Item | Value |
---|---|
geneid | 421 |
ensemblid | ENSG00000099889.14 |
hgncid | 728 |
symbol | ARVCF |
name | ARVCF delta catenin family member |
refseq_nuc | NM_001670.3 |
refseq_prot | NP_001661.1 |
ensembl_nuc | ENST00000263207.8 |
ensembl_prot | ENSP00000263207.3 |
mane_status | MANE Select |
chr | chr22 |
start | 19969896 |
end | 20016823 |
strand | - |
ver | v1.2 |
region | chr22:19969896-20016823 |
region5000 | chr22:19964896-20021823 |
regionname0 | ARVCF_chr22_19969896_20016823 |
regionname5000 | ARVCF_chr22_19964896_20021823 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 962 | 149 | 32 | 32 | 65 | 7 | 12 | 46 | ARVCF_chr22_19964896_20021823 | ARVCF | MEDCN others(957): Show |
chr22 | 19964896 | 20021823 |
a0002 | 0/0 | 962 | 76 | 9 | 20 | 36 | 2 | 9 | 26 | ARVCF_chr22_19964896_20021823 | ARVCF | MEDCN others(957): Show |
chr22 | 19964896 | 20021823 |
a0003 | 1/0 | 962 | 61 | 4 | 10 | 39 | 3 | 4 | 29 | ARVCF_chr22_19964896_20021823 | ARVCF | MEDCN others(957): Show |
chr22 | 19964896 | 20021823 |
a0004 | 0/0 | 962 | 29 | 15 | 6 | 3 | 0 | 5 | 1 | ARVCF_chr22_19964896_20021823 | ARVCF | MEDCN others(957): Show |
chr22 | 19964896 | 20021823 |
a0005 | 0/0 | 962 | 24 | 24 | 0 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | MEDCN others(957): Show |
chr22 | 19964896 | 20021823 |
a0006 | 0/0 | 962 | 9 | 0 | 0 | 7 | 0 | 2 | 7 | ARVCF_chr22_19964896_20021823 | ARVCF | MEDCN others(957): Show |
chr22 | 19964896 | 20021823 |
a0007 | 0/0 | 962 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | MEDCN others(957): Show |
chr22 | 19964896 | 20021823 |
a0008 | 0/0 | 962 | 2 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | MEDCN others(957): Show |
chr22 | 19964896 | 20021823 |
a0009 | 0/0 | 962 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | MEDCN others(957): Show |
chr22 | 19964896 | 20021823 |
a0010 | 0/0 | 962 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | MEDCN others(957): Show |
chr22 | 19964896 | 20021823 |
a0011 | 0/0 | 962 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ARVCF_chr22_19964896_20021823 | ARVCF | MEDCN others(957): Show |
chr22 | 19964896 | 20021823 |
a0012 | 0/0 | 962 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | MEDCN others(957): Show |
chr22 | 19964896 | 20021823 |
a0013 | 0/0 | 962 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | MEDCD others(957): Show |
chr22 | 19964896 | 20021823 |
a0014 | 0/0 | 962 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | MEDCN others(957): Show |
chr22 | 19964896 | 20021823 |
a0015 | 0/0 | 962 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | MEDCN others(957): Show |
chr22 | 19964896 | 20021823 |
a0016 | 0/0 | 962 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | MEDCN others(957): Show |
chr22 | 19964896 | 20021823 |
a0017 | 0/0 | 962 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | MEDCN others(957): Show |
chr22 | 19964896 | 20021823 |
a0018 | 0/0 | 962 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | MEDCN others(957): Show |
chr22 | 19964896 | 20021823 |
a0019 | 0/0 | 962 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | MEDCN others(957): Show |
chr22 | 19964896 | 20021823 |
a0020 | 0/0 | 962 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | MEDCN others(957): Show |
chr22 | 19964896 | 20021823 |
a0021 | 0/0 | 962 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARVCF_chr22_19964896_20021823 | ARVCF | MEDCN others(957): Show |
chr22 | 19964896 | 20021823 |
a0022 | 0/0 | 962 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARVCF_chr22_19964896_20021823 | ARVCF | MEDCD others(957): Show |
chr22 | 19964896 | 20021823 |
a0023 | 0/0 | 962 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARVCF_chr22_19964896_20021823 | ARVCF | MEDCN others(957): Show |
chr22 | 19964896 | 20021823 |
a0024 | 0/0 | 962 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARVCF_chr22_19964896_20021823 | ARVCF | MEDCN others(957): Show |
chr22 | 19964896 | 20021823 |
a0025 | 0/0 | 962 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARVCF_chr22_19964896_20021823 | ARVCF | MEDCN others(957): Show |
chr22 | 19964896 | 20021823 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2886 | 113 | 19 | 18 | 63 | 6 | 7 | ARVCF_chr22_19964896_20021823 | ARVCF | ATGGA others(2881): Show |
chr22 | 19964896 | 20021823 | ||
a0001c0004 | 0/1 | 2886 | 34 | 13 | 14 | 0 | 1 | 5 | ARVCF_chr22_19964896_20021823 | ARVCF | ATGGA others(2881): Show |
chr22 | 19964896 | 20021823 | ||
a0001c0033 | 0/0 | 2886 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | ATGGA others(2881): Show |
chr22 | 19964896 | 20021823 | ||
a0001c0035 | 0/0 | 2886 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | ATGGA others(2881): Show |
chr22 | 19964896 | 20021823 | ||
a0002c0002 | 0/0 | 2886 | 74 | 8 | 20 | 36 | 2 | 8 | ARVCF_chr22_19964896_20021823 | ARVCF | ATGGA others(2881): Show |
chr22 | 19964896 | 20021823 | ||
a0002c0032 | 0/0 | 2886 | 1 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | ATGGA others(2881): Show |
chr22 | 19964896 | 20021823 | ||
a0002c0040 | 0/0 | 2886 | 1 | 0 | 0 | 0 | 0 | 1 | ARVCF_chr22_19964896_20021823 | ARVCF | ATGGA others(2881): Show |
chr22 | 19964896 | 20021823 | ||
a0003c0003 | 1/0 | 2886 | 42 | 0 | 7 | 28 | 3 | 3 | ARVCF_chr22_19964896_20021823 | ARVCF | ATGGA others(2881): Show |
chr22 | 19964896 | 20021823 | ||
a0003c0008 | 0/0 | 2886 | 8 | 4 | 3 | 0 | 0 | 1 | ARVCF_chr22_19964896_20021823 | ARVCF | ATGGA others(2881): Show |
chr22 | 19964896 | 20021823 | ||
a0003c0014 | 0/0 | 2886 | 2 | 0 | 0 | 2 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | ATGGA others(2881): Show |
chr22 | 19964896 | 20021823 | ||
a0003c0015 | 0/0 | 2886 | 2 | 0 | 0 | 2 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | ATGGA others(2881): Show |
chr22 | 19964896 | 20021823 | ||
a0003c0017 | 0/0 | 2886 | 2 | 0 | 0 | 2 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | ATGGA others(2881): Show |
chr22 | 19964896 | 20021823 | ||
a0003c0019 | 0/0 | 2886 | 2 | 0 | 0 | 2 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | ATGGA others(2881): Show |
chr22 | 19964896 | 20021823 | ||
a0003c0020 | 0/0 | 2886 | 2 | 0 | 0 | 2 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | ATGGA others(2881): Show |
chr22 | 19964896 | 20021823 | ||
a0003c0038 | 0/0 | 2886 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | ATGGA others(2881): Show |
chr22 | 19964896 | 20021823 | ||
a0004c0006 | 0/0 | 2886 | 14 | 2 | 6 | 2 | 0 | 4 | ARVCF_chr22_19964896_20021823 | ARVCF | ATGGA others(2881): Show |
chr22 | 19964896 | 20021823 | ||
a0004c0009 | 0/0 | 2886 | 7 | 6 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | ATGGA others(2881): Show |
chr22 | 19964896 | 20021823 | ||
a0004c0011 | 0/0 | 2886 | 3 | 3 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | ATGGA others(2881): Show |
chr22 | 19964896 | 20021823 | ||
a0004c0012 | 0/0 | 2886 | 3 | 3 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | ATGGA others(2881): Show |
chr22 | 19964896 | 20021823 | ||
a0004c0026 | 0/0 | 2886 | 1 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | ATGGA others(2881): Show |
chr22 | 19964896 | 20021823 | ||
a0004c0041 | 0/0 | 2886 | 1 | 0 | 0 | 0 | 0 | 1 | ARVCF_chr22_19964896_20021823 | ARVCF | ATGGA others(2881): Show |
chr22 | 19964896 | 20021823 | ||
a0005c0005 | 0/0 | 2886 | 23 | 23 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | ATGGA others(2881): Show |
chr22 | 19964896 | 20021823 | ||
a0005c0025 | 0/0 | 2886 | 1 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | ATGGA others(2881): Show |
chr22 | 19964896 | 20021823 | ||
a0006c0007 | 0/0 | 2886 | 9 | 0 | 0 | 7 | 0 | 2 | ARVCF_chr22_19964896_20021823 | ARVCF | ATGGA others(2881): Show |
chr22 | 19964896 | 20021823 | ||
a0007c0010 | 0/0 | 2886 | 4 | 4 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | ATGGA others(2881): Show |
chr22 | 19964896 | 20021823 | ||
a0008c0016 | 0/0 | 2886 | 2 | 1 | 0 | 0 | 1 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | ATGGA others(2881): Show |
chr22 | 19964896 | 20021823 | ||
a0009c0013 | 0/0 | 2886 | 2 | 2 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | ATGGA others(2881): Show |
chr22 | 19964896 | 20021823 | ||
a0010c0021 | 0/0 | 2886 | 2 | 2 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | ATGGA others(2881): Show |
chr22 | 19964896 | 20021823 | ||
a0011c0018 | 0/0 | 2886 | 2 | 0 | 0 | 2 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | ATGGA others(2881): Show |
chr22 | 19964896 | 20021823 | ||
a0012c0022 | 0/0 | 2886 | 1 | 0 | 0 | 0 | 1 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | ATGGA others(2881): Show |
chr22 | 19964896 | 20021823 | ||
a0013c0042 | 0/0 | 2886 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | ATGGA others(2881): Show |
chr22 | 19964896 | 20021823 | ||
a0014c0039 | 0/0 | 2886 | 1 | 0 | 1 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | ATGGA others(2881): Show |
chr22 | 19964896 | 20021823 | ||
a0015c0029 | 0/0 | 2886 | 1 | 0 | 1 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | ATGGA others(2881): Show |
chr22 | 19964896 | 20021823 | ||
a0016c0036 | 0/0 | 2886 | 1 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | ATGGA others(2881): Show |
chr22 | 19964896 | 20021823 | ||
a0017c0037 | 0/0 | 2886 | 1 | 0 | 0 | 0 | 0 | 1 | ARVCF_chr22_19964896_20021823 | ARVCF | ATGGA others(2881): Show |
chr22 | 19964896 | 20021823 | ||
a0018c0034 | 0/0 | 2886 | 1 | 0 | 0 | 0 | 0 | 1 | ARVCF_chr22_19964896_20021823 | ARVCF | ATGGA others(2881): Show |
chr22 | 19964896 | 20021823 | ||
a0019c0024 | 0/0 | 2886 | 1 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | ATGGA others(2881): Show |
chr22 | 19964896 | 20021823 | ||
a0020c0031 | 0/0 | 2886 | 1 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | ATGGA others(2881): Show |
chr22 | 19964896 | 20021823 | ||
a0021c0028 | 0/0 | 2886 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | ATGGA others(2881): Show |
chr22 | 19964896 | 20021823 | ||
a0022c0043 | 0/0 | 2886 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | ATGGA others(2881): Show |
chr22 | 19964896 | 20021823 | ||
a0023c0023 | 0/0 | 2886 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | ATGGA others(2881): Show |
chr22 | 19964896 | 20021823 | ||
a0024c0030 | 0/0 | 2886 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | ATGGA others(2881): Show |
chr22 | 19964896 | 20021823 | ||
a0025c0027 | 0/0 | 2886 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | ATGGA others(2881): Show |
chr22 | 19964896 | 20021823 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4056 | 107 | 18 | 16 | 61 | 5 | 7 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4051): Show |
chr22 | 19964896 | 20021823 |
a0001c0001t0003 | 0/0 | 4056 | 1 | 0 | 1 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4051): Show |
chr22 | 19964896 | 20021823 |
a0001c0001t0013 | 0/0 | 4056 | 2 | 1 | 1 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4051): Show |
chr22 | 19964896 | 20021823 |
a0001c0001t0021 | 0/0 | 4056 | 1 | 0 | 0 | 0 | 1 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4051): Show |
chr22 | 19964896 | 20021823 |
a0001c0001t0023 | 0/0 | 4037 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4032): Show |
chr22 | 19964896 | 20021823 |
a0001c0001t0025 | 0/0 | 4056 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4051): Show |
chr22 | 19964896 | 20021823 |
a0001c0004t0004 | 0/0 | 4056 | 21 | 5 | 11 | 0 | 1 | 4 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4051): Show |
chr22 | 19964896 | 20021823 |
a0001c0004t0008 | 0/0 | 4051 | 6 | 4 | 2 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4046): Show |
chr22 | 19964896 | 20021823 |
a0001c0004t0009 | 0/0 | 4056 | 4 | 4 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4051): Show |
chr22 | 19964896 | 20021823 |
a0001c0004t0011 | 0/0 | 4056 | 1 | 0 | 1 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4051): Show |
chr22 | 19964896 | 20021823 |
a0001c0004t0016 | 0/0 | 4056 | 1 | 0 | 0 | 0 | 0 | 1 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4051): Show |
chr22 | 19964896 | 20021823 |
a0001c0004t0022 | 0/1 | 4056 | 1 | 0 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4051): Show |
chr22 | 19964896 | 20021823 |
a0001c0033t0024 | 0/0 | 4056 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4051): Show |
chr22 | 19964896 | 20021823 |
a0001c0035t0001 | 0/0 | 4056 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4051): Show |
chr22 | 19964896 | 20021823 |
a0002c0002t0001 | 0/0 | 4056 | 22 | 0 | 4 | 17 | 0 | 1 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4051): Show |
chr22 | 19964896 | 20021823 |
a0002c0002t0003 | 0/0 | 4056 | 50 | 8 | 16 | 17 | 2 | 7 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4051): Show |
chr22 | 19964896 | 20021823 |
a0002c0002t0014 | 0/0 | 4056 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4051): Show |
chr22 | 19964896 | 20021823 |
a0002c0002t0020 | 0/0 | 4056 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4051): Show |
chr22 | 19964896 | 20021823 |
a0002c0032t0004 | 0/0 | 4056 | 1 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4051): Show |
chr22 | 19964896 | 20021823 |
a0002c0040t0003 | 0/0 | 4056 | 1 | 0 | 0 | 0 | 0 | 1 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4051): Show |
chr22 | 19964896 | 20021823 |
a0003c0003t0002 | 1/0 | 4056 | 38 | 0 | 6 | 27 | 3 | 1 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4051): Show |
chr22 | 19964896 | 20021823 |
a0003c0003t0012 | 0/0 | 4056 | 2 | 0 | 0 | 0 | 0 | 2 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4051): Show |
chr22 | 19964896 | 20021823 |
a0003c0003t0018 | 0/0 | 4056 | 1 | 0 | 1 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4051): Show |
chr22 | 19964896 | 20021823 |
a0003c0003t0019 | 0/0 | 4056 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4051): Show |
chr22 | 19964896 | 20021823 |
a0003c0008t0004 | 0/0 | 4056 | 4 | 4 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4051): Show |
chr22 | 19964896 | 20021823 |
a0003c0008t0007 | 0/0 | 4056 | 4 | 0 | 3 | 0 | 0 | 1 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4051): Show |
chr22 | 19964896 | 20021823 |
a0003c0014t0006 | 0/0 | 4056 | 2 | 0 | 0 | 2 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4051): Show |
chr22 | 19964896 | 20021823 |
a0003c0015t0002 | 0/0 | 4056 | 2 | 0 | 0 | 2 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4051): Show |
chr22 | 19964896 | 20021823 |
a0003c0017t0006 | 0/0 | 4056 | 2 | 0 | 0 | 2 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4051): Show |
chr22 | 19964896 | 20021823 |
a0003c0019t0002 | 0/0 | 4056 | 2 | 0 | 0 | 2 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4051): Show |
chr22 | 19964896 | 20021823 |
a0003c0020t0002 | 0/0 | 4056 | 2 | 0 | 0 | 2 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4051): Show |
chr22 | 19964896 | 20021823 |
a0003c0038t0002 | 0/0 | 4056 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4051): Show |
chr22 | 19964896 | 20021823 |
a0004c0006t0005 | 0/0 | 4056 | 13 | 1 | 6 | 2 | 0 | 4 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4051): Show |
chr22 | 19964896 | 20021823 |
a0004c0006t0006 | 0/0 | 4056 | 1 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4051): Show |
chr22 | 19964896 | 20021823 |
a0004c0009t0002 | 0/0 | 4056 | 6 | 6 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4051): Show |
chr22 | 19964896 | 20021823 |
a0004c0009t0015 | 0/0 | 4056 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4051): Show |
chr22 | 19964896 | 20021823 |
a0004c0011t0006 | 0/0 | 4056 | 3 | 3 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4051): Show |
chr22 | 19964896 | 20021823 |
a0004c0012t0006 | 0/0 | 4056 | 3 | 3 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4051): Show |
chr22 | 19964896 | 20021823 |
a0004c0026t0006 | 0/0 | 4056 | 1 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4051): Show |
chr22 | 19964896 | 20021823 |
a0004c0041t0005 | 0/0 | 4056 | 1 | 0 | 0 | 0 | 0 | 1 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4051): Show |
chr22 | 19964896 | 20021823 |
a0005c0005t0004 | 0/0 | 4056 | 22 | 22 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4051): Show |
chr22 | 19964896 | 20021823 |
a0005c0005t0011 | 0/0 | 4056 | 1 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4051): Show |
chr22 | 19964896 | 20021823 |
a0005c0025t0004 | 0/0 | 4056 | 1 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4051): Show |
chr22 | 19964896 | 20021823 |
a0006c0007t0007 | 0/0 | 4056 | 8 | 0 | 0 | 6 | 0 | 2 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4051): Show |
chr22 | 19964896 | 20021823 |
a0006c0007t0017 | 0/0 | 4056 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4051): Show |
chr22 | 19964896 | 20021823 |
a0007c0010t0010 | 0/0 | 4056 | 4 | 4 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4051): Show |
chr22 | 19964896 | 20021823 |
a0008c0016t0006 | 0/0 | 4056 | 2 | 1 | 0 | 0 | 1 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4051): Show |
chr22 | 19964896 | 20021823 |
a0009c0013t0002 | 0/0 | 4056 | 2 | 2 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4051): Show |
chr22 | 19964896 | 20021823 |
a0010c0021t0002 | 0/0 | 4056 | 2 | 2 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4051): Show |
chr22 | 19964896 | 20021823 |
a0011c0018t0002 | 0/0 | 4056 | 2 | 0 | 0 | 2 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4051): Show |
chr22 | 19964896 | 20021823 |
a0012c0022t0005 | 0/0 | 4056 | 1 | 0 | 0 | 0 | 1 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4051): Show |
chr22 | 19964896 | 20021823 |
a0013c0042t0001 | 0/0 | 4056 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4051): Show |
chr22 | 19964896 | 20021823 |
a0014c0039t0004 | 0/0 | 4056 | 1 | 0 | 1 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4051): Show |
chr22 | 19964896 | 20021823 |
a0015c0029t0003 | 0/0 | 4056 | 1 | 0 | 1 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4051): Show |
chr22 | 19964896 | 20021823 |
a0016c0036t0004 | 0/0 | 4056 | 1 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4051): Show |
chr22 | 19964896 | 20021823 |
a0017c0037t0004 | 0/0 | 4056 | 1 | 0 | 0 | 0 | 0 | 1 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4051): Show |
chr22 | 19964896 | 20021823 |
a0018c0034t0001 | 0/0 | 4056 | 1 | 0 | 0 | 0 | 0 | 1 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4051): Show |
chr22 | 19964896 | 20021823 |
a0019c0024t0002 | 0/0 | 4056 | 1 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4051): Show |
chr22 | 19964896 | 20021823 |
a0020c0031t0003 | 0/0 | 4056 | 1 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4051): Show |
chr22 | 19964896 | 20021823 |
a0021c0028t0003 | 0/0 | 4056 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4051): Show |
chr22 | 19964896 | 20021823 |
a0022c0043t0002 | 0/0 | 4056 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4051): Show |
chr22 | 19964896 | 20021823 |
a0023c0023t0001 | 0/0 | 4056 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4051): Show |
chr22 | 19964896 | 20021823 |
a0024c0030t0001 | 0/0 | 4056 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4051): Show |
chr22 | 19964896 | 20021823 |
a0025c0027t0003 | 0/0 | 4056 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | GCGCA others(4051): Show |
chr22 | 19964896 | 20021823 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 7 | 0 | 1 | 5 | 0 | 1 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0005 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0012 | 0/0 | 4 | 1 | 2 | 0 | 1 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0013 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0050 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0003g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0013g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0013g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0021g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0023g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0001t0025g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0004t0004g0017 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0004t0004g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0004t0004g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0004t0004g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0004t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0004t0004g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0004t0004g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0004t0004g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0004t0004g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0004t0004g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0004t0004g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0004t0004g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0004t0004g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0004t0004g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0004t0004g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0004t0008g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0004t0008g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0004t0008g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0004t0008g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0004t0009g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0004t0009g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0004t0011g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0004t0016g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0004t0022g0111 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0033t0024g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0001c0035t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0002c0002t0001g0001 | 0/0 | 11 | 0 | 0 | 10 | 0 | 1 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0002c0002t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0002c0002t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0002c0002t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0002c0002t0003g0003 | 0/0 | 8 | 3 | 0 | 5 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0002c0002t0003g0006 | 0/0 | 6 | 0 | 2 | 1 | 1 | 2 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0002c0002t0003g0008 | 0/0 | 5 | 0 | 3 | 0 | 0 | 2 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0002c0002t0003g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0002c0002t0003g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0002c0002t0003g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0002c0002t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0002c0002t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0002c0002t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0002c0002t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0002c0002t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0002c0002t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0002c0002t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0002c0002t0003g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0002c0002t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0002c0002t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0002c0002t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0002c0002t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0002c0002t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0002c0002t0003g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0002c0002t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0002c0002t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0002c0002t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0002c0002t0003g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0002c0002t0003g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0002c0002t0003g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0002c0002t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0002c0002t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0002c0002t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0002c0002t0003g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0002c0002t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0002c0002t0014g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0002c0002t0020g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0002c0032t0004g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0002c0040t0003g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0003c0003t0002g0002 | 0/0 | 9 | 0 | 0 | 7 | 2 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0003c0003t0002g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0003c0003t0002g0039 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0003c0003t0002g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0003c0003t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0003c0003t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0003c0003t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0003c0003t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0003c0003t0002g0151 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0003c0003t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0003c0003t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0003c0003t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0003c0003t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0003c0003t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0003c0003t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0003c0003t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0003c0003t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0003c0003t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0003c0003t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0003c0003t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0003c0003t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0003c0003t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0003c0003t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0003c0003t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0003c0003t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0003c0003t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0003c0003t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0003c0003t0012g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0003c0003t0018g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0003c0003t0019g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0003c0008t0004g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0003c0008t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0003c0008t0004g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0003c0008t0007g0021 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0003c0008t0007g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0003c0014t0006g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0003c0014t0006g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0003c0015t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0003c0015t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0003c0017t0006g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0003c0017t0006g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0003c0019t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0003c0020t0002g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0003c0038t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0004c0006t0005g0014 | 0/0 | 4 | 1 | 1 | 0 | 0 | 2 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0004c0006t0005g0024 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0004c0006t0005g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0004c0006t0005g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0004c0006t0005g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0004c0006t0005g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0004c0006t0005g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0004c0006t0005g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0004c0006t0006g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0004c0009t0002g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0004c0009t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0004c0009t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0004c0009t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0004c0009t0015g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0004c0011t0006g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0004c0011t0006g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0004c0012t0006g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0004c0012t0006g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0004c0026t0006g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0004c0041t0005g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0005c0005t0004g0009 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0005c0005t0004g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0005c0005t0004g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0005c0005t0004g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0005c0005t0004g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0005c0005t0004g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0005c0005t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0005c0005t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0005c0005t0004g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0005c0005t0004g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0005c0005t0004g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0005c0005t0004g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0005c0005t0004g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0005c0005t0011g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0005c0025t0004g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0006c0007t0007g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0006c0007t0007g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0006c0007t0007g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0006c0007t0007g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0006c0007t0007g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0006c0007t0007g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0006c0007t0017g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0007c0010t0010g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0007c0010t0010g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0007c0010t0010g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0008c0016t0006g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0008c0016t0006g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0009c0013t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0009c0013t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0010c0021t0002g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0011c0018t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0012c0022t0005g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0013c0042t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0014c0039t0004g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0015c0029t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0016c0036t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0017c0037t0004g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0018c0034t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0019c0024t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0020c0031t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0021c0028t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0022c0043t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0023c0023t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0024c0030t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
a0025c0027t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | GBR | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG00099 | hp2 | a0001 | c0004 | t0004 | g0112 | EUR | GBR | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG00140 | hp1 | a0012 | c0022 | t0005 | g0246 | EUR | GBR | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0217 | EUR | GBR | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG00280 | hp1 | a0002 | c0002 | t0003 | g0077 | EUR | FIN | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG00280 | hp2 | a0003 | c0003 | t0002 | g0002 | EUR | FIN | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG00323 | hp1 | a0008 | c0016 | t0006 | g0178 | EUR | FIN | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG00323 | hp2 | a0003 | c0003 | t0002 | g0150 | EUR | FIN | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG00408 | hp1 | a0003 | c0017 | t0006 | g0243 | EAS | CHS | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG00408 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG00423 | hp1 | a0002 | c0002 | t0003 | g0025 | EAS | CHS | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG00423 | hp2 | a0002 | c0002 | t0003 | g0006 | EAS | CHS | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG00544 | hp1 | a0013 | c0042 | t0001 | g0164 | EAS | CHS | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | CHS | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | CHS | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG00597 | hp2 | a0001 | c0035 | t0001 | g0230 | EAS | CHS | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG00609 | hp2 | a0003 | c0019 | t0002 | g0041 | EAS | CHS | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG00621 | hp1 | a0003 | c0003 | t0002 | g0155 | EAS | CHS | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | CHS | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG00639 | hp1 | a0001 | c0004 | t0004 | g0110 | AMR | PUR | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG00639 | hp2 | a0002 | c0002 | t0003 | g0027 | AMR | PUR | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG00642 | hp1 | a0001 | c0004 | t0004 | g0109 | AMR | PUR | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG00735 | hp1 | a0002 | c0002 | t0003 | g0026 | AMR | PUR | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG00735 | hp2 | a0004 | c0006 | t0005 | g0024 | AMR | PUR | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG00741 | hp1 | a0014 | c0039 | t0004 | g0118 | AMR | PUR | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG01069 | hp1 | a0003 | c0003 | t0002 | g0149 | AMR | PUR | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG01069 | hp2 | a0001 | c0004 | t0004 | g0032 | AMR | PUR | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG01071 | hp1 | a0001 | c0004 | t0004 | g0032 | AMR | PUR | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG01071 | hp2 | a0001 | c0004 | t0004 | g0017 | AMR | PUR | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG01074 | hp1 | a0002 | c0002 | t0003 | g0055 | AMR | PUR | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG01081 | hp1 | a0002 | c0002 | t0003 | g0078 | AMR | PUR | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG01081 | hp2 | a0004 | c0006 | t0005 | g0247 | AMR | PUR | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG01099 | hp2 | a0015 | c0029 | t0003 | g0058 | AMR | PUR | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG01109 | hp2 | a0002 | c0002 | t0003 | g0072 | AMR | PUR | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG01167 | hp2 | a0001 | c0004 | t0004 | g0115 | AMR | PUR | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG01168 | hp1 | a0001 | c0004 | t0004 | g0044 | AMR | PUR | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG01168 | hp2 | a0002 | c0002 | t0003 | g0069 | AMR | PUR | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG01169 | hp1 | a0001 | c0004 | t0004 | g0044 | AMR | PUR | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG01175 | hp1 | a0002 | c0002 | t0003 | g0080 | AMR | PUR | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG01243 | hp2 | a0001 | c0001 | t0013 | g0256 | AMR | PUR | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG01256 | hp1 | a0004 | c0006 | t0005 | g0024 | AMR | CLM | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG01256 | hp2 | a0002 | c0002 | t0001 | g0185 | AMR | CLM | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG01257 | hp1 | a0001 | c0004 | t0008 | g0028 | AMR | CLM | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG01257 | hp2 | a0002 | c0002 | t0003 | g0008 | AMR | CLM | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG01258 | hp1 | a0004 | c0006 | t0005 | g0024 | AMR | CLM | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG01258 | hp2 | a0001 | c0004 | t0008 | g0028 | AMR | CLM | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | CLM | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG01261 | hp2 | a0002 | c0002 | t0003 | g0027 | AMR | CLM | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG01358 | hp1 | a0002 | c0002 | t0003 | g0079 | AMR | CLM | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG01358 | hp2 | a0001 | c0004 | t0004 | g0017 | AMR | CLM | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG01361 | hp1 | a0003 | c0003 | t0002 | g0038 | AMR | CLM | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG01361 | hp2 | a0001 | c0004 | t0004 | g0017 | AMR | CLM | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | CLM | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG01496 | hp1 | a0004 | c0006 | t0005 | g0250 | AMR | CLM | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG01496 | hp2 | a0002 | c0002 | t0003 | g0006 | AMR | CLM | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG01516 | hp1 | a0003 | c0003 | t0002 | g0002 | EUR | IBS | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0218 | EUR | IBS | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG01884 | hp2 | a0004 | c0009 | t0002 | g0105 | AFR | ACB | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG01891 | hp1 | a0007 | c0010 | t0010 | g0143 | AFR | ACB | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG01928 | hp1 | a0004 | c0006 | t0005 | g0014 | AMR | PEL | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG01928 | hp2 | a0003 | c0003 | t0002 | g0171 | AMR | PEL | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG01934 | hp1 | a0003 | c0003 | t0018 | g0091 | AMR | PEL | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG01934 | hp2 | a0001 | c0004 | t0004 | g0108 | AMR | PEL | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG01952 | hp1 | a0003 | c0003 | t0002 | g0038 | AMR | PEL | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG01952 | hp2 | a0003 | c0008 | t0007 | g0021 | AMR | PEL | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG01975 | hp1 | a0002 | c0002 | t0001 | g0036 | AMR | PEL | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG01975 | hp2 | a0002 | c0002 | t0003 | g0008 | AMR | PEL | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG01978 | hp1 | a0003 | c0008 | t0007 | g0189 | AMR | PEL | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG01978 | hp2 | a0002 | c0002 | t0003 | g0064 | AMR | PEL | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG01981 | hp1 | a0002 | c0002 | t0003 | g0070 | AMR | PEL | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG01981 | hp2 | a0001 | c0004 | t0011 | g0083 | AMR | PEL | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG01993 | hp1 | a0002 | c0002 | t0001 | g0146 | AMR | PEL | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG01993 | hp2 | a0003 | c0008 | t0007 | g0021 | AMR | PEL | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02004 | hp1 | a0002 | c0002 | t0001 | g0036 | AMR | PEL | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02004 | hp2 | a0003 | c0003 | t0002 | g0039 | AMR | PEL | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02027 | hp2 | a0002 | c0002 | t0001 | g0123 | EAS | KHV | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02040 | hp1 | a0003 | c0003 | t0002 | g0157 | EAS | KHV | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02040 | hp2 | a0002 | c0002 | t0001 | g0122 | EAS | KHV | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02055 | hp1 | a0004 | c0011 | t0006 | g0095 | AFR | ACB | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02056 | hp2 | a0003 | c0003 | t0002 | g0173 | EAS | KHV | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02071 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02074 | hp1 | a0003 | c0003 | t0002 | g0168 | EAS | KHV | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02083 | hp1 | a0003 | c0003 | t0002 | g0002 | EAS | KHV | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02129 | hp1 | a0002 | c0002 | t0003 | g0025 | EAS | KHV | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02129 | hp2 | a0003 | c0003 | t0002 | g0156 | EAS | KHV | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02132 | hp2 | a0003 | c0003 | t0002 | g0158 | EAS | KHV | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02135 | hp1 | a0003 | c0019 | t0002 | g0041 | EAS | KHV | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02145 | hp1 | a0004 | c0009 | t0002 | g0015 | AFR | ACB | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02145 | hp2 | a0001 | c0004 | t0004 | g0128 | AFR | ACB | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02155 | hp1 | a0004 | c0006 | t0005 | g0252 | EAS | CDX | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02155 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | CDX | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | CDX | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | CDX | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02258 | hp1 | a0004 | c0011 | t0006 | g0030 | AFR | ACB | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02280 | hp1 | a0001 | c0004 | t0009 | g0018 | AFR | ACB | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02280 | hp2 | a0001 | c0001 | t0013 | g0255 | AFR | ACB | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02300 | hp1 | a0003 | c0003 | t0002 | g0148 | AMR | PEL | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02300 | hp2 | a0002 | c0002 | t0003 | g0008 | AMR | PEL | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02451 | hp1 | a0005 | c0005 | t0004 | g0140 | AFR | ACB | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | ACB | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02523 | hp1 | a0002 | c0002 | t0001 | g0125 | EAS | KHV | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02523 | hp2 | a0001 | c0001 | t0025 | g0254 | EAS | KHV | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02602 | hp1 | a0002 | c0040 | t0003 | g0052 | SAS | PJL | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02602 | hp2 | a0001 | c0004 | t0004 | g0113 | SAS | PJL | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02615 | hp1 | a0005 | c0005 | t0004 | g0135 | AFR | GWD | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02622 | hp1 | a0005 | c0005 | t0004 | g0011 | AFR | GWD | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02622 | hp2 | a0004 | c0009 | t0002 | g0093 | AFR | GWD | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02630 | hp1 | a0001 | c0004 | t0004 | g0019 | AFR | GWD | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02630 | hp2 | a0003 | c0008 | t0004 | g0202 | AFR | GWD | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02647 | hp1 | a0016 | c0036 | t0004 | g0129 | AFR | GWD | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02647 | hp2 | a0003 | c0008 | t0004 | g0034 | AFR | GWD | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02698 | hp1 | a0004 | c0006 | t0005 | g0014 | SAS | PJL | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02717 | hp1 | a0001 | c0004 | t0008 | g0089 | AFR | GWD | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02717 | hp2 | a0005 | c0005 | t0004 | g0009 | AFR | GWD | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02723 | hp1 | a0005 | c0005 | t0004 | g0009 | AFR | GWD | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02723 | hp2 | a0002 | c0002 | t0003 | g0003 | AFR | GWD | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02735 | hp1 | a0004 | c0006 | t0005 | g0249 | SAS | PJL | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02735 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02738 | hp1 | a0002 | c0002 | t0003 | g0084 | SAS | PJL | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02809 | hp1 | a0005 | c0005 | t0004 | g0011 | AFR | GWD | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02809 | hp2 | a0001 | c0004 | t0008 | g0090 | AFR | GWD | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02818 | hp1 | a0002 | c0002 | t0003 | g0071 | AFR | GWD | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02818 | hp2 | a0007 | c0010 | t0010 | g0142 | AFR | GWD | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02886 | hp2 | a0009 | c0013 | t0002 | g0096 | AFR | GWD | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02895 | hp1 | a0005 | c0005 | t0004 | g0133 | AFR | GWD | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02895 | hp2 | a0002 | c0002 | t0003 | g0074 | AFR | GWD | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02896 | hp1 | a0010 | c0021 | t0002 | g0031 | AFR | GWD | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02896 | hp2 | a0004 | c0009 | t0002 | g0015 | AFR | GWD | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02897 | hp1 | a0002 | c0002 | t0003 | g0076 | AFR | GWD | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02897 | hp2 | a0010 | c0021 | t0002 | g0031 | AFR | GWD | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ESN | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02922 | hp2 | a0005 | c0005 | t0004 | g0009 | AFR | ESN | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02965 | hp1 | a0007 | c0010 | t0010 | g0035 | AFR | ESN | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02965 | hp2 | a0005 | c0005 | t0004 | g0137 | AFR | ESN | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02970 | hp1 | a0007 | c0010 | t0010 | g0035 | AFR | ESN | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ESN | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02976 | hp1 | a0002 | c0002 | t0003 | g0059 | AFR | ESN | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02976 | hp2 | a0002 | c0032 | t0004 | g0136 | AFR | ESN | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG03017 | hp1 | a0017 | c0037 | t0004 | g0116 | SAS | PJL | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG03017 | hp2 | a0002 | c0002 | t0003 | g0008 | SAS | PJL | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG03041 | hp1 | a0005 | c0005 | t0004 | g0020 | AFR | GWD | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG03041 | hp2 | a0004 | c0012 | t0006 | g0033 | AFR | GWD | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG03098 | hp1 | a0005 | c0005 | t0011 | g0067 | AFR | MSL | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG03098 | hp2 | a0005 | c0005 | t0004 | g0020 | AFR | MSL | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG03130 | hp1 | a0004 | c0012 | t0006 | g0120 | AFR | ESN | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG03130 | hp2 | a0001 | c0004 | t0009 | g0121 | AFR | ESN | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG03139 | hp1 | a0005 | c0005 | t0004 | g0226 | AFR | ESN | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG03139 | hp2 | a0004 | c0011 | t0006 | g0030 | AFR | ESN | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG03195 | hp1 | a0005 | c0005 | t0004 | g0020 | AFR | ESN | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG03195 | hp2 | a0004 | c0012 | t0006 | g0033 | AFR | ESN | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG03209 | hp1 | a0008 | c0016 | t0006 | g0177 | AFR | MSL | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG03209 | hp2 | a0005 | c0005 | t0004 | g0239 | AFR | MSL | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG03225 | hp1 | a0009 | c0013 | t0002 | g0098 | AFR | MSL | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG03225 | hp2 | a0001 | c0004 | t0004 | g0019 | AFR | MSL | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG03239 | hp1 | a0002 | c0002 | t0003 | g0068 | SAS | PJL | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG03239 | hp2 | a0018 | c0034 | t0001 | g0199 | SAS | PJL | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | MSL | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG03453 | hp2 | a0004 | c0009 | t0002 | g0015 | AFR | MSL | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG03486 | hp1 | a0019 | c0024 | t0002 | g0097 | AFR | MSL | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | MSL | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG03491 | hp1 | a0002 | c0002 | t0003 | g0008 | SAS | PJL | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG03491 | hp2 | a0003 | c0003 | t0012 | g0040 | SAS | PJL | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG03492 | hp1 | a0002 | c0002 | t0003 | g0006 | SAS | PJL | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG03492 | hp2 | a0003 | c0003 | t0012 | g0040 | SAS | PJL | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG03516 | hp1 | a0001 | c0004 | t0008 | g0029 | AFR | ESN | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG03516 | hp2 | a0005 | c0005 | t0004 | g0139 | AFR | ESN | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG03540 | hp1 | a0004 | c0009 | t0002 | g0094 | AFR | GWD | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG03540 | hp2 | a0005 | c0025 | t0004 | g0134 | AFR | GWD | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG03579 | hp1 | a0002 | c0002 | t0003 | g0075 | AFR | MSL | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG03579 | hp2 | a0020 | c0031 | t0003 | g0054 | AFR | MSL | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG03688 | hp1 | a0004 | c0006 | t0005 | g0014 | SAS | STU | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG03688 | hp2 | a0006 | c0007 | t0007 | g0102 | SAS | STU | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG03704 | hp1 | a0001 | c0004 | t0016 | g0087 | SAS | PJL | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG03704 | hp2 | a0003 | c0008 | t0007 | g0021 | SAS | PJL | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | BEB | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG03927 | hp2 | a0001 | c0004 | t0004 | g0117 | SAS | BEB | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG03942 | hp1 | a0003 | c0003 | t0002 | g0174 | SAS | BEB | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | BEB | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG04115 | hp1 | a0002 | c0002 | t0003 | g0006 | SAS | STU | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG04115 | hp2 | a0001 | c0004 | t0004 | g0119 | SAS | STU | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG04184 | hp1 | a0004 | c0041 | t0005 | g0251 | SAS | BEB | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | BEB | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG04199 | hp1 | a0002 | c0002 | t0003 | g0066 | SAS | STU | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | STU | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG04204 | hp1 | a0004 | c0006 | t0005 | g0253 | SAS | STU | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG04204 | hp2 | a0001 | c0004 | t0004 | g0114 | SAS | STU | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | STU | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG04228 | hp2 | a0006 | c0007 | t0007 | g0101 | SAS | STU | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | YRI | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18522 | hp2 | a0005 | c0005 | t0004 | g0011 | AFR | YRI | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | CHB | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18612 | hp2 | a0004 | c0006 | t0005 | g0248 | EAS | CHB | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | CHB | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18747 | hp2 | a0002 | c0002 | t0001 | g0126 | EAS | CHB | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18906 | hp1 | a0001 | c0004 | t0009 | g0018 | AFR | YRI | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18906 | hp2 | a0005 | c0005 | t0004 | g0009 | AFR | YRI | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18939 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18939 | hp2 | a0003 | c0003 | t0019 | g0092 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18940 | hp1 | a0003 | c0003 | t0002 | g0166 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18940 | hp2 | a0002 | c0002 | t0003 | g0003 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18941 | hp1 | a0002 | c0002 | t0014 | g0056 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18942 | hp1 | a0021 | c0028 | t0003 | g0065 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18942 | hp2 | a0003 | c0015 | t0002 | g0159 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18943 | hp1 | a0006 | c0007 | t0007 | g0016 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18943 | hp2 | a0003 | c0003 | t0002 | g0002 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18944 | hp1 | a0003 | c0003 | t0002 | g0042 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18947 | hp2 | a0011 | c0018 | t0002 | g0037 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18949 | hp1 | a0002 | c0002 | t0001 | g0130 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18949 | hp2 | a0001 | c0001 | t0023 | g0212 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18951 | hp2 | a0002 | c0002 | t0003 | g0003 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18956 | hp1 | a0003 | c0020 | t0002 | g0043 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18957 | hp1 | a0022 | c0043 | t0002 | g0165 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18959 | hp1 | a0002 | c0002 | t0003 | g0057 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18961 | hp1 | a0004 | c0009 | t0015 | g0061 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18964 | hp1 | a0003 | c0003 | t0002 | g0161 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18966 | hp2 | a0003 | c0003 | t0002 | g0002 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18967 | hp2 | a0003 | c0020 | t0002 | g0043 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18970 | hp1 | a0003 | c0003 | t0002 | g0152 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18973 | hp1 | a0002 | c0002 | t0001 | g0127 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18975 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18975 | hp2 | a0003 | c0003 | t0002 | g0002 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18977 | hp1 | a0002 | c0002 | t0003 | g0081 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18979 | hp1 | a0006 | c0007 | t0007 | g0106 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18979 | hp2 | a0002 | c0002 | t0003 | g0053 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18980 | hp1 | a0006 | c0007 | t0007 | g0016 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18983 | hp1 | a0003 | c0017 | t0006 | g0242 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18983 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18984 | hp1 | a0006 | c0007 | t0007 | g0016 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18984 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18985 | hp2 | a0003 | c0003 | t0002 | g0154 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18986 | hp1 | a0023 | c0023 | t0001 | g0100 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18989 | hp1 | a0003 | c0003 | t0002 | g0170 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18989 | hp2 | a0024 | c0030 | t0001 | g0145 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18997 | hp2 | a0003 | c0003 | t0002 | g0147 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18998 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA18999 | hp2 | a0002 | c0002 | t0003 | g0086 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA19000 | hp1 | a0002 | c0002 | t0003 | g0063 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA19000 | hp2 | a0003 | c0003 | t0002 | g0002 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA19003 | hp1 | a0003 | c0003 | t0002 | g0039 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA19005 | hp2 | a0003 | c0003 | t0002 | g0042 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA19011 | hp2 | a0006 | c0007 | t0007 | g0104 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA19012 | hp2 | a0003 | c0003 | t0002 | g0172 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA19043 | hp1 | a0002 | c0002 | t0003 | g0003 | AFR | LWK | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA19043 | hp2 | a0001 | c0004 | t0004 | g0103 | AFR | LWK | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA19054 | hp1 | a0003 | c0015 | t0002 | g0167 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA19054 | hp2 | a0002 | c0002 | t0003 | g0060 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA19057 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA19057 | hp2 | a0003 | c0014 | t0006 | g0240 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA19058 | hp1 | a0002 | c0002 | t0003 | g0003 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA19060 | hp1 | a0003 | c0003 | t0002 | g0002 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA19060 | hp2 | a0002 | c0002 | t0003 | g0062 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA19064 | hp2 | a0002 | c0002 | t0003 | g0082 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA19065 | hp2 | a0003 | c0038 | t0002 | g0162 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA19066 | hp2 | a0003 | c0003 | t0002 | g0169 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA19070 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA19074 | hp1 | a0003 | c0003 | t0002 | g0160 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA19074 | hp2 | a0002 | c0002 | t0003 | g0026 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA19077 | hp2 | a0002 | c0002 | t0001 | g0144 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA19079 | hp1 | a0002 | c0002 | t0003 | g0003 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA19079 | hp2 | a0002 | c0002 | t0020 | g0124 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA19080 | hp1 | a0025 | c0027 | t0003 | g0085 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA19081 | hp2 | a0011 | c0018 | t0002 | g0037 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA19082 | hp2 | a0006 | c0007 | t0017 | g0088 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA19084 | hp2 | a0006 | c0007 | t0007 | g0099 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA19085 | hp1 | a0003 | c0014 | t0006 | g0241 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA19087 | hp1 | a0003 | c0003 | t0002 | g0163 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA19088 | hp2 | a0002 | c0002 | t0003 | g0003 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA19089 | hp1 | a0003 | c0003 | t0002 | g0002 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA19090 | hp1 | a0001 | c0033 | t0024 | g0245 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA19090 | hp2 | a0003 | c0003 | t0002 | g0153 | EAS | JPT | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA19240 | hp1 | a0001 | c0004 | t0009 | g0018 | AFR | YRI | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | YRI | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ASW | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA20129 | hp2 | a0004 | c0026 | t0006 | g0107 | AFR | ASW | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA20752 | hp1 | a0002 | c0002 | t0003 | g0006 | EUR | TSI | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0179 | EUR | TSI | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0188 | EUR | TSI | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA20805 | hp2 | a0001 | c0001 | t0021 | g0220 | EUR | TSI | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG01123 | hp1 | a0002 | c0002 | t0003 | g0006 | AMR | CLM | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG01123 | hp2 | a0001 | c0001 | t0003 | g0073 | AMR | CLM | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02109 | hp1 | a0005 | c0005 | t0004 | g0011 | AFR | ACB | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02109 | hp2 | a0005 | c0005 | t0004 | g0138 | AFR | ACB | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02486 | hp1 | a0003 | c0008 | t0004 | g0131 | AFR | ACB | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | ACB | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02559 | hp1 | a0005 | c0005 | t0004 | g0132 | AFR | ACB | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG02559 | hp2 | a0003 | c0008 | t0004 | g0034 | AFR | ACB | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG03471 | hp1 | a0001 | c0004 | t0004 | g0019 | AFR | MSL | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG03471 | hp2 | a0001 | c0004 | t0008 | g0029 | AFR | MSL | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG06807 | hp1 | a0004 | c0006 | t0006 | g0175 | AFR | USA | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
HG06807 | hp2 | a0002 | c0002 | t0003 | g0003 | AFR | USA | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA20300 | hp1 | a0005 | c0005 | t0004 | g0141 | AFR | USA | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA20300 | hp2 | a0004 | c0006 | t0005 | g0014 | AFR | USA | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA21309 | hp1 | a0005 | c0005 | t0004 | g0009 | AFR | LWK | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | LWK | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
homoSapiens | chm13v2 | a0001 | c0004 | t0022 | g0111 | REF | REF | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
homoSapiens | grch38p0 | a0003 | c0003 | t0002 | g0151 | REF | REF | ARVCF_chr22_19964896_20021823 | ARVCF | chr22 | 19964896 | 20021823 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:19971933 | G | A | 1 | a0008 | 2 | HG00323.hp1 HG03209.hp1 |
missense_variant | MODERATE | c.2734C>T | p.Arg912Trp | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 18/20 | 3041/4056 | 2734/2889 | 912/962 | chr22 | 19971933 | |||
chr22:19971941 | C | T | 1 | a0008 | 2 | HG00323.hp1 HG03209.hp1 |
missense_variant | MODERATE | c.2726G>A | p.Arg909Gln | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 18/20 | 3033/4056 | 2726/2889 | 909/962 | chr22 | 19971941 | |||
chr22:19971950 | C | T | 13 | a0001 a0002 a0013 others(10): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
missense_variant | MODERATE | c.2717G>A | p.Arg906Gln | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 18/20 | 3024/4056 | 2717/2889 | 906/962 | chr22 | 19971950 | |||
chr22:19972803 | G | A | 1 | a0011 | 2 | NA18947.hp2 NA19081.hp2 |
missense_variant | MODERATE | c.2575C>T | p.Pro859Ser | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 16/20 | 2882/4056 | 2575/2889 | 859/962 | chr22 | 19972803 | |||
chr22:19972989 | A | G | 1 | a0015 | 1 | HG01099.hp2 | missense_variant | MODERATE | c.2486T>C | p.Val829Ala | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 15/20 | 2793/4056 | 2486/2889 | 829/962 | chr22 | 19972989 | |||
chr22:19973025 | C | G | 1 | a0021 | 1 | NA18942.hp1 | missense_variant | MODERATE | c.2450G>C | p.Arg817Pro | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 15/20 | 2757/4056 | 2450/2889 | 817/962 | chr22 | 19973025 | |||
chr22:19973143 | G | A | 1 | a0007 | 4 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(1): Show |
missense_variant | MODERATE | c.2414C>T | p.Ala805Val | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 14/20 | 2721/4056 | 2414/2889 | 805/962 | chr22 | 19973143 | |||
chr22:19973248 | C | A | 1 | a0024 | 1 | NA18989.hp2 | missense_variant | MODERATE | c.2309G>T | p.Cys770Phe | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 14/20 | 2616/4056 | 2309/2889 | 770/962 | chr22 | 19973248 | |||
chr22:19977463 | G | A | 1 | a0018 | 1 | HG03239.hp2 | missense_variant | MODERATE | c.1822C>T | p.Arg608Cys | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 9/20 | 2129/4056 | 1822/2889 | 608/962 | chr22 | 19977463 | |||
chr22:19977561 | A | G | 1 | a0025 | 1 | NA19080.hp1 | missense_variant | MODERATE | c.1724T>C | p.Met575Thr | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 9/20 | 2031/4056 | 1724/2889 | 575/962 | chr22 | 19977561 | |||
chr22:19978925 | C | T | 1 | a0017 | 1 | HG03017.hp1 | missense_variant | MODERATE | c.1552G>A | p.Val518Ile | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 7/20 | 1859/4056 | 1552/2889 | 518/962 | chr22 | 19978925 | |||
chr22:19979039 | C | T | 2 | a0009 a0019 |
3 | HG02886.hp2 HG03225.hp1 HG03486.hp1 |
missense_variant | MODERATE | c.1438G>A | p.Val480Ile | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 7/20 | 1745/4056 | 1438/2889 | 480/962 | chr22 | 19979039 | |||
chr22:19979056 | T | G | 1 | a0020 | 1 | HG03579.hp2 | missense_variant | MODERATE | c.1421A>C | p.Tyr474Ser | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 7/20 | 1728/4056 | 1421/2889 | 474/962 | chr22 | 19979056 | |||
chr22:19980091 | G | A | 1 | a0014 | 1 | HG00741.hp1 | missense_variant | MODERATE | c.1048C>T | p.Arg350Cys | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 6/20 | 1355/4056 | 1048/2889 | 350/962 | chr22 | 19980091 | |||
chr22:19980154 | C | T | 1 | a0016 | 1 | HG02647.hp1 | missense_variant | MODERATE | c.985G>A | p.Glu329Lys | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 6/20 | 1292/4056 | 985/2889 | 329/962 | chr22 | 19980154 | |||
chr22:19981410 | G | A | 1 | a0019 | 1 | HG03486.hp1 | missense_variant | MODERATE | c.697C>T | p.Arg233Trp | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 5/20 | 1004/4056 | 697/2889 | 233/962 | chr22 | 19981410 | |||
chr22:19981448 | G | A | 14 | a0002 a0004 a0006 others(11): Show |
130 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(127): Show |
missense_variant | MODERATE | c.659C>T | p.Pro220Leu | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 5/20 | 966/4056 | 659/2889 | 220/962 | chr22 | 19981448 | |||
chr22:19981520 | C | T | 4 | a0006 a0009 a0019 others(1): Show |
13 | HG02886.hp2 HG03225.hp1 HG03486.hp1 others(10): Show |
missense_variant | MODERATE | c.587G>A | p.Arg196Gln | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 5/20 | 894/4056 | 587/2889 | 196/962 | chr22 | 19981520 | |||
chr22:19981583 | A | G | 15 | a0002 a0004 a0005 others(12): Show |
154 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(151): Show |
missense_variant | MODERATE | c.524T>C | p.Val175Ala | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 5/20 | 831/4056 | 524/2889 | 175/962 | chr22 | 19981583 | |||
chr22:19981659 | C | T | 1 | a0012 | 1 | HG00140.hp1 | missense_variant | MODERATE | c.448G>A | p.Asp150Asn | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 5/20 | 755/4056 | 448/2889 | 150/962 | chr22 | 19981659 | |||
chr22:19990695 | G | A | 1 | a0010 | 2 | HG02896.hp1 HG02897.hp2 |
missense_variant | MODERATE | c.100C>T | p.Arg34Trp | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/20 | 407/4056 | 100/2889 | 34/962 | chr22 | 19990695 | |||
chr22:19990782 | T | C | 2 | a0013 a0022 |
2 | HG00544.hp1 NA18957.hp1 |
missense_variant | MODERATE | c.13A>G | p.Asn5Asp | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/20 | 320/4056 | 13/2889 | 5/962 | chr22 | 19990782 | |||
chr22:19990812 | G | A | 1 | a0007 | 4 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(1): Show |
splice_region_variant | LOW | c.-18C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/20 | chr22 | 19990812 | |||||||
chr22:20016590 | T | G | 1 | a0001 | 1 | NA19090.hp1 | splice_region_variant | LOW | c.-74A>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/20 | chr22 | 20016590 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:19971306 | G | A | 9 | a0003c0014 a0003c0017 a0004c0006 others(6): Show |
29 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(26): Show |
synonymous_variant | LOW | c.2811C>T | p.Pro937Pro | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 19/20 | 3118/4056 | 2811/2889 | 937/962 | chr22 | 19971306 | |||
chr22:19972976 | C | T | 1 | a0008c0016 | 2 | HG00323.hp1 HG03209.hp1 |
synonymous_variant | LOW | c.2499G>A | p.Lys833Lys | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 15/20 | 2806/4056 | 2499/2889 | 833/962 | chr22 | 19972976 | |||
chr22:19973199 | G | A | 1 | a0003c0019 | 2 | HG00609.hp2 HG02135.hp1 |
synonymous_variant | LOW | c.2358C>T | p.Ile786Ile | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 14/20 | 2665/4056 | 2358/2889 | 786/962 | chr22 | 19973199 | |||
chr22:19973701 | G | A | 1 | a0001c0033 | 1 | NA19090.hp1 | synonymous_variant | LOW | c.2181C>T | p.Arg727Arg | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 13/20 | 2488/4056 | 2181/2889 | 727/962 | chr22 | 19973701 | |||
chr22:19974217 | G | A | 1 | a0003c0020 | 2 | NA18956.hp1 NA18967.hp2 |
synonymous_variant | LOW | c.1983C>T | p.Pro661Pro | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 12/20 | 2290/4056 | 1983/2889 | 661/962 | chr22 | 19974217 | |||
chr22:19977524 | G | A | 1 | a0003c0038 | 1 | NA19065.hp2 | synonymous_variant | LOW | c.1761C>T | p.Pro587Pro | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 9/20 | 2068/4056 | 1761/2889 | 587/962 | chr22 | 19977524 | |||
chr22:19979807 | A | G | 1 | a0003c0015 | 2 | NA18942.hp2 NA19054.hp1 |
synonymous_variant | LOW | c.1332T>C | p.Gly444Gly | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 6/20 | 1639/4056 | 1332/2889 | 444/962 | chr22 | 19979807 | |||
chr22:19979828 | G | A | 1 | a0001c0035 | 1 | HG00597.hp2 | synonymous_variant | LOW | c.1311C>T | p.Ala437Ala | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 6/20 | 1618/4056 | 1311/2889 | 437/962 | chr22 | 19979828 | |||
chr22:19979957 | C | G | 4 | a0006c0007 a0009c0013 a0019c0024 others(1): Show |
13 | HG02886.hp2 HG03225.hp1 HG03486.hp1 others(10): Show |
synonymous_variant | LOW | c.1182G>C | p.Arg394Arg | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 6/20 | 1489/4056 | 1182/2889 | 394/962 | chr22 | 19979957 | |||
chr22:19980020 | G | A | 1 | a0005c0005 | 23 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(20): Show |
synonymous_variant | LOW | c.1119C>T | p.Pro373Pro | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 6/20 | 1426/4056 | 1119/2889 | 373/962 | chr22 | 19980020 | |||
chr22:19980044 | G | A | 2 | a0002c0032 a0004c0012 |
4 | HG02976.hp2 HG03041.hp2 HG03130.hp1 others(1): Show |
synonymous_variant | LOW | c.1095C>T | p.Ala365Ala | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 6/20 | 1402/4056 | 1095/2889 | 365/962 | chr22 | 19980044 | |||
chr22:19980125 | C | G | 1 | a0003c0014 | 2 | NA19057.hp2 NA19085.hp1 |
synonymous_variant | LOW | c.1014G>C | p.Arg338Arg | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 6/20 | 1321/4056 | 1014/2889 | 338/962 | chr22 | 19980125 | |||
chr22:19981270 | C | T | 1 | a0016c0036 | 1 | HG02647.hp1 | synonymous_variant | LOW | c.837G>A | p.Glu279Glu | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 5/20 | 1144/4056 | 837/2889 | 279/962 | chr22 | 19981270 | |||
chr22:19981333 | C | T | 1 | a0004c0026 | 1 | NA20129.hp2 | synonymous_variant | LOW | c.774G>A | p.Pro258Pro | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 5/20 | 1081/4056 | 774/2889 | 258/962 | chr22 | 19981333 | |||
chr22:19981552 | A | G | 28 | a0001c0001 a0001c0033 a0001c0035 others(25): Show |
278 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(275): Show |
synonymous_variant | LOW | c.555T>C | p.Ser185Ser | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 5/20 | 862/4056 | 555/2889 | 185/962 | chr22 | 19981552 | |||
chr22:19981654 | G | A | 1 | a0002c0040 | 1 | HG02602.hp1 | synonymous_variant | LOW | c.453C>T | p.Gly151Gly | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 5/20 | 760/4056 | 453/2889 | 151/962 | chr22 | 19981654 | |||
chr22:19981972 | G | T | 1 | a0004c0011 | 3 | HG02055.hp1 HG02258.hp1 HG03139.hp2 |
synonymous_variant | LOW | c.330C>A | p.Val110Val | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 4/20 | 637/4056 | 330/2889 | 110/962 | chr22 | 19981972 | |||
chr22:19982002 | G | A | 1 | a0004c0041 | 1 | HG04184.hp1 | synonymous_variant | LOW | c.300C>T | p.Pro100Pro | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 4/20 | 607/4056 | 300/2889 | 100/962 | chr22 | 19982002 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:19970108 | C | A | 21 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0013 others(18): Show |
198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
3_prime_UTR_variant | MODIFIER | c.*648G>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 20/20 | 1120 | chr22 | 19970108 | ||||||
chr22:19970110 | A | T | 3 | a0003c0008t0007 a0006c0007t0007 a0006c0007t0017 |
13 | HG01952.hp2 HG01978.hp1 HG01993.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*646T>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 20/20 | 1118 | chr22 | 19970110 | ||||||
chr22:19970163 | G | A | 1 | a0001c0001t0021 | 1 | NA20805.hp2 | 3_prime_UTR_variant | MODIFIER | c.*593C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 20/20 | 1065 | chr22 | 19970163 | ||||||
chr22:19970221 | G | C | 1 | a0001c0004t0009 | 4 | HG02280.hp1 HG03130.hp2 NA18906.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*535C>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 20/20 | 1007 | chr22 | 19970221 | ||||||
chr22:19970236 | G | C | 1 | a0007c0010t0010 | 4 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*520C>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 20/20 | 992 | chr22 | 19970236 | ||||||
chr22:19970240 | G | A | 21 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0013 others(18): Show |
198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
3_prime_UTR_variant | MODIFIER | c.*516C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 20/20 | 988 | chr22 | 19970240 | ||||||
chr22:19970264 | C | T | 45 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0013 others(42): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
3_prime_UTR_variant | MODIFIER | c.*492G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 20/20 | 964 | chr22 | 19970264 | ||||||
chr22:19970303 | C | T | 1 | a0002c0002t0014 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*453G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 20/20 | 925 | chr22 | 19970303 | ||||||
chr22:19970383 | C | G | 1 | a0002c0002t0020 | 1 | NA19079.hp2 | 3_prime_UTR_variant | MODIFIER | c.*373G>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 20/20 | 845 | chr22 | 19970383 | ||||||
chr22:19970499 | G | A | 12 | a0001c0004t0004 a0001c0004t0008 a0001c0004t0011 others(9): Show |
61 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*257C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 20/20 | 729 | chr22 | 19970499 | ||||||
chr22:19970514 | G | A | 1 | a0003c0003t0012 | 2 | HG03491.hp2 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*242C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 20/20 | 714 | chr22 | 19970514 | ||||||
chr22:19970672 | ACGGCACG others(12): Show |
A | 1 | a0001c0001t0023 | 1 | NA18949.hp2 | 3_prime_UTR_variant | MODIFIER | c.*65_*83delCCCTGAGC others(11): Show |
ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 20/20 | 537 | chr22 | 19970672 | ||||||
chr22:19970674 | G | A | 1 | a0007c0010t0010 | 4 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*82C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 20/20 | 554 | chr22 | 19970674 | ||||||
chr22:19970679 | G | A | 2 | a0004c0006t0006 a0012c0022t0005 |
2 | HG00140.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*77C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 20/20 | 549 | chr22 | 19970679 | ||||||
chr22:20016640 | C | A | 4 | a0001c0001t0025 a0004c0006t0005 a0004c0041t0005 others(1): Show |
16 | HG00140.hp1 HG00735.hp2 HG01081.hp2 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-124G>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/20 | 25846 | chr22 | 20016640 | ||||||
chr22:20016667 | A | C | 1 | a0003c0003t0019 | 1 | NA18939.hp2 | 5_prime_UTR_variant | MODIFIER | c.-151T>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/20 | 25873 | chr22 | 20016667 | ||||||
chr22:20016669 | C | T | 1 | a0003c0003t0018 | 1 | HG01934.hp1 | 5_prime_UTR_variant | MODIFIER | c.-153G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/20 | 25875 | chr22 | 20016669 | ||||||
chr22:20016693 | TGCGGC | T | 1 | a0001c0004t0008 | 6 | HG01257.hp1 HG01258.hp2 HG02717.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-182_-178delGCCGC | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/20 | 25900 | chr22 | 20016693 | ||||||
chr22:20016756 | T | C | 1 | a0006c0007t0017 | 1 | NA19082.hp2 | 5_prime_UTR_variant | MODIFIER | c.-240A>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/20 | 25962 | chr22 | 20016756 | ||||||
chr22:20016757 | C | T | 1 | a0006c0007t0017 | 1 | NA19082.hp2 | 5_prime_UTR_variant | MODIFIER | c.-241G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/20 | 25963 | chr22 | 20016757 | ||||||
chr22:20016780 | C | T | 1 | a0001c0004t0016 | 1 | HG03704.hp1 | 5_prime_UTR_variant | MODIFIER | c.-264G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/20 | 25986 | chr22 | 20016780 | ||||||
chr22:20016788 | C | T | 11 | a0001c0001t0003 a0001c0004t0011 a0002c0002t0003 others(8): Show |
60 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(57): Show |
5_prime_UTR_variant | MODIFIER | c.-272G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/20 | 25994 | chr22 | 20016788 | ||||||
chr22:20016789 | G | A | 1 | a0001c0001t0013 | 2 | HG01243.hp2 HG02280.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-273C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/20 | chr22 | 20016789 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:19970769 | C | T | 1 | a0004c0006t0005g0252 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.*13-26G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 19/19 | chr22 | 19970769 | |||||||
chr22:19971018 | G | A | 1 | a0005c0005t0004g0140 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.*12+198C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 19/19 | chr22 | 19971018 | |||||||
chr22:19971038 | C | T | 2 | a0004c0009t0002g0105 a0004c0012t0006g0033 |
3 | HG01884.hp2 HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.*12+178G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 19/19 | chr22 | 19971038 | |||||||
chr22:19971089 | G | A | 13 | a0003c0014t0006g0240 a0003c0014t0006g0241 a0003c0017t0006g0242 others(10): Show |
18 | HG00408.hp1 HG00735.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.*12+127C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 19/19 | chr22 | 19971089 | |||||||
chr22:19971145 | CGG | C | 9 | a0001c0001t0001g0046 a0001c0001t0001g0048 a0001c0001t0001g0182 others(6): Show |
11 | HG01346.hp2 HG01884.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.*12+69_*12+70delCC | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 19/19 | chr22 | 19971145 | |||||||
chr22:19971146 | G | A | 121 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(118): Show |
187 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.*12+70C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 19/19 | chr22 | 19971146 | |||||||
chr22:19971187 | T | A | 2 | a0001c0004t0009g0018 a0001c0004t0009g0121 |
4 | HG02280.hp1 HG03130.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.*12+29A>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 19/19 | chr22 | 19971187 | |||||||
chr22:19971471 | C | T | 2 | a0008c0016t0006g0177 a0008c0016t0006g0178 |
2 | HG00323.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2782-136G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 18/19 | chr22 | 19971471 | |||||||
chr22:19971488 | G | A | 26 | a0002c0002t0001g0001 a0002c0002t0001g0036 a0002c0002t0001g0122 others(23): Show |
43 | HG00280.hp1 HG00408.hp2 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.2782-153C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 18/19 | chr22 | 19971488 | |||||||
chr22:19971510 | G | A | 25 | a0001c0004t0004g0017 a0001c0004t0004g0019 a0001c0004t0004g0032 others(22): Show |
33 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.2782-175C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 18/19 | chr22 | 19971510 | |||||||
chr22:19971517 | C | T | 1 | a0005c0005t0004g0138 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2782-182G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 18/19 | chr22 | 19971517 | |||||||
chr22:19971704 | G | A | 5 | a0001c0001t0001g0012 a0001c0001t0001g0188 a0001c0001t0001g0194 others(2): Show |
8 | HG00099.hp1 HG00738.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.2781+182C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 18/19 | chr22 | 19971704 | |||||||
chr22:19971843 | G | A | 200 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(197): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.2781+43C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 18/19 | chr22 | 19971843 | |||||||
chr22:19971865 | C | T | 1 | a0002c0002t0001g0130 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2781+21G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 18/19 | chr22 | 19971865 | |||||||
chr22:19972044 | C | A | 1 | a0004c0012t0006g0033 | 2 | HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2696-73G>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 17/19 | chr22 | 19972044 | |||||||
chr22:19972223 | C | T | 41 | a0003c0008t0004g0034 a0003c0008t0004g0131 a0003c0008t0004g0202 others(38): Show |
59 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.2695+135G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 17/19 | chr22 | 19972223 | |||||||
chr22:19972432 | A | G | 194 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(191): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.2642-21T>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 16/19 | chr22 | 19972432 | |||||||
chr22:19972570 | G | A | 1 | a0002c0002t0001g0125 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2642-159C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 16/19 | chr22 | 19972570 | |||||||
chr22:19972617 | G | A | 25 | a0001c0004t0004g0017 a0001c0004t0004g0019 a0001c0004t0004g0032 others(22): Show |
33 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.2641+120C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 16/19 | chr22 | 19972617 | |||||||
chr22:19972661 | C | G | 51 | a0002c0002t0001g0001 a0002c0002t0001g0036 a0002c0002t0001g0122 others(48): Show |
81 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.2641+76G>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 16/19 | chr22 | 19972661 | |||||||
chr22:19972665 | T | C | 198 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(195): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.2641+72A>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 16/19 | chr22 | 19972665 | |||||||
chr22:19972675 | G | C | 51 | a0002c0002t0001g0001 a0002c0002t0001g0036 a0002c0002t0001g0122 others(48): Show |
81 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.2641+62C>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 16/19 | chr22 | 19972675 | |||||||
chr22:19972715 | C | T | 4 | a0001c0004t0008g0028 a0001c0004t0008g0029 a0001c0004t0008g0089 others(1): Show |
6 | HG01257.hp1 HG01258.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2641+22G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 16/19 | chr22 | 19972715 | |||||||
chr22:19972853 | G | A | 2 | a0002c0002t0003g0053 a0002c0002t0014g0056 |
2 | NA18941.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.2551-26C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 15/19 | chr22 | 19972853 | |||||||
chr22:19972871 | G | A | 41 | a0003c0008t0004g0034 a0003c0008t0004g0131 a0003c0008t0004g0202 others(38): Show |
59 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.2551-44C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 15/19 | chr22 | 19972871 | |||||||
chr22:19972898 | A | G | 1 | a0010c0021t0002g0031 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2550+27T>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 15/19 | chr22 | 19972898 | |||||||
chr22:19972906 | A | C | 1 | a0002c0002t0001g0130 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2550+19T>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 15/19 | chr22 | 19972906 | |||||||
chr22:19973052 | C | G | 1 | a0001c0001t0023g0212 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.2439-16G>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 14/19 | chr22 | 19973052 | |||||||
chr22:19973060 | G | T | 1 | a0004c0026t0006g0107 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2439-24C>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 14/19 | chr22 | 19973060 | |||||||
chr22:19973083 | G | C | 124 | a0001c0004t0004g0017 a0001c0004t0004g0019 a0001c0004t0004g0032 others(121): Show |
174 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.2438+36C>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 14/19 | chr22 | 19973083 | |||||||
chr22:19973404 | C | A | 1 | a0024c0030t0001g0145 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.2240-87G>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 13/19 | chr22 | 19973404 | |||||||
chr22:19973426 | C | T | 1 | a0002c0002t0003g0078 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2240-109G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 13/19 | chr22 | 19973426 | |||||||
chr22:19973484 | G | C | 25 | a0001c0004t0004g0017 a0001c0004t0004g0019 a0001c0004t0004g0032 others(22): Show |
33 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.2239+159C>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 13/19 | chr22 | 19973484 | |||||||
chr22:19973487 | C | CG | 18 | a0001c0001t0001g0211 a0001c0004t0004g0017 a0001c0004t0004g0032 others(15): Show |
22 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.2239+155dupC | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 13/19 | chr22 | 19973487 | |||||||
chr22:19973487 | C | T | 22 | a0003c0014t0006g0240 a0003c0014t0006g0241 a0003c0017t0006g0242 others(19): Show |
29 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(26): Show |
intron_variant | MODIFIER | c.2239+156G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 13/19 | chr22 | 19973487 | |||||||
chr22:19973548 | C | T | 1 | a0004c0009t0002g0105 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2239+95G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 13/19 | chr22 | 19973548 | |||||||
chr22:19973578 | C | T | 18 | a0003c0014t0006g0240 a0003c0014t0006g0241 a0003c0017t0006g0242 others(15): Show |
24 | HG00140.hp1 HG00408.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.2239+65G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 13/19 | chr22 | 19973578 | |||||||
chr22:19973910 | C | T | 12 | a0003c0008t0007g0021 a0003c0008t0007g0189 a0006c0007t0007g0016 others(9): Show |
16 | HG01952.hp2 HG01978.hp1 HG01993.hp2 others(13): Show |
intron_variant | MODIFIER | c.2089-117G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 12/19 | chr22 | 19973910 | |||||||
chr22:19974040 | G | A | 2 | a0001c0004t0009g0018 a0001c0004t0009g0121 |
4 | HG02280.hp1 HG03130.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.2088+72C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 12/19 | chr22 | 19974040 | |||||||
chr22:19974096 | C | G | 1 | a0004c0006t0005g0249 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2088+16G>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 12/19 | chr22 | 19974096 | |||||||
chr22:19974403 | G | A | 41 | a0003c0008t0004g0034 a0003c0008t0004g0131 a0003c0008t0004g0202 others(38): Show |
59 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.1961-164C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 11/19 | chr22 | 19974403 | |||||||
chr22:19974432 | A | G | 156 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(153): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.1961-193T>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 11/19 | chr22 | 19974432 | |||||||
chr22:19974550 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1961-311C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 11/19 | chr22 | 19974550 | |||||||
chr22:19974565 | C | A | 1 | a0003c0003t0002g0157 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1961-326G>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 11/19 | chr22 | 19974565 | |||||||
chr22:19974574 | C | T | 5 | a0003c0008t0004g0034 a0003c0008t0004g0131 a0003c0008t0004g0202 others(2): Show |
9 | HG02109.hp1 HG02486.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1961-335G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 11/19 | chr22 | 19974574 | |||||||
chr22:19974680 | T | G | 38 | a0003c0008t0004g0034 a0003c0008t0004g0131 a0003c0008t0004g0202 others(35): Show |
56 | HG00140.hp1 HG00408.hp1 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.1961-441A>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 11/19 | chr22 | 19974680 | |||||||
chr22:19974857 | C | T | 211 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(208): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.1961-618G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 11/19 | chr22 | 19974857 | |||||||
chr22:19975012 | G | A | 1 | a0002c0002t0003g0066 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1960+674C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 11/19 | chr22 | 19975012 | |||||||
chr22:19975148 | C | A | 18 | a0003c0008t0004g0034 a0003c0008t0004g0131 a0003c0008t0004g0202 others(15): Show |
28 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(25): Show |
intron_variant | MODIFIER | c.1960+538G>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 11/19 | chr22 | 19975148 | |||||||
chr22:19975246 | C | T | 161 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(158): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.1960+440G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 11/19 | chr22 | 19975246 | |||||||
chr22:19975264 | T | C | 212 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(209): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.1960+422A>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 11/19 | chr22 | 19975264 | |||||||
chr22:19975325 | C | T | 15 | a0004c0009t0002g0015 a0004c0009t0002g0093 a0004c0009t0002g0094 others(12): Show |
19 | HG01884.hp2 HG02145.hp1 HG02622.hp2 others(16): Show |
intron_variant | MODIFIER | c.1960+361G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 11/19 | chr22 | 19975325 | |||||||
chr22:19975419 | C | T | 1 | a0003c0003t0002g0160 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1960+267G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 11/19 | chr22 | 19975419 | |||||||
chr22:19975440 | G | T | 134 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(131): Show |
205 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.1960+246C>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 11/19 | chr22 | 19975440 | |||||||
chr22:19975496 | C | G | 1 | a0021c0028t0003g0065 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1960+190G>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 11/19 | chr22 | 19975496 | |||||||
chr22:19975900 | C | T | 17 | a0003c0014t0006g0240 a0003c0014t0006g0241 a0003c0017t0006g0242 others(14): Show |
23 | HG00140.hp1 HG00408.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.1889-143G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 10/19 | chr22 | 19975900 | |||||||
chr22:19976077 | G | A | 1 | a0005c0005t0004g0139 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1889-320C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 10/19 | chr22 | 19976077 | |||||||
chr22:19976143 | C | T | 161 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(158): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.1889-386G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 10/19 | chr22 | 19976143 | |||||||
chr22:19976477 | T | C | 15 | a0005c0005t0004g0009 a0005c0005t0004g0011 a0005c0005t0004g0020 others(12): Show |
24 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(21): Show |
intron_variant | MODIFIER | c.1888+229A>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 10/19 | chr22 | 19976477 | |||||||
chr22:19976484 | G | A | 3 | a0007c0010t0010g0035 a0007c0010t0010g0142 a0007c0010t0010g0143 |
4 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1888+222C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 10/19 | chr22 | 19976484 | |||||||
chr22:19976510 | C | A | 3 | a0007c0010t0010g0035 a0007c0010t0010g0142 a0007c0010t0010g0143 |
4 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1888+196G>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 10/19 | chr22 | 19976510 | |||||||
chr22:19976628 | G | T | 9 | a0004c0006t0005g0014 a0004c0006t0005g0024 a0004c0006t0005g0247 others(6): Show |
14 | HG00735.hp2 HG01081.hp2 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.1888+78C>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 10/19 | chr22 | 19976628 | |||||||
chr22:19976768 | C | T | 3 | a0004c0006t0005g0024 a0004c0006t0005g0247 a0004c0006t0005g0250 |
5 | HG00735.hp2 HG01081.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.1871-45G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 9/19 | chr22 | 19976768 | |||||||
chr22:19976841 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1871-118C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 9/19 | chr22 | 19976841 | |||||||
chr22:19976895 | T | G | 211 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(208): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.1871-172A>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 9/19 | chr22 | 19976895 | |||||||
chr22:19977034 | TG | T | 162 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(159): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.1871-312delC | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 9/19 | chr22 | 19977034 | |||||||
chr22:19977602 | A | G | 1 | a0003c0017t0006g0243 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1699-16T>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 8/19 | chr22 | 19977602 | |||||||
chr22:19977681 | G | A | 1 | a0003c0003t0002g0172 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1699-95C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 8/19 | chr22 | 19977681 | |||||||
chr22:19977690 | G | C | 1 | a0001c0004t0004g0113 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1699-104C>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 8/19 | chr22 | 19977690 | |||||||
chr22:19977720 | A | G | 4 | a0001c0001t0001g0005 a0001c0001t0001g0203 a0001c0001t0001g0231 others(1): Show |
10 | HG02071.hp1 HG02165.hp1 NA18944.hp2 others(7): Show |
intron_variant | MODIFIER | c.1699-134T>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 8/19 | chr22 | 19977720 | |||||||
chr22:19977772 | G | A | 1 | a0003c0003t0002g0161 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1698+186C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 8/19 | chr22 | 19977772 | |||||||
chr22:19977826 | G | A | 1 | a0002c0002t0003g0053 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1698+132C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 8/19 | chr22 | 19977826 | |||||||
chr22:19978109 | G | A | 1 | a0002c0002t0001g0126 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1581-34C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 7/19 | chr22 | 19978109 | |||||||
chr22:19978204 | G | A | 1 | a0003c0015t0002g0167 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1581-129C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 7/19 | chr22 | 19978204 | |||||||
chr22:19978206 | A | G | 1 | a0003c0015t0002g0167 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1581-131T>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 7/19 | chr22 | 19978206 | |||||||
chr22:19978207 | C | A | 1 | a0003c0015t0002g0167 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1581-132G>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 7/19 | chr22 | 19978207 | |||||||
chr22:19978366 | C | G | 15 | a0005c0005t0004g0009 a0005c0005t0004g0011 a0005c0005t0004g0020 others(12): Show |
24 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(21): Show |
intron_variant | MODIFIER | c.1581-291G>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 7/19 | chr22 | 19978366 | |||||||
chr22:19978408 | G | A | 4 | a0001c0001t0001g0022 a0001c0001t0001g0183 a0001c0001t0001g0205 others(1): Show |
6 | HG00558.hp1 NA18941.hp2 NA18949.hp2 others(3): Show |
intron_variant | MODIFIER | c.1581-333C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 7/19 | chr22 | 19978408 | |||||||
chr22:19978418 | T | C | 1 | a0003c0003t0002g0149 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1581-343A>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 7/19 | chr22 | 19978418 | |||||||
chr22:19978467 | G | A | 3 | a0004c0009t0002g0015 a0004c0009t0002g0093 a0004c0009t0002g0094 |
5 | HG02145.hp1 HG02622.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1581-392C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 7/19 | chr22 | 19978467 | |||||||
chr22:19978519 | G | A | 9 | a0001c0004t0004g0019 a0001c0004t0004g0103 a0001c0004t0004g0128 others(6): Show |
13 | HG01257.hp1 HG01258.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1580+378C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 7/19 | chr22 | 19978519 | |||||||
chr22:19978562 | G | A | 1 | a0004c0006t0005g0249 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1580+335C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 7/19 | chr22 | 19978562 | |||||||
chr22:19978721 | T | C | 1 | a0001c0001t0001g0223 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1580+176A>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 7/19 | chr22 | 19978721 | |||||||
chr22:19978797 | T | C | 15 | a0005c0005t0004g0009 a0005c0005t0004g0011 a0005c0005t0004g0020 others(12): Show |
24 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(21): Show |
intron_variant | MODIFIER | c.1580+100A>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 7/19 | chr22 | 19978797 | |||||||
chr22:19978802 | C | A | 4 | a0004c0009t0002g0015 a0004c0009t0002g0093 a0004c0009t0002g0094 others(1): Show |
6 | HG01884.hp2 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1580+95G>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 7/19 | chr22 | 19978802 | |||||||
chr22:19979087 | G | A | 3 | a0009c0013t0002g0096 a0009c0013t0002g0098 a0019c0024t0002g0097 |
3 | HG02886.hp2 HG03225.hp1 HG03486.hp1 |
splice_region_variant&intron_variant | LOW | c.1397-7C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 6/19 | chr22 | 19979087 | |||||||
chr22:19979123 | G | A | 1 | a0003c0003t0002g0147 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1397-43C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 6/19 | chr22 | 19979123 | |||||||
chr22:19979226 | C | T | 51 | a0002c0032t0004g0136 a0004c0006t0005g0014 a0004c0006t0005g0024 others(48): Show |
73 | HG00140.hp1 HG00735.hp2 HG01081.hp2 others(70): Show |
intron_variant | MODIFIER | c.1397-146G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 6/19 | chr22 | 19979226 | |||||||
chr22:19979436 | T | C | 1 | a0003c0038t0002g0162 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1396+307A>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 6/19 | chr22 | 19979436 | |||||||
chr22:19979490 | G | A | 1 | a0005c0005t0004g0139 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1396+253C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 6/19 | chr22 | 19979490 | |||||||
chr22:19979510 | G | A | 15 | a0005c0005t0004g0009 a0005c0005t0004g0011 a0005c0005t0004g0020 others(12): Show |
24 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(21): Show |
intron_variant | MODIFIER | c.1396+233C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 6/19 | chr22 | 19979510 | |||||||
chr22:19979533 | G | A | 1 | a0003c0017t0006g0243 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1396+210C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 6/19 | chr22 | 19979533 | |||||||
chr22:19979545 | G | A | 134 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(131): Show |
205 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.1396+198C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 6/19 | chr22 | 19979545 | |||||||
chr22:19979636 | C | A | 1 | a0001c0001t0001g0196 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1396+107G>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 6/19 | chr22 | 19979636 | |||||||
chr22:19979682 | C | T | 1 | a0003c0008t0004g0131 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1396+61G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 6/19 | chr22 | 19979682 | |||||||
chr22:19979703 | C | T | 13 | a0004c0006t0005g0014 a0004c0006t0005g0024 a0004c0006t0005g0247 others(10): Show |
19 | HG00140.hp1 HG00735.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.1396+40G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 6/19 | chr22 | 19979703 | |||||||
chr22:19979716 | A | T | 1 | a0002c0032t0004g0136 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1396+27T>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 6/19 | chr22 | 19979716 | |||||||
chr22:19979725 | T | C | 13 | a0004c0006t0005g0014 a0004c0006t0005g0024 a0004c0006t0005g0247 others(10): Show |
19 | HG00140.hp1 HG00735.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.1396+18A>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 6/19 | chr22 | 19979725 | |||||||
chr22:19980285 | G | T | 6 | a0001c0004t0004g0017 a0001c0004t0004g0110 a0001c0004t0004g0115 others(3): Show |
8 | HG00639.hp1 HG00741.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.897-43C>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 5/19 | chr22 | 19980285 | |||||||
chr22:19980457 | C | T | 67 | a0002c0002t0001g0001 a0002c0002t0001g0036 a0002c0002t0001g0122 others(64): Show |
102 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.897-215G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 5/19 | chr22 | 19980457 | |||||||
chr22:19980582 | G | A | 2 | a0001c0004t0008g0028 a0002c0002t0003g0062 |
3 | HG01257.hp1 HG01258.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.897-340C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 5/19 | chr22 | 19980582 | |||||||
chr22:19980671 | C | T | 1 | a0007c0010t0010g0143 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.897-429G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 5/19 | chr22 | 19980671 | |||||||
chr22:19980752 | A | G | 15 | a0005c0005t0004g0009 a0005c0005t0004g0011 a0005c0005t0004g0020 others(12): Show |
24 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(21): Show |
intron_variant | MODIFIER | c.896+459T>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 5/19 | chr22 | 19980752 | |||||||
chr22:19980790 | T | C | 2 | a0001c0001t0001g0046 a0001c0001t0001g0182 |
3 | HG03453.hp1 NA19240.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.896+421A>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 5/19 | chr22 | 19980790 | |||||||
chr22:19980979 | C | T | 2 | a0008c0016t0006g0177 a0008c0016t0006g0178 |
2 | HG00323.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.896+232G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 5/19 | chr22 | 19980979 | |||||||
chr22:19980980 | G | A | 1 | a0003c0003t0002g0163 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.896+231C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 5/19 | chr22 | 19980980 | |||||||
chr22:19981031 | C | T | 3 | a0002c0032t0004g0136 a0004c0012t0006g0033 a0004c0012t0006g0120 |
4 | HG02976.hp2 HG03041.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.896+180G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 5/19 | chr22 | 19981031 | |||||||
chr22:19981038 | C | T | 2 | a0001c0001t0013g0255 a0001c0001t0013g0256 |
2 | HG01243.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.896+173G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 5/19 | chr22 | 19981038 | |||||||
chr22:19981074 | C | T | 24 | a0001c0004t0004g0017 a0001c0004t0004g0019 a0001c0004t0004g0032 others(21): Show |
32 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.896+137G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 5/19 | chr22 | 19981074 | |||||||
chr22:19981105 | A | G | 1 | a0001c0001t0001g0047 | 2 | HG02257.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.896+106T>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 5/19 | chr22 | 19981105 | |||||||
chr22:19981196 | C | T | 1 | a0008c0016t0006g0177 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.896+15G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 5/19 | chr22 | 19981196 | |||||||
chr22:19981844 | C | A | 1 | a0001c0001t0001g0214 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.369+89G>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 4/19 | chr22 | 19981844 | |||||||
chr22:19981873 | G | C | 3 | a0009c0013t0002g0096 a0009c0013t0002g0098 a0019c0024t0002g0097 |
3 | HG02886.hp2 HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.369+60C>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 4/19 | chr22 | 19981873 | |||||||
chr22:19981877 | G | A | 5 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(2): Show |
5 | HG00642.hp2 HG00738.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.369+56C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 4/19 | chr22 | 19981877 | |||||||
chr22:19981897 | C | T | 3 | a0007c0010t0010g0035 a0007c0010t0010g0142 a0007c0010t0010g0143 |
4 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.369+36G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 4/19 | chr22 | 19981897 | |||||||
chr22:19982173 | C | T | 66 | a0002c0002t0001g0001 a0002c0002t0001g0036 a0002c0002t0001g0122 others(63): Show |
100 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.211-82G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19982173 | |||||||
chr22:19982180 | T | G | 1 | a0004c0006t0005g0248 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.211-89A>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19982180 | |||||||
chr22:19982202 | G | A | 13 | a0004c0006t0005g0014 a0004c0006t0005g0024 a0004c0006t0005g0247 others(10): Show |
19 | HG00140.hp1 HG00735.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.211-111C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19982202 | |||||||
chr22:19982388 | A | C | 1 | a0003c0008t0007g0189 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.211-297T>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19982388 | |||||||
chr22:19982424 | C | A | 18 | a0002c0032t0004g0136 a0004c0006t0005g0014 a0004c0006t0005g0024 others(15): Show |
26 | HG00140.hp1 HG00735.hp2 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.211-333G>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19982424 | |||||||
chr22:19982441 | G | T | 83 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(80): Show |
124 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.211-350C>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19982441 | |||||||
chr22:19982471 | G | A | 6 | a0001c0001t0001g0007 a0001c0001t0001g0187 a0001c0001t0001g0207 others(3): Show |
11 | HG02056.hp1 HG02135.hp2 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.211-380C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19982471 | |||||||
chr22:19982474 | G | A | 1 | a0001c0001t0001g0235 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.211-383C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19982474 | |||||||
chr22:19982491 | C | G | 211 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(208): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.211-400G>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19982491 | |||||||
chr22:19982644 | C | T | 1 | a0003c0015t0002g0159 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.211-553G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19982644 | |||||||
chr22:19982811 | G | T | 1 | a0002c0002t0001g0123 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.211-720C>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19982811 | |||||||
chr22:19982979 | G | A | 83 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(80): Show |
124 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.211-888C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19982979 | |||||||
chr22:19983024 | G | T | 87 | a0002c0002t0001g0001 a0002c0002t0001g0036 a0002c0002t0001g0122 others(84): Show |
130 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.211-933C>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19983024 | |||||||
chr22:19983038 | G | A | 3 | a0001c0004t0009g0018 a0001c0004t0009g0121 a0003c0003t0002g0152 |
5 | HG02280.hp1 HG03130.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.211-947C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19983038 | |||||||
chr22:19983060 | A | G | 102 | a0002c0002t0001g0001 a0002c0002t0001g0036 a0002c0002t0001g0122 others(99): Show |
154 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.211-969T>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19983060 | |||||||
chr22:19983078 | C | T | 1 | a0001c0035t0001g0230 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.211-987G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19983078 | |||||||
chr22:19983393 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.211-1302G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19983393 | |||||||
chr22:19983499 | T | G | 1 | a0001c0001t0001g0222 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.211-1408A>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19983499 | |||||||
chr22:19983579 | G | A | 2 | a0004c0011t0006g0030 a0004c0011t0006g0095 |
3 | HG02055.hp1 HG02258.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.211-1488C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19983579 | |||||||
chr22:19983868 | C | T | 24 | a0001c0004t0004g0017 a0001c0004t0004g0019 a0001c0004t0004g0032 others(21): Show |
32 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.211-1777G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19983868 | |||||||
chr22:19983884 | G | T | 1 | a0002c0002t0003g0059 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.211-1793C>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19983884 | |||||||
chr22:19983904 | C | T | 1 | a0005c0005t0011g0067 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.211-1813G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19983904 | |||||||
chr22:19984029 | T | C | 66 | a0002c0002t0001g0001 a0002c0002t0001g0036 a0002c0002t0001g0122 others(63): Show |
100 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.211-1938A>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19984029 | |||||||
chr22:19984195 | C | CA | 3 | a0004c0009t0002g0015 a0004c0009t0002g0093 a0004c0009t0002g0094 |
5 | HG02145.hp1 HG02622.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.211-2105dupT | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19984195 | |||||||
chr22:19984389 | C | T | 3 | a0007c0010t0010g0035 a0007c0010t0010g0142 a0007c0010t0010g0143 |
4 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.211-2298G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19984389 | |||||||
chr22:19984401 | TCAGCCCC others(7): Show |
T | 1 | a0001c0001t0001g0050 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.211-2324_211-2311d others(16): Show |
ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19984401 | |||||||
chr22:19984484 | G | A | 3 | a0007c0010t0010g0035 a0007c0010t0010g0142 a0007c0010t0010g0143 |
4 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.211-2393C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19984484 | |||||||
chr22:19984501 | G | A | 1 | a0001c0001t0001g0183 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.211-2410C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19984501 | |||||||
chr22:19984578 | G | A | 1 | a0003c0003t0002g0174 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.211-2487C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19984578 | |||||||
chr22:19984592 | C | T | 3 | a0004c0011t0006g0030 a0004c0011t0006g0095 a0007c0010t0010g0142 |
4 | HG02055.hp1 HG02258.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.211-2501G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19984592 | |||||||
chr22:19984595 | C | A | 54 | a0002c0002t0001g0001 a0002c0002t0001g0036 a0002c0002t0001g0122 others(51): Show |
86 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.211-2504G>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19984595 | |||||||
chr22:19984650 | G | A | 4 | a0001c0004t0008g0028 a0001c0004t0008g0029 a0001c0004t0008g0089 others(1): Show |
6 | HG01257.hp1 HG01258.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.211-2559C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19984650 | |||||||
chr22:19984842 | T | C | 13 | a0004c0006t0005g0014 a0004c0006t0005g0024 a0004c0006t0005g0247 others(10): Show |
19 | HG00140.hp1 HG00735.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.211-2751A>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19984842 | |||||||
chr22:19984929 | C | G | 102 | a0002c0002t0001g0001 a0002c0002t0001g0036 a0002c0002t0001g0122 others(99): Show |
154 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.211-2838G>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19984929 | |||||||
chr22:19985021 | G | T | 7 | a0001c0001t0001g0012 a0001c0001t0001g0188 a0001c0001t0001g0194 others(4): Show |
12 | HG00099.hp1 HG00738.hp1 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.211-2930C>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19985021 | |||||||
chr22:19985036 | G | A | 55 | a0002c0002t0001g0001 a0002c0002t0001g0036 a0002c0002t0001g0122 others(52): Show |
87 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.211-2945C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19985036 | |||||||
chr22:19985107 | C | T | 7 | a0001c0001t0001g0012 a0001c0001t0001g0188 a0001c0001t0001g0194 others(4): Show |
12 | HG00099.hp1 HG00738.hp1 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.211-3016G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19985107 | |||||||
chr22:19985214 | C | A | 15 | a0005c0005t0004g0009 a0005c0005t0004g0011 a0005c0005t0004g0020 others(12): Show |
24 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(21): Show |
intron_variant | MODIFIER | c.211-3123G>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19985214 | |||||||
chr22:19985258 | C | T | 2 | a0001c0001t0001g0209 a0001c0001t0001g0234 |
2 | HG03927.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.211-3167G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19985258 | |||||||
chr22:19985301 | T | C | 102 | a0002c0002t0001g0001 a0002c0002t0001g0036 a0002c0002t0001g0122 others(99): Show |
154 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.211-3210A>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19985301 | |||||||
chr22:19985486 | C | T | 3 | a0003c0003t0002g0038 a0003c0003t0002g0154 a0003c0003t0002g0171 |
4 | HG01361.hp1 HG01928.hp2 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.211-3395G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19985486 | |||||||
chr22:19985496 | C | A | 3 | a0009c0013t0002g0096 a0009c0013t0002g0098 a0019c0024t0002g0097 |
3 | HG02886.hp2 HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.211-3405G>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19985496 | |||||||
chr22:19985682 | T | G | 102 | a0002c0002t0001g0001 a0002c0002t0001g0036 a0002c0002t0001g0122 others(99): Show |
154 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.211-3591A>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19985682 | |||||||
chr22:19985704 | G | A | 3 | a0007c0010t0010g0035 a0007c0010t0010g0142 a0007c0010t0010g0143 |
4 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.211-3613C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19985704 | |||||||
chr22:19985718 | C | CACA | 102 | a0002c0002t0001g0001 a0002c0002t0001g0036 a0002c0002t0001g0122 others(99): Show |
154 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.211-3628_211-3627i others(5): Show |
ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19985718 | |||||||
chr22:19985877 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.211-3786C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19985877 | |||||||
chr22:19985994 | C | T | 1 | a0004c0009t0002g0105 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.211-3903G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19985994 | |||||||
chr22:19986074 | C | T | 16 | a0001c0004t0004g0017 a0001c0004t0004g0032 a0001c0004t0004g0044 others(13): Show |
20 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.211-3983G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19986074 | |||||||
chr22:19986509 | T | C | 94 | a0002c0002t0001g0001 a0002c0002t0001g0036 a0002c0002t0001g0122 others(91): Show |
144 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.210+4076A>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19986509 | |||||||
chr22:19986551 | T | C | 7 | a0001c0004t0004g0017 a0001c0004t0004g0110 a0001c0004t0004g0115 others(4): Show |
9 | HG00639.hp1 HG00741.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.210+4034A>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19986551 | |||||||
chr22:19986581 | C | T | 3 | a0007c0010t0010g0035 a0007c0010t0010g0142 a0007c0010t0010g0143 |
4 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.210+4004G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19986581 | |||||||
chr22:19986582 | G | A | 1 | a0004c0009t0002g0093 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.210+4003C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19986582 | |||||||
chr22:19986710 | G | A | 3 | a0009c0013t0002g0096 a0009c0013t0002g0098 a0019c0024t0002g0097 |
3 | HG02886.hp2 HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.210+3875C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19986710 | |||||||
chr22:19986766 | CGTCCATC others(2): Show |
C | 3 | a0007c0010t0010g0035 a0007c0010t0010g0142 a0007c0010t0010g0143 |
4 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.210+3810_210+3818d others(11): Show |
ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19986766 | |||||||
chr22:19986821 | A | C | 1 | a0002c0002t0003g0063 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.210+3764T>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19986821 | |||||||
chr22:19986821 | A | G | 93 | a0002c0002t0001g0001 a0002c0002t0001g0036 a0002c0002t0001g0122 others(90): Show |
143 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.210+3764T>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19986821 | |||||||
chr22:19986835 | C | G | 1 | a0001c0001t0001g0208 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.210+3750G>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19986835 | |||||||
chr22:19987060 | A | G | 94 | a0002c0002t0001g0001 a0002c0002t0001g0036 a0002c0002t0001g0122 others(91): Show |
144 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.210+3525T>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19987060 | |||||||
chr22:19987112 | G | T | 1 | a0002c0002t0003g0064 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.210+3473C>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19987112 | |||||||
chr22:19987127 | G | T | 1 | a0001c0004t0008g0028 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.210+3458C>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19987127 | |||||||
chr22:19987131 | G | A | 94 | a0002c0002t0001g0001 a0002c0002t0001g0036 a0002c0002t0001g0122 others(91): Show |
144 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.210+3454C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19987131 | |||||||
chr22:19987141 | C | T | 2 | a0001c0001t0001g0046 a0001c0001t0001g0182 |
3 | HG03453.hp1 NA19240.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.210+3444G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19987141 | |||||||
chr22:19987176 | G | A | 1 | a0004c0006t0005g0249 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.210+3409C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19987176 | |||||||
chr22:19987202 | C | T | 1 | a0001c0004t0004g0114 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.210+3383G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19987202 | |||||||
chr22:19987277 | G | A | 1 | a0001c0001t0001g0050 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.210+3308C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19987277 | |||||||
chr22:19987330 | C | T | 1 | a0002c0002t0001g0122 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.210+3255G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19987330 | |||||||
chr22:19987337 | AG | A | 8 | a0002c0032t0004g0136 a0004c0012t0006g0033 a0004c0012t0006g0120 others(5): Show |
12 | HG02559.hp1 HG02615.hp1 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.210+3247delC | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19987337 | |||||||
chr22:19987382 | T | C | 94 | a0002c0002t0001g0001 a0002c0002t0001g0036 a0002c0002t0001g0122 others(91): Show |
144 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.210+3203A>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19987382 | |||||||
chr22:19987474 | T | C | 1 | a0001c0001t0001g0204 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.210+3111A>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19987474 | |||||||
chr22:19987728 | G | A | 1 | a0005c0005t0011g0067 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.210+2857C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19987728 | |||||||
chr22:19987728 | G | C | 1 | a0001c0001t0023g0212 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.210+2857C>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19987728 | |||||||
chr22:19987767 | G | A | 1 | a0004c0006t0005g0250 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.210+2818C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19987767 | |||||||
chr22:19987775 | G | C | 2 | a0004c0011t0006g0030 a0004c0011t0006g0095 |
3 | HG02055.hp1 HG02258.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.210+2810C>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19987775 | |||||||
chr22:19987887 | G | A | 6 | a0001c0001t0001g0007 a0001c0001t0001g0187 a0001c0001t0001g0207 others(3): Show |
11 | HG02056.hp1 HG02135.hp2 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.210+2698C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19987887 | |||||||
chr22:19987911 | G | C | 2 | a0001c0001t0013g0255 a0001c0001t0013g0256 |
2 | HG01243.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.210+2674C>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19987911 | |||||||
chr22:19987911 | G | T | 1 | a0002c0002t0003g0075 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.210+2674C>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19987911 | |||||||
chr22:19987921 | A | G | 58 | a0002c0002t0001g0001 a0002c0002t0001g0036 a0002c0002t0001g0122 others(55): Show |
90 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.210+2664T>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19987921 | |||||||
chr22:19987967 | G | A | 1 | a0001c0001t0001g0188 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.210+2618C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19987967 | |||||||
chr22:19988169 | G | A | 1 | a0015c0029t0003g0058 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.210+2416C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19988169 | |||||||
chr22:19988189 | G | A | 3 | a0007c0010t0010g0035 a0007c0010t0010g0142 a0007c0010t0010g0143 |
4 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.210+2396C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19988189 | |||||||
chr22:19988336 | G | A | 1 | a0002c0002t0001g0146 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.210+2249C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19988336 | |||||||
chr22:19988448 | C | T | 2 | a0001c0001t0001g0180 a0004c0006t0005g0252 |
2 | HG00642.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.210+2137G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19988448 | |||||||
chr22:19988612 | T | TGGTTCCC others(13): Show |
1 | a0001c0001t0023g0212 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.210+1953_210+1972d others(22): Show |
ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19988612 | |||||||
chr22:19988841 | G | T | 2 | a0004c0006t0006g0175 a0012c0022t0005g0246 |
2 | HG00140.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.210+1744C>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19988841 | |||||||
chr22:19988883 | G | A | 58 | a0002c0002t0001g0001 a0002c0002t0001g0036 a0002c0002t0001g0122 others(55): Show |
90 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.210+1702C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19988883 | |||||||
chr22:19988918 | G | T | 1 | a0008c0016t0006g0178 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.210+1667C>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19988918 | |||||||
chr22:19988987 | C | A | 58 | a0002c0002t0001g0001 a0002c0002t0001g0036 a0002c0002t0001g0122 others(55): Show |
90 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.210+1598G>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19988987 | |||||||
chr22:19989020 | T | A | 1 | a0004c0026t0006g0107 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.210+1565A>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19989020 | |||||||
chr22:19989059 | C | G | 3 | a0009c0013t0002g0096 a0009c0013t0002g0098 a0019c0024t0002g0097 |
3 | HG02886.hp2 HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.210+1526G>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19989059 | |||||||
chr22:19989145 | G | A | 1 | a0001c0001t0001g0192 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.210+1440C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19989145 | |||||||
chr22:19989167 | C | CTA | 3 | a0009c0013t0002g0096 a0009c0013t0002g0098 a0019c0024t0002g0097 |
3 | HG02886.hp2 HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.210+1417_210+1418i others(4): Show |
ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19989167 | |||||||
chr22:19989309 | C | G | 1 | a0001c0001t0001g0183 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.210+1276G>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19989309 | |||||||
chr22:19989311 | C | G | 211 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(208): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.210+1274G>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19989311 | |||||||
chr22:19989316 | T | C | 1 | a0001c0001t0001g0213 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.210+1269A>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19989316 | |||||||
chr22:19989322 | G | A | 58 | a0002c0002t0001g0001 a0002c0002t0001g0036 a0002c0002t0001g0122 others(55): Show |
90 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.210+1263C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19989322 | |||||||
chr22:19989387 | C | T | 9 | a0004c0006t0005g0014 a0004c0006t0005g0024 a0004c0006t0005g0247 others(6): Show |
14 | HG00735.hp2 HG01081.hp2 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.210+1198G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19989387 | |||||||
chr22:19989455 | G | C | 2 | a0001c0001t0001g0051 a0001c0001t0001g0244 |
3 | HG01109.hp1 HG01891.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.210+1130C>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19989455 | |||||||
chr22:19989489 | G | A | 2 | a0001c0001t0001g0049 a0001c0001t0001g0236 |
3 | NA18950.hp1 NA18961.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.210+1096C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19989489 | |||||||
chr22:19989546 | T | G | 1 | a0003c0008t0004g0131 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.210+1039A>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19989546 | |||||||
chr22:19989658 | G | A | 15 | a0005c0005t0004g0009 a0005c0005t0004g0011 a0005c0005t0004g0020 others(12): Show |
24 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(21): Show |
intron_variant | MODIFIER | c.210+927C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19989658 | |||||||
chr22:19990042 | A | G | 2 | a0005c0005t0004g0011 a0005c0005t0004g0239 |
5 | HG02109.hp1 HG02622.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.210+543T>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19990042 | |||||||
chr22:19990124 | C | T | 79 | a0002c0002t0001g0001 a0002c0002t0001g0036 a0002c0002t0001g0122 others(76): Show |
120 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.210+461G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19990124 | |||||||
chr22:19990183 | A | C | 18 | a0002c0032t0004g0136 a0004c0006t0005g0014 a0004c0006t0005g0024 others(15): Show |
26 | HG00140.hp1 HG00735.hp2 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.210+402T>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19990183 | |||||||
chr22:19990211 | C | T | 1 | a0001c0004t0008g0090 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.210+374G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19990211 | |||||||
chr22:19990317 | C | T | 24 | a0001c0004t0004g0017 a0001c0004t0004g0019 a0001c0004t0004g0032 others(21): Show |
32 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.210+268G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19990317 | |||||||
chr22:19990467 | C | T | 17 | a0002c0032t0004g0136 a0004c0006t0005g0014 a0004c0006t0005g0024 others(14): Show |
24 | HG00140.hp1 HG00735.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.210+118G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19990467 | |||||||
chr22:19990499 | C | T | 94 | a0002c0002t0001g0001 a0002c0002t0001g0036 a0002c0002t0001g0122 others(91): Show |
144 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.210+86G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19990499 | |||||||
chr22:19990551 | A | T | 17 | a0002c0032t0004g0136 a0004c0006t0005g0014 a0004c0006t0005g0024 others(14): Show |
24 | HG00140.hp1 HG00735.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.210+34T>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 3/19 | chr22 | 19990551 | |||||||
chr22:19990857 | G | C | 4 | a0002c0032t0004g0136 a0004c0012t0006g0033 a0004c0012t0006g0120 others(1): Show |
6 | HG02896.hp1 HG02897.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18-45C>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19990857 | |||||||
chr22:19990947 | C | T | 2 | a0001c0004t0004g0103 a0016c0036t0004g0129 |
2 | HG02647.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-18-135G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19990947 | |||||||
chr22:19991035 | T | C | 195 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(192): Show |
294 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.-18-223A>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19991035 | |||||||
chr22:19991095 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-18-283C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19991095 | |||||||
chr22:19991225 | G | A | 2 | a0001c0004t0009g0018 a0001c0004t0009g0121 |
4 | HG02280.hp1 HG03130.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-413C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19991225 | |||||||
chr22:19991333 | C | A | 2 | a0001c0004t0004g0103 a0016c0036t0004g0129 |
2 | HG02647.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-18-521G>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19991333 | |||||||
chr22:19991344 | C | T | 1 | a0004c0006t0005g0247 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-18-532G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19991344 | |||||||
chr22:19991421 | T | C | 1 | a0001c0001t0001g0217 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-18-609A>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19991421 | |||||||
chr22:19991469 | G | A | 2 | a0004c0011t0006g0030 a0004c0011t0006g0095 |
3 | HG02055.hp1 HG02258.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-18-657C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19991469 | |||||||
chr22:19991518 | A | G | 1 | a0015c0029t0003g0058 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-18-706T>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19991518 | |||||||
chr22:19991524 | A | C | 1 | a0002c0002t0014g0056 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-18-712T>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19991524 | |||||||
chr22:19991625 | C | A | 1 | a0003c0003t0002g0154 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-18-813G>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19991625 | |||||||
chr22:19991725 | G | GC | 7 | a0001c0004t0004g0103 a0001c0004t0004g0128 a0001c0004t0008g0028 others(4): Show |
9 | HG01257.hp1 HG01258.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.-18-914dupG | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19991725 | |||||||
chr22:19991743 | A | G | 13 | a0004c0006t0005g0014 a0004c0006t0005g0024 a0004c0006t0005g0247 others(10): Show |
19 | HG00140.hp1 HG00735.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.-18-931T>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19991743 | |||||||
chr22:19991821 | A | G | 6 | a0001c0004t0009g0018 a0001c0004t0009g0121 a0002c0032t0004g0136 others(3): Show |
10 | HG02280.hp1 HG02896.hp1 HG02897.hp2 others(7): Show |
intron_variant | MODIFIER | c.-18-1009T>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19991821 | |||||||
chr22:19991828 | C | A | 1 | a0003c0003t0002g0166 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-18-1016G>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19991828 | |||||||
chr22:19991878 | G | C | 1 | a0002c0002t0001g0127 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-18-1066C>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19991878 | |||||||
chr22:19991964 | C | T | 1 | a0011c0018t0002g0037 | 2 | NA18947.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.-18-1152G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19991964 | |||||||
chr22:19991974 | A | T | 6 | a0001c0004t0009g0018 a0001c0004t0009g0121 a0002c0032t0004g0136 others(3): Show |
10 | HG02280.hp1 HG02896.hp1 HG02897.hp2 others(7): Show |
intron_variant | MODIFIER | c.-18-1162T>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19991974 | |||||||
chr22:19991993 | T | C | 15 | a0005c0005t0004g0009 a0005c0005t0004g0011 a0005c0005t0004g0020 others(12): Show |
24 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(21): Show |
intron_variant | MODIFIER | c.-18-1181A>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19991993 | |||||||
chr22:19991998 | A | G | 15 | a0005c0005t0004g0009 a0005c0005t0004g0011 a0005c0005t0004g0020 others(12): Show |
24 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(21): Show |
intron_variant | MODIFIER | c.-18-1186T>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19991998 | |||||||
chr22:19992190 | G | A | 5 | a0001c0004t0004g0110 a0001c0004t0004g0115 a0001c0004t0016g0087 others(2): Show |
5 | HG00639.hp1 HG00741.hp1 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.-18-1378C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19992190 | |||||||
chr22:19992272 | G | A | 1 | a0004c0011t0006g0095 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-18-1460C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19992272 | |||||||
chr22:19992350 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-18-1538C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19992350 | |||||||
chr22:19992410 | C | A | 13 | a0004c0006t0005g0014 a0004c0006t0005g0024 a0004c0006t0005g0247 others(10): Show |
19 | HG00140.hp1 HG00735.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.-18-1598G>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19992410 | |||||||
chr22:19992587 | C | G | 7 | a0001c0004t0009g0018 a0001c0004t0009g0121 a0002c0032t0004g0136 others(4): Show |
11 | HG02280.hp1 HG02896.hp1 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.-18-1775G>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19992587 | |||||||
chr22:19992761 | C | A | 1 | a0003c0003t0002g0169 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18-1949G>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19992761 | |||||||
chr22:19992764 | C | A | 1 | a0019c0024t0002g0097 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-18-1952G>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19992764 | |||||||
chr22:19992764 | C | T | 1 | a0002c0002t0003g0057 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-18-1952G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19992764 | |||||||
chr22:19992777 | C | T | 83 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(80): Show |
124 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.-18-1965G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19992777 | |||||||
chr22:19992888 | C | T | 1 | a0001c0001t0013g0256 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-18-2076G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19992888 | |||||||
chr22:19993025 | A | G | 211 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(208): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.-18-2213T>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19993025 | |||||||
chr22:19993213 | G | A | 1 | a0002c0002t0001g0185 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-18-2401C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19993213 | |||||||
chr22:19993587 | T | C | 4 | a0001c0001t0001g0198 a0009c0013t0002g0096 a0009c0013t0002g0098 others(1): Show |
4 | HG02165.hp2 HG02886.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-2775A>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19993587 | |||||||
chr22:19993757 | A | G | 3 | a0001c0001t0001g0184 a0001c0001t0001g0192 a0001c0001t0001g0193 |
3 | NA18973.hp2 NA18974.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.-18-2945T>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19993757 | |||||||
chr22:19993819 | G | A | 1 | a0004c0009t0002g0094 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-18-3007C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19993819 | |||||||
chr22:19993988 | C | T | 1 | a0002c0002t0001g0144 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-18-3176G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19993988 | |||||||
chr22:19994030 | C | T | 2 | a0004c0006t0006g0175 a0012c0022t0005g0246 |
2 | HG00140.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-18-3218G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19994030 | |||||||
chr22:19994076 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-18-3264G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19994076 | |||||||
chr22:19994143 | G | A | 3 | a0001c0004t0004g0110 a0014c0039t0004g0118 a0017c0037t0004g0116 |
3 | HG00639.hp1 HG00741.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.-18-3331C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19994143 | |||||||
chr22:19994159 | T | C | 1 | a0002c0032t0004g0136 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-18-3347A>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19994159 | |||||||
chr22:19994171 | C | T | 13 | a0004c0006t0005g0014 a0004c0006t0005g0024 a0004c0006t0005g0247 others(10): Show |
19 | HG00140.hp1 HG00735.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.-18-3359G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19994171 | |||||||
chr22:19994257 | G | A | 2 | a0001c0001t0013g0255 a0001c0001t0013g0256 |
2 | HG01243.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.-18-3445C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19994257 | |||||||
chr22:19994276 | G | T | 3 | a0007c0010t0010g0035 a0007c0010t0010g0142 a0007c0010t0010g0143 |
4 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-3464C>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19994276 | |||||||
chr22:19994329 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-18-3517C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19994329 | |||||||
chr22:19994441 | A | AGAACATA others(242): Show |
1 | a0005c0005t0004g0239 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-18-3878_-18-3630d others(251): Show |
ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19994441 | |||||||
chr22:19994550 | A | AGATGAAT others(43): Show |
1 | a0004c0026t0006g0107 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-18-3788_-18-3739d others(52): Show |
ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19994550 | |||||||
chr22:19994550 | AGATGAAT others(43): Show |
A | 4 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0238 others(1): Show |
4 | HG00558.hp2 HG00597.hp2 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-3788_-18-3739d others(52): Show |
ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19994550 | |||||||
chr22:19994597 | T | C | 4 | a0001c0004t0004g0019 a0007c0010t0010g0035 a0007c0010t0010g0142 others(1): Show |
5 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18-3785A>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19994597 | |||||||
chr22:19994610 | A | G | 3 | a0007c0010t0010g0035 a0007c0010t0010g0142 a0007c0010t0010g0143 |
4 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-3798T>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19994610 | |||||||
chr22:19994913 | TG | T | 29 | a0001c0001t0001g0005 a0001c0001t0001g0203 a0001c0001t0001g0206 others(26): Show |
43 | HG00140.hp1 HG00735.hp2 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.-18-4102delC | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19994913 | |||||||
chr22:19994955 | G | A | 43 | a0003c0003t0002g0002 a0003c0003t0002g0038 a0003c0003t0002g0039 others(40): Show |
58 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.-18-4143C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19994955 | |||||||
chr22:19995000 | G | A | 1 | a0002c0002t0003g0066 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-18-4188C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19995000 | |||||||
chr22:19995001 | G | T | 1 | a0002c0002t0003g0066 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-18-4189C>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19995001 | |||||||
chr22:19995109 | A | C | 1 | a0001c0001t0001g0215 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-18-4297T>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19995109 | |||||||
chr22:19995148 | G | C | 1 | a0001c0004t0009g0121 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-18-4336C>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19995148 | |||||||
chr22:19995159 | T | C | 7 | a0002c0002t0003g0006 a0002c0002t0003g0055 a0002c0002t0003g0070 others(4): Show |
12 | HG00423.hp2 HG01074.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.-18-4347A>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19995159 | |||||||
chr22:19995171 | A | G | 13 | a0004c0006t0005g0014 a0004c0006t0005g0024 a0004c0006t0005g0247 others(10): Show |
19 | HG00140.hp1 HG00735.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.-18-4359T>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19995171 | |||||||
chr22:19995199 | G | C | 3 | a0009c0013t0002g0096 a0009c0013t0002g0098 a0019c0024t0002g0097 |
3 | HG02886.hp2 HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-18-4387C>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19995199 | |||||||
chr22:19995332 | G | A | 1 | a0002c0002t0003g0066 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-18-4520C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19995332 | |||||||
chr22:19995491 | G | A | 149 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(146): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.-18-4679C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19995491 | |||||||
chr22:19995588 | C | A | 91 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(88): Show |
134 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(131): Show |
intron_variant | MODIFIER | c.-18-4776G>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19995588 | |||||||
chr22:19995673 | G | T | 1 | a0005c0005t0004g0139 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-18-4861C>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19995673 | |||||||
chr22:19995690 | C | T | 54 | a0002c0002t0001g0001 a0002c0002t0001g0036 a0002c0002t0001g0122 others(51): Show |
86 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.-18-4878G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19995690 | |||||||
chr22:19995780 | C | T | 39 | a0001c0004t0004g0017 a0001c0004t0004g0019 a0001c0004t0004g0032 others(36): Show |
56 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.-18-4968G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19995780 | |||||||
chr22:19995793 | C | A | 1 | a0003c0017t0006g0243 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-18-4981G>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19995793 | |||||||
chr22:19995986 | G | A | 1 | a0018c0034t0001g0199 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-18-5174C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19995986 | |||||||
chr22:19996149 | C | T | 1 | a0002c0002t0003g0066 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-18-5337G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19996149 | |||||||
chr22:19996284 | C | T | 1 | a0002c0002t0003g0066 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-18-5472G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19996284 | |||||||
chr22:19996313 | C | CA | 10 | a0001c0004t0009g0018 a0001c0004t0009g0121 a0002c0032t0004g0136 others(7): Show |
16 | HG02109.hp2 HG02280.hp1 HG02896.hp1 others(13): Show |
intron_variant | MODIFIER | c.-18-5502dupT | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19996313 | |||||||
chr22:19996373 | A | G | 1 | a0001c0001t0001g0050 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-18-5561T>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19996373 | |||||||
chr22:19996409 | C | T | 8 | a0006c0007t0007g0016 a0006c0007t0007g0099 a0006c0007t0007g0101 others(5): Show |
10 | HG03688.hp2 HG04228.hp2 NA18943.hp1 others(7): Show |
intron_variant | MODIFIER | c.-18-5597G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19996409 | |||||||
chr22:19996440 | C | G | 3 | a0007c0010t0010g0035 a0007c0010t0010g0142 a0007c0010t0010g0143 |
4 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-5628G>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19996440 | |||||||
chr22:19996467 | T | C | 4 | a0001c0004t0008g0028 a0001c0004t0008g0029 a0001c0004t0008g0089 others(1): Show |
6 | HG01257.hp1 HG01258.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18-5655A>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19996467 | |||||||
chr22:19996490 | C | T | 55 | a0002c0002t0001g0001 a0002c0002t0001g0036 a0002c0002t0001g0122 others(52): Show |
87 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.-18-5678G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19996490 | |||||||
chr22:19996504 | T | A | 13 | a0004c0006t0005g0014 a0004c0006t0005g0024 a0004c0006t0005g0247 others(10): Show |
19 | HG00140.hp1 HG00735.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.-18-5692A>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19996504 | |||||||
chr22:19996602 | G | T | 1 | a0002c0032t0004g0136 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-18-5790C>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19996602 | |||||||
chr22:19996677 | C | T | 5 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(2): Show |
5 | HG00642.hp2 HG00738.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18-5865G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19996677 | |||||||
chr22:19996680 | G | A | 13 | a0004c0006t0005g0014 a0004c0006t0005g0024 a0004c0006t0005g0247 others(10): Show |
19 | HG00140.hp1 HG00735.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.-18-5868C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19996680 | |||||||
chr22:19996686 | C | T | 1 | a0003c0003t0002g0158 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-18-5874G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19996686 | |||||||
chr22:19996688 | C | T | 49 | a0002c0002t0001g0185 a0002c0002t0003g0003 a0002c0002t0003g0006 others(46): Show |
71 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.-18-5876G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19996688 | |||||||
chr22:19996721 | T | C | 3 | a0002c0002t0003g0074 a0002c0002t0003g0075 a0002c0002t0003g0076 |
3 | HG02895.hp2 HG02897.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-18-5909A>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19996721 | |||||||
chr22:19996754 | C | T | 43 | a0002c0002t0001g0185 a0002c0002t0003g0003 a0002c0002t0003g0006 others(40): Show |
64 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.-18-5942G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19996754 | |||||||
chr22:19996755 | G | A | 2 | a0006c0007t0007g0101 a0006c0007t0007g0102 |
2 | HG03688.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-18-5943C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19996755 | |||||||
chr22:19996778 | C | T | 13 | a0004c0006t0005g0014 a0004c0006t0005g0024 a0004c0006t0005g0247 others(10): Show |
19 | HG00140.hp1 HG00735.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.-18-5966G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19996778 | |||||||
chr22:19996885 | C | T | 1 | a0001c0001t0001g0192 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-18-6073G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19996885 | |||||||
chr22:19996892 | G | A | 1 | a0004c0026t0006g0107 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-18-6080C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19996892 | |||||||
chr22:19997043 | A | T | 2 | a0004c0006t0006g0175 a0012c0022t0005g0246 |
2 | HG00140.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-18-6231T>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19997043 | |||||||
chr22:19997089 | C | G | 91 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(88): Show |
134 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(131): Show |
intron_variant | MODIFIER | c.-18-6277G>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19997089 | |||||||
chr22:19997175 | G | T | 2 | a0001c0004t0009g0018 a0001c0004t0009g0121 |
4 | HG02280.hp1 HG03130.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-6363C>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19997175 | |||||||
chr22:19997243 | G | A | 1 | a0002c0002t0003g0064 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-18-6431C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19997243 | |||||||
chr22:19997549 | G | A | 1 | a0002c0002t0003g0069 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-18-6737C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19997549 | |||||||
chr22:19997603 | G | A | 2 | a0001c0004t0009g0018 a0001c0004t0009g0121 |
4 | HG02280.hp1 HG03130.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-6791C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19997603 | |||||||
chr22:19997651 | T | G | 19 | a0001c0004t0009g0018 a0001c0004t0009g0121 a0002c0032t0004g0136 others(16): Show |
29 | HG00140.hp1 HG00735.hp2 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.-18-6839A>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19997651 | |||||||
chr22:19997826 | G | A | 14 | a0001c0001t0001g0013 a0001c0001t0001g0050 a0001c0001t0001g0176 others(11): Show |
18 | HG00140.hp2 HG00642.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.-18-7014C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19997826 | |||||||
chr22:19997861 | C | T | 3 | a0005c0005t0004g0137 a0005c0005t0004g0138 a0005c0005t0004g0226 |
3 | HG02109.hp2 HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-18-7049G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19997861 | |||||||
chr22:19997984 | G | A | 104 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(101): Show |
153 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.-18-7172C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19997984 | |||||||
chr22:19997987 | C | A | 1 | a0001c0001t0001g0238 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-18-7175G>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19997987 | |||||||
chr22:19998115 | G | A | 3 | a0009c0013t0002g0096 a0009c0013t0002g0098 a0019c0024t0002g0097 |
3 | HG02886.hp2 HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-18-7303C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19998115 | |||||||
chr22:19998221 | G | A | 13 | a0004c0006t0005g0014 a0004c0006t0005g0024 a0004c0006t0005g0247 others(10): Show |
19 | HG00140.hp1 HG00735.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.-18-7409C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19998221 | |||||||
chr22:19998259 | G | A | 2 | a0004c0011t0006g0030 a0004c0011t0006g0095 |
3 | HG02055.hp1 HG02258.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-18-7447C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19998259 | |||||||
chr22:19998268 | C | A | 1 | a0002c0002t0003g0072 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-18-7456G>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19998268 | |||||||
chr22:19998457 | C | T | 1 | a0004c0006t0006g0175 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-18-7645G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19998457 | |||||||
chr22:19998625 | C | T | 83 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(80): Show |
124 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.-18-7813G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19998625 | |||||||
chr22:19998786 | G | A | 13 | a0004c0006t0005g0014 a0004c0006t0005g0024 a0004c0006t0005g0247 others(10): Show |
19 | HG00140.hp1 HG00735.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.-18-7974C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19998786 | |||||||
chr22:19999237 | C | A | 1 | a0001c0001t0001g0200 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-18-8425G>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19999237 | |||||||
chr22:19999294 | C | G | 1 | a0004c0009t0002g0105 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-18-8482G>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19999294 | |||||||
chr22:19999475 | A | G | 1 | a0002c0002t0003g0077 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-18-8663T>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19999475 | |||||||
chr22:19999562 | T | C | 1 | a0001c0001t0001g0201 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-18-8750A>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19999562 | |||||||
chr22:19999679 | G | T | 44 | a0001c0001t0001g0204 a0002c0002t0001g0185 a0002c0002t0003g0003 others(41): Show |
65 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.-18-8867C>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19999679 | |||||||
chr22:19999801 | G | C | 1 | a0004c0009t0002g0105 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-18-8989C>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19999801 | |||||||
chr22:19999883 | C | G | 108 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(105): Show |
159 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.-18-9071G>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 19999883 | |||||||
chr22:20000091 | T | C | 1 | a0003c0015t0002g0167 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-18-9279A>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20000091 | |||||||
chr22:20000208 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-18-9396G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20000208 | |||||||
chr22:20000241 | A | C | 207 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(204): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.-18-9429T>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20000241 | |||||||
chr22:20000385 | C | T | 1 | a0001c0004t0004g0112 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-18-9573G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20000385 | |||||||
chr22:20000499 | GCTCCCAC others(3): Show |
G | 70 | a0001c0004t0004g0017 a0001c0004t0004g0019 a0001c0004t0004g0032 others(67): Show |
108 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.-18-9697_-18-9688d others(12): Show |
ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20000499 | |||||||
chr22:20000538 | C | T | 1 | a0004c0012t0006g0120 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-18-9726G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20000538 | |||||||
chr22:20000590 | G | C | 1 | a0004c0026t0006g0107 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-18-9778C>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20000590 | |||||||
chr22:20000644 | G | A | 39 | a0002c0002t0001g0185 a0002c0002t0003g0003 a0002c0002t0003g0006 others(36): Show |
58 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.-19+9811C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20000644 | |||||||
chr22:20000722 | G | A | 94 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(91): Show |
138 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(135): Show |
intron_variant | MODIFIER | c.-19+9733C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20000722 | |||||||
chr22:20000735 | G | T | 13 | a0004c0006t0005g0014 a0004c0006t0005g0024 a0004c0006t0005g0247 others(10): Show |
19 | HG00140.hp1 HG00735.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.-19+9720C>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20000735 | |||||||
chr22:20000842 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-19+9613G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20000842 | |||||||
chr22:20000994 | G | C | 213 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(210): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.-19+9461C>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20000994 | |||||||
chr22:20001027 | C | T | 1 | a0003c0003t0002g0147 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-19+9428G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20001027 | |||||||
chr22:20001035 | C | T | 3 | a0009c0013t0002g0096 a0009c0013t0002g0098 a0019c0024t0002g0097 |
3 | HG02886.hp2 HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-19+9420G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20001035 | |||||||
chr22:20001042 | A | G | 2 | a0003c0003t0002g0156 a0003c0003t0002g0157 |
2 | HG02040.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.-19+9413T>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20001042 | |||||||
chr22:20001089 | G | A | 3 | a0004c0009t0002g0015 a0004c0009t0002g0093 a0004c0009t0002g0094 |
5 | HG02145.hp1 HG02622.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.-19+9366C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20001089 | |||||||
chr22:20001126 | T | C | 1 | a0001c0001t0001g0179 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-19+9329A>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20001126 | |||||||
chr22:20001153 | T | C | 207 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(204): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.-19+9302A>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20001153 | |||||||
chr22:20001297 | G | A | 3 | a0007c0010t0010g0035 a0007c0010t0010g0142 a0007c0010t0010g0143 |
4 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+9158C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20001297 | |||||||
chr22:20001357 | G | A | 1 | a0008c0016t0006g0178 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-19+9098C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20001357 | |||||||
chr22:20001403 | G | T | 1 | a0016c0036t0004g0129 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-19+9052C>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20001403 | |||||||
chr22:20001440 | G | A | 1 | a0003c0008t0004g0202 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-19+9015C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20001440 | |||||||
chr22:20001573 | G | A | 1 | a0004c0006t0005g0253 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-19+8882C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20001573 | |||||||
chr22:20001573 | G | C | 1 | a0004c0012t0006g0120 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-19+8882C>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20001573 | |||||||
chr22:20001601 | C | T | 1 | a0003c0003t0002g0155 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-19+8854G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20001601 | |||||||
chr22:20002082 | C | T | 1 | a0001c0001t0001g0207 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-19+8373G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20002082 | |||||||
chr22:20002089 | C | G | 43 | a0002c0002t0001g0185 a0002c0002t0003g0003 a0002c0002t0003g0006 others(40): Show |
64 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.-19+8366G>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20002089 | |||||||
chr22:20002119 | A | G | 70 | a0001c0004t0004g0017 a0001c0004t0004g0019 a0001c0004t0004g0032 others(67): Show |
108 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.-19+8336T>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20002119 | |||||||
chr22:20002205 | G | A | 1 | a0001c0004t0004g0103 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-19+8250C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20002205 | |||||||
chr22:20002216 | T | C | 1 | a0002c0002t0003g0071 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-19+8239A>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20002216 | |||||||
chr22:20002367 | C | T | 70 | a0001c0004t0004g0017 a0001c0004t0004g0019 a0001c0004t0004g0032 others(67): Show |
108 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.-19+8088G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20002367 | |||||||
chr22:20002619 | G | A | 1 | a0021c0028t0003g0065 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-19+7836C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20002619 | |||||||
chr22:20002803 | ATTGATTT others(3): Show |
A | 1 | a0001c0001t0001g0206 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-19+7642_-19+7651d others(12): Show |
ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20002803 | |||||||
chr22:20002815 | A | T | 1 | a0001c0001t0001g0206 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-19+7640T>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20002815 | |||||||
chr22:20002905 | G | A | 1 | a0002c0002t0003g0072 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-19+7550C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20002905 | |||||||
chr22:20003027 | A | T | 1 | a0004c0026t0006g0107 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-19+7428T>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20003027 | |||||||
chr22:20003028 | A | C | 1 | a0001c0001t0001g0205 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-19+7427T>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20003028 | |||||||
chr22:20003261 | C | T | 1 | a0001c0004t0004g0103 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-19+7194G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20003261 | |||||||
chr22:20003266 | G | T | 56 | a0001c0004t0004g0017 a0001c0004t0004g0019 a0001c0004t0004g0032 others(53): Show |
87 | HG00099.hp2 HG00408.hp2 HG00639.hp1 others(84): Show |
intron_variant | MODIFIER | c.-19+7189C>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20003266 | |||||||
chr22:20003345 | C | G | 7 | a0006c0007t0007g0016 a0006c0007t0007g0099 a0006c0007t0007g0101 others(4): Show |
9 | HG03688.hp2 HG04228.hp2 NA18943.hp1 others(6): Show |
intron_variant | MODIFIER | c.-19+7110G>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20003345 | |||||||
chr22:20003437 | G | C | 1 | a0001c0001t0001g0225 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-19+7018C>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20003437 | |||||||
chr22:20003458 | C | G | 1 | a0010c0021t0002g0031 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-19+6997G>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20003458 | |||||||
chr22:20003460 | A | G | 3 | a0001c0001t0001g0012 a0001c0001t0001g0188 a0001c0001t0001g0228 |
6 | HG00099.hp1 HG00738.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19+6995T>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20003460 | |||||||
chr22:20003544 | T | C | 56 | a0001c0004t0004g0017 a0001c0004t0004g0019 a0001c0004t0004g0032 others(53): Show |
87 | HG00099.hp2 HG00408.hp2 HG00639.hp1 others(84): Show |
intron_variant | MODIFIER | c.-19+6911A>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20003544 | |||||||
chr22:20003597 | G | A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0218 |
5 | HG00741.hp2 HG01074.hp2 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19+6858C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20003597 | |||||||
chr22:20003865 | CAG | C | 70 | a0001c0004t0004g0017 a0001c0004t0004g0019 a0001c0004t0004g0032 others(67): Show |
108 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.-19+6588_-19+6589d others(4): Show |
ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20003865 | |||||||
chr22:20003940 | C | T | 13 | a0004c0006t0005g0014 a0004c0006t0005g0024 a0004c0006t0005g0247 others(10): Show |
19 | HG00140.hp1 HG00735.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.-19+6515G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20003940 | |||||||
chr22:20003948 | C | T | 1 | a0001c0004t0004g0108 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-19+6507G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20003948 | |||||||
chr22:20004088 | T | C | 5 | a0001c0001t0001g0005 a0001c0001t0001g0203 a0001c0001t0001g0231 others(2): Show |
11 | HG02071.hp1 HG02165.hp1 NA18944.hp2 others(8): Show |
intron_variant | MODIFIER | c.-19+6367A>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20004088 | |||||||
chr22:20004247 | T | C | 15 | a0005c0005t0004g0009 a0005c0005t0004g0011 a0005c0005t0004g0020 others(12): Show |
24 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(21): Show |
intron_variant | MODIFIER | c.-19+6208A>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20004247 | |||||||
chr22:20004299 | G | T | 1 | a0003c0003t0002g0172 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-19+6156C>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20004299 | |||||||
chr22:20004322 | C | T | 1 | a0001c0004t0004g0128 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-19+6133G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20004322 | |||||||
chr22:20004427 | G | A | 70 | a0001c0004t0004g0017 a0001c0004t0004g0019 a0001c0004t0004g0032 others(67): Show |
108 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.-19+6028C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20004427 | |||||||
chr22:20004492 | A | G | 95 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(92): Show |
139 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(136): Show |
intron_variant | MODIFIER | c.-19+5963T>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20004492 | |||||||
chr22:20004552 | T | C | 1 | a0006c0007t0007g0102 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-19+5903A>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20004552 | |||||||
chr22:20004600 | G | T | 1 | a0010c0021t0002g0031 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-19+5855C>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20004600 | |||||||
chr22:20004626 | C | A | 1 | a0001c0001t0001g0219 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-19+5829G>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20004626 | |||||||
chr22:20004763 | T | C | 1 | a0004c0009t0002g0105 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-19+5692A>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20004763 | |||||||
chr22:20004860 | C | A | 1 | a0003c0003t0002g0168 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-19+5595G>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20004860 | |||||||
chr22:20004929 | T | C | 1 | a0001c0001t0021g0220 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-19+5526A>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20004929 | |||||||
chr22:20005063 | G | C | 15 | a0005c0005t0004g0009 a0005c0005t0004g0011 a0005c0005t0004g0020 others(12): Show |
24 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(21): Show |
intron_variant | MODIFIER | c.-19+5392C>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20005063 | |||||||
chr22:20005087 | T | G | 1 | a0003c0003t0002g0169 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-19+5368A>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20005087 | |||||||
chr22:20005162 | T | C | 14 | a0004c0026t0006g0107 a0006c0007t0007g0016 a0006c0007t0007g0099 others(11): Show |
16 | HG00323.hp1 HG02886.hp2 HG03209.hp1 others(13): Show |
intron_variant | MODIFIER | c.-19+5293A>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20005162 | |||||||
chr22:20005332 | G | A | 1 | a0002c0002t0003g0066 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-19+5123C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20005332 | |||||||
chr22:20005372 | T | TA | 41 | a0002c0002t0001g0185 a0002c0002t0003g0003 a0002c0002t0003g0006 others(38): Show |
61 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.-19+5082dupT | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20005372 | |||||||
chr22:20005372 | TA | T | 6 | a0001c0001t0001g0045 a0003c0003t0002g0150 a0003c0003t0002g0174 others(3): Show |
7 | HG00323.hp2 HG02615.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19+5082delT | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20005372 | |||||||
chr22:20005372 | TAA | T | 14 | a0004c0026t0006g0107 a0006c0007t0007g0016 a0006c0007t0007g0099 others(11): Show |
16 | HG00323.hp1 HG02886.hp2 HG03209.hp1 others(13): Show |
intron_variant | MODIFIER | c.-19+5081_-19+5082d others(4): Show |
ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20005372 | |||||||
chr22:20005410 | A | G | 11 | a0006c0007t0007g0016 a0006c0007t0007g0099 a0006c0007t0007g0101 others(8): Show |
13 | HG02886.hp2 HG03225.hp1 HG03486.hp1 others(10): Show |
intron_variant | MODIFIER | c.-19+5045T>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20005410 | |||||||
chr22:20005415 | G | C | 15 | a0005c0005t0004g0009 a0005c0005t0004g0011 a0005c0005t0004g0020 others(12): Show |
24 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(21): Show |
intron_variant | MODIFIER | c.-19+5040C>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20005415 | |||||||
chr22:20005586 | G | A | 3 | a0007c0010t0010g0035 a0007c0010t0010g0142 a0007c0010t0010g0143 |
4 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+4869C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20005586 | |||||||
chr22:20005616 | G | A | 1 | a0001c0004t0004g0117 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-19+4839C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20005616 | |||||||
chr22:20005776 | G | A | 70 | a0001c0004t0004g0017 a0001c0004t0004g0019 a0001c0004t0004g0032 others(67): Show |
108 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.-19+4679C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20005776 | |||||||
chr22:20005794 | T | A | 1 | a0004c0026t0006g0107 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-19+4661A>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20005794 | |||||||
chr22:20005794 | T | TA | 32 | a0001c0001t0001g0233 a0001c0004t0004g0019 a0001c0004t0004g0103 others(29): Show |
49 | HG00408.hp2 HG01257.hp1 HG01258.hp2 others(46): Show |
intron_variant | MODIFIER | c.-19+4660dupT | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20005794 | |||||||
chr22:20006011 | C | T | 1 | a0003c0003t0002g0153 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-19+4444G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20006011 | |||||||
chr22:20006114 | G | C | 1 | a0005c0005t0004g0133 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-19+4341C>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20006114 | |||||||
chr22:20006115 | AGTTTTCT others(6): Show |
A | 1 | a0005c0005t0004g0133 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-19+4327_-19+4339d others(15): Show |
ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20006115 | |||||||
chr22:20006129 | T | A | 1 | a0005c0005t0004g0133 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-19+4326A>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20006129 | |||||||
chr22:20006145 | T | C | 1 | a0002c0002t0003g0070 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-19+4310A>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20006145 | |||||||
chr22:20006302 | G | C | 1 | a0001c0001t0001g0203 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-19+4153C>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20006302 | |||||||
chr22:20006334 | T | G | 1 | a0002c0002t0003g0086 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-19+4121A>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20006334 | |||||||
chr22:20006343 | C | T | 2 | a0001c0001t0001g0190 a0003c0003t0002g0174 |
2 | HG01346.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.-19+4112G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20006343 | |||||||
chr22:20006344 | A | G | 1 | a0003c0003t0002g0174 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-19+4111T>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20006344 | |||||||
chr22:20006349 | G | A | 1 | a0003c0003t0002g0174 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-19+4106C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20006349 | |||||||
chr22:20006353 | G | A | 1 | a0003c0003t0002g0174 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-19+4102C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20006353 | |||||||
chr22:20006360 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-19+4095C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20006360 | |||||||
chr22:20006373 | C | A | 1 | a0009c0013t0002g0098 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-19+4082G>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20006373 | |||||||
chr22:20006373 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-19+4082G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20006373 | |||||||
chr22:20006438 | G | A | 2 | a0002c0002t0003g0071 a0002c0002t0003g0072 |
2 | HG01109.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-19+4017C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20006438 | |||||||
chr22:20006527 | C | T | 20 | a0001c0004t0004g0019 a0001c0004t0004g0103 a0001c0004t0004g0128 others(17): Show |
35 | HG00408.hp2 HG01257.hp1 HG01258.hp2 others(32): Show |
intron_variant | MODIFIER | c.-19+3928G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20006527 | |||||||
chr22:20006562 | G | C | 11 | a0006c0007t0007g0016 a0006c0007t0007g0099 a0006c0007t0007g0101 others(8): Show |
13 | HG02886.hp2 HG03225.hp1 HG03486.hp1 others(10): Show |
intron_variant | MODIFIER | c.-19+3893C>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20006562 | |||||||
chr22:20006565 | C | T | 1 | a0002c0002t0003g0053 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-19+3890G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20006565 | |||||||
chr22:20006578 | CA | C | 157 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(154): Show |
230 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.-19+3876delT | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20006578 | |||||||
chr22:20006623 | A | G | 2 | a0001c0004t0004g0110 a0014c0039t0004g0118 |
2 | HG00639.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.-19+3832T>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20006623 | |||||||
chr22:20006657 | G | C | 15 | a0001c0004t0004g0017 a0001c0004t0004g0032 a0001c0004t0004g0044 others(12): Show |
19 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.-19+3798C>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20006657 | |||||||
chr22:20006779 | G | A | 1 | a0001c0004t0004g0032 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-19+3676C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20006779 | |||||||
chr22:20006820 | CG | C | 4 | a0006c0007t0007g0016 a0006c0007t0007g0106 a0006c0007t0017g0088 others(1): Show |
6 | NA18943.hp1 NA18979.hp1 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19+3634delC | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20006820 | |||||||
chr22:20007200 | A | G | 1 | a0001c0001t0013g0256 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-19+3255T>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20007200 | |||||||
chr22:20007310 | G | A | 13 | a0004c0006t0005g0014 a0004c0006t0005g0024 a0004c0006t0005g0247 others(10): Show |
19 | HG00140.hp1 HG00735.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.-19+3145C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20007310 | |||||||
chr22:20007503 | G | A | 1 | a0005c0005t0004g0226 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-19+2952C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20007503 | |||||||
chr22:20007511 | C | T | 2 | a0008c0016t0006g0177 a0008c0016t0006g0178 |
2 | HG00323.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-19+2944G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20007511 | |||||||
chr22:20007628 | G | A | 1 | a0005c0005t0004g0239 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-19+2827C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20007628 | |||||||
chr22:20007643 | G | A | 1 | a0005c0005t0004g0135 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-19+2812C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20007643 | |||||||
chr22:20007658 | G | A | 1 | a0004c0006t0005g0252 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-19+2797C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20007658 | |||||||
chr22:20007957 | T | G | 11 | a0006c0007t0007g0016 a0006c0007t0007g0099 a0006c0007t0007g0101 others(8): Show |
13 | HG02886.hp2 HG03225.hp1 HG03486.hp1 others(10): Show |
intron_variant | MODIFIER | c.-19+2498A>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20007957 | |||||||
chr22:20007991 | CAG | C | 42 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(39): Show |
60 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.-19+2462_-19+2463d others(4): Show |
ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20007991 | |||||||
chr22:20008111 | T | C | 15 | a0001c0004t0004g0019 a0001c0004t0004g0103 a0002c0002t0001g0001 others(12): Show |
28 | HG00408.hp2 HG01975.hp1 HG01993.hp1 others(25): Show |
intron_variant | MODIFIER | c.-19+2344A>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20008111 | |||||||
chr22:20008127 | T | C | 1 | a0014c0039t0004g0118 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-19+2328A>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20008127 | |||||||
chr22:20008243 | C | T | 3 | a0005c0005t0004g0020 a0005c0005t0004g0135 a0005c0025t0004g0134 |
5 | HG02615.hp1 HG03041.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-19+2212G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20008243 | |||||||
chr22:20008252 | C | T | 3 | a0009c0013t0002g0096 a0009c0013t0002g0098 a0019c0024t0002g0097 |
3 | HG02886.hp2 HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-19+2203G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20008252 | |||||||
chr22:20008313 | G | C | 102 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(99): Show |
150 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.-19+2142C>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20008313 | |||||||
chr22:20008355 | C | T | 5 | a0001c0001t0001g0012 a0001c0001t0001g0188 a0001c0001t0001g0228 others(2): Show |
10 | HG00099.hp1 HG00738.hp1 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.-19+2100G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20008355 | |||||||
chr22:20008429 | T | C | 1 | a0001c0001t0001g0223 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-19+2026A>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20008429 | |||||||
chr22:20008717 | A | G | 211 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(208): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.-19+1738T>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20008717 | |||||||
chr22:20008732 | A | G | 211 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(208): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.-19+1723T>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20008732 | |||||||
chr22:20008769 | G | A | 1 | a0001c0001t0001g0224 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-19+1686C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20008769 | |||||||
chr22:20008772 | C | T | 1 | a0004c0012t0006g0033 | 2 | HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-19+1683G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20008772 | |||||||
chr22:20008907 | G | A | 1 | a0001c0001t0001g0225 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-19+1548C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20008907 | |||||||
chr22:20008970 | G | A | 1 | a0002c0002t0001g0130 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-19+1485C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20008970 | |||||||
chr22:20009046 | G | T | 1 | a0001c0004t0004g0017 | 3 | HG01071.hp2 HG01358.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.-19+1409C>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20009046 | |||||||
chr22:20009047 | C | T | 152 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(149): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.-19+1408G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20009047 | |||||||
chr22:20009098 | G | A | 1 | a0004c0009t0002g0105 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-19+1357C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20009098 | |||||||
chr22:20009173 | G | A | 1 | a0004c0009t0002g0105 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-19+1282C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20009173 | |||||||
chr22:20009231 | G | A | 1 | a0004c0006t0005g0253 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-19+1224C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20009231 | |||||||
chr22:20009273 | C | T | 1 | a0001c0001t0013g0255 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-19+1182G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20009273 | |||||||
chr22:20009306 | G | A | 154 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(151): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.-19+1149C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20009306 | |||||||
chr22:20009355 | G | C | 45 | a0001c0001t0003g0073 a0001c0004t0011g0083 a0002c0002t0001g0185 others(42): Show |
66 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.-19+1100C>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20009355 | |||||||
chr22:20009661 | G | A | 3 | a0007c0010t0010g0035 a0007c0010t0010g0142 a0007c0010t0010g0143 |
4 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+794C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20009661 | |||||||
chr22:20009747 | C | T | 2 | a0004c0026t0006g0107 a0010c0021t0002g0031 |
3 | HG02896.hp1 HG02897.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-19+708G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20009747 | |||||||
chr22:20009829 | G | A | 2 | a0002c0002t0003g0068 a0002c0002t0003g0069 |
2 | HG01168.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.-19+626C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20009829 | |||||||
chr22:20010191 | A | G | 1 | a0012c0022t0005g0246 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-19+264T>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20010191 | |||||||
chr22:20010250 | A | G | 1 | a0002c0002t0003g0081 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-19+205T>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20010250 | |||||||
chr22:20010355 | G | A | 2 | a0006c0007t0007g0101 a0006c0007t0007g0102 |
2 | HG03688.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-19+100C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 2/19 | chr22 | 20010355 | |||||||
chr22:20010565 | G | A | 10 | a0001c0001t0003g0073 a0002c0002t0003g0006 a0002c0002t0003g0025 others(7): Show |
16 | HG00423.hp1 HG00423.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.-72-57C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20010565 | |||||||
chr22:20010590 | G | A | 4 | a0007c0010t0010g0035 a0007c0010t0010g0142 a0007c0010t0010g0143 others(1): Show |
6 | HG01891.hp1 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-72-82C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20010590 | |||||||
chr22:20010635 | G | A | 1 | a0010c0021t0002g0031 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-72-127C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20010635 | |||||||
chr22:20010681 | C | T | 15 | a0001c0004t0004g0017 a0001c0004t0004g0032 a0001c0004t0004g0044 others(12): Show |
19 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.-72-173G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20010681 | |||||||
chr22:20010717 | C | T | 2 | a0008c0016t0006g0177 a0008c0016t0006g0178 |
2 | HG00323.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-72-209G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20010717 | |||||||
chr22:20010858 | T | TC | 12 | a0004c0006t0005g0014 a0004c0006t0005g0024 a0004c0006t0005g0247 others(9): Show |
18 | HG00140.hp1 HG00735.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.-72-351dupG | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20010858 | |||||||
chr22:20010863 | T | C | 94 | a0001c0001t0003g0073 a0001c0004t0004g0017 a0001c0004t0004g0032 others(91): Show |
134 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.-72-355A>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20010863 | |||||||
chr22:20010915 | G | C | 3 | a0002c0002t0003g0074 a0002c0002t0003g0075 a0002c0002t0003g0076 |
3 | HG02895.hp2 HG02897.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-72-407C>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20010915 | |||||||
chr22:20010921 | G | A | 1 | a0004c0011t0006g0095 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-72-413C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20010921 | |||||||
chr22:20010963 | C | T | 11 | a0006c0007t0007g0016 a0006c0007t0007g0099 a0006c0007t0007g0101 others(8): Show |
13 | HG02886.hp2 HG03225.hp1 HG03486.hp1 others(10): Show |
intron_variant | MODIFIER | c.-72-455G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20010963 | |||||||
chr22:20011034 | G | T | 1 | a0004c0026t0006g0107 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-72-526C>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20011034 | |||||||
chr22:20011095 | C | G | 84 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(81): Show |
125 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.-72-587G>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20011095 | |||||||
chr22:20011132 | G | C | 157 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(154): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.-72-624C>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20011132 | |||||||
chr22:20011392 | TC | T | 11 | a0006c0007t0007g0016 a0006c0007t0007g0099 a0006c0007t0007g0101 others(8): Show |
13 | HG02886.hp2 HG03225.hp1 HG03486.hp1 others(10): Show |
intron_variant | MODIFIER | c.-72-885delG | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20011392 | |||||||
chr22:20011433 | C | T | 2 | a0002c0002t0003g0055 a0002c0002t0003g0080 |
2 | HG01074.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.-72-925G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20011433 | |||||||
chr22:20011440 | T | G | 12 | a0004c0006t0005g0014 a0004c0006t0005g0024 a0004c0006t0005g0247 others(9): Show |
18 | HG00140.hp1 HG00735.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.-72-932A>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20011440 | |||||||
chr22:20011550 | C | T | 13 | a0001c0004t0004g0019 a0002c0002t0001g0001 a0002c0002t0001g0036 others(10): Show |
26 | HG00408.hp2 HG01975.hp1 HG01993.hp1 others(23): Show |
intron_variant | MODIFIER | c.-72-1042G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20011550 | |||||||
chr22:20011571 | G | A | 1 | a0004c0026t0006g0107 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-72-1063C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20011571 | |||||||
chr22:20011641 | C | T | 190 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(187): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.-72-1133G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20011641 | |||||||
chr22:20011657 | AGT | A | 3 | a0002c0002t0003g0077 a0002c0002t0003g0078 a0002c0002t0003g0079 |
3 | HG00280.hp1 HG01081.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.-72-1151_-72-1150d others(4): Show |
ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20011657 | |||||||
chr22:20011748 | C | T | 12 | a0004c0006t0005g0014 a0004c0006t0005g0024 a0004c0006t0005g0247 others(9): Show |
18 | HG00140.hp1 HG00735.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.-72-1240G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20011748 | |||||||
chr22:20011894 | C | A | 1 | a0001c0001t0001g0227 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-72-1386G>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20011894 | |||||||
chr22:20011963 | C | T | 85 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(82): Show |
126 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.-72-1455G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20011963 | |||||||
chr22:20011969 | T | C | 211 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(208): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.-72-1461A>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20011969 | |||||||
chr22:20012016 | C | A | 1 | a0002c0002t0001g0130 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-72-1508G>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20012016 | |||||||
chr22:20012018 | A | G | 1 | a0004c0012t0006g0033 | 2 | HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-72-1510T>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20012018 | |||||||
chr22:20012079 | T | TC | 120 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(117): Show |
190 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.-72-1572dupG | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20012079 | |||||||
chr22:20012079 | T | TCC | 33 | a0001c0001t0001g0023 a0001c0001t0001g0176 a0001c0001t0001g0180 others(30): Show |
38 | HG00597.hp2 HG00639.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.-72-1573_-72-1572d others(4): Show |
ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20012079 | |||||||
chr22:20012085 | C | CG | 12 | a0004c0006t0005g0014 a0004c0006t0005g0024 a0004c0006t0005g0247 others(9): Show |
18 | HG00140.hp1 HG00735.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.-72-1578_-72-1577i others(3): Show |
ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20012085 | |||||||
chr22:20012088 | C | G | 1 | a0011c0018t0002g0037 | 2 | NA18947.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.-72-1580G>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20012088 | |||||||
chr22:20012090 | C | A | 12 | a0004c0006t0005g0014 a0004c0006t0005g0024 a0004c0006t0005g0247 others(9): Show |
18 | HG00140.hp1 HG00735.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.-72-1582G>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20012090 | |||||||
chr22:20012090 | C | CG | 13 | a0001c0004t0004g0017 a0001c0004t0004g0032 a0001c0004t0004g0110 others(10): Show |
16 | HG00099.hp2 HG00639.hp1 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.-72-1583_-72-1582i others(3): Show |
ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20012090 | |||||||
chr22:20012090 | C | G | 2 | a0001c0004t0004g0108 a0001c0004t0004g0109 |
2 | HG00642.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.-72-1582G>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20012090 | |||||||
chr22:20012237 | A | G | 57 | a0001c0001t0003g0073 a0001c0004t0011g0083 a0002c0002t0003g0003 others(54): Show |
81 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.-72-1729T>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20012237 | |||||||
chr22:20012623 | G | A | 2 | a0001c0004t0009g0018 a0001c0004t0009g0121 |
4 | HG02280.hp1 HG03130.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-72-2115C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20012623 | |||||||
chr22:20012905 | G | T | 33 | a0001c0004t0004g0017 a0001c0004t0004g0032 a0001c0004t0004g0108 others(30): Show |
48 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.-72-2397C>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20012905 | |||||||
chr22:20013248 | A | C | 3 | a0007c0010t0010g0035 a0007c0010t0010g0142 a0007c0010t0010g0143 |
4 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-72-2740T>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20013248 | |||||||
chr22:20013287 | C | T | 3 | a0007c0010t0010g0035 a0007c0010t0010g0142 a0007c0010t0010g0143 |
4 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-72-2779G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20013287 | |||||||
chr22:20013341 | G | A | 1 | a0025c0027t0003g0085 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-72-2833C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20013341 | |||||||
chr22:20013359 | C | G | 1 | a0005c0005t0004g0239 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-72-2851G>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20013359 | |||||||
chr22:20013427 | T | G | 251 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(248): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.-72-2919A>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20013427 | |||||||
chr22:20013452 | G | A | 1 | a0004c0012t0006g0033 | 2 | HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-72-2944C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20013452 | |||||||
chr22:20013483 | G | A | 213 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(210): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.-72-2975C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20013483 | |||||||
chr22:20013493 | C | T | 2 | a0003c0003t0002g0148 a0003c0003t0002g0149 |
2 | HG01069.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.-72-2985G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20013493 | |||||||
chr22:20013634 | G | A | 1 | a0002c0002t0003g0086 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-73+2955C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20013634 | |||||||
chr22:20013636 | C | T | 3 | a0007c0010t0010g0035 a0007c0010t0010g0142 a0007c0010t0010g0143 |
4 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-73+2953G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20013636 | |||||||
chr22:20013703 | A | G | 1 | a0002c0040t0003g0052 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-73+2886T>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20013703 | |||||||
chr22:20013810 | C | T | 17 | a0001c0001t0001g0051 a0001c0001t0001g0244 a0002c0032t0004g0136 others(14): Show |
28 | HG01109.hp1 HG01891.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.-73+2779G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20013810 | |||||||
chr22:20013927 | C | T | 1 | a0002c0040t0003g0052 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-73+2662G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20013927 | |||||||
chr22:20014020 | A | T | 1 | a0003c0003t0019g0092 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-73+2569T>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20014020 | |||||||
chr22:20014064 | CAG | C | 17 | a0001c0001t0001g0051 a0001c0001t0001g0244 a0002c0032t0004g0136 others(14): Show |
28 | HG01109.hp1 HG01891.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.-73+2523_-73+2524d others(4): Show |
ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20014064 | |||||||
chr22:20014077 | T | A | 3 | a0007c0010t0010g0035 a0007c0010t0010g0142 a0007c0010t0010g0143 |
4 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-73+2512A>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20014077 | |||||||
chr22:20014225 | C | T | 1 | a0001c0001t0001g0184 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-73+2364G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20014225 | |||||||
chr22:20014299 | A | G | 12 | a0004c0006t0005g0014 a0004c0006t0005g0024 a0004c0006t0005g0247 others(9): Show |
18 | HG00140.hp1 HG00735.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.-73+2290T>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20014299 | |||||||
chr22:20014426 | C | T | 1 | a0001c0001t0001g0183 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-73+2163G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20014426 | |||||||
chr22:20014581 | C | A | 1 | a0003c0003t0019g0092 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-73+2008G>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20014581 | |||||||
chr22:20014708 | C | T | 12 | a0004c0006t0005g0014 a0004c0006t0005g0024 a0004c0006t0005g0247 others(9): Show |
18 | HG00140.hp1 HG00735.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.-73+1881G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20014708 | |||||||
chr22:20014709 | G | A | 1 | a0001c0004t0016g0087 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-73+1880C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20014709 | |||||||
chr22:20014902 | A | T | 1 | a0003c0003t0002g0147 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-73+1687T>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20014902 | |||||||
chr22:20014971 | G | A | 1 | a0006c0007t0007g0104 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-73+1618C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20014971 | |||||||
chr22:20015119 | G | A | 1 | a0004c0009t0002g0105 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-73+1470C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20015119 | |||||||
chr22:20015268 | G | C | 4 | a0002c0002t0001g0036 a0002c0002t0001g0144 a0002c0002t0001g0146 others(1): Show |
5 | HG01975.hp1 HG01993.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.-73+1321C>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20015268 | |||||||
chr22:20015325 | G | T | 44 | a0001c0001t0003g0073 a0001c0004t0011g0083 a0002c0002t0003g0003 others(41): Show |
65 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.-73+1264C>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20015325 | |||||||
chr22:20015536 | C | T | 14 | a0001c0004t0004g0017 a0001c0004t0004g0032 a0001c0004t0004g0108 others(11): Show |
17 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.-73+1053G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20015536 | |||||||
chr22:20015629 | C | T | 11 | a0001c0001t0025g0254 a0004c0006t0005g0014 a0004c0006t0005g0024 others(8): Show |
16 | HG00140.hp1 HG00735.hp2 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.-73+960G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20015629 | |||||||
chr22:20015685 | C | T | 1 | a0003c0003t0019g0092 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-73+904G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20015685 | |||||||
chr22:20015688 | C | T | 1 | a0001c0001t0001g0182 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-73+901G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20015688 | |||||||
chr22:20015700 | G | A | 2 | a0008c0016t0006g0177 a0008c0016t0006g0178 |
2 | HG00323.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-73+889C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20015700 | |||||||
chr22:20015733 | T | A | 1 | a0006c0007t0007g0106 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-73+856A>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20015733 | |||||||
chr22:20015743 | C | G | 79 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(76): Show |
119 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.-73+846G>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20015743 | |||||||
chr22:20015811 | G | A | 80 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(77): Show |
120 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.-73+778C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20015811 | |||||||
chr22:20015964 | G | C | 2 | a0001c0004t0008g0029 a0001c0004t0008g0090 |
3 | HG02809.hp2 HG03471.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-73+625C>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20015964 | |||||||
chr22:20015967 | C | CAG | 209 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(206): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.-73+620_-73+621dup others(2): Show |
ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20015967 | |||||||
chr22:20016135 | T | A | 1 | a0006c0007t0007g0106 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-73+454A>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20016135 | |||||||
chr22:20016144 | C | T | 1 | a0001c0001t0001g0238 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-73+445G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20016144 | |||||||
chr22:20016182 | C | T | 3 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 |
3 | HG00642.hp2 HG01346.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-73+407G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20016182 | |||||||
chr22:20016186 | T | G | 1 | a0004c0026t0006g0107 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-73+403A>C | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20016186 | |||||||
chr22:20016208 | C | T | 151 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(148): Show |
221 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.-73+381G>A | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20016208 | |||||||
chr22:20016214 | C | A | 1 | a0001c0001t0001g0238 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-73+375G>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20016214 | |||||||
chr22:20016263 | G | A | 79 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(76): Show |
119 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.-73+326C>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20016263 | |||||||
chr22:20016310 | G | C | 2 | a0001c0001t0001g0051 a0001c0001t0001g0244 |
3 | HG01109.hp1 HG01891.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-73+279C>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20016310 | |||||||
chr22:20016313 | G | C | 1 | a0005c0005t0004g0239 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-73+276C>G | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20016313 | |||||||
chr22:20016351 | C | A | 4 | a0003c0014t0006g0240 a0003c0014t0006g0241 a0003c0017t0006g0242 others(1): Show |
4 | HG00408.hp1 NA18983.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.-73+238G>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20016351 | |||||||
chr22:20016551 | C | A | 1 | a0001c0001t0001g0244 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-73+38G>T | ARVCF | ENSG00000099889.14 | transcript | ENST00000263207.8 | protein_coding | 1/19 | chr22 | 20016551 |