0002c0003t0005g0048 others(64): Show |
72 | HG00673.hp1 HG01099.hp2 HG01256.hp1 others(69): Show |
intron_variant | MODIFIER | c.-8-3497T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20568350 | |||||||
chr16:20568444 | T | C | 12 | a0003c0007t0007g0313 a0003c0007t0014g0331 a0003c0007t0014g0332 others(9): Show |
13 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-8-3591A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20568444 | |||||||
chr16:20568470 | T | C | 1 | a0006c0020t0020g0042 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-8-3617A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20568470 | |||||||
chr16:20568484 | G | C | 1 | a0001c0002t0002g0249 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-8-3631C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20568484 | |||||||
chr16:20568611 | G | T | 3 | a0003c0008t0001g0310 a0003c0008t0015g0039 a0003c0008t0015g0309 |
4 | HG02615.hp1 HG02809.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-3758C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20568611 | |||||||
chr16:20568627 | T | C | 1 | a0001c0001t0001g0215 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-8-3774A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20568627 | |||||||
chr16:20568904 | T | C | 67 | a0002c0003t0005g0009 a0002c0003t0005g0010 a0002c0003t0005g0048 others(64): Show |
72 | HG00673.hp1 HG01099.hp2 HG01256.hp1 others(69): Show |
intron_variant | MODIFIER | c.-8-4051A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20568904 | |||||||
chr16:20569030 | G | T | 1 | a0001c0017t0004g0033 | 2 | HG02698.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.-8-4177C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20569030 | |||||||
chr16:20569042 | C | T | 1 | a0001c0001t0003g0162 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-8-4189G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20569042 | |||||||
chr16:20569090 | C | T | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(215): Show |
254 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(251): Show |
intron_variant | MODIFIER | c.-8-4237G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20569090 | |||||||
chr16:20569328 | C | T | 1 | a0001c0004t0002g0130 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-8-4475G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20569328 | |||||||
chr16:20569357 | G | A | 1 | a0004c0005t0006g0096 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-8-4504C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20569357 | |||||||
chr16:20569431 | C | T | 1 | a0001c0002t0003g0013 | 2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-8-4578G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20569431 | |||||||
chr16:20569499 | G | A | 1 | a0001c0002t0022g0302 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-8-4646C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20569499 | |||||||
chr16:20569519 | T | G | 2 | a0002c0003t0010g0005 a0002c0018t0010g0046 |
4 | HG02559.hp2 HG02970.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-4666A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20569519 | |||||||
chr16:20569530 | G | C | 1 | a0001c0002t0022g0302 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-8-4677C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20569530 | |||||||
chr16:20569566 | G | C | 3 | a0001c0001t0001g0027 a0001c0001t0001g0217 a0001c0004t0007g0216 |
4 | NA18943.hp1 NA19002.hp1 NA19072.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-4713C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20569566 | |||||||
chr16:20569594 | C | T | 311 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(308): Show |
362 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(359): Show |
intron_variant | MODIFIER | c.-8-4741G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20569594 | |||||||
chr16:20569648 | G | C | 1 | a0001c0002t0002g0249 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-8-4795C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20569648 | |||||||
chr16:20569791 | G | C | 1 | a0002c0003t0005g0090 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-8-4938C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20569791 | |||||||
chr16:20569878 | A | G | 1 | a0002c0003t0005g0050 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-8-5025T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20569878 | |||||||
chr16:20570006 | C | G | 1 | a0001c0001t0001g0161 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-8-5153G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20570006 | |||||||
chr16:20570010 | A | T | 1 | a0001c0001t0001g0161 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-8-5157T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20570010 | |||||||
chr16:20570266 | T | C | 1 | a0003c0007t0004g0303 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-8-5413A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20570266 | |||||||
chr16:20570294 | C | T | 15 | a0001c0002t0002g0118 a0001c0002t0003g0116 a0001c0006t0011g0115 others(12): Show |
16 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.-8-5441G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20570294 | |||||||
chr16:20570322 | G | T | 1 | a0002c0003t0005g0049 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-8-5469C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20570322 | |||||||
chr16:20570509 | G | T | 15 | a0001c0002t0002g0118 a0001c0002t0003g0116 a0001c0006t0011g0115 others(12): Show |
16 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.-8-5656C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20570509 | |||||||
chr16:20570534 | C | T | 1 | a0001c0002t0002g0227 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-9+5673G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20570534 | |||||||
chr16:20570551 | G | C | 15 | a0001c0002t0002g0118 a0001c0002t0003g0116 a0001c0006t0011g0115 others(12): Show |
16 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.-9+5656C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20570551 | |||||||
chr16:20570721 | A | G | 17 | a0001c0002t0002g0118 a0001c0002t0003g0116 a0001c0006t0011g0115 others(14): Show |
18 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.-9+5486T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20570721 | |||||||
chr16:20570796 | C | G | 3 | a0001c0001t0008g0326 a0001c0001t0008g0327 a0001c0001t0008g0328 |
3 | HG02155.hp1 NA18612.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.-9+5411G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20570796 | |||||||
chr16:20570800 | G | A | 2 | a0003c0008t0003g0125 a0003c0025t0003g0124 |
2 | HG03704.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-9+5407C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20570800 | |||||||
chr16:20570962 | TC | T | 10 | a0003c0007t0007g0313 a0003c0007t0014g0331 a0003c0007t0014g0332 others(7): Show |
11 | HG02055.hp2 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-9+5244delG | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20570962 | |||||||
chr16:20570963 | C | T | 2 | a0003c0008t0011g0311 a0003c0008t0011g0312 |
2 | HG02145.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-9+5244G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20570963 | |||||||
chr16:20571276 | G | A | 1 | a0003c0008t0011g0308 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-9+4931C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20571276 | |||||||
chr16:20571363 | T | C | 1 | a0003c0008t0011g0308 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-9+4844A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20571363 | |||||||
chr16:20571371 | T | C | 1 | a0003c0008t0011g0308 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-9+4836A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20571371 | |||||||
chr16:20571509 | A | C | 8 | a0001c0002t0002g0118 a0001c0002t0003g0116 a0001c0006t0011g0115 others(5): Show |
8 | HG02257.hp1 HG02717.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.-9+4698T>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20571509 | |||||||
chr16:20571539 | A | G | 1 | a0003c0007t0007g0313 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-9+4668T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20571539 | |||||||
chr16:20571540 | T | C | 3 | a0001c0002t0002g0250 a0001c0002t0002g0251 a0001c0002t0002g0252 |
3 | HG01167.hp1 HG01169.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.-9+4667A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20571540 | |||||||
chr16:20571550 | G | T | 1 | a0001c0004t0002g0129 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-9+4657C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20571550 | |||||||
chr16:20571597 | G | A | 5 | a0001c0002t0003g0013 a0003c0007t0003g0014 a0003c0008t0003g0125 others(2): Show |
7 | HG02486.hp2 HG02572.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9+4610C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20571597 | |||||||
chr16:20571646 | C | A | 1 | a0010c0023t0027g0323 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-9+4561G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20571646 | |||||||
chr16:20571756 | A | G | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(210): Show |
247 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(244): Show |
intron_variant | MODIFIER | c.-9+4451T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20571756 | |||||||
chr16:20571870 | G | T | 13 | a0005c0011t0008g0320 a0005c0011t0008g0321 a0005c0011t0008g0322 others(10): Show |
15 | HG01168.hp1 HG01169.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.-9+4337C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20571870 | |||||||
chr16:20571916 | G | T | 12 | a0003c0007t0007g0313 a0003c0007t0014g0331 a0003c0007t0014g0332 others(9): Show |
13 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-9+4291C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20571916 | |||||||
chr16:20572060 | A | G | 37 | a0001c0001t0001g0126 a0001c0001t0001g0135 a0001c0001t0001g0136 others(34): Show |
40 | HG00558.hp1 HG00597.hp1 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.-9+4147T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20572060 | |||||||
chr16:20572238 | G | C | 1 | a0001c0004t0002g0148 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-9+3969C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20572238 | |||||||
chr16:20572238 | G | T | 67 | a0002c0003t0005g0009 a0002c0003t0005g0010 a0002c0003t0005g0048 others(64): Show |
72 | HG00673.hp1 HG01099.hp2 HG01256.hp1 others(69): Show |
intron_variant | MODIFIER | c.-9+3969C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20572238 | |||||||
chr16:20572267 | C | A | 12 | a0004c0005t0006g0097 a0004c0005t0006g0098 a0004c0005t0006g0099 others(9): Show |
12 | HG01934.hp2 HG02258.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.-9+3940G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20572267 | |||||||
chr16:20572460 | T | C | 2 | a0006c0020t0003g0110 a0006c0020t0020g0042 |
2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-9+3747A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20572460 | |||||||
chr16:20572490 | T | C | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(216): Show |
256 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(253): Show |
intron_variant | MODIFIER | c.-9+3717A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20572490 | |||||||
chr16:20572509 | C | T | 1 | a0001c0002t0003g0255 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-9+3698G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20572509 | |||||||
chr16:20572572 | A | G | 3 | a0001c0002t0004g0257 a0001c0002t0004g0258 a0001c0002t0004g0259 |
3 | HG01167.hp2 HG02683.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-9+3635T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20572572 | |||||||
chr16:20572633 | T | C | 1 | a0001c0001t0001g0218 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-9+3574A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20572633 | |||||||
chr16:20572664 | T | C | 2 | a0003c0008t0003g0125 a0003c0025t0003g0124 |
2 | HG03704.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-9+3543A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20572664 | |||||||
chr16:20572667 | A | G | 65 | a0002c0003t0005g0009 a0002c0003t0005g0010 a0002c0003t0005g0048 others(62): Show |
68 | HG00673.hp1 HG01099.hp2 HG01256.hp1 others(65): Show |
intron_variant | MODIFIER | c.-9+3540T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20572667 | |||||||
chr16:20572774 | A | T | 66 | a0002c0003t0005g0009 a0002c0003t0005g0010 a0002c0003t0005g0048 others(63): Show |
71 | HG00673.hp1 HG01099.hp2 HG01256.hp1 others(68): Show |
intron_variant | MODIFIER | c.-9+3433T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20572774 | |||||||
chr16:20572775 | T | A | 2 | a0003c0008t0003g0125 a0003c0025t0003g0124 |
2 | HG03704.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-9+3432A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20572775 | |||||||
chr16:20572965 | A | C | 1 | a0001c0001t0001g0001 | 6 | NA18970.hp1 NA18972.hp2 NA18988.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9+3242T>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20572965 | |||||||
chr16:20572974 | A | AT | 65 | a0001c0002t0002g0118 a0001c0002t0003g0116 a0001c0002t0003g0255 others(62): Show |
71 | HG00673.hp1 HG01081.hp2 HG01256.hp1 others(68): Show |
intron_variant | MODIFIER | c.-9+3232dupA | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20572974 | |||||||
chr16:20572974 | AT | A | 128 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(125): Show |
156 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.-9+3232delA | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20572974 | |||||||
chr16:20572974 | ATT | A | 8 | a0001c0002t0003g0013 a0001c0004t0002g0149 a0003c0007t0003g0014 others(5): Show |
11 | HG00597.hp2 HG01891.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.-9+3231_-9+3232del others(2): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20572974 | |||||||
chr16:20572978 | T | C | 12 | a0003c0007t0007g0313 a0003c0007t0014g0331 a0003c0007t0014g0332 others(9): Show |
13 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-9+3229A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20572978 | |||||||
chr16:20572980 | T | C | 5 | a0001c0002t0003g0013 a0003c0007t0003g0014 a0003c0008t0003g0125 others(2): Show |
7 | HG02486.hp2 HG02572.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9+3227A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20572980 | |||||||
chr16:20573003 | C | A | 1 | a0001c0004t0002g0156 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-9+3204G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20573003 | |||||||
chr16:20573005 | C | G | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(126): Show |
157 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.-9+3202G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20573005 | |||||||
chr16:20573108 | A | G | 2 | a0001c0002t0003g0253 a0001c0002t0003g0254 |
2 | HG02451.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-9+3099T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20573108 | |||||||
chr16:20573119 | T | G | 3 | a0003c0008t0001g0310 a0003c0008t0015g0039 a0003c0008t0015g0309 |
4 | HG02615.hp1 HG02809.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+3088A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20573119 | |||||||
chr16:20573140 | C | T | 1 | a0007c0014t0001g0160 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-9+3067G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20573140 | |||||||
chr16:20573172 | T | A | 5 | a0001c0001t0001g0150 a0001c0001t0003g0151 a0001c0001t0003g0152 others(2): Show |
6 | HG00597.hp1 HG00621.hp1 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9+3035A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20573172 | |||||||
chr16:20573310 | G | T | 1 | a0001c0001t0003g0128 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-9+2897C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20573310 | |||||||
chr16:20573363 | G | A | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(114): Show |
144 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.-9+2844C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20573363 | |||||||
chr16:20573459 | T | C | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(210): Show |
247 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(244): Show |
intron_variant | MODIFIER | c.-9+2748A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20573459 | |||||||
chr16:20573525 | G | T | 2 | a0003c0008t0003g0125 a0003c0025t0003g0124 |
2 | HG03704.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-9+2682C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20573525 | |||||||
chr16:20573528 | T | A | 137 | a0001c0002t0002g0281 a0001c0002t0002g0284 a0001c0002t0002g0295 others(134): Show |
151 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.-9+2679A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20573528 | |||||||
chr16:20573661 | G | C | 1 | a0003c0007t0007g0313 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-9+2546C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20573661 | |||||||
chr16:20573681 | C | T | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(77): Show |
104 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.-9+2526G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20573681 | |||||||
chr16:20573759 | G | A | 1 | a0001c0002t0007g0220 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-9+2448C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20573759 | |||||||
chr16:20573822 | A | T | 1 | a0003c0008t0011g0307 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-9+2385T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20573822 | |||||||
chr16:20573890 | A | G | 2 | a0003c0008t0003g0125 a0003c0025t0003g0124 |
2 | HG03704.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-9+2317T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20573890 | |||||||
chr16:20573940 | T | C | 1 | a0001c0006t0003g0304 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-9+2267A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20573940 | |||||||
chr16:20573993 | G | A | 1 | a0005c0024t0016g0325 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-9+2214C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20573993 | |||||||
chr16:20574052 | C | T | 1 | a0001c0002t0004g0226 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-9+2155G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20574052 | |||||||
chr16:20574054 | A | G | 4 | a0001c0001t0001g0159 a0001c0006t0003g0224 a0001c0006t0003g0225 others(1): Show |
4 | HG00609.hp2 NA18961.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+2153T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20574054 | |||||||
chr16:20574145 | A | G | 2 | a0001c0012t0007g0028 a0001c0012t0007g0222 |
3 | HG02965.hp1 HG02970.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-9+2062T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20574145 | |||||||
chr16:20574242 | G | A | 2 | a0006c0020t0003g0110 a0006c0020t0020g0042 |
2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-9+1965C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20574242 | |||||||
chr16:20574309 | C | T | 12 | a0003c0007t0007g0313 a0003c0007t0014g0331 a0003c0007t0014g0332 others(9): Show |
13 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-9+1898G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20574309 | |||||||
chr16:20574311 | G | A | 2 | a0006c0020t0003g0110 a0006c0020t0020g0042 |
2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-9+1896C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20574311 | |||||||
chr16:20574358 | T | C | 2 | a0003c0008t0003g0125 a0003c0025t0003g0124 |
2 | HG03704.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-9+1849A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20574358 | |||||||
chr16:20574617 | C | T | 1 | a0006c0020t0020g0042 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-9+1590G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20574617 | |||||||
chr16:20574689 | C | T | 68 | a0001c0002t0007g0109 a0002c0003t0005g0009 a0002c0003t0005g0010 others(65): Show |
73 | HG00673.hp1 HG01099.hp2 HG01256.hp1 others(70): Show |
intron_variant | MODIFIER | c.-9+1518G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20574689 | |||||||
chr16:20574860 | T | C | 14 | a0001c0001t0003g0127 a0001c0004t0002g0154 a0003c0007t0007g0313 others(11): Show |
15 | HG01168.hp2 HG02055.hp2 HG02056.hp2 others(12): Show |
intron_variant | MODIFIER | c.-9+1347A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20574860 | |||||||
chr16:20574862 | G | T | 13 | a0001c0001t0003g0127 a0003c0007t0007g0313 a0003c0007t0014g0331 others(10): Show |
14 | HG02055.hp2 HG02056.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.-9+1345C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20574862 | |||||||
chr16:20574871 | A | T | 1 | a0001c0002t0002g0221 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-9+1336T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20574871 | |||||||
chr16:20574876 | C | T | 1 | a0003c0008t0011g0307 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-9+1331G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20574876 | |||||||
chr16:20574917 | A | T | 1 | a0002c0003t0005g0048 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-9+1290T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20574917 | |||||||
chr16:20574949 | A | G | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(210): Show |
247 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(244): Show |
intron_variant | MODIFIER | c.-9+1258T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20574949 | |||||||
chr16:20575140 | G | T | 12 | a0003c0007t0007g0313 a0003c0007t0014g0331 a0003c0007t0014g0332 others(9): Show |
13 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-9+1067C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20575140 | |||||||
chr16:20575174 | G | GAACTCCA others(12): Show |
2 | a0001c0004t0002g0155 a0001c0004t0002g0156 |
2 | HG01952.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.-9+1014_-9+1032dup others(19): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20575174 | |||||||
chr16:20575200 | T | G | 93 | a0001c0002t0002g0118 a0001c0002t0003g0116 a0001c0006t0011g0115 others(90): Show |
98 | HG00673.hp1 HG01099.hp2 HG01256.hp1 others(95): Show |
intron_variant | MODIFIER | c.-9+1007A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20575200 | |||||||
chr16:20575297 | A | G | 17 | a0001c0002t0002g0118 a0001c0002t0003g0116 a0001c0006t0011g0115 others(14): Show |
18 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.-9+910T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20575297 | |||||||
chr16:20575331 | A | G | 1 | a0001c0002t0007g0220 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-9+876T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20575331 | |||||||
chr16:20575338 | T | G | 1 | a0001c0006t0003g0305 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-9+869A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20575338 | |||||||
chr16:20575464 | GC | G | 17 | a0001c0002t0002g0118 a0001c0002t0003g0116 a0001c0006t0011g0115 others(14): Show |
18 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.-9+742delG | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20575464 | |||||||
chr16:20575465 | C | G | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(212): Show |
252 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(249): Show |
intron_variant | MODIFIER | c.-9+742G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20575465 | |||||||
chr16:20575476 | A | G | 2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | NA18951.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.-9+731T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20575476 | |||||||
chr16:20575534 | A | C | 1 | a0001c0002t0007g0109 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-9+673T>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20575534 | |||||||
chr16:20575538 | C | T | 1 | a0001c0002t0007g0109 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-9+669G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20575538 | |||||||
chr16:20575597 | C | G | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(215): Show |
254 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(251): Show |
intron_variant | MODIFIER | c.-9+610G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20575597 | |||||||
chr16:20575629 | G | T | 1 | a0001c0002t0004g0219 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-9+578C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20575629 | |||||||
chr16:20575714 | C | T | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(114): Show |
144 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.-9+493G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20575714 | |||||||
chr16:20575741 | A | G | 4 | a0003c0007t0014g0331 a0003c0007t0014g0332 a0003c0007t0014g0333 others(1): Show |
4 | HG02258.hp2 HG02717.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9+466T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20575741 | |||||||
chr16:20575784 | C | G | 37 | a0001c0001t0001g0126 a0001c0001t0001g0135 a0001c0001t0001g0136 others(34): Show |
40 | HG00558.hp1 HG00597.hp1 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.-9+423G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20575784 | |||||||
chr16:20575797 | T | G | 65 | a0002c0003t0005g0009 a0002c0003t0005g0010 a0002c0003t0005g0048 others(62): Show |
68 | HG00673.hp1 HG01099.hp2 HG01256.hp1 others(65): Show |
intron_variant | MODIFIER | c.-9+410A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20575797 | |||||||
chr16:20575806 | A | G | 17 | a0001c0002t0002g0118 a0001c0002t0003g0116 a0001c0006t0011g0115 others(14): Show |
18 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.-9+401T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20575806 | |||||||
chr16:20575809 | G | T | 2 | a0006c0020t0003g0110 a0006c0020t0020g0042 |
2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-9+398C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20575809 | |||||||
chr16:20575874 | G | T | 1 | a0001c0001t0001g0126 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-9+333C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20575874 | |||||||
chr16:20575932 | G | A | 1 | a0001c0002t0002g0306 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-9+275C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20575932 | |||||||
chr16:20575969 | C | A | 26 | a0001c0002t0007g0109 a0003c0007t0007g0313 a0003c0007t0014g0331 others(23): Show |
29 | HG01168.hp1 HG01169.hp1 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.-9+238G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20575969 | |||||||
chr16:20576003 | T | C | 1 | a0001c0002t0004g0314 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-9+204A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20576003 | |||||||
chr16:20576024 | C | G | 89 | a0001c0002t0002g0118 a0001c0002t0003g0013 a0001c0002t0003g0116 others(86): Show |
97 | HG00673.hp1 HG01099.hp2 HG01256.hp1 others(94): Show |
intron_variant | MODIFIER | c.-9+183G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20576024 | |||||||
chr16:20576039 | G | T | 1 | a0001c0002t0007g0109 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-9+168C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20576039 | |||||||
chr16:20576204 | C | T | 13 | a0005c0011t0008g0320 a0005c0011t0008g0321 a0005c0011t0008g0322 others(10): Show |
15 | HG01168.hp1 HG01169.hp1 HG01891.hp1 others(12): Show |
splice_region_variant&intron_variant | LOW | c.-9+3G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20576204 |