Item | Value |
---|---|
geneid | 79587 |
ensemblid | ENSG00000134905.17 |
hgncid | 25695 |
symbol | CARS2 |
name | cysteinyl-tRNA synthetase 2, mitochondrial |
refseq_nuc | NM_024537.4 |
refseq_prot | NP_078813.1 |
ensembl_nuc | ENST00000257347.9 |
ensembl_prot | ENSP00000257347.4 |
mane_status | MANE Select |
chr | chr13 |
start | 110641417 |
end | 110706116 |
strand | - |
ver | v1.2 |
region | chr13:110641417-110706116 |
region5000 | chr13:110636417-110711116 |
regionname0 | CARS2_chr13_110641417_110706116 |
regionname5000 | CARS2_chr13_110636417_110711116 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 564 | 282 | 73 | 52 | 116 | 10 | 29 | 96 | CARS2_chr13_110636417_110711116 | CARS2 | MLRTT others(559): Show |
chr13 | 110636417 | 110711116 |
a0002 | 0/0 | 564 | 43 | 6 | 11 | 19 | 2 | 5 | 15 | CARS2_chr13_110636417_110711116 | CARS2 | MLRTT others(559): Show |
chr13 | 110636417 | 110711116 |
a0003 | 0/0 | 564 | 26 | 3 | 9 | 12 | 2 | 0 | 6 | CARS2_chr13_110636417_110711116 | CARS2 | MLRTT others(559): Show |
chr13 | 110636417 | 110711116 |
a0004 | 0/0 | 564 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | MLRTT others(559): Show |
chr13 | 110636417 | 110711116 |
a0005 | 0/0 | 564 | 3 | 0 | 0 | 0 | 0 | 3 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | MLRTT others(559): Show |
chr13 | 110636417 | 110711116 |
a0006 | 0/0 | 564 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | MLRTT others(559): Show |
chr13 | 110636417 | 110711116 |
a0007 | 0/0 | 564 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | MLRTT others(559): Show |
chr13 | 110636417 | 110711116 |
a0008 | 0/0 | 564 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CARS2_chr13_110636417_110711116 | CARS2 | MLRTT others(559): Show |
chr13 | 110636417 | 110711116 |
a0009 | 0/0 | 564 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | MLRTT others(559): Show |
chr13 | 110636417 | 110711116 |
a0010 | 0/0 | 564 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | MLRTT others(559): Show |
chr13 | 110636417 | 110711116 |
a0011 | 0/0 | 564 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | MLRTT others(559): Show |
chr13 | 110636417 | 110711116 |
a0012 | 0/0 | 564 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | MLRTT others(559): Show |
chr13 | 110636417 | 110711116 |
a0013 | 0/0 | 564 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | MLRTT others(559): Show |
chr13 | 110636417 | 110711116 |
a0014 | 0/0 | 564 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | MLRTT others(559): Show |
chr13 | 110636417 | 110711116 |
a0015 | 0/0 | 564 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | MLRTT others(559): Show |
chr13 | 110636417 | 110711116 |
a0016 | 0/0 | 564 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | MLRTT others(559): Show |
chr13 | 110636417 | 110711116 |
a0017 | 0/0 | 564 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | MLRTT others(559): Show |
chr13 | 110636417 | 110711116 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1692 | 121 | 21 | 18 | 68 | 4 | 10 | CARS2_chr13_110636417_110711116 | CARS2 | ATGTT others(1687): Show |
chr13 | 110636417 | 110711116 | ||
a0001c0002 | 0/1 | 1692 | 72 | 18 | 18 | 27 | 1 | 7 | CARS2_chr13_110636417_110711116 | CARS2 | ATGTT others(1687): Show |
chr13 | 110636417 | 110711116 | ||
a0001c0003 | 0/0 | 1692 | 47 | 23 | 7 | 8 | 0 | 9 | CARS2_chr13_110636417_110711116 | CARS2 | ATGTT others(1687): Show |
chr13 | 110636417 | 110711116 | ||
a0001c0005 | 0/0 | 1692 | 27 | 2 | 6 | 12 | 5 | 2 | CARS2_chr13_110636417_110711116 | CARS2 | ATGTT others(1687): Show |
chr13 | 110636417 | 110711116 | ||
a0001c0007 | 1/0 | 1692 | 8 | 5 | 1 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | ATGTT others(1687): Show |
chr13 | 110636417 | 110711116 | ||
a0001c0009 | 0/0 | 1692 | 3 | 3 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | ATGTT others(1687): Show |
chr13 | 110636417 | 110711116 | ||
a0001c0019 | 0/0 | 1692 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | ATGTT others(1687): Show |
chr13 | 110636417 | 110711116 | ||
a0001c0020 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | ATGTT others(1687): Show |
chr13 | 110636417 | 110711116 | ||
a0001c0025 | 0/0 | 1692 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | ATGTT others(1687): Show |
chr13 | 110636417 | 110711116 | ||
a0001c0027 | 0/0 | 1692 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | ATGTT others(1687): Show |
chr13 | 110636417 | 110711116 | ||
a0002c0004 | 0/0 | 1692 | 38 | 4 | 9 | 19 | 2 | 4 | CARS2_chr13_110636417_110711116 | CARS2 | ATGTT others(1687): Show |
chr13 | 110636417 | 110711116 | ||
a0002c0008 | 0/0 | 1692 | 5 | 2 | 2 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | ATGTT others(1687): Show |
chr13 | 110636417 | 110711116 | ||
a0003c0006 | 0/0 | 1692 | 21 | 0 | 8 | 11 | 2 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | ATGTT others(1687): Show |
chr13 | 110636417 | 110711116 | ||
a0003c0011 | 0/0 | 1692 | 3 | 3 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | ATGTT others(1687): Show |
chr13 | 110636417 | 110711116 | ||
a0003c0024 | 0/0 | 1692 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | ATGTT others(1687): Show |
chr13 | 110636417 | 110711116 | ||
a0003c0028 | 0/0 | 1692 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | ATGTT others(1687): Show |
chr13 | 110636417 | 110711116 | ||
a0004c0012 | 0/0 | 1692 | 3 | 3 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | ATGTT others(1687): Show |
chr13 | 110636417 | 110711116 | ||
a0005c0010 | 0/0 | 1692 | 3 | 0 | 0 | 0 | 0 | 3 | CARS2_chr13_110636417_110711116 | CARS2 | ATGTT others(1687): Show |
chr13 | 110636417 | 110711116 | ||
a0006c0015 | 0/0 | 1692 | 2 | 2 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | ATGTT others(1687): Show |
chr13 | 110636417 | 110711116 | ||
a0007c0014 | 0/0 | 1692 | 2 | 2 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | ATGTT others(1687): Show |
chr13 | 110636417 | 110711116 | ||
a0008c0013 | 0/0 | 1692 | 2 | 0 | 0 | 2 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | ATGTT others(1687): Show |
chr13 | 110636417 | 110711116 | ||
a0009c0029 | 0/0 | 1692 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | ATGTT others(1687): Show |
chr13 | 110636417 | 110711116 | ||
a0010c0018 | 0/0 | 1692 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | ATGTT others(1687): Show |
chr13 | 110636417 | 110711116 | ||
a0011c0017 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | ATGTT others(1687): Show |
chr13 | 110636417 | 110711116 | ||
a0012c0030 | 0/0 | 1692 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | ATGTT others(1687): Show |
chr13 | 110636417 | 110711116 | ||
a0013c0023 | 0/0 | 1692 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | ATGTT others(1687): Show |
chr13 | 110636417 | 110711116 | ||
a0014c0022 | 0/0 | 1692 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | ATGTT others(1687): Show |
chr13 | 110636417 | 110711116 | ||
a0015c0021 | 0/0 | 1692 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | ATGTT others(1687): Show |
chr13 | 110636417 | 110711116 | ||
a0016c0026 | 0/0 | 1692 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | ATGTT others(1687): Show |
chr13 | 110636417 | 110711116 | ||
a0017c0016 | 0/0 | 1692 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | ATGTT others(1687): Show |
chr13 | 110636417 | 110711116 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 1838 | 106 | 16 | 18 | 58 | 4 | 10 | CARS2_chr13_110636417_110711116 | CARS2 | AGTCG others(1833): Show |
chr13 | 110636417 | 110711116 |
a0001c0001t0002 | 0/0 | 1838 | 15 | 5 | 0 | 10 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | AGTCG others(1833): Show |
chr13 | 110636417 | 110711116 |
a0001c0002t0001 | 0/1 | 1838 | 52 | 3 | 15 | 25 | 1 | 7 | CARS2_chr13_110636417_110711116 | CARS2 | AGTCG others(1833): Show |
chr13 | 110636417 | 110711116 |
a0001c0002t0002 | 0/0 | 1838 | 17 | 12 | 3 | 2 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | AGTCG others(1833): Show |
chr13 | 110636417 | 110711116 |
a0001c0002t0003 | 0/0 | 1838 | 3 | 3 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | AGTCG others(1833): Show |
chr13 | 110636417 | 110711116 |
a0001c0003t0001 | 0/0 | 1838 | 17 | 11 | 3 | 0 | 0 | 3 | CARS2_chr13_110636417_110711116 | CARS2 | AGTCG others(1833): Show |
chr13 | 110636417 | 110711116 |
a0001c0003t0002 | 0/0 | 1838 | 30 | 12 | 4 | 8 | 0 | 6 | CARS2_chr13_110636417_110711116 | CARS2 | AGTCG others(1833): Show |
chr13 | 110636417 | 110711116 |
a0001c0005t0001 | 0/0 | 1838 | 26 | 2 | 6 | 11 | 5 | 2 | CARS2_chr13_110636417_110711116 | CARS2 | AGTCG others(1833): Show |
chr13 | 110636417 | 110711116 |
a0001c0005t0002 | 0/0 | 1838 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | AGTCG others(1833): Show |
chr13 | 110636417 | 110711116 |
a0001c0007t0001 | 1/0 | 1838 | 7 | 4 | 1 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | AGTCG others(1833): Show |
chr13 | 110636417 | 110711116 |
a0001c0007t0002 | 0/0 | 1838 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | AGTCG others(1833): Show |
chr13 | 110636417 | 110711116 |
a0001c0009t0002 | 0/0 | 1838 | 3 | 3 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | AGTCG others(1833): Show |
chr13 | 110636417 | 110711116 |
a0001c0019t0001 | 0/0 | 1838 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | AGTCG others(1833): Show |
chr13 | 110636417 | 110711116 |
a0001c0020t0002 | 0/0 | 1838 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | AGTCG others(1833): Show |
chr13 | 110636417 | 110711116 |
a0001c0025t0001 | 0/0 | 1838 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | AGTCG others(1833): Show |
chr13 | 110636417 | 110711116 |
a0001c0027t0001 | 0/0 | 1838 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | AGTCG others(1833): Show |
chr13 | 110636417 | 110711116 |
a0002c0004t0001 | 0/0 | 1838 | 33 | 1 | 9 | 17 | 2 | 4 | CARS2_chr13_110636417_110711116 | CARS2 | AGTCG others(1833): Show |
chr13 | 110636417 | 110711116 |
a0002c0004t0002 | 0/0 | 1838 | 3 | 1 | 0 | 2 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | AGTCG others(1833): Show |
chr13 | 110636417 | 110711116 |
a0002c0004t0003 | 0/0 | 1838 | 2 | 2 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | AGTCG others(1833): Show |
chr13 | 110636417 | 110711116 |
a0002c0008t0001 | 0/0 | 1838 | 4 | 1 | 2 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | AGTCG others(1833): Show |
chr13 | 110636417 | 110711116 |
a0002c0008t0003 | 0/0 | 1838 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | AGTCG others(1833): Show |
chr13 | 110636417 | 110711116 |
a0003c0006t0002 | 0/0 | 1838 | 21 | 0 | 8 | 11 | 2 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | AGTCG others(1833): Show |
chr13 | 110636417 | 110711116 |
a0003c0011t0002 | 0/0 | 1838 | 3 | 3 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | AGTCG others(1833): Show |
chr13 | 110636417 | 110711116 |
a0003c0024t0001 | 0/0 | 1838 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | AGTCG others(1833): Show |
chr13 | 110636417 | 110711116 |
a0003c0028t0001 | 0/0 | 1838 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | AGTCG others(1833): Show |
chr13 | 110636417 | 110711116 |
a0004c0012t0002 | 0/0 | 1838 | 2 | 2 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | AGTCG others(1833): Show |
chr13 | 110636417 | 110711116 |
a0004c0012t0004 | 0/0 | 1888 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | AGTCG others(1883): Show |
chr13 | 110636417 | 110711116 |
a0005c0010t0001 | 0/0 | 1838 | 3 | 0 | 0 | 0 | 0 | 3 | CARS2_chr13_110636417_110711116 | CARS2 | AGTCG others(1833): Show |
chr13 | 110636417 | 110711116 |
a0006c0015t0002 | 0/0 | 1838 | 2 | 2 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | AGTCG others(1833): Show |
chr13 | 110636417 | 110711116 |
a0007c0014t0002 | 0/0 | 1838 | 2 | 2 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | AGTCG others(1833): Show |
chr13 | 110636417 | 110711116 |
a0008c0013t0001 | 0/0 | 1838 | 2 | 0 | 0 | 2 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | AGTCG others(1833): Show |
chr13 | 110636417 | 110711116 |
a0009c0029t0001 | 0/0 | 1838 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | AGTCG others(1833): Show |
chr13 | 110636417 | 110711116 |
a0010c0018t0002 | 0/0 | 1838 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | AGTCG others(1833): Show |
chr13 | 110636417 | 110711116 |
a0011c0017t0002 | 0/0 | 1838 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | AGTCG others(1833): Show |
chr13 | 110636417 | 110711116 |
a0012c0030t0001 | 0/0 | 1838 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | AGTCG others(1833): Show |
chr13 | 110636417 | 110711116 |
a0013c0023t0002 | 0/0 | 1838 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | AGTCG others(1833): Show |
chr13 | 110636417 | 110711116 |
a0014c0022t0001 | 0/0 | 1838 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | AGTCG others(1833): Show |
chr13 | 110636417 | 110711116 |
a0015c0021t0001 | 0/0 | 1838 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | AGTCG others(1833): Show |
chr13 | 110636417 | 110711116 |
a0016c0026t0001 | 0/0 | 1838 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | AGTCG others(1833): Show |
chr13 | 110636417 | 110711116 |
a0017c0016t0001 | 0/0 | 1838 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | AGTCG others(1833): Show |
chr13 | 110636417 | 110711116 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0001g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0001g0196 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0002g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0002g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0003g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0003g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0002t0003g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0003t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0003t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0003t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0003t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0003t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0003t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0003t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0003t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0003t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0003t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0003t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0003t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0003t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0003t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0003t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0003t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0003t0002g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0003t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0003t0002g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0003t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0003t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0003t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0003t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0003t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0003t0002g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0003t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0003t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0003t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0003t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0003t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0003t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0003t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0003t0002g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0003t0002g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0003t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0003t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0003t0002g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0003t0002g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0003t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0003t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0003t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0003t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0005t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0005t0001g0003 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0005t0001g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0005t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0005t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0005t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0005t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0005t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0005t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0005t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0005t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0005t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0005t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0005t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0005t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0005t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0005t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0005t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0005t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0005t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0005t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0005t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0007t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0007t0001g0257 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0007t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0007t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0007t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0007t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0007t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0007t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0009t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0009t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0009t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0019t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0020t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0025t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0001c0027t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0002c0004t0001g0008 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0002c0004t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0002c0004t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0002c0004t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0002c0004t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0002c0004t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0002c0004t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0002c0004t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0002c0004t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0002c0004t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0002c0004t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0002c0004t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0002c0004t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0002c0004t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0002c0004t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0002c0004t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0002c0004t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0002c0004t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0002c0004t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0002c0004t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0002c0004t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0002c0004t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0002c0004t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0002c0004t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0002c0004t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0002c0004t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0002c0004t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0002c0004t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0002c0004t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0002c0004t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0002c0004t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0002c0004t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0002c0004t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0002c0004t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0002c0004t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0002c0004t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0002c0004t0003g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0002c0008t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0002c0008t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0002c0008t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0002c0008t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0002c0008t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0003c0006t0002g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0003c0006t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0003c0006t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0003c0006t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0003c0006t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0003c0006t0002g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0003c0006t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0003c0006t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0003c0006t0002g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0003c0006t0002g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0003c0006t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0003c0006t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0003c0006t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0003c0006t0002g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0003c0006t0002g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0003c0006t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0003c0006t0002g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0003c0006t0002g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0003c0006t0002g0338 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0003c0006t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0003c0011t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0003c0011t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0003c0011t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0003c0024t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0003c0028t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0004c0012t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0004c0012t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0004c0012t0004g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0005c0010t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0005c0010t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0005c0010t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0006c0015t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0006c0015t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0007c0014t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0007c0014t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0008c0013t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0008c0013t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0009c0029t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0010c0018t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0011c0017t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0012c0030t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0013c0023t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0014c0022t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0015c0021t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0016c0026t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
a0017c0016t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | GBR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG00099 | hp2 | a0001 | c0005 | t0001 | g0334 | EUR | GBR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG00140 | hp1 | a0001 | c0005 | t0001 | g0136 | EUR | GBR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0128 | EUR | GBR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG00280 | hp1 | a0003 | c0006 | t0002 | g0335 | EUR | FIN | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | FIN | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG00408 | hp2 | a0003 | c0006 | t0002 | g0320 | EAS | CHS | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG00438 | hp1 | a0001 | c0003 | t0002 | g0301 | EAS | CHS | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG00558 | hp1 | a0003 | c0006 | t0002 | g0333 | EAS | CHS | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | CHS | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG00597 | hp1 | a0002 | c0004 | t0001 | g0044 | EAS | CHS | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG00609 | hp1 | a0001 | c0002 | t0001 | g0201 | EAS | CHS | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG00609 | hp2 | a0001 | c0025 | t0001 | g0113 | EAS | CHS | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG00621 | hp2 | a0001 | c0002 | t0001 | g0190 | EAS | CHS | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG00639 | hp2 | a0001 | c0027 | t0001 | g0172 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG00642 | hp2 | a0001 | c0003 | t0002 | g0286 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG00738 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG00738 | hp2 | a0002 | c0008 | t0001 | g0234 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01069 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01069 | hp2 | a0003 | c0006 | t0002 | g0025 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01070 | hp1 | a0001 | c0002 | t0001 | g0017 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01071 | hp1 | a0003 | c0006 | t0002 | g0025 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01071 | hp2 | a0001 | c0002 | t0001 | g0017 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01074 | hp1 | a0001 | c0003 | t0001 | g0246 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01074 | hp2 | a0001 | c0005 | t0001 | g0016 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01099 | hp2 | a0002 | c0004 | t0001 | g0047 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01106 | hp1 | a0001 | c0002 | t0001 | g0185 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01106 | hp2 | a0009 | c0029 | t0001 | g0173 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01109 | hp1 | a0002 | c0004 | t0001 | g0008 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01109 | hp2 | a0003 | c0006 | t0002 | g0326 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01167 | hp1 | a0001 | c0002 | t0001 | g0195 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01167 | hp2 | a0002 | c0004 | t0001 | g0039 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01168 | hp1 | a0002 | c0004 | t0001 | g0037 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01168 | hp2 | a0001 | c0005 | t0001 | g0168 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01169 | hp1 | a0001 | c0002 | t0001 | g0194 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01169 | hp2 | a0001 | c0005 | t0001 | g0169 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01192 | hp2 | a0010 | c0018 | t0002 | g0263 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01243 | hp1 | a0003 | c0006 | t0002 | g0337 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01243 | hp2 | a0001 | c0003 | t0001 | g0289 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01255 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | CLM | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01255 | hp2 | a0002 | c0004 | t0001 | g0038 | AMR | CLM | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01256 | hp1 | a0003 | c0006 | t0002 | g0332 | AMR | CLM | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01256 | hp2 | a0003 | c0028 | t0001 | g0132 | AMR | CLM | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01257 | hp1 | a0001 | c0002 | t0001 | g0074 | AMR | CLM | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01258 | hp2 | a0003 | c0006 | t0002 | g0331 | AMR | CLM | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01346 | hp1 | a0001 | c0002 | t0002 | g0019 | AMR | CLM | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01358 | hp1 | a0001 | c0002 | t0001 | g0187 | AMR | CLM | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01358 | hp2 | a0002 | c0004 | t0001 | g0049 | AMR | CLM | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01361 | hp1 | a0002 | c0004 | t0001 | g0042 | AMR | CLM | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01433 | hp1 | a0002 | c0008 | t0001 | g0035 | AMR | CLM | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01433 | hp2 | a0001 | c0005 | t0001 | g0175 | AMR | CLM | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01496 | hp1 | a0001 | c0005 | t0001 | g0129 | AMR | CLM | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01496 | hp2 | a0001 | c0002 | t0001 | g0177 | AMR | CLM | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01515 | hp1 | a0002 | c0004 | t0001 | g0043 | EUR | IBS | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01515 | hp2 | a0001 | c0002 | t0001 | g0181 | EUR | IBS | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01517 | hp1 | a0002 | c0004 | t0001 | g0041 | EUR | IBS | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01517 | hp2 | a0001 | c0005 | t0001 | g0133 | EUR | IBS | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01884 | hp2 | a0001 | c0003 | t0002 | g0007 | AFR | ACB | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01891 | hp1 | a0001 | c0002 | t0003 | g0266 | AFR | ACB | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01891 | hp2 | a0001 | c0020 | t0002 | g0300 | AFR | ACB | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01928 | hp2 | a0002 | c0004 | t0001 | g0048 | AMR | PEL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01943 | hp1 | a0001 | c0007 | t0001 | g0271 | AMR | PEL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01943 | hp2 | a0001 | c0019 | t0001 | g0205 | AMR | PEL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01952 | hp1 | a0001 | c0005 | t0001 | g0167 | AMR | PEL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01952 | hp2 | a0001 | c0002 | t0001 | g0209 | AMR | PEL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01975 | hp2 | a0001 | c0003 | t0001 | g0287 | AMR | PEL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01978 | hp1 | a0001 | c0002 | t0002 | g0019 | AMR | PEL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01981 | hp2 | a0001 | c0002 | t0001 | g0208 | AMR | PEL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01993 | hp1 | a0003 | c0006 | t0002 | g0323 | AMR | PEL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01993 | hp2 | a0001 | c0003 | t0002 | g0280 | AMR | PEL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02015 | hp1 | a0002 | c0004 | t0001 | g0033 | EAS | KHV | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02055 | hp1 | a0001 | c0007 | t0001 | g0273 | AFR | ACB | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02055 | hp2 | a0001 | c0003 | t0002 | g0295 | AFR | ACB | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02071 | hp2 | a0001 | c0002 | t0001 | g0214 | EAS | KHV | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02074 | hp1 | a0002 | c0004 | t0001 | g0218 | EAS | KHV | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02074 | hp2 | a0003 | c0006 | t0002 | g0321 | EAS | KHV | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02148 | hp1 | a0001 | c0002 | t0001 | g0183 | AMR | PEL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02148 | hp2 | a0002 | c0004 | t0001 | g0046 | AMR | PEL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | CDX | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02155 | hp2 | a0002 | c0004 | t0001 | g0058 | EAS | CDX | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02257 | hp2 | a0001 | c0003 | t0001 | g0297 | AFR | ACB | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02258 | hp1 | a0001 | c0002 | t0003 | g0267 | AFR | ACB | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02258 | hp2 | a0001 | c0003 | t0002 | g0007 | AFR | ACB | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02273 | hp1 | a0001 | c0003 | t0002 | g0024 | AMR | PEL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02273 | hp2 | a0001 | c0002 | t0002 | g0200 | AMR | PEL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02280 | hp1 | a0002 | c0008 | t0003 | g0243 | AFR | ACB | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02280 | hp2 | a0001 | c0002 | t0002 | g0022 | AFR | ACB | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02293 | hp2 | a0003 | c0006 | t0002 | g0327 | AMR | PEL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02300 | hp2 | a0001 | c0002 | t0001 | g0064 | AMR | PEL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02451 | hp1 | a0001 | c0003 | t0002 | g0285 | AFR | ACB | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02451 | hp2 | a0003 | c0011 | t0002 | g0253 | AFR | ACB | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02523 | hp2 | a0001 | c0002 | t0001 | g0184 | EAS | KHV | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02572 | hp1 | a0001 | c0009 | t0002 | g0279 | AFR | GWD | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02572 | hp2 | a0001 | c0003 | t0002 | g0296 | AFR | GWD | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02602 | hp1 | a0001 | c0002 | t0001 | g0188 | SAS | PJL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02622 | hp1 | a0004 | c0012 | t0004 | g0259 | AFR | GWD | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02622 | hp2 | a0001 | c0002 | t0002 | g0256 | AFR | GWD | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | GWD | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02630 | hp2 | a0001 | c0003 | t0001 | g0237 | AFR | GWD | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02647 | hp1 | a0001 | c0002 | t0002 | g0241 | AFR | GWD | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02647 | hp2 | a0001 | c0003 | t0001 | g0248 | AFR | GWD | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02717 | hp1 | a0001 | c0002 | t0002 | g0251 | AFR | GWD | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02723 | hp2 | a0001 | c0003 | t0001 | g0020 | AFR | GWD | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02735 | hp2 | a0001 | c0002 | t0001 | g0182 | SAS | PJL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02809 | hp1 | a0003 | c0011 | t0002 | g0240 | AFR | GWD | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02809 | hp2 | a0011 | c0017 | t0002 | g0264 | AFR | GWD | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02818 | hp2 | a0001 | c0009 | t0002 | g0277 | AFR | GWD | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02886 | hp2 | a0001 | c0007 | t0001 | g0275 | AFR | GWD | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02896 | hp1 | a0001 | c0002 | t0002 | g0268 | AFR | GWD | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02896 | hp2 | a0001 | c0003 | t0001 | g0020 | AFR | GWD | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02897 | hp1 | a0001 | c0003 | t0001 | g0231 | AFR | GWD | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02897 | hp2 | a0001 | c0002 | t0002 | g0269 | AFR | GWD | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02922 | hp1 | a0001 | c0002 | t0001 | g0262 | AFR | ESN | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02922 | hp2 | a0001 | c0003 | t0002 | g0293 | AFR | ESN | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02970 | hp1 | a0002 | c0004 | t0001 | g0235 | AFR | ESN | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02970 | hp2 | a0006 | c0015 | t0002 | g0066 | AFR | ESN | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02976 | hp1 | a0004 | c0012 | t0002 | g0260 | AFR | ESN | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02976 | hp2 | a0007 | c0014 | t0002 | g0249 | AFR | ESN | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG03017 | hp1 | a0001 | c0003 | t0001 | g0322 | SAS | PJL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG03017 | hp2 | a0001 | c0002 | t0001 | g0186 | SAS | PJL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG03041 | hp2 | a0002 | c0004 | t0003 | g0299 | AFR | GWD | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG03098 | hp1 | a0001 | c0002 | t0002 | g0258 | AFR | MSL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG03098 | hp2 | a0001 | c0007 | t0001 | g0272 | AFR | MSL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ESN | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG03130 | hp2 | a0007 | c0014 | t0002 | g0250 | AFR | ESN | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG03139 | hp1 | a0001 | c0003 | t0002 | g0290 | AFR | ESN | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0084 | AFR | ESN | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG03195 | hp1 | a0001 | c0003 | t0001 | g0247 | AFR | ESN | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0086 | AFR | ESN | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0154 | AFR | MSL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | MSL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | MSL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0076 | AFR | MSL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG03239 | hp2 | a0005 | c0010 | t0001 | g0097 | SAS | PJL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | MSL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG03453 | hp2 | a0001 | c0002 | t0002 | g0239 | AFR | MSL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG03486 | hp1 | a0006 | c0015 | t0002 | g0067 | AFR | MSL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG03486 | hp2 | a0002 | c0008 | t0001 | g0233 | AFR | MSL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG03491 | hp1 | a0001 | c0003 | t0002 | g0281 | SAS | PJL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG03491 | hp2 | a0002 | c0004 | t0001 | g0040 | SAS | PJL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG03492 | hp1 | a0001 | c0003 | t0002 | g0282 | SAS | PJL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG03516 | hp1 | a0001 | c0002 | t0002 | g0245 | AFR | ESN | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG03516 | hp2 | a0001 | c0007 | t0001 | g0274 | AFR | ESN | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG03540 | hp2 | a0001 | c0002 | t0002 | g0022 | AFR | GWD | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG03579 | hp1 | a0004 | c0012 | t0002 | g0261 | AFR | MSL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG03579 | hp2 | a0001 | c0003 | t0002 | g0288 | AFR | MSL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG03654 | hp1 | a0001 | c0003 | t0002 | g0284 | SAS | PJL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG03654 | hp2 | a0001 | c0003 | t0002 | g0306 | SAS | PJL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG03669 | hp1 | a0001 | c0007 | t0001 | g0189 | SAS | PJL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG03669 | hp2 | a0001 | c0002 | t0001 | g0192 | SAS | PJL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG03688 | hp1 | a0001 | c0003 | t0001 | g0216 | SAS | STU | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG03688 | hp2 | a0002 | c0004 | t0001 | g0052 | SAS | STU | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG03704 | hp2 | a0005 | c0010 | t0001 | g0096 | SAS | PJL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG03927 | hp1 | a0001 | c0003 | t0002 | g0310 | SAS | BEB | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG03942 | hp1 | a0002 | c0004 | t0001 | g0219 | SAS | BEB | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG03942 | hp2 | a0001 | c0005 | t0001 | g0135 | SAS | BEB | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG04115 | hp1 | a0001 | c0003 | t0002 | g0283 | SAS | STU | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG04115 | hp2 | a0012 | c0030 | t0001 | g0134 | SAS | STU | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG04184 | hp1 | a0002 | c0008 | t0001 | g0036 | SAS | BEB | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0225 | SAS | BEB | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | STU | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG04199 | hp2 | a0001 | c0005 | t0001 | g0003 | SAS | STU | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG04204 | hp1 | a0001 | c0002 | t0001 | g0193 | SAS | STU | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG04204 | hp2 | a0001 | c0003 | t0001 | g0217 | SAS | STU | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG04228 | hp1 | a0005 | c0010 | t0001 | g0103 | SAS | STU | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG04228 | hp2 | a0002 | c0004 | t0001 | g0008 | SAS | STU | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18522 | hp1 | a0001 | c0002 | t0002 | g0242 | AFR | YRI | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0291 | AFR | YRI | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18612 | hp1 | a0003 | c0006 | t0002 | g0329 | EAS | CHB | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18612 | hp2 | a0001 | c0005 | t0001 | g0149 | EAS | CHB | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18747 | hp1 | a0003 | c0024 | t0001 | g0141 | EAS | CHB | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18747 | hp2 | a0003 | c0006 | t0002 | g0319 | EAS | CHB | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18906 | hp1 | a0001 | c0007 | t0002 | g0270 | AFR | YRI | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18906 | hp2 | a0001 | c0002 | t0003 | g0265 | AFR | YRI | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18941 | hp1 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18941 | hp2 | a0001 | c0003 | t0002 | g0313 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18942 | hp2 | a0001 | c0002 | t0001 | g0197 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18943 | hp2 | a0002 | c0004 | t0001 | g0051 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18945 | hp1 | a0001 | c0005 | t0001 | g0131 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18945 | hp2 | a0001 | c0003 | t0002 | g0023 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18946 | hp1 | a0001 | c0002 | t0001 | g0213 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18949 | hp1 | a0001 | c0002 | t0001 | g0207 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18949 | hp2 | a0013 | c0023 | t0002 | g0336 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18950 | hp2 | a0003 | c0006 | t0002 | g0325 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18951 | hp1 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18954 | hp1 | a0001 | c0005 | t0001 | g0145 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18954 | hp2 | a0001 | c0002 | t0001 | g0211 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18956 | hp1 | a0014 | c0022 | t0001 | g0117 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18956 | hp2 | a0001 | c0003 | t0002 | g0317 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18957 | hp1 | a0001 | c0002 | t0002 | g0198 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18957 | hp2 | a0002 | c0004 | t0001 | g0050 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18959 | hp1 | a0008 | c0013 | t0001 | g0027 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18959 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18963 | hp1 | a0002 | c0004 | t0001 | g0056 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18963 | hp2 | a0001 | c0005 | t0001 | g0003 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18964 | hp1 | a0003 | c0006 | t0002 | g0328 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18967 | hp1 | a0002 | c0004 | t0001 | g0032 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18969 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18969 | hp2 | a0001 | c0005 | t0001 | g0003 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18972 | hp1 | a0003 | c0006 | t0002 | g0339 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18973 | hp2 | a0001 | c0005 | t0001 | g0229 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18975 | hp2 | a0015 | c0021 | t0001 | g0203 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18977 | hp1 | a0001 | c0002 | t0001 | g0062 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18979 | hp1 | a0002 | c0004 | t0001 | g0030 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18980 | hp2 | a0001 | c0003 | t0002 | g0311 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18984 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18990 | hp1 | a0001 | c0005 | t0001 | g0002 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18993 | hp2 | a0002 | c0004 | t0002 | g0060 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18994 | hp1 | a0002 | c0004 | t0001 | g0031 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18994 | hp2 | a0016 | c0026 | t0001 | g0091 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18997 | hp1 | a0001 | c0005 | t0001 | g0146 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA18997 | hp2 | a0002 | c0004 | t0001 | g0034 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA19000 | hp1 | a0003 | c0006 | t0002 | g0330 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA19001 | hp1 | a0001 | c0002 | t0002 | g0199 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA19002 | hp2 | a0002 | c0004 | t0001 | g0055 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA19003 | hp2 | a0001 | c0002 | t0001 | g0176 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA19004 | hp2 | a0001 | c0002 | t0001 | g0202 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA19005 | hp2 | a0001 | c0002 | t0001 | g0204 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA19007 | hp1 | a0001 | c0003 | t0002 | g0023 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA19007 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA19009 | hp1 | a0001 | c0002 | t0001 | g0210 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA19009 | hp2 | a0001 | c0005 | t0001 | g0080 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA19010 | hp1 | a0001 | c0002 | t0001 | g0206 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA19010 | hp2 | a0002 | c0004 | t0001 | g0053 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA19011 | hp2 | a0001 | c0002 | t0001 | g0212 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA19030 | hp1 | a0001 | c0003 | t0002 | g0068 | AFR | LWK | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA19030 | hp2 | a0002 | c0004 | t0002 | g0238 | AFR | LWK | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA19043 | hp1 | a0001 | c0002 | t0001 | g0276 | AFR | LWK | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA19043 | hp2 | a0001 | c0002 | t0001 | g0230 | AFR | LWK | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA19055 | hp2 | a0001 | c0003 | t0002 | g0316 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA19056 | hp1 | a0001 | c0002 | t0001 | g0221 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA19060 | hp1 | a0001 | c0005 | t0001 | g0002 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA19064 | hp1 | a0001 | c0003 | t0002 | g0302 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA19064 | hp2 | a0008 | c0013 | t0001 | g0028 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA19065 | hp2 | a0002 | c0004 | t0002 | g0045 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA19068 | hp2 | a0003 | c0006 | t0002 | g0324 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA19070 | hp1 | a0002 | c0004 | t0001 | g0059 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA19074 | hp1 | a0001 | c0005 | t0002 | g0130 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA19074 | hp2 | a0001 | c0002 | t0001 | g0178 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA19078 | hp1 | a0002 | c0004 | t0001 | g0029 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA19079 | hp2 | a0003 | c0006 | t0002 | g0318 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA19085 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA19086 | hp1 | a0017 | c0016 | t0001 | g0026 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA19086 | hp2 | a0001 | c0005 | t0001 | g0002 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA19087 | hp1 | a0002 | c0004 | t0001 | g0054 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA19091 | hp1 | a0002 | c0004 | t0001 | g0057 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA19091 | hp2 | a0001 | c0002 | t0001 | g0191 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0148 | AFR | YRI | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA19240 | hp2 | a0001 | c0003 | t0001 | g0244 | AFR | YRI | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | ASW | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA20129 | hp2 | a0001 | c0002 | t0002 | g0255 | AFR | ASW | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA20752 | hp1 | a0001 | c0005 | t0001 | g0174 | EUR | TSI | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA20752 | hp2 | a0003 | c0006 | t0002 | g0338 | EUR | TSI | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | TSI | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA20805 | hp2 | a0001 | c0005 | t0001 | g0170 | EUR | TSI | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA20905 | hp1 | a0001 | c0002 | t0001 | g0180 | SAS | GIH | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA20905 | hp2 | a0001 | c0002 | t0001 | g0179 | SAS | GIH | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01123 | hp1 | a0001 | c0003 | t0002 | g0024 | AMR | CLM | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | CLM | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02109 | hp1 | a0001 | c0005 | t0001 | g0016 | AFR | ACB | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02109 | hp2 | a0001 | c0003 | t0002 | g0298 | AFR | ACB | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02486 | hp1 | a0001 | c0009 | t0002 | g0278 | AFR | ACB | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02486 | hp2 | a0001 | c0005 | t0001 | g0171 | AFR | ACB | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02559 | hp1 | a0001 | c0003 | t0002 | g0007 | AFR | ACB | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG02559 | hp2 | a0001 | c0003 | t0001 | g0155 | AFR | ACB | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG03471 | hp1 | a0001 | c0003 | t0001 | g0294 | AFR | MSL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | MSL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG06807 | hp1 | a0002 | c0004 | t0003 | g0236 | AFR | USA | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
HG06807 | hp2 | a0001 | c0003 | t0001 | g0340 | AFR | USA | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA20300 | hp1 | a0003 | c0011 | t0002 | g0252 | AFR | USA | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
NA20300 | hp2 | a0001 | c0003 | t0002 | g0292 | AFR | USA | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0196 | REF | REF | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
homoSapiens | grch38p0 | a0001 | c0007 | t0001 | g0257 | REF | REF | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:110641551 | T | C | 2 | a0004 a0010 |
4 | HG01192.hp2 HG02622.hp1 HG02976.hp1 others(1): Show |
missense_variant | MODERATE | c.1681A>G | p.Lys561Glu | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 15/15 | 1704/1838 | 1681/1695 | 561/564 | chr13 | 110641551 | |||
chr13:110641568 | T | G | 2 | a0003 a0013 |
27 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(24): Show |
missense_variant | MODERATE | c.1664A>C | p.Gln555Pro | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 15/15 | 1687/1838 | 1664/1695 | 555/564 | chr13 | 110641568 | |||
chr13:110641600 | G | T | 1 | a0011 | 1 | HG02809.hp2 | missense_variant | MODERATE | c.1632C>A | p.Ser544Arg | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 15/15 | 1655/1838 | 1632/1695 | 544/564 | chr13 | 110641600 | |||
chr13:110642347 | G | A | 1 | a0013 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.1591C>T | p.Arg531Trp | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/15 | 1614/1838 | 1591/1695 | 531/564 | chr13 | 110642347 | |||
chr13:110642400 | C | T | 1 | a0007 | 2 | HG02976.hp2 HG03130.hp2 |
missense_variant | MODERATE | c.1538G>A | p.Arg513Gln | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/15 | 1561/1838 | 1538/1695 | 513/564 | chr13 | 110642400 | |||
chr13:110642404 | G | A | 1 | a0009 | 1 | HG01106.hp2 | missense_variant | MODERATE | c.1534C>T | p.Arg512Trp | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/15 | 1557/1838 | 1534/1695 | 512/564 | chr13 | 110642404 | |||
chr13:110642449 | C | T | 1 | a0010 | 1 | HG01192.hp2 | missense_variant | MODERATE | c.1489G>A | p.Val497Ile | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/15 | 1512/1838 | 1489/1695 | 497/564 | chr13 | 110642449 | |||
chr13:110645977 | G | A | 1 | a0012 | 1 | HG04115.hp2 | missense_variant | MODERATE | c.1307C>T | p.Ala436Val | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 12/15 | 1330/1838 | 1307/1695 | 436/564 | chr13 | 110645977 | |||
chr13:110646048 | A | C | 1 | a0014 | 1 | NA18956.hp1 | missense_variant | MODERATE | c.1236T>G | p.Asp412Glu | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 12/15 | 1259/1838 | 1236/1695 | 412/564 | chr13 | 110646048 | |||
chr13:110647162 | G | A | 1 | a0006 | 2 | HG02970.hp2 HG03486.hp1 |
missense_variant | MODERATE | c.1132C>T | p.Arg378Cys | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/15 | 1155/1838 | 1132/1695 | 378/564 | chr13 | 110647162 | |||
chr13:110667379 | G | A | 1 | a0015 | 1 | NA18975.hp2 | missense_variant | MODERATE | c.880C>T | p.His294Tyr | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/15 | 903/1838 | 880/1695 | 294/564 | chr13 | 110667379 | |||
chr13:110683120 | C | T | 1 | a0005 | 3 | HG03239.hp2 HG03704.hp2 HG04228.hp1 |
missense_variant | MODERATE | c.586G>A | p.Asp196Asn | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/15 | 609/1838 | 586/1695 | 196/564 | chr13 | 110683120 | |||
chr13:110687727 | C | T | 1 | a0016 | 1 | NA18994.hp2 | missense_variant | MODERATE | c.565G>A | p.Ala189Thr | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/15 | 588/1838 | 565/1695 | 189/564 | chr13 | 110687727 | |||
chr13:110687754 | T | A | 1 | a0002 | 43 | HG00597.hp1 HG00738.hp2 HG01099.hp2 others(40): Show |
missense_variant | MODERATE | c.538A>T | p.Ile180Phe | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/15 | 561/1838 | 538/1695 | 180/564 | chr13 | 110687754 | |||
chr13:110705916 | C | G | 1 | a0008 | 2 | NA18959.hp1 NA19064.hp2 |
missense_variant | MODERATE | c.178G>C | p.Gly60Arg | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 1/15 | 201/1838 | 178/1695 | 60/564 | chr13 | 110705916 | |||
chr13:110705951 | C | T | 1 | a0017 | 1 | NA19086.hp1 | missense_variant | MODERATE | c.143G>A | p.Arg48Gln | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 1/15 | 166/1838 | 143/1695 | 48/564 | chr13 | 110705951 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:110646045 | A | G | 16 | a0001c0002 a0001c0003 a0001c0009 others(13): Show |
197 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(194): Show |
synonymous_variant | LOW | c.1239T>C | p.Asp413Asp | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 12/15 | 1262/1838 | 1239/1695 | 413/564 | chr13 | 110646045 | |||
chr13:110647235 | G | A | 1 | a0001c0025 | 1 | HG00609.hp2 | synonymous_variant | LOW | c.1059C>T | p.Ile353Ile | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/15 | 1082/1838 | 1059/1695 | 353/564 | chr13 | 110647235 | |||
chr13:110663475 | T | C | 1 | a0001c0019 | 1 | HG01943.hp2 | synonymous_variant | LOW | c.963A>G | p.Ser321Ser | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/15 | 986/1838 | 963/1695 | 321/564 | chr13 | 110663475 | |||
chr13:110663508 | G | A | 1 | a0001c0020 | 1 | HG01891.hp2 | synonymous_variant | LOW | c.930C>T | p.His310His | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/15 | 953/1838 | 930/1695 | 310/564 | chr13 | 110663508 | |||
chr13:110667407 | T | C | 21 | a0001c0001 a0001c0003 a0001c0005 others(18): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
synonymous_variant | LOW | c.852A>G | p.Glu284Glu | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/15 | 875/1838 | 852/1695 | 284/564 | chr13 | 110667407 | |||
chr13:110687728 | C | T | 1 | a0001c0009 | 3 | HG02486.hp1 HG02572.hp1 HG02818.hp2 |
synonymous_variant | LOW | c.564G>A | p.Thr188Thr | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/15 | 587/1838 | 564/1695 | 188/564 | chr13 | 110687728 | |||
chr13:110687995 | G | A | 7 | a0001c0005 a0001c0027 a0003c0028 others(4): Show |
34 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(31): Show |
synonymous_variant | LOW | c.417C>T | p.Leu139Leu | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 4/15 | 440/1838 | 417/1695 | 139/564 | chr13 | 110687995 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:110641483 | C | G | 3 | a0001c0002t0003 a0002c0004t0003 a0002c0008t0003 |
6 | HG01891.hp1 HG02258.hp1 HG02280.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*54G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 15/15 | 54 | chr13 | 110641483 | ||||||
chr13:110641500 | G | A | 20 | a0001c0001t0002 a0001c0002t0002 a0001c0002t0003 others(17): Show |
111 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*37C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 15/15 | 37 | chr13 | 110641500 | ||||||
chr13:110641504 | T | TGTCGTGA others(43): Show |
1 | a0004c0012t0004 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*32_*33insCAAGAATC others(42): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 15/15 | 32 | chr13 | 110641504 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:110641620 | G | C | 1 | a0006c0015t0002g0067 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1624-12C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/14 | chr13 | 110641620 | |||||||
chr13:110641641 | A | G | 3 | a0001c0002t0001g0179 a0001c0002t0001g0181 a0001c0002t0001g0182 |
3 | HG01515.hp2 HG02735.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1624-33T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/14 | chr13 | 110641641 | |||||||
chr13:110641708 | C | T | 1 | a0002c0008t0001g0234 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1624-100G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/14 | chr13 | 110641708 | |||||||
chr13:110641979 | ATCACCTG others(11): Show |
A | 1 | a0001c0001t0001g0069 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1623+318_1623+335d others(20): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/14 | chr13 | 110641979 | |||||||
chr13:110641991 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1623+324G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/14 | chr13 | 110641991 | |||||||
chr13:110641999 | T | C | 38 | a0001c0001t0001g0072 a0001c0001t0001g0093 a0001c0001t0001g0137 others(35): Show |
40 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.1623+316A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/14 | chr13 | 110641999 | |||||||
chr13:110642005 | C | A | 1 | a0001c0002t0002g0258 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1623+310G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/14 | chr13 | 110642005 | |||||||
chr13:110642012 | A | G | 1 | a0001c0002t0002g0258 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1623+303T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/14 | chr13 | 110642012 | |||||||
chr13:110642015 | C | A | 1 | a0001c0002t0002g0258 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1623+300G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/14 | chr13 | 110642015 | |||||||
chr13:110642017 | C | T | 1 | a0001c0002t0002g0258 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1623+298G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/14 | chr13 | 110642017 | |||||||
chr13:110642018 | G | A | 1 | a0001c0002t0002g0258 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1623+297C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/14 | chr13 | 110642018 | |||||||
chr13:110642022 | A | T | 1 | a0001c0002t0002g0258 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1623+293T>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/14 | chr13 | 110642022 | |||||||
chr13:110642027 | A | C | 1 | a0001c0002t0002g0258 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1623+288T>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/14 | chr13 | 110642027 | |||||||
chr13:110642033 | C | G | 1 | a0001c0002t0002g0258 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1623+282G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/14 | chr13 | 110642033 | |||||||
chr13:110642046 | A | C | 1 | a0001c0002t0002g0258 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1623+269T>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/14 | chr13 | 110642046 | |||||||
chr13:110642053 | C | T | 1 | a0001c0002t0002g0258 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1623+262G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/14 | chr13 | 110642053 | |||||||
chr13:110642056 | C | T | 1 | a0001c0002t0002g0258 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1623+259G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/14 | chr13 | 110642056 | |||||||
chr13:110642058 | G | A | 1 | a0001c0002t0002g0258 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1623+257C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/14 | chr13 | 110642058 | |||||||
chr13:110642059 | A | G | 1 | a0001c0002t0002g0258 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1623+256T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/14 | chr13 | 110642059 | |||||||
chr13:110642061 | C | T | 1 | a0001c0002t0002g0258 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1623+254G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/14 | chr13 | 110642061 | |||||||
chr13:110642062 | A | G | 1 | a0001c0002t0002g0258 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1623+253T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/14 | chr13 | 110642062 | |||||||
chr13:110642066 | G | T | 1 | a0001c0002t0002g0258 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1623+249C>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/14 | chr13 | 110642066 | |||||||
chr13:110642067 | A | G | 1 | a0001c0002t0002g0258 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1623+248T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/14 | chr13 | 110642067 | |||||||
chr13:110642073 | T | C | 1 | a0001c0002t0002g0258 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1623+242A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/14 | chr13 | 110642073 | |||||||
chr13:110642074 | G | A | 1 | a0001c0002t0002g0258 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1623+241C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/14 | chr13 | 110642074 | |||||||
chr13:110642078 | G | A | 1 | a0001c0002t0002g0258 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1623+237C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/14 | chr13 | 110642078 | |||||||
chr13:110642085 | T | C | 1 | a0001c0002t0002g0258 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1623+230A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/14 | chr13 | 110642085 | |||||||
chr13:110642202 | C | T | 1 | a0001c0003t0001g0289 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1623+113G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/14 | chr13 | 110642202 | |||||||
chr13:110642226 | C | T | 1 | a0001c0002t0002g0256 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1623+89G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/14 | chr13 | 110642226 | |||||||
chr13:110642256 | C | T | 3 | a0001c0001t0001g0156 a0001c0001t0001g0161 a0010c0018t0002g0263 |
3 | HG01192.hp2 NA18971.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.1623+59G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/14 | chr13 | 110642256 | |||||||
chr13:110642538 | G | A | 1 | a0010c0018t0002g0263 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1417-17C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 13/14 | chr13 | 110642538 | |||||||
chr13:110642573 | G | GC | 327 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(324): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.1417-53dupG | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 13/14 | chr13 | 110642573 | |||||||
chr13:110642581 | C | A | 2 | a0003c0006t0002g0330 a0003c0006t0002g0339 |
2 | NA18972.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.1417-60G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 13/14 | chr13 | 110642581 | |||||||
chr13:110642652 | C | T | 19 | a0001c0001t0001g0087 a0001c0001t0001g0110 a0001c0001t0002g0076 others(16): Show |
23 | HG00642.hp2 HG01123.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.1417-131G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 13/14 | chr13 | 110642652 | |||||||
chr13:110642798 | G | A | 1 | a0002c0004t0001g0039 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1417-277C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 13/14 | chr13 | 110642798 | |||||||
chr13:110642802 | C | T | 1 | a0001c0007t0001g0275 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1417-281G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 13/14 | chr13 | 110642802 | |||||||
chr13:110642841 | G | C | 16 | a0001c0003t0001g0322 a0003c0006t0002g0025 a0003c0006t0002g0318 others(13): Show |
17 | HG00280.hp1 HG00558.hp1 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.1417-320C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 13/14 | chr13 | 110642841 | |||||||
chr13:110642869 | C | T | 24 | a0001c0001t0002g0150 a0001c0003t0001g0322 a0001c0007t0001g0189 others(21): Show |
24 | HG00280.hp1 HG00558.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1417-348G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 13/14 | chr13 | 110642869 | |||||||
chr13:110642893 | C | T | 1 | a0001c0002t0001g0188 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1417-372G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 13/14 | chr13 | 110642893 | |||||||
chr13:110642912 | G | A | 1 | a0001c0002t0001g0177 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1417-391C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 13/14 | chr13 | 110642912 | |||||||
chr13:110642950 | G | A | 8 | a0001c0001t0001g0254 a0001c0002t0002g0022 a0001c0002t0002g0241 others(5): Show |
9 | HG02280.hp2 HG02451.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1417-429C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 13/14 | chr13 | 110642950 | |||||||
chr13:110642970 | G | A | 1 | a0011c0017t0002g0264 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1417-449C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 13/14 | chr13 | 110642970 | |||||||
chr13:110643056 | T | C | 1 | a0001c0001t0001g0078 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1417-535A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 13/14 | chr13 | 110643056 | |||||||
chr13:110643097 | CAAACTAC others(2): Show |
C | 2 | a0001c0003t0001g0020 a0001c0003t0001g0231 |
3 | HG02723.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1417-585_1417-577d others(11): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 13/14 | chr13 | 110643097 | |||||||
chr13:110643130 | T | C | 1 | a0001c0005t0001g0175 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1417-609A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 13/14 | chr13 | 110643130 | |||||||
chr13:110643348 | C | A | 36 | a0001c0001t0001g0126 a0001c0001t0001g0142 a0001c0001t0001g0162 others(33): Show |
37 | HG00597.hp1 HG01099.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.1417-827G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 13/14 | chr13 | 110643348 | |||||||
chr13:110643485 | C | T | 3 | a0001c0002t0003g0265 a0001c0002t0003g0266 a0001c0002t0003g0267 |
3 | HG01891.hp1 HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1416+900G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 13/14 | chr13 | 110643485 | |||||||
chr13:110643515 | C | G | 1 | a0001c0001t0001g0111 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1416+870G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 13/14 | chr13 | 110643515 | |||||||
chr13:110643523 | T | C | 12 | a0001c0002t0001g0276 a0001c0003t0001g0020 a0001c0003t0001g0155 others(9): Show |
13 | HG01074.hp1 HG02257.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.1416+862A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 13/14 | chr13 | 110643523 | |||||||
chr13:110643543 | C | T | 2 | a0001c0002t0001g0230 a0002c0004t0001g0235 |
2 | HG02970.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1416+842G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 13/14 | chr13 | 110643543 | |||||||
chr13:110643606 | C | T | 1 | a0001c0002t0001g0204 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1416+779G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 13/14 | chr13 | 110643606 | |||||||
chr13:110643677 | G | A | 61 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0017 others(58): Show |
69 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(66): Show |
intron_variant | MODIFIER | c.1416+708C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 13/14 | chr13 | 110643677 | |||||||
chr13:110643746 | TTAAGAA | T | 51 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(48): Show |
52 | HG00438.hp1 HG00597.hp1 HG01099.hp2 others(49): Show |
intron_variant | MODIFIER | c.1416+633_1416+638d others(8): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 13/14 | chr13 | 110643746 | |||||||
chr13:110643777 | A | G | 51 | a0001c0001t0002g0086 a0001c0001t0002g0148 a0001c0002t0001g0005 others(48): Show |
58 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.1416+608T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 13/14 | chr13 | 110643777 | |||||||
chr13:110643823 | C | T | 48 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0017 others(45): Show |
55 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.1416+562G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 13/14 | chr13 | 110643823 | |||||||
chr13:110643988 | T | G | 32 | a0002c0004t0001g0008 a0002c0004t0001g0029 a0002c0004t0001g0030 others(29): Show |
33 | HG00597.hp1 HG01099.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.1416+397A>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 13/14 | chr13 | 110643988 | |||||||
chr13:110644339 | C | T | 2 | a0002c0004t0001g0055 a0002c0004t0001g0056 |
2 | NA18963.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.1416+46G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 13/14 | chr13 | 110644339 | |||||||
chr13:110644541 | A | G | 1 | a0001c0001t0001g0012 | 2 | NA18983.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1318-58T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 12/14 | chr13 | 110644541 | |||||||
chr13:110644625 | G | A | 2 | a0006c0015t0002g0066 a0006c0015t0002g0067 |
2 | HG02970.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1318-142C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 12/14 | chr13 | 110644625 | |||||||
chr13:110645057 | C | T | 220 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(217): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1318-574G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 12/14 | chr13 | 110645057 | |||||||
chr13:110645074 | G | A | 1 | a0001c0002t0001g0209 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1318-591C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 12/14 | chr13 | 110645074 | |||||||
chr13:110645101 | G | T | 133 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(130): Show |
141 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(138): Show |
intron_variant | MODIFIER | c.1318-618C>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 12/14 | chr13 | 110645101 | |||||||
chr13:110645104 | A | C | 1 | a0014c0022t0001g0117 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1318-621T>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 12/14 | chr13 | 110645104 | |||||||
chr13:110645264 | C | T | 31 | a0001c0003t0001g0294 a0001c0003t0001g0322 a0001c0003t0001g0340 others(28): Show |
32 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.1317+703G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 12/14 | chr13 | 110645264 | |||||||
chr13:110645297 | A | T | 1 | a0014c0022t0001g0117 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1317+670T>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 12/14 | chr13 | 110645297 | |||||||
chr13:110645352 | C | A | 98 | a0001c0001t0001g0073 a0001c0001t0002g0303 a0001c0001t0002g0304 others(95): Show |
101 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.1317+615G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 12/14 | chr13 | 110645352 | |||||||
chr13:110645390 | C | T | 3 | a0001c0005t0001g0129 a0001c0005t0001g0133 a0003c0028t0001g0132 |
3 | HG01256.hp2 HG01496.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1317+577G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 12/14 | chr13 | 110645390 | |||||||
chr13:110645413 | C | A | 2 | a0001c0002t0002g0256 a0001c0002t0002g0258 |
2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1317+554G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 12/14 | chr13 | 110645413 | |||||||
chr13:110645415 | C | T | 1 | a0010c0018t0002g0263 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1317+552G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 12/14 | chr13 | 110645415 | |||||||
chr13:110645488 | C | T | 1 | a0001c0003t0002g0306 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1317+479G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 12/14 | chr13 | 110645488 | |||||||
chr13:110645523 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1317+444A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 12/14 | chr13 | 110645523 | |||||||
chr13:110645548 | A | C | 1 | a0014c0022t0001g0117 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1317+419T>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 12/14 | chr13 | 110645548 | |||||||
chr13:110645605 | C | A | 293 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(290): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.1317+362G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 12/14 | chr13 | 110645605 | |||||||
chr13:110645630 | A | C | 12 | a0001c0001t0001g0110 a0001c0001t0001g0254 a0001c0002t0001g0276 others(9): Show |
12 | HG00738.hp2 HG01943.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1317+337T>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 12/14 | chr13 | 110645630 | |||||||
chr13:110645723 | T | G | 50 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0017 others(47): Show |
57 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.1317+244A>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 12/14 | chr13 | 110645723 | |||||||
chr13:110645854 | C | T | 15 | a0001c0003t0001g0287 a0001c0003t0001g0289 a0001c0003t0002g0023 others(12): Show |
17 | HG00642.hp2 HG01123.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.1317+113G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 12/14 | chr13 | 110645854 | |||||||
chr13:110645940 | C | T | 3 | a0001c0009t0002g0277 a0001c0009t0002g0278 a0001c0009t0002g0279 |
3 | HG02486.hp1 HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1317+27G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 12/14 | chr13 | 110645940 | |||||||
chr13:110645943 | A | G | 8 | a0001c0001t0001g0110 a0001c0009t0002g0277 a0001c0009t0002g0278 others(5): Show |
8 | HG02486.hp1 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1317+24T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 12/14 | chr13 | 110645943 | |||||||
chr13:110645957 | G | A | 1 | a0003c0006t0002g0338 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1317+10C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 12/14 | chr13 | 110645957 | |||||||
chr13:110646123 | G | A | 1 | a0001c0003t0001g0237 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1194-33C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110646123 | |||||||
chr13:110646185 | G | A | 10 | a0001c0002t0001g0262 a0001c0002t0003g0265 a0001c0002t0003g0266 others(7): Show |
10 | HG01192.hp2 HG01891.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.1194-95C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110646185 | |||||||
chr13:110646412 | G | C | 26 | a0001c0001t0001g0115 a0001c0001t0001g0140 a0001c0001t0002g0308 others(23): Show |
27 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(24): Show |
intron_variant | MODIFIER | c.1194-322C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110646412 | |||||||
chr13:110646422 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1194-332C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110646422 | |||||||
chr13:110646435 | C | T | 1 | a0001c0002t0002g0245 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1194-345G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110646435 | |||||||
chr13:110646468 | C | T | 2 | a0001c0002t0002g0251 a0001c0002t0002g0255 |
2 | HG02717.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1194-378G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110646468 | |||||||
chr13:110646471 | G | A | 2 | a0001c0002t0002g0268 a0001c0002t0002g0269 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1194-381C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110646471 | |||||||
chr13:110646490 | C | CCCACCAC others(10): Show |
1 | a0014c0022t0001g0117 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1194-401_1194-400i others(19): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110646490 | |||||||
chr13:110646492 | A | C | 1 | a0014c0022t0001g0117 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1194-402T>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110646492 | |||||||
chr13:110646513 | A | T | 1 | a0014c0022t0001g0117 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1194-423T>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110646513 | |||||||
chr13:110646517 | G | C | 1 | a0014c0022t0001g0117 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1194-427C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110646517 | |||||||
chr13:110646520 | G | A | 1 | a0014c0022t0001g0117 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1194-430C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110646520 | |||||||
chr13:110646522 | G | A | 1 | a0014c0022t0001g0117 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1194-432C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110646522 | |||||||
chr13:110646525 | G | C | 1 | a0014c0022t0001g0117 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1194-435C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110646525 | |||||||
chr13:110646526 | G | C | 1 | a0014c0022t0001g0117 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1194-436C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110646526 | |||||||
chr13:110646528 | T | G | 1 | a0014c0022t0001g0117 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1194-438A>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110646528 | |||||||
chr13:110646529 | T | A | 1 | a0014c0022t0001g0117 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1194-439A>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110646529 | |||||||
chr13:110646533 | A | T | 1 | a0014c0022t0001g0117 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1194-443T>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110646533 | |||||||
chr13:110646534 | C | G | 1 | a0014c0022t0001g0117 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1194-444G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110646534 | |||||||
chr13:110646543 | T | G | 1 | a0014c0022t0001g0117 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1194-453A>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110646543 | |||||||
chr13:110646559 | T | C | 158 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0014 others(155): Show |
168 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.1194-469A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110646559 | |||||||
chr13:110646560 | G | A | 4 | a0001c0003t0001g0294 a0001c0003t0002g0295 a0001c0003t0002g0296 others(1): Show |
4 | HG02055.hp2 HG02109.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1194-470C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110646560 | |||||||
chr13:110646579 | G | A | 3 | a0001c0003t0002g0007 a0001c0003t0002g0292 a0001c0003t0002g0293 |
5 | HG01884.hp2 HG02258.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1194-489C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110646579 | |||||||
chr13:110646614 | G | A | 8 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0307 others(5): Show |
9 | HG01109.hp1 HG03491.hp2 HG03942.hp1 others(6): Show |
intron_variant | MODIFIER | c.1193+487C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110646614 | |||||||
chr13:110646630 | G | T | 2 | a0001c0002t0001g0230 a0002c0004t0001g0235 |
2 | HG02970.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1193+471C>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110646630 | |||||||
chr13:110646714 | C | T | 145 | a0001c0001t0001g0085 a0001c0001t0001g0094 a0001c0001t0001g0124 others(142): Show |
156 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.1193+387G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110646714 | |||||||
chr13:110646736 | G | A | 4 | a0001c0002t0001g0262 a0001c0002t0003g0265 a0001c0002t0003g0266 others(1): Show |
4 | HG01891.hp1 HG02258.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1193+365C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110646736 | |||||||
chr13:110646747 | C | T | 1 | a0010c0018t0002g0263 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1193+354G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110646747 | |||||||
chr13:110646748 | G | A | 1 | a0001c0005t0001g0334 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1193+353C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110646748 | |||||||
chr13:110646871 | C | G | 1 | a0001c0003t0001g0237 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1193+230G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110646871 | |||||||
chr13:110647076 | G | A | 1 | a0001c0003t0001g0237 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1193+25C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110647076 | |||||||
chr13:110647078 | C | T | 1 | a0001c0001t0001g0114 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1193+23G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110647078 | |||||||
chr13:110647371 | C | T | 56 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(53): Show |
57 | HG00438.hp1 HG00597.hp1 HG01099.hp2 others(54): Show |
intron_variant | MODIFIER | c.1055-132G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110647371 | |||||||
chr13:110647372 | G | A | 4 | a0001c0002t0001g0262 a0001c0002t0003g0265 a0001c0002t0003g0266 others(1): Show |
4 | HG01891.hp1 HG02258.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1055-133C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110647372 | |||||||
chr13:110647466 | G | A | 124 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(121): Show |
131 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.1055-227C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110647466 | |||||||
chr13:110647516 | C | CGGA | 124 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(121): Show |
131 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.1055-278_1055-277i others(5): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110647516 | |||||||
chr13:110647557 | G | A | 17 | a0001c0001t0002g0086 a0001c0001t0002g0148 a0001c0003t0001g0020 others(14): Show |
18 | HG01074.hp1 HG02257.hp2 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.1055-318C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110647557 | |||||||
chr13:110647574 | G | C | 1 | a0001c0002t0001g0213 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1055-335C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110647574 | |||||||
chr13:110647653 | T | C | 63 | a0001c0001t0001g0159 a0001c0001t0002g0303 a0001c0001t0002g0304 others(60): Show |
64 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.1055-414A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110647653 | |||||||
chr13:110647654 | C | G | 6 | a0002c0004t0001g0029 a0002c0004t0001g0030 a0002c0004t0001g0031 others(3): Show |
6 | HG02015.hp1 NA18967.hp1 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.1055-415G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110647654 | |||||||
chr13:110647684 | C | CAAGCCCC others(74): Show |
1 | a0001c0001t0002g0303 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1055-446_1055-445i others(83): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110647684 | |||||||
chr13:110647694 | A | G | 124 | a0001c0001t0001g0159 a0001c0001t0002g0304 a0001c0001t0002g0305 others(121): Show |
131 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.1055-455T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110647694 | |||||||
chr13:110647694 | A | T | 1 | a0001c0001t0002g0303 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1055-455T>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110647694 | |||||||
chr13:110647697 | G | A | 1 | a0001c0001t0002g0303 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1055-458C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110647697 | |||||||
chr13:110647697 | G | GAGGGAGG others(72): Show |
124 | a0001c0001t0001g0159 a0001c0001t0002g0304 a0001c0001t0002g0305 others(121): Show |
131 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.1055-459_1055-458i others(81): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110647697 | |||||||
chr13:110647782 | C | T | 15 | a0001c0003t0001g0287 a0001c0003t0001g0289 a0001c0003t0002g0007 others(12): Show |
19 | HG00642.hp2 HG01123.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.1055-543G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110647782 | |||||||
chr13:110647790 | C | T | 3 | a0001c0009t0002g0277 a0001c0009t0002g0278 a0001c0009t0002g0279 |
3 | HG02486.hp1 HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1055-551G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110647790 | |||||||
chr13:110647862 | A | G | 3 | a0002c0004t0001g0041 a0002c0004t0001g0042 a0002c0004t0001g0043 |
3 | HG01361.hp1 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1055-623T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110647862 | |||||||
chr13:110647979 | C | T | 3 | a0001c0001t0001g0093 a0001c0001t0001g0137 a0001c0001t0001g0138 |
3 | HG00438.hp2 HG00544.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1055-740G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110647979 | |||||||
chr13:110648031 | G | C | 123 | a0001c0001t0001g0159 a0001c0001t0002g0303 a0001c0001t0002g0304 others(120): Show |
130 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.1055-792C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110648031 | |||||||
chr13:110648310 | A | C | 1 | a0001c0001t0001g0158 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1055-1071T>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110648310 | |||||||
chr13:110648345 | C | A | 1 | a0001c0002t0001g0193 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1055-1106G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110648345 | |||||||
chr13:110648452 | A | G | 128 | a0001c0001t0001g0159 a0001c0001t0002g0303 a0001c0001t0002g0304 others(125): Show |
135 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.1055-1213T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110648452 | |||||||
chr13:110648532 | G | C | 67 | a0001c0002t0001g0230 a0001c0002t0001g0262 a0001c0002t0002g0022 others(64): Show |
73 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.1055-1293C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110648532 | |||||||
chr13:110648550 | C | T | 68 | a0001c0002t0001g0230 a0001c0002t0001g0262 a0001c0002t0002g0022 others(65): Show |
74 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.1055-1311G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110648550 | |||||||
chr13:110648596 | G | A | 62 | a0001c0002t0001g0230 a0001c0002t0002g0022 a0001c0002t0002g0239 others(59): Show |
68 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.1055-1357C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110648596 | |||||||
chr13:110648602 | G | T | 15 | a0001c0003t0001g0287 a0001c0003t0001g0289 a0001c0003t0002g0007 others(12): Show |
19 | HG00642.hp2 HG01123.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.1055-1363C>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110648602 | |||||||
chr13:110648610 | A | T | 188 | a0001c0001t0001g0159 a0001c0001t0002g0303 a0001c0001t0002g0304 others(185): Show |
203 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(200): Show |
intron_variant | MODIFIER | c.1055-1371T>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110648610 | |||||||
chr13:110648621 | G | A | 1 | a0003c0006t0002g0328 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1055-1382C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110648621 | |||||||
chr13:110648630 | G | A | 64 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0017 others(61): Show |
75 | HG00609.hp1 HG00621.hp2 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.1055-1391C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110648630 | |||||||
chr13:110648661 | C | T | 12 | a0001c0002t0002g0022 a0001c0002t0002g0239 a0001c0002t0002g0241 others(9): Show |
13 | HG02280.hp2 HG02451.hp2 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.1055-1422G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110648661 | |||||||
chr13:110648689 | G | A | 15 | a0001c0003t0001g0287 a0001c0003t0001g0289 a0001c0003t0002g0007 others(12): Show |
19 | HG00642.hp2 HG01123.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.1055-1450C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110648689 | |||||||
chr13:110648693 | T | C | 62 | a0001c0002t0001g0230 a0001c0002t0002g0022 a0001c0002t0002g0239 others(59): Show |
68 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.1055-1454A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110648693 | |||||||
chr13:110648701 | T | C | 125 | a0001c0001t0001g0159 a0001c0001t0002g0303 a0001c0001t0002g0304 others(122): Show |
132 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.1055-1462A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110648701 | |||||||
chr13:110648709 | C | G | 3 | a0001c0009t0002g0277 a0001c0009t0002g0278 a0001c0009t0002g0279 |
3 | HG02486.hp1 HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1055-1470G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110648709 | |||||||
chr13:110648710 | G | GGTGCCTC others(6): Show |
1 | a0014c0022t0001g0117 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1055-1484_1055-147 others(17): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110648710 | |||||||
chr13:110648830 | C | T | 15 | a0001c0003t0001g0287 a0001c0003t0001g0289 a0001c0003t0002g0007 others(12): Show |
19 | HG00642.hp2 HG01123.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.1055-1591G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110648830 | |||||||
chr13:110648931 | C | T | 124 | a0001c0001t0001g0159 a0001c0001t0002g0303 a0001c0001t0002g0304 others(121): Show |
131 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.1055-1692G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110648931 | |||||||
chr13:110648994 | A | G | 137 | a0001c0001t0001g0159 a0001c0001t0002g0303 a0001c0001t0002g0304 others(134): Show |
145 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.1055-1755T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110648994 | |||||||
chr13:110649010 | C | T | 1 | a0001c0001t0001g0012 | 2 | NA18983.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1055-1771G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649010 | |||||||
chr13:110649098 | C | A | 1 | a0004c0012t0002g0261 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1055-1859G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649098 | |||||||
chr13:110649140 | C | T | 2 | a0001c0001t0001g0120 a0001c0001t0001g0144 |
2 | HG03704.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.1054+1894G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649140 | |||||||
chr13:110649196 | C | G | 86 | a0001c0001t0001g0159 a0001c0001t0002g0303 a0001c0001t0002g0304 others(83): Show |
88 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.1054+1838G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649196 | |||||||
chr13:110649218 | G | T | 1 | a0001c0005t0001g0129 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1054+1816C>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649218 | |||||||
chr13:110649265 | C | G | 63 | a0001c0001t0001g0159 a0001c0001t0002g0303 a0001c0001t0002g0304 others(60): Show |
64 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.1054+1769G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649265 | |||||||
chr13:110649321 | C | T | 1 | a0001c0001t0002g0312 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1054+1713G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649321 | |||||||
chr13:110649414 | AG | A | 70 | a0001c0001t0001g0159 a0001c0001t0002g0303 a0001c0001t0002g0304 others(67): Show |
71 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.1054+1619delC | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649414 | |||||||
chr13:110649429 | G | C | 1 | a0001c0002t0001g0214 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1054+1605C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649429 | |||||||
chr13:110649469 | TA | T | 188 | a0001c0001t0001g0159 a0001c0001t0002g0303 a0001c0001t0002g0304 others(185): Show |
203 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(200): Show |
intron_variant | MODIFIER | c.1054+1564delT | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649469 | |||||||
chr13:110649535 | C | T | 76 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0017 others(73): Show |
85 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(82): Show |
intron_variant | MODIFIER | c.1054+1499G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649535 | |||||||
chr13:110649649 | C | A | 70 | a0001c0001t0001g0159 a0001c0001t0002g0303 a0001c0001t0002g0304 others(67): Show |
71 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.1054+1385G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649649 | |||||||
chr13:110649862 | A | C | 1 | a0001c0001t0002g0303 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1054+1172T>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649862 | |||||||
chr13:110649931 | C | CTGTTTTT others(3): Show |
1 | a0001c0003t0002g0306 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1054+1102_1054+110 others(14): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649931 | |||||||
chr13:110649931 | C | CTGTTTTT others(7): Show |
1 | a0001c0001t0002g0309 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1054+1102_1054+110 others(18): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649931 | |||||||
chr13:110649931 | C | CTGTTTTT others(8): Show |
1 | a0001c0001t0002g0312 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1054+1102_1054+110 others(19): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649931 | |||||||
chr13:110649931 | C | CTGTTTTT others(11): Show |
2 | a0002c0004t0002g0045 a0002c0004t0002g0060 |
2 | NA18993.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1054+1102_1054+110 others(22): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649931 | |||||||
chr13:110649931 | C | CTGTTTTT others(10): Show |
3 | a0002c0004t0002g0238 a0006c0015t0002g0066 a0006c0015t0002g0067 |
3 | HG02970.hp2 HG03486.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1054+1102_1054+110 others(21): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649931 | |||||||
chr13:110649931 | C | CTGTTTTT others(11): Show |
9 | a0002c0004t0001g0033 a0002c0004t0001g0034 a0002c0004t0001g0037 others(6): Show |
9 | HG01168.hp1 HG01515.hp1 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.1054+1102_1054+110 others(22): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649931 | |||||||
chr13:110649931 | C | CTGTTTTT others(12): Show |
13 | a0002c0004t0001g0008 a0002c0004t0001g0029 a0002c0004t0001g0030 others(10): Show |
14 | HG01109.hp1 HG01255.hp2 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.1054+1102_1054+110 others(23): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649931 | |||||||
chr13:110649931 | C | CTGTTTTT others(15): Show |
1 | a0002c0004t0001g0047 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1054+1102_1054+110 others(26): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649931 | |||||||
chr13:110649931 | C | CTGTTTTT others(16): Show |
3 | a0002c0004t0001g0046 a0002c0004t0001g0048 a0002c0004t0001g0049 |
3 | HG01358.hp2 HG01928.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.1054+1102_1054+110 others(27): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649931 | |||||||
chr13:110649931 | C | CTGTTTTT others(17): Show |
3 | a0002c0004t0001g0039 a0002c0004t0001g0050 a0002c0004t0001g0057 |
3 | HG01167.hp2 NA18957.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1054+1102_1054+110 others(28): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649931 | |||||||
chr13:110649931 | C | CTGTTTTT others(18): Show |
4 | a0001c0001t0002g0305 a0001c0001t0002g0308 a0001c0001t0002g0314 others(1): Show |
4 | NA18939.hp1 NA18941.hp2 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.1054+1102_1054+110 others(29): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649931 | |||||||
chr13:110649931 | C | CTGTTTTT others(19): Show |
6 | a0001c0001t0002g0304 a0001c0001t0002g0307 a0001c0001t0002g0315 others(3): Show |
6 | HG00438.hp1 HG02074.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.1054+1102_1054+110 others(30): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649931 | |||||||
chr13:110649931 | C | CTGTTTTT others(20): Show |
1 | a0001c0003t0002g0302 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1054+1102_1054+110 others(31): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649931 | |||||||
chr13:110649931 | C | CTGTTTTT others(23): Show |
1 | a0002c0004t0001g0054 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1054+1102_1054+110 others(34): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649931 | |||||||
chr13:110649931 | C | CTGTTTTT others(24): Show |
1 | a0002c0004t0001g0059 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1054+1102_1054+110 others(35): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649931 | |||||||
chr13:110649931 | C | CTGTTTTT others(25): Show |
1 | a0001c0001t0002g0303 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1054+1102_1054+110 others(36): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649931 | |||||||
chr13:110649931 | C | CTGTTTTT others(28): Show |
1 | a0001c0003t0001g0237 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1054+1102_1054+110 others(39): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649931 | |||||||
chr13:110649931 | C | CTT | 7 | a0001c0002t0001g0230 a0001c0002t0002g0251 a0001c0002t0002g0255 others(4): Show |
7 | HG01891.hp2 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1054+1101_1054+110 others(6): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649931 | |||||||
chr13:110649931 | C | CTTTTTTT others(7): Show |
1 | a0010c0018t0002g0263 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1054+1089_1054+110 others(18): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649931 | |||||||
chr13:110649931 | CT | C | 135 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(132): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.1054+1102delA | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649931 | |||||||
chr13:110649931 | CTT | C | 111 | a0001c0001t0001g0015 a0001c0001t0001g0118 a0001c0001t0001g0119 others(108): Show |
123 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.1054+1101_1054+110 others(6): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649931 | |||||||
chr13:110649931 | CTTT | C | 6 | a0001c0002t0002g0198 a0001c0003t0001g0322 a0001c0003t0002g0281 others(3): Show |
6 | HG00597.hp1 HG01256.hp1 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.1054+1100_1054+110 others(7): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649931 | |||||||
chr13:110649931 | CTTTTT | C | 6 | a0001c0002t0001g0262 a0001c0002t0003g0266 a0001c0002t0003g0267 others(3): Show |
6 | HG01891.hp1 HG02258.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1054+1098_1054+110 others(9): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649931 | |||||||
chr13:110649936 | T | G | 1 | a0002c0004t0001g0044 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1054+1098A>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649936 | |||||||
chr13:110649937 | T | G | 1 | a0001c0003t0002g0068 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1054+1097A>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649937 | |||||||
chr13:110649938 | T | G | 3 | a0001c0003t0002g0311 a0001c0003t0002g0316 a0001c0003t0002g0317 |
3 | NA18956.hp2 NA18980.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.1054+1096A>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649938 | |||||||
chr13:110649987 | G | T | 1 | a0001c0001t0001g0073 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1054+1047C>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649987 | |||||||
chr13:110650006 | C | T | 7 | a0001c0002t0001g0230 a0001c0002t0002g0251 a0001c0002t0002g0255 others(4): Show |
7 | HG01891.hp2 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1054+1028G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110650006 | |||||||
chr13:110650007 | A | G | 69 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(66): Show |
70 | HG00438.hp1 HG00597.hp1 HG01099.hp2 others(67): Show |
intron_variant | MODIFIER | c.1054+1027T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110650007 | |||||||
chr13:110650032 | G | A | 69 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(66): Show |
70 | HG00438.hp1 HG00597.hp1 HG01099.hp2 others(67): Show |
intron_variant | MODIFIER | c.1054+1002C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110650032 | |||||||
chr13:110650061 | T | C | 69 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(66): Show |
70 | HG00438.hp1 HG00597.hp1 HG01099.hp2 others(67): Show |
intron_variant | MODIFIER | c.1054+973A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110650061 | |||||||
chr13:110650077 | C | T | 20 | a0001c0003t0001g0287 a0001c0003t0001g0289 a0001c0003t0001g0294 others(17): Show |
24 | HG00642.hp2 HG01123.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.1054+957G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110650077 | |||||||
chr13:110650082 | G | A | 2 | a0001c0003t0001g0155 a0001c0003t0001g0297 |
2 | HG02257.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1054+952C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110650082 | |||||||
chr13:110650225 | G | C | 69 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(66): Show |
70 | HG00438.hp1 HG00597.hp1 HG01099.hp2 others(67): Show |
intron_variant | MODIFIER | c.1054+809C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110650225 | |||||||
chr13:110650238 | C | T | 69 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(66): Show |
70 | HG00438.hp1 HG00597.hp1 HG01099.hp2 others(67): Show |
intron_variant | MODIFIER | c.1054+796G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110650238 | |||||||
chr13:110650300 | G | A | 3 | a0001c0002t0001g0006 a0001c0002t0001g0204 a0001c0002t0001g0213 |
5 | NA18946.hp1 NA18959.hp2 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.1054+734C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110650300 | |||||||
chr13:110650381 | A | G | 68 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(65): Show |
69 | HG00438.hp1 HG00597.hp1 HG01099.hp2 others(66): Show |
intron_variant | MODIFIER | c.1054+653T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110650381 | |||||||
chr13:110650564 | G | A | 1 | a0001c0002t0002g0256 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1054+470C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110650564 | |||||||
chr13:110650567 | G | A | 7 | a0001c0002t0001g0230 a0001c0002t0002g0251 a0001c0002t0002g0255 others(4): Show |
7 | HG01891.hp2 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1054+467C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110650567 | |||||||
chr13:110650575 | T | C | 187 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(184): Show |
202 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(199): Show |
intron_variant | MODIFIER | c.1054+459A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110650575 | |||||||
chr13:110650676 | T | G | 1 | a0002c0004t0001g0037 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1054+358A>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110650676 | |||||||
chr13:110650766 | G | A | 69 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(66): Show |
70 | HG00438.hp1 HG00597.hp1 HG01099.hp2 others(67): Show |
intron_variant | MODIFIER | c.1054+268C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110650766 | |||||||
chr13:110650846 | C | G | 7 | a0001c0002t0001g0230 a0001c0002t0002g0251 a0001c0002t0002g0255 others(4): Show |
7 | HG01891.hp2 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1054+188G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110650846 | |||||||
chr13:110650847 | G | A | 1 | a0002c0004t0001g0057 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1054+187C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110650847 | |||||||
chr13:110650853 | A | G | 187 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(184): Show |
202 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(199): Show |
intron_variant | MODIFIER | c.1054+181T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110650853 | |||||||
chr13:110650873 | C | T | 68 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(65): Show |
69 | HG00438.hp1 HG00597.hp1 HG01099.hp2 others(66): Show |
intron_variant | MODIFIER | c.1054+161G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110650873 | |||||||
chr13:110650893 | A | T | 12 | a0001c0002t0002g0022 a0001c0002t0002g0239 a0001c0002t0002g0241 others(9): Show |
13 | HG02280.hp2 HG02451.hp2 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.1054+141T>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110650893 | |||||||
chr13:110650924 | C | T | 1 | a0011c0017t0002g0264 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1054+110G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110650924 | |||||||
chr13:110650993 | C | T | 1 | a0001c0020t0002g0300 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1054+41G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110650993 | |||||||
chr13:110651026 | C | T | 1 | a0010c0018t0002g0263 | 1 | HG01192.hp2 | splice_region_variant&intron_variant | LOW | c.1054+8G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110651026 | |||||||
chr13:110651198 | A | G | 1 | a0002c0004t0003g0236 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.988-98T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110651198 | |||||||
chr13:110651263 | C | A | 1 | a0002c0004t0001g0053 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.988-163G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110651263 | |||||||
chr13:110651291 | C | T | 2 | a0001c0002t0001g0230 a0002c0004t0001g0235 |
2 | HG02970.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.988-191G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110651291 | |||||||
chr13:110651318 | G | A | 1 | a0003c0006t0002g0338 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.988-218C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110651318 | |||||||
chr13:110651380 | G | C | 2 | a0001c0002t0002g0268 a0001c0002t0002g0269 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.988-280C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110651380 | |||||||
chr13:110651381 | T | C | 2 | a0001c0002t0002g0268 a0001c0002t0002g0269 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.988-281A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110651381 | |||||||
chr13:110651412 | C | T | 2 | a0001c0002t0001g0230 a0002c0004t0001g0235 |
2 | HG02970.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.988-312G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110651412 | |||||||
chr13:110651532 | C | T | 2 | a0001c0002t0001g0017 a0001c0002t0001g0185 |
3 | HG01070.hp1 HG01071.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.988-432G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110651532 | |||||||
chr13:110651538 | A | G | 2 | a0001c0002t0002g0251 a0001c0002t0002g0255 |
2 | HG02717.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.988-438T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110651538 | |||||||
chr13:110651590 | C | A | 5 | a0001c0001t0001g0013 a0001c0001t0001g0082 a0001c0001t0001g0083 others(2): Show |
6 | NA18946.hp2 NA18964.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.988-490G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110651590 | |||||||
chr13:110651703 | C | A | 3 | a0001c0001t0001g0156 a0001c0001t0001g0161 a0001c0001t0001g0164 |
3 | NA18971.hp1 NA19000.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.988-603G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110651703 | |||||||
chr13:110651704 | C | T | 1 | a0001c0002t0001g0214 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.988-604G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110651704 | |||||||
chr13:110651955 | C | T | 43 | a0001c0003t0001g0287 a0001c0003t0001g0289 a0001c0003t0001g0294 others(40): Show |
48 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.988-855G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110651955 | |||||||
chr13:110652103 | C | T | 5 | a0001c0002t0001g0006 a0001c0002t0001g0204 a0001c0002t0001g0213 others(2): Show |
7 | HG01943.hp2 NA18946.hp1 NA18959.hp2 others(4): Show |
intron_variant | MODIFIER | c.988-1003G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110652103 | |||||||
chr13:110652142 | T | G | 50 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0017 others(47): Show |
57 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.988-1042A>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110652142 | |||||||
chr13:110652160 | C | T | 1 | a0002c0004t0001g0054 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.988-1060G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110652160 | |||||||
chr13:110652162 | G | A | 73 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0017 others(70): Show |
82 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(79): Show |
intron_variant | MODIFIER | c.988-1062C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110652162 | |||||||
chr13:110652453 | G | A | 2 | a0001c0003t0001g0020 a0001c0003t0001g0231 |
3 | HG02723.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.988-1353C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110652453 | |||||||
chr13:110652489 | T | G | 144 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(141): Show |
154 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(151): Show |
intron_variant | MODIFIER | c.988-1389A>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110652489 | |||||||
chr13:110652597 | T | C | 189 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(186): Show |
204 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(201): Show |
intron_variant | MODIFIER | c.988-1497A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110652597 | |||||||
chr13:110652845 | G | A | 2 | a0006c0015t0002g0066 a0006c0015t0002g0067 |
2 | HG02970.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.988-1745C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110652845 | |||||||
chr13:110652869 | G | T | 1 | a0001c0003t0002g0313 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.988-1769C>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110652869 | |||||||
chr13:110652995 | C | T | 73 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0017 others(70): Show |
82 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(79): Show |
intron_variant | MODIFIER | c.988-1895G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110652995 | |||||||
chr13:110653059 | C | T | 73 | a0001c0001t0001g0014 a0001c0001t0001g0151 a0001c0001t0001g0153 others(70): Show |
75 | HG00438.hp1 HG00597.hp1 HG01099.hp2 others(72): Show |
intron_variant | MODIFIER | c.988-1959G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110653059 | |||||||
chr13:110653116 | G | A | 45 | a0001c0001t0001g0011 a0001c0001t0001g0090 a0001c0003t0001g0287 others(42): Show |
51 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(48): Show |
intron_variant | MODIFIER | c.988-2016C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110653116 | |||||||
chr13:110653185 | A | AG | 187 | a0001c0001t0001g0119 a0001c0001t0002g0303 a0001c0001t0002g0304 others(184): Show |
202 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(199): Show |
intron_variant | MODIFIER | c.988-2086dupC | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110653185 | |||||||
chr13:110653199 | A | ATG | 163 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0002g0303 others(160): Show |
174 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(171): Show |
intron_variant | MODIFIER | c.988-2101_988-2100d others(4): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110653199 | |||||||
chr13:110653199 | A | ATGTG | 16 | a0001c0002t0001g0191 a0001c0003t0001g0287 a0001c0003t0001g0289 others(13): Show |
20 | HG00642.hp2 HG01123.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.988-2103_988-2100d others(6): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110653199 | |||||||
chr13:110653199 | A | ATGTGTG | 6 | a0001c0002t0001g0230 a0001c0003t0001g0294 a0001c0003t0002g0281 others(3): Show |
6 | HG03471.hp1 HG03491.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.988-2105_988-2100d others(8): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110653199 | |||||||
chr13:110653211 | G | GTGTGTT | 3 | a0002c0004t0001g0037 a0002c0004t0001g0038 a0002c0004t0001g0039 |
3 | HG01167.hp2 HG01168.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.988-2112_988-2111i others(8): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110653211 | |||||||
chr13:110653215 | T | G | 3 | a0002c0004t0001g0037 a0002c0004t0001g0038 a0002c0004t0001g0039 |
3 | HG01167.hp2 HG01168.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.988-2115A>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110653215 | |||||||
chr13:110653291 | G | A | 1 | a0001c0005t0001g0175 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.988-2191C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110653291 | |||||||
chr13:110653440 | C | T | 184 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(181): Show |
199 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(196): Show |
intron_variant | MODIFIER | c.988-2340G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110653440 | |||||||
chr13:110653528 | C | A | 1 | a0001c0002t0001g0211 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.988-2428G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110653528 | |||||||
chr13:110653608 | A | G | 4 | a0001c0002t0002g0255 a0001c0002t0002g0256 a0001c0002t0002g0258 others(1): Show |
4 | HG01891.hp2 HG02622.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.988-2508T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110653608 | |||||||
chr13:110653760 | A | C | 142 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(139): Show |
152 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(149): Show |
intron_variant | MODIFIER | c.988-2660T>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110653760 | |||||||
chr13:110653926 | C | T | 1 | a0001c0005t0001g0129 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.988-2826G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110653926 | |||||||
chr13:110653974 | T | C | 4 | a0001c0002t0001g0262 a0001c0002t0003g0265 a0001c0002t0003g0266 others(1): Show |
4 | HG01891.hp1 HG02258.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.988-2874A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110653974 | |||||||
chr13:110653975 | G | GT | 4 | a0001c0002t0001g0006 a0001c0002t0001g0204 a0001c0002t0001g0207 others(1): Show |
6 | NA18946.hp1 NA18949.hp1 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.988-2876dupA | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110653975 | |||||||
chr13:110653984 | T | C | 4 | a0001c0002t0002g0255 a0001c0002t0002g0256 a0001c0002t0002g0258 others(1): Show |
4 | HG01891.hp2 HG02622.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.988-2884A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110653984 | |||||||
chr13:110654092 | G | A | 13 | a0001c0002t0002g0022 a0001c0002t0002g0239 a0001c0002t0002g0241 others(10): Show |
14 | HG02280.hp2 HG02451.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.988-2992C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110654092 | |||||||
chr13:110654134 | C | G | 1 | a0001c0002t0003g0267 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.988-3034G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110654134 | |||||||
chr13:110654165 | C | T | 1 | a0001c0001t0001g0232 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.988-3065G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110654165 | |||||||
chr13:110654263 | A | G | 2 | a0001c0003t0001g0216 a0001c0003t0001g0217 |
2 | HG03688.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.988-3163T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110654263 | |||||||
chr13:110654264 | G | A | 2 | a0001c0003t0001g0216 a0001c0003t0001g0217 |
2 | HG03688.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.988-3164C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110654264 | |||||||
chr13:110654582 | C | G | 142 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(139): Show |
152 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(149): Show |
intron_variant | MODIFIER | c.988-3482G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110654582 | |||||||
chr13:110654761 | T | C | 79 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0017 others(76): Show |
88 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(85): Show |
intron_variant | MODIFIER | c.988-3661A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110654761 | |||||||
chr13:110654788 | T | C | 142 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(139): Show |
152 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(149): Show |
intron_variant | MODIFIER | c.988-3688A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110654788 | |||||||
chr13:110654871 | G | A | 142 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(139): Show |
152 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(149): Show |
intron_variant | MODIFIER | c.988-3771C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110654871 | |||||||
chr13:110654880 | G | GCCACTGC others(8): Show |
1 | a0001c0003t0002g0290 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.988-3795_988-3781d others(17): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110654880 | |||||||
chr13:110654921 | C | CA | 70 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0017 others(67): Show |
79 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(76): Show |
intron_variant | MODIFIER | c.988-3822dupT | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110654921 | |||||||
chr13:110654921 | C | CAA | 59 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(56): Show |
60 | HG00438.hp1 HG00597.hp1 HG01109.hp1 others(57): Show |
intron_variant | MODIFIER | c.988-3823_988-3822d others(4): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110654921 | |||||||
chr13:110654921 | C | CAAA | 7 | a0002c0004t0001g0046 a0002c0004t0001g0047 a0002c0004t0001g0048 others(4): Show |
7 | HG01099.hp2 HG01192.hp2 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.988-3824_988-3822d others(5): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110654921 | |||||||
chr13:110654921 | CA | C | 40 | a0001c0003t0001g0287 a0001c0003t0001g0289 a0001c0003t0001g0322 others(37): Show |
45 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.988-3822delT | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110654921 | |||||||
chr13:110654926 | A | AAAAAAAA others(9): Show |
1 | a0001c0001t0002g0076 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.988-3842_988-3827d others(18): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110654926 | |||||||
chr13:110654926 | AAAAAAAA others(9): Show |
A | 1 | a0001c0001t0001g0070 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.988-3842_988-3827d others(18): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110654926 | |||||||
chr13:110654932 | AAAAGAAA others(13): Show |
A | 4 | a0001c0002t0001g0262 a0001c0002t0003g0265 a0001c0002t0003g0266 others(1): Show |
4 | HG01891.hp1 HG02258.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.988-3852_988-3833d others(22): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110654932 | |||||||
chr13:110654950 | AAG | A | 60 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(57): Show |
61 | HG00438.hp1 HG00597.hp1 HG01099.hp2 others(58): Show |
intron_variant | MODIFIER | c.988-3852_988-3851d others(4): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110654950 | |||||||
chr13:110654951 | AG | A | 77 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0017 others(74): Show |
86 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(83): Show |
intron_variant | MODIFIER | c.988-3852delC | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110654951 | |||||||
chr13:110654952 | G | A | 4 | a0001c0002t0001g0207 a0001c0003t0002g0295 a0001c0003t0002g0296 others(1): Show |
4 | HG02055.hp2 HG02109.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.988-3852C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110654952 | |||||||
chr13:110655064 | G | A | 142 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(139): Show |
152 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(149): Show |
intron_variant | MODIFIER | c.988-3964C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110655064 | |||||||
chr13:110655088 | A | G | 142 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(139): Show |
152 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(149): Show |
intron_variant | MODIFIER | c.988-3988T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110655088 | |||||||
chr13:110655234 | CACAA | C | 23 | a0001c0003t0001g0322 a0001c0003t0001g0340 a0003c0006t0002g0025 others(20): Show |
24 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.988-4138_988-4135d others(6): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110655234 | |||||||
chr13:110655277 | C | A | 142 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(139): Show |
152 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(149): Show |
intron_variant | MODIFIER | c.988-4177G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110655277 | |||||||
chr13:110655298 | G | A | 6 | a0001c0002t0001g0005 a0001c0002t0001g0074 a0001c0002t0001g0177 others(3): Show |
8 | HG00738.hp1 HG01069.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.988-4198C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110655298 | |||||||
chr13:110655434 | A | G | 132 | a0001c0001t0001g0075 a0001c0001t0002g0303 a0001c0001t0002g0304 others(129): Show |
141 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(138): Show |
intron_variant | MODIFIER | c.988-4334T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110655434 | |||||||
chr13:110655439 | C | T | 1 | a0001c0005t0001g0170 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.988-4339G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110655439 | |||||||
chr13:110655478 | G | T | 134 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(131): Show |
143 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(140): Show |
intron_variant | MODIFIER | c.988-4378C>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110655478 | |||||||
chr13:110655506 | G | A | 134 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(131): Show |
143 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(140): Show |
intron_variant | MODIFIER | c.988-4406C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110655506 | |||||||
chr13:110655519 | C | T | 1 | a0002c0004t0001g0050 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.988-4419G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110655519 | |||||||
chr13:110655693 | G | C | 188 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(185): Show |
203 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(200): Show |
intron_variant | MODIFIER | c.988-4593C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110655693 | |||||||
chr13:110655699 | T | C | 134 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(131): Show |
143 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(140): Show |
intron_variant | MODIFIER | c.988-4599A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110655699 | |||||||
chr13:110655737 | C | G | 4 | a0001c0002t0001g0180 a0001c0002t0001g0183 a0001c0002t0001g0194 others(1): Show |
4 | HG01167.hp1 HG01169.hp1 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.988-4637G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110655737 | |||||||
chr13:110655863 | C | T | 151 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(148): Show |
164 | HG00140.hp1 HG00438.hp1 HG00597.hp1 others(161): Show |
intron_variant | MODIFIER | c.988-4763G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110655863 | |||||||
chr13:110655878 | T | C | 134 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(131): Show |
143 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(140): Show |
intron_variant | MODIFIER | c.988-4778A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110655878 | |||||||
chr13:110655932 | C | T | 4 | a0001c0002t0002g0255 a0001c0002t0002g0256 a0001c0002t0002g0258 others(1): Show |
4 | HG01891.hp2 HG02622.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.988-4832G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110655932 | |||||||
chr13:110656122 | G | A | 134 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(131): Show |
143 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(140): Show |
intron_variant | MODIFIER | c.988-5022C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110656122 | |||||||
chr13:110656124 | G | A | 3 | a0001c0001t0001g0014 a0001c0001t0001g0151 a0001c0001t0001g0228 |
4 | HG02040.hp2 HG02071.hp1 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.988-5024C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110656124 | |||||||
chr13:110656229 | G | C | 1 | a0010c0018t0002g0263 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.988-5129C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110656229 | |||||||
chr13:110656265 | T | C | 11 | a0001c0003t0001g0020 a0001c0003t0001g0155 a0001c0003t0001g0231 others(8): Show |
12 | HG01074.hp1 HG02257.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.988-5165A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110656265 | |||||||
chr13:110656268 | A | G | 1 | a0001c0003t0001g0322 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.988-5168T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110656268 | |||||||
chr13:110656318 | G | A | 2 | a0001c0003t0002g0302 a0001c0003t0002g0313 |
2 | NA18941.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.988-5218C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110656318 | |||||||
chr13:110656410 | C | T | 5 | a0001c0002t0001g0018 a0001c0002t0001g0176 a0001c0002t0001g0178 others(2): Show |
6 | HG00609.hp1 NA18984.hp1 NA19003.hp2 others(3): Show |
intron_variant | MODIFIER | c.988-5310G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110656410 | |||||||
chr13:110656428 | C | A | 1 | a0002c0004t0001g0037 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.988-5328G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110656428 | |||||||
chr13:110656446 | G | A | 37 | a0002c0004t0001g0008 a0002c0004t0001g0029 a0002c0004t0001g0030 others(34): Show |
38 | HG00597.hp1 HG01099.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.988-5346C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110656446 | |||||||
chr13:110656456 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0090 |
3 | HG00099.hp1 HG01081.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.988-5356G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110656456 | |||||||
chr13:110656515 | G | A | 58 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(55): Show |
59 | HG00438.hp1 HG00597.hp1 HG01099.hp2 others(56): Show |
intron_variant | MODIFIER | c.988-5415C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110656515 | |||||||
chr13:110656528 | G | T | 13 | a0001c0002t0002g0022 a0001c0002t0002g0239 a0001c0002t0002g0241 others(10): Show |
14 | HG02280.hp2 HG02451.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.988-5428C>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110656528 | |||||||
chr13:110656569 | C | T | 134 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(131): Show |
143 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(140): Show |
intron_variant | MODIFIER | c.988-5469G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110656569 | |||||||
chr13:110656586 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.988-5486T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110656586 | |||||||
chr13:110656618 | C | G | 16 | a0001c0003t0001g0287 a0001c0003t0001g0289 a0001c0003t0002g0007 others(13): Show |
20 | HG00642.hp2 HG01123.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.988-5518G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110656618 | |||||||
chr13:110656637 | C | T | 1 | a0001c0003t0001g0322 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.988-5537G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110656637 | |||||||
chr13:110656656 | A | G | 1 | a0002c0004t0003g0236 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.988-5556T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110656656 | |||||||
chr13:110656726 | T | C | 1 | a0001c0003t0002g0068 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.988-5626A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110656726 | |||||||
chr13:110656728 | C | T | 1 | a0001c0003t0001g0237 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.988-5628G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110656728 | |||||||
chr13:110656757 | G | T | 134 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(131): Show |
143 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(140): Show |
intron_variant | MODIFIER | c.988-5657C>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110656757 | |||||||
chr13:110656815 | C | T | 134 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(131): Show |
143 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(140): Show |
intron_variant | MODIFIER | c.988-5715G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110656815 | |||||||
chr13:110656889 | G | T | 1 | a0001c0001t0001g0095 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.988-5789C>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110656889 | |||||||
chr13:110656889 | GA | G | 182 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(179): Show |
197 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(194): Show |
intron_variant | MODIFIER | c.988-5790delT | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110656889 | |||||||
chr13:110656890 | A | T | 1 | a0001c0001t0001g0095 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.988-5790T>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110656890 | |||||||
chr13:110656920 | C | G | 177 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(174): Show |
191 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(188): Show |
intron_variant | MODIFIER | c.988-5820G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110656920 | |||||||
chr13:110656924 | T | A | 1 | a0001c0003t0002g0068 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.988-5824A>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110656924 | |||||||
chr13:110657051 | T | A | 1 | a0001c0001t0001g0225 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.988-5951A>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110657051 | |||||||
chr13:110657144 | T | TATAAG | 188 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(185): Show |
203 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(200): Show |
intron_variant | MODIFIER | c.988-6045_988-6044i others(7): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110657144 | |||||||
chr13:110657199 | A | AAATTTTA others(1): Show |
134 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(131): Show |
143 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(140): Show |
intron_variant | MODIFIER | c.988-6107_988-6100d others(10): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110657199 | |||||||
chr13:110657270 | C | T | 134 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(131): Show |
143 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(140): Show |
intron_variant | MODIFIER | c.988-6170G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110657270 | |||||||
chr13:110657324 | A | G | 1 | a0004c0012t0002g0261 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.987+6127T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110657324 | |||||||
chr13:110657377 | G | C | 3 | a0002c0004t0001g0037 a0002c0004t0001g0038 a0002c0004t0001g0039 |
3 | HG01167.hp2 HG01168.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.987+6074C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110657377 | |||||||
chr13:110657464 | T | C | 134 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(131): Show |
143 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(140): Show |
intron_variant | MODIFIER | c.987+5987A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110657464 | |||||||
chr13:110657615 | A | G | 4 | a0001c0001t0001g0098 a0001c0001t0001g0104 a0001c0001t0001g0105 others(1): Show |
4 | HG01928.hp1 HG01975.hp1 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.987+5836T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110657615 | |||||||
chr13:110657710 | G | A | 21 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(18): Show |
21 | HG00438.hp1 HG02630.hp2 HG02970.hp2 others(18): Show |
intron_variant | MODIFIER | c.987+5741C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110657710 | |||||||
chr13:110657739 | C | G | 177 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(174): Show |
191 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(188): Show |
intron_variant | MODIFIER | c.987+5712G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110657739 | |||||||
chr13:110657768 | T | A | 1 | a0001c0002t0001g0062 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.987+5683A>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110657768 | |||||||
chr13:110657774 | C | T | 1 | a0001c0002t0001g0062 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.987+5677G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110657774 | |||||||
chr13:110657775 | T | G | 1 | a0001c0002t0001g0062 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.987+5676A>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110657775 | |||||||
chr13:110657811 | T | G | 1 | a0001c0002t0001g0062 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.987+5640A>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110657811 | |||||||
chr13:110657827 | C | A | 58 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(55): Show |
59 | HG00438.hp1 HG00597.hp1 HG01099.hp2 others(56): Show |
intron_variant | MODIFIER | c.987+5624G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110657827 | |||||||
chr13:110657864 | T | C | 1 | a0001c0003t0001g0294 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.987+5587A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110657864 | |||||||
chr13:110657873 | G | A | 17 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(14): Show |
17 | HG00438.hp1 HG03654.hp2 HG03927.hp1 others(14): Show |
intron_variant | MODIFIER | c.987+5578C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110657873 | |||||||
chr13:110658001 | C | T | 134 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(131): Show |
143 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(140): Show |
intron_variant | MODIFIER | c.987+5450G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110658001 | |||||||
chr13:110658094 | T | G | 21 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(18): Show |
21 | HG00438.hp1 HG02630.hp2 HG02970.hp2 others(18): Show |
intron_variant | MODIFIER | c.987+5357A>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110658094 | |||||||
chr13:110658119 | GA | G | 6 | a0001c0001t0001g0021 a0001c0001t0001g0069 a0001c0001t0001g0079 others(3): Show |
7 | HG01346.hp2 HG01884.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.987+5331delT | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110658119 | |||||||
chr13:110658349 | G | C | 1 | a0001c0001t0002g0076 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.987+5102C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110658349 | |||||||
chr13:110658509 | C | T | 134 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(131): Show |
143 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(140): Show |
intron_variant | MODIFIER | c.987+4942G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110658509 | |||||||
chr13:110658569 | T | C | 134 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(131): Show |
143 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(140): Show |
intron_variant | MODIFIER | c.987+4882A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110658569 | |||||||
chr13:110658650 | C | T | 17 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(14): Show |
17 | HG00438.hp1 HG03654.hp2 HG03927.hp1 others(14): Show |
intron_variant | MODIFIER | c.987+4801G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110658650 | |||||||
chr13:110658651 | A | G | 134 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(131): Show |
143 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(140): Show |
intron_variant | MODIFIER | c.987+4800T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110658651 | |||||||
chr13:110658759 | C | A | 3 | a0001c0003t0002g0295 a0001c0003t0002g0296 a0001c0003t0002g0298 |
3 | HG02055.hp2 HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.987+4692G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110658759 | |||||||
chr13:110658761 | A | G | 134 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(131): Show |
143 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(140): Show |
intron_variant | MODIFIER | c.987+4690T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110658761 | |||||||
chr13:110658834 | C | T | 63 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(60): Show |
64 | HG00438.hp1 HG00597.hp1 HG01099.hp2 others(61): Show |
intron_variant | MODIFIER | c.987+4617G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110658834 | |||||||
chr13:110658883 | C | G | 1 | a0001c0002t0001g0262 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.987+4568G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110658883 | |||||||
chr13:110658886 | G | A | 3 | a0001c0009t0002g0277 a0001c0009t0002g0278 a0001c0009t0002g0279 |
3 | HG02486.hp1 HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.987+4565C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110658886 | |||||||
chr13:110659116 | G | A | 2 | a0001c0003t0001g0020 a0001c0003t0001g0231 |
3 | HG02723.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.987+4335C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110659116 | |||||||
chr13:110659468 | T | C | 2 | a0006c0015t0002g0066 a0006c0015t0002g0067 |
2 | HG02970.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.987+3983A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110659468 | |||||||
chr13:110659497 | CT | C | 187 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(184): Show |
202 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(199): Show |
intron_variant | MODIFIER | c.987+3953delA | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110659497 | |||||||
chr13:110659550 | T | C | 2 | a0001c0002t0001g0017 a0001c0002t0001g0185 |
3 | HG01070.hp1 HG01071.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.987+3901A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110659550 | |||||||
chr13:110659582 | C | T | 34 | a0002c0004t0001g0008 a0002c0004t0001g0029 a0002c0004t0001g0030 others(31): Show |
35 | HG00597.hp1 HG01099.hp2 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.987+3869G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110659582 | |||||||
chr13:110659709 | G | A | 3 | a0001c0002t0001g0064 a0001c0002t0002g0019 a0001c0002t0002g0200 |
4 | HG01346.hp1 HG01978.hp1 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.987+3742C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110659709 | |||||||
chr13:110659767 | G | A | 1 | a0010c0018t0002g0263 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.987+3684C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110659767 | |||||||
chr13:110659814 | T | C | 1 | a0001c0005t0001g0136 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.987+3637A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110659814 | |||||||
chr13:110659873 | C | T | 71 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0017 others(68): Show |
79 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(76): Show |
intron_variant | MODIFIER | c.987+3578G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110659873 | |||||||
chr13:110659874 | A | G | 134 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(131): Show |
143 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(140): Show |
intron_variant | MODIFIER | c.987+3577T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110659874 | |||||||
chr13:110659943 | T | C | 134 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(131): Show |
143 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(140): Show |
intron_variant | MODIFIER | c.987+3508A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110659943 | |||||||
chr13:110659993 | A | G | 134 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(131): Show |
143 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(140): Show |
intron_variant | MODIFIER | c.987+3458T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110659993 | |||||||
chr13:110660012 | T | C | 134 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(131): Show |
143 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(140): Show |
intron_variant | MODIFIER | c.987+3439A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110660012 | |||||||
chr13:110660051 | T | C | 134 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(131): Show |
143 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(140): Show |
intron_variant | MODIFIER | c.987+3400A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110660051 | |||||||
chr13:110660070 | G | C | 1 | a0001c0002t0001g0184 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.987+3381C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110660070 | |||||||
chr13:110660132 | T | A | 1 | a0001c0001t0001g0001 | 3 | HG01257.hp2 HG01258.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.987+3319A>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110660132 | |||||||
chr13:110660136 | A | G | 63 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(60): Show |
64 | HG00438.hp1 HG00597.hp1 HG01099.hp2 others(61): Show |
intron_variant | MODIFIER | c.987+3315T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110660136 | |||||||
chr13:110660139 | C | T | 1 | a0003c0006t0002g0326 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.987+3312G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110660139 | |||||||
chr13:110660306 | A | G | 134 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(131): Show |
143 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(140): Show |
intron_variant | MODIFIER | c.987+3145T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110660306 | |||||||
chr13:110660712 | C | G | 134 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(131): Show |
143 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(140): Show |
intron_variant | MODIFIER | c.987+2739G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110660712 | |||||||
chr13:110660763 | C | CT | 11 | a0001c0001t0001g0128 a0001c0003t0001g0020 a0001c0003t0001g0155 others(8): Show |
12 | HG00140.hp2 HG01074.hp1 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.987+2687dupA | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110660763 | |||||||
chr13:110660763 | C | CTT | 142 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(139): Show |
159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.987+2686_987+2687d others(4): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110660763 | |||||||
chr13:110660763 | CTTT | C | 125 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(122): Show |
134 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(131): Show |
intron_variant | MODIFIER | c.987+2685_987+2687d others(5): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110660763 | |||||||
chr13:110660847 | C | T | 17 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(14): Show |
17 | HG00438.hp1 HG03654.hp2 HG03927.hp1 others(14): Show |
intron_variant | MODIFIER | c.987+2604G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110660847 | |||||||
chr13:110660856 | G | C | 11 | a0001c0003t0001g0020 a0001c0003t0001g0155 a0001c0003t0001g0231 others(8): Show |
12 | HG01074.hp1 HG02257.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.987+2595C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110660856 | |||||||
chr13:110660864 | T | C | 130 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(127): Show |
139 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(136): Show |
intron_variant | MODIFIER | c.987+2587A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110660864 | |||||||
chr13:110660950 | T | C | 134 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(131): Show |
143 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(140): Show |
intron_variant | MODIFIER | c.987+2501A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110660950 | |||||||
chr13:110661066 | G | A | 37 | a0002c0004t0001g0008 a0002c0004t0001g0029 a0002c0004t0001g0030 others(34): Show |
38 | HG00597.hp1 HG01099.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.987+2385C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110661066 | |||||||
chr13:110661075 | T | G | 134 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(131): Show |
143 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(140): Show |
intron_variant | MODIFIER | c.987+2376A>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110661075 | |||||||
chr13:110661151 | A | G | 1 | a0002c0004t0001g0038 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.987+2300T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110661151 | |||||||
chr13:110661202 | C | A | 1 | a0001c0002t0001g0230 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.987+2249G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110661202 | |||||||
chr13:110661202 | C | T | 53 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0017 others(50): Show |
60 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(57): Show |
intron_variant | MODIFIER | c.987+2249G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110661202 | |||||||
chr13:110661269 | C | A | 1 | a0003c0006t0002g0323 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.987+2182G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110661269 | |||||||
chr13:110661327 | C | T | 159 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(156): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.987+2124G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110661327 | |||||||
chr13:110661515 | G | A | 4 | a0001c0002t0001g0262 a0001c0002t0003g0265 a0001c0002t0003g0266 others(1): Show |
4 | HG01891.hp1 HG02258.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.987+1936C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110661515 | |||||||
chr13:110661782 | T | C | 23 | a0001c0003t0001g0322 a0001c0003t0001g0340 a0003c0006t0002g0025 others(20): Show |
24 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.987+1669A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110661782 | |||||||
chr13:110661904 | G | C | 76 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0017 others(73): Show |
84 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(81): Show |
intron_variant | MODIFIER | c.987+1547C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110661904 | |||||||
chr13:110661920 | G | A | 2 | a0006c0015t0002g0066 a0006c0015t0002g0067 |
2 | HG02970.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.987+1531C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110661920 | |||||||
chr13:110662108 | T | C | 1 | a0003c0006t0002g0338 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.987+1343A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110662108 | |||||||
chr13:110662181 | CCATGCAA others(31): Show |
C | 5 | a0001c0002t0001g0262 a0001c0002t0003g0265 a0001c0002t0003g0266 others(2): Show |
5 | HG01192.hp2 HG01891.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.987+1232_987+1269d others(40): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110662181 | |||||||
chr13:110662194 | TGGTCGGG others(31): Show |
T | 71 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0017 others(68): Show |
79 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(76): Show |
intron_variant | MODIFIER | c.987+1219_987+1256d others(40): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110662194 | |||||||
chr13:110662283 | G | GAC | 75 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0017 others(72): Show |
83 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(80): Show |
intron_variant | MODIFIER | c.987+1166_987+1167d others(4): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110662283 | |||||||
chr13:110662286 | C | G | 75 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0017 others(72): Show |
83 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(80): Show |
intron_variant | MODIFIER | c.987+1165G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110662286 | |||||||
chr13:110662291 | T | C | 76 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0017 others(73): Show |
84 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(81): Show |
intron_variant | MODIFIER | c.987+1160A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110662291 | |||||||
chr13:110662293 | T | C | 76 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0017 others(73): Show |
84 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(81): Show |
intron_variant | MODIFIER | c.987+1158A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110662293 | |||||||
chr13:110662294 | G | A | 76 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0017 others(73): Show |
84 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(81): Show |
intron_variant | MODIFIER | c.987+1157C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110662294 | |||||||
chr13:110662296 | G | A | 76 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0017 others(73): Show |
84 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(81): Show |
intron_variant | MODIFIER | c.987+1155C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110662296 | |||||||
chr13:110662309 | A | G | 76 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0017 others(73): Show |
84 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(81): Show |
intron_variant | MODIFIER | c.987+1142T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110662309 | |||||||
chr13:110662317 | C | G | 76 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0017 others(73): Show |
84 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(81): Show |
intron_variant | MODIFIER | c.987+1134G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110662317 | |||||||
chr13:110662318 | T | C | 76 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0017 others(73): Show |
84 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(81): Show |
intron_variant | MODIFIER | c.987+1133A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110662318 | |||||||
chr13:110662321 | G | T | 76 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0017 others(73): Show |
84 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(81): Show |
intron_variant | MODIFIER | c.987+1130C>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110662321 | |||||||
chr13:110662323 | A | G | 76 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0017 others(73): Show |
84 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(81): Show |
intron_variant | MODIFIER | c.987+1128T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110662323 | |||||||
chr13:110662328 | C | A | 76 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0017 others(73): Show |
84 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(81): Show |
intron_variant | MODIFIER | c.987+1123G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110662328 | |||||||
chr13:110662329 | T | C | 76 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0017 others(73): Show |
84 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(81): Show |
intron_variant | MODIFIER | c.987+1122A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110662329 | |||||||
chr13:110662332 | T | C | 1 | a0012c0030t0001g0134 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.987+1119A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110662332 | |||||||
chr13:110662335 | G | A | 76 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0017 others(73): Show |
84 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(81): Show |
intron_variant | MODIFIER | c.987+1116C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110662335 | |||||||
chr13:110662349 | T | A | 2 | a0001c0002t0001g0017 a0001c0002t0001g0185 |
3 | HG01070.hp1 HG01071.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.987+1102A>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110662349 | |||||||
chr13:110662349 | T | C | 74 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0018 others(71): Show |
81 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(78): Show |
intron_variant | MODIFIER | c.987+1102A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110662349 | |||||||
chr13:110662557 | C | T | 258 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(255): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.987+894G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110662557 | |||||||
chr13:110662603 | G | A | 24 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(21): Show |
24 | HG00438.hp1 HG02622.hp1 HG02630.hp2 others(21): Show |
intron_variant | MODIFIER | c.987+848C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110662603 | |||||||
chr13:110662647 | C | T | 258 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(255): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.987+804G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110662647 | |||||||
chr13:110662666 | T | C | 49 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0017 others(46): Show |
56 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.987+785A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110662666 | |||||||
chr13:110662902 | G | A | 179 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(176): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.987+549C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110662902 | |||||||
chr13:110662940 | C | T | 76 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0065 others(73): Show |
84 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(81): Show |
intron_variant | MODIFIER | c.987+511G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110662940 | |||||||
chr13:110662952 | T | C | 292 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(289): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(321): Show |
intron_variant | MODIFIER | c.987+499A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110662952 | |||||||
chr13:110662971 | C | T | 1 | a0002c0004t0001g0040 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.987+480G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110662971 | |||||||
chr13:110663058 | G | A | 256 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(253): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.987+393C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110663058 | |||||||
chr13:110663072 | A | G | 1 | a0002c0004t0001g0054 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.987+379T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110663072 | |||||||
chr13:110663142 | A | G | 261 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(258): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.987+309T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110663142 | |||||||
chr13:110663159 | A | C | 271 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(268): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.987+292T>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110663159 | |||||||
chr13:110663175 | G | C | 1 | a0001c0005t0001g0135 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.987+276C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110663175 | |||||||
chr13:110663204 | A | G | 257 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(254): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.987+247T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110663204 | |||||||
chr13:110663248 | A | G | 44 | a0001c0001t0001g0072 a0001c0001t0001g0092 a0001c0001t0001g0106 others(41): Show |
45 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.987+203T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110663248 | |||||||
chr13:110663254 | G | A | 10 | a0001c0002t0001g0262 a0001c0002t0003g0265 a0001c0002t0003g0266 others(7): Show |
10 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.987+197C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110663254 | |||||||
chr13:110663696 | G | A | 1 | a0001c0007t0001g0271 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.920-178C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110663696 | |||||||
chr13:110663696 | G | C | 257 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(254): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.920-178C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110663696 | |||||||
chr13:110663714 | C | T | 257 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(254): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.920-196G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110663714 | |||||||
chr13:110663937 | A | G | 1 | a0001c0001t0002g0150 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.920-419T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110663937 | |||||||
chr13:110664084 | TTAAGGAA others(4): Show |
T | 23 | a0001c0003t0001g0322 a0001c0003t0001g0340 a0003c0006t0002g0025 others(20): Show |
24 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.920-577_920-567del others(11): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110664084 | |||||||
chr13:110664102 | T | G | 1 | a0001c0003t0001g0294 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.920-584A>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110664102 | |||||||
chr13:110664118 | C | G | 4 | a0001c0003t0002g0281 a0001c0003t0002g0282 a0001c0003t0002g0283 others(1): Show |
4 | HG03491.hp1 HG03492.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.920-600G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110664118 | |||||||
chr13:110664243 | A | G | 260 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(257): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.920-725T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110664243 | |||||||
chr13:110664462 | A | G | 1 | a0003c0006t0002g0329 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.920-944T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110664462 | |||||||
chr13:110664536 | C | A | 255 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(252): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.920-1018G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110664536 | |||||||
chr13:110664585 | C | T | 6 | a0001c0001t0001g0021 a0001c0001t0001g0069 a0001c0001t0001g0079 others(3): Show |
7 | HG01346.hp2 HG01884.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.920-1067G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110664585 | |||||||
chr13:110664768 | T | C | 1 | a0001c0003t0001g0237 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.920-1250A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110664768 | |||||||
chr13:110664791 | T | A | 68 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0017 others(65): Show |
76 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(73): Show |
intron_variant | MODIFIER | c.920-1273A>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110664791 | |||||||
chr13:110664924 | G | A | 3 | a0001c0005t0001g0167 a0001c0005t0001g0170 a0001c0005t0001g0171 |
3 | HG01952.hp1 HG02486.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.920-1406C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110664924 | |||||||
chr13:110665058 | C | T | 1 | a0001c0002t0003g0267 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.920-1540G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110665058 | |||||||
chr13:110665171 | G | A | 1 | a0003c0011t0002g0240 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.920-1653C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110665171 | |||||||
chr13:110665189 | A | G | 258 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(255): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.920-1671T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110665189 | |||||||
chr13:110665252 | C | A | 1 | a0001c0002t0001g0190 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.920-1734G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110665252 | |||||||
chr13:110665302 | T | C | 258 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(255): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.920-1784A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110665302 | |||||||
chr13:110665384 | T | G | 1 | a0001c0020t0002g0300 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.920-1866A>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110665384 | |||||||
chr13:110665425 | G | A | 257 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(254): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.920-1907C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110665425 | |||||||
chr13:110665813 | C | T | 63 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(60): Show |
64 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.919+1527G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110665813 | |||||||
chr13:110666139 | C | G | 11 | a0001c0002t0001g0262 a0001c0002t0001g0276 a0001c0002t0003g0265 others(8): Show |
11 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.919+1201G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110666139 | |||||||
chr13:110666267 | G | A | 4 | a0001c0002t0001g0180 a0001c0002t0001g0183 a0001c0002t0001g0194 others(1): Show |
4 | HG01167.hp1 HG01169.hp1 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.919+1073C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110666267 | |||||||
chr13:110666284 | C | T | 2 | a0003c0006t0002g0330 a0003c0006t0002g0339 |
2 | NA18972.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.919+1056G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110666284 | |||||||
chr13:110666294 | G | A | 1 | a0001c0002t0001g0208 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.919+1046C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110666294 | |||||||
chr13:110666352 | T | C | 258 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(255): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.919+988A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110666352 | |||||||
chr13:110666447 | T | C | 258 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(255): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.919+893A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110666447 | |||||||
chr13:110666484 | T | C | 258 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(255): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.919+856A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110666484 | |||||||
chr13:110666489 | G | A | 50 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0017 others(47): Show |
57 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.919+851C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110666489 | |||||||
chr13:110666508 | G | A | 1 | a0001c0003t0001g0287 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.919+832C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110666508 | |||||||
chr13:110666681 | T | C | 3 | a0001c0009t0002g0277 a0001c0009t0002g0278 a0001c0009t0002g0279 |
3 | HG02486.hp1 HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.919+659A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110666681 | |||||||
chr13:110666944 | T | C | 1 | a0001c0003t0001g0294 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.919+396A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110666944 | |||||||
chr13:110667009 | C | T | 257 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(254): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.919+331G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110667009 | |||||||
chr13:110667175 | A | C | 1 | a0004c0012t0002g0261 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.919+165T>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110667175 | |||||||
chr13:110667537 | G | A | 148 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(145): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.786-64C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110667537 | |||||||
chr13:110667598 | A | G | 1 | a0001c0005t0001g0175 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.786-125T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110667598 | |||||||
chr13:110667731 | C | G | 148 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(145): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.786-258G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110667731 | |||||||
chr13:110668024 | G | A | 2 | a0002c0004t0001g0031 a0002c0004t0001g0032 |
2 | NA18967.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.786-551C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110668024 | |||||||
chr13:110668073 | G | A | 17 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(14): Show |
17 | HG00438.hp1 HG03654.hp2 HG03927.hp1 others(14): Show |
intron_variant | MODIFIER | c.786-600C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110668073 | |||||||
chr13:110668125 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.786-652G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110668125 | |||||||
chr13:110668269 | C | T | 63 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(60): Show |
64 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.786-796G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110668269 | |||||||
chr13:110668270 | G | A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0090 |
3 | HG00099.hp1 HG01081.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.786-797C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110668270 | |||||||
chr13:110668271 | C | T | 63 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(60): Show |
64 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.786-798G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110668271 | |||||||
chr13:110668399 | G | A | 3 | a0001c0009t0002g0277 a0001c0009t0002g0278 a0001c0009t0002g0279 |
3 | HG02486.hp1 HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.786-926C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110668399 | |||||||
chr13:110668401 | G | T | 1 | a0001c0002t0001g0262 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.786-928C>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110668401 | |||||||
chr13:110668497 | G | A | 1 | a0002c0004t0002g0060 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.786-1024C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110668497 | |||||||
chr13:110668520 | T | C | 269 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(266): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.786-1047A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110668520 | |||||||
chr13:110668521 | G | A | 139 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(136): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.786-1048C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110668521 | |||||||
chr13:110668536 | C | T | 2 | a0002c0004t0001g0055 a0002c0004t0001g0056 |
2 | NA18963.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.786-1063G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110668536 | |||||||
chr13:110668541 | C | CA | 255 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(252): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.786-1069dupT | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110668541 | |||||||
chr13:110668578 | T | C | 2 | a0001c0001t0002g0307 a0001c0001t0002g0314 |
2 | NA18939.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.786-1105A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110668578 | |||||||
chr13:110668579 | C | T | 1 | a0001c0003t0001g0237 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.786-1106G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110668579 | |||||||
chr13:110668662 | G | C | 1 | a0001c0003t0002g0290 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.786-1189C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110668662 | |||||||
chr13:110668722 | G | A | 2 | a0001c0003t0001g0216 a0001c0003t0001g0217 |
2 | HG03688.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.786-1249C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110668722 | |||||||
chr13:110668725 | G | A | 50 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0017 others(47): Show |
57 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.786-1252C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110668725 | |||||||
chr13:110669036 | T | C | 4 | a0001c0003t0002g0281 a0001c0003t0002g0282 a0001c0003t0002g0283 others(1): Show |
4 | HG03491.hp1 HG03492.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.786-1563A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110669036 | |||||||
chr13:110669071 | C | G | 1 | a0002c0004t0001g0034 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.786-1598G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110669071 | |||||||
chr13:110669204 | A | C | 139 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(136): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.786-1731T>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110669204 | |||||||
chr13:110669410 | C | T | 148 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(145): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.786-1937G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110669410 | |||||||
chr13:110669416 | G | A | 1 | a0001c0019t0001g0205 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.786-1943C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110669416 | |||||||
chr13:110669624 | C | T | 46 | a0001c0001t0001g0291 a0001c0003t0001g0155 a0001c0003t0001g0287 others(43): Show |
51 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.786-2151G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110669624 | |||||||
chr13:110669648 | G | A | 1 | a0002c0008t0001g0036 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.786-2175C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110669648 | |||||||
chr13:110669735 | G | A | 1 | a0001c0003t0002g0285 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.786-2262C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110669735 | |||||||
chr13:110669764 | C | T | 2 | a0001c0001t0001g0128 a0003c0006t0002g0025 |
3 | HG00140.hp2 HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.786-2291G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110669764 | |||||||
chr13:110669893 | C | T | 1 | a0001c0003t0002g0068 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.786-2420G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110669893 | |||||||
chr13:110669919 | G | T | 1 | a0001c0003t0001g0294 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.786-2446C>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110669919 | |||||||
chr13:110669993 | C | T | 3 | a0001c0009t0002g0277 a0001c0009t0002g0278 a0001c0009t0002g0279 |
3 | HG02486.hp1 HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.786-2520G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110669993 | |||||||
chr13:110669995 | G | A | 3 | a0001c0002t0002g0239 a0001c0002t0002g0241 a0001c0002t0002g0242 |
3 | HG02647.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.786-2522C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110669995 | |||||||
chr13:110670003 | G | C | 1 | a0001c0002t0003g0267 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.786-2530C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110670003 | |||||||
chr13:110670066 | C | T | 2 | a0001c0001t0001g0010 a0001c0001t0001g0099 |
3 | HG00280.hp2 HG01192.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.786-2593G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110670066 | |||||||
chr13:110670266 | G | T | 2 | a0001c0003t0001g0216 a0001c0003t0001g0217 |
2 | HG03688.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.786-2793C>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110670266 | |||||||
chr13:110670430 | T | C | 1 | a0001c0003t0002g0283 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.786-2957A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110670430 | |||||||
chr13:110670612 | G | C | 1 | a0001c0003t0001g0294 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.786-3139C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110670612 | |||||||
chr13:110670658 | C | G | 46 | a0001c0001t0001g0291 a0001c0003t0001g0155 a0001c0003t0001g0287 others(43): Show |
51 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.786-3185G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110670658 | |||||||
chr13:110670934 | C | T | 139 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(136): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.786-3461G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110670934 | |||||||
chr13:110670958 | G | T | 63 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(60): Show |
64 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.786-3485C>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110670958 | |||||||
chr13:110670976 | C | T | 23 | a0001c0003t0001g0322 a0001c0003t0001g0340 a0003c0006t0002g0025 others(20): Show |
24 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.786-3503G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110670976 | |||||||
chr13:110671049 | A | G | 2 | a0001c0001t0001g0143 a0001c0001t0001g0157 |
2 | NA19055.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.786-3576T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110671049 | |||||||
chr13:110671232 | C | T | 23 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(20): Show |
23 | HG00438.hp1 HG02622.hp1 HG02970.hp2 others(20): Show |
intron_variant | MODIFIER | c.786-3759G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110671232 | |||||||
chr13:110671320 | T | C | 257 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(254): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.786-3847A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110671320 | |||||||
chr13:110671336 | G | A | 23 | a0001c0003t0001g0322 a0001c0003t0001g0340 a0003c0006t0002g0025 others(20): Show |
24 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.786-3863C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110671336 | |||||||
chr13:110671472 | T | C | 3 | a0002c0004t0001g0031 a0002c0004t0001g0032 a0002c0004t0001g0034 |
3 | NA18967.hp1 NA18994.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.786-3999A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110671472 | |||||||
chr13:110671660 | C | G | 1 | a0001c0001t0001g0082 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.786-4187G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110671660 | |||||||
chr13:110671915 | C | G | 257 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(254): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.786-4442G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110671915 | |||||||
chr13:110671950 | G | A | 257 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(254): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.786-4477C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110671950 | |||||||
chr13:110671982 | T | C | 1 | a0011c0017t0002g0264 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.786-4509A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110671982 | |||||||
chr13:110672047 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.786-4574C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110672047 | |||||||
chr13:110672436 | G | A | 148 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(145): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.785+4538C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110672436 | |||||||
chr13:110672473 | C | T | 2 | a0006c0015t0002g0066 a0006c0015t0002g0067 |
2 | HG02970.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.785+4501G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110672473 | |||||||
chr13:110672514 | C | T | 1 | a0001c0003t0001g0294 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.785+4460G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110672514 | |||||||
chr13:110672570 | G | C | 1 | a0004c0012t0002g0261 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.785+4404C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110672570 | |||||||
chr13:110673079 | C | G | 11 | a0001c0002t0001g0262 a0001c0002t0001g0276 a0001c0002t0003g0265 others(8): Show |
11 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.785+3895G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110673079 | |||||||
chr13:110673087 | C | T | 46 | a0001c0001t0001g0291 a0001c0003t0001g0155 a0001c0003t0001g0287 others(43): Show |
51 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.785+3887G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110673087 | |||||||
chr13:110673134 | G | A | 3 | a0001c0009t0002g0277 a0001c0009t0002g0278 a0001c0009t0002g0279 |
3 | HG02486.hp1 HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.785+3840C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110673134 | |||||||
chr13:110673164 | T | G | 139 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(136): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.785+3810A>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110673164 | |||||||
chr13:110673169 | T | C | 269 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(266): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.785+3805A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110673169 | |||||||
chr13:110673182 | C | T | 269 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(266): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.785+3792G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110673182 | |||||||
chr13:110673297 | G | A | 2 | a0001c0001t0001g0085 a0001c0001t0001g0094 |
2 | HG02886.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.785+3677C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110673297 | |||||||
chr13:110673557 | C | T | 1 | a0001c0005t0001g0167 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.785+3417G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110673557 | |||||||
chr13:110673563 | T | G | 139 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(136): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.785+3411A>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110673563 | |||||||
chr13:110673602 | A | G | 11 | a0001c0002t0001g0262 a0001c0002t0001g0276 a0001c0002t0003g0265 others(8): Show |
11 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.785+3372T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110673602 | |||||||
chr13:110673605 | T | A | 17 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(14): Show |
17 | HG00438.hp1 HG03654.hp2 HG03927.hp1 others(14): Show |
intron_variant | MODIFIER | c.785+3369A>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110673605 | |||||||
chr13:110673681 | C | A | 2 | a0001c0002t0002g0268 a0001c0002t0002g0269 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.785+3293G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110673681 | |||||||
chr13:110673752 | T | G | 1 | a0001c0003t0002g0298 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.785+3222A>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110673752 | |||||||
chr13:110673762 | A | G | 258 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(255): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.785+3212T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110673762 | |||||||
chr13:110673943 | G | C | 1 | a0001c0003t0001g0237 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.785+3031C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110673943 | |||||||
chr13:110674055 | A | T | 1 | a0001c0003t0001g0237 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.785+2919T>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110674055 | |||||||
chr13:110674078 | A | G | 257 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(254): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.785+2896T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110674078 | |||||||
chr13:110674148 | T | G | 4 | a0001c0002t0001g0061 a0001c0002t0001g0062 a0001c0002t0001g0063 others(1): Show |
4 | HG00621.hp2 NA18941.hp1 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.785+2826A>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110674148 | |||||||
chr13:110674224 | T | C | 50 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0017 others(47): Show |
57 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.785+2750A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110674224 | |||||||
chr13:110674241 | A | C | 1 | a0001c0002t0001g0230 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.785+2733T>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110674241 | |||||||
chr13:110674251 | A | G | 1 | a0001c0002t0001g0062 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.785+2723T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110674251 | |||||||
chr13:110674297 | T | C | 2 | a0001c0027t0001g0172 a0009c0029t0001g0173 |
2 | HG00639.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.785+2677A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110674297 | |||||||
chr13:110674420 | A | ACAACCAT others(323): Show |
9 | a0001c0003t0001g0322 a0003c0006t0002g0025 a0003c0006t0002g0323 others(6): Show |
10 | HG00280.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.785+2553_785+2554i others(332): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110674420 | |||||||
chr13:110674420 | A | ACAACCAT others(324): Show |
3 | a0001c0003t0001g0340 a0003c0006t0002g0325 a0003c0006t0002g0326 |
3 | HG01109.hp2 HG06807.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.785+2553_785+2554i others(333): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110674420 | |||||||
chr13:110674420 | A | ACAACCAT others(325): Show |
7 | a0003c0006t0002g0318 a0003c0006t0002g0319 a0003c0006t0002g0320 others(4): Show |
7 | HG00408.hp2 HG00558.hp1 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.785+2553_785+2554i others(334): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110674420 | |||||||
chr13:110674420 | A | ACAACCAT others(326): Show |
4 | a0003c0006t0002g0328 a0003c0006t0002g0329 a0003c0006t0002g0330 others(1): Show |
4 | NA18612.hp1 NA18964.hp1 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.785+2553_785+2554i others(335): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110674420 | |||||||
chr13:110674569 | A | G | 1 | a0001c0002t0002g0255 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.785+2405T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110674569 | |||||||
chr13:110674616 | C | T | 38 | a0002c0004t0001g0008 a0002c0004t0001g0029 a0002c0004t0001g0030 others(35): Show |
39 | HG00597.hp1 HG01099.hp2 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.785+2358G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110674616 | |||||||
chr13:110674677 | G | A | 1 | a0002c0004t0001g0218 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.785+2297C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110674677 | |||||||
chr13:110675023 | C | G | 11 | a0001c0002t0001g0262 a0001c0002t0001g0276 a0001c0002t0003g0265 others(8): Show |
11 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.785+1951G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110675023 | |||||||
chr13:110675032 | T | C | 63 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0017 others(60): Show |
71 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(68): Show |
intron_variant | MODIFIER | c.785+1942A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110675032 | |||||||
chr13:110675042 | T | TA | 337 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(334): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.785+1931dupT | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110675042 | |||||||
chr13:110675047 | C | G | 337 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(334): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.785+1927G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110675047 | |||||||
chr13:110675418 | T | C | 257 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(254): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.785+1556A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110675418 | |||||||
chr13:110675425 | G | A | 12 | a0001c0002t0001g0262 a0001c0002t0001g0276 a0001c0002t0003g0265 others(9): Show |
12 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.785+1549C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110675425 | |||||||
chr13:110675495 | A | G | 269 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(266): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.785+1479T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110675495 | |||||||
chr13:110675551 | C | T | 1 | a0001c0003t0001g0237 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.785+1423G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110675551 | |||||||
chr13:110675718 | C | A | 1 | a0001c0001t0002g0150 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.785+1256G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110675718 | |||||||
chr13:110675744 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.785+1230C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110675744 | |||||||
chr13:110675745 | C | T | 1 | a0001c0002t0001g0230 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.785+1229G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110675745 | |||||||
chr13:110675799 | C | T | 5 | a0001c0001t0001g0098 a0001c0001t0001g0104 a0001c0001t0001g0105 others(2): Show |
5 | HG01928.hp1 HG01975.hp1 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.785+1175G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110675799 | |||||||
chr13:110675851 | A | C | 1 | a0001c0002t0001g0230 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.785+1123T>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110675851 | |||||||
chr13:110675910 | C | T | 1 | a0002c0004t0001g0050 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.785+1064G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110675910 | |||||||
chr13:110675968 | C | T | 7 | a0001c0005t0001g0002 a0001c0005t0001g0080 a0001c0005t0001g0145 others(4): Show |
9 | NA18954.hp1 NA18973.hp2 NA18990.hp1 others(6): Show |
intron_variant | MODIFIER | c.785+1006G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110675968 | |||||||
chr13:110676057 | G | A | 2 | a0001c0001t0001g0021 a0001c0001t0001g0079 |
3 | HG01346.hp2 HG01884.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.785+917C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110676057 | |||||||
chr13:110676216 | C | T | 12 | a0001c0002t0001g0262 a0001c0002t0001g0276 a0001c0002t0003g0265 others(9): Show |
12 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.785+758G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110676216 | |||||||
chr13:110676272 | T | C | 257 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(254): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.785+702A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110676272 | |||||||
chr13:110676273 | G | A | 1 | a0003c0011t0002g0240 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.785+701C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110676273 | |||||||
chr13:110676300 | C | G | 257 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(254): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.785+674G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110676300 | |||||||
chr13:110676381 | G | C | 257 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(254): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.785+593C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110676381 | |||||||
chr13:110676418 | C | T | 40 | a0002c0004t0001g0008 a0002c0004t0001g0029 a0002c0004t0001g0030 others(37): Show |
41 | HG00597.hp1 HG00738.hp2 HG01099.hp2 others(38): Show |
intron_variant | MODIFIER | c.785+556G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110676418 | |||||||
chr13:110676500 | T | A | 1 | a0003c0011t0002g0240 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.785+474A>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110676500 | |||||||
chr13:110676580 | C | T | 1 | a0002c0004t0001g0219 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.785+394G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110676580 | |||||||
chr13:110676632 | G | A | 1 | a0001c0003t0001g0297 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.785+342C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110676632 | |||||||
chr13:110676743 | C | A | 6 | a0001c0003t0001g0020 a0001c0003t0001g0231 a0001c0003t0001g0244 others(3): Show |
7 | HG01074.hp1 HG02647.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.785+231G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110676743 | |||||||
chr13:110676752 | C | T | 11 | a0001c0002t0001g0262 a0001c0002t0001g0276 a0001c0002t0003g0265 others(8): Show |
11 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.785+222G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110676752 | |||||||
chr13:110676772 | G | A | 46 | a0001c0001t0001g0291 a0001c0003t0001g0155 a0001c0003t0001g0287 others(43): Show |
51 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.785+202C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110676772 | |||||||
chr13:110676852 | CA | C | 50 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0017 others(47): Show |
57 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.785+121delT | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110676852 | |||||||
chr13:110676867 | G | T | 11 | a0001c0002t0001g0262 a0001c0002t0001g0276 a0001c0002t0003g0265 others(8): Show |
11 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.785+107C>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110676867 | |||||||
chr13:110677232 | A | C | 1 | a0001c0003t0001g0237 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.656-129T>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677232 | |||||||
chr13:110677242 | C | T | 11 | a0001c0002t0001g0262 a0001c0002t0001g0276 a0001c0002t0003g0265 others(8): Show |
11 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.656-139G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677242 | |||||||
chr13:110677242 | CCAGACAG others(69): Show |
C | 139 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(136): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.656-215_656-140del others(76): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677242 | |||||||
chr13:110677263 | A | G | 11 | a0001c0002t0001g0262 a0001c0002t0001g0276 a0001c0002t0003g0265 others(8): Show |
11 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.656-160T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677263 | |||||||
chr13:110677265 | A | G | 11 | a0001c0002t0001g0262 a0001c0002t0001g0276 a0001c0002t0003g0265 others(8): Show |
11 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.656-162T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677265 | |||||||
chr13:110677265 | AGACCCAG others(69): Show |
A | 9 | a0001c0003t0001g0020 a0001c0003t0001g0231 a0001c0003t0001g0244 others(6): Show |
10 | HG01074.hp1 HG02486.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.656-238_656-163del others(76): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677265 | |||||||
chr13:110677308 | A | C | 11 | a0001c0002t0001g0262 a0001c0002t0001g0276 a0001c0002t0003g0265 others(8): Show |
11 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.656-205T>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677308 | |||||||
chr13:110677308 | ACATGGAA others(69): Show |
A | 63 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0017 others(60): Show |
71 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(68): Show |
intron_variant | MODIFIER | c.656-281_656-206del others(76): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677308 | |||||||
chr13:110677332 | C | T | 63 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(60): Show |
64 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.656-229G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677332 | |||||||
chr13:110677333 | C | T | 63 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(60): Show |
64 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.656-230G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677333 | |||||||
chr13:110677341 | G | A | 64 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(61): Show |
65 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(62): Show |
intron_variant | MODIFIER | c.656-238C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677341 | |||||||
chr13:110677342 | G | A | 63 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(60): Show |
64 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.656-239C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677342 | |||||||
chr13:110677342 | G | C | 1 | a0001c0003t0001g0237 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.656-239C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677342 | |||||||
chr13:110677348 | G | A | 63 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(60): Show |
64 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.656-245C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677348 | |||||||
chr13:110677361 | C | T | 63 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(60): Show |
64 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.656-258G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677361 | |||||||
chr13:110677366 | A | ATACAATC others(79): Show |
1 | a0002c0004t0002g0238 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.656-264_656-263ins others(86): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677366 | |||||||
chr13:110677368 | A | ACAATCAC others(87): Show |
62 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(59): Show |
63 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(60): Show |
intron_variant | MODIFIER | c.656-266_656-265ins others(94): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677368 | |||||||
chr13:110677373 | A | C | 62 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(59): Show |
63 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(60): Show |
intron_variant | MODIFIER | c.656-270T>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677373 | |||||||
chr13:110677375 | A | C | 1 | a0002c0004t0002g0238 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.656-272T>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677375 | |||||||
chr13:110677375 | A | G | 62 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(59): Show |
63 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(60): Show |
intron_variant | MODIFIER | c.656-272T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677375 | |||||||
chr13:110677376 | T | C | 62 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(59): Show |
63 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(60): Show |
intron_variant | MODIFIER | c.656-273A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677376 | |||||||
chr13:110677383 | A | G | 63 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(60): Show |
64 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.656-280T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677383 | |||||||
chr13:110677387 | T | C | 63 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(60): Show |
64 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.656-284A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677387 | |||||||
chr13:110677402 | T | C | 63 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(60): Show |
64 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.656-299A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677402 | |||||||
chr13:110677407 | CT | C | 63 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(60): Show |
64 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.656-305delA | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677407 | |||||||
chr13:110677410 | A | G | 63 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(60): Show |
64 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.656-307T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677410 | |||||||
chr13:110677415 | G | A | 1 | a0001c0002t0001g0276 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.656-312C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677415 | |||||||
chr13:110677421 | C | CCAGA | 63 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(60): Show |
64 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.656-319_656-318ins others(4): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677421 | |||||||
chr13:110677424 | A | G | 63 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(60): Show |
64 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.656-321T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677424 | |||||||
chr13:110677424 | ATCACCCC others(140): Show |
A | 64 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0017 others(61): Show |
72 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(69): Show |
intron_variant | MODIFIER | c.656-468_656-322del | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677424 | |||||||
chr13:110677491 | C | T | 1 | a0001c0003t0002g0068 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.656-388G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677491 | |||||||
chr13:110677538 | T | TCAGACAG others(339): Show |
1 | a0001c0003t0001g0237 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.656-436_656-435ins others(346): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677538 | |||||||
chr13:110677538 | T | TCAGACAG others(45): Show |
9 | a0001c0003t0001g0020 a0001c0003t0001g0231 a0001c0003t0001g0244 others(6): Show |
10 | HG01074.hp1 HG02486.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.656-436_656-435ins others(52): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677538 | |||||||
chr13:110677538 | TCAGACAG others(166): Show |
T | 196 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(193): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.656-608_656-436del | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677538 | |||||||
chr13:110677557 | C | T | 3 | a0002c0004t0001g0041 a0002c0004t0001g0042 a0002c0004t0001g0043 |
3 | HG01361.hp1 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.656-454G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677557 | |||||||
chr13:110677564 | C | CCAGACAG others(20): Show |
63 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(60): Show |
64 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.656-488_656-462dup others(27): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677564 | |||||||
chr13:110677685 | TCAGACAG others(19): Show |
T | 15 | a0001c0003t0001g0020 a0001c0003t0001g0231 a0001c0003t0001g0244 others(12): Show |
16 | HG01074.hp1 HG01099.hp2 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.656-608_656-583del others(26): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677685 | |||||||
chr13:110677705 | G | A | 1 | a0003c0011t0002g0240 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.656-602C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677705 | |||||||
chr13:110677725 | C | T | 1 | a0001c0002t0003g0266 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.656-622G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677725 | |||||||
chr13:110677731 | G | A | 1 | a0001c0002t0002g0199 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.656-628C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677731 | |||||||
chr13:110677779 | C | T | 50 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0017 others(47): Show |
57 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.656-676G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677779 | |||||||
chr13:110677856 | C | T | 18 | a0001c0001t0001g0291 a0001c0003t0001g0155 a0001c0003t0001g0287 others(15): Show |
22 | HG00642.hp2 HG01123.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.656-753G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677856 | |||||||
chr13:110677940 | C | T | 3 | a0001c0003t0002g0068 a0006c0015t0002g0066 a0006c0015t0002g0067 |
3 | HG02970.hp2 HG03486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.656-837G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677940 | |||||||
chr13:110677947 | G | A | 1 | a0001c0002t0003g0265 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.656-844C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677947 | |||||||
chr13:110677948 | G | A | 75 | a0001c0001t0001g0291 a0001c0001t0002g0303 a0001c0001t0002g0304 others(72): Show |
80 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.656-845C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677948 | |||||||
chr13:110678020 | G | A | 4 | a0001c0003t0001g0297 a0001c0003t0002g0295 a0001c0003t0002g0296 others(1): Show |
4 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.656-917C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110678020 | |||||||
chr13:110678021 | T | C | 196 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(193): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.656-918A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110678021 | |||||||
chr13:110678024 | A | G | 196 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(193): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.656-921T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110678024 | |||||||
chr13:110678058 | C | T | 139 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(136): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.656-955G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110678058 | |||||||
chr13:110678081 | C | T | 1 | a0001c0002t0001g0204 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.656-978G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110678081 | |||||||
chr13:110678087 | C | T | 1 | a0002c0008t0003g0243 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.656-984G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110678087 | |||||||
chr13:110678129 | T | C | 23 | a0001c0003t0001g0322 a0001c0003t0001g0340 a0003c0006t0002g0025 others(20): Show |
24 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.656-1026A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110678129 | |||||||
chr13:110678153 | A | G | 266 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(263): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.656-1050T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110678153 | |||||||
chr13:110678175 | C | T | 34 | a0001c0001t0001g0291 a0001c0002t0001g0262 a0001c0002t0001g0276 others(31): Show |
38 | HG00642.hp2 HG01123.hp1 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.656-1072G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110678175 | |||||||
chr13:110678189 | C | T | 1 | a0001c0005t0001g0129 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.656-1086G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110678189 | |||||||
chr13:110678270 | C | T | 13 | a0001c0002t0002g0022 a0001c0002t0002g0239 a0001c0002t0002g0241 others(10): Show |
14 | HG02280.hp2 HG02451.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.656-1167G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110678270 | |||||||
chr13:110678288 | C | T | 2 | a0001c0002t0003g0265 a0001c0002t0003g0266 |
2 | HG01891.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.656-1185G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110678288 | |||||||
chr13:110678358 | C | G | 1 | a0001c0001t0001g0106 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.656-1255G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110678358 | |||||||
chr13:110678411 | A | G | 4 | a0001c0002t0002g0255 a0001c0002t0002g0256 a0001c0002t0002g0258 others(1): Show |
4 | HG01891.hp2 HG02622.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.656-1308T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110678411 | |||||||
chr13:110678455 | C | T | 3 | a0001c0003t0002g0311 a0001c0003t0002g0316 a0001c0003t0002g0317 |
3 | NA18956.hp2 NA18980.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.656-1352G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110678455 | |||||||
chr13:110678456 | G | A | 1 | a0001c0002t0001g0204 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.656-1353C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110678456 | |||||||
chr13:110678471 | T | C | 1 | a0001c0001t0001g0142 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.656-1368A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110678471 | |||||||
chr13:110678555 | A | G | 1 | a0001c0001t0001g0116 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.656-1452T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110678555 | |||||||
chr13:110678712 | C | T | 4 | a0001c0002t0001g0061 a0001c0002t0001g0062 a0001c0002t0001g0063 others(1): Show |
4 | HG00621.hp2 NA18941.hp1 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.656-1609G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110678712 | |||||||
chr13:110678744 | A | G | 1 | a0001c0003t0001g0237 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.656-1641T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110678744 | |||||||
chr13:110678833 | G | A | 50 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0017 others(47): Show |
57 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.656-1730C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110678833 | |||||||
chr13:110678841 | G | C | 13 | a0001c0002t0001g0262 a0001c0002t0001g0276 a0001c0002t0002g0268 others(10): Show |
13 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.656-1738C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110678841 | |||||||
chr13:110678869 | G | C | 1 | a0001c0001t0001g0092 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.656-1766C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110678869 | |||||||
chr13:110678891 | A | G | 23 | a0001c0001t0001g0291 a0001c0003t0001g0155 a0001c0003t0001g0287 others(20): Show |
27 | HG00642.hp2 HG01123.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.656-1788T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110678891 | |||||||
chr13:110678928 | C | T | 1 | a0001c0003t0002g0068 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.656-1825G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110678928 | |||||||
chr13:110679026 | G | A | 1 | a0001c0002t0003g0267 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.656-1923C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679026 | |||||||
chr13:110679034 | T | TAAAGGCT others(25): Show |
245 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(242): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.656-1932_656-1931i others(34): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679034 | |||||||
chr13:110679051 | G | T | 60 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(57): Show |
61 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.656-1948C>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679051 | |||||||
chr13:110679118 | G | A | 22 | a0001c0002t0001g0262 a0001c0002t0001g0276 a0001c0002t0002g0268 others(19): Show |
23 | HG01074.hp1 HG01891.hp1 HG01943.hp1 others(20): Show |
intron_variant | MODIFIER | c.656-2015C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679118 | |||||||
chr13:110679138 | G | A | 1 | a0001c0001t0001g0114 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.656-2035C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679138 | |||||||
chr13:110679206 | C | T | 1 | a0001c0003t0001g0237 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.656-2103G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679206 | |||||||
chr13:110679358 | C | T | 23 | a0001c0001t0001g0291 a0001c0003t0001g0155 a0001c0003t0001g0287 others(20): Show |
27 | HG00642.hp2 HG01123.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.656-2255G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679358 | |||||||
chr13:110679386 | C | T | 1 | a0001c0002t0001g0061 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.656-2283G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679386 | |||||||
chr13:110679455 | G | A | 1 | a0001c0002t0003g0267 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.656-2352C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679455 | |||||||
chr13:110679511 | C | T | 60 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(57): Show |
61 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.656-2408G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679511 | |||||||
chr13:110679549 | A | AAAAG | 14 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(11): Show |
14 | HG03654.hp2 NA18939.hp1 NA18941.hp2 others(11): Show |
intron_variant | MODIFIER | c.656-2450_656-2447d others(6): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679549 | |||||||
chr13:110679549 | A | AAAAGAAA others(19): Show |
6 | a0001c0002t0002g0022 a0001c0002t0002g0251 a0003c0011t0002g0252 others(3): Show |
7 | HG02280.hp2 HG02451.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.656-2472_656-2447d others(28): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679549 | |||||||
chr13:110679567 | A | G | 3 | a0001c0003t0001g0297 a0001c0003t0002g0295 a0001c0003t0002g0296 |
3 | HG02055.hp2 HG02257.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.656-2464T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679567 | |||||||
chr13:110679567 | AAGAG | A | 7 | a0002c0004t0001g0030 a0002c0004t0001g0031 a0002c0004t0001g0032 others(4): Show |
7 | HG02015.hp1 HG02155.hp2 HG04184.hp1 others(4): Show |
intron_variant | MODIFIER | c.656-2468_656-2465d others(6): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679567 | |||||||
chr13:110679569 | G | A | 3 | a0001c0003t0001g0297 a0001c0003t0002g0295 a0001c0003t0002g0296 |
3 | HG02055.hp2 HG02257.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.656-2466C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679569 | |||||||
chr13:110679569 | GAGAGAGA others(1): Show |
G | 3 | a0001c0009t0002g0277 a0001c0009t0002g0278 a0001c0009t0002g0279 |
3 | HG02486.hp1 HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.656-2474_656-2467d others(10): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679569 | |||||||
chr13:110679569 | GAGAGAGA others(9): Show |
G | 1 | a0001c0001t0001g0128 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.656-2482_656-2467d others(18): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679569 | |||||||
chr13:110679571 | G | A | 6 | a0001c0001t0002g0312 a0001c0003t0002g0301 a0001c0003t0002g0310 others(3): Show |
6 | HG00438.hp1 HG02970.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.656-2468C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679571 | |||||||
chr13:110679573 | G | A | 215 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(212): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.656-2470C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679573 | |||||||
chr13:110679573 | G | GAGAAAGA others(23): Show |
1 | a0004c0012t0002g0261 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.656-2471_656-2470i others(32): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679573 | |||||||
chr13:110679573 | G | GAGAAAGA others(23): Show |
6 | a0001c0002t0001g0005 a0001c0002t0001g0074 a0001c0002t0001g0177 others(3): Show |
8 | HG00738.hp1 HG01069.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.656-2471_656-2470i others(32): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679573 | |||||||
chr13:110679573 | G | GAGAAAGA others(27): Show |
25 | a0001c0002t0001g0006 a0001c0002t0001g0017 a0001c0002t0001g0064 others(22): Show |
29 | HG00621.hp2 HG01070.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.656-2471_656-2470i others(36): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679573 | |||||||
chr13:110679573 | G | GAGAAAGA others(31): Show |
3 | a0001c0002t0001g0193 a0001c0002t0001g0213 a0001c0002t0002g0199 |
3 | HG04204.hp1 NA18946.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.656-2471_656-2470i others(40): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679573 | |||||||
chr13:110679573 | G | GAGAAAGA others(35): Show |
1 | a0001c0002t0001g0206 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.656-2471_656-2470i others(44): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679573 | |||||||
chr13:110679573 | G | GAGAAAGA others(29): Show |
1 | a0001c0002t0001g0207 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.656-2471_656-2470i others(38): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679573 | |||||||
chr13:110679573 | G | GAGAAAGA others(22): Show |
1 | a0001c0002t0001g0187 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.656-2471_656-2470i others(31): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679573 | |||||||
chr13:110679573 | G | GAGAAAGA others(23): Show |
1 | a0001c0002t0001g0188 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.656-2471_656-2470i others(32): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679573 | |||||||
chr13:110679573 | G | GAGAAAGA others(27): Show |
9 | a0001c0002t0001g0018 a0001c0002t0001g0061 a0001c0002t0001g0063 others(6): Show |
10 | HG00609.hp1 HG03669.hp1 NA18941.hp1 others(7): Show |
intron_variant | MODIFIER | c.656-2471_656-2470i others(36): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679573 | |||||||
chr13:110679573 | G | GAGAAAGA others(28): Show |
1 | a0001c0002t0001g0062 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.656-2471_656-2470i others(37): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679573 | |||||||
chr13:110679577 | A | AAGAAAGA others(15): Show |
1 | a0001c0002t0002g0239 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.656-2475_656-2474i others(24): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679577 | |||||||
chr13:110679581 | A | AAGAAAGA others(11): Show |
1 | a0011c0017t0002g0264 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.656-2479_656-2478i others(20): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679581 | |||||||
chr13:110679585 | AAGAAAGA others(7): Show |
A | 137 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(134): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.656-2496_656-2483d others(16): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679585 | |||||||
chr13:110679585 | AAGAAAGA others(11): Show |
A | 1 | a0001c0001t0001g0115 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.656-2500_656-2483d others(20): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679585 | |||||||
chr13:110679589 | AAGAAAGA others(3): Show |
A | 1 | a0001c0003t0001g0237 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.656-2496_656-2487d others(12): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679589 | |||||||
chr13:110679591 | G | GAGAGAGA others(33): Show |
1 | a0001c0002t0001g0186 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.656-2489_656-2488i others(42): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679591 | |||||||
chr13:110679593 | A | AAG | 3 | a0002c0004t0001g0037 a0002c0004t0001g0038 a0002c0008t0001g0035 |
3 | HG01168.hp1 HG01255.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.656-2492_656-2491d others(4): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679593 | |||||||
chr13:110679593 | A | G | 1 | a0001c0002t0001g0186 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.656-2490T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679593 | |||||||
chr13:110679593 | AAGAAAGA others(1): Show |
A | 22 | a0001c0003t0001g0322 a0001c0003t0001g0340 a0003c0006t0002g0025 others(19): Show |
23 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(20): Show |
intron_variant | MODIFIER | c.656-2498_656-2491d others(10): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679593 | |||||||
chr13:110679593 | AAGAAAGA others(3): Show |
A | 1 | a0003c0006t0002g0338 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.656-2500_656-2491d others(12): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679593 | |||||||
chr13:110679597 | A | AAG | 39 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0017 others(36): Show |
46 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.656-2496_656-2495d others(4): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679597 | |||||||
chr13:110679597 | A | AAGAAAG | 13 | a0001c0002t0001g0262 a0001c0002t0001g0276 a0001c0002t0002g0268 others(10): Show |
13 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.656-2495_656-2494i others(8): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679597 | |||||||
chr13:110679597 | A | G | 45 | a0001c0002t0001g0186 a0001c0002t0001g0193 a0001c0002t0001g0202 others(42): Show |
46 | HG00597.hp1 HG01099.hp2 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.656-2494T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679597 | |||||||
chr13:110679597 | AAGAGAG | A | 20 | a0001c0001t0001g0291 a0001c0003t0001g0155 a0001c0003t0001g0287 others(17): Show |
24 | HG00642.hp2 HG01123.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.656-2500_656-2495d others(8): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679597 | |||||||
chr13:110679597 | AAGAGAGA others(1): Show |
A | 6 | a0001c0003t0001g0020 a0001c0003t0001g0231 a0001c0003t0001g0244 others(3): Show |
7 | HG01074.hp1 HG02647.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.656-2502_656-2495d others(10): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679597 | |||||||
chr13:110679597 | AAGAGAGA others(3): Show |
A | 2 | a0001c0003t0002g0295 a0001c0003t0002g0296 |
2 | HG02055.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.656-2504_656-2495d others(12): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679597 | |||||||
chr13:110679597 | AAGAGAGA others(7): Show |
A | 1 | a0001c0003t0001g0297 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.656-2508_656-2495d others(16): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679597 | |||||||
chr13:110679599 | G | GAA | 7 | a0001c0002t0001g0194 a0001c0002t0001g0195 a0001c0002t0002g0255 others(4): Show |
7 | HG01167.hp1 HG01169.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.656-2497_656-2496i others(4): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679599 | |||||||
chr13:110679599 | G | GAGAAAGA others(13): Show |
2 | a0004c0012t0002g0260 a0004c0012t0004g0259 |
2 | HG02622.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.656-2497_656-2496i others(22): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679599 | |||||||
chr13:110679599 | G | GAGAAAGA others(17): Show |
4 | a0001c0002t0002g0241 a0001c0002t0002g0242 a0001c0002t0002g0245 others(1): Show |
4 | HG02647.hp1 HG02809.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.656-2497_656-2496i others(26): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679599 | |||||||
chr13:110679601 | G | A | 24 | a0001c0001t0001g0128 a0001c0001t0002g0303 a0001c0001t0002g0304 others(21): Show |
24 | HG00140.hp2 HG00438.hp1 HG02486.hp1 others(21): Show |
intron_variant | MODIFIER | c.656-2498C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679601 | |||||||
chr13:110679603 | G | A | 3 | a0004c0012t0002g0260 a0004c0012t0004g0259 a0011c0017t0002g0264 |
3 | HG02622.hp1 HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.656-2500C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679603 | |||||||
chr13:110679605 | G | A | 1 | a0001c0001t0002g0312 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.656-2502C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679605 | |||||||
chr13:110679607 | G | A | 21 | a0001c0001t0001g0291 a0001c0003t0001g0155 a0001c0003t0001g0287 others(18): Show |
25 | HG00642.hp2 HG01123.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.656-2504C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679607 | |||||||
chr13:110679618 | A | G | 1 | a0001c0003t0001g0237 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.656-2515T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679618 | |||||||
chr13:110679622 | A | G | 1 | a0001c0003t0001g0237 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.656-2519T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679622 | |||||||
chr13:110679640 | C | T | 23 | a0001c0001t0001g0291 a0001c0003t0001g0155 a0001c0003t0001g0287 others(20): Show |
27 | HG00642.hp2 HG01123.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.656-2537G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679640 | |||||||
chr13:110679650 | C | CGGAG | 153 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(150): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.656-2551_656-2548d others(6): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679650 | |||||||
chr13:110679650 | C | CGGAGGGA others(1): Show |
18 | a0001c0001t0001g0001 a0001c0001t0001g0070 a0001c0001t0001g0071 others(15): Show |
20 | HG01257.hp2 HG01258.hp1 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.656-2555_656-2548d others(10): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679650 | |||||||
chr13:110679650 | C | CGGAGGGA others(5): Show |
31 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0082 others(28): Show |
37 | HG00642.hp2 HG01123.hp1 HG01243.hp2 others(34): Show |
intron_variant | MODIFIER | c.656-2559_656-2548d others(14): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679650 | |||||||
chr13:110679650 | C | CGGAGGGA others(9): Show |
2 | a0001c0001t0002g0150 a0001c0003t0001g0297 |
2 | HG02257.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.656-2563_656-2548d others(18): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679650 | |||||||
chr13:110679650 | C | CGGGGAGG others(7): Show |
1 | a0001c0003t0002g0283 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.656-2548_656-2547i others(16): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679650 | |||||||
chr13:110679650 | CGGAG | C | 11 | a0001c0002t0002g0022 a0001c0002t0002g0239 a0001c0002t0002g0241 others(8): Show |
12 | HG02280.hp2 HG02451.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.656-2551_656-2548d others(6): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679650 | |||||||
chr13:110679674 | G | A | 1 | a0001c0002t0002g0241 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.656-2571C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679674 | |||||||
chr13:110679689 | G | A | 1 | a0001c0003t0002g0316 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.656-2586C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679689 | |||||||
chr13:110679732 | G | C | 5 | a0001c0003t0001g0287 a0001c0003t0001g0289 a0001c0003t0002g0024 others(2): Show |
6 | HG00642.hp2 HG01123.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.656-2629C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679732 | |||||||
chr13:110679786 | A | G | 96 | a0001c0001t0001g0291 a0001c0001t0002g0303 a0001c0001t0002g0304 others(93): Show |
101 | HG00438.hp1 HG00597.hp1 HG00642.hp2 others(98): Show |
intron_variant | MODIFIER | c.656-2683T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679786 | |||||||
chr13:110679864 | G | A | 1 | a0002c0008t0003g0243 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.656-2761C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679864 | |||||||
chr13:110679884 | T | C | 36 | a0001c0001t0001g0291 a0001c0002t0001g0262 a0001c0002t0001g0276 others(33): Show |
40 | HG00642.hp2 HG01123.hp1 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.656-2781A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679884 | |||||||
chr13:110679947 | A | G | 23 | a0001c0001t0001g0291 a0001c0003t0001g0155 a0001c0003t0001g0287 others(20): Show |
27 | HG00642.hp2 HG01123.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.656-2844T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679947 | |||||||
chr13:110680147 | AGGGGG | A | 20 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0075 others(17): Show |
20 | HG00597.hp2 HG01099.hp1 HG02040.hp2 others(17): Show |
intron_variant | MODIFIER | c.655+2899_655+2903d others(7): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110680147 | |||||||
chr13:110680147 | AGGGGGG | A | 73 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0013 others(70): Show |
80 | HG00280.hp1 HG00609.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.655+2898_655+2903d others(8): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110680147 | |||||||
chr13:110680147 | AGGGGGGG | A | 194 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(191): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.655+2897_655+2903d others(9): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110680147 | |||||||
chr13:110680147 | AGGGGGGG others(1): Show |
A | 47 | a0001c0003t0001g0244 a0001c0003t0001g0246 a0001c0003t0001g0247 others(44): Show |
48 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.655+2896_655+2903d others(10): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110680147 | |||||||
chr13:110680156 | G | C | 1 | a0001c0001t0001g0072 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.655+2895C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110680156 | |||||||
chr13:110680156 | G | T | 1 | a0002c0004t0001g0037 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.655+2895C>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110680156 | |||||||
chr13:110680157 | G | C | 32 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0070 others(29): Show |
34 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.655+2894C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110680157 | |||||||
chr13:110680157 | G | T | 1 | a0001c0003t0001g0237 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.655+2894C>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110680157 | |||||||
chr13:110680158 | G | C | 2 | a0001c0002t0001g0208 a0001c0005t0001g0016 |
3 | HG01074.hp2 HG01981.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.655+2893C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110680158 | |||||||
chr13:110680206 | A | G | 139 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(136): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.655+2845T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110680206 | |||||||
chr13:110680323 | G | A | 139 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(136): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.655+2728C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110680323 | |||||||
chr13:110680341 | C | T | 60 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(57): Show |
61 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.655+2710G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110680341 | |||||||
chr13:110680388 | G | A | 1 | a0001c0002t0001g0184 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.655+2663C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110680388 | |||||||
chr13:110680451 | G | T | 6 | a0002c0004t0001g0029 a0002c0004t0001g0030 a0002c0004t0001g0031 others(3): Show |
6 | HG02015.hp1 NA18967.hp1 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.655+2600C>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110680451 | |||||||
chr13:110680501 | C | T | 139 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(136): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.655+2550G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110680501 | |||||||
chr13:110680539 | G | A | 139 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(136): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.655+2512C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110680539 | |||||||
chr13:110680578 | T | C | 9 | a0001c0003t0001g0020 a0001c0003t0001g0231 a0001c0003t0001g0244 others(6): Show |
10 | HG01074.hp1 HG02486.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.655+2473A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110680578 | |||||||
chr13:110680630 | CA | C | 333 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(330): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.655+2420delT | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110680630 | |||||||
chr13:110680712 | G | T | 3 | a0001c0003t0002g0281 a0001c0003t0002g0282 a0001c0003t0002g0283 |
3 | HG03491.hp1 HG03492.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.655+2339C>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110680712 | |||||||
chr13:110680832 | C | T | 2 | a0006c0015t0002g0066 a0006c0015t0002g0067 |
2 | HG02970.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.655+2219G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110680832 | |||||||
chr13:110680959 | G | A | 1 | a0001c0002t0003g0265 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.655+2092C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110680959 | |||||||
chr13:110680968 | G | A | 51 | a0001c0001t0001g0011 a0001c0001t0001g0090 a0001c0002t0001g0005 others(48): Show |
59 | HG00099.hp1 HG00609.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.655+2083C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110680968 | |||||||
chr13:110681235 | T | C | 1 | a0002c0004t0001g0049 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.655+1816A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110681235 | |||||||
chr13:110681444 | T | C | 1 | a0002c0008t0001g0036 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.655+1607A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110681444 | |||||||
chr13:110681624 | C | T | 13 | a0001c0001t0001g0122 a0001c0002t0001g0276 a0001c0002t0002g0268 others(10): Show |
13 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.655+1427G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110681624 | |||||||
chr13:110681625 | G | A | 1 | a0001c0005t0001g0136 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.655+1426C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110681625 | |||||||
chr13:110682000 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.655+1051A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110682000 | |||||||
chr13:110682004 | G | A | 337 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(334): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.655+1047C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110682004 | |||||||
chr13:110682011 | A | G | 4 | a0001c0002t0002g0255 a0001c0002t0002g0256 a0001c0002t0002g0258 others(1): Show |
4 | HG01891.hp2 HG02622.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.655+1040T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110682011 | |||||||
chr13:110682091 | A | G | 3 | a0001c0009t0002g0277 a0001c0009t0002g0278 a0001c0009t0002g0279 |
3 | HG02486.hp1 HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.655+960T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110682091 | |||||||
chr13:110682206 | T | C | 1 | a0001c0002t0001g0230 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.655+845A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110682206 | |||||||
chr13:110682367 | G | A | 60 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(57): Show |
61 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.655+684C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110682367 | |||||||
chr13:110682753 | T | C | 2 | a0002c0004t0001g0058 a0002c0004t0001g0059 |
2 | HG02155.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.655+298A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110682753 | |||||||
chr13:110682761 | G | A | 61 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(58): Show |
62 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(59): Show |
intron_variant | MODIFIER | c.655+290C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110682761 | |||||||
chr13:110682768 | A | C | 1 | a0001c0002t0001g0230 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.655+283T>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110682768 | |||||||
chr13:110682837 | C | T | 1 | a0007c0014t0002g0250 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.655+214G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110682837 | |||||||
chr13:110682972 | C | T | 24 | a0001c0003t0001g0322 a0001c0003t0001g0340 a0001c0003t0002g0285 others(21): Show |
25 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(22): Show |
intron_variant | MODIFIER | c.655+79G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110682972 | |||||||
chr13:110683135 | CTG | C | 4 | a0001c0002t0002g0255 a0001c0002t0002g0256 a0001c0002t0002g0258 others(1): Show |
4 | HG01891.hp2 HG02622.hp2 HG03098.hp1 others(1): Show |
splice_acceptor_variant&splice_region_variant&intron_variant | HIGH | c.572-3_572-2delCA | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110683135 | |||||||
chr13:110683286 | G | T | 13 | a0001c0002t0001g0262 a0001c0002t0001g0276 a0001c0002t0002g0268 others(10): Show |
13 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.572-152C>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110683286 | |||||||
chr13:110683382 | C | A | 73 | a0001c0001t0001g0291 a0001c0002t0001g0005 a0001c0002t0001g0006 others(70): Show |
84 | HG00609.hp1 HG00621.hp2 HG00642.hp2 others(81): Show |
intron_variant | MODIFIER | c.572-248G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110683382 | |||||||
chr13:110683410 | C | T | 3 | a0001c0009t0002g0277 a0001c0009t0002g0278 a0001c0009t0002g0279 |
3 | HG02486.hp1 HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.572-276G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110683410 | |||||||
chr13:110683602 | G | A | 3 | a0001c0009t0002g0277 a0001c0009t0002g0278 a0001c0009t0002g0279 |
3 | HG02486.hp1 HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.572-468C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110683602 | |||||||
chr13:110683696 | T | G | 3 | a0003c0006t0002g0324 a0003c0006t0002g0330 a0003c0006t0002g0339 |
3 | NA18972.hp1 NA19000.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.572-562A>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110683696 | |||||||
chr13:110683740 | GGT | G | 4 | a0001c0002t0002g0255 a0001c0002t0002g0256 a0001c0002t0002g0258 others(1): Show |
4 | HG01891.hp2 HG02622.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.572-608_572-607del others(2): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110683740 | |||||||
chr13:110683874 | A | G | 1 | a0010c0018t0002g0263 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.572-740T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110683874 | |||||||
chr13:110684041 | T | C | 184 | a0001c0001t0001g0291 a0001c0001t0002g0303 a0001c0001t0002g0304 others(181): Show |
199 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(196): Show |
intron_variant | MODIFIER | c.572-907A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110684041 | |||||||
chr13:110684054 | G | A | 13 | a0001c0002t0001g0262 a0001c0002t0001g0276 a0001c0002t0002g0268 others(10): Show |
13 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.572-920C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110684054 | |||||||
chr13:110684056 | A | G | 333 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(330): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.572-922T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110684056 | |||||||
chr13:110684336 | C | T | 23 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(20): Show |
23 | HG00438.hp1 HG02622.hp1 HG02970.hp2 others(20): Show |
intron_variant | MODIFIER | c.572-1202G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110684336 | |||||||
chr13:110684368 | T | C | 1 | a0001c0003t0001g0237 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.572-1234A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110684368 | |||||||
chr13:110684519 | G | C | 23 | a0001c0003t0001g0322 a0001c0003t0001g0340 a0003c0006t0002g0025 others(20): Show |
24 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.572-1385C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110684519 | |||||||
chr13:110684616 | C | T | 2 | a0001c0001t0001g0143 a0001c0001t0001g0157 |
2 | NA19055.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.572-1482G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110684616 | |||||||
chr13:110684617 | C | T | 17 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(14): Show |
17 | HG00438.hp1 HG03654.hp2 HG03927.hp1 others(14): Show |
intron_variant | MODIFIER | c.572-1483G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110684617 | |||||||
chr13:110684709 | C | T | 1 | a0001c0003t0002g0310 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.572-1575G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110684709 | |||||||
chr13:110684927 | T | G | 333 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(330): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.572-1793A>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110684927 | |||||||
chr13:110684937 | G | T | 2 | a0001c0002t0002g0268 a0001c0002t0002g0269 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.572-1803C>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110684937 | |||||||
chr13:110684998 | C | T | 2 | a0002c0008t0001g0233 a0002c0008t0001g0234 |
2 | HG00738.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.572-1864G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110684998 | |||||||
chr13:110685010 | C | G | 1 | a0001c0003t0001g0294 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.572-1876G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110685010 | |||||||
chr13:110685078 | C | A | 4 | a0001c0001t0001g0101 a0001c0001t0001g0122 a0001c0001t0001g0123 others(1): Show |
4 | NA18943.hp1 NA18966.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.572-1944G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110685078 | |||||||
chr13:110685102 | A | G | 1 | a0001c0001t0001g0102 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.572-1968T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110685102 | |||||||
chr13:110685221 | A | G | 1 | a0001c0002t0001g0262 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.572-2087T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110685221 | |||||||
chr13:110685259 | A | G | 14 | a0001c0002t0001g0230 a0001c0002t0001g0262 a0001c0002t0001g0276 others(11): Show |
14 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.572-2125T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110685259 | |||||||
chr13:110685277 | T | G | 4 | a0001c0003t0001g0244 a0001c0003t0001g0246 a0001c0003t0001g0247 others(1): Show |
4 | HG01074.hp1 HG02647.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.572-2143A>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110685277 | |||||||
chr13:110685295 | G | A | 1 | a0003c0024t0001g0141 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.572-2161C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110685295 | |||||||
chr13:110685309 | C | CA | 13 | a0001c0002t0001g0262 a0001c0002t0001g0276 a0001c0002t0002g0268 others(10): Show |
13 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.572-2176dupT | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110685309 | |||||||
chr13:110685430 | T | C | 139 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(136): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.571+2291A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110685430 | |||||||
chr13:110685454 | G | A | 1 | a0001c0002t0001g0221 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.571+2267C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110685454 | |||||||
chr13:110685517 | T | C | 2 | a0002c0008t0001g0233 a0002c0008t0001g0234 |
2 | HG00738.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.571+2204A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110685517 | |||||||
chr13:110685519 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.571+2202G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110685519 | |||||||
chr13:110685547 | T | G | 2 | a0001c0003t0001g0340 a0003c0006t0002g0025 |
3 | HG01069.hp2 HG01071.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.571+2174A>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110685547 | |||||||
chr13:110685798 | T | C | 6 | a0001c0003t0001g0020 a0001c0003t0001g0231 a0001c0003t0001g0244 others(3): Show |
7 | HG01074.hp1 HG02647.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.571+1923A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110685798 | |||||||
chr13:110685882 | A | G | 1 | a0001c0003t0002g0068 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.571+1839T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110685882 | |||||||
chr13:110685935 | C | T | 1 | a0002c0004t0001g0218 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.571+1786G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110685935 | |||||||
chr13:110685963 | G | C | 9 | a0001c0001t0001g0100 a0001c0001t0001g0124 a0001c0001t0001g0125 others(6): Show |
9 | HG00597.hp2 HG02040.hp1 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.571+1758C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110685963 | |||||||
chr13:110685992 | G | GA | 200 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(197): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.571+1728dupT | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110685992 | |||||||
chr13:110685992 | G | GAA | 76 | a0001c0001t0001g0128 a0001c0001t0001g0291 a0001c0002t0001g0005 others(73): Show |
88 | HG00140.hp2 HG00609.hp1 HG00621.hp2 others(85): Show |
intron_variant | MODIFIER | c.571+1727_571+1728d others(4): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110685992 | |||||||
chr13:110686006 | A | AG | 13 | a0001c0002t0001g0262 a0001c0002t0001g0276 a0001c0002t0002g0268 others(10): Show |
13 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.571+1714_571+1715i others(3): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110686006 | |||||||
chr13:110686189 | G | A | 1 | a0002c0004t0001g0051 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.571+1532C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110686189 | |||||||
chr13:110686242 | C | CT | 28 | a0001c0001t0002g0309 a0001c0002t0001g0176 a0001c0002t0001g0183 others(25): Show |
29 | HG00609.hp1 HG01243.hp2 HG01433.hp1 others(26): Show |
intron_variant | MODIFIER | c.571+1478dupA | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110686242 | |||||||
chr13:110686242 | CT | C | 27 | a0001c0001t0001g0075 a0001c0001t0001g0092 a0001c0001t0001g0098 others(24): Show |
27 | HG00438.hp2 HG00597.hp2 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.571+1478delA | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110686242 | |||||||
chr13:110686242 | CTT | C | 127 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(124): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.571+1477_571+1478d others(4): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110686242 | |||||||
chr13:110686264 | C | T | 13 | a0001c0002t0001g0262 a0001c0002t0001g0276 a0001c0002t0002g0268 others(10): Show |
13 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.571+1457G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110686264 | |||||||
chr13:110686343 | A | G | 2 | a0005c0010t0001g0096 a0005c0010t0001g0097 |
2 | HG03239.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.571+1378T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110686343 | |||||||
chr13:110686391 | C | T | 1 | a0001c0002t0001g0230 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.571+1330G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110686391 | |||||||
chr13:110686572 | T | A | 6 | a0001c0003t0001g0020 a0001c0003t0001g0231 a0001c0003t0001g0244 others(3): Show |
7 | HG01074.hp1 HG02647.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.571+1149A>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110686572 | |||||||
chr13:110686703 | C | T | 4 | a0002c0004t0001g0050 a0002c0004t0001g0051 a0002c0004t0001g0055 others(1): Show |
4 | NA18943.hp2 NA18957.hp2 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.571+1018G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110686703 | |||||||
chr13:110686777 | C | T | 9 | a0001c0003t0001g0020 a0001c0003t0001g0231 a0001c0003t0001g0244 others(6): Show |
10 | HG01074.hp1 HG02486.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.571+944G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110686777 | |||||||
chr13:110686899 | G | A | 1 | a0003c0006t0002g0325 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.571+822C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110686899 | |||||||
chr13:110686979 | G | A | 1 | a0001c0019t0001g0205 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.571+742C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110686979 | |||||||
chr13:110687016 | G | C | 3 | a0001c0009t0002g0277 a0001c0009t0002g0278 a0001c0009t0002g0279 |
3 | HG02486.hp1 HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.571+705C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110687016 | |||||||
chr13:110687189 | G | T | 2 | a0001c0001t0001g0009 a0001c0001t0001g0095 |
3 | HG00642.hp1 HG03927.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.571+532C>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110687189 | |||||||
chr13:110687387 | C | T | 1 | a0001c0002t0001g0230 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.571+334G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110687387 | |||||||
chr13:110687422 | C | G | 13 | a0001c0002t0001g0262 a0001c0002t0001g0276 a0001c0002t0002g0268 others(10): Show |
13 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.571+299G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110687422 | |||||||
chr13:110687468 | G | T | 2 | a0001c0001t0001g0085 a0001c0001t0001g0094 |
2 | HG02886.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.571+253C>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110687468 | |||||||
chr13:110687692 | G | A | 1 | a0002c0004t0001g0059 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.571+29C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110687692 | |||||||
chr13:110687692 | G | GA | 43 | a0001c0001t0002g0308 a0001c0002t0001g0214 a0001c0005t0001g0146 others(40): Show |
44 | HG00597.hp1 HG01099.hp2 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.571+28dupT | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110687692 | |||||||
chr13:110687692 | GAA | G | 13 | a0001c0002t0001g0262 a0001c0002t0001g0276 a0001c0002t0002g0268 others(10): Show |
13 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.571+27_571+28delTT | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110687692 | |||||||
chr13:110687695 | A | C | 23 | a0001c0003t0001g0322 a0001c0003t0001g0340 a0003c0006t0002g0025 others(20): Show |
24 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.571+26T>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110687695 | |||||||
chr13:110688097 | T | C | 1 | a0002c0008t0001g0036 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.394-79A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110688097 | |||||||
chr13:110688142 | G | A | 1 | a0001c0002t0001g0180 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.394-124C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110688142 | |||||||
chr13:110688175 | G | A | 11 | a0001c0002t0002g0022 a0001c0002t0002g0239 a0001c0002t0002g0241 others(8): Show |
12 | HG02280.hp2 HG02451.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.394-157C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110688175 | |||||||
chr13:110688245 | CT | C | 11 | a0001c0002t0002g0022 a0001c0002t0002g0239 a0001c0002t0002g0241 others(8): Show |
12 | HG02280.hp2 HG02451.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.394-228delA | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110688245 | |||||||
chr13:110688389 | C | T | 6 | a0001c0003t0001g0020 a0001c0003t0001g0231 a0001c0003t0001g0244 others(3): Show |
7 | HG01074.hp1 HG02647.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.394-371G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110688389 | |||||||
chr13:110688696 | G | A | 1 | a0001c0002t0001g0230 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.394-678C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110688696 | |||||||
chr13:110688739 | G | A | 3 | a0001c0001t0001g0093 a0001c0001t0001g0137 a0001c0001t0001g0138 |
3 | HG00438.hp2 HG00544.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.394-721C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110688739 | |||||||
chr13:110688883 | C | A | 14 | a0001c0002t0001g0230 a0001c0002t0001g0262 a0001c0002t0001g0276 others(11): Show |
14 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.394-865G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110688883 | |||||||
chr13:110689202 | C | A | 1 | a0001c0002t0001g0197 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.394-1184G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110689202 | |||||||
chr13:110689281 | C | G | 10 | a0001c0002t0002g0022 a0001c0002t0002g0239 a0001c0002t0002g0241 others(7): Show |
11 | HG02280.hp2 HG02451.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.394-1263G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110689281 | |||||||
chr13:110689300 | T | C | 333 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(330): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.394-1282A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110689300 | |||||||
chr13:110689404 | C | T | 139 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(136): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.394-1386G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110689404 | |||||||
chr13:110689567 | T | C | 1 | a0001c0003t0002g0288 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.394-1549A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110689567 | |||||||
chr13:110689900 | G | A | 1 | a0003c0006t0002g0328 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.394-1882C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110689900 | |||||||
chr13:110689902 | A | C | 1 | a0001c0002t0001g0230 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.394-1884T>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110689902 | |||||||
chr13:110689951 | G | A | 23 | a0001c0003t0001g0322 a0001c0003t0001g0340 a0003c0006t0002g0025 others(20): Show |
24 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.394-1933C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110689951 | |||||||
chr13:110690187 | T | C | 337 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(334): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.394-2169A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110690187 | |||||||
chr13:110690585 | G | A | 2 | a0001c0002t0002g0198 a0001c0002t0002g0199 |
2 | NA18957.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.394-2567C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110690585 | |||||||
chr13:110690600 | T | C | 4 | a0001c0001t0001g0021 a0001c0001t0001g0069 a0001c0001t0001g0079 others(1): Show |
5 | HG01346.hp2 HG01884.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.394-2582A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110690600 | |||||||
chr13:110690627 | A | G | 1 | a0001c0001t0001g0075 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.394-2609T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110690627 | |||||||
chr13:110690885 | T | C | 2 | a0001c0001t0001g0142 a0001c0001t0001g0162 |
2 | HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.394-2867A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110690885 | |||||||
chr13:110691060 | C | T | 13 | a0001c0002t0001g0262 a0001c0002t0001g0276 a0001c0002t0002g0268 others(10): Show |
13 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.394-3042G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110691060 | |||||||
chr13:110691267 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.394-3249G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110691267 | |||||||
chr13:110691392 | A | G | 1 | a0001c0003t0002g0068 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.394-3374T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110691392 | |||||||
chr13:110691427 | T | C | 23 | a0001c0003t0001g0322 a0001c0003t0001g0340 a0003c0006t0002g0025 others(20): Show |
24 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.394-3409A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110691427 | |||||||
chr13:110691541 | C | T | 137 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(134): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.394-3523G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110691541 | |||||||
chr13:110691585 | G | A | 1 | a0001c0003t0001g0294 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.394-3567C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110691585 | |||||||
chr13:110691781 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.394-3763G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110691781 | |||||||
chr13:110691856 | C | T | 26 | a0001c0001t0001g0156 a0001c0001t0001g0161 a0001c0001t0001g0164 others(23): Show |
26 | HG00438.hp1 HG02622.hp1 HG02970.hp2 others(23): Show |
intron_variant | MODIFIER | c.394-3838G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110691856 | |||||||
chr13:110691880 | C | G | 333 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(330): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.394-3862G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110691880 | |||||||
chr13:110691987 | GA | G | 73 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(70): Show |
78 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.394-3970delT | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110691987 | |||||||
chr13:110691987 | GAA | G | 7 | a0001c0002t0001g0061 a0001c0002t0003g0265 a0001c0002t0003g0266 others(4): Show |
7 | HG00738.hp2 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.394-3971_394-3970d others(4): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110691987 | |||||||
chr13:110692001 | A | AT | 3 | a0001c0003t0001g0020 a0001c0003t0001g0231 a0001c0003t0001g0294 |
4 | HG02723.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.394-3984_394-3983i others(3): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692001 | |||||||
chr13:110692001 | A | ATAT | 3 | a0003c0006t0002g0319 a0003c0006t0002g0320 a0003c0006t0002g0329 |
3 | HG00408.hp2 NA18612.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.394-3984_394-3983i others(5): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692001 | |||||||
chr13:110692001 | A | T | 18 | a0001c0001t0001g0291 a0001c0002t0001g0230 a0001c0002t0003g0265 others(15): Show |
22 | HG00642.hp2 HG01123.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.394-3983T>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692001 | |||||||
chr13:110692003 | A | AT | 7 | a0001c0002t0003g0267 a0001c0003t0001g0247 a0001c0003t0001g0248 others(4): Show |
7 | HG01192.hp2 HG02257.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.394-3986_394-3985i others(3): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692003 | |||||||
chr13:110692003 | A | ATAT | 15 | a0001c0003t0001g0244 a0001c0003t0001g0322 a0001c0003t0001g0340 others(12): Show |
16 | HG00558.hp1 HG01069.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.394-3986_394-3985i others(5): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692003 | |||||||
chr13:110692003 | A | T | 42 | a0001c0001t0001g0291 a0001c0002t0001g0179 a0001c0002t0001g0180 others(39): Show |
47 | HG00408.hp2 HG00642.hp2 HG01074.hp1 others(44): Show |
intron_variant | MODIFIER | c.394-3985T>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692003 | |||||||
chr13:110692004 | AT | A | 130 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(127): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.394-3987delA | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692004 | |||||||
chr13:110692005 | T | A | 31 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0069 others(28): Show |
34 | HG01257.hp2 HG01258.hp1 HG01346.hp2 others(31): Show |
intron_variant | MODIFIER | c.394-3987A>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692005 | |||||||
chr13:110692007 | T | A | 126 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(123): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.394-3989A>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692007 | |||||||
chr13:110692009 | T | A | 11 | a0001c0001t0001g0012 a0001c0001t0001g0073 a0001c0001t0001g0139 others(8): Show |
12 | HG01070.hp2 HG01081.hp2 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.394-3991A>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692009 | |||||||
chr13:110692023 | T | C | 18 | a0001c0003t0001g0020 a0001c0003t0001g0155 a0001c0003t0001g0231 others(15): Show |
21 | HG01074.hp1 HG01884.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.394-4005A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692023 | |||||||
chr13:110692023 | TAC | T | 20 | a0001c0001t0002g0309 a0001c0001t0002g0312 a0001c0002t0002g0022 others(17): Show |
21 | HG01099.hp2 HG01358.hp2 HG01928.hp2 others(18): Show |
intron_variant | MODIFIER | c.394-4007_394-4006d others(4): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692023 | |||||||
chr13:110692025 | C | T | 203 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(200): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.394-4007G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692025 | |||||||
chr13:110692027 | C | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(131): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.394-4009G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692027 | |||||||
chr13:110692035 | C | CAT | 38 | a0001c0001t0001g0291 a0001c0002t0001g0230 a0001c0003t0001g0287 others(35): Show |
41 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.394-4019_394-4018d others(4): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692035 | |||||||
chr13:110692035 | C | T | 10 | a0001c0003t0001g0155 a0001c0003t0001g0294 a0001c0003t0001g0297 others(7): Show |
10 | HG01256.hp1 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.394-4017G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692035 | |||||||
chr13:110692035 | CAT | C | 16 | a0001c0001t0001g0021 a0001c0001t0001g0069 a0001c0001t0001g0079 others(13): Show |
17 | HG01346.hp2 HG01884.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.394-4019_394-4018d others(4): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692035 | |||||||
chr13:110692037 | T | C | 139 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(136): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.394-4019A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692037 | |||||||
chr13:110692047 | T | C | 5 | a0001c0001t0001g0087 a0001c0009t0002g0277 a0001c0009t0002g0278 others(2): Show |
5 | HG02486.hp1 HG02572.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.394-4029A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692047 | |||||||
chr13:110692051 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.394-4033G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692051 | |||||||
chr13:110692055 | T | C | 1 | a0001c0001t0001g0087 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.394-4037A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692055 | |||||||
chr13:110692057 | C | CAT | 74 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(71): Show |
76 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.394-4041_394-4040d others(4): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692057 | |||||||
chr13:110692057 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.394-4039G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692057 | |||||||
chr13:110692113 | T | C | 1 | a0001c0005t0001g0149 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.394-4095A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692113 | |||||||
chr13:110692118 | A | C | 9 | a0001c0003t0001g0020 a0001c0003t0001g0231 a0001c0003t0001g0244 others(6): Show |
10 | HG01074.hp1 HG02486.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.394-4100T>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692118 | |||||||
chr13:110692119 | CACATATA others(3): Show |
C | 13 | a0001c0002t0001g0262 a0001c0002t0001g0276 a0001c0002t0002g0268 others(10): Show |
13 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.394-4111_394-4102d others(12): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692119 | |||||||
chr13:110692313 | T | C | 7 | a0001c0003t0001g0020 a0001c0003t0001g0231 a0001c0003t0001g0244 others(4): Show |
8 | HG01074.hp1 HG02451.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.394-4295A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692313 | |||||||
chr13:110692385 | C | A | 9 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0082 others(6): Show |
11 | HG02040.hp2 HG02071.hp1 NA18939.hp2 others(8): Show |
intron_variant | MODIFIER | c.394-4367G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692385 | |||||||
chr13:110692560 | C | T | 1 | a0002c0004t0001g0030 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.394-4542G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692560 | |||||||
chr13:110692561 | C | CT | 8 | a0001c0002t0001g0179 a0001c0002t0001g0180 a0001c0002t0002g0255 others(5): Show |
8 | HG01891.hp2 HG02622.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.394-4544dupA | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692561 | |||||||
chr13:110692561 | CT | C | 135 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(132): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.394-4544delA | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692561 | |||||||
chr13:110692595 | T | G | 1 | a0001c0005t0001g0174 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.394-4577A>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692595 | |||||||
chr13:110692607 | T | C | 13 | a0001c0002t0001g0262 a0001c0002t0001g0276 a0001c0002t0002g0268 others(10): Show |
13 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.394-4589A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692607 | |||||||
chr13:110692776 | C | T | 1 | a0001c0001t0001g0073 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.394-4758G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692776 | |||||||
chr13:110692809 | G | T | 1 | a0001c0002t0001g0208 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.394-4791C>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692809 | |||||||
chr13:110692837 | C | T | 1 | a0001c0002t0003g0265 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.394-4819G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692837 | |||||||
chr13:110692878 | A | G | 13 | a0001c0002t0001g0262 a0001c0002t0001g0276 a0001c0002t0002g0268 others(10): Show |
13 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.394-4860T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692878 | |||||||
chr13:110692919 | G | A | 13 | a0001c0002t0001g0262 a0001c0002t0001g0276 a0001c0002t0002g0268 others(10): Show |
13 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.394-4901C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692919 | |||||||
chr13:110692997 | C | T | 1 | a0001c0003t0002g0285 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.394-4979G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692997 | |||||||
chr13:110693084 | TG | T | 13 | a0001c0002t0001g0262 a0001c0002t0001g0276 a0001c0002t0002g0268 others(10): Show |
13 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.394-5067delC | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110693084 | |||||||
chr13:110693096 | C | T | 2 | a0001c0001t0002g0084 a0001c0001t0002g0154 |
2 | HG03139.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.394-5078G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110693096 | |||||||
chr13:110693109 | C | CA | 72 | a0001c0001t0001g0072 a0001c0001t0001g0161 a0001c0001t0002g0314 others(69): Show |
75 | HG00597.hp1 HG01099.hp2 HG01109.hp1 others(72): Show |
intron_variant | MODIFIER | c.394-5092dupT | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110693109 | |||||||
chr13:110693109 | C | CAA | 9 | a0001c0007t0001g0273 a0001c0007t0001g0274 a0001c0007t0001g0275 others(6): Show |
9 | HG00738.hp2 HG02015.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.394-5093_394-5092d others(4): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110693109 | |||||||
chr13:110693109 | CA | C | 132 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(129): Show |
149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.394-5092delT | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110693109 | |||||||
chr13:110693209 | A | G | 2 | a0001c0003t0002g0281 a0001c0003t0002g0282 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.394-5191T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110693209 | |||||||
chr13:110693265 | C | T | 75 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(72): Show |
77 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(74): Show |
intron_variant | MODIFIER | c.394-5247G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110693265 | |||||||
chr13:110693421 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.394-5403C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110693421 | |||||||
chr13:110693804 | A | G | 106 | a0001c0001t0001g0291 a0001c0002t0001g0005 a0001c0002t0001g0006 others(103): Show |
119 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.394-5786T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110693804 | |||||||
chr13:110693924 | T | C | 1 | a0001c0003t0002g0290 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.394-5906A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110693924 | |||||||
chr13:110694018 | G | GT | 6 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(3): Show |
6 | HG01891.hp2 HG02300.hp1 NA18972.hp2 others(3): Show |
intron_variant | MODIFIER | c.394-6001dupA | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110694018 | |||||||
chr13:110694107 | A | C | 52 | a0001c0002t0002g0022 a0001c0002t0002g0239 a0001c0002t0002g0241 others(49): Show |
54 | HG00597.hp1 HG00738.hp2 HG01099.hp2 others(51): Show |
intron_variant | MODIFIER | c.394-6089T>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110694107 | |||||||
chr13:110694108 | A | T | 1 | a0001c0005t0001g0080 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.394-6090T>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110694108 | |||||||
chr13:110694169 | G | A | 1 | a0001c0003t0001g0237 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.394-6151C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110694169 | |||||||
chr13:110694305 | C | T | 13 | a0001c0002t0001g0262 a0001c0002t0001g0276 a0001c0002t0002g0268 others(10): Show |
13 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.394-6287G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110694305 | |||||||
chr13:110694367 | G | T | 73 | a0001c0001t0001g0291 a0001c0002t0001g0005 a0001c0002t0001g0006 others(70): Show |
84 | HG00609.hp1 HG00621.hp2 HG00642.hp2 others(81): Show |
intron_variant | MODIFIER | c.394-6349C>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110694367 | |||||||
chr13:110694368 | T | C | 1 | a0001c0001t0001g0291 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.394-6350A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110694368 | |||||||
chr13:110694568 | C | A | 1 | a0002c0004t0003g0299 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.394-6550G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110694568 | |||||||
chr13:110694579 | C | G | 333 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(330): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.394-6561G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110694579 | |||||||
chr13:110694581 | G | A | 96 | a0001c0001t0001g0291 a0001c0002t0001g0005 a0001c0002t0001g0006 others(93): Show |
108 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.394-6563C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110694581 | |||||||
chr13:110694713 | A | T | 138 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(135): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.394-6695T>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110694713 | |||||||
chr13:110695331 | C | T | 139 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(136): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.393+6107G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110695331 | |||||||
chr13:110695448 | G | A | 138 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(135): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.393+5990C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110695448 | |||||||
chr13:110695475 | G | A | 2 | a0003c0006t0002g0331 a0003c0006t0002g0332 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.393+5963C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110695475 | |||||||
chr13:110695775 | C | CT | 71 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(68): Show |
73 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(70): Show |
intron_variant | MODIFIER | c.393+5662dupA | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110695775 | |||||||
chr13:110695789 | A | T | 54 | a0001c0002t0002g0022 a0001c0002t0002g0239 a0001c0002t0002g0241 others(51): Show |
56 | HG00597.hp1 HG00738.hp2 HG01099.hp2 others(53): Show |
intron_variant | MODIFIER | c.393+5649T>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110695789 | |||||||
chr13:110695858 | A | G | 1 | a0001c0003t0001g0246 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.393+5580T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110695858 | |||||||
chr13:110695887 | C | A | 1 | a0001c0001t0001g0163 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.393+5551G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110695887 | |||||||
chr13:110695933 | C | T | 138 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(135): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.393+5505G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110695933 | |||||||
chr13:110695941 | T | C | 258 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(255): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.393+5497A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110695941 | |||||||
chr13:110696026 | G | A | 1 | a0001c0001t0001g0164 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.393+5412C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110696026 | |||||||
chr13:110696032 | C | T | 4 | a0001c0003t0002g0281 a0001c0003t0002g0282 a0001c0003t0002g0283 others(1): Show |
4 | HG03491.hp1 HG03492.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.393+5406G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110696032 | |||||||
chr13:110696105 | G | A | 5 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0065 others(2): Show |
8 | NA18942.hp1 NA18944.hp2 NA18952.hp1 others(5): Show |
intron_variant | MODIFIER | c.393+5333C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110696105 | |||||||
chr13:110696233 | G | A | 1 | a0003c0006t0002g0333 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.393+5205C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110696233 | |||||||
chr13:110696276 | GTA | G | 75 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(72): Show |
77 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(74): Show |
intron_variant | MODIFIER | c.393+5160_393+5161d others(4): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110696276 | |||||||
chr13:110696413 | C | T | 75 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(72): Show |
77 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(74): Show |
intron_variant | MODIFIER | c.393+5025G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110696413 | |||||||
chr13:110696780 | T | C | 227 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(224): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.393+4658A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110696780 | |||||||
chr13:110696846 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.393+4592A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110696846 | |||||||
chr13:110696942 | A | G | 337 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(334): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.393+4496T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110696942 | |||||||
chr13:110696987 | T | C | 75 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(72): Show |
77 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(74): Show |
intron_variant | MODIFIER | c.393+4451A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110696987 | |||||||
chr13:110697243 | G | T | 333 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(330): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.393+4195C>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110697243 | |||||||
chr13:110697244 | A | G | 333 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(330): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.393+4194T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110697244 | |||||||
chr13:110697265 | C | A | 1 | a0001c0003t0002g0068 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.393+4173G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110697265 | |||||||
chr13:110697506 | G | C | 2 | a0002c0004t0001g0235 a0002c0008t0003g0243 |
2 | HG02280.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.393+3932C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110697506 | |||||||
chr13:110697520 | G | A | 1 | a0001c0003t0001g0237 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.393+3918C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110697520 | |||||||
chr13:110697547 | C | A | 75 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(72): Show |
77 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(74): Show |
intron_variant | MODIFIER | c.393+3891G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110697547 | |||||||
chr13:110697662 | C | T | 73 | a0001c0001t0001g0291 a0001c0002t0001g0005 a0001c0002t0001g0006 others(70): Show |
84 | HG00609.hp1 HG00621.hp2 HG00642.hp2 others(81): Show |
intron_variant | MODIFIER | c.393+3776G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110697662 | |||||||
chr13:110697722 | T | C | 11 | a0001c0005t0001g0016 a0001c0005t0001g0167 a0001c0005t0001g0168 others(8): Show |
12 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.393+3716A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110697722 | |||||||
chr13:110697858 | C | T | 23 | a0001c0003t0001g0322 a0001c0003t0001g0340 a0003c0006t0002g0025 others(20): Show |
24 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.393+3580G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110697858 | |||||||
chr13:110697888 | C | T | 2 | a0001c0001t0001g0021 a0001c0001t0001g0079 |
3 | HG01346.hp2 HG01884.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.393+3550G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110697888 | |||||||
chr13:110697934 | C | T | 73 | a0001c0001t0001g0291 a0001c0002t0001g0005 a0001c0002t0001g0006 others(70): Show |
84 | HG00609.hp1 HG00621.hp2 HG00642.hp2 others(81): Show |
intron_variant | MODIFIER | c.393+3504G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110697934 | |||||||
chr13:110698228 | A | C | 2 | a0001c0001t0001g0077 a0001c0001t0001g0078 |
2 | NA18974.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.393+3210T>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110698228 | |||||||
chr13:110698467 | C | T | 1 | a0001c0001t0002g0076 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.393+2971G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110698467 | |||||||
chr13:110698520 | C | CA | 15 | a0001c0002t0001g0262 a0001c0002t0001g0276 a0001c0002t0002g0268 others(12): Show |
15 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.393+2917dupT | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110698520 | |||||||
chr13:110698702 | C | A | 1 | a0001c0005t0001g0175 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.393+2736G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110698702 | |||||||
chr13:110698831 | G | A | 3 | a0001c0009t0002g0277 a0001c0009t0002g0278 a0001c0009t0002g0279 |
3 | HG02486.hp1 HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.393+2607C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110698831 | |||||||
chr13:110699013 | A | G | 1 | a0001c0003t0002g0301 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.393+2425T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110699013 | |||||||
chr13:110699022 | G | A | 1 | a0002c0004t0002g0060 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.393+2416C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110699022 | |||||||
chr13:110699022 | GA | G | 286 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(283): Show |
313 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(310): Show |
intron_variant | MODIFIER | c.393+2415delT | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110699022 | |||||||
chr13:110699023 | A | G | 1 | a0002c0004t0002g0060 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.393+2415T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110699023 | |||||||
chr13:110699187 | G | A | 199 | a0001c0001t0001g0215 a0001c0001t0001g0291 a0001c0001t0002g0303 others(196): Show |
214 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(211): Show |
intron_variant | MODIFIER | c.393+2251C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110699187 | |||||||
chr13:110699213 | C | T | 24 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(21): Show |
24 | HG00438.hp1 HG02622.hp1 HG02630.hp2 others(21): Show |
intron_variant | MODIFIER | c.393+2225G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110699213 | |||||||
chr13:110699371 | T | C | 1 | a0001c0001t0001g0220 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.393+2067A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110699371 | |||||||
chr13:110699447 | C | T | 1 | a0002c0004t0003g0236 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.393+1991G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110699447 | |||||||
chr13:110699726 | C | T | 23 | a0001c0003t0001g0322 a0001c0003t0001g0340 a0001c0005t0001g0334 others(20): Show |
24 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.393+1712G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110699726 | |||||||
chr13:110699762 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.393+1676G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110699762 | |||||||
chr13:110699788 | C | T | 1 | a0001c0002t0001g0074 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.393+1650G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110699788 | |||||||
chr13:110699804 | G | A | 50 | a0001c0001t0001g0021 a0001c0002t0001g0230 a0001c0002t0001g0276 others(47): Show |
54 | HG00597.hp1 HG01074.hp1 HG01099.hp2 others(51): Show |
intron_variant | MODIFIER | c.393+1634C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110699804 | |||||||
chr13:110699860 | C | T | 21 | a0001c0001t0001g0291 a0001c0003t0001g0287 a0001c0003t0001g0289 others(18): Show |
25 | HG00642.hp2 HG01123.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.393+1578G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110699860 | |||||||
chr13:110699972 | C | T | 2 | a0001c0003t0002g0280 a0010c0018t0002g0263 |
2 | HG01192.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.393+1466G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110699972 | |||||||
chr13:110700005 | C | T | 1 | a0001c0001t0001g0073 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.393+1433G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110700005 | |||||||
chr13:110700007 | C | T | 142 | a0001c0001t0001g0021 a0001c0001t0001g0291 a0001c0001t0002g0303 others(139): Show |
150 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.393+1431G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110700007 | |||||||
chr13:110700061 | T | C | 121 | a0001c0001t0001g0021 a0001c0001t0001g0291 a0001c0002t0001g0262 others(118): Show |
129 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.393+1377A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110700061 | |||||||
chr13:110700062 | G | A | 1 | a0013c0023t0002g0336 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.393+1376C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110700062 | |||||||
chr13:110700080 | C | CT | 3 | a0001c0009t0002g0277 a0001c0009t0002g0278 a0001c0009t0002g0279 |
3 | HG02486.hp1 HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.393+1357dupA | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110700080 | |||||||
chr13:110700113 | C | T | 80 | a0001c0001t0001g0021 a0001c0002t0002g0022 a0001c0002t0002g0239 others(77): Show |
84 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.393+1325G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110700113 | |||||||
chr13:110700149 | T | G | 1 | a0003c0006t0002g0337 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.393+1289A>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110700149 | |||||||
chr13:110700202 | T | G | 1 | a0001c0002t0001g0221 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.393+1236A>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110700202 | |||||||
chr13:110700253 | G | A | 76 | a0001c0001t0001g0021 a0001c0002t0002g0022 a0001c0002t0002g0239 others(73): Show |
80 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.393+1185C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110700253 | |||||||
chr13:110700576 | C | T | 3 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 |
3 | HG02735.hp1 HG02738.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.393+862G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110700576 | |||||||
chr13:110700656 | C | A | 1 | a0003c0006t0002g0338 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.393+782G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110700656 | |||||||
chr13:110700656 | C | T | 5 | a0001c0001t0001g0254 a0001c0002t0002g0255 a0001c0002t0002g0256 others(2): Show |
5 | HG01891.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.393+782G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110700656 | |||||||
chr13:110700697 | T | C | 1 | a0001c0002t0002g0258 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.393+741A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110700697 | |||||||
chr13:110700764 | C | T | 121 | a0001c0001t0001g0021 a0001c0001t0001g0291 a0001c0002t0001g0262 others(118): Show |
129 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.393+674G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110700764 | |||||||
chr13:110700872 | A | G | 1 | a0001c0003t0001g0244 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.393+566T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110700872 | |||||||
chr13:110700926 | T | C | 1 | a0001c0003t0002g0293 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.393+512A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110700926 | |||||||
chr13:110700968 | T | C | 56 | a0001c0001t0001g0021 a0001c0002t0002g0022 a0001c0002t0002g0239 others(53): Show |
59 | HG00597.hp1 HG00738.hp2 HG01074.hp1 others(56): Show |
intron_variant | MODIFIER | c.393+470A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110700968 | |||||||
chr13:110701159 | G | A | 3 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 |
3 | NA18966.hp1 NA18981.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.393+279C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110701159 | |||||||
chr13:110701356 | G | A | 11 | a0001c0002t0002g0022 a0001c0002t0002g0245 a0001c0002t0002g0251 others(8): Show |
12 | HG01074.hp1 HG02280.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.393+82C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110701356 | |||||||
chr13:110701602 | A | G | 1 | a0001c0002t0001g0262 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.276-47T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 2/14 | chr13 | 110701602 | |||||||
chr13:110701666 | C | CA | 11 | a0001c0002t0002g0022 a0001c0002t0002g0245 a0001c0002t0002g0251 others(8): Show |
12 | HG01074.hp1 HG02280.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.276-112dupT | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 2/14 | chr13 | 110701666 | |||||||
chr13:110701757 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.276-202G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 2/14 | chr13 | 110701757 | |||||||
chr13:110701763 | T | C | 186 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(183): Show |
209 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.276-208A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 2/14 | chr13 | 110701763 | |||||||
chr13:110701798 | T | G | 1 | a0001c0003t0002g0317 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.276-243A>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 2/14 | chr13 | 110701798 | |||||||
chr13:110701867 | A | G | 26 | a0001c0001t0001g0291 a0001c0003t0001g0287 a0001c0003t0001g0289 others(23): Show |
30 | HG00642.hp2 HG01123.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.276-312T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 2/14 | chr13 | 110701867 | |||||||
chr13:110702057 | T | C | 1 | a0002c0004t0003g0299 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.276-502A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 2/14 | chr13 | 110702057 | |||||||
chr13:110702064 | G | A | 3 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 |
3 | HG01081.hp2 HG01123.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.276-509C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 2/14 | chr13 | 110702064 | |||||||
chr13:110702441 | C | A | 212 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(209): Show |
236 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.276-886G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 2/14 | chr13 | 110702441 | |||||||
chr13:110702733 | T | C | 15 | a0001c0002t0001g0262 a0001c0002t0001g0276 a0001c0002t0002g0268 others(12): Show |
15 | HG01192.hp2 HG01891.hp1 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.276-1178A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 2/14 | chr13 | 110702733 | |||||||
chr13:110702823 | G | T | 1 | a0001c0001t0001g0065 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.276-1268C>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 2/14 | chr13 | 110702823 | |||||||
chr13:110702862 | T | C | 1 | a0001c0001t0001g0228 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.276-1307A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 2/14 | chr13 | 110702862 | |||||||
chr13:110703149 | T | C | 1 | a0001c0005t0001g0229 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.276-1594A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 2/14 | chr13 | 110703149 | |||||||
chr13:110703207 | A | G | 56 | a0001c0001t0001g0021 a0001c0002t0002g0022 a0001c0002t0002g0239 others(53): Show |
59 | HG00597.hp1 HG00738.hp2 HG01074.hp1 others(56): Show |
intron_variant | MODIFIER | c.276-1652T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 2/14 | chr13 | 110703207 | |||||||
chr13:110703755 | G | A | 23 | a0001c0001t0001g0291 a0001c0003t0001g0287 a0001c0003t0001g0289 others(20): Show |
27 | HG00642.hp2 HG01123.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.275+1766C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 2/14 | chr13 | 110703755 | |||||||
chr13:110703967 | T | A | 3 | a0001c0002t0001g0230 a0001c0003t0001g0020 a0001c0003t0001g0231 |
4 | HG02723.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.275+1554A>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 2/14 | chr13 | 110703967 | |||||||
chr13:110703982 | G | A | 6 | a0001c0003t0001g0294 a0001c0003t0001g0297 a0001c0003t0002g0295 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.275+1539C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 2/14 | chr13 | 110703982 | |||||||
chr13:110704239 | T | C | 26 | a0001c0001t0001g0291 a0001c0003t0001g0287 a0001c0003t0001g0289 others(23): Show |
30 | HG00642.hp2 HG01123.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.275+1282A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 2/14 | chr13 | 110704239 | |||||||
chr13:110704445 | C | T | 56 | a0001c0001t0001g0021 a0001c0002t0002g0022 a0001c0002t0002g0239 others(53): Show |
59 | HG00597.hp1 HG00738.hp2 HG01074.hp1 others(56): Show |
intron_variant | MODIFIER | c.275+1076G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 2/14 | chr13 | 110704445 | |||||||
chr13:110704453 | G | A | 209 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(206): Show |
233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.275+1068C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 2/14 | chr13 | 110704453 | |||||||
chr13:110704494 | C | A | 1 | a0003c0006t0002g0339 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.275+1027G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 2/14 | chr13 | 110704494 | |||||||
chr13:110704500 | G | A | 1 | a0001c0001t0001g0232 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.275+1021C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 2/14 | chr13 | 110704500 | |||||||
chr13:110704544 | T | C | 1 | a0001c0020t0002g0300 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.275+977A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 2/14 | chr13 | 110704544 | |||||||
chr13:110704552 | C | T | 1 | a0001c0002t0001g0064 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.275+969G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 2/14 | chr13 | 110704552 | |||||||
chr13:110704617 | C | T | 209 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(206): Show |
233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.275+904G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 2/14 | chr13 | 110704617 | |||||||
chr13:110704800 | T | C | 2 | a0001c0003t0001g0340 a0003c0006t0002g0025 |
3 | HG01069.hp2 HG01071.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.275+721A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 2/14 | chr13 | 110704800 | |||||||
chr13:110704859 | C | T | 3 | a0001c0002t0001g0061 a0001c0002t0001g0062 a0001c0002t0001g0063 |
3 | NA18941.hp1 NA18951.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.275+662G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 2/14 | chr13 | 110704859 | |||||||
chr13:110704860 | A | G | 209 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(206): Show |
233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.275+661T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 2/14 | chr13 | 110704860 | |||||||
chr13:110704906 | C | T | 33 | a0002c0004t0001g0008 a0002c0004t0001g0029 a0002c0004t0001g0030 others(30): Show |
34 | HG00597.hp1 HG01099.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.275+615G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 2/14 | chr13 | 110704906 | |||||||
chr13:110705406 | G | A | 17 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(14): Show |
17 | HG00438.hp1 HG03654.hp2 HG03927.hp1 others(14): Show |
intron_variant | MODIFIER | c.275+115C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 2/14 | chr13 | 110705406 | |||||||
chr13:110705653 | T | G | 24 | a0001c0003t0001g0322 a0001c0003t0001g0340 a0001c0005t0001g0334 others(21): Show |
25 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(22): Show |
intron_variant | MODIFIER | c.225-82A>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 1/14 | chr13 | 110705653 |