Item | Value |
---|---|
geneid | 64098 |
ensemblid | ENSG00000138964.17 |
hgncid | 14654 |
symbol | PARVG |
name | parvin gamma |
refseq_nuc | NM_022141.7 |
refseq_prot | NP_071424.1 |
ensembl_nuc | ENST00000444313.8 |
ensembl_prot | ENSP00000391583.2 |
mane_status | MANE Select |
chr | chr22 |
start | 44180925 |
end | 44208469 |
strand | + |
ver | v1.2 |
region | chr22:44180925-44208469 |
region5000 | chr22:44175925-44213469 |
regionname0 | PARVG_chr22_44180925_44208469 |
regionname5000 | PARVG_chr22_44175925_44213469 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 331 | 413 | 89 | 74 | 186 | 18 | 44 | 138 | PARVG_chr22_44175925_44213469 | PARVG | MEPEF others(326): Show |
chr22 | 44175925 | 44213469 |
a0002 | 0/0 | 331 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | MEPEF others(326): Show |
chr22 | 44175925 | 44213469 |
a0003 | 0/0 | 317 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | MEPEF others(312): Show |
chr22 | 44175925 | 44213469 |
a0004 | 0/0 | 331 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | MEPEF others(326): Show |
chr22 | 44175925 | 44213469 |
a0005 | 0/0 | 331 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PARVG_chr22_44175925_44213469 | PARVG | MEPEF others(326): Show |
chr22 | 44175925 | 44213469 |
a0006 | 0/0 | 331 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PARVG_chr22_44175925_44213469 | PARVG | MEPEF others(326): Show |
chr22 | 44175925 | 44213469 |
a0007 | 0/0 | 331 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | MEPEF others(326): Show |
chr22 | 44175925 | 44213469 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 993 | 207 | 66 | 39 | 69 | 9 | 23 | PARVG_chr22_44175925_44213469 | PARVG | ATGGA others(988): Show |
chr22 | 44175925 | 44213469 | ||
a0001c0002 | 1/0 | 993 | 135 | 15 | 20 | 82 | 3 | 14 | PARVG_chr22_44175925_44213469 | PARVG | ATGGA others(988): Show |
chr22 | 44175925 | 44213469 | ||
a0001c0003 | 0/0 | 993 | 31 | 2 | 9 | 13 | 3 | 4 | PARVG_chr22_44175925_44213469 | PARVG | ATGGA others(988): Show |
chr22 | 44175925 | 44213469 | ||
a0001c0004 | 0/0 | 993 | 25 | 1 | 2 | 19 | 2 | 1 | PARVG_chr22_44175925_44213469 | PARVG | ATGGA others(988): Show |
chr22 | 44175925 | 44213469 | ||
a0001c0005 | 0/0 | 993 | 13 | 5 | 3 | 3 | 0 | 2 | PARVG_chr22_44175925_44213469 | PARVG | ATGGA others(988): Show |
chr22 | 44175925 | 44213469 | ||
a0001c0012 | 0/0 | 993 | 1 | 0 | 1 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | ATGGA others(988): Show |
chr22 | 44175925 | 44213469 | ||
a0001c0013 | 0/0 | 993 | 1 | 0 | 0 | 0 | 1 | 0 | PARVG_chr22_44175925_44213469 | PARVG | ATGGA others(988): Show |
chr22 | 44175925 | 44213469 | ||
a0002c0006 | 0/0 | 993 | 3 | 3 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | ATGGA others(988): Show |
chr22 | 44175925 | 44213469 | ||
a0003c0007 | 0/0 | 993 | 2 | 2 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | ATGGA others(988): Show |
chr22 | 44175925 | 44213469 | ||
a0004c0010 | 0/0 | 993 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | ATGGA others(988): Show |
chr22 | 44175925 | 44213469 | ||
a0005c0011 | 0/0 | 993 | 1 | 0 | 0 | 0 | 0 | 1 | PARVG_chr22_44175925_44213469 | PARVG | ATGGA others(988): Show |
chr22 | 44175925 | 44213469 | ||
a0006c0008 | 0/0 | 993 | 1 | 0 | 0 | 0 | 0 | 1 | PARVG_chr22_44175925_44213469 | PARVG | ATGGA others(988): Show |
chr22 | 44175925 | 44213469 | ||
a0007c0009 | 0/0 | 993 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | ATGGA others(988): Show |
chr22 | 44175925 | 44213469 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3488 | 1 | 0 | 0 | 0 | 0 | 1 | PARVG_chr22_44175925_44213469 | PARVG | AGCTT others(3483): Show |
chr22 | 44175925 | 44213469 |
a0001c0001t0002 | 0/0 | 3488 | 87 | 25 | 7 | 39 | 5 | 11 | PARVG_chr22_44175925_44213469 | PARVG | AGCTT others(3483): Show |
chr22 | 44175925 | 44213469 |
a0001c0001t0003 | 0/1 | 3488 | 64 | 17 | 23 | 18 | 0 | 5 | PARVG_chr22_44175925_44213469 | PARVG | AGCTT others(3483): Show |
chr22 | 44175925 | 44213469 |
a0001c0001t0004 | 0/0 | 3469 | 5 | 0 | 0 | 3 | 0 | 2 | PARVG_chr22_44175925_44213469 | PARVG | AGCTT others(3464): Show |
chr22 | 44175925 | 44213469 |
a0001c0001t0007 | 0/0 | 3488 | 10 | 6 | 0 | 4 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | AGCTT others(3483): Show |
chr22 | 44175925 | 44213469 |
a0001c0001t0008 | 0/0 | 3488 | 5 | 1 | 3 | 0 | 1 | 0 | PARVG_chr22_44175925_44213469 | PARVG | AGCTT others(3483): Show |
chr22 | 44175925 | 44213469 |
a0001c0001t0009 | 0/0 | 3488 | 2 | 1 | 1 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | AGCTT others(3483): Show |
chr22 | 44175925 | 44213469 |
a0001c0001t0010 | 0/0 | 3488 | 5 | 4 | 1 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | AGCTT others(3483): Show |
chr22 | 44175925 | 44213469 |
a0001c0001t0011 | 0/0 | 3488 | 4 | 0 | 1 | 0 | 3 | 0 | PARVG_chr22_44175925_44213469 | PARVG | AGCTT others(3483): Show |
chr22 | 44175925 | 44213469 |
a0001c0001t0012 | 0/0 | 3488 | 4 | 1 | 1 | 1 | 0 | 1 | PARVG_chr22_44175925_44213469 | PARVG | AGCTT others(3483): Show |
chr22 | 44175925 | 44213469 |
a0001c0001t0013 | 0/0 | 3488 | 2 | 0 | 1 | 0 | 0 | 1 | PARVG_chr22_44175925_44213469 | PARVG | AGCTT others(3483): Show |
chr22 | 44175925 | 44213469 |
a0001c0001t0014 | 0/0 | 3488 | 3 | 2 | 1 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | AGCTT others(3483): Show |
chr22 | 44175925 | 44213469 |
a0001c0001t0015 | 0/0 | 3488 | 2 | 0 | 0 | 0 | 0 | 2 | PARVG_chr22_44175925_44213469 | PARVG | AGCTT others(3483): Show |
chr22 | 44175925 | 44213469 |
a0001c0001t0016 | 0/0 | 3488 | 2 | 2 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | AGCTT others(3483): Show |
chr22 | 44175925 | 44213469 |
a0001c0001t0018 | 0/0 | 3488 | 2 | 2 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | AGCTT others(3483): Show |
chr22 | 44175925 | 44213469 |
a0001c0001t0020 | 0/0 | 3488 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | AGCCT others(3483): Show |
chr22 | 44175925 | 44213469 |
a0001c0001t0021 | 0/0 | 3488 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | AGCTT others(3483): Show |
chr22 | 44175925 | 44213469 |
a0001c0001t0025 | 0/0 | 3488 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | AGCTT others(3483): Show |
chr22 | 44175925 | 44213469 |
a0001c0001t0027 | 0/0 | 3488 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | AGCTT others(3483): Show |
chr22 | 44175925 | 44213469 |
a0001c0001t0029 | 0/0 | 3488 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | AGCTT others(3483): Show |
chr22 | 44175925 | 44213469 |
a0001c0001t0030 | 0/0 | 3488 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | AGCTT others(3483): Show |
chr22 | 44175925 | 44213469 |
a0001c0001t0032 | 0/0 | 3488 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | AGCTT others(3483): Show |
chr22 | 44175925 | 44213469 |
a0001c0001t0033 | 0/0 | 3469 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | AGCTT others(3464): Show |
chr22 | 44175925 | 44213469 |
a0001c0001t0035 | 0/0 | 3504 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | AGCTT others(3499): Show |
chr22 | 44175925 | 44213469 |
a0001c0002t0001 | 1/0 | 3488 | 101 | 15 | 18 | 52 | 3 | 12 | PARVG_chr22_44175925_44213469 | PARVG | AGCTT others(3483): Show |
chr22 | 44175925 | 44213469 |
a0001c0002t0005 | 0/0 | 3488 | 28 | 0 | 2 | 25 | 0 | 1 | PARVG_chr22_44175925_44213469 | PARVG | AGCTT others(3483): Show |
chr22 | 44175925 | 44213469 |
a0001c0002t0017 | 0/0 | 3488 | 2 | 0 | 0 | 2 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | AGCTT others(3483): Show |
chr22 | 44175925 | 44213469 |
a0001c0002t0019 | 0/0 | 3488 | 2 | 0 | 0 | 2 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | AGCTT others(3483): Show |
chr22 | 44175925 | 44213469 |
a0001c0002t0023 | 0/0 | 3488 | 1 | 0 | 0 | 0 | 0 | 1 | PARVG_chr22_44175925_44213469 | PARVG | AGCTT others(3483): Show |
chr22 | 44175925 | 44213469 |
a0001c0002t0028 | 0/0 | 3488 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | AGCTT others(3483): Show |
chr22 | 44175925 | 44213469 |
a0001c0003t0003 | 0/0 | 3488 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | AGCTT others(3483): Show |
chr22 | 44175925 | 44213469 |
a0001c0003t0004 | 0/0 | 3469 | 25 | 2 | 7 | 10 | 2 | 4 | PARVG_chr22_44175925_44213469 | PARVG | AGCTT others(3464): Show |
chr22 | 44175925 | 44213469 |
a0001c0003t0006 | 0/0 | 3469 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | AGCTT others(3464): Show |
chr22 | 44175925 | 44213469 |
a0001c0003t0007 | 0/0 | 3488 | 1 | 0 | 1 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | AGCTT others(3483): Show |
chr22 | 44175925 | 44213469 |
a0001c0003t0022 | 0/0 | 3469 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | AGCTT others(3464): Show |
chr22 | 44175925 | 44213469 |
a0001c0003t0024 | 0/0 | 3469 | 1 | 0 | 0 | 0 | 1 | 0 | PARVG_chr22_44175925_44213469 | PARVG | AGCTT others(3464): Show |
chr22 | 44175925 | 44213469 |
a0001c0003t0034 | 0/0 | 3469 | 1 | 0 | 1 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | AGCTT others(3464): Show |
chr22 | 44175925 | 44213469 |
a0001c0004t0002 | 0/0 | 3488 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | AGCTT others(3483): Show |
chr22 | 44175925 | 44213469 |
a0001c0004t0004 | 0/0 | 3469 | 12 | 1 | 1 | 9 | 1 | 0 | PARVG_chr22_44175925_44213469 | PARVG | AGCTT others(3464): Show |
chr22 | 44175925 | 44213469 |
a0001c0004t0006 | 0/0 | 3469 | 11 | 0 | 1 | 9 | 1 | 0 | PARVG_chr22_44175925_44213469 | PARVG | AGCTT others(3464): Show |
chr22 | 44175925 | 44213469 |
a0001c0004t0026 | 0/0 | 3469 | 1 | 0 | 0 | 0 | 0 | 1 | PARVG_chr22_44175925_44213469 | PARVG | AGCTT others(3464): Show |
chr22 | 44175925 | 44213469 |
a0001c0005t0002 | 0/0 | 3488 | 6 | 1 | 1 | 3 | 0 | 1 | PARVG_chr22_44175925_44213469 | PARVG | AGCTT others(3483): Show |
chr22 | 44175925 | 44213469 |
a0001c0005t0003 | 0/0 | 3488 | 3 | 3 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | AGCTT others(3483): Show |
chr22 | 44175925 | 44213469 |
a0001c0005t0009 | 0/0 | 3488 | 3 | 0 | 2 | 0 | 0 | 1 | PARVG_chr22_44175925_44213469 | PARVG | AGCTT others(3483): Show |
chr22 | 44175925 | 44213469 |
a0001c0005t0031 | 0/0 | 3488 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | AGCTT others(3483): Show |
chr22 | 44175925 | 44213469 |
a0001c0012t0001 | 0/0 | 3488 | 1 | 0 | 1 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | AGCTT others(3483): Show |
chr22 | 44175925 | 44213469 |
a0001c0013t0001 | 0/0 | 3488 | 1 | 0 | 0 | 0 | 1 | 0 | PARVG_chr22_44175925_44213469 | PARVG | AGCTT others(3483): Show |
chr22 | 44175925 | 44213469 |
a0002c0006t0002 | 0/0 | 3488 | 3 | 3 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | AGCTT others(3483): Show |
chr22 | 44175925 | 44213469 |
a0003c0007t0002 | 0/0 | 3488 | 2 | 2 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | AGCTT others(3483): Show |
chr22 | 44175925 | 44213469 |
a0004c0010t0002 | 0/0 | 3488 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | AGCTT others(3483): Show |
chr22 | 44175925 | 44213469 |
a0005c0011t0002 | 0/0 | 3488 | 1 | 0 | 0 | 0 | 0 | 1 | PARVG_chr22_44175925_44213469 | PARVG | AGCTT others(3483): Show |
chr22 | 44175925 | 44213469 |
a0006c0008t0013 | 0/0 | 3488 | 1 | 0 | 0 | 0 | 0 | 1 | PARVG_chr22_44175925_44213469 | PARVG | AGCTT others(3483): Show |
chr22 | 44175925 | 44213469 |
a0007c0009t0003 | 0/0 | 3488 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | AGCTT others(3483): Show |
chr22 | 44175925 | 44213469 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0009 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0030 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0002g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0003g0001 | 0/0 | 6 | 1 | 2 | 2 | 0 | 1 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0003g0002 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0003g0016 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0003g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0003g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0003g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0003g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0003g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0003g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0003g0171 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0003g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0003g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0003g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0003g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0003g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0003g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0003g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0003g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0003g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0003g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0003g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0003g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0003g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0004g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0004g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0004g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0004g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0004g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0007g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0007g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0007g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0007g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0007g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0007g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0007g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0007g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0007g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0007g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0008g0007 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0008g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0008g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0009g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0009g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0010g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0010g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0010g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0010g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0010g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0011g0032 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0011g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0011g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0012g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0012g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0012g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0012g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0013g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0013g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0014g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0014g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0014g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0015g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0015g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0016g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0016g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0018g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0018g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0020g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0021g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0025g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0027g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0029g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0030g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0032g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0033g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0001t0035g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0013 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0023 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0029 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0182 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0001g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0005g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0005g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0005g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0005g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0005g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0005g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0005g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0005g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0005g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0005g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0005g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0005g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0005g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0005g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0005g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0005g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0005g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0005g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0005g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0005g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0017g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0017g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0019g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0019g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0023g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0002t0028g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0003t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0003t0004g0005 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0003t0004g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0003t0004g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0003t0004g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0003t0004g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0003t0004g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0003t0004g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0003t0004g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0003t0004g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0003t0004g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0003t0004g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0003t0004g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0003t0004g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0003t0004g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0003t0004g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0003t0004g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0003t0004g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0003t0004g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0003t0004g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0003t0004g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0003t0006g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0003t0007g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0003t0022g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0003t0024g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0003t0034g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0004t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0004t0004g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0004t0004g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0004t0004g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0004t0004g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0004t0004g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0004t0004g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0004t0004g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0004t0004g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0004t0004g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0004t0004g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0004t0004g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0004t0006g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0004t0006g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0004t0006g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0004t0006g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0004t0006g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0004t0006g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0004t0006g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0004t0006g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0004t0026g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0005t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0005t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0005t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0005t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0005t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0005t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0005t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0005t0003g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0005t0003g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0005t0009g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0005t0009g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0005t0031g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0012t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0001c0013t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0002c0006t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0002c0006t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0002c0006t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0003c0007t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0003c0007t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0004c0010t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0005c0011t0002g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0006c0008t0013g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
a0007c0009t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0008 | g0119 | EUR | GBR | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG00099 | hp2 | a0001 | c0001 | t0011 | g0232 | EUR | GBR | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG00140 | hp1 | a0001 | c0004 | t0004 | g0004 | EUR | GBR | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG00140 | hp2 | a0001 | c0003 | t0004 | g0145 | EUR | GBR | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG00280 | hp1 | a0001 | c0003 | t0024 | g0219 | EUR | FIN | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0266 | EUR | FIN | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG00323 | hp1 | a0001 | c0013 | t0001 | g0062 | EUR | FIN | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0192 | EUR | FIN | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG00408 | hp1 | a0001 | c0004 | t0004 | g0310 | EAS | CHS | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG00408 | hp2 | a0001 | c0003 | t0004 | g0190 | EAS | CHS | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG00423 | hp1 | a0001 | c0001 | t0012 | g0058 | EAS | CHS | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG00423 | hp2 | a0001 | c0001 | t0030 | g0247 | EAS | CHS | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG00438 | hp1 | a0001 | c0004 | t0006 | g0129 | EAS | CHS | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | CHS | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG00544 | hp1 | a0001 | c0004 | t0006 | g0019 | EAS | CHS | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG00544 | hp2 | a0001 | c0004 | t0006 | g0121 | EAS | CHS | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG00558 | hp1 | a0001 | c0002 | t0001 | g0268 | EAS | CHS | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | CHS | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0335 | EAS | CHS | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | CHS | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG00609 | hp1 | a0001 | c0004 | t0004 | g0342 | EAS | CHS | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | CHS | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | CHS | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG00621 | hp2 | a0001 | c0002 | t0005 | g0034 | EAS | CHS | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG00639 | hp1 | a0001 | c0012 | t0001 | g0100 | AMR | PUR | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG00639 | hp2 | a0001 | c0002 | t0001 | g0166 | AMR | PUR | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG00642 | hp1 | a0001 | c0003 | t0004 | g0005 | AMR | PUR | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0305 | AMR | PUR | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG00673 | hp1 | a0001 | c0002 | t0017 | g0275 | EAS | CHS | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG00673 | hp2 | a0001 | c0004 | t0004 | g0259 | EAS | CHS | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG00733 | hp1 | a0001 | c0002 | t0001 | g0027 | AMR | PUR | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG00733 | hp2 | a0001 | c0003 | t0004 | g0149 | AMR | PUR | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG00735 | hp1 | a0001 | c0005 | t0002 | g0174 | AMR | PUR | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG00735 | hp2 | a0001 | c0001 | t0003 | g0076 | AMR | PUR | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0164 | AMR | PUR | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0151 | AMR | PUR | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG00741 | hp1 | a0001 | c0002 | t0001 | g0337 | AMR | PUR | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG00741 | hp2 | a0001 | c0003 | t0004 | g0005 | AMR | PUR | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01069 | hp1 | a0001 | c0002 | t0001 | g0013 | AMR | PUR | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01069 | hp2 | a0001 | c0001 | t0003 | g0073 | AMR | PUR | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01071 | hp1 | a0001 | c0001 | t0011 | g0209 | AMR | PUR | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01071 | hp2 | a0001 | c0002 | t0001 | g0013 | AMR | PUR | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01074 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01074 | hp2 | a0001 | c0002 | t0001 | g0023 | AMR | PUR | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01081 | hp1 | a0001 | c0001 | t0003 | g0309 | AMR | PUR | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01081 | hp2 | a0001 | c0001 | t0003 | g0016 | AMR | PUR | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01099 | hp1 | a0001 | c0004 | t0006 | g0117 | AMR | PUR | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01099 | hp2 | a0001 | c0001 | t0009 | g0150 | AMR | PUR | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01106 | hp1 | a0001 | c0003 | t0034 | g0189 | AMR | PUR | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0306 | AMR | PUR | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01109 | hp1 | a0001 | c0001 | t0003 | g0349 | AMR | PUR | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0170 | AMR | PUR | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01167 | hp1 | a0001 | c0005 | t0009 | g0014 | AMR | PUR | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01167 | hp2 | a0001 | c0001 | t0013 | g0242 | AMR | PUR | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0301 | AMR | PUR | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01168 | hp2 | a0001 | c0001 | t0008 | g0007 | AMR | PUR | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01169 | hp1 | a0001 | c0001 | t0008 | g0007 | AMR | PUR | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01169 | hp2 | a0001 | c0005 | t0009 | g0014 | AMR | PUR | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01175 | hp1 | a0001 | c0001 | t0008 | g0118 | AMR | PUR | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01175 | hp2 | a0001 | c0003 | t0004 | g0005 | AMR | PUR | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01192 | hp1 | a0001 | c0004 | t0004 | g0302 | AMR | PUR | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01192 | hp2 | a0001 | c0002 | t0001 | g0307 | AMR | PUR | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01243 | hp1 | a0001 | c0001 | t0010 | g0048 | AMR | PUR | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01243 | hp2 | a0001 | c0001 | t0003 | g0290 | AMR | PUR | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01255 | hp1 | a0001 | c0003 | t0004 | g0303 | AMR | CLM | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01256 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01256 | hp2 | a0001 | c0003 | t0004 | g0147 | AMR | CLM | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01258 | hp1 | a0001 | c0003 | t0007 | g0115 | AMR | CLM | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01258 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0208 | AMR | CLM | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01261 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01346 | hp1 | a0001 | c0002 | t0001 | g0027 | AMR | CLM | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01346 | hp2 | a0001 | c0002 | t0001 | g0040 | AMR | CLM | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01358 | hp1 | a0001 | c0002 | t0001 | g0040 | AMR | CLM | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01358 | hp2 | a0001 | c0001 | t0003 | g0336 | AMR | CLM | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0049 | AMR | CLM | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01433 | hp2 | a0001 | c0002 | t0001 | g0024 | AMR | CLM | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01496 | hp1 | a0001 | c0001 | t0012 | g0105 | AMR | CLM | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01496 | hp2 | a0001 | c0001 | t0003 | g0064 | AMR | CLM | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0070 | EUR | IBS | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01515 | hp2 | a0001 | c0002 | t0001 | g0022 | EUR | IBS | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0021 | EUR | IBS | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01516 | hp2 | a0001 | c0003 | t0004 | g0146 | EUR | IBS | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0021 | EUR | IBS | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01517 | hp2 | a0001 | c0002 | t0001 | g0022 | EUR | IBS | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0350 | AFR | ACB | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01884 | hp2 | a0001 | c0001 | t0003 | g0285 | AFR | ACB | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01891 | hp1 | a0001 | c0001 | t0007 | g0109 | AFR | ACB | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01891 | hp2 | a0001 | c0001 | t0003 | g0282 | AFR | ACB | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01928 | hp1 | a0001 | c0002 | t0005 | g0111 | AMR | PEL | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01928 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01934 | hp1 | a0001 | c0002 | t0001 | g0207 | AMR | PEL | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01934 | hp2 | a0001 | c0001 | t0014 | g0108 | AMR | PEL | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01943 | hp1 | a0001 | c0003 | t0004 | g0005 | AMR | PEL | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01943 | hp2 | a0001 | c0002 | t0001 | g0323 | AMR | PEL | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01952 | hp1 | a0001 | c0001 | t0003 | g0185 | AMR | PEL | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01952 | hp2 | a0001 | c0002 | t0005 | g0101 | AMR | PEL | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01975 | hp1 | a0001 | c0002 | t0001 | g0188 | AMR | PEL | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01975 | hp2 | a0001 | c0001 | t0003 | g0317 | AMR | PEL | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01978 | hp1 | a0001 | c0002 | t0001 | g0184 | AMR | PEL | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG01978 | hp2 | a0001 | c0002 | t0001 | g0322 | AMR | PEL | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02004 | hp1 | a0001 | c0002 | t0001 | g0013 | AMR | PEL | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02004 | hp2 | a0001 | c0001 | t0003 | g0162 | AMR | PEL | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02015 | hp1 | a0001 | c0001 | t0004 | g0245 | EAS | KHV | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02015 | hp2 | a0001 | c0004 | t0006 | g0125 | EAS | KHV | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | KHV | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02027 | hp2 | a0001 | c0002 | t0001 | g0163 | EAS | KHV | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02040 | hp1 | a0001 | c0002 | t0001 | g0039 | EAS | KHV | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0284 | EAS | KHV | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02055 | hp1 | a0003 | c0007 | t0002 | g0067 | AFR | ACB | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0072 | AFR | ACB | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02056 | hp1 | a0001 | c0004 | t0004 | g0212 | EAS | KHV | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | KHV | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02071 | hp1 | a0001 | c0002 | t0005 | g0113 | EAS | KHV | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02071 | hp2 | a0001 | c0002 | t0005 | g0092 | EAS | KHV | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02074 | hp1 | a0001 | c0002 | t0001 | g0261 | EAS | KHV | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02074 | hp2 | a0001 | c0002 | t0001 | g0331 | EAS | KHV | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02080 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | KHV | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02080 | hp2 | a0001 | c0002 | t0005 | g0008 | EAS | KHV | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | KHV | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02083 | hp2 | a0001 | c0003 | t0003 | g0300 | EAS | KHV | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02129 | hp1 | a0001 | c0002 | t0005 | g0008 | EAS | KHV | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02129 | hp2 | a0001 | c0004 | t0006 | g0004 | EAS | KHV | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02132 | hp1 | a0001 | c0003 | t0004 | g0201 | EAS | KHV | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02132 | hp2 | a0001 | c0002 | t0001 | g0054 | EAS | KHV | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02135 | hp1 | a0001 | c0002 | t0001 | g0204 | EAS | KHV | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | KHV | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02145 | hp1 | a0001 | c0001 | t0014 | g0107 | AFR | ACB | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02145 | hp2 | a0001 | c0002 | t0001 | g0029 | AFR | ACB | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02155 | hp1 | a0001 | c0002 | t0001 | g0258 | EAS | CDX | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02155 | hp2 | a0001 | c0002 | t0017 | g0324 | EAS | CDX | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | CDX | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02165 | hp2 | a0001 | c0003 | t0004 | g0220 | EAS | CDX | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0214 | AFR | ACB | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0099 | AFR | ACB | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0060 | AFR | ACB | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0308 | AFR | ACB | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02273 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02273 | hp2 | a0001 | c0001 | t0003 | g0320 | AMR | PEL | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0041 | AFR | ACB | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02280 | hp2 | a0001 | c0002 | t0001 | g0288 | AFR | ACB | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02293 | hp1 | a0001 | c0001 | t0003 | g0143 | AMR | PEL | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02293 | hp2 | a0001 | c0001 | t0003 | g0165 | AMR | PEL | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02300 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0304 | AMR | PEL | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02451 | hp1 | a0001 | c0002 | t0001 | g0292 | AFR | ACB | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02451 | hp2 | a0001 | c0001 | t0003 | g0090 | AFR | ACB | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02523 | hp1 | a0001 | c0001 | t0007 | g0103 | EAS | KHV | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02523 | hp2 | a0001 | c0002 | t0001 | g0029 | EAS | KHV | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0339 | AFR | GWD | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0043 | AFR | GWD | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02602 | hp1 | a0001 | c0001 | t0015 | g0218 | SAS | PJL | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02602 | hp2 | a0001 | c0003 | t0004 | g0148 | SAS | PJL | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02615 | hp1 | a0001 | c0001 | t0003 | g0358 | AFR | GWD | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02615 | hp2 | a0001 | c0001 | t0010 | g0089 | AFR | GWD | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0315 | AFR | GWD | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02622 | hp2 | a0001 | c0002 | t0001 | g0346 | AFR | GWD | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02630 | hp1 | a0001 | c0001 | t0007 | g0116 | AFR | GWD | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02630 | hp2 | a0001 | c0002 | t0001 | g0264 | AFR | GWD | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02647 | hp1 | a0001 | c0002 | t0001 | g0299 | AFR | GWD | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0050 | AFR | GWD | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02683 | hp1 | a0001 | c0005 | t0009 | g0057 | SAS | PJL | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02683 | hp2 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02698 | hp1 | a0001 | c0002 | t0001 | g0244 | SAS | PJL | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02698 | hp2 | a0001 | c0005 | t0002 | g0224 | SAS | PJL | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02717 | hp1 | a0001 | c0002 | t0001 | g0066 | AFR | GWD | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02717 | hp2 | a0001 | c0001 | t0003 | g0065 | AFR | GWD | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02723 | hp1 | a0001 | c0001 | t0010 | g0262 | AFR | GWD | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02723 | hp2 | a0001 | c0005 | t0031 | g0215 | AFR | GWD | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02735 | hp1 | a0001 | c0001 | t0015 | g0205 | SAS | PJL | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02735 | hp2 | a0001 | c0001 | t0013 | g0193 | SAS | PJL | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02738 | hp1 | a0001 | c0002 | t0001 | g0172 | SAS | PJL | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0230 | SAS | PJL | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02809 | hp1 | a0001 | c0001 | t0003 | g0254 | AFR | GWD | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02809 | hp2 | a0001 | c0001 | t0018 | g0096 | AFR | GWD | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02818 | hp1 | a0001 | c0001 | t0007 | g0160 | AFR | GWD | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02818 | hp2 | a0001 | c0002 | t0001 | g0079 | AFR | GWD | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02886 | hp1 | a0001 | c0005 | t0002 | g0216 | AFR | GWD | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02886 | hp2 | a0002 | c0006 | t0002 | g0250 | AFR | GWD | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | GWD | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0047 | AFR | GWD | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02897 | hp1 | a0001 | c0005 | t0003 | g0298 | AFR | GWD | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | GWD | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02922 | hp1 | a0001 | c0001 | t0012 | g0106 | AFR | ESN | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02922 | hp2 | a0001 | c0001 | t0016 | g0210 | AFR | ESN | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02965 | hp1 | a0001 | c0001 | t0003 | g0156 | AFR | ESN | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0053 | AFR | ESN | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02970 | hp1 | a0002 | c0006 | t0002 | g0251 | AFR | ESN | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02970 | hp2 | a0001 | c0001 | t0029 | g0340 | AFR | ESN | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02976 | hp1 | a0001 | c0001 | t0007 | g0110 | AFR | ESN | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02976 | hp2 | a0001 | c0001 | t0003 | g0095 | AFR | ESN | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG03017 | hp1 | a0001 | c0001 | t0012 | g0120 | SAS | PJL | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0152 | SAS | PJL | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG03041 | hp1 | a0001 | c0001 | t0003 | g0045 | AFR | GWD | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG03041 | hp2 | a0001 | c0005 | t0003 | g0061 | AFR | GWD | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG03098 | hp1 | a0001 | c0002 | t0001 | g0357 | AFR | MSL | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG03098 | hp2 | a0001 | c0001 | t0014 | g0348 | AFR | MSL | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG03130 | hp1 | a0001 | c0001 | t0027 | g0341 | AFR | ESN | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG03130 | hp2 | a0001 | c0002 | t0001 | g0159 | AFR | ESN | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG03139 | hp1 | a0001 | c0001 | t0003 | g0046 | AFR | ESN | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG03139 | hp2 | a0001 | c0002 | t0001 | g0293 | AFR | ESN | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG03209 | hp1 | a0002 | c0006 | t0002 | g0052 | AFR | MSL | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0265 | AFR | MSL | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG03225 | hp1 | a0001 | c0001 | t0007 | g0267 | AFR | MSL | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG03225 | hp2 | a0001 | c0002 | t0001 | g0094 | AFR | MSL | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG03239 | hp1 | a0001 | c0002 | t0001 | g0296 | SAS | PJL | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0249 | SAS | PJL | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG03453 | hp1 | a0001 | c0001 | t0003 | g0200 | AFR | MSL | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG03453 | hp2 | a0001 | c0001 | t0007 | g0124 | AFR | MSL | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0289 | AFR | MSL | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG03486 | hp2 | a0001 | c0001 | t0010 | g0093 | AFR | MSL | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG03491 | hp1 | a0001 | c0001 | t0004 | g0154 | SAS | PJL | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0295 | SAS | PJL | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG03492 | hp1 | a0001 | c0001 | t0004 | g0155 | SAS | PJL | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG03492 | hp2 | a0005 | c0011 | t0002 | g0006 | SAS | PJL | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG03516 | hp1 | a0001 | c0001 | t0020 | g0055 | AFR | ESN | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG03516 | hp2 | a0001 | c0003 | t0004 | g0294 | AFR | ESN | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG03540 | hp1 | a0001 | c0005 | t0003 | g0316 | AFR | GWD | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG03540 | hp2 | a0001 | c0001 | t0003 | g0042 | AFR | GWD | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0044 | AFR | MSL | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0353 | AFR | MSL | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG03654 | hp1 | a0006 | c0008 | t0013 | g0194 | SAS | PJL | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG03654 | hp2 | a0001 | c0002 | t0001 | g0153 | SAS | PJL | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG03669 | hp1 | a0001 | c0003 | t0004 | g0173 | SAS | PJL | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG03669 | hp2 | a0001 | c0001 | t0003 | g0142 | SAS | PJL | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0237 | SAS | STU | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG03688 | hp2 | a0001 | c0003 | t0004 | g0222 | SAS | STU | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG03704 | hp1 | a0001 | c0002 | t0001 | g0181 | SAS | PJL | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG03704 | hp2 | a0001 | c0002 | t0023 | g0167 | SAS | PJL | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0169 | SAS | PJL | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG03710 | hp2 | a0001 | c0002 | t0001 | g0179 | SAS | PJL | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG03831 | hp1 | a0001 | c0001 | t0003 | g0144 | SAS | BEB | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0243 | SAS | BEB | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG03834 | hp1 | a0001 | c0002 | t0001 | g0255 | SAS | BEB | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0075 | SAS | BEB | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG03927 | hp1 | a0001 | c0002 | t0001 | g0175 | SAS | BEB | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | BEB | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG03942 | hp1 | a0001 | c0002 | t0005 | g0131 | SAS | BEB | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG03942 | hp2 | a0001 | c0004 | t0026 | g0127 | SAS | BEB | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG04115 | hp1 | a0001 | c0002 | t0001 | g0256 | SAS | STU | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG04115 | hp2 | a0001 | c0003 | t0004 | g0223 | SAS | STU | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG04184 | hp1 | a0001 | c0002 | t0001 | g0024 | SAS | BEB | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG04184 | hp2 | a0001 | c0001 | t0003 | g0239 | SAS | BEB | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0009 | SAS | STU | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG04199 | hp2 | a0001 | c0002 | t0001 | g0344 | SAS | STU | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0030 | SAS | STU | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0257 | SAS | STU | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0297 | SAS | STU | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG04228 | hp2 | a0001 | c0002 | t0001 | g0180 | SAS | STU | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0354 | AFR | YRI | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0068 | AFR | YRI | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | CHB | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18612 | hp2 | a0001 | c0001 | t0003 | g0279 | EAS | CHB | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18906 | hp1 | a0001 | c0001 | t0003 | g0356 | AFR | YRI | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18906 | hp2 | a0001 | c0002 | t0001 | g0199 | AFR | YRI | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18941 | hp1 | a0001 | c0004 | t0004 | g0228 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18941 | hp2 | a0001 | c0002 | t0001 | g0345 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18942 | hp1 | a0001 | c0002 | t0005 | g0015 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18942 | hp2 | a0001 | c0002 | t0005 | g0132 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18943 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18944 | hp1 | a0001 | c0002 | t0005 | g0137 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18945 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18947 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18947 | hp2 | a0001 | c0004 | t0006 | g0004 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18949 | hp1 | a0001 | c0001 | t0007 | g0123 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18949 | hp2 | a0001 | c0002 | t0001 | g0071 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18950 | hp1 | a0001 | c0002 | t0028 | g0253 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18950 | hp2 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18951 | hp1 | a0001 | c0002 | t0001 | g0333 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18952 | hp1 | a0001 | c0002 | t0005 | g0134 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18952 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18953 | hp2 | a0001 | c0002 | t0001 | g0158 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18954 | hp1 | a0001 | c0002 | t0001 | g0217 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18954 | hp2 | a0001 | c0001 | t0004 | g0235 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18959 | hp1 | a0001 | c0002 | t0001 | g0272 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18960 | hp1 | a0001 | c0001 | t0003 | g0088 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18960 | hp2 | a0001 | c0003 | t0004 | g0260 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18962 | hp1 | a0001 | c0003 | t0022 | g0102 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18962 | hp2 | a0001 | c0002 | t0001 | g0187 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18963 | hp1 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18963 | hp2 | a0001 | c0002 | t0001 | g0319 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18964 | hp1 | a0001 | c0005 | t0002 | g0195 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18964 | hp2 | a0001 | c0003 | t0004 | g0026 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18966 | hp1 | a0001 | c0001 | t0003 | g0269 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18966 | hp2 | a0001 | c0002 | t0001 | g0183 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18967 | hp1 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18967 | hp2 | a0001 | c0002 | t0001 | g0338 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18968 | hp1 | a0001 | c0002 | t0001 | g0186 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18968 | hp2 | a0001 | c0001 | t0035 | g0059 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18969 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18971 | hp1 | a0001 | c0002 | t0001 | g0311 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18972 | hp1 | a0001 | c0002 | t0019 | g0278 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18972 | hp2 | a0001 | c0002 | t0001 | g0326 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18973 | hp1 | a0001 | c0003 | t0004 | g0025 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18974 | hp1 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18975 | hp1 | a0001 | c0001 | t0032 | g0206 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18975 | hp2 | a0001 | c0002 | t0005 | g0003 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18977 | hp1 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0330 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18980 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18980 | hp2 | a0001 | c0002 | t0005 | g0114 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18981 | hp1 | a0001 | c0002 | t0005 | g0135 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18981 | hp2 | a0001 | c0005 | t0002 | g0196 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18982 | hp1 | a0001 | c0002 | t0001 | g0334 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18983 | hp2 | a0001 | c0003 | t0004 | g0026 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18984 | hp1 | a0001 | c0001 | t0003 | g0233 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18984 | hp2 | a0001 | c0001 | t0003 | g0280 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18986 | hp1 | a0001 | c0002 | t0005 | g0020 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18986 | hp2 | a0001 | c0004 | t0006 | g0004 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0321 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18988 | hp2 | a0001 | c0002 | t0001 | g0226 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18989 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18990 | hp1 | a0001 | c0002 | t0001 | g0328 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18991 | hp1 | a0001 | c0003 | t0006 | g0122 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18991 | hp2 | a0001 | c0002 | t0001 | g0227 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18994 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18995 | hp1 | a0001 | c0002 | t0001 | g0202 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18995 | hp2 | a0001 | c0002 | t0005 | g0003 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18998 | hp1 | a0001 | c0002 | t0001 | g0325 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18998 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA19000 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA19000 | hp2 | a0001 | c0002 | t0001 | g0203 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA19002 | hp2 | a0001 | c0002 | t0001 | g0286 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA19005 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA19009 | hp1 | a0001 | c0003 | t0004 | g0221 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA19009 | hp2 | a0001 | c0002 | t0005 | g0008 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA19010 | hp1 | a0001 | c0001 | t0007 | g0138 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA19010 | hp2 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA19011 | hp1 | a0001 | c0003 | t0004 | g0025 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA19012 | hp1 | a0001 | c0002 | t0005 | g0112 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA19012 | hp2 | a0001 | c0004 | t0004 | g0036 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA19030 | hp1 | a0001 | c0001 | t0003 | g0098 | AFR | LWK | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0078 | AFR | LWK | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA19043 | hp1 | a0001 | c0001 | t0033 | g0343 | AFR | LWK | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA19043 | hp2 | a0007 | c0009 | t0003 | g0091 | AFR | LWK | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA19054 | hp1 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA19054 | hp2 | a0001 | c0002 | t0005 | g0003 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA19057 | hp2 | a0001 | c0002 | t0001 | g0178 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA19058 | hp1 | a0001 | c0001 | t0004 | g0332 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA19058 | hp2 | a0001 | c0002 | t0005 | g0020 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA19060 | hp1 | a0001 | c0002 | t0005 | g0015 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA19060 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA19062 | hp1 | a0001 | c0002 | t0019 | g0271 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA19062 | hp2 | a0001 | c0002 | t0001 | g0273 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA19063 | hp1 | a0001 | c0001 | t0021 | g0248 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA19063 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA19064 | hp1 | a0001 | c0002 | t0005 | g0126 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA19064 | hp2 | a0001 | c0004 | t0006 | g0019 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA19066 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA19066 | hp2 | a0001 | c0001 | t0007 | g0139 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA19067 | hp1 | a0001 | c0002 | t0001 | g0177 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA19067 | hp2 | a0001 | c0002 | t0001 | g0287 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA19068 | hp1 | a0001 | c0002 | t0001 | g0327 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA19068 | hp2 | a0001 | c0004 | t0006 | g0128 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA19074 | hp1 | a0001 | c0001 | t0003 | g0211 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA19075 | hp1 | a0001 | c0002 | t0005 | g0133 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA19075 | hp2 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA19077 | hp1 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA19079 | hp1 | a0001 | c0003 | t0004 | g0312 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA19080 | hp1 | a0001 | c0001 | t0003 | g0276 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA19080 | hp2 | a0001 | c0002 | t0005 | g0003 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA19081 | hp1 | a0001 | c0005 | t0002 | g0191 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA19081 | hp2 | a0001 | c0004 | t0004 | g0036 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA19083 | hp1 | a0001 | c0002 | t0005 | g0069 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA19085 | hp1 | a0001 | c0004 | t0002 | g0329 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA19086 | hp1 | a0001 | c0001 | t0003 | g0277 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA19086 | hp2 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA19090 | hp1 | a0001 | c0004 | t0004 | g0198 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA19090 | hp2 | a0001 | c0002 | t0005 | g0136 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA19091 | hp1 | a0001 | c0004 | t0004 | g0270 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA19091 | hp2 | a0001 | c0002 | t0001 | g0157 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA19240 | hp1 | a0003 | c0007 | t0002 | g0161 | AFR | YRI | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA19240 | hp2 | a0001 | c0003 | t0004 | g0355 | AFR | YRI | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA20129 | hp1 | a0001 | c0002 | t0001 | g0352 | AFR | ASW | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0252 | AFR | ASW | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA20752 | hp1 | a0001 | c0004 | t0006 | g0130 | EUR | TSI | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA20752 | hp2 | a0001 | c0001 | t0011 | g0032 | EUR | TSI | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA20805 | hp1 | a0001 | c0002 | t0001 | g0023 | EUR | TSI | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA20805 | hp2 | a0001 | c0001 | t0011 | g0032 | EUR | TSI | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02109 | hp1 | a0001 | c0001 | t0009 | g0051 | AFR | ACB | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0140 | AFR | ACB | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02486 | hp1 | a0004 | c0010 | t0002 | g0097 | AFR | ACB | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02486 | hp2 | a0001 | c0001 | t0010 | g0056 | AFR | ACB | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0141 | AFR | ACB | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG02559 | hp2 | a0001 | c0001 | t0016 | g0318 | AFR | ACB | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG03471 | hp1 | a0001 | c0001 | t0003 | g0263 | AFR | MSL | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG03471 | hp2 | a0001 | c0001 | t0018 | g0351 | AFR | MSL | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG06807 | hp1 | a0001 | c0001 | t0008 | g0007 | AFR | USA | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
HG06807 | hp2 | a0001 | c0001 | t0025 | g0104 | AFR | USA | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18955 | hp1 | a0001 | c0002 | t0005 | g0003 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA18955 | hp2 | a0001 | c0002 | t0001 | g0283 | EAS | JPT | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA20300 | hp1 | a0001 | c0002 | t0001 | g0291 | AFR | USA | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA20300 | hp2 | a0001 | c0001 | t0003 | g0001 | AFR | USA | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA21309 | hp1 | a0001 | c0004 | t0004 | g0213 | AFR | LWK | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0347 | AFR | LWK | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0171 | REF | REF | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0182 | REF | REF | PARVG_chr22_44175925_44213469 | PARVG | chr22 | 44175925 | 44213469 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:44185850 | C | A | 1 | a0006 | 1 | HG03654.hp1 | missense_variant | MODERATE | c.122C>A | p.Pro41His | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 4/14 | 571/3488 | 122/996 | 41/331 | chr22 | 44185850 | |||
chr22:44190639 | C | A | 1 | a0002 | 3 | HG02886.hp2 HG02970.hp1 HG03209.hp1 |
missense_variant | MODERATE | c.477C>A | p.Asn159Lys | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 7/14 | 926/3488 | 477/996 | 159/331 | chr22 | 44190639 | |||
chr22:44193814 | G | A | 1 | a0007 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.574G>A | p.Glu192Lys | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 9/14 | 1023/3488 | 574/996 | 192/331 | chr22 | 44193814 | |||
chr22:44196202 | G | C | 1 | a0004 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.631G>C | p.Ala211Pro | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 10/14 | 1080/3488 | 631/996 | 211/331 | chr22 | 44196202 | |||
chr22:44196371 | A | G | 1 | a0005 | 1 | HG03492.hp2 | missense_variant | MODERATE | c.667A>G | p.Lys223Glu | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 11/14 | 1116/3488 | 667/996 | 223/331 | chr22 | 44196371 | |||
chr22:44206382 | C | T | 1 | a0003 | 2 | HG02055.hp1 NA19240.hp1 |
stop_gained | HIGH | c.952C>T | p.Gln318* | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 14/14 | 1401/3488 | 952/996 | 318/331 | chr22 | 44206382 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:44190642 | C | T | 4 | a0001c0003 a0001c0005 a0001c0012 others(1): Show |
46 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(43): Show |
synonymous_variant | LOW | c.480C>T | p.Val160Val | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 7/14 | 929/3488 | 480/996 | 160/331 | chr22 | 44190642 | |||
chr22:44198704 | C | G | 3 | a0001c0003 a0001c0004 a0001c0013 |
57 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(54): Show |
synonymous_variant | LOW | c.795C>G | p.Pro265Pro | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/14 | 1244/3488 | 795/996 | 265/331 | chr22 | 44198704 | |||
chr22:44206349 | A | C | 10 | a0001c0001 a0001c0003 a0001c0004 others(7): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
synonymous_variant | LOW | c.919A>C | p.Arg307Arg | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 14/14 | 1368/3488 | 919/996 | 307/331 | chr22 | 44206349 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:44180928 | T | C | 1 | a0001c0001t0020 | 1 | HG03516.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-446T>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 1/14 | chr22 | 44180928 | |||||||
chr22:44181063 | A | C | 1 | a0001c0001t0035 | 1 | NA18968.hp2 | 5_prime_UTR_variant | MODIFIER | c.-311A>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 1/14 | 2267 | chr22 | 44181063 | ||||||
chr22:44181064 | C | T | 1 | a0001c0001t0035 | 1 | NA18968.hp2 | 5_prime_UTR_variant | MODIFIER | c.-310C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 1/14 | 2266 | chr22 | 44181064 | ||||||
chr22:44181082 | G | T | 1 | a0001c0001t0035 | 1 | NA18968.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-292G>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 1/14 | chr22 | 44181082 | |||||||
chr22:44181092 | T | G | 1 | a0001c0001t0035 | 1 | NA18968.hp2 | 5_prime_UTR_variant | MODIFIER | c.-282T>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 1/14 | 2238 | chr22 | 44181092 | ||||||
chr22:44181093 | C | A | 1 | a0001c0001t0035 | 1 | NA18968.hp2 | 5_prime_UTR_variant | MODIFIER | c.-281C>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 1/14 | 2237 | chr22 | 44181093 | ||||||
chr22:44181096 | C | A | 1 | a0001c0001t0035 | 1 | NA18968.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-278C>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 1/14 | chr22 | 44181096 | |||||||
chr22:44181097 | T | G | 1 | a0001c0001t0035 | 1 | NA18968.hp2 | 5_prime_UTR_variant | MODIFIER | c.-277T>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 1/14 | 2233 | chr22 | 44181097 | ||||||
chr22:44181098 | G | A | 1 | a0001c0001t0035 | 1 | NA18968.hp2 | 5_prime_UTR_variant | MODIFIER | c.-276G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 1/14 | 2232 | chr22 | 44181098 | ||||||
chr22:44181104 | C | T | 1 | a0001c0001t0035 | 1 | NA18968.hp2 | 5_prime_UTR_variant | MODIFIER | c.-270C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 1/14 | 2226 | chr22 | 44181104 | ||||||
chr22:44181105 | C | CAATTATT others(9): Show |
1 | a0001c0001t0035 | 1 | NA18968.hp2 | 5_prime_UTR_variant | MODIFIER | c.-269_-268insAATTAT others(10): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 1/14 | 2224 | chr22 | 44181105 | ||||||
chr22:44181108 | C | A | 1 | a0001c0001t0035 | 1 | NA18968.hp2 | 5_prime_UTR_variant | MODIFIER | c.-266C>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 1/14 | 2222 | chr22 | 44181108 | ||||||
chr22:44181109 | C | T | 1 | a0001c0001t0035 | 1 | NA18968.hp2 | 5_prime_UTR_variant | MODIFIER | c.-265C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 1/14 | 2221 | chr22 | 44181109 | ||||||
chr22:44181114 | C | T | 1 | a0001c0001t0035 | 1 | NA18968.hp2 | 5_prime_UTR_variant | MODIFIER | c.-260C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 1/14 | 2216 | chr22 | 44181114 | ||||||
chr22:44181115 | C | A | 1 | a0001c0001t0035 | 1 | NA18968.hp2 | 5_prime_UTR_variant | MODIFIER | c.-259C>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 1/14 | 2215 | chr22 | 44181115 | ||||||
chr22:44181116 | C | A | 1 | a0001c0001t0035 | 1 | NA18968.hp2 | 5_prime_UTR_variant | MODIFIER | c.-258C>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 1/14 | 2214 | chr22 | 44181116 | ||||||
chr22:44181117 | C | T | 1 | a0001c0001t0035 | 1 | NA18968.hp2 | 5_prime_UTR_variant | MODIFIER | c.-257C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 1/14 | 2213 | chr22 | 44181117 | ||||||
chr22:44181119 | T | A | 1 | a0001c0001t0035 | 1 | NA18968.hp2 | 5_prime_UTR_variant | MODIFIER | c.-255T>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 1/14 | 2211 | chr22 | 44181119 | ||||||
chr22:44181120 | G | A | 1 | a0001c0001t0021 | 1 | NA19063.hp1 | 5_prime_UTR_variant | MODIFIER | c.-254G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 1/14 | 2210 | chr22 | 44181120 | ||||||
chr22:44181124 | A | T | 1 | a0001c0001t0035 | 1 | NA18968.hp2 | 5_prime_UTR_variant | MODIFIER | c.-250A>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 1/14 | 2206 | chr22 | 44181124 | ||||||
chr22:44181125 | C | G | 1 | a0001c0001t0035 | 1 | NA18968.hp2 | 5_prime_UTR_variant | MODIFIER | c.-249C>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 1/14 | 2205 | chr22 | 44181125 | ||||||
chr22:44181127 | A | T | 1 | a0001c0001t0035 | 1 | NA18968.hp2 | 5_prime_UTR_variant | MODIFIER | c.-247A>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 1/14 | 2203 | chr22 | 44181127 | ||||||
chr22:44181761 | G | A | 1 | a0001c0003t0022 | 1 | NA18962.hp1 | 5_prime_UTR_variant | MODIFIER | c.-169G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 2/14 | 1569 | chr22 | 44181761 | ||||||
chr22:44181769 | G | C | 6 | a0001c0001t0011 a0001c0001t0013 a0001c0001t0015 others(3): Show |
11 | HG00099.hp2 HG00280.hp1 HG01071.hp1 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-161G>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 2/14 | 1561 | chr22 | 44181769 | ||||||
chr22:44181803 | T | A | 11 | a0001c0001t0007 a0001c0001t0008 a0001c0001t0012 others(8): Show |
66 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(63): Show |
5_prime_UTR_variant | MODIFIER | c.-127T>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 2/14 | 1527 | chr22 | 44181803 | ||||||
chr22:44206526 | C | A | 3 | a0001c0001t0009 a0001c0001t0011 a0001c0005t0009 |
9 | HG00099.hp2 HG01071.hp1 HG01099.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*100C>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 14/14 | 100 | chr22 | 44206526 | ||||||
chr22:44206669 | A | C | 9 | a0001c0001t0004 a0001c0003t0004 a0001c0003t0006 others(6): Show |
58 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*243A>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 14/14 | 243 | chr22 | 44206669 | ||||||
chr22:44206713 | T | A | 2 | a0001c0001t0010 a0001c0001t0014 |
8 | HG01243.hp1 HG01934.hp2 HG02145.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*287T>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 14/14 | 287 | chr22 | 44206713 | ||||||
chr22:44206767 | G | A | 1 | a0001c0004t0026 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*341G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 14/14 | 341 | chr22 | 44206767 | ||||||
chr22:44206778 | T | G | 1 | a0001c0001t0025 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*352T>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 14/14 | 352 | chr22 | 44206778 | ||||||
chr22:44206824 | C | A | 1 | a0001c0001t0016 | 2 | HG02559.hp2 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*398C>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 14/14 | 398 | chr22 | 44206824 | ||||||
chr22:44206958 | G | A | 1 | a0001c0001t0027 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*532G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 14/14 | 532 | chr22 | 44206958 | ||||||
chr22:44207272 | G | A | 1 | a0001c0002t0017 | 2 | HG00673.hp1 HG02155.hp2 |
3_prime_UTR_variant | MODIFIER | c.*846G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 14/14 | 846 | chr22 | 44207272 | ||||||
chr22:44207289 | TGGGGAGG others(12): Show |
T | 1 | a0001c0001t0033 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*894_*912delAGGCTG others(13): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 14/14 | 894 | INFO_REALIGN_3_PRIME | chr22 | 44207289 | |||||
chr22:44207295 | GGGGTGAG others(67): Show |
G | 3 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0016 |
5 | HG02258.hp1 HG02559.hp2 HG02895.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*892_*965delTGAGGC others(68): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 14/14 | 892 | INFO_REALIGN_3_PRIME | chr22 | 44207295 | |||||
chr22:44207328 | G | A | 1 | a0001c0001t0018 | 2 | HG02809.hp2 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*902G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 14/14 | 902 | chr22 | 44207328 | ||||||
chr22:44207369 | C | T | 10 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0012 others(7): Show |
82 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*943C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 14/14 | 943 | chr22 | 44207369 | ||||||
chr22:44207400 | TGGGGACG others(12): Show |
T | 9 | a0001c0001t0004 a0001c0003t0004 a0001c0003t0006 others(6): Show |
58 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*980_*998delCGGGTG others(13): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 14/14 | 980 | INFO_REALIGN_3_PRIME | chr22 | 44207400 | |||||
chr22:44207406 | CGGGTGAG others(12): Show |
C | 1 | a0001c0002t0028 | 1 | NA18950.hp1 | 3_prime_UTR_variant | MODIFIER | c.*993_*1011delCGGGG others(14): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 14/14 | 993 | INFO_REALIGN_3_PRIME | chr22 | 44207406 | |||||
chr22:44207425 | G | T | 9 | a0001c0001t0004 a0001c0003t0004 a0001c0003t0006 others(6): Show |
58 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*999G>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 14/14 | 999 | chr22 | 44207425 | ||||||
chr22:44207477 | T | C | 10 | a0001c0001t0004 a0001c0002t0028 a0001c0003t0004 others(7): Show |
59 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*1051T>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 14/14 | 1051 | chr22 | 44207477 | ||||||
chr22:44207647 | A | G | 1 | a0001c0001t0008 | 5 | HG00099.hp1 HG01168.hp2 HG01169.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1221A>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 14/14 | 1221 | chr22 | 44207647 | ||||||
chr22:44207702 | G | A | 10 | a0001c0001t0004 a0001c0002t0028 a0001c0003t0004 others(7): Show |
59 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*1276G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 14/14 | 1276 | chr22 | 44207702 | ||||||
chr22:44207713 | C | T | 2 | a0001c0001t0030 a0001c0001t0032 |
2 | HG00423.hp2 NA18975.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1287C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 14/14 | 1287 | chr22 | 44207713 | ||||||
chr22:44207804 | T | C | 45 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(42): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
3_prime_UTR_variant | MODIFIER | c.*1378T>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 14/14 | 1378 | chr22 | 44207804 | ||||||
chr22:44207845 | C | T | 1 | a0001c0005t0031 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1419C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 14/14 | 1419 | chr22 | 44207845 | ||||||
chr22:44207990 | T | C | 11 | a0001c0001t0004 a0001c0001t0029 a0001c0002t0028 others(8): Show |
60 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*1564T>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 14/14 | 1564 | chr22 | 44207990 | ||||||
chr22:44208099 | G | A | 1 | a0001c0002t0019 | 2 | NA18972.hp1 NA19062.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1673G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 14/14 | 1673 | chr22 | 44208099 | ||||||
chr22:44208325 | G | A | 1 | a0001c0003t0034 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1899G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 14/14 | 1899 | chr22 | 44208325 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:44181197 | C | T | 13 | a0001c0001t0002g0347 a0001c0001t0002g0350 a0001c0001t0002g0353 others(10): Show |
13 | HG01109.hp1 HG01884.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.-189+12C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 1/13 | chr22 | 44181197 | |||||||
chr22:44181206 | G | C | 24 | a0001c0001t0002g0041 a0001c0001t0002g0043 a0001c0001t0002g0044 others(21): Show |
24 | HG01109.hp1 HG01243.hp1 HG01433.hp1 others(21): Show |
intron_variant | MODIFIER | c.-189+21G>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 1/13 | chr22 | 44181206 | |||||||
chr22:44181221 | C | G | 1 | a0001c0001t0003g0358 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-189+36C>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 1/13 | chr22 | 44181221 | |||||||
chr22:44181255 | C | T | 1 | a0001c0002t0001g0345 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-189+70C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 1/13 | chr22 | 44181255 | |||||||
chr22:44181270 | G | T | 21 | a0001c0001t0002g0041 a0001c0001t0002g0043 a0001c0001t0002g0044 others(18): Show |
21 | HG01109.hp1 HG01243.hp1 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.-189+85G>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 1/13 | chr22 | 44181270 | |||||||
chr22:44181278 | G | A | 1 | a0001c0001t0002g0053 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-189+93G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 1/13 | chr22 | 44181278 | |||||||
chr22:44181280 | T | A | 29 | a0001c0001t0002g0041 a0001c0001t0002g0043 a0001c0001t0002g0044 others(26): Show |
30 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(27): Show |
intron_variant | MODIFIER | c.-189+95T>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 1/13 | chr22 | 44181280 | |||||||
chr22:44181296 | TCCTCCGA others(13): Show |
T | 3 | a0001c0001t0012g0058 a0001c0002t0005g0003 a0001c0002t0005g0015 |
8 | HG00423.hp1 NA18942.hp1 NA18955.hp1 others(5): Show |
intron_variant | MODIFIER | c.-189+116_-189+135d others(22): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr22 | 44181296 | ||||||
chr22:44181332 | G | C | 1 | a0001c0001t0035g0059 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-189+147G>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 1/13 | chr22 | 44181332 | |||||||
chr22:44181387 | T | A | 1 | a0001c0001t0035g0059 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-189+202T>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 1/13 | chr22 | 44181387 | |||||||
chr22:44181419 | G | T | 1 | a0001c0001t0035g0059 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-189+234G>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 1/13 | chr22 | 44181419 | |||||||
chr22:44181427 | T | G | 1 | a0001c0001t0035g0059 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-189+242T>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 1/13 | chr22 | 44181427 | |||||||
chr22:44181446 | G | GGTGGAGG others(5): Show |
1 | a0001c0001t0035g0059 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-189+261_-189+262i others(14): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 1/13 | chr22 | 44181446 | |||||||
chr22:44181451 | G | A | 1 | a0001c0001t0035g0059 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-189+266G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 1/13 | chr22 | 44181451 | |||||||
chr22:44181453 | A | G | 1 | a0001c0001t0035g0059 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-189+268A>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 1/13 | chr22 | 44181453 | |||||||
chr22:44181458 | G | T | 1 | a0001c0001t0035g0059 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-189+273G>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 1/13 | chr22 | 44181458 | |||||||
chr22:44181461 | T | A | 1 | a0001c0001t0035g0059 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-189+276T>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 1/13 | chr22 | 44181461 | |||||||
chr22:44181464 | A | T | 1 | a0001c0001t0035g0059 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-188-278A>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 1/13 | chr22 | 44181464 | |||||||
chr22:44181639 | G | C | 2 | a0001c0001t0002g0060 a0001c0005t0003g0061 |
2 | HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-188-103G>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 1/13 | chr22 | 44181639 | |||||||
chr22:44181698 | A | G | 1 | a0001c0002t0001g0344 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-188-44A>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 1/13 | chr22 | 44181698 | |||||||
chr22:44181725 | C | A | 1 | a0001c0013t0001g0062 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-188-17C>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 1/13 | chr22 | 44181725 | |||||||
chr22:44182090 | A | G | 1 | a0001c0001t0014g0348 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-13+173A>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 2/13 | chr22 | 44182090 | |||||||
chr22:44182151 | C | T | 3 | a0001c0001t0003g0356 a0001c0002t0001g0357 a0001c0003t0004g0355 |
3 | HG03098.hp1 NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-13+234C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 2/13 | chr22 | 44182151 | |||||||
chr22:44182162 | G | A | 1 | a0001c0002t0001g0346 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-13+245G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 2/13 | chr22 | 44182162 | |||||||
chr22:44182214 | C | T | 1 | a0001c0001t0033g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-13+297C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 2/13 | chr22 | 44182214 | |||||||
chr22:44182348 | A | ACGCCCAG others(33): Show |
1 | a0001c0001t0002g0063 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-13+432_-13+471dup others(40): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr22 | 44182348 | ||||||
chr22:44182408 | G | T | 2 | a0001c0005t0009g0014 a0001c0005t0009g0057 |
3 | HG01167.hp1 HG01169.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.-13+491G>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 2/13 | chr22 | 44182408 | |||||||
chr22:44182432 | C | T | 1 | a0001c0004t0004g0342 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-13+515C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 2/13 | chr22 | 44182432 | |||||||
chr22:44182608 | T | C | 1 | a0001c0001t0003g0064 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-13+691T>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 2/13 | chr22 | 44182608 | |||||||
chr22:44182618 | C | G | 7 | a0001c0001t0002g0350 a0001c0001t0002g0353 a0001c0001t0002g0354 others(4): Show |
7 | HG01884.hp1 HG02970.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.-12-700C>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 2/13 | chr22 | 44182618 | |||||||
chr22:44182667 | G | A | 1 | a0001c0001t0003g0065 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-12-651G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 2/13 | chr22 | 44182667 | |||||||
chr22:44182685 | G | A | 2 | a0001c0002t0001g0066 a0003c0007t0002g0067 |
2 | HG02055.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-12-633G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 2/13 | chr22 | 44182685 | |||||||
chr22:44182728 | G | A | 1 | a0001c0001t0002g0068 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-12-590G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 2/13 | chr22 | 44182728 | |||||||
chr22:44182759 | C | G | 37 | a0001c0001t0002g0063 a0001c0001t0002g0313 a0001c0001t0002g0314 others(34): Show |
41 | HG00408.hp1 HG00597.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.-12-559C>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 2/13 | chr22 | 44182759 | |||||||
chr22:44182901 | C | T | 1 | a0001c0001t0014g0348 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-12-417C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 2/13 | chr22 | 44182901 | |||||||
chr22:44182983 | T | TG | 32 | a0001c0001t0002g0017 a0001c0001t0002g0070 a0001c0001t0002g0072 others(29): Show |
40 | HG00597.hp2 HG00735.hp2 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.-12-329dupG | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr22 | 44182983 | ||||||
chr22:44183170 | G | A | 1 | a0001c0002t0005g0092 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-12-148G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 2/13 | chr22 | 44183170 | |||||||
chr22:44183182 | T | C | 1 | a0001c0001t0014g0348 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-12-136T>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 2/13 | chr22 | 44183182 | |||||||
chr22:44183513 | C | T | 1 | a0007c0009t0003g0091 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.79+105C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 3/13 | chr22 | 44183513 | |||||||
chr22:44183620 | C | A | 20 | a0001c0001t0002g0018 a0001c0001t0002g0041 a0001c0001t0002g0043 others(17): Show |
21 | HG01243.hp1 HG01433.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.79+212C>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 3/13 | chr22 | 44183620 | |||||||
chr22:44183815 | G | A | 133 | a0001c0001t0002g0018 a0001c0001t0002g0021 a0001c0001t0002g0041 others(130): Show |
155 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.79+407G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 3/13 | chr22 | 44183815 | |||||||
chr22:44183856 | T | C | 133 | a0001c0001t0002g0018 a0001c0001t0002g0021 a0001c0001t0002g0041 others(130): Show |
155 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.79+448T>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 3/13 | chr22 | 44183856 | |||||||
chr22:44183875 | C | T | 1 | a0003c0007t0002g0161 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.79+467C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 3/13 | chr22 | 44183875 | |||||||
chr22:44183911 | G | T | 5 | a0001c0001t0002g0047 a0001c0001t0003g0045 a0001c0001t0003g0046 others(2): Show |
5 | HG01243.hp1 HG02257.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+503G>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 3/13 | chr22 | 44183911 | |||||||
chr22:44183927 | G | A | 1 | a0001c0001t0014g0348 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.79+519G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 3/13 | chr22 | 44183927 | |||||||
chr22:44183951 | C | T | 132 | a0001c0001t0002g0018 a0001c0001t0002g0021 a0001c0001t0002g0041 others(129): Show |
154 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.79+543C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 3/13 | chr22 | 44183951 | |||||||
chr22:44184002 | C | T | 1 | a0001c0001t0002g0308 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.79+594C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 3/13 | chr22 | 44184002 | |||||||
chr22:44184003 | G | A | 1 | a0001c0001t0003g0162 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.79+595G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 3/13 | chr22 | 44184003 | |||||||
chr22:44184031 | G | A | 1 | a0001c0012t0001g0100 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.79+623G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 3/13 | chr22 | 44184031 | |||||||
chr22:44184177 | C | T | 1 | a0001c0001t0007g0160 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.79+769C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 3/13 | chr22 | 44184177 | |||||||
chr22:44184269 | A | G | 9 | a0001c0001t0002g0301 a0001c0001t0002g0304 a0001c0001t0002g0305 others(6): Show |
9 | HG00642.hp2 HG01106.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.79+861A>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 3/13 | chr22 | 44184269 | |||||||
chr22:44184381 | C | T | 86 | a0001c0001t0002g0021 a0001c0001t0002g0041 a0001c0001t0002g0043 others(83): Show |
94 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.79+973C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 3/13 | chr22 | 44184381 | |||||||
chr22:44184467 | T | C | 1 | a0001c0001t0014g0348 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.79+1059T>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 3/13 | chr22 | 44184467 | |||||||
chr22:44184469 | G | A | 3 | a0001c0001t0002g0347 a0001c0001t0003g0349 a0001c0002t0001g0346 |
3 | HG01109.hp1 HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.79+1061G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 3/13 | chr22 | 44184469 | |||||||
chr22:44184497 | C | T | 3 | a0001c0001t0002g0347 a0001c0001t0003g0349 a0001c0002t0001g0346 |
3 | HG01109.hp1 HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.79+1089C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 3/13 | chr22 | 44184497 | |||||||
chr22:44184527 | C | T | 1 | a0001c0003t0003g0300 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.79+1119C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 3/13 | chr22 | 44184527 | |||||||
chr22:44184552 | C | T | 3 | a0001c0001t0002g0347 a0001c0001t0003g0349 a0001c0002t0001g0346 |
3 | HG01109.hp1 HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.79+1144C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 3/13 | chr22 | 44184552 | |||||||
chr22:44184586 | G | A | 1 | a0001c0001t0010g0093 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.79+1178G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 3/13 | chr22 | 44184586 | |||||||
chr22:44184590 | C | T | 64 | a0001c0001t0002g0021 a0001c0001t0002g0063 a0001c0001t0002g0141 others(61): Show |
72 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.79+1182C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 3/13 | chr22 | 44184590 | |||||||
chr22:44184907 | A | G | 307 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(304): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.80-901A>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 3/13 | chr22 | 44184907 | |||||||
chr22:44184908 | T | A | 307 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(304): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.80-900T>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 3/13 | chr22 | 44184908 | |||||||
chr22:44185038 | C | T | 1 | a0001c0001t0002g0140 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.80-770C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 3/13 | chr22 | 44185038 | |||||||
chr22:44185056 | A | G | 41 | a0001c0001t0002g0038 a0001c0001t0002g0086 a0001c0001t0002g0295 others(38): Show |
54 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.80-752A>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 3/13 | chr22 | 44185056 | |||||||
chr22:44185091 | A | G | 1 | a0001c0001t0002g0080 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.80-717A>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 3/13 | chr22 | 44185091 | |||||||
chr22:44185102 | C | T | 2 | a0001c0001t0007g0116 a0001c0003t0004g0294 |
2 | HG02630.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.80-706C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 3/13 | chr22 | 44185102 | |||||||
chr22:44185166 | C | T | 283 | a0001c0001t0002g0006 a0001c0001t0002g0017 a0001c0001t0002g0018 others(280): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.80-642C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 3/13 | chr22 | 44185166 | |||||||
chr22:44185241 | T | C | 1 | a0001c0001t0011g0209 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.80-567T>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 3/13 | chr22 | 44185241 | |||||||
chr22:44185264 | C | A | 1 | a0001c0001t0033g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.80-544C>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 3/13 | chr22 | 44185264 | |||||||
chr22:44185270 | A | G | 1 | a0001c0003t0007g0115 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.80-538A>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 3/13 | chr22 | 44185270 | |||||||
chr22:44185310 | G | A | 1 | a0001c0001t0033g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.80-498G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 3/13 | chr22 | 44185310 | |||||||
chr22:44185406 | T | C | 2 | a0001c0004t0004g0302 a0001c0004t0006g0117 |
2 | HG01099.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.80-402T>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 3/13 | chr22 | 44185406 | |||||||
chr22:44185409 | G | A | 1 | a0001c0002t0001g0337 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.80-399G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 3/13 | chr22 | 44185409 | |||||||
chr22:44185445 | A | G | 1 | a0001c0001t0027g0341 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.80-363A>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 3/13 | chr22 | 44185445 | |||||||
chr22:44185490 | C | G | 1 | a0001c0001t0002g0297 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.80-318C>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 3/13 | chr22 | 44185490 | |||||||
chr22:44185523 | A | G | 110 | a0001c0001t0002g0041 a0001c0001t0002g0053 a0001c0001t0002g0063 others(107): Show |
127 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.80-285A>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 3/13 | chr22 | 44185523 | |||||||
chr22:44185544 | T | C | 1 | a0001c0001t0016g0210 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.80-264T>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 3/13 | chr22 | 44185544 | |||||||
chr22:44185596 | A | G | 1 | a0001c0001t0007g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.80-212A>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 3/13 | chr22 | 44185596 | |||||||
chr22:44185603 | A | C | 1 | a0001c0002t0001g0066 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.80-205A>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 3/13 | chr22 | 44185603 | |||||||
chr22:44185669 | G | A | 97 | a0001c0001t0002g0053 a0001c0001t0002g0063 a0001c0001t0002g0078 others(94): Show |
112 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.80-139G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 3/13 | chr22 | 44185669 | |||||||
chr22:44185718 | C | T | 6 | a0001c0001t0002g0308 a0001c0001t0007g0109 a0001c0001t0007g0110 others(3): Show |
6 | HG01891.hp1 HG02258.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.80-90C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 3/13 | chr22 | 44185718 | |||||||
chr22:44185930 | G | A | 1 | a0001c0002t0001g0163 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.144+58G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 4/13 | chr22 | 44185930 | |||||||
chr22:44185943 | C | T | 2 | a0001c0001t0002g0339 a0001c0001t0009g0051 |
2 | HG02109.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.144+71C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 4/13 | chr22 | 44185943 | |||||||
chr22:44185983 | G | T | 1 | a0001c0001t0016g0210 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.144+111G>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 4/13 | chr22 | 44185983 | |||||||
chr22:44186015 | C | T | 3 | a0001c0001t0003g0200 a0001c0001t0012g0105 a0001c0001t0014g0108 |
3 | HG01496.hp1 HG01934.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.144+143C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 4/13 | chr22 | 44186015 | |||||||
chr22:44186209 | C | A | 1 | a0001c0001t0002g0214 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.144+337C>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 4/13 | chr22 | 44186209 | |||||||
chr22:44186211 | C | T | 2 | a0001c0002t0001g0049 a0001c0002t0001g0292 |
2 | HG01433.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.144+339C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 4/13 | chr22 | 44186211 | |||||||
chr22:44186212 | G | A | 4 | a0001c0001t0010g0093 a0001c0005t0002g0216 a0001c0005t0003g0316 others(1): Show |
4 | HG02723.hp2 HG02886.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.144+340G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 4/13 | chr22 | 44186212 | |||||||
chr22:44186225 | G | A | 110 | a0001c0001t0002g0063 a0001c0001t0002g0078 a0001c0001t0002g0080 others(107): Show |
134 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.144+353G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 4/13 | chr22 | 44186225 | |||||||
chr22:44186256 | G | A | 30 | a0001c0001t0009g0150 a0001c0001t0029g0340 a0001c0003t0003g0300 others(27): Show |
36 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(33): Show |
intron_variant | MODIFIER | c.144+384G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 4/13 | chr22 | 44186256 | |||||||
chr22:44186384 | G | A | 81 | a0001c0001t0001g0168 a0001c0001t0002g0006 a0001c0001t0002g0009 others(78): Show |
98 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.144+512G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 4/13 | chr22 | 44186384 | |||||||
chr22:44186388 | C | A | 2 | a0001c0001t0007g0124 a0001c0001t0016g0210 |
2 | HG02922.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.144+516C>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 4/13 | chr22 | 44186388 | |||||||
chr22:44186411 | T | G | 2 | a0001c0004t0006g0019 a0001c0004t0006g0125 |
3 | HG00544.hp1 HG02015.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.144+539T>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 4/13 | chr22 | 44186411 | |||||||
chr22:44186448 | C | T | 2 | a0001c0001t0010g0093 a0001c0005t0003g0061 |
2 | HG03041.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.144+576C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 4/13 | chr22 | 44186448 | |||||||
chr22:44186455 | G | A | 3 | a0002c0006t0002g0052 a0002c0006t0002g0250 a0002c0006t0002g0251 |
3 | HG02886.hp2 HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.144+583G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 4/13 | chr22 | 44186455 | |||||||
chr22:44186554 | C | T | 5 | a0001c0001t0010g0093 a0001c0005t0002g0216 a0001c0005t0003g0061 others(2): Show |
5 | HG02723.hp2 HG02886.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.144+682C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 4/13 | chr22 | 44186554 | |||||||
chr22:44186619 | T | C | 291 | a0001c0001t0001g0168 a0001c0001t0002g0006 a0001c0001t0002g0009 others(288): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.144+747T>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 4/13 | chr22 | 44186619 | |||||||
chr22:44186631 | C | T | 6 | a0001c0001t0007g0109 a0001c0001t0007g0110 a0001c0001t0025g0104 others(3): Show |
6 | HG01891.hp1 HG02647.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.144+759C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 4/13 | chr22 | 44186631 | |||||||
chr22:44186684 | G | A | 1 | a0001c0003t0004g0312 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.144+812G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 4/13 | chr22 | 44186684 | |||||||
chr22:44186685 | C | G | 1 | a0001c0003t0004g0312 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.144+813C>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 4/13 | chr22 | 44186685 | |||||||
chr22:44186870 | G | C | 5 | a0001c0001t0010g0093 a0001c0005t0002g0216 a0001c0005t0003g0061 others(2): Show |
5 | HG02723.hp2 HG02886.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.145-906G>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 4/13 | chr22 | 44186870 | |||||||
chr22:44186935 | G | A | 2 | a0001c0002t0001g0049 a0001c0002t0001g0292 |
2 | HG01433.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.145-841G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 4/13 | chr22 | 44186935 | |||||||
chr22:44186940 | T | G | 132 | a0001c0001t0002g0018 a0001c0001t0002g0063 a0001c0001t0002g0068 others(129): Show |
157 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.145-836T>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 4/13 | chr22 | 44186940 | |||||||
chr22:44187013 | G | A | 2 | a0001c0002t0001g0049 a0001c0002t0001g0292 |
2 | HG01433.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.145-763G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 4/13 | chr22 | 44187013 | |||||||
chr22:44187049 | A | C | 196 | a0001c0001t0002g0018 a0001c0001t0002g0033 a0001c0001t0002g0047 others(193): Show |
231 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.145-727A>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 4/13 | chr22 | 44187049 | |||||||
chr22:44187316 | T | C | 12 | a0001c0001t0002g0053 a0001c0001t0002g0308 a0001c0001t0003g0254 others(9): Show |
12 | HG01891.hp1 HG02258.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.145-460T>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 4/13 | chr22 | 44187316 | |||||||
chr22:44187327 | G | A | 1 | a0001c0002t0001g0334 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.145-449G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 4/13 | chr22 | 44187327 | |||||||
chr22:44187366 | A | C | 281 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(278): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.145-410A>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 4/13 | chr22 | 44187366 | |||||||
chr22:44187494 | T | C | 1 | a0001c0001t0027g0341 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.145-282T>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 4/13 | chr22 | 44187494 | |||||||
chr22:44187553 | C | T | 2 | a0001c0002t0001g0094 a0001c0002t0001g0288 |
2 | HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.145-223C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 4/13 | chr22 | 44187553 | |||||||
chr22:44187555 | G | A | 5 | a0001c0001t0002g0053 a0001c0001t0003g0254 a0001c0001t0003g0356 others(2): Show |
5 | HG02809.hp1 HG02965.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.145-221G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 4/13 | chr22 | 44187555 | |||||||
chr22:44187596 | C | A | 3 | a0001c0001t0002g0028 a0001c0001t0002g0225 a0001c0002t0001g0226 |
4 | NA18971.hp2 NA18973.hp2 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.145-180C>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 4/13 | chr22 | 44187596 | |||||||
chr22:44187679 | T | C | 3 | a0001c0001t0002g0295 a0001c0002t0001g0175 a0001c0002t0005g0131 |
3 | HG03491.hp2 HG03927.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.145-97T>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 4/13 | chr22 | 44187679 | |||||||
chr22:44187691 | G | A | 3 | a0001c0001t0003g0200 a0001c0001t0012g0105 a0001c0001t0014g0108 |
3 | HG01496.hp1 HG01934.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.145-85G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 4/13 | chr22 | 44187691 | |||||||
chr22:44187770 | C | T | 2 | a0001c0001t0018g0096 a0001c0001t0018g0351 |
2 | HG02809.hp2 HG03471.hp2 |
splice_region_variant&intron_variant | LOW | c.145-6C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 4/13 | chr22 | 44187770 | |||||||
chr22:44187984 | C | T | 2 | a0001c0002t0001g0049 a0001c0002t0001g0292 |
2 | HG01433.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.247+106C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 5/13 | chr22 | 44187984 | |||||||
chr22:44188010 | T | A | 1 | a0001c0001t0002g0060 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.247+132T>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 5/13 | chr22 | 44188010 | |||||||
chr22:44188180 | G | A | 2 | a0001c0003t0004g0294 a0001c0003t0024g0219 |
2 | HG00280.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.247+302G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 5/13 | chr22 | 44188180 | |||||||
chr22:44188278 | T | C | 288 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(285): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.247+400T>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 5/13 | chr22 | 44188278 | |||||||
chr22:44188365 | T | C | 1 | a0001c0001t0003g0073 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.247+487T>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 5/13 | chr22 | 44188365 | |||||||
chr22:44188382 | A | C | 1 | a0001c0005t0002g0216 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.247+504A>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 5/13 | chr22 | 44188382 | |||||||
chr22:44188497 | G | A | 30 | a0001c0001t0002g0197 a0001c0002t0001g0034 a0001c0002t0001g0035 others(27): Show |
39 | HG00621.hp2 HG02027.hp2 HG02056.hp2 others(36): Show |
intron_variant | MODIFIER | c.248-617G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 5/13 | chr22 | 44188497 | |||||||
chr22:44188977 | C | G | 216 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(213): Show |
258 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(255): Show |
intron_variant | MODIFIER | c.248-137C>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 5/13 | chr22 | 44188977 | |||||||
chr22:44188977 | C | T | 3 | a0001c0001t0027g0341 a0001c0002t0001g0049 a0001c0002t0001g0292 |
3 | HG01433.hp1 HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.248-137C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 5/13 | chr22 | 44188977 | |||||||
chr22:44189079 | G | A | 1 | a0001c0001t0003g0099 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.248-35G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 5/13 | chr22 | 44189079 | |||||||
chr22:44189107 | C | T | 1 | a0001c0001t0027g0341 | 1 | HG03130.hp1 | splice_region_variant&intron_variant | LOW | c.248-7C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 5/13 | chr22 | 44189107 | |||||||
chr22:44189587 | G | A | 5 | a0001c0005t0002g0216 a0001c0005t0003g0061 a0001c0005t0003g0298 others(2): Show |
5 | HG02723.hp2 HG02886.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.388+333G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 6/13 | chr22 | 44189587 | |||||||
chr22:44189641 | G | A | 65 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(62): Show |
78 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.388+387G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 6/13 | chr22 | 44189641 | |||||||
chr22:44189649 | T | G | 278 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(275): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.388+395T>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 6/13 | chr22 | 44189649 | |||||||
chr22:44189656 | C | T | 1 | a0001c0002t0005g0113 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.388+402C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 6/13 | chr22 | 44189656 | |||||||
chr22:44189682 | C | T | 1 | a0001c0002t0001g0283 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.388+428C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 6/13 | chr22 | 44189682 | |||||||
chr22:44190019 | T | A | 132 | a0001c0001t0002g0018 a0001c0001t0002g0053 a0001c0001t0002g0063 others(129): Show |
157 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.389-532T>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 6/13 | chr22 | 44190019 | |||||||
chr22:44190053 | T | C | 1 | a0001c0001t0014g0107 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.389-498T>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 6/13 | chr22 | 44190053 | |||||||
chr22:44190061 | A | G | 137 | a0001c0001t0002g0018 a0001c0001t0002g0053 a0001c0001t0002g0063 others(134): Show |
162 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.389-490A>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 6/13 | chr22 | 44190061 | |||||||
chr22:44190078 | A | C | 103 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(100): Show |
119 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.389-473A>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 6/13 | chr22 | 44190078 | |||||||
chr22:44190104 | G | A | 1 | a0001c0001t0027g0341 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.389-447G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 6/13 | chr22 | 44190104 | |||||||
chr22:44190196 | A | C | 1 | a0001c0001t0002g0266 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.389-355A>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 6/13 | chr22 | 44190196 | |||||||
chr22:44190237 | T | C | 21 | a0001c0001t0002g0043 a0001c0001t0002g0050 a0001c0001t0002g0353 others(18): Show |
21 | HG01243.hp1 HG01243.hp2 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.389-314T>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 6/13 | chr22 | 44190237 | |||||||
chr22:44190340 | C | T | 1 | a0001c0001t0021g0248 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.389-211C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 6/13 | chr22 | 44190340 | |||||||
chr22:44190484 | A | T | 1 | a0001c0002t0001g0175 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.389-67A>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 6/13 | chr22 | 44190484 | |||||||
chr22:44190798 | A | G | 1 | a0001c0001t0003g0282 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.504+132A>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 7/13 | chr22 | 44190798 | |||||||
chr22:44190925 | G | A | 44 | a0001c0001t0025g0104 a0001c0001t0027g0341 a0001c0002t0001g0049 others(41): Show |
50 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.504+259G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 7/13 | chr22 | 44190925 | |||||||
chr22:44191005 | T | G | 2 | a0001c0001t0002g0033 a0001c0004t0004g0342 |
3 | HG00609.hp1 NA18953.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.504+339T>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 7/13 | chr22 | 44191005 | |||||||
chr22:44191235 | G | A | 1 | a0001c0001t0002g0229 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.504+569G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 7/13 | chr22 | 44191235 | |||||||
chr22:44191338 | G | A | 1 | a0001c0004t0004g0342 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.504+672G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 7/13 | chr22 | 44191338 | |||||||
chr22:44191353 | G | A | 1 | a0001c0005t0009g0057 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.504+687G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 7/13 | chr22 | 44191353 | |||||||
chr22:44191388 | A | AT | 171 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(168): Show |
206 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(203): Show |
intron_variant | MODIFIER | c.505-634dupT | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr22 | 44191388 | ||||||
chr22:44191388 | A | ATT | 30 | a0001c0001t0002g0078 a0001c0001t0002g0140 a0001c0001t0002g0170 others(27): Show |
33 | HG00423.hp2 HG00597.hp1 HG01106.hp2 others(30): Show |
intron_variant | MODIFIER | c.505-635_505-634dup others(2): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr22 | 44191388 | ||||||
chr22:44191388 | AT | A | 27 | a0001c0001t0003g0164 a0001c0001t0010g0262 a0001c0001t0012g0105 others(24): Show |
29 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.505-634delT | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr22 | 44191388 | ||||||
chr22:44191388 | ATT | A | 5 | a0001c0003t0004g0145 a0001c0003t0004g0146 a0001c0003t0004g0201 others(2): Show |
6 | HG00140.hp2 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.505-635_505-634del others(2): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr22 | 44191388 | ||||||
chr22:44191388 | ATTTTTTT others(2): Show |
A | 7 | a0001c0001t0002g0053 a0001c0001t0002g0308 a0001c0001t0007g0109 others(4): Show |
7 | HG01891.hp1 HG02258.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.505-642_505-634del others(9): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr22 | 44191388 | ||||||
chr22:44191388 | ATTTTTTT others(7): Show |
A | 1 | a0001c0001t0002g0021 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.505-647_505-634del others(14): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr22 | 44191388 | ||||||
chr22:44191537 | A | G | 1 | a0001c0001t0002g0060 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.505-512A>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 7/13 | chr22 | 44191537 | |||||||
chr22:44191628 | A | G | 3 | a0002c0006t0002g0052 a0002c0006t0002g0250 a0002c0006t0002g0251 |
3 | HG02886.hp2 HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.505-421A>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 7/13 | chr22 | 44191628 | |||||||
chr22:44191967 | C | T | 4 | a0001c0001t0002g0047 a0001c0001t0002g0315 a0001c0001t0007g0124 others(1): Show |
4 | HG02622.hp1 HG02895.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.505-82C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 7/13 | chr22 | 44191967 | |||||||
chr22:44192044 | C | G | 1 | a0001c0002t0001g0293 | 1 | HG03139.hp2 | splice_region_variant&intron_variant | LOW | c.505-5C>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 7/13 | chr22 | 44192044 | |||||||
chr22:44192160 | G | A | 2 | a0001c0001t0018g0096 a0001c0001t0018g0351 |
2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.560+56G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 8/13 | chr22 | 44192160 | |||||||
chr22:44192325 | G | C | 3 | a0001c0002t0001g0027 a0001c0002t0001g0094 a0001c0002t0001g0288 |
4 | HG00733.hp1 HG01346.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.560+221G>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 8/13 | chr22 | 44192325 | |||||||
chr22:44192436 | A | G | 2 | a0001c0003t0004g0294 a0001c0003t0024g0219 |
2 | HG00280.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.560+332A>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 8/13 | chr22 | 44192436 | |||||||
chr22:44192480 | C | T | 1 | a0001c0001t0003g0074 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.560+376C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 8/13 | chr22 | 44192480 | |||||||
chr22:44192535 | T | C | 358 | a0001c0001t0001g0168 a0001c0001t0002g0006 a0001c0001t0002g0009 others(355): Show |
419 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(416): Show |
intron_variant | MODIFIER | c.560+431T>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 8/13 | chr22 | 44192535 | |||||||
chr22:44192579 | T | C | 61 | a0001c0001t0002g0033 a0001c0001t0003g0233 a0001c0001t0004g0154 others(58): Show |
72 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.560+475T>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 8/13 | chr22 | 44192579 | |||||||
chr22:44192626 | C | T | 2 | a0001c0002t0001g0035 a0001c0002t0005g0136 |
3 | NA18974.hp1 NA18977.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.560+522C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 8/13 | chr22 | 44192626 | |||||||
chr22:44192645 | C | A | 1 | a0001c0004t0026g0127 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.560+541C>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 8/13 | chr22 | 44192645 | |||||||
chr22:44192767 | G | T | 2 | a0001c0001t0007g0138 a0001c0001t0007g0139 |
2 | NA19010.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.560+663G>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 8/13 | chr22 | 44192767 | |||||||
chr22:44192916 | G | T | 86 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(83): Show |
102 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.560+812G>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 8/13 | chr22 | 44192916 | |||||||
chr22:44192942 | T | C | 1 | a0001c0001t0004g0235 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.560+838T>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 8/13 | chr22 | 44192942 | |||||||
chr22:44193128 | T | C | 85 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(82): Show |
101 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.561-673T>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 8/13 | chr22 | 44193128 | |||||||
chr22:44193221 | CA | C | 87 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(84): Show |
103 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.561-570delA | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr22 | 44193221 | ||||||
chr22:44193483 | G | A | 5 | a0001c0002t0001g0085 a0001c0002t0001g0272 a0001c0002t0001g0273 others(2): Show |
6 | NA18942.hp1 NA18959.hp1 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.561-318G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 8/13 | chr22 | 44193483 | |||||||
chr22:44193493 | G | A | 4 | a0001c0005t0003g0061 a0001c0005t0003g0298 a0001c0005t0003g0316 others(1): Show |
4 | HG02723.hp2 HG02897.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.561-308G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 8/13 | chr22 | 44193493 | |||||||
chr22:44193856 | C | T | 7 | a0001c0001t0002g0308 a0001c0001t0007g0109 a0001c0001t0007g0110 others(4): Show |
7 | HG01891.hp1 HG02258.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.583+33C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 9/13 | chr22 | 44193856 | |||||||
chr22:44193868 | G | A | 1 | a0001c0001t0029g0340 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.583+45G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 9/13 | chr22 | 44193868 | |||||||
chr22:44193977 | T | G | 195 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(192): Show |
235 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(232): Show |
intron_variant | MODIFIER | c.583+154T>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 9/13 | chr22 | 44193977 | |||||||
chr22:44193981 | G | A | 3 | a0001c0001t0002g0078 a0001c0001t0002g0140 a0001c0001t0002g0141 |
3 | HG02109.hp2 HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.583+158G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 9/13 | chr22 | 44193981 | |||||||
chr22:44194128 | C | T | 2 | a0001c0001t0018g0096 a0001c0001t0018g0351 |
2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.583+305C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 9/13 | chr22 | 44194128 | |||||||
chr22:44194173 | G | A | 1 | a0001c0001t0004g0245 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.583+350G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 9/13 | chr22 | 44194173 | |||||||
chr22:44194190 | TCTATAAA others(11): Show |
T | 3 | a0001c0001t0018g0096 a0001c0001t0018g0351 a0001c0001t0033g0343 |
3 | HG02809.hp2 HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.583+370_583+387del others(18): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr22 | 44194190 | ||||||
chr22:44194251 | T | A | 4 | a0001c0005t0003g0061 a0001c0005t0003g0298 a0001c0005t0003g0316 others(1): Show |
4 | HG02723.hp2 HG02897.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.583+428T>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 9/13 | chr22 | 44194251 | |||||||
chr22:44194406 | C | T | 1 | a0001c0003t0004g0146 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.583+583C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 9/13 | chr22 | 44194406 | |||||||
chr22:44194490 | C | T | 1 | a0001c0001t0002g0068 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.583+667C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 9/13 | chr22 | 44194490 | |||||||
chr22:44194533 | A | G | 28 | a0001c0001t0002g0018 a0001c0001t0002g0047 a0001c0001t0002g0053 others(25): Show |
29 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.583+710A>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 9/13 | chr22 | 44194533 | |||||||
chr22:44194617 | A | G | 4 | a0001c0005t0003g0061 a0001c0005t0003g0298 a0001c0005t0003g0316 others(1): Show |
4 | HG02723.hp2 HG02897.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.583+794A>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 9/13 | chr22 | 44194617 | |||||||
chr22:44194667 | T | TATCC | 15 | a0001c0001t0002g0060 a0001c0001t0002g0068 a0001c0001t0002g0308 others(12): Show |
15 | HG01891.hp1 HG02258.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.583+866_583+869dup others(4): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr22 | 44194667 | ||||||
chr22:44194702 | C | T | 4 | a0001c0005t0003g0061 a0001c0005t0003g0298 a0001c0005t0003g0316 others(1): Show |
4 | HG02723.hp2 HG02897.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.583+879C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 9/13 | chr22 | 44194702 | |||||||
chr22:44194709 | C | T | 7 | a0001c0001t0018g0096 a0001c0001t0018g0351 a0001c0001t0033g0343 others(4): Show |
7 | HG02723.hp2 HG02809.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.583+886C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 9/13 | chr22 | 44194709 | |||||||
chr22:44194714 | TCATCCAT others(1): Show |
T | 7 | a0001c0001t0018g0096 a0001c0001t0018g0351 a0001c0001t0033g0343 others(4): Show |
7 | HG02723.hp2 HG02809.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.583+901_583+908del others(8): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr22 | 44194714 | ||||||
chr22:44194728 | ATCCC | A | 6 | a0001c0003t0004g0005 a0001c0003t0004g0147 a0001c0003t0004g0149 others(3): Show |
9 | HG00323.hp1 HG00642.hp1 HG00733.hp2 others(6): Show |
intron_variant | MODIFIER | c.583+909_583+912del others(4): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr22 | 44194728 | ||||||
chr22:44194732 | C | A | 1 | a0001c0003t0004g0303 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.583+909C>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 9/13 | chr22 | 44194732 | |||||||
chr22:44194767 | C | T | 2 | a0001c0001t0001g0168 a0001c0002t0023g0167 |
2 | HG03704.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.583+944C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 9/13 | chr22 | 44194767 | |||||||
chr22:44194788 | T | C | 1 | a0001c0001t0033g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.583+965T>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 9/13 | chr22 | 44194788 | |||||||
chr22:44194825 | T | TCATC | 3 | a0001c0001t0003g0075 a0001c0001t0018g0096 a0001c0001t0018g0351 |
3 | HG02809.hp2 HG03471.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.583+1019_583+1022d others(6): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr22 | 44194825 | ||||||
chr22:44194825 | T | TCATCCAT others(5): Show |
1 | a0001c0001t0033g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.583+1011_583+1022d others(14): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr22 | 44194825 | ||||||
chr22:44194842 | CATCT | C | 5 | a0001c0002t0005g0113 a0001c0005t0003g0061 a0001c0005t0003g0298 others(2): Show |
5 | HG02071.hp1 HG02723.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.583+1023_583+1026d others(6): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr22 | 44194842 | ||||||
chr22:44194846 | T | C | 132 | a0001c0001t0002g0018 a0001c0001t0002g0047 a0001c0001t0002g0060 others(129): Show |
159 | HG00099.hp1 HG00423.hp1 HG00544.hp2 others(156): Show |
intron_variant | MODIFIER | c.583+1023T>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 9/13 | chr22 | 44194846 | |||||||
chr22:44194847 | A | G | 1 | a0001c0001t0010g0262 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.583+1024A>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 9/13 | chr22 | 44194847 | |||||||
chr22:44195074 | C | T | 3 | a0001c0001t0025g0104 a0001c0002t0001g0049 a0001c0002t0001g0292 |
3 | HG01433.hp1 HG02451.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.584-1081C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 9/13 | chr22 | 44195074 | |||||||
chr22:44195112 | G | A | 56 | a0001c0001t0002g0236 a0001c0001t0003g0233 a0001c0002t0001g0307 others(53): Show |
66 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(63): Show |
intron_variant | MODIFIER | c.584-1043G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 9/13 | chr22 | 44195112 | |||||||
chr22:44195235 | C | T | 1 | a0001c0004t0004g0213 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.584-920C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 9/13 | chr22 | 44195235 | |||||||
chr22:44195280 | A | C | 1 | a0001c0001t0025g0104 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.584-875A>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 9/13 | chr22 | 44195280 | |||||||
chr22:44195526 | G | A | 3 | a0002c0006t0002g0052 a0002c0006t0002g0250 a0002c0006t0002g0251 |
3 | HG02886.hp2 HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.584-629G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 9/13 | chr22 | 44195526 | |||||||
chr22:44195554 | G | C | 2 | a0001c0001t0003g0046 a0001c0001t0003g0065 |
2 | HG02717.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.584-601G>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 9/13 | chr22 | 44195554 | |||||||
chr22:44195882 | C | G | 5 | a0001c0002t0001g0357 a0001c0005t0003g0061 a0001c0005t0003g0298 others(2): Show |
5 | HG02723.hp2 HG02897.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.584-273C>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 9/13 | chr22 | 44195882 | |||||||
chr22:44195980 | C | T | 1 | a0001c0001t0014g0108 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.584-175C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 9/13 | chr22 | 44195980 | |||||||
chr22:44196311 | C | T | 1 | a0001c0001t0032g0206 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.643-36C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 10/13 | chr22 | 44196311 | |||||||
chr22:44196431 | C | T | 1 | a0001c0001t0002g0053 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.711+16C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 11/13 | chr22 | 44196431 | |||||||
chr22:44196514 | G | T | 2 | a0001c0004t0006g0019 a0001c0004t0006g0125 |
3 | HG00544.hp1 HG02015.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.711+99G>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 11/13 | chr22 | 44196514 | |||||||
chr22:44196523 | AC | A | 4 | a0001c0002t0001g0022 a0001c0002t0001g0023 a0001c0002t0001g0024 others(1): Show |
7 | HG01074.hp2 HG01433.hp2 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.711+110delC | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr22 | 44196523 | ||||||
chr22:44196530 | G | A | 3 | a0002c0006t0002g0052 a0002c0006t0002g0250 a0002c0006t0002g0251 |
3 | HG02886.hp2 HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.711+115G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 11/13 | chr22 | 44196530 | |||||||
chr22:44196553 | G | A | 1 | a0001c0002t0001g0357 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.711+138G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 11/13 | chr22 | 44196553 | |||||||
chr22:44196578 | A | G | 11 | a0001c0001t0002g0041 a0001c0001t0002g0044 a0001c0001t0002g0265 others(8): Show |
11 | HG02109.hp1 HG02280.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.711+163A>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 11/13 | chr22 | 44196578 | |||||||
chr22:44196606 | C | CG | 143 | a0001c0001t0002g0018 a0001c0001t0002g0033 a0001c0001t0002g0043 others(140): Show |
171 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(168): Show |
intron_variant | MODIFIER | c.711+196dupG | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr22 | 44196606 | ||||||
chr22:44196606 | C | CGG | 67 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(64): Show |
82 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.711+195_711+196dup others(2): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr22 | 44196606 | ||||||
chr22:44196607 | G | A | 2 | a0001c0002t0001g0049 a0001c0002t0001g0292 |
2 | HG01433.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.711+192G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 11/13 | chr22 | 44196607 | |||||||
chr22:44196612 | T | G | 216 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(213): Show |
259 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.711+197T>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 11/13 | chr22 | 44196612 | |||||||
chr22:44196866 | T | C | 1 | a0001c0001t0002g0313 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.711+451T>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 11/13 | chr22 | 44196866 | |||||||
chr22:44196992 | G | C | 1 | a0001c0003t0004g0149 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.711+577G>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 11/13 | chr22 | 44196992 | |||||||
chr22:44197000 | GGTGCACA others(22): Show |
G | 1 | a0001c0003t0004g0149 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.711+587_711+615del others(29): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr22 | 44197000 | ||||||
chr22:44197016 | C | G | 5 | a0001c0002t0001g0357 a0001c0005t0003g0061 a0001c0005t0003g0298 others(2): Show |
5 | HG02723.hp2 HG02897.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.711+601C>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 11/13 | chr22 | 44197016 | |||||||
chr22:44197182 | G | A | 1 | a0001c0001t0002g0353 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.711+767G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 11/13 | chr22 | 44197182 | |||||||
chr22:44197291 | A | G | 2 | a0001c0001t0007g0109 a0001c0001t0007g0110 |
2 | HG01891.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.711+876A>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 11/13 | chr22 | 44197291 | |||||||
chr22:44197391 | A | C | 1 | a0001c0002t0001g0328 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.711+976A>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 11/13 | chr22 | 44197391 | |||||||
chr22:44197442 | A | G | 1 | a0001c0001t0002g0021 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.711+1027A>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 11/13 | chr22 | 44197442 | |||||||
chr22:44197608 | C | G | 52 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0016 others(49): Show |
65 | HG00099.hp1 HG00735.hp2 HG00738.hp1 others(62): Show |
intron_variant | MODIFIER | c.712-1013C>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 11/13 | chr22 | 44197608 | |||||||
chr22:44197665 | C | G | 1 | a0001c0003t0004g0026 | 2 | NA18964.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.712-956C>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 11/13 | chr22 | 44197665 | |||||||
chr22:44197669 | G | A | 4 | a0001c0001t0025g0104 a0001c0001t0029g0340 a0001c0002t0001g0049 others(1): Show |
4 | HG01433.hp1 HG02451.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.712-952G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 11/13 | chr22 | 44197669 | |||||||
chr22:44197691 | A | G | 1 | a0001c0001t0003g0279 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.712-930A>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 11/13 | chr22 | 44197691 | |||||||
chr22:44197743 | A | T | 1 | a0001c0002t0001g0311 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.712-878A>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 11/13 | chr22 | 44197743 | |||||||
chr22:44197744 | T | C | 64 | a0001c0001t0002g0018 a0001c0001t0002g0072 a0001c0001t0002g0252 others(61): Show |
78 | HG00099.hp1 HG00735.hp2 HG00738.hp1 others(75): Show |
intron_variant | MODIFIER | c.712-877T>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 11/13 | chr22 | 44197744 | |||||||
chr22:44197950 | A | C | 1 | a0001c0002t0005g0135 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.712-671A>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 11/13 | chr22 | 44197950 | |||||||
chr22:44198111 | T | G | 3 | a0001c0002t0001g0357 a0001c0005t0003g0298 a0001c0005t0031g0215 |
3 | HG02723.hp2 HG02897.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.712-510T>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 11/13 | chr22 | 44198111 | |||||||
chr22:44198153 | T | A | 231 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(228): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.712-468T>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 11/13 | chr22 | 44198153 | |||||||
chr22:44198244 | A | G | 1 | a0001c0001t0002g0305 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.712-377A>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 11/13 | chr22 | 44198244 | |||||||
chr22:44198255 | A | G | 224 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(221): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.712-366A>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 11/13 | chr22 | 44198255 | |||||||
chr22:44198257 | C | T | 13 | a0001c0002t0001g0082 a0001c0002t0001g0085 a0001c0002t0001g0217 others(10): Show |
14 | HG00558.hp1 HG02074.hp2 NA18942.hp1 others(11): Show |
intron_variant | MODIFIER | c.712-364C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 11/13 | chr22 | 44198257 | |||||||
chr22:44198328 | C | T | 1 | a0001c0001t0003g0144 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.712-293C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 11/13 | chr22 | 44198328 | |||||||
chr22:44198329 | T | G | 62 | a0001c0001t0002g0018 a0001c0001t0002g0072 a0001c0001t0002g0252 others(59): Show |
76 | HG00099.hp1 HG00735.hp2 HG00738.hp1 others(73): Show |
intron_variant | MODIFIER | c.712-292T>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 11/13 | chr22 | 44198329 | |||||||
chr22:44198576 | G | A | 1 | a0001c0001t0002g0266 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.712-45G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 11/13 | chr22 | 44198576 | |||||||
chr22:44198596 | T | C | 342 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(339): Show |
403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.712-25T>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 11/13 | chr22 | 44198596 | |||||||
chr22:44198597 | T | A | 1 | a0001c0002t0001g0082 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.712-24T>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 11/13 | chr22 | 44198597 | |||||||
chr22:44198600 | C | T | 2 | a0003c0007t0002g0067 a0003c0007t0002g0161 |
2 | HG02055.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.712-21C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 11/13 | chr22 | 44198600 | |||||||
chr22:44198771 | A | T | 1 | a0001c0001t0002g0060 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.813+49A>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44198771 | |||||||
chr22:44198831 | G | A | 3 | a0002c0006t0002g0052 a0002c0006t0002g0250 a0002c0006t0002g0251 |
3 | HG02886.hp2 HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.813+109G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44198831 | |||||||
chr22:44198859 | T | TATCC | 54 | a0001c0001t0002g0225 a0001c0001t0003g0001 a0001c0001t0003g0002 others(51): Show |
67 | HG00099.hp1 HG00735.hp2 HG00738.hp1 others(64): Show |
intron_variant | MODIFIER | c.813+159_813+162dup others(4): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198859 | ||||||
chr22:44198914 | C | A | 1 | a0001c0001t0003g0320 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.813+192C>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44198914 | |||||||
chr22:44198921 | T | C | 51 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0016 others(48): Show |
64 | HG00099.hp1 HG00735.hp2 HG00738.hp1 others(61): Show |
intron_variant | MODIFIER | c.813+199T>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44198921 | |||||||
chr22:44198923 | T | C | 52 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0016 others(49): Show |
65 | HG00099.hp1 HG00735.hp2 HG00738.hp1 others(62): Show |
intron_variant | MODIFIER | c.813+201T>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44198923 | |||||||
chr22:44198923 | T | TACCCATC others(65): Show |
1 | a0001c0003t0004g0149 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.813+218_813+219ins others(72): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198923 | ||||||
chr22:44198933 | T | TCCACCCA others(105): Show |
1 | a0001c0002t0001g0184 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.813+214_813+215ins others(112): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198933 | ||||||
chr22:44198936 | A | ATCCATCC others(109): Show |
1 | a0001c0001t0003g0088 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.813+218_813+219ins others(116): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198936 | ||||||
chr22:44198936 | A | ATCCATCC others(109): Show |
1 | a0001c0005t0003g0316 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.813+218_813+219ins others(116): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198936 | ||||||
chr22:44198936 | A | ATCCATCC others(105): Show |
1 | a0001c0001t0003g0087 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.813+218_813+219ins others(112): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198936 | ||||||
chr22:44198936 | A | ATCCATCC others(97): Show |
1 | a0001c0001t0003g0065 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.813+218_813+219ins others(104): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198936 | ||||||
chr22:44198937 | T | C | 1 | a0001c0002t0001g0184 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.813+215T>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44198937 | |||||||
chr22:44198937 | T | TCCACACC others(110): Show |
1 | a0001c0002t0001g0082 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.813+219_813+220ins others(117): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198937 | ||||||
chr22:44198937 | T | TCCACCCA others(105): Show |
1 | a0001c0002t0001g0345 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.813+266_813+267ins others(112): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198937 | ||||||
chr22:44198937 | T | TCCACCCA others(85): Show |
1 | a0001c0002t0005g0135 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.813+266_813+267ins others(92): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198937 | ||||||
chr22:44198937 | T | TCCACCCA others(109): Show |
17 | a0001c0002t0001g0029 a0001c0002t0001g0034 a0001c0002t0001g0035 others(14): Show |
24 | HG00621.hp2 HG02027.hp2 HG02071.hp2 others(21): Show |
intron_variant | MODIFIER | c.813+266_813+267ins others(116): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198937 | ||||||
chr22:44198937 | T | TCCACCCA others(93): Show |
1 | a0001c0002t0001g0227 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.813+266_813+267ins others(100): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198937 | ||||||
chr22:44198937 | T | TCCACCCA others(117): Show |
1 | a0001c0002t0001g0323 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.813+268_813+269ins others(124): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198937 | ||||||
chr22:44198937 | T | TCCACCCA others(113): Show |
5 | a0001c0001t0002g0041 a0001c0001t0002g0044 a0001c0001t0002g0265 others(2): Show |
5 | HG02280.hp1 HG03209.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.813+268_813+269ins others(120): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198937 | ||||||
chr22:44198937 | T | TCCACCCA others(117): Show |
1 | a0001c0001t0003g0239 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.813+268_813+269ins others(124): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198937 | ||||||
chr22:44198937 | T | TCCACCCA others(105): Show |
1 | a0001c0002t0001g0179 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.813+268_813+269ins others(112): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198937 | ||||||
chr22:44198937 | T | TCCACCCA others(109): Show |
1 | a0001c0002t0001g0344 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.813+268_813+269ins others(116): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198937 | ||||||
chr22:44198937 | T | TCCACCCA others(113): Show |
1 | a0001c0002t0001g0286 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.813+222_813+223ins others(120): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198937 | ||||||
chr22:44198937 | T | TCCATCCA others(69): Show |
4 | a0001c0003t0004g0145 a0001c0003t0004g0146 a0001c0003t0004g0148 others(1): Show |
4 | HG00140.hp2 HG01106.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.813+218_813+219ins others(76): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198937 | ||||||
chr22:44198937 | T | TCCATCCA others(69): Show |
27 | a0001c0001t0002g0053 a0001c0003t0003g0300 a0001c0003t0004g0005 others(24): Show |
33 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(30): Show |
intron_variant | MODIFIER | c.813+218_813+219ins others(76): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198937 | ||||||
chr22:44198937 | T | TCCATCCA others(73): Show |
2 | a0001c0003t0004g0222 a0001c0003t0004g0260 |
2 | HG03688.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.813+218_813+219ins others(80): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198937 | ||||||
chr22:44198937 | T | TCCATCCA others(73): Show |
15 | a0001c0004t0004g0004 a0001c0004t0004g0198 a0001c0004t0004g0212 others(12): Show |
18 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(15): Show |
intron_variant | MODIFIER | c.813+218_813+219ins others(80): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198937 | ||||||
chr22:44198937 | T | TCCATCCA others(61): Show |
1 | a0001c0001t0002g0047 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.813+218_813+219ins others(68): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198937 | ||||||
chr22:44198937 | T | TCCATCCA others(65): Show |
1 | a0001c0001t0016g0210 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.813+218_813+219ins others(72): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198937 | ||||||
chr22:44198937 | T | TCCATCCA others(85): Show |
2 | a0001c0001t0018g0096 a0001c0001t0018g0351 |
2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.813+218_813+219ins others(92): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198937 | ||||||
chr22:44198937 | T | TCCATCCA others(89): Show |
1 | a0001c0001t0002g0060 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.813+218_813+219ins others(96): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198937 | ||||||
chr22:44198940 | A | ATCCATCC others(101): Show |
1 | a0001c0001t0003g0076 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.813+218_813+219ins others(108): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44198940 | |||||||
chr22:44198940 | A | ATCCATCC others(109): Show |
2 | a0001c0001t0003g0095 a0001c0001t0003g0349 |
2 | HG01109.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.813+218_813+219ins others(116): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44198940 | |||||||
chr22:44198940 | A | ATCCATCC others(105): Show |
2 | a0001c0001t0003g0165 a0001c0001t0020g0055 |
2 | HG02293.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.813+218_813+219ins others(112): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44198940 | |||||||
chr22:44198940 | A | ATCCATCC others(104): Show |
1 | a0001c0001t0003g0081 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.813+218_813+219ins others(111): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44198940 | |||||||
chr22:44198940 | A | ATCCATCC others(105): Show |
22 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0016 others(19): Show |
33 | HG00738.hp1 HG01069.hp2 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.813+218_813+219ins others(112): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44198940 | |||||||
chr22:44198940 | A | ATCCATCC others(93): Show |
1 | a0001c0001t0003g0046 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.813+218_813+219ins others(100): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44198940 | |||||||
chr22:44198940 | A | ATCCATCC others(109): Show |
1 | a0001c0001t0003g0077 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.813+218_813+219ins others(116): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44198940 | |||||||
chr22:44198941 | C | T | 170 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(167): Show |
202 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.813+219C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44198941 | |||||||
chr22:44198944 | A | ATCCATCC others(97): Show |
3 | a0001c0001t0008g0007 a0001c0001t0008g0118 a0001c0001t0008g0119 |
5 | HG00099.hp1 HG01168.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.813+222_813+223ins others(104): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44198944 | |||||||
chr22:44198944 | A | ATCCATCC others(97): Show |
3 | a0001c0001t0003g0099 a0001c0001t0003g0200 a0001c0001t0012g0105 |
3 | HG01496.hp1 HG02257.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.813+222_813+223ins others(104): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44198944 | |||||||
chr22:44198944 | A | ATCCATCC others(101): Show |
6 | a0001c0001t0003g0142 a0001c0001t0003g0144 a0001c0001t0003g0285 others(3): Show |
6 | HG01884.hp2 HG02135.hp1 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.813+222_813+223ins others(108): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44198944 | |||||||
chr22:44198944 | A | ATCCATCC others(105): Show |
3 | a0001c0002t0001g0357 a0001c0005t0003g0298 a0001c0005t0031g0215 |
3 | HG02723.hp2 HG02897.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.813+222_813+223ins others(112): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44198944 | |||||||
chr22:44198944 | A | ATCCATCC others(97): Show |
1 | a0001c0001t0003g0143 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.813+222_813+223ins others(104): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44198944 | |||||||
chr22:44198945 | C | CCCATCCA others(101): Show |
1 | a0001c0001t0027g0341 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.813+250_813+251ins others(108): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198945 | ||||||
chr22:44198945 | C | CCCATCCA others(105): Show |
1 | a0001c0002t0001g0346 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.813+258_813+259ins others(112): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198945 | ||||||
chr22:44198945 | C | CCCATCCA others(113): Show |
2 | a0001c0001t0002g0339 a0001c0002t0001g0264 |
2 | HG02572.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.813+266_813+267ins others(120): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198945 | ||||||
chr22:44198945 | C | CCCATCCA others(89): Show |
1 | a0001c0002t0005g0134 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.813+266_813+267ins others(96): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198945 | ||||||
chr22:44198945 | C | CCCATCCA others(73): Show |
1 | a0004c0010t0002g0097 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.813+266_813+267ins others(80): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198945 | ||||||
chr22:44198945 | C | CCCATCCA others(113): Show |
1 | a0001c0002t0023g0167 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.813+266_813+267ins others(120): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198945 | ||||||
chr22:44198945 | C | CCCATCCA others(101): Show |
1 | a0001c0002t0001g0217 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.813+266_813+267ins others(108): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198945 | ||||||
chr22:44198945 | C | CCCATCCA others(113): Show |
18 | a0001c0001t0001g0168 a0001c0001t0002g0080 a0001c0001t0002g0234 others(15): Show |
18 | HG00639.hp1 HG00741.hp1 HG02738.hp1 others(15): Show |
intron_variant | MODIFIER | c.813+266_813+267ins others(120): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198945 | ||||||
chr22:44198945 | C | CCCATCCA others(117): Show |
1 | a0001c0002t0001g0186 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.813+266_813+267ins others(124): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198945 | ||||||
chr22:44198945 | C | CCCATCCA others(109): Show |
1 | a0001c0002t0001g0054 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.813+266_813+267ins others(116): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198945 | ||||||
chr22:44198945 | C | CCCATCCA others(113): Show |
1 | a0001c0002t0001g0066 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.813+266_813+267ins others(120): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198945 | ||||||
chr22:44198945 | C | CCCATCCA others(109): Show |
1 | a0001c0002t0005g0137 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.813+266_813+267ins others(116): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198945 | ||||||
chr22:44198945 | C | CCCATCCA others(109): Show |
1 | a0002c0006t0002g0052 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.813+266_813+267ins others(116): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198945 | ||||||
chr22:44198945 | C | CCCATCCA others(113): Show |
2 | a0002c0006t0002g0250 a0002c0006t0002g0251 |
2 | HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.813+266_813+267ins others(120): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198945 | ||||||
chr22:44198945 | C | CCCATCCA others(101): Show |
1 | a0001c0002t0001g0326 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.813+266_813+267ins others(108): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198945 | ||||||
chr22:44198945 | C | CCCATCCA others(77): Show |
1 | a0001c0001t0003g0042 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.813+268_813+269ins others(84): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198945 | ||||||
chr22:44198945 | C | CCCATCCA others(105): Show |
2 | a0001c0001t0003g0358 a0001c0002t0001g0331 |
2 | HG02074.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.813+268_813+269ins others(112): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198945 | ||||||
chr22:44198945 | C | CCCATCCA others(109): Show |
6 | a0001c0001t0003g0098 a0001c0001t0003g0290 a0001c0001t0010g0048 others(3): Show |
6 | HG01243.hp1 HG01243.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.813+268_813+269ins others(116): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198945 | ||||||
chr22:44198945 | C | CCCATCCA others(117): Show |
16 | a0001c0001t0003g0037 a0001c0001t0003g0233 a0001c0001t0003g0276 others(13): Show |
21 | HG00423.hp1 HG00673.hp1 HG02040.hp1 others(18): Show |
intron_variant | MODIFIER | c.813+268_813+269ins others(124): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198945 | ||||||
chr22:44198945 | C | CCCATCCA others(121): Show |
2 | a0001c0002t0001g0157 a0001c0002t0001g0158 |
2 | NA18953.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.813+268_813+269ins others(128): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198945 | ||||||
chr22:44198945 | C | CCCATCCA others(125): Show |
1 | a0001c0002t0001g0181 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.813+268_813+269ins others(132): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198945 | ||||||
chr22:44198945 | C | CCCATCCA others(113): Show |
5 | a0001c0002t0001g0010 a0001c0002t0001g0203 a0001c0002t0001g0273 others(2): Show |
7 | HG02080.hp1 NA18943.hp2 NA18955.hp2 others(4): Show |
intron_variant | MODIFIER | c.813+268_813+269ins others(120): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198945 | ||||||
chr22:44198945 | C | CCCATCCA others(118): Show |
1 | a0001c0001t0003g0277 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.813+268_813+269ins others(125): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198945 | ||||||
chr22:44198945 | C | CCCATCCA others(101): Show |
1 | a0001c0001t0010g0262 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.813+268_813+269ins others(108): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198945 | ||||||
chr22:44198945 | C | CCCATCCA others(105): Show |
1 | a0001c0001t0014g0348 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.813+268_813+269ins others(112): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198945 | ||||||
chr22:44198945 | C | CCCATCCA others(113): Show |
1 | a0001c0002t0005g0113 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.813+268_813+269ins others(120): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198945 | ||||||
chr22:44198945 | C | CCCATCCA others(105): Show |
4 | a0001c0002t0001g0268 a0001c0002t0001g0319 a0001c0002t0001g0327 others(1): Show |
4 | HG00558.hp1 NA18963.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.813+268_813+269ins others(112): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198945 | ||||||
chr22:44198945 | C | CCCATCCA others(121): Show |
1 | a0001c0001t0003g0279 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.813+268_813+269ins others(128): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198945 | ||||||
chr22:44198945 | C | CCCATCCA others(113): Show |
1 | a0001c0001t0014g0108 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.813+268_813+269ins others(120): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198945 | ||||||
chr22:44198945 | C | CCCATCCA others(121): Show |
5 | a0001c0001t0009g0051 a0001c0002t0001g0079 a0001c0002t0001g0159 others(2): Show |
5 | HG02109.hp1 HG02818.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.813+268_813+269ins others(128): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198945 | ||||||
chr22:44198945 | C | CCCATCCA others(117): Show |
1 | a0001c0002t0001g0011 | 3 | NA18945.hp2 NA18969.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.813+268_813+269ins others(124): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198945 | ||||||
chr22:44198945 | C | T | 172 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(169): Show |
204 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.813+223C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44198945 | |||||||
chr22:44198948 | A | ATCCATCC others(89): Show |
1 | a0001c0005t0003g0061 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.813+242_813+243ins others(96): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198948 | ||||||
chr22:44198949 | T | C | 55 | a0001c0001t0002g0047 a0001c0001t0002g0053 a0001c0001t0002g0060 others(52): Show |
64 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.813+227T>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44198949 | |||||||
chr22:44198949 | T | TCCATCCA others(105): Show |
5 | a0001c0002t0001g0188 a0001c0002t0001g0226 a0001c0002t0001g0322 others(2): Show |
7 | HG01975.hp1 HG01978.hp2 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.813+266_813+267ins others(112): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198949 | ||||||
chr22:44198949 | T | TCCATCCA others(109): Show |
6 | a0001c0002t0001g0013 a0001c0002t0001g0166 a0001c0002t0001g0207 others(3): Show |
8 | HG00639.hp2 HG01069.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.813+268_813+269ins others(116): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198949 | ||||||
chr22:44198949 | T | TCCATCCA others(69): Show |
2 | a0003c0007t0002g0067 a0003c0007t0002g0161 |
2 | HG02055.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.813+263_813+264ins others(76): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198949 | ||||||
chr22:44198953 | T | C | 53 | a0001c0001t0002g0047 a0001c0001t0002g0053 a0001c0001t0002g0060 others(50): Show |
62 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.813+231T>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44198953 | |||||||
chr22:44198953 | T | TCCATCCA others(197): Show |
2 | a0001c0001t0004g0154 a0001c0001t0004g0155 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.813+266_813+267ins others(204): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198953 | ||||||
chr22:44198956 | A | ATCCATCC others(89): Show |
1 | a0001c0001t0003g0280 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.813+246_813+247ins others(96): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198956 | ||||||
chr22:44198957 | T | TCCATCCA others(73): Show |
6 | a0001c0001t0002g0068 a0001c0001t0002g0308 a0001c0002t0001g0293 others(3): Show |
6 | HG02258.hp2 HG02647.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.813+246_813+247ins others(80): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198957 | ||||||
chr22:44198957 | T | TCCATCCA others(73): Show |
1 | a0001c0002t0001g0027 | 2 | HG00733.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.813+250_813+251ins others(80): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198957 | ||||||
chr22:44198957 | T | TCCATCCA others(73): Show |
1 | a0001c0001t0002g0354 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.813+250_813+251ins others(80): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198957 | ||||||
chr22:44198957 | T | TCCATCCA others(77): Show |
1 | a0001c0001t0007g0109 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.813+250_813+251ins others(84): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198957 | ||||||
chr22:44198957 | T | TCCATCCA others(77): Show |
2 | a0001c0002t0001g0094 a0001c0002t0001g0288 |
2 | HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.813+254_813+255ins others(84): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198957 | ||||||
chr22:44198957 | T | TCCATCCA others(77): Show |
5 | a0001c0001t0002g0078 a0001c0001t0002g0140 a0001c0001t0002g0141 others(2): Show |
6 | HG01346.hp2 HG01358.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.813+254_813+255ins others(84): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198957 | ||||||
chr22:44198957 | T | TCCATCCA others(77): Show |
9 | a0001c0001t0002g0018 a0001c0001t0002g0072 a0001c0001t0002g0252 others(6): Show |
10 | HG01884.hp1 HG02055.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.813+254_813+255ins others(84): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198957 | ||||||
chr22:44198957 | T | TCCATCCA others(81): Show |
3 | a0001c0001t0003g0254 a0001c0001t0007g0110 a0007c0009t0003g0091 |
3 | HG02809.hp1 HG02976.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.813+254_813+255ins others(88): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198957 | ||||||
chr22:44198957 | T | TCCATCCA others(61): Show |
1 | a0001c0001t0007g0124 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.813+254_813+255ins others(68): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198957 | ||||||
chr22:44198957 | T | TCCATCCA others(85): Show |
1 | a0001c0001t0003g0356 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.813+258_813+259ins others(92): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198957 | ||||||
chr22:44198957 | T | TCCATCCA others(61): Show |
1 | a0001c0001t0033g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.813+263_813+264ins others(68): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198957 | ||||||
chr22:44198961 | T | TCCATCCA others(53): Show |
1 | a0001c0001t0002g0043 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.813+246_813+247ins others(60): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198961 | ||||||
chr22:44198961 | T | TCCATCCA others(49): Show |
9 | a0001c0001t0002g0021 a0001c0001t0002g0030 a0001c0001t0002g0070 others(6): Show |
11 | HG00735.hp1 HG00738.hp2 HG01515.hp1 others(8): Show |
intron_variant | MODIFIER | c.813+246_813+247ins others(56): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198961 | ||||||
chr22:44198961 | T | TCCATCCA others(53): Show |
4 | a0001c0002t0001g0022 a0001c0002t0001g0023 a0001c0002t0001g0024 others(1): Show |
7 | HG01074.hp2 HG01433.hp2 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.813+250_813+251ins others(60): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198961 | ||||||
chr22:44198961 | T | TCCATCCA others(53): Show |
64 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(61): Show |
73 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.813+250_813+251ins others(60): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198961 | ||||||
chr22:44198961 | T | TCCATCCA others(57): Show |
1 | a0001c0001t0004g0245 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.813+250_813+251ins others(64): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198961 | ||||||
chr22:44198961 | T | TCCATCCA others(57): Show |
7 | a0001c0001t0009g0150 a0001c0001t0011g0032 a0001c0001t0011g0209 others(4): Show |
9 | HG00099.hp2 HG01071.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.813+254_813+255ins others(64): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198961 | ||||||
chr22:44198961 | T | TCCATCCA others(61): Show |
1 | a0001c0001t0007g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.813+258_813+259ins others(68): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198961 | ||||||
chr22:44198963 | C | CATCCATC others(109): Show |
4 | a0001c0001t0025g0104 a0001c0001t0029g0340 a0001c0002t0001g0049 others(1): Show |
4 | HG01433.hp1 HG02451.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.813+266_813+267ins others(116): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198963 | ||||||
chr22:44198969 | T | TCCATCCA others(49): Show |
1 | a0001c0001t0002g0315 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.813+254_813+255ins others(56): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44198969 | ||||||
chr22:44199112 | T | A | 52 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0016 others(49): Show |
65 | HG00099.hp1 HG00735.hp2 HG00738.hp1 others(62): Show |
intron_variant | MODIFIER | c.813+390T>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44199112 | |||||||
chr22:44199121 | C | T | 1 | a0001c0002t0001g0082 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.813+399C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44199121 | |||||||
chr22:44199122 | T | C | 1 | a0001c0002t0001g0082 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.813+400T>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44199122 | |||||||
chr22:44199190 | TACCCAGT others(18): Show |
T | 1 | a0001c0003t0004g0222 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.813+474_813+498del others(25): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44199190 | ||||||
chr22:44199310 | G | A | 5 | a0001c0002t0001g0027 a0001c0002t0001g0040 a0001c0002t0001g0094 others(2): Show |
7 | HG00733.hp1 HG01346.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.813+588G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44199310 | |||||||
chr22:44199331 | T | C | 10 | a0001c0001t0002g0018 a0001c0001t0002g0072 a0001c0001t0002g0252 others(7): Show |
11 | HG01884.hp1 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.813+609T>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44199331 | |||||||
chr22:44199338 | C | G | 1 | a0001c0013t0001g0062 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.813+616C>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44199338 | |||||||
chr22:44199359 | A | G | 124 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(121): Show |
143 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.813+637A>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44199359 | |||||||
chr22:44199436 | C | T | 1 | a0001c0001t0002g0047 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.813+714C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44199436 | |||||||
chr22:44199462 | T | C | 1 | a0001c0001t0003g0077 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.813+740T>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44199462 | |||||||
chr22:44199559 | C | T | 52 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0016 others(49): Show |
65 | HG00099.hp1 HG00735.hp2 HG00738.hp1 others(62): Show |
intron_variant | MODIFIER | c.813+837C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44199559 | |||||||
chr22:44199612 | G | T | 2 | a0003c0007t0002g0067 a0003c0007t0002g0161 |
2 | HG02055.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.813+890G>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44199612 | |||||||
chr22:44199628 | C | T | 3 | a0002c0006t0002g0052 a0002c0006t0002g0250 a0002c0006t0002g0251 |
3 | HG02886.hp2 HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.813+906C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44199628 | |||||||
chr22:44199655 | T | C | 1 | a0001c0002t0019g0271 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.813+933T>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44199655 | |||||||
chr22:44199682 | C | A | 52 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0016 others(49): Show |
65 | HG00099.hp1 HG00735.hp2 HG00738.hp1 others(62): Show |
intron_variant | MODIFIER | c.813+960C>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44199682 | |||||||
chr22:44199711 | G | A | 103 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0016 others(100): Show |
125 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.813+989G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44199711 | |||||||
chr22:44199722 | C | T | 103 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0016 others(100): Show |
125 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.813+1000C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44199722 | |||||||
chr22:44199733 | T | C | 1 | a0001c0001t0002g0301 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.813+1011T>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44199733 | |||||||
chr22:44199902 | C | T | 1 | a0001c0005t0003g0061 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.813+1180C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44199902 | |||||||
chr22:44199959 | T | C | 125 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(122): Show |
144 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.813+1237T>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44199959 | |||||||
chr22:44200074 | C | T | 1 | a0001c0001t0003g0276 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.813+1352C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44200074 | |||||||
chr22:44200093 | C | T | 1 | a0001c0002t0001g0337 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.813+1371C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44200093 | |||||||
chr22:44200205 | A | C | 239 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(236): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.813+1483A>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44200205 | |||||||
chr22:44200286 | C | T | 1 | a0001c0004t0006g0130 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.813+1564C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44200286 | |||||||
chr22:44200287 | G | A | 2 | a0001c0001t0002g0083 a0001c0001t0002g0246 |
2 | NA18974.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.813+1565G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44200287 | |||||||
chr22:44200327 | G | A | 233 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(230): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.813+1605G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44200327 | |||||||
chr22:44200342 | C | G | 1 | a0001c0002t0001g0273 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.813+1620C>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44200342 | |||||||
chr22:44200573 | G | A | 1 | a0001c0002t0023g0167 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.813+1851G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44200573 | |||||||
chr22:44200825 | C | T | 1 | a0004c0010t0002g0097 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.813+2103C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44200825 | |||||||
chr22:44200850 | C | T | 2 | a0001c0005t0003g0061 a0001c0005t0003g0316 |
2 | HG03041.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.813+2128C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44200850 | |||||||
chr22:44200863 | C | A | 52 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0016 others(49): Show |
65 | HG00099.hp1 HG00735.hp2 HG00738.hp1 others(62): Show |
intron_variant | MODIFIER | c.813+2141C>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44200863 | |||||||
chr22:44200966 | C | T | 1 | a0004c0010t0002g0097 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.813+2244C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44200966 | |||||||
chr22:44201074 | C | G | 1 | a0004c0010t0002g0097 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.813+2352C>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44201074 | |||||||
chr22:44201304 | G | A | 1 | a0004c0010t0002g0097 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.813+2582G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44201304 | |||||||
chr22:44201421 | G | A | 3 | a0002c0006t0002g0052 a0002c0006t0002g0250 a0002c0006t0002g0251 |
3 | HG02886.hp2 HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.813+2699G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44201421 | |||||||
chr22:44201422 | C | T | 102 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0016 others(99): Show |
124 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.813+2700C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44201422 | |||||||
chr22:44201436 | C | T | 1 | a0001c0001t0002g0214 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.813+2714C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44201436 | |||||||
chr22:44201521 | G | A | 2 | a0001c0001t0002g0308 a0001c0001t0027g0341 |
2 | HG02258.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.813+2799G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44201521 | |||||||
chr22:44201542 | C | T | 78 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0021 others(75): Show |
94 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.813+2820C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44201542 | |||||||
chr22:44201624 | T | C | 178 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(175): Show |
206 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.813+2902T>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44201624 | |||||||
chr22:44201632 | C | T | 1 | a0001c0002t0001g0325 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.813+2910C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44201632 | |||||||
chr22:44201671 | G | A | 1 | a0006c0008t0013g0194 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.813+2949G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44201671 | |||||||
chr22:44201716 | G | A | 51 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0016 others(48): Show |
64 | HG00099.hp1 HG00735.hp2 HG00738.hp1 others(61): Show |
intron_variant | MODIFIER | c.813+2994G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44201716 | |||||||
chr22:44201763 | A | G | 2 | a0001c0005t0002g0195 a0001c0005t0002g0196 |
2 | NA18964.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.813+3041A>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44201763 | |||||||
chr22:44201867 | C | T | 35 | a0001c0001t0003g0001 a0001c0001t0003g0016 a0001c0001t0003g0045 others(32): Show |
43 | HG00099.hp1 HG00735.hp2 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.813+3145C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44201867 | |||||||
chr22:44202008 | T | G | 1 | a0001c0001t0003g0077 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.813+3286T>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44202008 | |||||||
chr22:44202037 | C | G | 1 | a0001c0001t0032g0206 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.813+3315C>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44202037 | |||||||
chr22:44202049 | G | A | 52 | a0001c0001t0004g0154 a0001c0001t0004g0155 a0001c0001t0004g0235 others(49): Show |
61 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.813+3327G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44202049 | |||||||
chr22:44202057 | G | A | 1 | a0001c0001t0029g0340 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.813+3335G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44202057 | |||||||
chr22:44202142 | G | C | 4 | a0001c0001t0002g0053 a0002c0006t0002g0052 a0002c0006t0002g0250 others(1): Show |
4 | HG02886.hp2 HG02965.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.813+3420G>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44202142 | |||||||
chr22:44202208 | A | G | 238 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(235): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.813+3486A>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44202208 | |||||||
chr22:44202317 | G | A | 1 | a0001c0003t0004g0190 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.814-3440G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44202317 | |||||||
chr22:44202349 | C | T | 1 | a0001c0001t0002g0197 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.814-3408C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44202349 | |||||||
chr22:44202370 | G | A | 14 | a0001c0001t0003g0037 a0001c0001t0003g0233 a0001c0001t0003g0239 others(11): Show |
17 | HG00423.hp1 HG02080.hp1 HG02083.hp2 others(14): Show |
intron_variant | MODIFIER | c.814-3387G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44202370 | |||||||
chr22:44202421 | G | T | 52 | a0001c0001t0004g0154 a0001c0001t0004g0155 a0001c0001t0004g0235 others(49): Show |
61 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.814-3336G>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44202421 | |||||||
chr22:44202726 | C | T | 59 | a0001c0001t0002g0041 a0001c0001t0002g0044 a0001c0001t0002g0053 others(56): Show |
68 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.814-3031C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44202726 | |||||||
chr22:44202812 | G | A | 69 | a0001c0001t0002g0068 a0001c0001t0003g0001 a0001c0001t0003g0002 others(66): Show |
83 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(80): Show |
intron_variant | MODIFIER | c.814-2945G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44202812 | |||||||
chr22:44202862 | C | T | 1 | a0001c0002t0001g0023 | 2 | HG01074.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.814-2895C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44202862 | |||||||
chr22:44202903 | G | A | 1 | a0001c0001t0002g0214 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.814-2854G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44202903 | |||||||
chr22:44202907 | T | G | 1 | a0001c0004t0006g0128 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.814-2850T>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44202907 | |||||||
chr22:44203051 | T | C | 3 | a0001c0001t0002g0028 a0001c0001t0002g0225 a0001c0001t0007g0123 |
4 | NA18949.hp1 NA18971.hp2 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.814-2706T>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44203051 | |||||||
chr22:44203052 | A | T | 2 | a0001c0001t0007g0116 a0004c0010t0002g0097 |
2 | HG02486.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.814-2705A>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44203052 | |||||||
chr22:44203210 | G | C | 1 | a0001c0001t0013g0193 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.814-2547G>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44203210 | |||||||
chr22:44203243 | T | C | 104 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(101): Show |
118 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.814-2514T>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44203243 | |||||||
chr22:44203284 | G | A | 1 | a0001c0001t0029g0340 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.814-2473G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44203284 | |||||||
chr22:44203378 | C | A | 173 | a0001c0001t0001g0168 a0001c0001t0002g0006 a0001c0001t0002g0009 others(170): Show |
201 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.814-2379C>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44203378 | |||||||
chr22:44203380 | G | A | 239 | a0001c0001t0001g0168 a0001c0001t0002g0006 a0001c0001t0002g0009 others(236): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.814-2377G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44203380 | |||||||
chr22:44203533 | T | C | 1 | a0001c0001t0033g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.814-2224T>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44203533 | |||||||
chr22:44203545 | G | A | 1 | a0001c0003t0004g0201 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.814-2212G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44203545 | |||||||
chr22:44203572 | C | T | 172 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(169): Show |
200 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.814-2185C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44203572 | |||||||
chr22:44203651 | G | A | 172 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(169): Show |
200 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.814-2106G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44203651 | |||||||
chr22:44203664 | G | A | 1 | a0001c0001t0013g0242 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.814-2093G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44203664 | |||||||
chr22:44203773 | G | A | 96 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0016 others(93): Show |
116 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.814-1984G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44203773 | |||||||
chr22:44203776 | G | A | 68 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0016 others(65): Show |
82 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(79): Show |
intron_variant | MODIFIER | c.814-1981G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44203776 | |||||||
chr22:44203819 | C | T | 4 | a0001c0001t0025g0104 a0001c0001t0029g0340 a0003c0007t0002g0067 others(1): Show |
4 | HG02055.hp1 HG02970.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.814-1938C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44203819 | |||||||
chr22:44203856 | G | C | 6 | a0001c0003t0004g0005 a0001c0003t0004g0147 a0001c0003t0004g0149 others(3): Show |
9 | HG00642.hp1 HG00733.hp2 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.814-1901G>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44203856 | |||||||
chr22:44203901 | G | A | 172 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(169): Show |
200 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.814-1856G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44203901 | |||||||
chr22:44204042 | A | G | 180 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(177): Show |
208 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.814-1715A>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44204042 | |||||||
chr22:44204043 | C | A | 8 | a0001c0001t0010g0048 a0001c0001t0010g0056 a0001c0001t0010g0089 others(5): Show |
8 | HG01243.hp1 HG01934.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.814-1714C>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44204043 | |||||||
chr22:44204068 | C | T | 1 | a0001c0001t0002g0240 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.814-1689C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44204068 | |||||||
chr22:44204136 | T | G | 1 | a0001c0001t0002g0347 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.814-1621T>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44204136 | |||||||
chr22:44204229 | A | AC | 5 | a0001c0001t0002g0246 a0001c0001t0008g0118 a0001c0003t0004g0294 others(2): Show |
5 | HG00438.hp1 HG01175.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.814-1525dupC | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44204229 | ||||||
chr22:44204255 | C | A | 172 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(169): Show |
200 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.814-1502C>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44204255 | |||||||
chr22:44204292 | A | G | 180 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(177): Show |
208 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.814-1465A>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44204292 | |||||||
chr22:44204295 | C | T | 172 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(169): Show |
200 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.814-1462C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44204295 | |||||||
chr22:44204356 | T | C | 1 | a0001c0001t0003g0358 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.814-1401T>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44204356 | |||||||
chr22:44204361 | C | T | 4 | a0001c0001t0025g0104 a0001c0001t0029g0340 a0003c0007t0002g0067 others(1): Show |
4 | HG02055.hp1 HG02970.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.814-1396C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44204361 | |||||||
chr22:44204395 | G | A | 2 | a0001c0001t0007g0116 a0004c0010t0002g0097 |
2 | HG02486.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.814-1362G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44204395 | |||||||
chr22:44204481 | A | G | 8 | a0001c0001t0010g0048 a0001c0001t0010g0056 a0001c0001t0010g0089 others(5): Show |
8 | HG01243.hp1 HG01934.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.814-1276A>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44204481 | |||||||
chr22:44204535 | G | A | 2 | a0001c0002t0001g0040 a0001c0002t0001g0153 |
3 | HG01346.hp2 HG01358.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.814-1222G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44204535 | |||||||
chr22:44204620 | C | T | 68 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0016 others(65): Show |
82 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(79): Show |
intron_variant | MODIFIER | c.814-1137C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44204620 | |||||||
chr22:44204631 | G | GCCCCCCC others(5): Show |
1 | a0001c0002t0001g0273 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.814-1124_814-1123i others(14): Show |
PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr22 | 44204631 | ||||||
chr22:44204633 | C | G | 8 | a0001c0001t0003g0254 a0001c0001t0003g0263 a0001c0001t0003g0356 others(5): Show |
8 | HG02723.hp2 HG02809.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.814-1124C>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44204633 | |||||||
chr22:44204638 | G | A | 1 | a0001c0002t0017g0324 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.814-1119G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44204638 | |||||||
chr22:44204663 | C | G | 1 | a0001c0001t0003g0349 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.814-1094C>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44204663 | |||||||
chr22:44204734 | G | A | 5 | a0001c0001t0002g0047 a0001c0001t0002g0060 a0001c0001t0007g0124 others(2): Show |
5 | HG02258.hp1 HG02559.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.814-1023G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44204734 | |||||||
chr22:44204753 | G | C | 72 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0016 others(69): Show |
86 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(83): Show |
intron_variant | MODIFIER | c.814-1004G>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44204753 | |||||||
chr22:44204772 | G | A | 28 | a0001c0003t0004g0005 a0001c0003t0004g0025 a0001c0003t0004g0026 others(25): Show |
34 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(31): Show |
intron_variant | MODIFIER | c.814-985G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44204772 | |||||||
chr22:44204790 | A | G | 1 | a0001c0001t0002g0053 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.814-967A>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44204790 | |||||||
chr22:44204946 | C | T | 104 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(101): Show |
118 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.814-811C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44204946 | |||||||
chr22:44205061 | A | G | 1 | a0001c0002t0001g0163 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.814-696A>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44205061 | |||||||
chr22:44205074 | T | C | 79 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0016 others(76): Show |
93 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(90): Show |
intron_variant | MODIFIER | c.814-683T>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44205074 | |||||||
chr22:44205115 | C | A | 68 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0016 others(65): Show |
82 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(79): Show |
intron_variant | MODIFIER | c.814-642C>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44205115 | |||||||
chr22:44205229 | G | A | 2 | a0001c0001t0002g0080 a0001c0001t0002g0234 |
2 | NA18943.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.814-528G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44205229 | |||||||
chr22:44205242 | C | T | 1 | a0001c0001t0033g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.814-515C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44205242 | |||||||
chr22:44205359 | T | C | 4 | a0001c0001t0025g0104 a0001c0001t0029g0340 a0003c0007t0002g0067 others(1): Show |
4 | HG02055.hp1 HG02970.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.814-398T>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44205359 | |||||||
chr22:44205402 | C | T | 8 | a0001c0001t0010g0048 a0001c0001t0010g0056 a0001c0001t0010g0089 others(5): Show |
8 | HG01243.hp1 HG01934.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.814-355C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44205402 | |||||||
chr22:44205511 | C | T | 1 | a0001c0003t0007g0115 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.814-246C>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44205511 | |||||||
chr22:44205619 | C | G | 173 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(170): Show |
201 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.814-138C>G | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 12/13 | chr22 | 44205619 | |||||||
chr22:44205980 | G | A | 1 | a0001c0001t0016g0318 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.886+151G>A | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 13/13 | chr22 | 44205980 | |||||||
chr22:44206121 | G | T | 49 | a0001c0001t0004g0154 a0001c0001t0004g0155 a0001c0001t0004g0235 others(46): Show |
58 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.887-196G>T | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 13/13 | chr22 | 44206121 | |||||||
chr22:44206292 | T | C | 6 | a0001c0003t0004g0005 a0001c0003t0004g0147 a0001c0003t0004g0149 others(3): Show |
9 | HG00642.hp1 HG00733.hp2 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.887-25T>C | PARVG | ENSG00000138964.17 | transcript | ENST00000444313.8 | protein_coding | 13/13 | chr22 | 44206292 |