Item | Value |
---|---|
geneid | 196740 |
ensemblid | ENSG00000165633.13 |
hgncid | 26470 |
symbol | VSTM4 |
name | V-set and transmembrane domain containing 4 |
refseq_nuc | NM_001031746.5 |
refseq_prot | NP_001026916.2 |
ensembl_nuc | ENST00000332853.9 |
ensembl_prot | ENSP00000331062.3 |
mane_status | MANE Select |
chr | chr10 |
start | 49014236 |
end | 49115522 |
strand | - |
ver | v1.2 |
region | chr10:49014236-49115522 |
region5000 | chr10:49009236-49120522 |
regionname0 | VSTM4_chr10_49014236_49115522 |
regionname5000 | VSTM4_chr10_49009236_49120522 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 320 | 154 | 60 | 33 | 39 | 7 | 14 | 30 | VSTM4_chr10_49009236_49120522 | VSTM4 | MRLLA others(315): Show |
chr10 | 49009236 | 49120522 |
a0002 | 1/0 | 320 | 121 | 23 | 19 | 59 | 3 | 16 | 42 | VSTM4_chr10_49009236_49120522 | VSTM4 | MRLLA others(315): Show |
chr10 | 49009236 | 49120522 |
a0003 | 0/0 | 320 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | MRLLA others(315): Show |
chr10 | 49009236 | 49120522 |
a0004 | 0/0 | 320 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | MRLLA others(315): Show |
chr10 | 49009236 | 49120522 |
a0005 | 0/0 | 320 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | MRLLA others(315): Show |
chr10 | 49009236 | 49120522 |
a0006 | 0/0 | 320 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | MRLLA others(315): Show |
chr10 | 49009236 | 49120522 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 960 | 126 | 39 | 29 | 37 | 7 | 13 | VSTM4_chr10_49009236_49120522 | VSTM4 | ATGCG others(955): Show |
chr10 | 49009236 | 49120522 | ||
a0001c0003 | 0/0 | 960 | 19 | 16 | 3 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | ATGCG others(955): Show |
chr10 | 49009236 | 49120522 | ||
a0001c0004 | 0/0 | 960 | 4 | 1 | 0 | 2 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | ATGCG others(955): Show |
chr10 | 49009236 | 49120522 | ||
a0001c0005 | 0/0 | 960 | 4 | 4 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | ATGCG others(955): Show |
chr10 | 49009236 | 49120522 | ||
a0001c0008 | 0/0 | 960 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | ATGCG others(955): Show |
chr10 | 49009236 | 49120522 | ||
a0002c0002 | 0/0 | 960 | 120 | 23 | 19 | 59 | 3 | 16 | VSTM4_chr10_49009236_49120522 | VSTM4 | ATGCG others(955): Show |
chr10 | 49009236 | 49120522 | ||
a0002c0010 | 1/0 | 960 | 1 | 0 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | ATGCG others(955): Show |
chr10 | 49009236 | 49120522 | ||
a0003c0006 | 0/0 | 960 | 2 | 0 | 0 | 0 | 0 | 2 | VSTM4_chr10_49009236_49120522 | VSTM4 | ATGCG others(955): Show |
chr10 | 49009236 | 49120522 | ||
a0004c0011 | 0/0 | 960 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | ATGCG others(955): Show |
chr10 | 49009236 | 49120522 | ||
a0005c0009 | 0/0 | 960 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | ATGCG others(955): Show |
chr10 | 49009236 | 49120522 | ||
a0006c0007 | 0/0 | 960 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | ATGCG others(955): Show |
chr10 | 49009236 | 49120522 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6408 | 16 | 4 | 4 | 2 | 3 | 3 | VSTM4_chr10_49009236_49120522 | VSTM4 | GCTCT others(6403): Show |
chr10 | 49009236 | 49120522 |
a0001c0001t0002 | 0/0 | 6406 | 26 | 2 | 9 | 8 | 1 | 6 | VSTM4_chr10_49009236_49120522 | VSTM4 | GCTCT others(6401): Show |
chr10 | 49009236 | 49120522 |
a0001c0001t0003 | 0/0 | 6410 | 16 | 13 | 0 | 3 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | GCTCT others(6405): Show |
chr10 | 49009236 | 49120522 |
a0001c0001t0005 | 0/0 | 6408 | 13 | 0 | 0 | 13 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | GCTCT others(6403): Show |
chr10 | 49009236 | 49120522 |
a0001c0001t0007 | 0/0 | 6408 | 8 | 0 | 4 | 0 | 2 | 2 | VSTM4_chr10_49009236_49120522 | VSTM4 | GCTCT others(6403): Show |
chr10 | 49009236 | 49120522 |
a0001c0001t0008 | 0/0 | 6405 | 6 | 6 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | GCTCT others(6400): Show |
chr10 | 49009236 | 49120522 |
a0001c0001t0009 | 0/0 | 6406 | 5 | 0 | 0 | 5 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | GCTCT others(6401): Show |
chr10 | 49009236 | 49120522 |
a0001c0001t0010 | 0/0 | 6405 | 5 | 5 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | GCTCT others(6400): Show |
chr10 | 49009236 | 49120522 |
a0001c0001t0014 | 0/0 | 6406 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | GCTCT others(6401): Show |
chr10 | 49009236 | 49120522 |
a0001c0001t0015 | 0/0 | 6408 | 3 | 1 | 2 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | GCTCT others(6403): Show |
chr10 | 49009236 | 49120522 |
a0001c0001t0016 | 0/0 | 6408 | 3 | 0 | 1 | 0 | 1 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | GCTCT others(6403): Show |
chr10 | 49009236 | 49120522 |
a0001c0001t0017 | 0/0 | 6408 | 2 | 2 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | GCTCT others(6403): Show |
chr10 | 49009236 | 49120522 |
a0001c0001t0018 | 0/0 | 6408 | 2 | 0 | 2 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | GCTCT others(6403): Show |
chr10 | 49009236 | 49120522 |
a0001c0001t0019 | 0/0 | 6406 | 2 | 0 | 0 | 2 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | GCTCT others(6401): Show |
chr10 | 49009236 | 49120522 |
a0001c0001t0020 | 0/0 | 6406 | 2 | 0 | 0 | 2 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | GCTCT others(6401): Show |
chr10 | 49009236 | 49120522 |
a0001c0001t0021 | 0/0 | 6408 | 2 | 2 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | GCTCT others(6403): Show |
chr10 | 49009236 | 49120522 |
a0001c0001t0022 | 0/0 | 6405 | 2 | 0 | 2 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | GCTCT others(6400): Show |
chr10 | 49009236 | 49120522 |
a0001c0001t0023 | 0/0 | 6410 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | GCTCT others(6405): Show |
chr10 | 49009236 | 49120522 |
a0001c0001t0024 | 0/0 | 6408 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | GCTCT others(6403): Show |
chr10 | 49009236 | 49120522 |
a0001c0001t0026 | 0/0 | 6410 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | GCTCT others(6405): Show |
chr10 | 49009236 | 49120522 |
a0001c0001t0027 | 0/0 | 6408 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | GCTCT others(6403): Show |
chr10 | 49009236 | 49120522 |
a0001c0001t0031 | 0/0 | 6408 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | GCTCT others(6403): Show |
chr10 | 49009236 | 49120522 |
a0001c0001t0032 | 0/0 | 6406 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | GCTCT others(6401): Show |
chr10 | 49009236 | 49120522 |
a0001c0001t0034 | 0/0 | 6408 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | GCTCT others(6403): Show |
chr10 | 49009236 | 49120522 |
a0001c0001t0035 | 0/0 | 6406 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | GCTCT others(6401): Show |
chr10 | 49009236 | 49120522 |
a0001c0001t0038 | 0/0 | 6410 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | GCTCT others(6405): Show |
chr10 | 49009236 | 49120522 |
a0001c0001t0039 | 0/1 | 6406 | 1 | 0 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | GCTCT others(6401): Show |
chr10 | 49009236 | 49120522 |
a0001c0001t0041 | 0/0 | 6408 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | GCTCT others(6403): Show |
chr10 | 49009236 | 49120522 |
a0001c0001t0042 | 0/0 | 6408 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | GCTCT others(6403): Show |
chr10 | 49009236 | 49120522 |
a0001c0003t0004 | 0/0 | 6414 | 18 | 16 | 2 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | GCTCT others(6409): Show |
chr10 | 49009236 | 49120522 |
a0001c0003t0036 | 0/0 | 6414 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | GCTCT others(6409): Show |
chr10 | 49009236 | 49120522 |
a0001c0004t0006 | 0/0 | 6406 | 4 | 1 | 0 | 2 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | GCTCT others(6401): Show |
chr10 | 49009236 | 49120522 |
a0001c0005t0001 | 0/0 | 6408 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | GCTCT others(6403): Show |
chr10 | 49009236 | 49120522 |
a0001c0005t0008 | 0/0 | 6405 | 3 | 3 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | GCTCT others(6400): Show |
chr10 | 49009236 | 49120522 |
a0001c0008t0006 | 0/0 | 6406 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | GCTCT others(6401): Show |
chr10 | 49009236 | 49120522 |
a0002c0002t0001 | 0/0 | 6408 | 68 | 13 | 10 | 34 | 2 | 9 | VSTM4_chr10_49009236_49120522 | VSTM4 | GCTCT others(6403): Show |
chr10 | 49009236 | 49120522 |
a0002c0002t0002 | 0/0 | 6406 | 11 | 1 | 1 | 8 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | GCTCT others(6401): Show |
chr10 | 49009236 | 49120522 |
a0002c0002t0003 | 0/0 | 6410 | 11 | 0 | 0 | 9 | 0 | 2 | VSTM4_chr10_49009236_49120522 | VSTM4 | GCTCT others(6405): Show |
chr10 | 49009236 | 49120522 |
a0002c0002t0005 | 0/0 | 6408 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | GCTCT others(6403): Show |
chr10 | 49009236 | 49120522 |
a0002c0002t0006 | 0/0 | 6406 | 4 | 0 | 0 | 1 | 1 | 2 | VSTM4_chr10_49009236_49120522 | VSTM4 | GCTCT others(6401): Show |
chr10 | 49009236 | 49120522 |
a0002c0002t0007 | 0/0 | 6408 | 2 | 0 | 2 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | GCTCT others(6403): Show |
chr10 | 49009236 | 49120522 |
a0002c0002t0009 | 0/0 | 6406 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | GCTCT others(6401): Show |
chr10 | 49009236 | 49120522 |
a0002c0002t0011 | 0/0 | 6408 | 4 | 0 | 2 | 2 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | GCTCT others(6403): Show |
chr10 | 49009236 | 49120522 |
a0002c0002t0012 | 0/0 | 6407 | 4 | 4 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | GCTCT others(6402): Show |
chr10 | 49009236 | 49120522 |
a0002c0002t0013 | 0/0 | 6408 | 4 | 0 | 3 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | GCTCT others(6403): Show |
chr10 | 49009236 | 49120522 |
a0002c0002t0014 | 0/0 | 6406 | 3 | 3 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | GCTCT others(6401): Show |
chr10 | 49009236 | 49120522 |
a0002c0002t0023 | 0/0 | 6410 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | GCTCT others(6405): Show |
chr10 | 49009236 | 49120522 |
a0002c0002t0025 | 0/0 | 6408 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | GCTCT others(6403): Show |
chr10 | 49009236 | 49120522 |
a0002c0002t0028 | 0/0 | 6408 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | GCTCT others(6403): Show |
chr10 | 49009236 | 49120522 |
a0002c0002t0029 | 0/0 | 6408 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | GCTCT others(6403): Show |
chr10 | 49009236 | 49120522 |
a0002c0002t0030 | 0/0 | 6406 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | GCTCT others(6401): Show |
chr10 | 49009236 | 49120522 |
a0002c0002t0033 | 0/0 | 6406 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | GCTCT others(6401): Show |
chr10 | 49009236 | 49120522 |
a0002c0002t0040 | 0/0 | 6406 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | GCTCT others(6401): Show |
chr10 | 49009236 | 49120522 |
a0002c0010t0004 | 1/0 | 6414 | 1 | 0 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | GCTCT others(6409): Show |
chr10 | 49009236 | 49120522 |
a0003c0006t0006 | 0/0 | 6406 | 2 | 0 | 0 | 0 | 0 | 2 | VSTM4_chr10_49009236_49120522 | VSTM4 | GCTCT others(6401): Show |
chr10 | 49009236 | 49120522 |
a0004c0011t0037 | 0/0 | 6410 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | GCTCT others(6405): Show |
chr10 | 49009236 | 49120522 |
a0005c0009t0001 | 0/0 | 6408 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | GCTCT others(6403): Show |
chr10 | 49009236 | 49120522 |
a0006c0007t0003 | 0/0 | 6410 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | GCTCT others(6405): Show |
chr10 | 49009236 | 49120522 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 4 | 0 | 1 | 0 | 2 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0002g0002 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0003g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0003g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0003g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0003g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0003g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0005g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0005g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0005g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0005g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0005g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0005g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0005g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0005g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0005g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0005g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0005g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0007g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0007g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0007g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0007g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0007g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0007g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0007g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0007g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0008g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0008g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0008g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0008g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0008g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0008g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0009g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0009g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0009g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0010g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0010g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0010g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0010g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0010g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0014g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0015g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0015g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0016g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0016g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0016g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0017g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0017g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0018g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0018g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0019g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0019g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0020g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0020g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0021g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0021g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0022g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0022g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0023g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0024g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0026g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0027g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0031g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0032g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0034g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0035g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0038g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0039g0193 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0041g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0001t0042g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0003t0004g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0003t0004g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0003t0004g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0003t0004g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0003t0004g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0003t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0003t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0003t0004g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0003t0004g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0003t0004g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0003t0004g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0003t0004g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0003t0004g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0003t0004g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0003t0004g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0003t0004g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0003t0004g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0003t0004g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0003t0036g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0004t0006g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0004t0006g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0004t0006g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0004t0006g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0005t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0005t0008g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0005t0008g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0005t0008g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0001c0008t0006g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0003g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0003g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0005g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0006g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0006g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0006g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0006g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0007g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0007g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0009g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0011g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0011g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0011g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0012g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0012g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0012g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0013g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0013g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0013g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0013g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0014g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0014g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0023g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0025g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0028g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0029g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0030g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0033g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0002t0040g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0002c0010t0004g0134 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0003c0006t0006g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0004c0011t0037g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0005c0009t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
a0006c0007t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0007 | g0192 | EUR | GBR | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0256 | EUR | GBR | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG00280 | hp1 | a0002 | c0002 | t0001 | g0105 | EUR | FIN | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG00323 | hp1 | a0002 | c0002 | t0006 | g0102 | EUR | FIN | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG00423 | hp1 | a0002 | c0002 | t0009 | g0141 | EAS | CHS | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG00423 | hp2 | a0001 | c0001 | t0005 | g0065 | EAS | CHS | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG00438 | hp2 | a0002 | c0002 | t0011 | g0012 | EAS | CHS | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG00558 | hp1 | a0002 | c0002 | t0003 | g0162 | EAS | CHS | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG00558 | hp2 | a0001 | c0001 | t0003 | g0213 | EAS | CHS | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG00597 | hp1 | a0001 | c0001 | t0003 | g0035 | EAS | CHS | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG00597 | hp2 | a0002 | c0002 | t0001 | g0126 | EAS | CHS | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | CHS | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG00621 | hp2 | a0002 | c0002 | t0001 | g0043 | EAS | CHS | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG00639 | hp1 | a0002 | c0002 | t0007 | g0143 | AMR | PUR | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG00639 | hp2 | a0001 | c0008 | t0006 | g0023 | AMR | PUR | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG00642 | hp1 | a0001 | c0001 | t0022 | g0183 | AMR | PUR | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG00642 | hp2 | a0002 | c0002 | t0001 | g0061 | AMR | PUR | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG00741 | hp1 | a0002 | c0002 | t0001 | g0060 | AMR | PUR | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG00741 | hp2 | a0002 | c0002 | t0029 | g0096 | AMR | PUR | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG01069 | hp1 | a0001 | c0001 | t0038 | g0243 | AMR | PUR | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG01069 | hp2 | a0001 | c0001 | t0015 | g0013 | AMR | PUR | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG01070 | hp1 | a0001 | c0001 | t0007 | g0189 | AMR | PUR | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG01070 | hp2 | a0001 | c0001 | t0018 | g0236 | AMR | PUR | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG01071 | hp1 | a0001 | c0001 | t0015 | g0013 | AMR | PUR | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG01071 | hp2 | a0001 | c0001 | t0018 | g0237 | AMR | PUR | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG01074 | hp1 | a0001 | c0001 | t0007 | g0188 | AMR | PUR | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0235 | AMR | PUR | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG01081 | hp1 | a0002 | c0002 | t0013 | g0094 | AMR | PUR | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG01081 | hp2 | a0001 | c0001 | t0024 | g0190 | AMR | PUR | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG01106 | hp1 | a0001 | c0001 | t0026 | g0174 | AMR | PUR | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG01106 | hp2 | a0002 | c0002 | t0001 | g0128 | AMR | PUR | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG01109 | hp1 | a0001 | c0003 | t0004 | g0198 | AMR | PUR | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG01109 | hp2 | a0002 | c0002 | t0007 | g0131 | AMR | PUR | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG01175 | hp1 | a0002 | c0002 | t0001 | g0135 | AMR | PUR | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG01192 | hp1 | a0001 | c0001 | t0007 | g0186 | AMR | PUR | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG01243 | hp1 | a0001 | c0001 | t0034 | g0194 | AMR | PUR | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG01243 | hp2 | a0001 | c0001 | t0022 | g0181 | AMR | PUR | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0231 | AMR | CLM | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG01255 | hp2 | a0002 | c0002 | t0001 | g0137 | AMR | CLM | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG01256 | hp1 | a0002 | c0002 | t0001 | g0140 | AMR | CLM | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0233 | AMR | CLM | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0221 | AMR | CLM | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG01257 | hp2 | a0002 | c0002 | t0001 | g0130 | AMR | CLM | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG01346 | hp1 | a0001 | c0001 | t0032 | g0220 | AMR | CLM | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG01346 | hp2 | a0002 | c0002 | t0001 | g0067 | AMR | CLM | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG01496 | hp1 | a0001 | c0001 | t0007 | g0185 | AMR | CLM | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0218 | AMR | CLM | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG01884 | hp1 | a0001 | c0001 | t0008 | g0031 | AFR | ACB | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG01884 | hp2 | a0001 | c0001 | t0010 | g0182 | AFR | ACB | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG01952 | hp1 | a0002 | c0002 | t0002 | g0095 | AMR | PEL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0212 | AMR | PEL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG01975 | hp1 | a0002 | c0002 | t0013 | g0098 | AMR | PEL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PEL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0225 | AMR | PEL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG01978 | hp2 | a0001 | c0001 | t0016 | g0166 | AMR | PEL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG01981 | hp1 | a0001 | c0003 | t0036 | g0197 | AMR | PEL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG01993 | hp1 | a0002 | c0002 | t0001 | g0107 | AMR | PEL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG01993 | hp2 | a0002 | c0002 | t0011 | g0070 | AMR | PEL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | KHV | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02015 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | KHV | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02027 | hp1 | a0002 | c0002 | t0001 | g0255 | EAS | KHV | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02027 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02056 | hp1 | a0002 | c0002 | t0002 | g0122 | EAS | KHV | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02056 | hp2 | a0001 | c0001 | t0019 | g0050 | EAS | KHV | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02074 | hp1 | a0002 | c0002 | t0028 | g0044 | EAS | KHV | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | KHV | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02080 | hp1 | a0002 | c0002 | t0002 | g0113 | EAS | KHV | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02080 | hp2 | a0002 | c0002 | t0006 | g0078 | EAS | KHV | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02083 | hp1 | a0002 | c0002 | t0001 | g0069 | EAS | KHV | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02083 | hp2 | a0001 | c0001 | t0020 | g0036 | EAS | KHV | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02135 | hp1 | a0002 | c0002 | t0002 | g0125 | EAS | KHV | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02135 | hp2 | a0002 | c0002 | t0030 | g0046 | EAS | KHV | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02145 | hp1 | a0001 | c0003 | t0004 | g0196 | AFR | ACB | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02148 | hp1 | a0002 | c0002 | t0011 | g0127 | AMR | PEL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02257 | hp1 | a0002 | c0002 | t0001 | g0086 | AFR | ACB | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02257 | hp2 | a0001 | c0001 | t0010 | g0015 | AFR | ACB | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02258 | hp1 | a0001 | c0001 | t0014 | g0169 | AFR | ACB | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02258 | hp2 | a0001 | c0001 | t0003 | g0252 | AFR | ACB | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02273 | hp1 | a0002 | c0002 | t0001 | g0091 | AMR | PEL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02273 | hp2 | a0002 | c0002 | t0013 | g0099 | AMR | PEL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02451 | hp1 | a0001 | c0003 | t0004 | g0209 | AFR | ACB | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02451 | hp2 | a0002 | c0002 | t0001 | g0085 | AFR | ACB | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02572 | hp1 | a0001 | c0005 | t0008 | g0173 | AFR | GWD | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02572 | hp2 | a0001 | c0001 | t0003 | g0203 | AFR | GWD | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0232 | SAS | PJL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02602 | hp2 | a0002 | c0002 | t0001 | g0090 | SAS | PJL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0216 | AFR | GWD | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02615 | hp2 | a0001 | c0005 | t0008 | g0171 | AFR | GWD | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02622 | hp1 | a0002 | c0002 | t0014 | g0073 | AFR | GWD | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02622 | hp2 | a0002 | c0002 | t0012 | g0009 | AFR | GWD | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02630 | hp1 | a0001 | c0003 | t0004 | g0200 | AFR | GWD | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02630 | hp2 | a0001 | c0001 | t0017 | g0240 | AFR | GWD | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02647 | hp1 | a0001 | c0003 | t0004 | g0205 | AFR | GWD | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02647 | hp2 | a0001 | c0001 | t0003 | g0254 | AFR | GWD | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02683 | hp2 | a0002 | c0002 | t0013 | g0151 | SAS | PJL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0178 | SAS | PJL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02698 | hp2 | a0002 | c0002 | t0001 | g0097 | SAS | PJL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02717 | hp2 | a0001 | c0001 | t0035 | g0165 | AFR | GWD | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02723 | hp1 | a0001 | c0003 | t0004 | g0199 | AFR | GWD | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02723 | hp2 | a0001 | c0001 | t0010 | g0179 | AFR | GWD | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02735 | hp1 | a0001 | c0001 | t0007 | g0234 | SAS | PJL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0040 | SAS | PJL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02738 | hp1 | a0002 | c0002 | t0001 | g0093 | SAS | PJL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0239 | SAS | PJL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02809 | hp1 | a0001 | c0001 | t0027 | g0028 | AFR | GWD | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02809 | hp2 | a0001 | c0005 | t0008 | g0170 | AFR | GWD | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02818 | hp1 | a0002 | c0002 | t0012 | g0074 | AFR | GWD | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02818 | hp2 | a0001 | c0001 | t0003 | g0244 | AFR | GWD | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02895 | hp1 | a0001 | c0001 | t0003 | g0246 | AFR | GWD | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02896 | hp1 | a0001 | c0001 | t0008 | g0034 | AFR | GWD | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0249 | AFR | GWD | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02897 | hp1 | a0001 | c0001 | t0003 | g0247 | AFR | GWD | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02897 | hp2 | a0001 | c0001 | t0008 | g0033 | AFR | GWD | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02922 | hp1 | a0002 | c0002 | t0001 | g0082 | AFR | ESN | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02922 | hp2 | a0001 | c0003 | t0004 | g0195 | AFR | ESN | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02965 | hp1 | a0001 | c0001 | t0010 | g0201 | AFR | ESN | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02965 | hp2 | a0001 | c0003 | t0004 | g0241 | AFR | ESN | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02970 | hp1 | a0004 | c0011 | t0037 | g0259 | AFR | ESN | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02970 | hp2 | a0001 | c0003 | t0004 | g0250 | AFR | ESN | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02976 | hp1 | a0001 | c0001 | t0010 | g0184 | AFR | ESN | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02976 | hp2 | a0001 | c0001 | t0003 | g0248 | AFR | ESN | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG03017 | hp1 | a0002 | c0002 | t0001 | g0124 | SAS | PJL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG03017 | hp2 | a0002 | c0002 | t0001 | g0104 | SAS | PJL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG03041 | hp2 | a0001 | c0004 | t0006 | g0020 | AFR | GWD | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG03098 | hp1 | a0001 | c0003 | t0004 | g0202 | AFR | MSL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG03098 | hp2 | a0001 | c0003 | t0004 | g0210 | AFR | MSL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG03130 | hp1 | a0001 | c0003 | t0004 | g0206 | AFR | ESN | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG03130 | hp2 | a0001 | c0001 | t0017 | g0251 | AFR | ESN | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG03139 | hp1 | a0001 | c0001 | t0003 | g0253 | AFR | ESN | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG03139 | hp2 | a0002 | c0002 | t0001 | g0146 | AFR | ESN | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG03195 | hp1 | a0001 | c0001 | t0021 | g0017 | AFR | ESN | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG03195 | hp2 | a0001 | c0001 | t0008 | g0032 | AFR | ESN | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG03225 | hp1 | a0001 | c0001 | t0023 | g0175 | AFR | MSL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG03225 | hp2 | a0001 | c0003 | t0004 | g0208 | AFR | MSL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG03239 | hp2 | a0002 | c0002 | t0006 | g0100 | SAS | PJL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG03453 | hp1 | a0001 | c0005 | t0001 | g0172 | AFR | MSL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG03453 | hp2 | a0001 | c0003 | t0004 | g0204 | AFR | MSL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG03486 | hp1 | a0001 | c0003 | t0004 | g0180 | AFR | MSL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG03486 | hp2 | a0001 | c0001 | t0008 | g0029 | AFR | MSL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG03491 | hp1 | a0002 | c0002 | t0001 | g0139 | SAS | PJL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG03491 | hp2 | a0003 | c0006 | t0006 | g0005 | SAS | PJL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0258 | SAS | PJL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG03492 | hp2 | a0003 | c0006 | t0006 | g0005 | SAS | PJL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG03516 | hp1 | a0002 | c0002 | t0014 | g0008 | AFR | ESN | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG03516 | hp2 | a0002 | c0002 | t0001 | g0083 | AFR | ESN | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG03540 | hp1 | a0001 | c0001 | t0015 | g0167 | AFR | GWD | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG03540 | hp2 | a0002 | c0002 | t0001 | g0076 | AFR | GWD | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG03579 | hp1 | a0002 | c0002 | t0001 | g0145 | AFR | MSL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG03579 | hp2 | a0002 | c0002 | t0001 | g0079 | AFR | MSL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0038 | SAS | PJL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG03654 | hp2 | a0002 | c0002 | t0006 | g0092 | SAS | PJL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG03704 | hp1 | a0002 | c0002 | t0003 | g0161 | SAS | PJL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG03704 | hp2 | a0001 | c0001 | t0007 | g0191 | SAS | PJL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0018 | SAS | BEB | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG03927 | hp2 | a0002 | c0002 | t0001 | g0123 | SAS | BEB | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG03942 | hp1 | a0001 | c0004 | t0006 | g0019 | SAS | BEB | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG03942 | hp2 | a0002 | c0002 | t0001 | g0118 | SAS | BEB | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG04199 | hp1 | a0002 | c0002 | t0002 | g0153 | SAS | STU | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG04199 | hp2 | a0002 | c0002 | t0040 | g0149 | SAS | STU | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG04204 | hp1 | a0002 | c0002 | t0003 | g0159 | SAS | STU | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG04204 | hp2 | a0001 | c0001 | t0031 | g0229 | SAS | STU | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA18612 | hp1 | a0002 | c0002 | t0001 | g0115 | EAS | CHB | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA18612 | hp2 | a0002 | c0002 | t0002 | g0111 | EAS | CHB | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA18906 | hp1 | a0001 | c0001 | t0003 | g0014 | AFR | YRI | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA18906 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | YRI | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA18941 | hp1 | a0001 | c0004 | t0006 | g0022 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA18941 | hp2 | a0001 | c0001 | t0042 | g0057 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA18944 | hp1 | a0001 | c0001 | t0009 | g0004 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA18944 | hp2 | a0002 | c0002 | t0001 | g0106 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA18947 | hp1 | a0001 | c0001 | t0005 | g0053 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA18947 | hp2 | a0002 | c0002 | t0001 | g0068 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA18948 | hp1 | a0001 | c0001 | t0005 | g0058 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA18948 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA18952 | hp1 | a0002 | c0002 | t0001 | g0121 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA18952 | hp2 | a0001 | c0001 | t0005 | g0066 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA18963 | hp2 | a0002 | c0002 | t0003 | g0157 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA18965 | hp1 | a0001 | c0001 | t0009 | g0227 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA18965 | hp2 | a0002 | c0002 | t0025 | g0117 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA18966 | hp1 | a0001 | c0001 | t0005 | g0006 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA18966 | hp2 | a0002 | c0002 | t0001 | g0042 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA18967 | hp1 | a0002 | c0002 | t0001 | g0133 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA18967 | hp2 | a0001 | c0001 | t0009 | g0223 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA18970 | hp1 | a0001 | c0001 | t0041 | g0056 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA18970 | hp2 | a0002 | c0002 | t0001 | g0138 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA18977 | hp1 | a0002 | c0002 | t0001 | g0132 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA18977 | hp2 | a0001 | c0001 | t0005 | g0051 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA18979 | hp1 | a0002 | c0002 | t0003 | g0156 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA18979 | hp2 | a0002 | c0002 | t0001 | g0103 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA18983 | hp1 | a0001 | c0001 | t0005 | g0007 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA18983 | hp2 | a0001 | c0001 | t0009 | g0004 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA18984 | hp1 | a0002 | c0002 | t0011 | g0012 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA18984 | hp2 | a0002 | c0002 | t0002 | g0155 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA18985 | hp1 | a0002 | c0002 | t0003 | g0109 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA18985 | hp2 | a0002 | c0002 | t0001 | g0158 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA18989 | hp1 | a0002 | c0002 | t0002 | g0112 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA18989 | hp2 | a0001 | c0001 | t0005 | g0064 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA18990 | hp1 | a0001 | c0001 | t0005 | g0006 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA18990 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA18993 | hp2 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA18994 | hp1 | a0005 | c0009 | t0001 | g0041 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA18994 | hp2 | a0001 | c0001 | t0005 | g0054 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA18995 | hp1 | a0002 | c0002 | t0002 | g0154 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA18995 | hp2 | a0002 | c0002 | t0001 | g0089 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA18999 | hp2 | a0002 | c0002 | t0003 | g0164 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA19002 | hp1 | a0001 | c0001 | t0019 | g0048 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA19002 | hp2 | a0002 | c0002 | t0005 | g0120 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA19003 | hp1 | a0006 | c0007 | t0003 | g0152 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA19003 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA19004 | hp1 | a0002 | c0002 | t0001 | g0119 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA19004 | hp2 | a0001 | c0001 | t0005 | g0055 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA19010 | hp2 | a0002 | c0002 | t0001 | g0072 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA19011 | hp1 | a0002 | c0002 | t0002 | g0114 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA19011 | hp2 | a0002 | c0002 | t0001 | g0062 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA19012 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA19030 | hp1 | a0002 | c0002 | t0033 | g0084 | AFR | LWK | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA19030 | hp2 | a0002 | c0002 | t0023 | g0144 | AFR | LWK | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA19058 | hp1 | a0002 | c0002 | t0001 | g0063 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA19058 | hp2 | a0001 | c0004 | t0006 | g0059 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA19062 | hp1 | a0002 | c0002 | t0001 | g0071 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA19062 | hp2 | a0001 | c0001 | t0020 | g0049 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA19065 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA19068 | hp1 | a0001 | c0001 | t0005 | g0007 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA19068 | hp2 | a0002 | c0002 | t0001 | g0129 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA19070 | hp1 | a0002 | c0002 | t0001 | g0045 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA19070 | hp2 | a0002 | c0002 | t0003 | g0142 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA19082 | hp1 | a0002 | c0002 | t0003 | g0160 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA19082 | hp2 | a0002 | c0002 | t0001 | g0148 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA19085 | hp1 | a0002 | c0002 | t0001 | g0147 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA19085 | hp2 | a0002 | c0002 | t0003 | g0163 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA19087 | hp1 | a0001 | c0001 | t0009 | g0004 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA19087 | hp2 | a0002 | c0002 | t0001 | g0047 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA19088 | hp1 | a0002 | c0002 | t0001 | g0150 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA19088 | hp2 | a0002 | c0002 | t0003 | g0110 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA19240 | hp1 | a0002 | c0002 | t0001 | g0077 | AFR | YRI | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA19240 | hp2 | a0001 | c0003 | t0004 | g0168 | AFR | YRI | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA20129 | hp1 | a0002 | c0002 | t0002 | g0108 | AFR | ASW | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA20129 | hp2 | a0002 | c0002 | t0014 | g0008 | AFR | ASW | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA20752 | hp1 | a0001 | c0001 | t0007 | g0187 | EUR | TSI | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA20752 | hp2 | a0001 | c0001 | t0016 | g0177 | EUR | TSI | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0228 | EUR | TSI | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA20805 | hp2 | a0002 | c0002 | t0001 | g0116 | EUR | TSI | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA20905 | hp1 | a0002 | c0002 | t0001 | g0136 | SAS | GIH | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA20905 | hp2 | a0001 | c0001 | t0016 | g0176 | SAS | GIH | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG01123 | hp1 | a0001 | c0003 | t0004 | g0211 | AMR | CLM | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02109 | hp1 | a0001 | c0003 | t0004 | g0207 | AFR | ACB | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02109 | hp2 | a0002 | c0002 | t0001 | g0101 | AFR | ACB | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02486 | hp1 | a0002 | c0002 | t0001 | g0081 | AFR | ACB | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02486 | hp2 | a0002 | c0002 | t0012 | g0009 | AFR | ACB | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02559 | hp1 | a0002 | c0002 | t0001 | g0080 | AFR | ACB | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG02559 | hp2 | a0001 | c0001 | t0003 | g0245 | AFR | ACB | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG06807 | hp1 | a0001 | c0001 | t0008 | g0030 | AFR | USA | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
HG06807 | hp2 | a0002 | c0002 | t0012 | g0075 | AFR | USA | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA18955 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA18955 | hp2 | a0001 | c0001 | t0005 | g0052 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0224 | AFR | USA | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA20300 | hp2 | a0001 | c0001 | t0003 | g0014 | AFR | USA | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA21309 | hp1 | a0002 | c0002 | t0001 | g0087 | AFR | LWK | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
NA21309 | hp2 | a0001 | c0001 | t0021 | g0242 | AFR | LWK | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
homoSapiens | chm13v2 | a0001 | c0001 | t0039 | g0193 | REF | REF | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
homoSapiens | grch38p0 | a0002 | c0010 | t0004 | g0134 | REF | REF | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:49077267 | T | G | 1 | a0003 | 2 | HG03491.hp2 HG03492.hp2 |
missense_variant | MODERATE | c.586A>C | p.Met196Leu | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/8 | 623/6414 | 586/963 | 196/320 | chr10 | 49077267 | |||
chr10:49107734 | C | T | 1 | a0005 | 1 | NA18994.hp1 | missense_variant | MODERATE | c.317G>A | p.Arg106Gln | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/8 | 354/6414 | 317/963 | 106/320 | chr10 | 49107734 | |||
chr10:49107848 | A | G | 3 | a0001 a0003 a0004 |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(153): Show |
missense_variant | MODERATE | c.203T>C | p.Phe68Ser | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/8 | 240/6414 | 203/963 | 68/320 | chr10 | 49107848 | |||
chr10:49107893 | C | T | 1 | a0006 | 1 | NA19003.hp1 | missense_variant | MODERATE | c.158G>A | p.Arg53Gln | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/8 | 195/6414 | 158/963 | 53/320 | chr10 | 49107893 | |||
chr10:49115463 | G | A | 1 | a0004 | 1 | HG02970.hp1 | missense_variant | MODERATE | c.23C>T | p.Ala8Val | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/8 | 60/6414 | 23/963 | 8/320 | chr10 | 49115463 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:49019740 | T | C | 9 | a0001c0001 a0001c0004 a0001c0005 others(6): Show |
259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
synonymous_variant | LOW | c.873A>G | p.Glu291Glu | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 910/6414 | 873/963 | 291/320 | chr10 | 49019740 | |||
chr10:49048503 | G | A | 3 | a0001c0004 a0001c0008 a0003c0006 |
7 | HG00639.hp2 HG03041.hp2 HG03491.hp2 others(4): Show |
synonymous_variant | LOW | c.750C>T | p.Asp250Asp | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 6/8 | 787/6414 | 750/963 | 250/320 | chr10 | 49048503 | |||
chr10:49107676 | G | A | 2 | a0001c0008 a0004c0011 |
2 | HG00639.hp2 HG02970.hp1 |
synonymous_variant | LOW | c.375C>T | p.Tyr125Tyr | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/8 | 412/6414 | 375/963 | 125/320 | chr10 | 49107676 | |||
chr10:49107772 | G | A | 1 | a0001c0005 | 4 | HG02572.hp1 HG02615.hp2 HG02809.hp2 others(1): Show |
synonymous_variant | LOW | c.279C>T | p.Ser93Ser | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/8 | 316/6414 | 279/963 | 93/320 | chr10 | 49107772 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:49014382 | T | C | 3 | a0001c0001t0015 a0001c0001t0016 a0001c0001t0018 |
8 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5268A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 5268 | chr10 | 49014382 | ||||||
chr10:49014516 | C | T | 1 | a0001c0001t0042 | 1 | NA18941.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5134G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 5134 | chr10 | 49014516 | ||||||
chr10:49014516 | CCT | C | 19 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0009 others(16): Show |
76 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*5132_*5133delAG | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 5132 | chr10 | 49014516 | ||||||
chr10:49014540 | G | T | 18 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0015 others(15): Show |
122 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(119): Show |
3_prime_UTR_variant | MODIFIER | c.*5110C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 5110 | chr10 | 49014540 | ||||||
chr10:49014609 | GTT | G | 46 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(43): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
3_prime_UTR_variant | MODIFIER | c.*5039_*5040delAA | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 5039 | chr10 | 49014609 | ||||||
chr10:49014724 | T | G | 46 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(43): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
3_prime_UTR_variant | MODIFIER | c.*4926A>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 4926 | chr10 | 49014724 | ||||||
chr10:49014953 | G | A | 2 | a0001c0001t0010 a0001c0001t0022 |
7 | HG00642.hp1 HG01243.hp2 HG01884.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4697C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 4697 | chr10 | 49014953 | ||||||
chr10:49015020 | A | G | 4 | a0001c0001t0005 a0001c0001t0041 a0001c0001t0042 others(1): Show |
16 | HG00423.hp2 NA18941.hp2 NA18947.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*4630T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 4630 | chr10 | 49015020 | ||||||
chr10:49015118 | CATT | C | 2 | a0001c0001t0010 a0001c0001t0022 |
7 | HG00642.hp1 HG01243.hp2 HG01884.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4529_*4531delAAT | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 4529 | chr10 | 49015118 | ||||||
chr10:49015119 | A | ATT | 8 | a0001c0001t0005 a0001c0001t0015 a0001c0001t0016 others(5): Show |
25 | HG00423.hp2 HG01069.hp2 HG01070.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*4529_*4530dupAA | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 4530 | chr10 | 49015119 | ||||||
chr10:49015119 | AT | A | 18 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0026 others(15): Show |
111 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*4530delA | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 4530 | chr10 | 49015119 | ||||||
chr10:49015119 | ATT | A | 7 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0024 others(4): Show |
27 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*4529_*4530delAA | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 4529 | chr10 | 49015119 | ||||||
chr10:49015119 | ATTT | A | 4 | a0001c0001t0007 a0001c0001t0008 a0002c0002t0001 others(1): Show |
8 | HG01074.hp1 HG02622.hp1 HG02698.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4528_*4530delAAA | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 4528 | chr10 | 49015119 | ||||||
chr10:49015119 | ATTTT | A | 18 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0009 others(15): Show |
72 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*4527_*4530delAAAA | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 4527 | chr10 | 49015119 | ||||||
chr10:49015122 | T | G | 2 | a0001c0001t0010 a0001c0001t0022 |
7 | HG00642.hp1 HG01243.hp2 HG01884.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4528A>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 4528 | chr10 | 49015122 | ||||||
chr10:49015144 | C | G | 1 | a0001c0001t0015 | 3 | HG01069.hp2 HG01071.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4506G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 4506 | chr10 | 49015144 | ||||||
chr10:49015368 | G | A | 2 | a0001c0001t0010 a0001c0001t0022 |
7 | HG00642.hp1 HG01243.hp2 HG01884.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4282C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 4282 | chr10 | 49015368 | ||||||
chr10:49015411 | G | A | 4 | a0001c0004t0006 a0001c0008t0006 a0002c0002t0006 others(1): Show |
11 | HG00323.hp1 HG00639.hp2 HG02080.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4239C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 4239 | chr10 | 49015411 | ||||||
chr10:49015454 | G | C | 1 | a0001c0003t0036 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4196C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 4196 | chr10 | 49015454 | ||||||
chr10:49015478 | G | A | 1 | a0001c0001t0027 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4172C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 4172 | chr10 | 49015478 | ||||||
chr10:49015481 | C | T | 3 | a0001c0001t0015 a0001c0001t0016 a0001c0001t0018 |
8 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4169G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 4169 | chr10 | 49015481 | ||||||
chr10:49015569 | G | A | 19 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0015 others(16): Show |
123 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*4081C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 4081 | chr10 | 49015569 | ||||||
chr10:49015792 | G | A | 7 | a0001c0001t0003 a0001c0001t0023 a0001c0001t0038 others(4): Show |
32 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*3858C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 3858 | chr10 | 49015792 | ||||||
chr10:49015849 | C | T | 1 | a0001c0001t0041 | 1 | NA18970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3801G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 3801 | chr10 | 49015849 | ||||||
chr10:49015851 | C | T | 1 | a0001c0001t0026 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3799G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 3799 | chr10 | 49015851 | ||||||
chr10:49015862 | C | T | 1 | a0001c0001t0035 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3788G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 3788 | chr10 | 49015862 | ||||||
chr10:49016027 | C | G | 1 | a0001c0001t0017 | 2 | HG02630.hp2 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3623G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 3623 | chr10 | 49016027 | ||||||
chr10:49016090 | T | C | 1 | a0004c0011t0037 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3560A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 3560 | chr10 | 49016090 | ||||||
chr10:49016118 | TTTTG | T | 54 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(51): Show |
259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
3_prime_UTR_variant | MODIFIER | c.*3528_*3531delCAAA | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 3528 | chr10 | 49016118 | ||||||
chr10:49016359 | G | T | 20 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0009 others(17): Show |
77 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*3291C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 3291 | chr10 | 49016359 | ||||||
chr10:49016710 | C | T | 1 | a0002c0002t0030 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2940G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 2940 | chr10 | 49016710 | ||||||
chr10:49016721 | C | T | 15 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0024 others(12): Show |
114 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*2929G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 2929 | chr10 | 49016721 | ||||||
chr10:49016740 | C | T | 1 | a0001c0001t0019 | 2 | HG02056.hp2 NA19002.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2910G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 2910 | chr10 | 49016740 | ||||||
chr10:49016811 | C | T | 22 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0009 others(19): Show |
80 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*2839G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 2839 | chr10 | 49016811 | ||||||
chr10:49016989 | C | G | 45 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(42): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
3_prime_UTR_variant | MODIFIER | c.*2661G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 2661 | chr10 | 49016989 | ||||||
chr10:49017018 | T | C | 9 | a0001c0001t0008 a0001c0001t0014 a0001c0001t0035 others(6): Show |
25 | HG00323.hp1 HG00639.hp2 HG01884.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*2632A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 2632 | chr10 | 49017018 | ||||||
chr10:49017077 | CA | C | 1 | a0002c0002t0012 | 4 | HG02486.hp2 HG02622.hp2 HG02818.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2572delT | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 2572 | chr10 | 49017077 | ||||||
chr10:49017406 | T | C | 1 | a0001c0001t0038 | 1 | HG01069.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2244A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 2244 | chr10 | 49017406 | ||||||
chr10:49017421 | G | A | 1 | a0001c0001t0032 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2229C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 2229 | chr10 | 49017421 | ||||||
chr10:49017425 | A | G | 10 | a0001c0001t0008 a0001c0001t0014 a0001c0001t0034 others(7): Show |
26 | HG00323.hp1 HG00639.hp2 HG01243.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*2225T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 2225 | chr10 | 49017425 | ||||||
chr10:49017437 | A | G | 2 | a0001c0001t0023 a0002c0002t0023 |
2 | HG03225.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2213T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 2213 | chr10 | 49017437 | ||||||
chr10:49017531 | T | C | 1 | a0001c0001t0022 | 2 | HG00642.hp1 HG01243.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2119A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 2119 | chr10 | 49017531 | ||||||
chr10:49017598 | G | C | 7 | a0001c0001t0003 a0001c0001t0023 a0001c0001t0038 others(4): Show |
32 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*2052C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 2052 | chr10 | 49017598 | ||||||
chr10:49017624 | T | C | 1 | a0002c0002t0028 | 1 | HG02074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2026A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 2026 | chr10 | 49017624 | ||||||
chr10:49017629 | G | A | 2 | a0001c0001t0019 a0001c0001t0020 |
4 | HG02056.hp2 HG02083.hp2 NA19002.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2021C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 2021 | chr10 | 49017629 | ||||||
chr10:49017690 | G | A | 15 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0024 others(12): Show |
114 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*1960C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 1960 | chr10 | 49017690 | ||||||
chr10:49017709 | C | T | 21 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0009 others(18): Show |
79 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*1941G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 1941 | chr10 | 49017709 | ||||||
chr10:49017829 | T | C | 1 | a0002c0002t0029 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1821A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 1821 | chr10 | 49017829 | ||||||
chr10:49017834 | T | C | 4 | a0001c0004t0006 a0001c0008t0006 a0002c0002t0006 others(1): Show |
11 | HG00323.hp1 HG00639.hp2 HG02080.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1816A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 1816 | chr10 | 49017834 | ||||||
chr10:49018186 | T | C | 1 | a0002c0002t0033 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1464A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 1464 | chr10 | 49018186 | ||||||
chr10:49018258 | A | G | 1 | a0002c0002t0033 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1392T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 1392 | chr10 | 49018258 | ||||||
chr10:49018289 | T | G | 15 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0024 others(12): Show |
114 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*1361A>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 1361 | chr10 | 49018289 | ||||||
chr10:49018540 | C | T | 2 | a0001c0001t0009 a0002c0002t0009 |
6 | HG00423.hp1 NA18944.hp1 NA18965.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1110G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 1110 | chr10 | 49018540 | ||||||
chr10:49018549 | A | G | 5 | a0001c0001t0005 a0001c0001t0021 a0001c0001t0041 others(2): Show |
18 | HG00423.hp2 HG03195.hp1 NA18941.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1101T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 1101 | chr10 | 49018549 | ||||||
chr10:49018673 | CA | C | 2 | a0001c0001t0008 a0001c0005t0008 |
9 | HG01884.hp1 HG02572.hp1 HG02615.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*976delT | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 976 | chr10 | 49018673 | ||||||
chr10:49018759 | C | A | 3 | a0001c0001t0007 a0001c0001t0024 a0002c0002t0007 |
11 | HG00099.hp1 HG00639.hp1 HG01070.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*891G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 891 | chr10 | 49018759 | ||||||
chr10:49018807 | T | C | 45 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(42): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
3_prime_UTR_variant | MODIFIER | c.*843A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 843 | chr10 | 49018807 | ||||||
chr10:49019084 | C | T | 22 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0009 others(19): Show |
80 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*566G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 566 | chr10 | 49019084 | ||||||
chr10:49019246 | C | G | 1 | a0002c0002t0025 | 1 | NA18965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*404G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 404 | chr10 | 49019246 | ||||||
chr10:49019278 | A | G | 11 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0018 others(8): Show |
53 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*372T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 372 | chr10 | 49019278 | ||||||
chr10:49019339 | G | A | 1 | a0002c0002t0040 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*311C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 311 | chr10 | 49019339 | ||||||
chr10:49019363 | G | A | 1 | a0002c0002t0013 | 4 | HG01081.hp1 HG01975.hp1 HG02273.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*287C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 287 | chr10 | 49019363 | ||||||
chr10:49019411 | G | A | 4 | a0001c0001t0005 a0001c0001t0041 a0001c0001t0042 others(1): Show |
16 | HG00423.hp2 NA18941.hp2 NA18947.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*239C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 239 | chr10 | 49019411 | ||||||
chr10:49019431 | C | T | 1 | a0001c0001t0017 | 2 | HG02630.hp2 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*219G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 219 | chr10 | 49019431 | ||||||
chr10:49019470 | C | T | 12 | a0001c0001t0001 a0001c0001t0026 a0001c0001t0027 others(9): Show |
103 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*180G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 180 | chr10 | 49019470 | ||||||
chr10:49019514 | C | T | 2 | a0002c0002t0011 a0002c0002t0025 |
5 | HG00438.hp2 HG01993.hp2 HG02148.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*136G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 136 | chr10 | 49019514 | ||||||
chr10:49019538 | C | T | 1 | a0001c0001t0024 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*112G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 112 | chr10 | 49019538 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:49019825 | C | T | 210 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0024 others(207): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.838-50G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49019825 | |||||||
chr10:49019882 | C | A | 238 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0024 others(235): Show |
259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.838-107G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49019882 | |||||||
chr10:49020060 | C | T | 1 | a0002c0002t0012g0074 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.838-285G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49020060 | |||||||
chr10:49020221 | C | T | 1 | a0002c0002t0001g0121 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.838-446G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49020221 | |||||||
chr10:49020530 | AC | A | 12 | a0001c0001t0010g0015 a0001c0001t0010g0179 a0001c0001t0010g0182 others(9): Show |
13 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.838-756delG | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49020530 | |||||||
chr10:49020568 | A | G | 2 | a0001c0004t0006g0022 a0001c0004t0006g0059 |
2 | NA18941.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.838-793T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49020568 | |||||||
chr10:49020703 | A | C | 93 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0024 others(90): Show |
103 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.838-928T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49020703 | |||||||
chr10:49020727 | A | AGAAG | 97 | a0001c0001t0002g0002 a0001c0001t0002g0018 a0001c0001t0002g0038 others(94): Show |
107 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.838-956_838-953dup others(4): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49020727 | |||||||
chr10:49020727 | A | AGGAAG | 3 | a0001c0005t0001g0172 a0002c0002t0001g0077 a0002c0002t0001g0105 |
3 | HG00280.hp1 HG03453.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.838-953_838-952ins others(5): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49020727 | |||||||
chr10:49020727 | A | AGGAAGGA others(2): Show |
38 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(35): Show |
42 | HG00099.hp1 HG00639.hp1 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.838-953_838-952ins others(9): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49020727 | |||||||
chr10:49020727 | A | AGGAAGGA others(6): Show |
44 | a0001c0001t0024g0190 a0002c0002t0001g0010 a0002c0002t0001g0011 others(41): Show |
46 | HG00597.hp2 HG00621.hp2 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.838-953_838-952ins others(13): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49020727 | |||||||
chr10:49020727 | A | AGGAAGGA others(10): Show |
19 | a0001c0001t0001g0003 a0001c0001t0001g0088 a0001c0001t0001g0217 others(16): Show |
23 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.838-953_838-952ins others(17): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49020727 | |||||||
chr10:49020727 | AGAAG | A | 31 | a0001c0001t0003g0014 a0001c0001t0003g0021 a0001c0001t0003g0035 others(28): Show |
32 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.838-956_838-953del others(4): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49020727 | |||||||
chr10:49020743 | G | A | 2 | a0001c0001t0017g0240 a0001c0001t0017g0251 |
2 | HG02630.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.838-968C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49020743 | |||||||
chr10:49020753 | G | A | 106 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0024 others(103): Show |
116 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.838-978C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49020753 | |||||||
chr10:49020757 | G | A | 6 | a0001c0001t0001g0037 a0002c0002t0001g0001 a0002c0002t0001g0106 others(3): Show |
9 | HG01106.hp2 HG02027.hp2 NA18612.hp1 others(6): Show |
intron_variant | MODIFIER | c.838-982C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49020757 | |||||||
chr10:49020835 | G | C | 1 | a0001c0001t0010g0179 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.838-1060C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49020835 | |||||||
chr10:49020871 | G | A | 104 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0024 others(101): Show |
114 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.838-1096C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49020871 | |||||||
chr10:49020877 | T | C | 104 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0024 others(101): Show |
114 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.838-1102A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49020877 | |||||||
chr10:49021038 | A | C | 2 | a0002c0002t0014g0008 a0002c0002t0014g0073 |
3 | HG02622.hp1 HG03516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.838-1263T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49021038 | |||||||
chr10:49021151 | C | CCTAAAAG others(2228): Show |
1 | a0001c0001t0017g0240 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.838-1377_838-1376i others(2237): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49021151 | |||||||
chr10:49021151 | C | CCTAAAAG others(2235): Show |
1 | a0001c0001t0017g0251 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.838-1377_838-1376i others(2244): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49021151 | |||||||
chr10:49021204 | GA | G | 10 | a0001c0004t0006g0019 a0001c0004t0006g0020 a0001c0004t0006g0022 others(7): Show |
11 | HG00323.hp1 HG00639.hp2 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.838-1430delT | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49021204 | |||||||
chr10:49021445 | A | T | 2 | a0001c0003t0004g0207 a0001c0003t0004g0209 |
2 | HG02109.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.838-1670T>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49021445 | |||||||
chr10:49021493 | A | C | 226 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0024 others(223): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.838-1718T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49021493 | |||||||
chr10:49021593 | T | A | 104 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0024 others(101): Show |
114 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.838-1818A>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49021593 | |||||||
chr10:49021620 | C | T | 3 | a0001c0005t0008g0170 a0001c0005t0008g0171 a0001c0005t0008g0173 |
3 | HG02572.hp1 HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.838-1845G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49021620 | |||||||
chr10:49021709 | T | G | 1 | a0001c0001t0002g0228 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.838-1934A>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49021709 | |||||||
chr10:49021717 | A | G | 1 | a0002c0002t0001g0083 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.838-1942T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49021717 | |||||||
chr10:49021921 | T | C | 31 | a0001c0001t0003g0014 a0001c0001t0003g0021 a0001c0001t0003g0035 others(28): Show |
32 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.838-2146A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49021921 | |||||||
chr10:49021976 | C | T | 2 | a0001c0001t0002g0228 a0002c0002t0002g0095 |
2 | HG01952.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.838-2201G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49021976 | |||||||
chr10:49022082 | A | C | 11 | a0001c0001t0007g0185 a0001c0001t0007g0186 a0001c0001t0007g0187 others(8): Show |
11 | HG00099.hp1 HG00639.hp1 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.838-2307T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49022082 | |||||||
chr10:49022111 | T | A | 1 | a0002c0002t0001g0097 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.838-2336A>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49022111 | |||||||
chr10:49022118 | TTTA | T | 72 | a0001c0001t0002g0002 a0001c0001t0002g0018 a0001c0001t0002g0038 others(69): Show |
78 | HG00323.hp1 HG00423.hp1 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.838-2346_838-2344d others(5): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49022118 | |||||||
chr10:49022121 | A | AT | 9 | a0001c0001t0007g0185 a0001c0001t0007g0186 a0001c0001t0007g0187 others(6): Show |
9 | HG00099.hp1 HG00639.hp1 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.838-2347dupA | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49022121 | |||||||
chr10:49022195 | T | C | 31 | a0001c0001t0003g0014 a0001c0001t0003g0021 a0001c0001t0003g0035 others(28): Show |
32 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.838-2420A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49022195 | |||||||
chr10:49022293 | G | T | 245 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0024 others(242): Show |
266 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.838-2518C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49022293 | |||||||
chr10:49022302 | A | T | 11 | a0001c0001t0007g0185 a0001c0001t0007g0186 a0001c0001t0007g0187 others(8): Show |
11 | HG00099.hp1 HG00639.hp1 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.838-2527T>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49022302 | |||||||
chr10:49022471 | A | T | 1 | a0001c0001t0001g0016 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.838-2696T>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49022471 | |||||||
chr10:49022473 | A | C | 2 | a0002c0002t0014g0008 a0002c0002t0014g0073 |
3 | HG02622.hp1 HG03516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.838-2698T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49022473 | |||||||
chr10:49022705 | T | C | 1 | a0001c0001t0008g0031 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.838-2930A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49022705 | |||||||
chr10:49022878 | C | T | 3 | a0001c0001t0010g0184 a0001c0001t0010g0201 a0001c0001t0022g0183 |
3 | HG00642.hp1 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.838-3103G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49022878 | |||||||
chr10:49022981 | C | T | 2 | a0001c0001t0008g0033 a0001c0001t0008g0034 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.838-3206G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49022981 | |||||||
chr10:49023110 | T | C | 6 | a0001c0001t0008g0029 a0001c0001t0008g0030 a0001c0001t0008g0031 others(3): Show |
6 | HG01884.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.838-3335A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49023110 | |||||||
chr10:49023127 | T | C | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG01192.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.838-3352A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49023127 | |||||||
chr10:49023139 | A | G | 1 | a0002c0002t0001g0104 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.838-3364T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49023139 | |||||||
chr10:49023270 | T | C | 1 | a0002c0002t0006g0102 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.838-3495A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49023270 | |||||||
chr10:49023305 | A | G | 1 | a0001c0001t0026g0174 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.838-3530T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49023305 | |||||||
chr10:49023407 | G | A | 1 | a0002c0002t0003g0163 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.838-3632C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49023407 | |||||||
chr10:49023509 | T | C | 14 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0051 others(11): Show |
16 | HG00423.hp2 NA18941.hp2 NA18947.hp1 others(13): Show |
intron_variant | MODIFIER | c.838-3734A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49023509 | |||||||
chr10:49023623 | C | A | 1 | a0001c0001t0002g0218 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.838-3848G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49023623 | |||||||
chr10:49023684 | C | G | 1 | a0001c0001t0017g0240 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.838-3909G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49023684 | |||||||
chr10:49023738 | T | C | 1 | a0004c0011t0037g0259 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.838-3963A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49023738 | |||||||
chr10:49023739 | G | A | 1 | a0004c0011t0037g0259 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.838-3964C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49023739 | |||||||
chr10:49023795 | C | T | 118 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0024 others(115): Show |
130 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.838-4020G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49023795 | |||||||
chr10:49023824 | G | T | 1 | a0002c0002t0001g0104 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.838-4049C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49023824 | |||||||
chr10:49023827 | G | A | 14 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0051 others(11): Show |
16 | HG00423.hp2 NA18941.hp2 NA18947.hp1 others(13): Show |
intron_variant | MODIFIER | c.838-4052C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49023827 | |||||||
chr10:49023835 | G | A | 31 | a0001c0001t0003g0014 a0001c0001t0003g0021 a0001c0001t0003g0035 others(28): Show |
32 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.838-4060C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49023835 | |||||||
chr10:49023837 | T | C | 2 | a0001c0001t0003g0244 a0001c0001t0003g0248 |
2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.838-4062A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49023837 | |||||||
chr10:49024074 | T | C | 1 | a0001c0001t0001g0226 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.838-4299A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49024074 | |||||||
chr10:49024134 | C | T | 3 | a0001c0001t0002g0216 a0001c0001t0002g0239 a0002c0002t0002g0153 |
3 | HG02615.hp1 HG02738.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.838-4359G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49024134 | |||||||
chr10:49024135 | A | G | 210 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0024 others(207): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.838-4360T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49024135 | |||||||
chr10:49024195 | CT | C | 32 | a0001c0001t0003g0014 a0001c0001t0003g0021 a0001c0001t0003g0035 others(29): Show |
33 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.838-4421delA | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49024195 | |||||||
chr10:49024241 | T | C | 104 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0024 others(101): Show |
114 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.838-4466A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49024241 | |||||||
chr10:49024367 | G | C | 34 | a0001c0001t0003g0014 a0001c0001t0003g0021 a0001c0001t0003g0035 others(31): Show |
36 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.838-4592C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49024367 | |||||||
chr10:49024381 | C | T | 1 | a0001c0001t0034g0194 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.838-4606G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49024381 | |||||||
chr10:49024440 | A | G | 1 | a0001c0001t0023g0175 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.838-4665T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49024440 | |||||||
chr10:49024496 | G | C | 1 | a0002c0002t0002g0125 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.838-4721C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49024496 | |||||||
chr10:49024811 | C | T | 1 | a0001c0001t0001g0258 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.838-5036G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49024811 | |||||||
chr10:49024827 | C | G | 1 | a0001c0001t0035g0165 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.838-5052G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49024827 | |||||||
chr10:49024838 | C | T | 104 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0024 others(101): Show |
114 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.838-5063G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49024838 | |||||||
chr10:49024944 | GT | G | 104 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0024 others(101): Show |
114 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.838-5170delA | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49024944 | |||||||
chr10:49024959 | T | C | 5 | a0001c0001t0015g0013 a0001c0001t0015g0167 a0001c0001t0016g0166 others(2): Show |
6 | HG01069.hp2 HG01071.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.838-5184A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49024959 | |||||||
chr10:49025076 | C | T | 104 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0024 others(101): Show |
114 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.838-5301G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49025076 | |||||||
chr10:49025232 | G | A | 1 | a0001c0001t0003g0253 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.838-5457C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49025232 | |||||||
chr10:49025429 | T | C | 12 | a0001c0001t0010g0015 a0001c0001t0010g0179 a0001c0001t0010g0182 others(9): Show |
13 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.838-5654A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49025429 | |||||||
chr10:49025476 | C | T | 1 | a0001c0001t0002g0224 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.838-5701G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49025476 | |||||||
chr10:49025524 | C | T | 31 | a0001c0001t0003g0014 a0001c0001t0003g0021 a0001c0001t0003g0035 others(28): Show |
32 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.838-5749G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49025524 | |||||||
chr10:49025538 | C | T | 1 | a0001c0003t0004g0196 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.838-5763G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49025538 | |||||||
chr10:49025552 | T | C | 1 | a0002c0002t0014g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.838-5777A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49025552 | |||||||
chr10:49025794 | G | A | 1 | a0001c0001t0007g0186 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.838-6019C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49025794 | |||||||
chr10:49025932 | C | T | 72 | a0001c0001t0002g0002 a0001c0001t0002g0018 a0001c0001t0002g0038 others(69): Show |
79 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.838-6157G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49025932 | |||||||
chr10:49026034 | C | T | 3 | a0001c0001t0001g0016 a0001c0001t0017g0240 a0001c0001t0017g0251 |
3 | HG02145.hp2 HG02630.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.838-6259G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49026034 | |||||||
chr10:49026300 | C | T | 103 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0025 others(100): Show |
113 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.838-6525G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49026300 | |||||||
chr10:49026355 | T | C | 76 | a0001c0001t0001g0016 a0001c0001t0002g0002 a0001c0001t0002g0018 others(73): Show |
83 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.838-6580A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49026355 | |||||||
chr10:49026356 | G | A | 1 | a0002c0002t0033g0084 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.838-6581C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49026356 | |||||||
chr10:49026376 | T | C | 49 | a0001c0001t0002g0002 a0001c0001t0002g0018 a0001c0001t0002g0038 others(46): Show |
54 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.838-6601A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49026376 | |||||||
chr10:49026492 | G | T | 1 | a0001c0001t0001g0217 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.838-6717C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49026492 | |||||||
chr10:49026618 | G | T | 2 | a0002c0002t0011g0070 a0002c0002t0011g0127 |
2 | HG01993.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.838-6843C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49026618 | |||||||
chr10:49026841 | C | T | 16 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0051 others(13): Show |
18 | HG00423.hp2 HG03195.hp1 NA18941.hp2 others(15): Show |
intron_variant | MODIFIER | c.838-7066G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49026841 | |||||||
chr10:49026990 | A | C | 32 | a0001c0001t0003g0014 a0001c0001t0003g0021 a0001c0001t0003g0035 others(29): Show |
33 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.838-7215T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49026990 | |||||||
chr10:49026999 | G | A | 3 | a0001c0001t0005g0064 a0001c0001t0005g0065 a0001c0001t0005g0066 |
3 | HG00423.hp2 NA18952.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.838-7224C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49026999 | |||||||
chr10:49027087 | T | C | 1 | a0002c0002t0001g0115 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.838-7312A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49027087 | |||||||
chr10:49027290 | G | A | 103 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0025 others(100): Show |
113 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.838-7515C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49027290 | |||||||
chr10:49027467 | T | C | 1 | a0001c0005t0008g0173 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.838-7692A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49027467 | |||||||
chr10:49027574 | C | T | 48 | a0001c0001t0002g0002 a0001c0001t0002g0018 a0001c0001t0002g0038 others(45): Show |
53 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.838-7799G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49027574 | |||||||
chr10:49027590 | C | T | 75 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0088 others(72): Show |
84 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.838-7815G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49027590 | |||||||
chr10:49027653 | A | G | 92 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0025 others(89): Show |
102 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.838-7878T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49027653 | |||||||
chr10:49027670 | A | C | 238 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0024 others(235): Show |
259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.838-7895T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49027670 | |||||||
chr10:49027786 | C | T | 92 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0025 others(89): Show |
102 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.838-8011G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49027786 | |||||||
chr10:49027893 | G | C | 1 | a0001c0008t0006g0023 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.838-8118C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49027893 | |||||||
chr10:49028135 | C | T | 1 | a0002c0002t0001g0097 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.838-8360G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49028135 | |||||||
chr10:49028323 | C | A | 1 | a0001c0001t0008g0030 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.838-8548G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49028323 | |||||||
chr10:49028323 | C | T | 11 | a0001c0001t0007g0185 a0001c0001t0007g0186 a0001c0001t0007g0187 others(8): Show |
11 | HG00099.hp1 HG00639.hp1 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.838-8548G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49028323 | |||||||
chr10:49028435 | C | A | 75 | a0001c0001t0001g0016 a0001c0001t0002g0002 a0001c0001t0002g0018 others(72): Show |
82 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.838-8660G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49028435 | |||||||
chr10:49028534 | T | C | 178 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0024 others(175): Show |
195 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.838-8759A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49028534 | |||||||
chr10:49028584 | T | A | 103 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0025 others(100): Show |
113 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.838-8809A>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49028584 | |||||||
chr10:49028586 | G | C | 103 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0025 others(100): Show |
113 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.838-8811C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49028586 | |||||||
chr10:49028644 | T | C | 32 | a0001c0001t0003g0014 a0001c0001t0003g0021 a0001c0001t0003g0035 others(29): Show |
33 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.838-8869A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49028644 | |||||||
chr10:49028847 | T | G | 103 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0025 others(100): Show |
113 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.838-9072A>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49028847 | |||||||
chr10:49029143 | A | T | 103 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0025 others(100): Show |
113 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.838-9368T>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49029143 | |||||||
chr10:49029394 | G | A | 1 | a0001c0003t0004g0198 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.838-9619C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49029394 | |||||||
chr10:49029415 | C | A | 1 | a0001c0003t0004g0199 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.838-9640G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49029415 | |||||||
chr10:49029562 | C | T | 32 | a0001c0001t0003g0014 a0001c0001t0003g0021 a0001c0001t0003g0035 others(29): Show |
33 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.838-9787G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49029562 | |||||||
chr10:49029715 | G | T | 1 | a0002c0002t0033g0084 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.838-9940C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49029715 | |||||||
chr10:49029739 | C | T | 11 | a0001c0001t0007g0185 a0001c0001t0007g0186 a0001c0001t0007g0187 others(8): Show |
11 | HG00099.hp1 HG00639.hp1 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.838-9964G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49029739 | |||||||
chr10:49029775 | G | C | 1 | a0001c0003t0036g0197 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.838-10000C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49029775 | |||||||
chr10:49030072 | G | A | 75 | a0001c0001t0001g0016 a0001c0001t0002g0002 a0001c0001t0002g0018 others(72): Show |
82 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.838-10297C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49030072 | |||||||
chr10:49030137 | A | G | 1 | a0004c0011t0037g0259 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.838-10362T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49030137 | |||||||
chr10:49030227 | C | T | 103 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0025 others(100): Show |
113 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.838-10452G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49030227 | |||||||
chr10:49030234 | C | A | 2 | a0002c0002t0006g0100 a0002c0002t0006g0102 |
2 | HG00323.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.838-10459G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49030234 | |||||||
chr10:49030309 | C | T | 1 | a0002c0002t0001g0079 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.838-10534G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49030309 | |||||||
chr10:49030310 | A | G | 103 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0025 others(100): Show |
113 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.838-10535T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49030310 | |||||||
chr10:49030408 | A | G | 98 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0025 others(95): Show |
108 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.838-10633T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49030408 | |||||||
chr10:49030525 | C | T | 68 | a0001c0001t0002g0002 a0001c0001t0002g0018 a0001c0001t0002g0038 others(65): Show |
75 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.838-10750G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49030525 | |||||||
chr10:49030618 | C | T | 32 | a0001c0001t0003g0014 a0001c0001t0003g0021 a0001c0001t0003g0035 others(29): Show |
33 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.838-10843G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49030618 | |||||||
chr10:49030633 | T | C | 1 | a0001c0001t0035g0165 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.838-10858A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49030633 | |||||||
chr10:49030648 | C | T | 1 | a0001c0003t0004g0196 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.838-10873G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49030648 | |||||||
chr10:49030654 | A | T | 12 | a0001c0001t0010g0015 a0001c0001t0010g0179 a0001c0001t0010g0182 others(9): Show |
13 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.838-10879T>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49030654 | |||||||
chr10:49030829 | T | C | 103 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0025 others(100): Show |
113 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.838-11054A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49030829 | |||||||
chr10:49030874 | A | G | 2 | a0002c0002t0014g0008 a0002c0002t0014g0073 |
3 | HG02622.hp1 HG03516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.838-11099T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49030874 | |||||||
chr10:49030917 | G | C | 1 | a0002c0002t0001g0140 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.838-11142C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49030917 | |||||||
chr10:49031008 | T | C | 79 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0088 others(76): Show |
88 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.838-11233A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49031008 | |||||||
chr10:49031096 | T | C | 1 | a0001c0001t0002g0221 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.838-11321A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49031096 | |||||||
chr10:49031116 | T | C | 75 | a0001c0001t0001g0016 a0001c0001t0002g0002 a0001c0001t0002g0018 others(72): Show |
82 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.838-11341A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49031116 | |||||||
chr10:49031200 | C | G | 32 | a0001c0001t0003g0014 a0001c0001t0003g0021 a0001c0001t0003g0035 others(29): Show |
33 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.838-11425G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49031200 | |||||||
chr10:49031209 | C | T | 2 | a0002c0002t0002g0154 a0002c0002t0002g0155 |
2 | NA18984.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.838-11434G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49031209 | |||||||
chr10:49031430 | A | G | 75 | a0001c0001t0001g0016 a0001c0001t0002g0002 a0001c0001t0002g0018 others(72): Show |
82 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.838-11655T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49031430 | |||||||
chr10:49031450 | C | T | 3 | a0001c0001t0014g0169 a0002c0002t0014g0008 a0002c0002t0014g0073 |
4 | HG02258.hp1 HG02622.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.838-11675G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49031450 | |||||||
chr10:49031798 | C | T | 4 | a0001c0001t0002g0178 a0001c0001t0018g0236 a0001c0001t0018g0237 others(1): Show |
4 | HG01070.hp2 HG01071.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.838-12023G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49031798 | |||||||
chr10:49031885 | C | A | 1 | a0001c0001t0001g0217 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.838-12110G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49031885 | |||||||
chr10:49031891 | A | G | 103 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0025 others(100): Show |
113 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.838-12116T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49031891 | |||||||
chr10:49031952 | C | G | 75 | a0001c0001t0001g0016 a0001c0001t0002g0002 a0001c0001t0002g0018 others(72): Show |
82 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.838-12177G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49031952 | |||||||
chr10:49032120 | A | C | 211 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0024 others(208): Show |
229 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.838-12345T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49032120 | |||||||
chr10:49032163 | C | T | 211 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0024 others(208): Show |
229 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.838-12388G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49032163 | |||||||
chr10:49032195 | G | T | 3 | a0001c0001t0021g0242 a0001c0001t0023g0175 a0002c0002t0023g0144 |
3 | HG03225.hp1 NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.838-12420C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49032195 | |||||||
chr10:49032234 | C | T | 1 | a0002c0002t0013g0151 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.838-12459G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49032234 | |||||||
chr10:49032264 | G | A | 12 | a0001c0001t0010g0015 a0001c0001t0010g0179 a0001c0001t0010g0182 others(9): Show |
13 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.838-12489C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49032264 | |||||||
chr10:49032294 | T | G | 238 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0024 others(235): Show |
259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.838-12519A>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49032294 | |||||||
chr10:49032316 | T | C | 4 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(1): Show |
4 | HG01192.hp2 HG02717.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.838-12541A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49032316 | |||||||
chr10:49032493 | A | G | 1 | a0002c0002t0001g0062 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.838-12718T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49032493 | |||||||
chr10:49032517 | G | A | 2 | a0001c0001t0001g0016 a0001c0001t0017g0240 |
2 | HG02145.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.838-12742C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49032517 | |||||||
chr10:49032572 | A | C | 1 | a0001c0001t0015g0167 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.838-12797T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49032572 | |||||||
chr10:49032767 | C | T | 1 | a0002c0002t0001g0105 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.838-12992G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49032767 | |||||||
chr10:49032872 | C | CAG | 6 | a0001c0001t0007g0185 a0001c0001t0007g0187 a0001c0001t0007g0192 others(3): Show |
6 | HG00099.hp1 HG00639.hp1 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.838-13099_838-1309 others(6): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49032872 | |||||||
chr10:49032909 | G | A | 3 | a0001c0001t0014g0169 a0002c0002t0014g0008 a0002c0002t0014g0073 |
4 | HG02258.hp1 HG02622.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.838-13134C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49032909 | |||||||
chr10:49032938 | CT | C | 104 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0025 others(101): Show |
114 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.838-13164delA | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49032938 | |||||||
chr10:49033277 | A | G | 12 | a0001c0001t0010g0015 a0001c0001t0010g0179 a0001c0001t0010g0182 others(9): Show |
13 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.838-13502T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49033277 | |||||||
chr10:49033293 | A | G | 10 | a0001c0004t0006g0019 a0001c0004t0006g0020 a0001c0004t0006g0022 others(7): Show |
11 | HG00323.hp1 HG00639.hp2 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.838-13518T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49033293 | |||||||
chr10:49033359 | T | C | 2 | a0002c0002t0001g0135 a0002c0002t0001g0136 |
2 | HG01175.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.838-13584A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49033359 | |||||||
chr10:49033492 | G | C | 1 | a0004c0011t0037g0259 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.837+13491C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49033492 | |||||||
chr10:49033743 | C | T | 1 | a0001c0004t0006g0019 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.837+13240G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49033743 | |||||||
chr10:49033745 | G | C | 1 | a0002c0002t0033g0084 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.837+13238C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49033745 | |||||||
chr10:49033893 | C | T | 76 | a0001c0001t0001g0016 a0001c0001t0002g0002 a0001c0001t0002g0018 others(73): Show |
83 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.837+13090G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49033893 | |||||||
chr10:49033962 | TCAC | T | 76 | a0001c0001t0001g0016 a0001c0001t0002g0002 a0001c0001t0002g0018 others(73): Show |
83 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.837+13018_837+1302 others(7): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49033962 | |||||||
chr10:49033970 | A | T | 76 | a0001c0001t0001g0016 a0001c0001t0002g0002 a0001c0001t0002g0018 others(73): Show |
83 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.837+13013T>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49033970 | |||||||
chr10:49034157 | C | T | 1 | a0001c0004t0006g0022 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.837+12826G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49034157 | |||||||
chr10:49034190 | CCACCATC others(2): Show |
C | 102 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0025 others(99): Show |
112 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.837+12784_837+1279 others(13): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49034190 | |||||||
chr10:49034275 | T | C | 73 | a0001c0001t0002g0002 a0001c0001t0002g0018 a0001c0001t0002g0038 others(70): Show |
80 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.837+12708A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49034275 | |||||||
chr10:49034362 | G | A | 1 | a0002c0002t0001g0105 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.837+12621C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49034362 | |||||||
chr10:49034404 | C | G | 246 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0024 others(243): Show |
267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.837+12579G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49034404 | |||||||
chr10:49034462 | C | T | 9 | a0001c0001t0008g0029 a0001c0001t0008g0030 a0001c0001t0008g0031 others(6): Show |
9 | HG01884.hp1 HG02572.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.837+12521G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49034462 | |||||||
chr10:49034465 | T | A | 3 | a0001c0001t0010g0184 a0001c0001t0010g0201 a0001c0001t0022g0183 |
3 | HG00642.hp1 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.837+12518A>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49034465 | |||||||
chr10:49034736 | C | T | 1 | a0002c0002t0001g0079 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.837+12247G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49034736 | |||||||
chr10:49034763 | T | C | 102 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0025 others(99): Show |
112 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.837+12220A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49034763 | |||||||
chr10:49035066 | C | T | 3 | a0001c0001t0010g0184 a0001c0001t0010g0201 a0001c0001t0022g0183 |
3 | HG00642.hp1 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.837+11917G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49035066 | |||||||
chr10:49035067 | G | A | 17 | a0001c0001t0003g0035 a0001c0001t0003g0039 a0001c0001t0003g0213 others(14): Show |
17 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(14): Show |
intron_variant | MODIFIER | c.837+11916C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49035067 | |||||||
chr10:49035192 | C | T | 14 | a0001c0001t0001g0217 a0002c0002t0001g0060 a0002c0002t0001g0061 others(11): Show |
14 | HG00280.hp1 HG00642.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.837+11791G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49035192 | |||||||
chr10:49035254 | T | A | 3 | a0001c0001t0003g0252 a0001c0001t0003g0254 a0001c0001t0017g0251 |
3 | HG02258.hp2 HG02647.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.837+11729A>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49035254 | |||||||
chr10:49035291 | A | C | 49 | a0001c0001t0002g0002 a0001c0001t0002g0018 a0001c0001t0002g0038 others(46): Show |
54 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.837+11692T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49035291 | |||||||
chr10:49035346 | G | T | 76 | a0001c0001t0001g0016 a0001c0001t0002g0002 a0001c0001t0002g0018 others(73): Show |
83 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.837+11637C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49035346 | |||||||
chr10:49035448 | G | A | 1 | a0001c0001t0021g0017 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.837+11535C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49035448 | |||||||
chr10:49035462 | G | A | 1 | a0002c0002t0033g0084 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.837+11521C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49035462 | |||||||
chr10:49035494 | C | T | 77 | a0001c0001t0001g0016 a0001c0001t0002g0002 a0001c0001t0002g0018 others(74): Show |
84 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.837+11489G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49035494 | |||||||
chr10:49035553 | G | A | 2 | a0002c0002t0014g0008 a0002c0002t0014g0073 |
3 | HG02622.hp1 HG03516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.837+11430C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49035553 | |||||||
chr10:49035657 | A | C | 10 | a0001c0004t0006g0019 a0001c0004t0006g0020 a0001c0004t0006g0022 others(7): Show |
11 | HG00323.hp1 HG00639.hp2 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.837+11326T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49035657 | |||||||
chr10:49035669 | C | CA | 53 | a0001c0001t0001g0026 a0001c0001t0003g0014 a0001c0001t0003g0021 others(50): Show |
56 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.837+11313dupT | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49035669 | |||||||
chr10:49035669 | C | CAA | 164 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0025 others(161): Show |
181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.837+11312_837+1131 others(6): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49035669 | |||||||
chr10:49035669 | C | CAAA | 13 | a0001c0001t0002g0222 a0001c0004t0006g0059 a0001c0008t0006g0023 others(10): Show |
14 | HG00323.hp1 HG00621.hp2 HG00639.hp2 others(11): Show |
intron_variant | MODIFIER | c.837+11311_837+1131 others(7): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49035669 | |||||||
chr10:49035687 | A | AAAAAAAA others(3): Show |
3 | a0001c0005t0008g0170 a0001c0005t0008g0171 a0001c0005t0008g0173 |
3 | HG02572.hp1 HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.837+11295_837+1129 others(14): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49035687 | |||||||
chr10:49035722 | C | A | 1 | a0002c0002t0003g0163 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.837+11261G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49035722 | |||||||
chr10:49035723 | A | G | 1 | a0002c0002t0001g0076 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.837+11260T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49035723 | |||||||
chr10:49035788 | C | T | 3 | a0001c0001t0010g0015 a0001c0001t0010g0182 a0001c0001t0022g0181 |
3 | HG01243.hp2 HG01884.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.837+11195G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49035788 | |||||||
chr10:49035915 | G | T | 49 | a0001c0001t0002g0002 a0001c0001t0002g0018 a0001c0001t0002g0038 others(46): Show |
54 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.837+11068C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49035915 | |||||||
chr10:49035988 | G | C | 1 | a0001c0001t0002g0178 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.837+10995C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49035988 | |||||||
chr10:49036103 | A | G | 169 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0024 others(166): Show |
186 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.837+10880T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49036103 | |||||||
chr10:49036118 | C | T | 4 | a0002c0002t0001g0077 a0002c0002t0001g0079 a0002c0002t0001g0082 others(1): Show |
4 | HG02922.hp1 HG03579.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.837+10865G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49036118 | |||||||
chr10:49036123 | A | G | 31 | a0001c0001t0003g0014 a0001c0001t0003g0021 a0001c0001t0003g0035 others(28): Show |
32 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.837+10860T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49036123 | |||||||
chr10:49036138 | G | A | 12 | a0002c0002t0001g0060 a0002c0002t0001g0061 a0002c0002t0001g0090 others(9): Show |
12 | HG00642.hp2 HG00741.hp1 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.837+10845C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49036138 | |||||||
chr10:49036197 | G | A | 1 | a0001c0003t0004g0199 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.837+10786C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49036197 | |||||||
chr10:49036228 | C | T | 3 | a0001c0001t0007g0188 a0001c0001t0007g0189 a0001c0001t0007g0191 |
3 | HG01070.hp1 HG01074.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.837+10755G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49036228 | |||||||
chr10:49036326 | G | A | 9 | a0001c0001t0010g0015 a0001c0001t0010g0182 a0001c0001t0010g0184 others(6): Show |
10 | HG00642.hp1 HG01243.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.837+10657C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49036326 | |||||||
chr10:49036605 | G | T | 1 | a0002c0002t0001g0083 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.837+10378C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49036605 | |||||||
chr10:49036757 | A | G | 1 | a0002c0002t0033g0084 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.837+10226T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49036757 | |||||||
chr10:49036779 | G | C | 4 | a0002c0002t0001g0077 a0002c0002t0001g0079 a0002c0002t0001g0082 others(1): Show |
4 | HG02922.hp1 HG03579.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.837+10204C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49036779 | |||||||
chr10:49037437 | A | G | 1 | a0001c0001t0017g0240 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.837+9546T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49037437 | |||||||
chr10:49037512 | T | C | 20 | a0001c0001t0007g0185 a0001c0001t0007g0186 a0001c0001t0007g0187 others(17): Show |
20 | HG00099.hp1 HG00558.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.837+9471A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49037512 | |||||||
chr10:49037518 | T | C | 10 | a0002c0002t0003g0109 a0002c0002t0003g0156 a0002c0002t0003g0157 others(7): Show |
10 | HG00558.hp1 HG03704.hp1 HG04204.hp1 others(7): Show |
intron_variant | MODIFIER | c.837+9465A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49037518 | |||||||
chr10:49037531 | C | A | 16 | a0001c0001t0003g0014 a0001c0001t0003g0021 a0001c0001t0003g0244 others(13): Show |
17 | HG01069.hp1 HG02258.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.837+9452G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49037531 | |||||||
chr10:49037562 | A | T | 1 | a0001c0001t0001g0217 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.837+9421T>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49037562 | |||||||
chr10:49037936 | C | CA | 14 | a0001c0001t0002g0178 a0001c0001t0002g0214 a0001c0001t0003g0213 others(11): Show |
14 | HG00558.hp2 HG01071.hp2 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.837+9046dupT | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49037936 | |||||||
chr10:49037940 | G | A | 237 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0024 others(234): Show |
258 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.837+9043C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49037940 | |||||||
chr10:49038021 | T | C | 3 | a0001c0005t0008g0170 a0001c0005t0008g0171 a0001c0005t0008g0173 |
3 | HG02572.hp1 HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.837+8962A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49038021 | |||||||
chr10:49038524 | G | A | 1 | a0001c0001t0038g0243 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.837+8459C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49038524 | |||||||
chr10:49038643 | G | A | 1 | a0004c0011t0037g0259 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.837+8340C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49038643 | |||||||
chr10:49038793 | A | T | 26 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0051 others(23): Show |
28 | HG00423.hp2 HG00558.hp1 HG02723.hp2 others(25): Show |
intron_variant | MODIFIER | c.837+8190T>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49038793 | |||||||
chr10:49038834 | C | T | 1 | a0004c0011t0037g0259 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.837+8149G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49038834 | |||||||
chr10:49038965 | C | G | 23 | a0001c0001t0003g0014 a0001c0001t0003g0244 a0001c0001t0003g0245 others(20): Show |
24 | HG01069.hp1 HG01070.hp1 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.837+8018G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49038965 | |||||||
chr10:49039076 | C | A | 10 | a0002c0002t0003g0109 a0002c0002t0003g0156 a0002c0002t0003g0157 others(7): Show |
10 | HG00558.hp1 HG03704.hp1 HG04204.hp1 others(7): Show |
intron_variant | MODIFIER | c.837+7907G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49039076 | |||||||
chr10:49039206 | G | A | 100 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0025 others(97): Show |
110 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.837+7777C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49039206 | |||||||
chr10:49039247 | C | A | 1 | a0002c0002t0001g0118 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.837+7736G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49039247 | |||||||
chr10:49039484 | C | T | 10 | a0002c0002t0003g0109 a0002c0002t0003g0156 a0002c0002t0003g0157 others(7): Show |
10 | HG00558.hp1 HG03704.hp1 HG04204.hp1 others(7): Show |
intron_variant | MODIFIER | c.837+7499G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49039484 | |||||||
chr10:49039728 | G | C | 1 | a0001c0004t0006g0019 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.837+7255C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49039728 | |||||||
chr10:49039995 | G | A | 1 | a0001c0001t0021g0242 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.837+6988C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49039995 | |||||||
chr10:49040182 | C | T | 10 | a0002c0002t0003g0109 a0002c0002t0003g0156 a0002c0002t0003g0157 others(7): Show |
10 | HG00558.hp1 HG03704.hp1 HG04204.hp1 others(7): Show |
intron_variant | MODIFIER | c.837+6801G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49040182 | |||||||
chr10:49040444 | G | A | 1 | a0001c0001t0034g0194 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.837+6539C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49040444 | |||||||
chr10:49040495 | G | A | 10 | a0001c0001t0010g0015 a0001c0001t0010g0182 a0001c0001t0010g0184 others(7): Show |
11 | HG00642.hp1 HG01243.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.837+6488C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49040495 | |||||||
chr10:49040497 | G | A | 6 | a0001c0001t0002g0178 a0001c0001t0015g0013 a0001c0001t0015g0167 others(3): Show |
7 | HG01069.hp2 HG01071.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.837+6486C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49040497 | |||||||
chr10:49040539 | G | A | 8 | a0001c0001t0002g0178 a0001c0001t0015g0013 a0001c0001t0015g0167 others(5): Show |
9 | HG01069.hp2 HG01071.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.837+6444C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49040539 | |||||||
chr10:49040606 | CCTA | C | 7 | a0001c0001t0017g0240 a0001c0004t0006g0019 a0001c0004t0006g0020 others(4): Show |
8 | HG00639.hp2 HG02630.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.837+6374_837+6376d others(5): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49040606 | |||||||
chr10:49040741 | C | T | 3 | a0001c0001t0019g0048 a0001c0001t0019g0050 a0001c0001t0020g0049 |
3 | HG02056.hp2 NA19002.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.837+6242G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49040741 | |||||||
chr10:49040777 | C | T | 1 | a0001c0001t0027g0028 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.837+6206G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49040777 | |||||||
chr10:49040833 | C | T | 107 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0025 others(104): Show |
117 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.837+6150G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49040833 | |||||||
chr10:49040879 | G | A | 30 | a0001c0001t0003g0014 a0001c0001t0003g0244 a0001c0001t0003g0245 others(27): Show |
32 | HG00099.hp1 HG00639.hp2 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.837+6104C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49040879 | |||||||
chr10:49040927 | C | T | 1 | a0004c0011t0037g0259 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.837+6056G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49040927 | |||||||
chr10:49040981 | T | C | 48 | a0001c0001t0001g0037 a0001c0001t0001g0217 a0001c0001t0001g0226 others(45): Show |
53 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.837+6002A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49040981 | |||||||
chr10:49041033 | C | A | 48 | a0001c0001t0001g0037 a0001c0001t0001g0217 a0001c0001t0001g0226 others(45): Show |
53 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.837+5950G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49041033 | |||||||
chr10:49041191 | G | T | 1 | a0001c0001t0001g0016 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.837+5792C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49041191 | |||||||
chr10:49041464 | T | C | 107 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0025 others(104): Show |
117 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.837+5519A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49041464 | |||||||
chr10:49041641 | G | T | 1 | a0001c0004t0006g0059 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.837+5342C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49041641 | |||||||
chr10:49041950 | T | C | 3 | a0002c0002t0002g0111 a0002c0002t0002g0112 a0002c0002t0002g0122 |
3 | HG02056.hp1 NA18612.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.837+5033A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49041950 | |||||||
chr10:49041951 | G | A | 10 | a0002c0002t0003g0109 a0002c0002t0003g0156 a0002c0002t0003g0157 others(7): Show |
10 | HG00558.hp1 HG03704.hp1 HG04204.hp1 others(7): Show |
intron_variant | MODIFIER | c.837+5032C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49041951 | |||||||
chr10:49042559 | G | T | 68 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0217 others(65): Show |
74 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.837+4424C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49042559 | |||||||
chr10:49042679 | C | T | 1 | a0001c0001t0002g0235 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.837+4304G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49042679 | |||||||
chr10:49042687 | A | C | 145 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0025 others(142): Show |
158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.837+4296T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49042687 | |||||||
chr10:49042700 | T | C | 1 | a0002c0002t0001g0069 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.837+4283A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49042700 | |||||||
chr10:49042721 | G | A | 1 | a0002c0002t0025g0117 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.837+4262C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49042721 | |||||||
chr10:49042855 | G | A | 1 | a0001c0001t0001g0016 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.837+4128C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49042855 | |||||||
chr10:49042918 | G | A | 2 | a0001c0001t0034g0194 a0004c0011t0037g0259 |
2 | HG01243.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.837+4065C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49042918 | |||||||
chr10:49042918 | G | C | 2 | a0002c0002t0001g0145 a0002c0002t0001g0146 |
2 | HG03139.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.837+4065C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49042918 | |||||||
chr10:49043048 | A | G | 107 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0025 others(104): Show |
117 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.837+3935T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49043048 | |||||||
chr10:49043056 | T | C | 145 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0025 others(142): Show |
158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.837+3927A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49043056 | |||||||
chr10:49043445 | T | C | 1 | a0002c0002t0001g0121 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.837+3538A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49043445 | |||||||
chr10:49043584 | T | G | 1 | a0001c0001t0021g0017 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.837+3399A>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49043584 | |||||||
chr10:49043620 | A | G | 4 | a0001c0001t0010g0015 a0001c0001t0010g0182 a0001c0001t0022g0181 others(1): Show |
4 | HG01243.hp2 HG01884.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.837+3363T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49043620 | |||||||
chr10:49043622 | A | G | 2 | a0001c0001t0034g0194 a0004c0011t0037g0259 |
2 | HG01243.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.837+3361T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49043622 | |||||||
chr10:49043721 | A | G | 1 | a0001c0001t0027g0028 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.837+3262T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49043721 | |||||||
chr10:49043966 | T | C | 1 | a0001c0001t0002g0232 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.837+3017A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49043966 | |||||||
chr10:49044018 | G | A | 1 | a0001c0001t0017g0240 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.837+2965C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49044018 | |||||||
chr10:49044090 | C | T | 1 | a0001c0001t0008g0030 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.837+2893G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49044090 | |||||||
chr10:49044119 | T | G | 2 | a0001c0001t0007g0188 a0001c0001t0007g0189 |
2 | HG01070.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.837+2864A>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49044119 | |||||||
chr10:49044213 | C | T | 21 | a0001c0001t0003g0014 a0001c0001t0003g0244 a0001c0001t0003g0246 others(18): Show |
22 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.837+2770G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49044213 | |||||||
chr10:49044395 | G | A | 1 | a0002c0002t0003g0162 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.837+2588C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49044395 | |||||||
chr10:49044409 | AAGAG | A | 2 | a0002c0002t0014g0008 a0002c0002t0014g0073 |
3 | HG02622.hp1 HG03516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.837+2570_837+2573d others(6): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49044409 | |||||||
chr10:49044431 | AAAG | A | 6 | a0001c0001t0001g0037 a0001c0001t0003g0039 a0001c0001t0019g0048 others(3): Show |
6 | HG02056.hp2 HG02083.hp2 NA18993.hp2 others(3): Show |
intron_variant | MODIFIER | c.837+2549_837+2551d others(5): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49044431 | |||||||
chr10:49044448 | GAGAA | G | 49 | a0001c0001t0001g0037 a0001c0001t0001g0217 a0001c0001t0001g0226 others(46): Show |
54 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.837+2531_837+2534d others(6): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49044448 | |||||||
chr10:49044526 | GA | G | 33 | a0001c0001t0003g0014 a0001c0001t0003g0244 a0001c0001t0003g0245 others(30): Show |
34 | HG00099.hp1 HG00558.hp1 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.837+2456delT | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49044526 | |||||||
chr10:49044583 | A | AAAG | 41 | a0001c0001t0002g0178 a0001c0001t0003g0014 a0001c0001t0003g0244 others(38): Show |
45 | HG00099.hp1 HG00639.hp2 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.837+2399_837+2400i others(5): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49044583 | |||||||
chr10:49044740 | C | T | 37 | a0001c0001t0002g0178 a0001c0001t0003g0014 a0001c0001t0003g0244 others(34): Show |
40 | HG00099.hp1 HG00639.hp2 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.837+2243G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49044740 | |||||||
chr10:49044813 | G | A | 46 | a0001c0001t0001g0037 a0001c0001t0001g0217 a0001c0001t0001g0226 others(43): Show |
51 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.837+2170C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49044813 | |||||||
chr10:49044891 | G | A | 21 | a0001c0001t0003g0014 a0001c0001t0003g0244 a0001c0001t0003g0245 others(18): Show |
22 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.837+2092C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49044891 | |||||||
chr10:49044956 | C | G | 1 | a0001c0001t0010g0179 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.837+2027G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49044956 | |||||||
chr10:49044977 | T | C | 1 | a0001c0001t0035g0165 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.837+2006A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49044977 | |||||||
chr10:49044983 | T | C | 2 | a0001c0001t0010g0179 a0001c0001t0021g0017 |
2 | HG02723.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.837+2000A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49044983 | |||||||
chr10:49045142 | C | T | 123 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0025 others(120): Show |
136 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.837+1841G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49045142 | |||||||
chr10:49045157 | A | G | 1 | a0004c0011t0037g0259 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.837+1826T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49045157 | |||||||
chr10:49045158 | T | C | 22 | a0001c0001t0003g0021 a0001c0001t0008g0029 a0001c0001t0008g0030 others(19): Show |
23 | HG00642.hp1 HG01106.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.837+1825A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49045158 | |||||||
chr10:49045202 | T | TTC | 119 | a0001c0001t0001g0003 a0001c0001t0001g0026 a0001c0001t0001g0027 others(116): Show |
132 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.837+1779_837+1780d others(4): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49045202 | |||||||
chr10:49045202 | T | TTCTC | 4 | a0001c0005t0001g0172 a0002c0002t0001g0083 a0002c0002t0001g0086 others(1): Show |
4 | HG00423.hp1 HG02257.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.837+1777_837+1780d others(6): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49045202 | |||||||
chr10:49045415 | G | C | 5 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(2): Show |
5 | HG01192.hp2 HG02717.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.837+1568C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49045415 | |||||||
chr10:49045623 | C | T | 246 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0024 others(243): Show |
267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.837+1360G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49045623 | |||||||
chr10:49045666 | C | T | 46 | a0001c0001t0001g0037 a0001c0001t0001g0217 a0001c0001t0001g0226 others(43): Show |
51 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.837+1317G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49045666 | |||||||
chr10:49045794 | C | T | 1 | a0002c0002t0001g0130 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.837+1189G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49045794 | |||||||
chr10:49045845 | A | T | 1 | a0002c0002t0003g0110 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.837+1138T>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49045845 | |||||||
chr10:49045849 | C | T | 7 | a0001c0001t0010g0015 a0001c0001t0010g0182 a0001c0001t0010g0184 others(4): Show |
7 | HG00642.hp1 HG01243.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.837+1134G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49045849 | |||||||
chr10:49045875 | T | A | 1 | a0001c0001t0023g0175 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.837+1108A>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49045875 | |||||||
chr10:49046051 | G | A | 7 | a0002c0002t0001g0077 a0002c0002t0001g0079 a0002c0002t0001g0080 others(4): Show |
7 | HG02080.hp2 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.837+932C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49046051 | |||||||
chr10:49046118 | A | C | 83 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0217 others(80): Show |
89 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.837+865T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49046118 | |||||||
chr10:49046221 | C | T | 123 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0025 others(120): Show |
136 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.837+762G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49046221 | |||||||
chr10:49046254 | A | T | 1 | a0001c0008t0006g0023 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.837+729T>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49046254 | |||||||
chr10:49046335 | C | T | 8 | a0001c0001t0010g0179 a0001c0001t0021g0017 a0001c0004t0006g0019 others(5): Show |
9 | HG00639.hp2 HG02723.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.837+648G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49046335 | |||||||
chr10:49046534 | C | A | 154 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0025 others(151): Show |
169 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.837+449G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49046534 | |||||||
chr10:49046602 | A | T | 8 | a0001c0001t0010g0179 a0001c0001t0021g0017 a0001c0004t0006g0019 others(5): Show |
9 | HG00639.hp2 HG02723.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.837+381T>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49046602 | |||||||
chr10:49046605 | C | T | 14 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0051 others(11): Show |
16 | HG00423.hp2 NA18941.hp2 NA18947.hp1 others(13): Show |
intron_variant | MODIFIER | c.837+378G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49046605 | |||||||
chr10:49046894 | A | G | 1 | a0001c0001t0017g0240 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.837+89T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49046894 | |||||||
chr10:49047206 | G | A | 1 | a0002c0002t0003g0164 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.776-162C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 6/7 | chr10 | 49047206 | |||||||
chr10:49047267 | T | G | 1 | a0002c0002t0023g0144 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.776-223A>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 6/7 | chr10 | 49047267 | |||||||
chr10:49047273 | TA | T | 5 | a0001c0001t0003g0021 a0001c0001t0026g0174 a0001c0005t0008g0170 others(2): Show |
5 | HG01106.hp1 HG02572.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.776-230delT | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 6/7 | chr10 | 49047273 | |||||||
chr10:49047523 | T | G | 21 | a0001c0001t0003g0014 a0001c0001t0003g0244 a0001c0001t0003g0245 others(18): Show |
22 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.776-479A>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 6/7 | chr10 | 49047523 | |||||||
chr10:49047878 | T | C | 3 | a0001c0001t0003g0252 a0001c0001t0003g0254 a0001c0001t0017g0251 |
3 | HG02258.hp2 HG02647.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.775+600A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 6/7 | chr10 | 49047878 | |||||||
chr10:49047887 | C | T | 2 | a0001c0001t0002g0239 a0002c0002t0002g0153 |
2 | HG02738.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.775+591G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 6/7 | chr10 | 49047887 | |||||||
chr10:49047893 | T | A | 5 | a0001c0001t0003g0021 a0001c0001t0026g0174 a0001c0005t0008g0170 others(2): Show |
5 | HG01106.hp1 HG02572.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.775+585A>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 6/7 | chr10 | 49047893 | |||||||
chr10:49047920 | T | C | 3 | a0001c0001t0014g0169 a0002c0002t0014g0008 a0002c0002t0014g0073 |
4 | HG02258.hp1 HG02622.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.775+558A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 6/7 | chr10 | 49047920 | |||||||
chr10:49048025 | G | A | 8 | a0001c0001t0010g0179 a0001c0001t0021g0017 a0001c0004t0006g0019 others(5): Show |
9 | HG00639.hp2 HG02723.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.775+453C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 6/7 | chr10 | 49048025 | |||||||
chr10:49048067 | T | C | 6 | a0001c0001t0010g0015 a0001c0001t0010g0182 a0001c0001t0010g0184 others(3): Show |
6 | HG00642.hp1 HG01243.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.775+411A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 6/7 | chr10 | 49048067 | |||||||
chr10:49048189 | T | C | 201 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0024 others(198): Show |
221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.775+289A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 6/7 | chr10 | 49048189 | |||||||
chr10:49048209 | A | G | 3 | a0001c0005t0008g0170 a0001c0005t0008g0171 a0001c0005t0008g0173 |
3 | HG02572.hp1 HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.775+269T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 6/7 | chr10 | 49048209 | |||||||
chr10:49048220 | C | T | 6 | a0001c0004t0006g0019 a0001c0004t0006g0020 a0001c0004t0006g0022 others(3): Show |
7 | HG00639.hp2 HG03041.hp2 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.775+258G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 6/7 | chr10 | 49048220 | |||||||
chr10:49048385 | T | G | 1 | a0001c0003t0004g0206 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.775+93A>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 6/7 | chr10 | 49048385 | |||||||
chr10:49048642 | G | GA | 6 | a0001c0001t0003g0021 a0001c0001t0026g0174 a0001c0005t0008g0170 others(3): Show |
6 | HG01106.hp1 HG02572.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.669-59dupT | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49048642 | |||||||
chr10:49048758 | G | T | 1 | a0002c0002t0006g0100 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.669-174C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49048758 | |||||||
chr10:49048833 | T | G | 1 | a0001c0001t0001g0016 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.669-249A>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49048833 | |||||||
chr10:49048870 | C | T | 123 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0025 others(120): Show |
136 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.669-286G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49048870 | |||||||
chr10:49048898 | G | C | 6 | a0001c0001t0002g0178 a0001c0001t0015g0013 a0001c0001t0015g0167 others(3): Show |
7 | HG01069.hp2 HG01071.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.669-314C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49048898 | |||||||
chr10:49049280 | G | A | 123 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0025 others(120): Show |
136 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.669-696C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49049280 | |||||||
chr10:49049304 | A | C | 14 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0051 others(11): Show |
16 | HG00423.hp2 NA18941.hp2 NA18947.hp1 others(13): Show |
intron_variant | MODIFIER | c.669-720T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49049304 | |||||||
chr10:49049418 | G | A | 8 | a0001c0001t0010g0179 a0001c0001t0021g0017 a0001c0004t0006g0019 others(5): Show |
9 | HG00639.hp2 HG02723.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.669-834C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49049418 | |||||||
chr10:49049491 | G | T | 1 | a0002c0002t0009g0141 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.669-907C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49049491 | |||||||
chr10:49049685 | C | T | 124 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0025 others(121): Show |
137 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.669-1101G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49049685 | |||||||
chr10:49049755 | CT | C | 153 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0025 others(150): Show |
168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.669-1172delA | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49049755 | |||||||
chr10:49049833 | G | C | 1 | a0001c0004t0006g0059 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.669-1249C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49049833 | |||||||
chr10:49050062 | A | AG | 160 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0025 others(157): Show |
175 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.669-1479dupC | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49050062 | |||||||
chr10:49050095 | G | A | 1 | a0004c0011t0037g0259 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.669-1511C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49050095 | |||||||
chr10:49050311 | A | C | 14 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0051 others(11): Show |
16 | HG00423.hp2 NA18941.hp2 NA18947.hp1 others(13): Show |
intron_variant | MODIFIER | c.669-1727T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49050311 | |||||||
chr10:49050438 | C | A | 1 | a0002c0002t0003g0142 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.669-1854G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49050438 | |||||||
chr10:49050660 | C | T | 2 | a0001c0001t0010g0179 a0001c0001t0021g0017 |
2 | HG02723.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.669-2076G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49050660 | |||||||
chr10:49050686 | A | G | 2 | a0002c0002t0014g0008 a0002c0002t0014g0073 |
3 | HG02622.hp1 HG03516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.669-2102T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49050686 | |||||||
chr10:49050690 | C | T | 104 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0025 others(101): Show |
114 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.669-2106G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49050690 | |||||||
chr10:49050784 | G | T | 2 | a0001c0005t0008g0170 a0001c0005t0008g0171 |
2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.669-2200C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49050784 | |||||||
chr10:49050947 | T | C | 47 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0217 others(44): Show |
52 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.669-2363A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49050947 | |||||||
chr10:49050962 | C | G | 22 | a0001c0001t0003g0014 a0001c0001t0003g0244 a0001c0001t0003g0245 others(19): Show |
23 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.669-2378G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49050962 | |||||||
chr10:49051023 | G | T | 6 | a0001c0001t0002g0178 a0001c0001t0015g0013 a0001c0001t0015g0167 others(3): Show |
7 | HG01069.hp2 HG01071.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.669-2439C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49051023 | |||||||
chr10:49051325 | C | A | 1 | a0002c0002t0001g0126 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.669-2741G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49051325 | |||||||
chr10:49051390 | C | CT | 36 | a0001c0001t0002g0178 a0001c0001t0003g0014 a0001c0001t0003g0244 others(33): Show |
38 | HG00099.hp1 HG01069.hp1 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.669-2807dupA | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49051390 | |||||||
chr10:49051390 | CT | C | 45 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(42): Show |
46 | HG00558.hp1 HG00639.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.669-2807delA | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49051390 | |||||||
chr10:49051665 | G | A | 1 | a0002c0002t0023g0144 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.669-3081C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49051665 | |||||||
chr10:49051883 | T | C | 1 | a0002c0002t0002g0112 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.669-3299A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49051883 | |||||||
chr10:49051955 | T | TTG | 161 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0025 others(158): Show |
176 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.669-3372_669-3371i others(4): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49051955 | |||||||
chr10:49052043 | G | A | 1 | a0001c0001t0007g0186 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.669-3459C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49052043 | |||||||
chr10:49052243 | T | G | 17 | a0002c0002t0001g0060 a0002c0002t0001g0061 a0002c0002t0001g0090 others(14): Show |
17 | HG00323.hp1 HG00642.hp2 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.669-3659A>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49052243 | |||||||
chr10:49052268 | A | G | 1 | a0001c0001t0038g0243 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.669-3684T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49052268 | |||||||
chr10:49052275 | C | T | 237 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0024 others(234): Show |
258 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.669-3691G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49052275 | |||||||
chr10:49052433 | A | AT | 41 | a0001c0001t0003g0014 a0001c0001t0003g0244 a0001c0001t0003g0245 others(38): Show |
44 | HG00099.hp1 HG00423.hp2 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.669-3850dupA | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49052433 | |||||||
chr10:49052433 | A | ATT | 114 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0025 others(111): Show |
125 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.669-3851_669-3850d others(4): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49052433 | |||||||
chr10:49052433 | A | ATTTT | 4 | a0001c0001t0002g0178 a0001c0001t0015g0013 a0001c0001t0015g0167 others(1): Show |
5 | HG01069.hp2 HG01071.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.669-3853_669-3850d others(6): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49052433 | |||||||
chr10:49052433 | AT | A | 11 | a0002c0002t0002g0154 a0002c0002t0002g0155 a0002c0002t0003g0156 others(8): Show |
11 | HG00558.hp1 HG03704.hp1 HG04204.hp1 others(8): Show |
intron_variant | MODIFIER | c.669-3850delA | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49052433 | |||||||
chr10:49052542 | A | G | 1 | a0001c0001t0035g0165 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.669-3958T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49052542 | |||||||
chr10:49052551 | GA | G | 237 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0024 others(234): Show |
258 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.669-3968delT | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49052551 | |||||||
chr10:49052558 | A | C | 1 | a0001c0001t0002g0219 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.669-3974T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49052558 | |||||||
chr10:49052693 | C | T | 13 | a0001c0001t0008g0029 a0001c0001t0008g0030 a0001c0001t0008g0031 others(10): Show |
14 | HG00639.hp2 HG01243.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.669-4109G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49052693 | |||||||
chr10:49052808 | T | C | 1 | a0002c0002t0006g0078 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.669-4224A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49052808 | |||||||
chr10:49052831 | G | A | 120 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0217 others(117): Show |
127 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.669-4247C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49052831 | |||||||
chr10:49053090 | G | A | 1 | a0004c0011t0037g0259 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.669-4506C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49053090 | |||||||
chr10:49053199 | G | A | 1 | a0001c0001t0002g0178 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.669-4615C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49053199 | |||||||
chr10:49053380 | C | T | 5 | a0001c0001t0003g0021 a0001c0001t0026g0174 a0001c0005t0008g0170 others(2): Show |
5 | HG01106.hp1 HG02572.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.669-4796G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49053380 | |||||||
chr10:49053388 | T | C | 1 | a0004c0011t0037g0259 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.669-4804A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49053388 | |||||||
chr10:49053482 | C | T | 13 | a0001c0001t0008g0029 a0001c0001t0008g0030 a0001c0001t0008g0031 others(10): Show |
14 | HG00639.hp2 HG01243.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.669-4898G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49053482 | |||||||
chr10:49053558 | G | A | 1 | a0001c0001t0007g0187 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.669-4974C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49053558 | |||||||
chr10:49053562 | G | C | 2 | a0001c0001t0010g0179 a0001c0001t0021g0017 |
2 | HG02723.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.669-4978C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49053562 | |||||||
chr10:49053629 | A | G | 1 | a0001c0001t0035g0165 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.669-5045T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49053629 | |||||||
chr10:49053684 | G | T | 4 | a0001c0001t0001g0003 a0001c0001t0001g0256 a0001c0001t0001g0257 others(1): Show |
7 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(4): Show |
intron_variant | MODIFIER | c.669-5100C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49053684 | |||||||
chr10:49053714 | G | T | 2 | a0001c0001t0010g0179 a0001c0001t0021g0017 |
2 | HG02723.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.669-5130C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49053714 | |||||||
chr10:49053732 | T | G | 22 | a0001c0001t0003g0014 a0001c0001t0003g0244 a0001c0001t0003g0245 others(19): Show |
23 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.669-5148A>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49053732 | |||||||
chr10:49053835 | C | T | 23 | a0001c0001t0003g0014 a0001c0001t0003g0244 a0001c0001t0003g0245 others(20): Show |
24 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.669-5251G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49053835 | |||||||
chr10:49053884 | G | A | 13 | a0001c0001t0023g0175 a0002c0002t0002g0154 a0002c0002t0002g0155 others(10): Show |
13 | HG00558.hp1 HG03225.hp1 HG03704.hp1 others(10): Show |
intron_variant | MODIFIER | c.669-5300C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49053884 | |||||||
chr10:49053910 | G | A | 3 | a0002c0002t0001g0001 a0002c0002t0001g0106 a0002c0002t0001g0115 |
6 | HG02027.hp2 NA18612.hp1 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.669-5326C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49053910 | |||||||
chr10:49053914 | A | C | 1 | a0001c0001t0015g0013 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.669-5330T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49053914 | |||||||
chr10:49054065 | C | A | 22 | a0001c0001t0003g0014 a0001c0001t0003g0244 a0001c0001t0003g0245 others(19): Show |
23 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.669-5481G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49054065 | |||||||
chr10:49054099 | T | C | 120 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0217 others(117): Show |
127 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.669-5515A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49054099 | |||||||
chr10:49054193 | C | T | 1 | a0001c0001t0023g0175 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.669-5609G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49054193 | |||||||
chr10:49054257 | G | A | 1 | a0002c0002t0001g0150 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.669-5673C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49054257 | |||||||
chr10:49054426 | G | A | 1 | a0001c0001t0015g0013 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.669-5842C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49054426 | |||||||
chr10:49054561 | A | G | 1 | a0002c0002t0001g0146 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.669-5977T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49054561 | |||||||
chr10:49054643 | G | C | 4 | a0002c0002t0001g0076 a0002c0002t0012g0009 a0002c0002t0012g0074 others(1): Show |
5 | HG02486.hp2 HG02622.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.669-6059C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49054643 | |||||||
chr10:49054907 | T | C | 1 | a0001c0001t0034g0194 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.669-6323A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49054907 | |||||||
chr10:49054938 | AG | A | 118 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0217 others(115): Show |
125 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(122): Show |
intron_variant | MODIFIER | c.669-6355delC | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49054938 | |||||||
chr10:49054991 | G | A | 1 | a0001c0001t0002g0018 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.669-6407C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49054991 | |||||||
chr10:49055033 | T | A | 1 | a0001c0001t0021g0017 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.669-6449A>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49055033 | |||||||
chr10:49055049 | G | C | 46 | a0001c0001t0001g0037 a0001c0001t0001g0217 a0001c0001t0001g0226 others(43): Show |
51 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.669-6465C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49055049 | |||||||
chr10:49055085 | T | C | 1 | a0001c0001t0001g0217 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.669-6501A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49055085 | |||||||
chr10:49055156 | A | G | 73 | a0001c0001t0003g0014 a0001c0001t0003g0021 a0001c0001t0003g0203 others(70): Show |
75 | HG00099.hp1 HG00558.hp1 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.669-6572T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49055156 | |||||||
chr10:49055168 | G | A | 10 | a0001c0001t0001g0217 a0001c0001t0001g0226 a0001c0001t0002g0212 others(7): Show |
10 | HG01952.hp2 HG01975.hp2 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.669-6584C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49055168 | |||||||
chr10:49055232 | C | A | 3 | a0001c0005t0008g0170 a0001c0005t0008g0171 a0001c0005t0008g0173 |
3 | HG02572.hp1 HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.669-6648G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49055232 | |||||||
chr10:49055264 | T | C | 1 | a0002c0002t0003g0142 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.669-6680A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49055264 | |||||||
chr10:49055278 | C | T | 5 | a0001c0001t0003g0021 a0001c0001t0026g0174 a0001c0005t0008g0170 others(2): Show |
5 | HG01106.hp1 HG02572.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.669-6694G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49055278 | |||||||
chr10:49055285 | G | A | 1 | a0002c0002t0001g0104 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.669-6701C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49055285 | |||||||
chr10:49055498 | G | A | 52 | a0001c0001t0001g0037 a0001c0001t0001g0217 a0001c0001t0001g0226 others(49): Show |
58 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.669-6914C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49055498 | |||||||
chr10:49055569 | C | G | 14 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0051 others(11): Show |
16 | HG00423.hp2 NA18941.hp2 NA18947.hp1 others(13): Show |
intron_variant | MODIFIER | c.669-6985G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49055569 | |||||||
chr10:49055831 | G | A | 22 | a0001c0001t0003g0014 a0001c0001t0003g0244 a0001c0001t0003g0245 others(19): Show |
23 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.669-7247C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49055831 | |||||||
chr10:49055871 | A | G | 10 | a0001c0001t0010g0015 a0001c0001t0010g0182 a0001c0001t0010g0184 others(7): Show |
11 | HG00642.hp1 HG01243.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.669-7287T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49055871 | |||||||
chr10:49055928 | G | A | 16 | a0001c0001t0003g0021 a0001c0001t0010g0015 a0001c0001t0010g0182 others(13): Show |
17 | HG00642.hp1 HG01106.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.669-7344C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49055928 | |||||||
chr10:49056002 | C | T | 154 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0217 others(151): Show |
165 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.669-7418G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49056002 | |||||||
chr10:49056050 | G | C | 16 | a0001c0001t0003g0021 a0001c0001t0010g0015 a0001c0001t0010g0182 others(13): Show |
17 | HG00642.hp1 HG01106.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.669-7466C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49056050 | |||||||
chr10:49056159 | C | G | 22 | a0001c0001t0003g0014 a0001c0001t0003g0244 a0001c0001t0003g0245 others(19): Show |
23 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.669-7575G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49056159 | |||||||
chr10:49056203 | A | G | 1 | a0001c0001t0003g0213 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.669-7619T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49056203 | |||||||
chr10:49056350 | G | A | 2 | a0001c0001t0003g0021 a0001c0001t0026g0174 |
2 | HG01106.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.669-7766C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49056350 | |||||||
chr10:49056496 | G | A | 2 | a0001c0001t0010g0179 a0001c0001t0021g0017 |
2 | HG02723.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.669-7912C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49056496 | |||||||
chr10:49056762 | C | T | 1 | a0001c0001t0002g0219 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.668+7941G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49056762 | |||||||
chr10:49056918 | T | C | 22 | a0001c0001t0003g0014 a0001c0001t0003g0244 a0001c0001t0003g0245 others(19): Show |
23 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.668+7785A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49056918 | |||||||
chr10:49056985 | C | T | 22 | a0001c0001t0003g0014 a0001c0001t0003g0244 a0001c0001t0003g0245 others(19): Show |
23 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.668+7718G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49056985 | |||||||
chr10:49056986 | G | A | 96 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0217 others(93): Show |
102 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.668+7717C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49056986 | |||||||
chr10:49057000 | G | A | 96 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0217 others(93): Show |
102 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.668+7703C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49057000 | |||||||
chr10:49057005 | G | T | 3 | a0001c0001t0007g0188 a0001c0001t0007g0189 a0001c0001t0007g0191 |
3 | HG01070.hp1 HG01074.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.668+7698C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49057005 | |||||||
chr10:49057022 | G | A | 1 | a0002c0002t0001g0089 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.668+7681C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49057022 | |||||||
chr10:49057251 | G | C | 1 | a0002c0002t0001g0104 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.668+7452C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49057251 | |||||||
chr10:49057340 | A | G | 1 | a0001c0001t0010g0015 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.668+7363T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49057340 | |||||||
chr10:49057545 | G | T | 16 | a0001c0001t0003g0021 a0001c0001t0010g0015 a0001c0001t0010g0182 others(13): Show |
17 | HG00642.hp1 HG01106.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.668+7158C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49057545 | |||||||
chr10:49057547 | C | T | 1 | a0002c0002t0003g0159 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.668+7156G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49057547 | |||||||
chr10:49057670 | G | T | 12 | a0002c0002t0002g0154 a0002c0002t0002g0155 a0002c0002t0003g0109 others(9): Show |
12 | HG00558.hp1 HG03704.hp1 HG04204.hp1 others(9): Show |
intron_variant | MODIFIER | c.668+7033C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49057670 | |||||||
chr10:49057864 | A | C | 1 | a0002c0002t0023g0144 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.668+6839T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49057864 | |||||||
chr10:49058154 | C | T | 2 | a0001c0001t0010g0179 a0001c0001t0021g0017 |
2 | HG02723.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.668+6549G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49058154 | |||||||
chr10:49058244 | G | A | 118 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0217 others(115): Show |
125 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(122): Show |
intron_variant | MODIFIER | c.668+6459C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49058244 | |||||||
chr10:49058354 | A | G | 1 | a0001c0003t0004g0168 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.668+6349T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49058354 | |||||||
chr10:49058589 | AG | A | 13 | a0001c0001t0008g0029 a0001c0001t0008g0030 a0001c0001t0008g0031 others(10): Show |
14 | HG00639.hp2 HG01243.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.668+6113delC | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49058589 | |||||||
chr10:49058885 | G | T | 21 | a0001c0001t0003g0014 a0001c0001t0003g0244 a0001c0001t0003g0245 others(18): Show |
22 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.668+5818C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49058885 | |||||||
chr10:49058905 | T | C | 13 | a0001c0001t0008g0029 a0001c0001t0008g0030 a0001c0001t0008g0031 others(10): Show |
14 | HG00639.hp2 HG01243.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.668+5798A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49058905 | |||||||
chr10:49058937 | G | T | 45 | a0001c0001t0001g0037 a0001c0001t0001g0217 a0001c0001t0001g0226 others(42): Show |
50 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.668+5766C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49058937 | |||||||
chr10:49059010 | C | T | 2 | a0001c0001t0003g0021 a0001c0001t0026g0174 |
2 | HG01106.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.668+5693G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49059010 | |||||||
chr10:49059046 | A | G | 1 | a0001c0001t0003g0253 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.668+5657T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49059046 | |||||||
chr10:49059053 | C | A | 1 | a0002c0002t0001g0093 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.668+5650G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49059053 | |||||||
chr10:49059448 | A | G | 121 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0217 others(118): Show |
128 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.668+5255T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49059448 | |||||||
chr10:49059526 | C | T | 1 | a0002c0002t0001g0087 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.668+5177G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49059526 | |||||||
chr10:49059597 | A | C | 6 | a0002c0002t0001g0076 a0002c0002t0001g0085 a0002c0002t0012g0009 others(3): Show |
7 | HG02451.hp2 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.668+5106T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49059597 | |||||||
chr10:49059608 | C | G | 1 | a0002c0002t0006g0102 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.668+5095G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49059608 | |||||||
chr10:49059734 | T | C | 20 | a0001c0001t0016g0176 a0001c0001t0016g0177 a0002c0002t0001g0060 others(17): Show |
20 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.668+4969A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49059734 | |||||||
chr10:49059742 | G | A | 1 | a0001c0001t0017g0240 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.668+4961C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49059742 | |||||||
chr10:49059851 | G | A | 3 | a0001c0001t0002g0214 a0001c0001t0003g0213 a0002c0002t0002g0125 |
3 | HG00558.hp2 HG02015.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.668+4852C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49059851 | |||||||
chr10:49060230 | C | T | 2 | a0002c0002t0001g0135 a0002c0002t0001g0136 |
2 | HG01175.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.668+4473G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49060230 | |||||||
chr10:49060231 | G | A | 7 | a0001c0004t0006g0019 a0001c0004t0006g0020 a0001c0004t0006g0022 others(4): Show |
8 | HG00639.hp2 HG03041.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.668+4472C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49060231 | |||||||
chr10:49060387 | T | C | 1 | a0001c0001t0002g0230 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.668+4316A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49060387 | |||||||
chr10:49060397 | A | C | 47 | a0001c0001t0001g0037 a0001c0001t0001g0217 a0001c0001t0001g0226 others(44): Show |
52 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.668+4306T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49060397 | |||||||
chr10:49060535 | T | G | 1 | a0001c0004t0006g0022 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.668+4168A>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49060535 | |||||||
chr10:49060554 | T | A | 96 | a0001c0001t0001g0037 a0001c0001t0001g0217 a0001c0001t0001g0226 others(93): Show |
102 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.668+4149A>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49060554 | |||||||
chr10:49060572 | G | A | 96 | a0001c0001t0001g0037 a0001c0001t0001g0217 a0001c0001t0001g0226 others(93): Show |
102 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.668+4131C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49060572 | |||||||
chr10:49060655 | T | G | 1 | a0002c0002t0001g0063 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.668+4048A>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49060655 | |||||||
chr10:49060718 | T | C | 153 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0217 others(150): Show |
164 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(161): Show |
intron_variant | MODIFIER | c.668+3985A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49060718 | |||||||
chr10:49060878 | A | G | 4 | a0001c0001t0001g0003 a0001c0001t0001g0256 a0001c0001t0001g0257 others(1): Show |
7 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(4): Show |
intron_variant | MODIFIER | c.668+3825T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49060878 | |||||||
chr10:49060893 | T | G | 46 | a0001c0001t0001g0037 a0001c0001t0001g0217 a0001c0001t0001g0226 others(43): Show |
51 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.668+3810A>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49060893 | |||||||
chr10:49061052 | A | G | 1 | a0001c0001t0005g0052 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.668+3651T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49061052 | |||||||
chr10:49061077 | T | C | 1 | a0001c0001t0035g0165 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.668+3626A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49061077 | |||||||
chr10:49061162 | A | T | 1 | a0004c0011t0037g0259 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.668+3541T>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49061162 | |||||||
chr10:49061205 | T | C | 1 | a0001c0001t0021g0017 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.668+3498A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49061205 | |||||||
chr10:49061238 | G | A | 3 | a0001c0003t0004g0207 a0001c0003t0004g0208 a0001c0003t0004g0209 |
3 | HG02109.hp1 HG02451.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.668+3465C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49061238 | |||||||
chr10:49061442 | T | G | 23 | a0001c0001t0001g0016 a0001c0001t0003g0014 a0001c0001t0003g0244 others(20): Show |
24 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.668+3261A>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49061442 | |||||||
chr10:49061496 | C | T | 175 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(172): Show |
187 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(184): Show |
intron_variant | MODIFIER | c.668+3207G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49061496 | |||||||
chr10:49061556 | T | G | 13 | a0001c0001t0008g0029 a0001c0001t0008g0030 a0001c0001t0008g0031 others(10): Show |
14 | HG00639.hp2 HG01243.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.668+3147A>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49061556 | |||||||
chr10:49061572 | G | A | 1 | a0002c0002t0001g0093 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.668+3131C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49061572 | |||||||
chr10:49061601 | C | A | 7 | a0001c0001t0034g0194 a0001c0004t0006g0019 a0001c0004t0006g0020 others(4): Show |
8 | HG00639.hp2 HG01243.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.668+3102G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49061601 | |||||||
chr10:49061639 | G | A | 119 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0217 others(116): Show |
126 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.668+3064C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49061639 | |||||||
chr10:49061668 | A | C | 120 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0217 others(117): Show |
127 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.668+3035T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49061668 | |||||||
chr10:49061907 | A | G | 1 | a0004c0011t0037g0259 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.668+2796T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49061907 | |||||||
chr10:49062177 | C | T | 2 | a0002c0002t0001g0135 a0002c0002t0001g0136 |
2 | HG01175.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.668+2526G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49062177 | |||||||
chr10:49062312 | ATT | A | 119 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0217 others(116): Show |
126 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.668+2389_668+2390d others(4): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49062312 | |||||||
chr10:49062321 | T | C | 1 | a0005c0009t0001g0041 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.668+2382A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49062321 | |||||||
chr10:49062332 | T | A | 119 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0217 others(116): Show |
126 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.668+2371A>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49062332 | |||||||
chr10:49062335 | ATTTTAGT others(87): Show |
A | 2 | a0002c0002t0001g0060 a0002c0002t0001g0061 |
2 | HG00642.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.668+2274_668+2367d others(96): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49062335 | |||||||
chr10:49062418 | T | C | 119 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0217 others(116): Show |
126 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.668+2285A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49062418 | |||||||
chr10:49062777 | T | C | 1 | a0001c0001t0021g0017 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.668+1926A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49062777 | |||||||
chr10:49062965 | T | C | 1 | a0002c0002t0001g0090 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.668+1738A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49062965 | |||||||
chr10:49063025 | C | CTT | 6 | a0001c0001t0002g0178 a0001c0001t0015g0013 a0001c0001t0015g0167 others(3): Show |
7 | HG01069.hp2 HG01071.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.668+1676_668+1677d others(4): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49063025 | |||||||
chr10:49063025 | CT | C | 40 | a0001c0001t0002g0212 a0001c0001t0003g0021 a0001c0001t0003g0203 others(37): Show |
41 | HG00642.hp1 HG01106.hp1 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.668+1677delA | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49063025 | |||||||
chr10:49063190 | T | A | 154 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0217 others(151): Show |
165 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.668+1513A>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49063190 | |||||||
chr10:49063364 | T | G | 1 | a0001c0001t0021g0017 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.668+1339A>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49063364 | |||||||
chr10:49063627 | G | C | 3 | a0001c0005t0008g0170 a0001c0005t0008g0171 a0001c0005t0008g0173 |
3 | HG02572.hp1 HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.668+1076C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49063627 | |||||||
chr10:49063755 | G | A | 96 | a0001c0001t0001g0037 a0001c0001t0001g0217 a0001c0001t0001g0226 others(93): Show |
102 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.668+948C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49063755 | |||||||
chr10:49063812 | G | C | 120 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0217 others(117): Show |
127 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.668+891C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49063812 | |||||||
chr10:49063947 | G | A | 2 | a0002c0002t0001g0150 a0002c0002t0011g0012 |
3 | HG00438.hp2 NA18984.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.668+756C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49063947 | |||||||
chr10:49064037 | C | T | 22 | a0001c0001t0001g0003 a0001c0001t0001g0256 a0001c0001t0001g0257 others(19): Show |
25 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(22): Show |
intron_variant | MODIFIER | c.668+666G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49064037 | |||||||
chr10:49064174 | G | T | 1 | a0001c0001t0001g0016 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.668+529C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49064174 | |||||||
chr10:49064261 | CT | C | 3 | a0001c0001t0005g0064 a0001c0001t0005g0065 a0001c0001t0005g0066 |
3 | HG00423.hp2 NA18952.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.668+441delA | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49064261 | |||||||
chr10:49064336 | C | T | 1 | a0001c0001t0002g0038 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.668+367G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49064336 | |||||||
chr10:49064427 | T | C | 97 | a0001c0001t0001g0037 a0001c0001t0001g0217 a0001c0001t0001g0226 others(94): Show |
103 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.668+276A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49064427 | |||||||
chr10:49065142 | C | A | 3 | a0001c0005t0001g0172 a0002c0002t0001g0083 a0002c0002t0001g0086 |
3 | HG02257.hp1 HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.635-406G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49065142 | |||||||
chr10:49065204 | C | T | 1 | a0001c0001t0021g0017 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.635-468G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49065204 | |||||||
chr10:49065356 | G | T | 1 | a0001c0001t0019g0050 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.635-620C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49065356 | |||||||
chr10:49065747 | T | C | 7 | a0002c0002t0001g0077 a0002c0002t0001g0079 a0002c0002t0001g0080 others(4): Show |
7 | HG02080.hp2 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.635-1011A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49065747 | |||||||
chr10:49065759 | G | A | 1 | a0002c0002t0012g0075 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.635-1023C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49065759 | |||||||
chr10:49066196 | A | G | 154 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0217 others(151): Show |
165 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.635-1460T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49066196 | |||||||
chr10:49066241 | T | C | 14 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0051 others(11): Show |
16 | HG00423.hp2 NA18941.hp2 NA18947.hp1 others(13): Show |
intron_variant | MODIFIER | c.635-1505A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49066241 | |||||||
chr10:49066281 | C | G | 1 | a0001c0003t0004g0204 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.635-1545G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49066281 | |||||||
chr10:49066553 | T | C | 14 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(11): Show |
15 | HG01192.hp2 HG02257.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.635-1817A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49066553 | |||||||
chr10:49066628 | T | A | 1 | a0001c0001t0003g0253 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.635-1892A>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49066628 | |||||||
chr10:49066683 | C | T | 97 | a0001c0001t0001g0037 a0001c0001t0001g0217 a0001c0001t0001g0226 others(94): Show |
103 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.635-1947G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49066683 | |||||||
chr10:49066734 | A | T | 1 | a0002c0002t0002g0095 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.635-1998T>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49066734 | |||||||
chr10:49067014 | A | G | 120 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0217 others(117): Show |
127 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.635-2278T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49067014 | |||||||
chr10:49067049 | C | A | 1 | a0001c0001t0034g0194 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.635-2313G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49067049 | |||||||
chr10:49067115 | C | A | 1 | a0001c0001t0017g0251 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.635-2379G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49067115 | |||||||
chr10:49067204 | ATGAT | A | 49 | a0001c0001t0003g0021 a0001c0001t0003g0203 a0001c0001t0010g0015 others(46): Show |
50 | HG00558.hp1 HG00642.hp1 HG01106.hp1 others(47): Show |
intron_variant | MODIFIER | c.635-2472_635-2469d others(6): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49067204 | |||||||
chr10:49067208 | T | A | 1 | a0004c0011t0037g0259 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.635-2472A>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49067208 | |||||||
chr10:49067250 | C | G | 13 | a0001c0001t0008g0029 a0001c0001t0008g0030 a0001c0001t0008g0031 others(10): Show |
14 | HG00639.hp2 HG01243.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.635-2514G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49067250 | |||||||
chr10:49067317 | T | C | 10 | a0001c0003t0004g0195 a0001c0003t0004g0196 a0001c0003t0004g0198 others(7): Show |
10 | HG01109.hp1 HG02145.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.635-2581A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49067317 | |||||||
chr10:49067487 | T | C | 25 | a0001c0001t0001g0016 a0001c0001t0003g0014 a0001c0001t0003g0244 others(22): Show |
27 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.635-2751A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49067487 | |||||||
chr10:49067518 | C | G | 47 | a0001c0001t0001g0037 a0001c0001t0001g0217 a0001c0001t0001g0226 others(44): Show |
52 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.635-2782G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49067518 | |||||||
chr10:49067669 | T | C | 1 | a0002c0002t0011g0070 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.635-2933A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49067669 | |||||||
chr10:49067936 | C | T | 17 | a0002c0002t0001g0060 a0002c0002t0001g0061 a0002c0002t0001g0090 others(14): Show |
17 | HG00323.hp1 HG00642.hp2 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.635-3200G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49067936 | |||||||
chr10:49068017 | T | C | 3 | a0001c0001t0005g0064 a0001c0001t0005g0065 a0001c0001t0005g0066 |
3 | HG00423.hp2 NA18952.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.635-3281A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49068017 | |||||||
chr10:49068049 | T | C | 1 | a0001c0001t0010g0201 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.635-3313A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49068049 | |||||||
chr10:49068066 | A | G | 2 | a0001c0001t0003g0021 a0001c0001t0026g0174 |
2 | HG01106.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.635-3330T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49068066 | |||||||
chr10:49068252 | A | G | 134 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0217 others(131): Show |
142 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.635-3516T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49068252 | |||||||
chr10:49068325 | C | T | 1 | a0001c0003t0036g0197 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.635-3589G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49068325 | |||||||
chr10:49068407 | C | T | 1 | a0001c0003t0004g0168 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.635-3671G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49068407 | |||||||
chr10:49068462 | T | G | 1 | a0001c0001t0008g0030 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.635-3726A>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49068462 | |||||||
chr10:49068528 | G | A | 1 | a0002c0002t0001g0137 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.635-3792C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49068528 | |||||||
chr10:49068690 | G | A | 17 | a0002c0002t0001g0060 a0002c0002t0001g0061 a0002c0002t0001g0090 others(14): Show |
17 | HG00323.hp1 HG00642.hp2 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.635-3954C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49068690 | |||||||
chr10:49068780 | C | G | 120 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0217 others(117): Show |
127 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.635-4044G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49068780 | |||||||
chr10:49068879 | C | T | 1 | a0001c0001t0021g0017 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.635-4143G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49068879 | |||||||
chr10:49068924 | A | T | 2 | a0001c0001t0001g0026 a0001c0001t0001g0027 |
2 | HG02717.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.635-4188T>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49068924 | |||||||
chr10:49069530 | G | T | 23 | a0001c0001t0001g0016 a0001c0001t0003g0014 a0001c0001t0003g0244 others(20): Show |
24 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.635-4794C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49069530 | |||||||
chr10:49069540 | C | T | 23 | a0001c0001t0001g0016 a0001c0001t0003g0014 a0001c0001t0003g0244 others(20): Show |
24 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.635-4804G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49069540 | |||||||
chr10:49069548 | G | C | 1 | a0001c0001t0010g0201 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.635-4812C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49069548 | |||||||
chr10:49069630 | A | G | 1 | a0002c0002t0001g0115 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.635-4894T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49069630 | |||||||
chr10:49069653 | G | C | 119 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0217 others(116): Show |
125 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(122): Show |
intron_variant | MODIFIER | c.635-4917C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49069653 | |||||||
chr10:49069684 | A | G | 8 | a0001c0001t0010g0015 a0001c0001t0010g0179 a0001c0001t0010g0182 others(5): Show |
8 | HG00642.hp1 HG01243.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.635-4948T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49069684 | |||||||
chr10:49069870 | C | T | 1 | a0002c0002t0001g0145 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.635-5134G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49069870 | |||||||
chr10:49069970 | CGGCCGGG others(310): Show |
C | 121 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0217 others(118): Show |
127 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.635-5551_635-5235d others(2): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49069970 | |||||||
chr10:49070027 | C | T | 1 | a0002c0002t0001g0147 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.635-5291G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49070027 | |||||||
chr10:49070049 | G | A | 6 | a0001c0001t0002g0178 a0001c0001t0015g0013 a0001c0001t0015g0167 others(3): Show |
7 | HG01069.hp2 HG01071.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.635-5313C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49070049 | |||||||
chr10:49070068 | C | T | 6 | a0001c0001t0002g0178 a0001c0001t0015g0013 a0001c0001t0015g0167 others(3): Show |
7 | HG01069.hp2 HG01071.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.635-5332G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49070068 | |||||||
chr10:49070105 | C | T | 56 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(53): Show |
62 | HG00423.hp2 HG00639.hp2 HG01069.hp2 others(59): Show |
intron_variant | MODIFIER | c.635-5369G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49070105 | |||||||
chr10:49070126 | G | A | 1 | a0002c0002t0001g0071 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.635-5390C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49070126 | |||||||
chr10:49070178 | G | A | 1 | a0001c0004t0006g0019 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.635-5442C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49070178 | |||||||
chr10:49070252 | C | CA | 15 | a0001c0001t0001g0257 a0001c0004t0006g0022 a0002c0002t0001g0001 others(12): Show |
15 | HG00323.hp1 HG01106.hp2 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.635-5517dupT | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49070252 | |||||||
chr10:49070252 | C | CAA | 8 | a0001c0001t0008g0029 a0001c0001t0008g0030 a0001c0001t0008g0031 others(5): Show |
8 | HG01884.hp1 HG02622.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.635-5518_635-5517d others(4): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49070252 | |||||||
chr10:49070252 | C | CAAAA | 6 | a0001c0001t0005g0006 a0002c0002t0001g0077 a0002c0002t0001g0079 others(3): Show |
7 | HG02559.hp1 HG02922.hp1 HG03579.hp2 others(4): Show |
intron_variant | MODIFIER | c.635-5520_635-5517d others(6): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49070252 | |||||||
chr10:49070252 | C | CAAAAA | 7 | a0001c0001t0002g0178 a0001c0001t0015g0013 a0001c0001t0015g0167 others(4): Show |
7 | HG01071.hp1 HG02080.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.635-5521_635-5517d others(7): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49070252 | |||||||
chr10:49070252 | C | CAAAAAAA others(4): Show |
10 | a0001c0001t0005g0007 a0001c0001t0005g0051 a0001c0001t0005g0052 others(7): Show |
11 | NA18941.hp2 NA18948.hp1 NA18952.hp2 others(8): Show |
intron_variant | MODIFIER | c.635-5527_635-5517d others(13): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49070252 | |||||||
chr10:49070252 | C | CAAAAAAA others(5): Show |
2 | a0001c0001t0005g0053 a0001c0001t0005g0055 |
2 | NA18947.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.635-5528_635-5517d others(14): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49070252 | |||||||
chr10:49070252 | C | CAAAAAAA others(6): Show |
1 | a0001c0001t0005g0065 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.635-5529_635-5517d others(15): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49070252 | |||||||
chr10:49070252 | CAA | C | 6 | a0002c0002t0001g0076 a0002c0002t0001g0085 a0002c0002t0012g0009 others(3): Show |
7 | HG02451.hp2 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.635-5518_635-5517d others(4): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49070252 | |||||||
chr10:49070287 | G | C | 133 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0025 others(130): Show |
148 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.635-5551C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49070287 | |||||||
chr10:49070346 | G | A | 2 | a0001c0001t0014g0169 a0004c0011t0037g0259 |
2 | HG02258.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.635-5610C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49070346 | |||||||
chr10:49070412 | TA | T | 119 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0217 others(116): Show |
125 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(122): Show |
intron_variant | MODIFIER | c.635-5677delT | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49070412 | |||||||
chr10:49070489 | T | C | 7 | a0002c0002t0001g0077 a0002c0002t0001g0079 a0002c0002t0001g0080 others(4): Show |
7 | HG02080.hp2 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.635-5753A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49070489 | |||||||
chr10:49070581 | C | T | 1 | a0002c0002t0001g0132 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.635-5845G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49070581 | |||||||
chr10:49070631 | G | C | 1 | a0001c0001t0023g0175 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.635-5895C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49070631 | |||||||
chr10:49070803 | C | T | 1 | a0002c0002t0013g0099 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.635-6067G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49070803 | |||||||
chr10:49071343 | G | A | 1 | a0001c0001t0038g0243 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.634+5876C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49071343 | |||||||
chr10:49071458 | A | G | 1 | a0001c0001t0003g0253 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.634+5761T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49071458 | |||||||
chr10:49071682 | C | A | 1 | a0001c0001t0002g0040 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.634+5537G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49071682 | |||||||
chr10:49071750 | T | G | 1 | a0001c0001t0001g0025 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.634+5469A>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49071750 | |||||||
chr10:49071910 | C | G | 1 | a0001c0001t0014g0169 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.634+5309G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49071910 | |||||||
chr10:49071994 | C | T | 14 | a0001c0001t0003g0203 a0001c0001t0010g0201 a0001c0003t0004g0195 others(11): Show |
14 | HG01109.hp1 HG01981.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.634+5225G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49071994 | |||||||
chr10:49072044 | A | G | 1 | a0002c0002t0002g0122 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.634+5175T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49072044 | |||||||
chr10:49072193 | C | T | 21 | a0001c0001t0003g0014 a0001c0001t0003g0244 a0001c0001t0003g0245 others(18): Show |
22 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.634+5026G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49072193 | |||||||
chr10:49072211 | G | A | 1 | a0004c0011t0037g0259 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.634+5008C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49072211 | |||||||
chr10:49072432 | G | A | 1 | a0001c0001t0005g0052 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.634+4787C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49072432 | |||||||
chr10:49072598 | G | A | 14 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0051 others(11): Show |
16 | HG00423.hp2 NA18941.hp2 NA18947.hp1 others(13): Show |
intron_variant | MODIFIER | c.634+4621C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49072598 | |||||||
chr10:49072747 | C | T | 23 | a0001c0001t0001g0016 a0001c0001t0003g0014 a0001c0001t0003g0244 others(20): Show |
24 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.634+4472G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49072747 | |||||||
chr10:49072882 | C | A | 120 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0217 others(117): Show |
127 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.634+4337G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49072882 | |||||||
chr10:49072883 | A | G | 120 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0217 others(117): Show |
127 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.634+4336T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49072883 | |||||||
chr10:49072989 | C | A | 122 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0217 others(119): Show |
129 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.634+4230G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49072989 | |||||||
chr10:49073044 | G | A | 120 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0217 others(117): Show |
127 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.634+4175C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49073044 | |||||||
chr10:49073069 | G | A | 20 | a0001c0001t0003g0203 a0001c0001t0010g0201 a0001c0003t0004g0168 others(17): Show |
20 | HG01109.hp1 HG01123.hp1 HG01981.hp1 others(17): Show |
intron_variant | MODIFIER | c.634+4150C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49073069 | |||||||
chr10:49073180 | G | T | 6 | a0001c0004t0006g0019 a0001c0004t0006g0020 a0001c0004t0006g0022 others(3): Show |
7 | HG00639.hp2 HG03041.hp2 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.634+4039C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49073180 | |||||||
chr10:49073311 | C | T | 97 | a0001c0001t0001g0037 a0001c0001t0001g0217 a0001c0001t0001g0226 others(94): Show |
103 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.634+3908G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49073311 | |||||||
chr10:49073346 | G | A | 1 | a0001c0005t0008g0173 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.634+3873C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49073346 | |||||||
chr10:49073394 | C | A | 1 | a0002c0002t0001g0083 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.634+3825G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49073394 | |||||||
chr10:49073455 | C | T | 4 | a0001c0001t0008g0030 a0001c0001t0008g0032 a0001c0001t0008g0033 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.634+3764G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49073455 | |||||||
chr10:49073602 | C | G | 7 | a0002c0002t0001g0077 a0002c0002t0001g0079 a0002c0002t0001g0080 others(4): Show |
7 | HG02080.hp2 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.634+3617G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49073602 | |||||||
chr10:49073665 | C | T | 1 | a0001c0003t0004g0211 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.634+3554G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49073665 | |||||||
chr10:49073835 | A | G | 120 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0217 others(117): Show |
127 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.634+3384T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49073835 | |||||||
chr10:49073846 | C | T | 4 | a0001c0001t0001g0003 a0001c0001t0001g0256 a0001c0001t0001g0257 others(1): Show |
7 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(4): Show |
intron_variant | MODIFIER | c.634+3373G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49073846 | |||||||
chr10:49073851 | A | G | 1 | a0001c0001t0021g0017 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.634+3368T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49073851 | |||||||
chr10:49073900 | C | T | 13 | a0001c0001t0008g0029 a0001c0001t0008g0030 a0001c0001t0008g0031 others(10): Show |
14 | HG00639.hp2 HG01243.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.634+3319G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49073900 | |||||||
chr10:49073946 | T | C | 2 | a0002c0002t0001g0135 a0002c0002t0001g0136 |
2 | HG01175.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.634+3273A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49073946 | |||||||
chr10:49074184 | A | G | 23 | a0001c0001t0001g0016 a0001c0001t0003g0014 a0001c0001t0003g0244 others(20): Show |
24 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.634+3035T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49074184 | |||||||
chr10:49074331 | G | C | 3 | a0001c0001t0019g0048 a0001c0001t0019g0050 a0001c0001t0020g0049 |
3 | HG02056.hp2 NA19002.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.634+2888C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49074331 | |||||||
chr10:49074478 | C | T | 1 | a0002c0002t0001g0121 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.634+2741G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49074478 | |||||||
chr10:49074497 | G | A | 1 | a0001c0001t0002g0232 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.634+2722C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49074497 | |||||||
chr10:49074503 | G | A | 20 | a0001c0001t0003g0203 a0001c0001t0010g0201 a0001c0003t0004g0168 others(17): Show |
20 | HG01109.hp1 HG01123.hp1 HG01981.hp1 others(17): Show |
intron_variant | MODIFIER | c.634+2716C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49074503 | |||||||
chr10:49074727 | T | G | 18 | a0002c0002t0001g0060 a0002c0002t0001g0061 a0002c0002t0001g0090 others(15): Show |
18 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.634+2492A>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49074727 | |||||||
chr10:49074828 | G | A | 13 | a0001c0001t0008g0029 a0001c0001t0008g0030 a0001c0001t0008g0031 others(10): Show |
14 | HG00639.hp2 HG01243.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.634+2391C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49074828 | |||||||
chr10:49075047 | G | A | 9 | a0001c0001t0007g0185 a0001c0001t0007g0186 a0001c0001t0007g0187 others(6): Show |
9 | HG00099.hp1 HG01070.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.634+2172C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49075047 | |||||||
chr10:49075109 | A | G | 104 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0217 others(101): Show |
106 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.634+2110T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49075109 | |||||||
chr10:49075199 | T | C | 120 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0217 others(117): Show |
127 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.634+2020A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49075199 | |||||||
chr10:49075249 | T | C | 1 | a0001c0001t0021g0017 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.634+1970A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49075249 | |||||||
chr10:49075282 | A | T | 2 | a0001c0001t0017g0240 a0001c0001t0021g0242 |
2 | HG02630.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.634+1937T>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49075282 | |||||||
chr10:49075378 | G | A | 14 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0051 others(11): Show |
16 | HG00423.hp2 NA18941.hp2 NA18947.hp1 others(13): Show |
intron_variant | MODIFIER | c.634+1841C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49075378 | |||||||
chr10:49075480 | C | T | 1 | a0001c0001t0002g0230 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.634+1739G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49075480 | |||||||
chr10:49075494 | T | C | 1 | a0001c0001t0034g0194 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.634+1725A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49075494 | |||||||
chr10:49075619 | C | T | 1 | a0001c0001t0003g0035 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.634+1600G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49075619 | |||||||
chr10:49075721 | T | C | 1 | a0002c0002t0001g0147 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.634+1498A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49075721 | |||||||
chr10:49075771 | T | C | 1 | a0001c0001t0009g0227 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.634+1448A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49075771 | |||||||
chr10:49075851 | G | A | 1 | a0001c0001t0005g0065 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.634+1368C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49075851 | |||||||
chr10:49075862 | A | G | 120 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0217 others(117): Show |
127 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.634+1357T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49075862 | |||||||
chr10:49076109 | C | T | 97 | a0001c0001t0001g0037 a0001c0001t0001g0217 a0001c0001t0001g0226 others(94): Show |
103 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.634+1110G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49076109 | |||||||
chr10:49076426 | G | A | 1 | a0002c0002t0040g0149 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.634+793C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49076426 | |||||||
chr10:49076428 | C | CGGAAGTA others(36): Show |
1 | a0002c0002t0040g0149 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.634+790_634+791ins others(43): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49076428 | |||||||
chr10:49076430 | C | A | 1 | a0002c0002t0040g0149 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.634+789G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49076430 | |||||||
chr10:49076458 | G | A | 1 | a0001c0001t0002g0232 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.634+761C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49076458 | |||||||
chr10:49076600 | A | C | 124 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(121): Show |
131 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(128): Show |
intron_variant | MODIFIER | c.634+619T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49076600 | |||||||
chr10:49076615 | A | G | 1 | a0001c0001t0001g0257 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.634+604T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49076615 | |||||||
chr10:49076651 | T | C | 12 | a0002c0002t0002g0154 a0002c0002t0002g0155 a0002c0002t0003g0109 others(9): Show |
12 | HG00558.hp1 HG03704.hp1 HG04204.hp1 others(9): Show |
intron_variant | MODIFIER | c.634+568A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49076651 | |||||||
chr10:49076897 | C | A | 6 | a0001c0001t0008g0029 a0001c0001t0008g0030 a0001c0001t0008g0031 others(3): Show |
6 | HG01884.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.634+322G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49076897 | |||||||
chr10:49077001 | C | T | 23 | a0001c0001t0001g0016 a0001c0001t0003g0014 a0001c0001t0003g0244 others(20): Show |
24 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.634+218G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49077001 | |||||||
chr10:49077002 | G | A | 1 | a0001c0001t0014g0169 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.634+217C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49077002 | |||||||
chr10:49077039 | A | C | 46 | a0001c0001t0001g0037 a0001c0001t0001g0217 a0001c0001t0001g0226 others(43): Show |
51 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.634+180T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49077039 | |||||||
chr10:49077090 | A | G | 1 | a0004c0011t0037g0259 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.634+129T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49077090 | |||||||
chr10:49077432 | A | T | 1 | a0001c0001t0008g0030 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.527-106T>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49077432 | |||||||
chr10:49077597 | T | G | 1 | a0002c0002t0023g0144 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.527-271A>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49077597 | |||||||
chr10:49077614 | G | A | 2 | a0002c0002t0014g0008 a0002c0002t0014g0073 |
3 | HG02622.hp1 HG03516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.527-288C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49077614 | |||||||
chr10:49077712 | G | GA | 4 | a0001c0001t0001g0003 a0001c0001t0001g0256 a0001c0001t0001g0257 others(1): Show |
7 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(4): Show |
intron_variant | MODIFIER | c.527-387dupT | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49077712 | |||||||
chr10:49077832 | A | T | 1 | a0001c0004t0006g0019 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.527-506T>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49077832 | |||||||
chr10:49077861 | A | G | 84 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0217 others(81): Show |
91 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.527-535T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49077861 | |||||||
chr10:49077993 | GA | G | 101 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0217 others(98): Show |
110 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.527-668delT | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49077993 | |||||||
chr10:49078477 | GAC | G | 22 | a0001c0001t0001g0016 a0001c0001t0003g0014 a0001c0001t0003g0244 others(19): Show |
23 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.527-1153_527-1152d others(4): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49078477 | |||||||
chr10:49078497 | T | A | 1 | a0001c0001t0002g0221 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.527-1171A>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49078497 | |||||||
chr10:49078500 | A | C | 1 | a0001c0001t0008g0030 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.527-1174T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49078500 | |||||||
chr10:49078523 | G | GA | 29 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0051 others(26): Show |
31 | HG00423.hp2 HG00558.hp1 HG02451.hp1 others(28): Show |
intron_variant | MODIFIER | c.527-1198dupT | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49078523 | |||||||
chr10:49078523 | G | GAA | 90 | a0001c0001t0001g0037 a0001c0001t0001g0217 a0001c0001t0001g0226 others(87): Show |
97 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.527-1199_527-1198d others(4): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49078523 | |||||||
chr10:49078523 | GA | G | 13 | a0001c0001t0001g0026 a0001c0001t0008g0029 a0001c0001t0008g0030 others(10): Show |
14 | HG00639.hp2 HG01884.hp1 HG02895.hp2 others(11): Show |
intron_variant | MODIFIER | c.527-1198delT | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49078523 | |||||||
chr10:49078575 | T | C | 83 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0217 others(80): Show |
90 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.527-1249A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49078575 | |||||||
chr10:49078580 | G | C | 1 | a0001c0001t0034g0194 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.527-1254C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49078580 | |||||||
chr10:49078826 | T | C | 1 | a0002c0002t0001g0128 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.527-1500A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49078826 | |||||||
chr10:49078849 | A | AT | 49 | a0001c0001t0001g0037 a0001c0001t0001g0217 a0001c0001t0001g0226 others(46): Show |
55 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.527-1524dupA | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49078849 | |||||||
chr10:49078984 | G | A | 1 | a0002c0002t0001g0137 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.527-1658C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49078984 | |||||||
chr10:49079109 | G | A | 3 | a0002c0002t0001g0107 a0002c0002t0001g0128 a0002c0002t0011g0127 |
3 | HG01106.hp2 HG01993.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.527-1783C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49079109 | |||||||
chr10:49079183 | G | C | 1 | a0001c0001t0001g0016 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.527-1857C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49079183 | |||||||
chr10:49079437 | C | T | 1 | a0002c0002t0001g0083 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.527-2111G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49079437 | |||||||
chr10:49079502 | A | G | 2 | a0002c0002t0014g0008 a0002c0002t0014g0073 |
3 | HG02622.hp1 HG03516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.527-2176T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49079502 | |||||||
chr10:49079527 | A | G | 22 | a0001c0001t0001g0016 a0001c0001t0003g0014 a0001c0001t0003g0244 others(19): Show |
23 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.527-2201T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49079527 | |||||||
chr10:49079642 | A | T | 2 | a0001c0001t0017g0251 a0001c0003t0004g0250 |
2 | HG02970.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.527-2316T>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49079642 | |||||||
chr10:49079753 | G | A | 131 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0217 others(128): Show |
139 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(136): Show |
intron_variant | MODIFIER | c.527-2427C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49079753 | |||||||
chr10:49079808 | GA | G | 82 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0217 others(79): Show |
89 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.527-2483delT | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49079808 | |||||||
chr10:49079822 | C | T | 82 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0217 others(79): Show |
89 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.527-2496G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49079822 | |||||||
chr10:49079845 | AACT | A | 6 | a0001c0001t0008g0029 a0001c0001t0008g0030 a0001c0001t0008g0031 others(3): Show |
6 | HG01884.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.527-2522_527-2520d others(5): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49079845 | |||||||
chr10:49079924 | C | CT | 82 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0217 others(79): Show |
89 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.527-2599dupA | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49079924 | |||||||
chr10:49080216 | G | A | 28 | a0001c0001t0003g0021 a0001c0001t0008g0029 a0001c0001t0008g0030 others(25): Show |
29 | HG00639.hp2 HG00642.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.527-2890C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49080216 | |||||||
chr10:49080273 | A | C | 1 | a0001c0001t0034g0194 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.527-2947T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49080273 | |||||||
chr10:49080358 | C | T | 7 | a0002c0002t0001g0077 a0002c0002t0001g0079 a0002c0002t0001g0080 others(4): Show |
7 | HG02080.hp2 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.527-3032G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49080358 | |||||||
chr10:49080571 | T | A | 1 | a0002c0002t0001g0071 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.527-3245A>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49080571 | |||||||
chr10:49080754 | C | A | 1 | a0001c0001t0021g0017 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.527-3428G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49080754 | |||||||
chr10:49080778 | G | T | 1 | a0001c0001t0034g0194 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.527-3452C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49080778 | |||||||
chr10:49080886 | G | T | 83 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0217 others(80): Show |
90 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.527-3560C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49080886 | |||||||
chr10:49081083 | A | G | 16 | a0001c0001t0003g0021 a0001c0001t0010g0015 a0001c0001t0010g0179 others(13): Show |
16 | HG00642.hp1 HG01106.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.527-3757T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49081083 | |||||||
chr10:49081180 | C | A | 1 | a0006c0007t0003g0152 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.527-3854G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49081180 | |||||||
chr10:49081551 | C | T | 2 | a0002c0002t0003g0110 a0002c0002t0003g0142 |
2 | NA19070.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.527-4225G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49081551 | |||||||
chr10:49081583 | C | G | 83 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0217 others(80): Show |
90 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.527-4257G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49081583 | |||||||
chr10:49081597 | G | T | 1 | a0001c0001t0002g0222 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.527-4271C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49081597 | |||||||
chr10:49081616 | G | T | 1 | a0001c0001t0002g0214 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.527-4290C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49081616 | |||||||
chr10:49081940 | C | T | 83 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0217 others(80): Show |
90 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.526+4015G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49081940 | |||||||
chr10:49082131 | G | A | 1 | a0001c0001t0021g0017 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.526+3824C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49082131 | |||||||
chr10:49082379 | T | C | 1 | a0002c0002t0001g0119 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.526+3576A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49082379 | |||||||
chr10:49082400 | A | T | 6 | a0001c0001t0003g0021 a0001c0001t0026g0174 a0001c0005t0001g0172 others(3): Show |
6 | HG01106.hp1 HG02572.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.526+3555T>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49082400 | |||||||
chr10:49082437 | A | G | 83 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0217 others(80): Show |
90 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.526+3518T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49082437 | |||||||
chr10:49082451 | G | A | 83 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0217 others(80): Show |
90 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.526+3504C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49082451 | |||||||
chr10:49082460 | T | C | 47 | a0001c0001t0001g0037 a0001c0001t0001g0217 a0001c0001t0001g0226 others(44): Show |
52 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.526+3495A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49082460 | |||||||
chr10:49082473 | T | G | 83 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0217 others(80): Show |
90 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.526+3482A>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49082473 | |||||||
chr10:49082497 | T | C | 5 | a0001c0003t0004g0207 a0001c0003t0004g0208 a0001c0003t0004g0209 others(2): Show |
5 | HG01123.hp1 HG02109.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.526+3458A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49082497 | |||||||
chr10:49082511 | C | T | 2 | a0002c0002t0014g0008 a0002c0002t0014g0073 |
3 | HG02622.hp1 HG03516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.526+3444G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49082511 | |||||||
chr10:49082547 | T | C | 83 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0217 others(80): Show |
90 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.526+3408A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49082547 | |||||||
chr10:49082603 | A | T | 83 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0217 others(80): Show |
90 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.526+3352T>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49082603 | |||||||
chr10:49082631 | T | C | 83 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0217 others(80): Show |
90 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.526+3324A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49082631 | |||||||
chr10:49082674 | A | G | 1 | a0001c0001t0035g0165 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.526+3281T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49082674 | |||||||
chr10:49082690 | G | GA | 5 | a0001c0001t0021g0017 a0001c0001t0035g0165 a0001c0003t0036g0197 others(2): Show |
5 | HG01981.hp1 HG02717.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.526+3264dupT | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49082690 | |||||||
chr10:49082690 | G | T | 49 | a0001c0001t0001g0037 a0001c0001t0001g0217 a0001c0001t0001g0226 others(46): Show |
55 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.526+3265C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49082690 | |||||||
chr10:49082921 | T | A | 2 | a0001c0001t0018g0236 a0001c0001t0018g0237 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.526+3034A>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49082921 | |||||||
chr10:49083169 | T | A | 1 | a0001c0001t0035g0165 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.526+2786A>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49083169 | |||||||
chr10:49083355 | C | G | 88 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(85): Show |
95 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.526+2600G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49083355 | |||||||
chr10:49083521 | G | A | 2 | a0002c0002t0014g0008 a0002c0002t0014g0073 |
3 | HG02622.hp1 HG03516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.526+2434C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49083521 | |||||||
chr10:49083806 | G | A | 12 | a0002c0002t0002g0154 a0002c0002t0002g0155 a0002c0002t0003g0109 others(9): Show |
12 | HG00558.hp1 HG03704.hp1 HG04204.hp1 others(9): Show |
intron_variant | MODIFIER | c.526+2149C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49083806 | |||||||
chr10:49083845 | T | C | 1 | a0002c0002t0002g0112 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.526+2110A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49083845 | |||||||
chr10:49083888 | C | G | 49 | a0001c0001t0001g0037 a0001c0001t0001g0217 a0001c0001t0001g0226 others(46): Show |
55 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.526+2067G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49083888 | |||||||
chr10:49083917 | C | T | 1 | a0002c0002t0001g0130 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.526+2038G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49083917 | |||||||
chr10:49084169 | A | G | 1 | a0002c0002t0001g0083 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.526+1786T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49084169 | |||||||
chr10:49084401 | C | T | 28 | a0001c0001t0003g0021 a0001c0001t0008g0029 a0001c0001t0008g0030 others(25): Show |
29 | HG00639.hp2 HG00642.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.526+1554G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49084401 | |||||||
chr10:49084438 | A | C | 1 | a0001c0001t0023g0175 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.526+1517T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49084438 | |||||||
chr10:49084765 | G | C | 1 | a0002c0002t0001g0139 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.526+1190C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49084765 | |||||||
chr10:49084780 | G | A | 1 | a0002c0002t0013g0151 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.526+1175C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49084780 | |||||||
chr10:49084965 | C | A | 1 | a0002c0002t0001g0063 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.526+990G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49084965 | |||||||
chr10:49085014 | A | C | 83 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0217 others(80): Show |
90 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.526+941T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49085014 | |||||||
chr10:49085058 | T | A | 1 | a0002c0002t0001g0063 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.526+897A>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49085058 | |||||||
chr10:49085112 | G | T | 1 | a0002c0002t0003g0163 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.526+843C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49085112 | |||||||
chr10:49085213 | C | T | 131 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0217 others(128): Show |
139 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(136): Show |
intron_variant | MODIFIER | c.526+742G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49085213 | |||||||
chr10:49085269 | C | T | 4 | a0001c0005t0001g0172 a0001c0005t0008g0170 a0001c0005t0008g0171 others(1): Show |
4 | HG02572.hp1 HG02615.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.526+686G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49085269 | |||||||
chr10:49085411 | A | G | 151 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0217 others(148): Show |
162 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.526+544T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49085411 | |||||||
chr10:49085522 | G | A | 48 | a0001c0001t0001g0037 a0001c0001t0001g0217 a0001c0001t0001g0226 others(45): Show |
54 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.526+433C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49085522 | |||||||
chr10:49085855 | G | A | 1 | a0002c0002t0028g0044 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.526+100C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49085855 | |||||||
chr10:49085891 | T | A | 28 | a0001c0001t0003g0021 a0001c0001t0008g0029 a0001c0001t0008g0030 others(25): Show |
29 | HG00639.hp2 HG00642.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.526+64A>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49085891 | |||||||
chr10:49085909 | A | C | 14 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0051 others(11): Show |
16 | HG00423.hp2 NA18941.hp2 NA18947.hp1 others(13): Show |
intron_variant | MODIFIER | c.526+46T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49085909 | |||||||
chr10:49085928 | TA | T | 6 | a0001c0001t0008g0029 a0001c0001t0008g0030 a0001c0001t0008g0031 others(3): Show |
6 | HG01884.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.526+26delT | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49085928 | |||||||
chr10:49086217 | C | T | 12 | a0002c0002t0002g0154 a0002c0002t0002g0155 a0002c0002t0003g0109 others(9): Show |
12 | HG00558.hp1 HG03704.hp1 HG04204.hp1 others(9): Show |
intron_variant | MODIFIER | c.458-194G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49086217 | |||||||
chr10:49086218 | A | G | 113 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0217 others(110): Show |
121 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.458-195T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49086218 | |||||||
chr10:49086387 | C | T | 16 | a0001c0001t0003g0021 a0001c0001t0010g0015 a0001c0001t0010g0179 others(13): Show |
16 | HG00642.hp1 HG01106.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.458-364G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49086387 | |||||||
chr10:49086398 | T | C | 1 | a0001c0001t0001g0016 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.458-375A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49086398 | |||||||
chr10:49086444 | T | C | 1 | a0001c0001t0008g0029 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.458-421A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49086444 | |||||||
chr10:49086625 | G | A | 196 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0024 others(193): Show |
211 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.458-602C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49086625 | |||||||
chr10:49086630 | C | T | 31 | a0001c0001t0003g0203 a0001c0001t0010g0201 a0001c0003t0004g0168 others(28): Show |
31 | HG00558.hp1 HG01109.hp1 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.458-607G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49086630 | |||||||
chr10:49086683 | C | T | 33 | a0001c0001t0003g0203 a0001c0001t0010g0201 a0001c0001t0021g0017 others(30): Show |
33 | HG00558.hp1 HG01109.hp1 HG01123.hp1 others(30): Show |
intron_variant | MODIFIER | c.458-660G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49086683 | |||||||
chr10:49086860 | T | C | 33 | a0001c0001t0003g0203 a0001c0001t0010g0201 a0001c0001t0021g0017 others(30): Show |
33 | HG00558.hp1 HG01109.hp1 HG01123.hp1 others(30): Show |
intron_variant | MODIFIER | c.458-837A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49086860 | |||||||
chr10:49086966 | A | C | 152 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0217 others(149): Show |
163 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.458-943T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49086966 | |||||||
chr10:49087009 | C | T | 28 | a0001c0001t0003g0021 a0001c0001t0008g0029 a0001c0001t0008g0030 others(25): Show |
29 | HG00639.hp2 HG00642.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.458-986G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49087009 | |||||||
chr10:49087347 | C | T | 6 | a0001c0001t0008g0029 a0001c0001t0008g0030 a0001c0001t0008g0031 others(3): Show |
6 | HG01884.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.458-1324G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49087347 | |||||||
chr10:49087412 | T | A | 1 | a0002c0002t0023g0144 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.458-1389A>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49087412 | |||||||
chr10:49087786 | G | A | 33 | a0001c0001t0003g0203 a0001c0001t0010g0201 a0001c0001t0021g0017 others(30): Show |
33 | HG00558.hp1 HG01109.hp1 HG01123.hp1 others(30): Show |
intron_variant | MODIFIER | c.458-1763C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49087786 | |||||||
chr10:49087881 | C | T | 16 | a0001c0001t0003g0021 a0001c0001t0010g0015 a0001c0001t0010g0179 others(13): Show |
16 | HG00642.hp1 HG01106.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.458-1858G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49087881 | |||||||
chr10:49087894 | TTA | T | 33 | a0001c0001t0003g0203 a0001c0001t0010g0201 a0001c0001t0021g0017 others(30): Show |
33 | HG00558.hp1 HG01109.hp1 HG01123.hp1 others(30): Show |
intron_variant | MODIFIER | c.458-1873_458-1872d others(4): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49087894 | |||||||
chr10:49087911 | G | GTA | 4 | a0001c0001t0001g0088 a0002c0002t0001g0089 a0002c0002t0001g0119 others(1): Show |
4 | NA18970.hp2 NA18993.hp1 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-1890_458-1889d others(4): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49087911 | |||||||
chr10:49087913 | A | ATATATAT others(18): Show |
1 | a0001c0001t0014g0169 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.458-1915_458-1891d others(27): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49087913 | |||||||
chr10:49087927 | GTAATATA others(2): Show |
G | 3 | a0001c0001t0007g0188 a0001c0001t0007g0189 a0001c0001t0007g0191 |
3 | HG01070.hp1 HG01074.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.458-1913_458-1905d others(11): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49087927 | |||||||
chr10:49087936 | ATGTATAT others(20): Show |
A | 20 | a0001c0001t0003g0203 a0001c0001t0010g0201 a0001c0001t0035g0165 others(17): Show |
20 | HG01109.hp1 HG01123.hp1 HG01981.hp1 others(17): Show |
intron_variant | MODIFIER | c.458-1940_458-1914d others(29): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49087936 | |||||||
chr10:49087975 | A | C | 1 | a0004c0011t0037g0259 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.458-1952T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49087975 | |||||||
chr10:49087976 | T | C | 1 | a0001c0003t0004g0205 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.458-1953A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49087976 | |||||||
chr10:49087988 | A | G | 3 | a0001c0001t0007g0188 a0001c0001t0007g0189 a0001c0001t0007g0191 |
3 | HG01070.hp1 HG01074.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.458-1965T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49087988 | |||||||
chr10:49087992 | G | A | 131 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0217 others(128): Show |
139 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(136): Show |
intron_variant | MODIFIER | c.458-1969C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49087992 | |||||||
chr10:49087995 | T | C | 28 | a0001c0001t0003g0021 a0001c0001t0008g0029 a0001c0001t0008g0030 others(25): Show |
29 | HG00639.hp2 HG00642.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.458-1972A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49087995 | |||||||
chr10:49088299 | T | G | 1 | a0001c0001t0021g0017 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.458-2276A>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49088299 | |||||||
chr10:49088336 | C | A | 6 | a0001c0001t0001g0037 a0001c0001t0003g0039 a0001c0001t0019g0048 others(3): Show |
6 | HG02056.hp2 HG02083.hp2 NA18993.hp2 others(3): Show |
intron_variant | MODIFIER | c.458-2313G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49088336 | |||||||
chr10:49088481 | A | G | 14 | a0001c0001t0021g0017 a0001c0001t0035g0165 a0002c0002t0002g0154 others(11): Show |
14 | HG00558.hp1 HG02717.hp2 HG03195.hp1 others(11): Show |
intron_variant | MODIFIER | c.458-2458T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49088481 | |||||||
chr10:49088571 | A | G | 2 | a0002c0002t0001g0010 a0002c0002t0001g0129 |
3 | NA18955.hp1 NA18990.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.458-2548T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49088571 | |||||||
chr10:49088577 | G | T | 118 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0217 others(115): Show |
126 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(123): Show |
intron_variant | MODIFIER | c.458-2554C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49088577 | |||||||
chr10:49088667 | C | T | 3 | a0002c0002t0001g0107 a0002c0002t0001g0128 a0002c0002t0011g0127 |
3 | HG01106.hp2 HG01993.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.458-2644G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49088667 | |||||||
chr10:49088723 | A | T | 8 | a0001c0001t0010g0015 a0001c0001t0010g0179 a0001c0001t0010g0182 others(5): Show |
8 | HG00642.hp1 HG01243.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.458-2700T>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49088723 | |||||||
chr10:49088846 | C | A | 2 | a0001c0001t0003g0246 a0001c0001t0003g0247 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.458-2823G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49088846 | |||||||
chr10:49088867 | G | A | 1 | a0001c0001t0002g0228 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.458-2844C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49088867 | |||||||
chr10:49088875 | T | C | 1 | a0002c0002t0001g0104 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.458-2852A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49088875 | |||||||
chr10:49088901 | C | T | 4 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(1): Show |
4 | HG01192.hp2 HG02717.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-2878G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49088901 | |||||||
chr10:49088936 | C | T | 49 | a0001c0001t0001g0037 a0001c0001t0001g0217 a0001c0001t0001g0226 others(46): Show |
55 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.458-2913G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49088936 | |||||||
chr10:49088975 | C | T | 49 | a0001c0001t0001g0037 a0001c0001t0001g0217 a0001c0001t0001g0226 others(46): Show |
55 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.458-2952G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49088975 | |||||||
chr10:49089104 | T | C | 13 | a0001c0001t0003g0014 a0001c0001t0003g0244 a0001c0001t0003g0245 others(10): Show |
14 | HG01069.hp1 HG02258.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.458-3081A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49089104 | |||||||
chr10:49089182 | G | A | 1 | a0001c0001t0021g0017 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.458-3159C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49089182 | |||||||
chr10:49089265 | C | G | 49 | a0001c0001t0001g0037 a0001c0001t0001g0217 a0001c0001t0001g0226 others(46): Show |
55 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.458-3242G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49089265 | |||||||
chr10:49089352 | C | T | 1 | a0001c0001t0023g0175 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.458-3329G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49089352 | |||||||
chr10:49089390 | T | G | 1 | a0001c0003t0004g0205 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.458-3367A>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49089390 | |||||||
chr10:49089427 | C | T | 21 | a0001c0001t0002g0178 a0001c0001t0005g0006 a0001c0001t0005g0007 others(18): Show |
24 | HG00423.hp2 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.458-3404G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49089427 | |||||||
chr10:49089495 | C | G | 1 | a0001c0001t0001g0016 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.458-3472G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49089495 | |||||||
chr10:49089520 | C | A | 49 | a0001c0001t0001g0037 a0001c0001t0001g0217 a0001c0001t0001g0226 others(46): Show |
55 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.458-3497G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49089520 | |||||||
chr10:49089662 | C | T | 1 | a0002c0002t0003g0109 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.458-3639G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49089662 | |||||||
chr10:49089663 | T | A | 1 | a0001c0001t0003g0253 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.458-3640A>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49089663 | |||||||
chr10:49089767 | G | T | 50 | a0001c0001t0001g0037 a0001c0001t0001g0217 a0001c0001t0001g0226 others(47): Show |
56 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.458-3744C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49089767 | |||||||
chr10:49090014 | G | A | 21 | a0001c0001t0003g0014 a0001c0001t0003g0244 a0001c0001t0003g0245 others(18): Show |
22 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.458-3991C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49090014 | |||||||
chr10:49090038 | T | C | 1 | a0002c0002t0001g0139 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.458-4015A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49090038 | |||||||
chr10:49090146 | G | T | 21 | a0001c0001t0003g0014 a0001c0001t0003g0244 a0001c0001t0003g0245 others(18): Show |
22 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.458-4123C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49090146 | |||||||
chr10:49090305 | G | A | 1 | a0001c0001t0023g0175 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.458-4282C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49090305 | |||||||
chr10:49090476 | A | G | 101 | a0001c0001t0001g0037 a0001c0001t0001g0217 a0001c0001t0001g0226 others(98): Show |
110 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.458-4453T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49090476 | |||||||
chr10:49090494 | G | A | 49 | a0001c0001t0001g0037 a0001c0001t0001g0217 a0001c0001t0001g0226 others(46): Show |
55 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.458-4471C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49090494 | |||||||
chr10:49090524 | T | C | 1 | a0001c0001t0001g0016 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.458-4501A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49090524 | |||||||
chr10:49090690 | C | T | 49 | a0001c0001t0001g0037 a0001c0001t0001g0217 a0001c0001t0001g0226 others(46): Show |
55 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.458-4667G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49090690 | |||||||
chr10:49090836 | G | C | 52 | a0001c0001t0002g0178 a0001c0001t0003g0203 a0001c0001t0005g0006 others(49): Show |
55 | HG00423.hp2 HG00558.hp1 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.458-4813C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49090836 | |||||||
chr10:49090884 | C | T | 1 | a0002c0002t0013g0094 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.458-4861G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49090884 | |||||||
chr10:49090987 | C | T | 1 | a0002c0002t0003g0161 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.458-4964G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49090987 | |||||||
chr10:49091016 | C | A | 4 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(1): Show |
4 | HG01192.hp2 HG02717.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-4993G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49091016 | |||||||
chr10:49091016 | C | G | 153 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0217 others(150): Show |
164 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(161): Show |
intron_variant | MODIFIER | c.458-4993G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49091016 | |||||||
chr10:49091117 | G | A | 1 | a0002c0002t0028g0044 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.458-5094C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49091117 | |||||||
chr10:49091156 | G | C | 2 | a0002c0002t0014g0008 a0002c0002t0014g0073 |
3 | HG02622.hp1 HG03516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.458-5133C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49091156 | |||||||
chr10:49091588 | A | G | 52 | a0001c0001t0002g0178 a0001c0001t0003g0203 a0001c0001t0005g0006 others(49): Show |
55 | HG00423.hp2 HG00558.hp1 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.458-5565T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49091588 | |||||||
chr10:49091602 | C | G | 1 | a0002c0002t0001g0126 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.458-5579G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49091602 | |||||||
chr10:49091634 | C | T | 1 | a0001c0001t0001g0016 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.458-5611G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49091634 | |||||||
chr10:49091913 | G | A | 49 | a0001c0001t0001g0037 a0001c0001t0001g0217 a0001c0001t0001g0226 others(46): Show |
55 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.458-5890C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49091913 | |||||||
chr10:49091914 | GA | G | 4 | a0001c0005t0001g0172 a0001c0005t0008g0170 a0001c0005t0008g0171 others(1): Show |
4 | HG02572.hp1 HG02615.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-5892delT | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49091914 | |||||||
chr10:49091975 | G | A | 52 | a0001c0001t0002g0178 a0001c0001t0003g0203 a0001c0001t0005g0006 others(49): Show |
55 | HG00423.hp2 HG00558.hp1 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.458-5952C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49091975 | |||||||
chr10:49092134 | C | A | 101 | a0001c0001t0001g0037 a0001c0001t0001g0217 a0001c0001t0001g0226 others(98): Show |
110 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.458-6111G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49092134 | |||||||
chr10:49092135 | T | A | 1 | a0001c0001t0021g0017 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.458-6112A>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49092135 | |||||||
chr10:49092201 | C | T | 157 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(154): Show |
168 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(165): Show |
intron_variant | MODIFIER | c.458-6178G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49092201 | |||||||
chr10:49092348 | C | T | 101 | a0001c0001t0001g0037 a0001c0001t0001g0217 a0001c0001t0001g0226 others(98): Show |
110 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.458-6325G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49092348 | |||||||
chr10:49092420 | C | T | 1 | a0002c0002t0001g0043 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.458-6397G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49092420 | |||||||
chr10:49092460 | C | A | 52 | a0001c0001t0002g0178 a0001c0001t0003g0203 a0001c0001t0005g0006 others(49): Show |
55 | HG00423.hp2 HG00558.hp1 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.458-6437G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49092460 | |||||||
chr10:49092724 | C | G | 12 | a0002c0002t0002g0154 a0002c0002t0002g0155 a0002c0002t0003g0109 others(9): Show |
12 | HG00558.hp1 HG03704.hp1 HG04204.hp1 others(9): Show |
intron_variant | MODIFIER | c.458-6701G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49092724 | |||||||
chr10:49092761 | C | A | 1 | a0001c0001t0003g0253 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.458-6738G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49092761 | |||||||
chr10:49092968 | A | T | 19 | a0001c0001t0003g0203 a0001c0001t0010g0201 a0001c0003t0004g0168 others(16): Show |
19 | HG01109.hp1 HG01123.hp1 HG01981.hp1 others(16): Show |
intron_variant | MODIFIER | c.458-6945T>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49092968 | |||||||
chr10:49093001 | A | G | 8 | a0001c0001t0010g0015 a0001c0001t0010g0179 a0001c0001t0010g0182 others(5): Show |
8 | HG00642.hp1 HG01243.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.458-6978T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49093001 | |||||||
chr10:49093009 | C | T | 6 | a0001c0004t0006g0019 a0001c0004t0006g0020 a0001c0004t0006g0022 others(3): Show |
7 | HG00639.hp2 HG03041.hp2 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.458-6986G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49093009 | |||||||
chr10:49093029 | T | C | 195 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0024 others(192): Show |
210 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.458-7006A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49093029 | |||||||
chr10:49093032 | T | C | 54 | a0001c0001t0002g0178 a0001c0001t0003g0203 a0001c0001t0005g0006 others(51): Show |
58 | HG00423.hp2 HG00558.hp1 HG01069.hp2 others(55): Show |
intron_variant | MODIFIER | c.458-7009A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49093032 | |||||||
chr10:49093044 | G | C | 1 | a0001c0001t0021g0242 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.458-7021C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49093044 | |||||||
chr10:49093330 | G | T | 52 | a0001c0001t0002g0178 a0001c0001t0003g0203 a0001c0001t0005g0006 others(49): Show |
55 | HG00423.hp2 HG00558.hp1 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.458-7307C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49093330 | |||||||
chr10:49093489 | G | A | 1 | a0001c0001t0035g0165 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.458-7466C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49093489 | |||||||
chr10:49093620 | T | C | 52 | a0001c0001t0002g0178 a0001c0001t0003g0203 a0001c0001t0005g0006 others(49): Show |
55 | HG00423.hp2 HG00558.hp1 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.458-7597A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49093620 | |||||||
chr10:49093687 | T | C | 14 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0051 others(11): Show |
16 | HG00423.hp2 NA18941.hp2 NA18947.hp1 others(13): Show |
intron_variant | MODIFIER | c.458-7664A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49093687 | |||||||
chr10:49093704 | A | G | 1 | a0001c0001t0035g0165 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.458-7681T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49093704 | |||||||
chr10:49093742 | C | CT | 17 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0027 others(14): Show |
18 | HG01069.hp2 HG01071.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.458-7720dupA | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49093742 | |||||||
chr10:49093742 | C | CTT | 12 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0051 others(9): Show |
14 | HG00423.hp2 HG03195.hp1 NA18941.hp2 others(11): Show |
intron_variant | MODIFIER | c.458-7721_458-7720d others(4): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49093742 | |||||||
chr10:49093742 | C | CTTT | 12 | a0001c0001t0005g0052 a0002c0002t0002g0154 a0002c0002t0002g0155 others(9): Show |
12 | HG00558.hp1 HG03704.hp1 HG04204.hp1 others(9): Show |
intron_variant | MODIFIER | c.458-7722_458-7720d others(5): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49093742 | |||||||
chr10:49093742 | CT | C | 19 | a0001c0001t0003g0247 a0001c0001t0007g0189 a0001c0001t0008g0031 others(16): Show |
19 | HG00323.hp1 HG01070.hp1 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.458-7720delA | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49093742 | |||||||
chr10:49093742 | CTT | C | 53 | a0001c0001t0001g0037 a0001c0001t0001g0217 a0001c0001t0001g0226 others(50): Show |
60 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.458-7721_458-7720d others(4): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49093742 | |||||||
chr10:49093784 | G | C | 48 | a0001c0001t0001g0037 a0001c0001t0001g0217 a0001c0001t0001g0226 others(45): Show |
54 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.458-7761C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49093784 | |||||||
chr10:49093847 | A | G | 28 | a0001c0001t0001g0016 a0001c0001t0003g0014 a0001c0001t0003g0244 others(25): Show |
29 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.458-7824T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49093847 | |||||||
chr10:49093905 | G | T | 1 | a0001c0001t0035g0165 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.458-7882C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49093905 | |||||||
chr10:49093982 | C | T | 48 | a0001c0001t0001g0037 a0001c0001t0001g0217 a0001c0001t0001g0226 others(45): Show |
54 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.458-7959G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49093982 | |||||||
chr10:49093989 | C | T | 13 | a0002c0002t0001g0079 a0002c0002t0002g0154 a0002c0002t0002g0155 others(10): Show |
13 | HG00558.hp1 HG03579.hp2 HG03704.hp1 others(10): Show |
intron_variant | MODIFIER | c.458-7966G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49093989 | |||||||
chr10:49093990 | A | G | 173 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(170): Show |
185 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(182): Show |
intron_variant | MODIFIER | c.458-7967T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49093990 | |||||||
chr10:49094047 | G | A | 1 | a0002c0002t0009g0141 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.458-8024C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49094047 | |||||||
chr10:49094135 | G | A | 1 | a0001c0001t0014g0169 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.458-8112C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49094135 | |||||||
chr10:49094160 | CA | C | 48 | a0001c0001t0001g0037 a0001c0001t0001g0217 a0001c0001t0001g0226 others(45): Show |
54 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.458-8138delT | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49094160 | |||||||
chr10:49094223 | G | A | 2 | a0002c0002t0006g0100 a0002c0002t0006g0102 |
2 | HG00323.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.458-8200C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49094223 | |||||||
chr10:49094251 | T | A | 12 | a0002c0002t0002g0154 a0002c0002t0002g0155 a0002c0002t0003g0109 others(9): Show |
12 | HG00558.hp1 HG03704.hp1 HG04204.hp1 others(9): Show |
intron_variant | MODIFIER | c.458-8228A>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49094251 | |||||||
chr10:49094536 | A | G | 1 | a0001c0001t0023g0175 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.458-8513T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49094536 | |||||||
chr10:49094662 | A | G | 2 | a0001c0001t0005g0051 a0001c0001t0005g0055 |
2 | NA18977.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.458-8639T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49094662 | |||||||
chr10:49094769 | ATTCTCAG others(2): Show |
A | 46 | a0001c0001t0001g0037 a0001c0001t0001g0217 a0001c0001t0001g0226 others(43): Show |
51 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.458-8755_458-8747d others(11): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49094769 | |||||||
chr10:49094787 | T | C | 52 | a0001c0001t0002g0178 a0001c0001t0003g0203 a0001c0001t0005g0006 others(49): Show |
55 | HG00423.hp2 HG00558.hp1 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.458-8764A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49094787 | |||||||
chr10:49094792 | G | C | 1 | a0001c0001t0002g0040 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.458-8769C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49094792 | |||||||
chr10:49094795 | G | T | 1 | a0001c0001t0026g0174 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.458-8772C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49094795 | |||||||
chr10:49094849 | C | T | 1 | a0001c0001t0023g0175 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.458-8826G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49094849 | |||||||
chr10:49094850 | A | G | 157 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(154): Show |
168 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(165): Show |
intron_variant | MODIFIER | c.458-8827T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49094850 | |||||||
chr10:49094911 | C | G | 52 | a0001c0001t0002g0178 a0001c0001t0003g0203 a0001c0001t0005g0006 others(49): Show |
55 | HG00423.hp2 HG00558.hp1 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.458-8888G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49094911 | |||||||
chr10:49095044 | A | C | 12 | a0002c0002t0002g0154 a0002c0002t0002g0155 a0002c0002t0003g0109 others(9): Show |
12 | HG00558.hp1 HG03704.hp1 HG04204.hp1 others(9): Show |
intron_variant | MODIFIER | c.458-9021T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49095044 | |||||||
chr10:49095107 | G | A | 1 | a0004c0011t0037g0259 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.458-9084C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49095107 | |||||||
chr10:49095129 | C | G | 48 | a0001c0001t0001g0037 a0001c0001t0001g0217 a0001c0001t0001g0226 others(45): Show |
54 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.458-9106G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49095129 | |||||||
chr10:49095410 | C | T | 40 | a0001c0001t0002g0178 a0001c0001t0003g0203 a0001c0001t0005g0006 others(37): Show |
43 | HG00423.hp2 HG01069.hp2 HG01071.hp1 others(40): Show |
intron_variant | MODIFIER | c.458-9387G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49095410 | |||||||
chr10:49095418 | C | T | 14 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0051 others(11): Show |
16 | HG00423.hp2 NA18941.hp2 NA18947.hp1 others(13): Show |
intron_variant | MODIFIER | c.458-9395G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49095418 | |||||||
chr10:49095421 | G | A | 46 | a0001c0001t0001g0037 a0001c0001t0001g0217 a0001c0001t0001g0226 others(43): Show |
52 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.458-9398C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49095421 | |||||||
chr10:49095491 | C | T | 73 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(70): Show |
77 | HG00099.hp1 HG00639.hp2 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.458-9468G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49095491 | |||||||
chr10:49095532 | G | A | 9 | a0001c0003t0004g0195 a0001c0003t0004g0196 a0001c0003t0004g0198 others(6): Show |
9 | HG01109.hp1 HG02145.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.458-9509C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49095532 | |||||||
chr10:49095594 | T | C | 1 | a0001c0001t0023g0175 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.458-9571A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49095594 | |||||||
chr10:49095751 | T | C | 1 | a0001c0001t0010g0184 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.458-9728A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49095751 | |||||||
chr10:49095802 | C | G | 1 | a0002c0002t0001g0087 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.458-9779G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49095802 | |||||||
chr10:49096013 | T | C | 1 | a0004c0011t0037g0259 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.458-9990A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49096013 | |||||||
chr10:49096334 | G | A | 5 | a0001c0001t0001g0003 a0001c0001t0001g0256 a0001c0001t0001g0257 others(2): Show |
8 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(5): Show |
intron_variant | MODIFIER | c.458-10311C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49096334 | |||||||
chr10:49096412 | A | G | 1 | a0001c0001t0008g0031 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.458-10389T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49096412 | |||||||
chr10:49096468 | G | A | 1 | a0001c0001t0010g0182 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.458-10445C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49096468 | |||||||
chr10:49096494 | A | C | 7 | a0001c0001t0003g0021 a0001c0004t0006g0019 a0001c0004t0006g0020 others(4): Show |
8 | HG00639.hp2 HG03041.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.458-10471T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49096494 | |||||||
chr10:49096622 | C | CGT | 55 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0026 others(52): Show |
62 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.458-10601_458-1060 others(6): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49096622 | |||||||
chr10:49096622 | C | CGTGT | 28 | a0001c0001t0001g0037 a0001c0001t0002g0018 a0001c0001t0002g0040 others(25): Show |
29 | HG00558.hp2 HG01069.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.458-10603_458-1060 others(8): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49096622 | |||||||
chr10:49096622 | C | CGTGTGT | 32 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0002g0002 others(29): Show |
36 | HG00438.hp1 HG00621.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.458-10605_458-1060 others(10): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49096622 | |||||||
chr10:49096622 | C | CGTGTGTG others(1): Show |
20 | a0001c0001t0002g0215 a0001c0001t0002g0218 a0001c0001t0002g0230 others(17): Show |
21 | HG00642.hp1 HG01074.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.458-10607_458-1060 others(12): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49096622 | |||||||
chr10:49096622 | C | CGTGTGTG others(3): Show |
6 | a0001c0001t0008g0031 a0001c0003t0004g0168 a0001c0003t0004g0205 others(3): Show |
6 | HG01884.hp1 HG02602.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.458-10609_458-1060 others(14): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49096622 | |||||||
chr10:49096622 | C | CGTGTGTG others(5): Show |
8 | a0001c0001t0003g0021 a0001c0001t0008g0029 a0001c0001t0008g0030 others(5): Show |
8 | HG00639.hp2 HG02717.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.458-10611_458-1060 others(16): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49096622 | |||||||
chr10:49096622 | C | CGTGTGTG others(7): Show |
2 | a0001c0001t0003g0203 a0001c0003t0004g0204 |
2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.458-10613_458-1060 others(18): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49096622 | |||||||
chr10:49096622 | C | CGTGTGTG others(9): Show |
5 | a0001c0001t0010g0201 a0001c0003t0004g0202 a0001c0003t0004g0209 others(2): Show |
5 | HG02451.hp1 HG02965.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.458-10615_458-1060 others(20): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49096622 | |||||||
chr10:49096622 | C | CGTGTGTG others(11): Show |
4 | a0001c0003t0004g0199 a0001c0003t0004g0200 a0001c0003t0004g0207 others(1): Show |
4 | HG02109.hp1 HG02630.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.458-10617_458-1060 others(22): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49096622 | |||||||
chr10:49096622 | C | CGTGTGTG others(15): Show |
3 | a0001c0003t0004g0198 a0001c0003t0004g0206 a0001c0003t0036g0197 |
3 | HG01109.hp1 HG01981.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.458-10621_458-1060 others(26): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49096622 | |||||||
chr10:49096622 | C | CGTGTGTG others(17): Show |
1 | a0001c0003t0004g0196 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.458-10623_458-1060 others(28): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49096622 | |||||||
chr10:49096622 | CGT | C | 6 | a0001c0001t0002g0214 a0001c0001t0005g0058 a0001c0001t0007g0192 others(3): Show |
6 | HG00099.hp1 HG02015.hp1 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.458-10601_458-1060 others(6): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49096622 | |||||||
chr10:49096622 | CGTGT | C | 10 | a0001c0001t0003g0253 a0001c0001t0021g0017 a0001c0005t0001g0172 others(7): Show |
10 | HG02135.hp2 HG02273.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.458-10603_458-1060 others(8): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49096622 | |||||||
chr10:49096622 | CGTGTGT | C | 7 | a0001c0001t0002g0178 a0001c0001t0015g0013 a0001c0001t0015g0167 others(4): Show |
8 | HG01069.hp2 HG01071.hp1 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.458-10605_458-1060 others(10): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49096622 | |||||||
chr10:49096622 | CGTGTGTG others(5): Show |
C | 1 | a0004c0011t0037g0259 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.458-10611_458-1060 others(16): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49096622 | |||||||
chr10:49096622 | CGTGTGTG others(11): Show |
C | 1 | a0002c0002t0007g0143 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.458-10617_458-1060 others(22): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49096622 | |||||||
chr10:49096677 | G | A | 58 | a0001c0001t0001g0003 a0001c0001t0001g0256 a0001c0001t0001g0257 others(55): Show |
65 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.458-10654C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49096677 | |||||||
chr10:49096749 | G | A | 13 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0051 others(10): Show |
15 | HG00423.hp2 NA18941.hp2 NA18947.hp1 others(12): Show |
intron_variant | MODIFIER | c.458-10726C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49096749 | |||||||
chr10:49096804 | G | A | 2 | a0002c0002t0001g0091 a0002c0002t0001g0147 |
2 | HG02273.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.458-10781C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49096804 | |||||||
chr10:49096921 | A | G | 59 | a0001c0001t0001g0003 a0001c0001t0001g0256 a0001c0001t0001g0257 others(56): Show |
66 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.457+10673T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49096921 | |||||||
chr10:49096953 | A | G | 153 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0024 others(150): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.457+10641T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49096953 | |||||||
chr10:49096971 | A | G | 104 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0217 others(101): Show |
116 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.457+10623T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49096971 | |||||||
chr10:49097150 | C | T | 1 | a0001c0001t0016g0166 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.457+10444G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49097150 | |||||||
chr10:49097194 | C | A | 1 | a0002c0002t0001g0148 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.457+10400G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49097194 | |||||||
chr10:49097209 | T | C | 1 | a0002c0002t0003g0163 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.457+10385A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49097209 | |||||||
chr10:49097350 | C | T | 12 | a0002c0002t0002g0154 a0002c0002t0002g0155 a0002c0002t0003g0109 others(9): Show |
12 | HG00558.hp1 HG03704.hp1 HG04204.hp1 others(9): Show |
intron_variant | MODIFIER | c.457+10244G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49097350 | |||||||
chr10:49097450 | T | TA | 46 | a0001c0001t0003g0014 a0001c0001t0003g0203 a0001c0001t0003g0244 others(43): Show |
49 | HG00423.hp2 HG01069.hp1 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.457+10143dupT | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49097450 | |||||||
chr10:49097635 | G | A | 2 | a0001c0001t0010g0184 a0001c0001t0022g0183 |
2 | HG00642.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.457+9959C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49097635 | |||||||
chr10:49097645 | T | C | 1 | a0001c0001t0002g0230 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.457+9949A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49097645 | |||||||
chr10:49097834 | G | T | 1 | a0001c0003t0004g0195 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.457+9760C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49097834 | |||||||
chr10:49097977 | C | T | 41 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(38): Show |
42 | HG00099.hp1 HG00639.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.457+9617G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49097977 | |||||||
chr10:49098084 | C | G | 58 | a0001c0001t0001g0003 a0001c0001t0001g0256 a0001c0001t0001g0257 others(55): Show |
65 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.457+9510G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49098084 | |||||||
chr10:49098085 | T | G | 58 | a0001c0001t0001g0003 a0001c0001t0001g0256 a0001c0001t0001g0257 others(55): Show |
65 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.457+9509A>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49098085 | |||||||
chr10:49098152 | G | A | 1 | a0001c0001t0001g0016 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.457+9442C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49098152 | |||||||
chr10:49098341 | C | T | 26 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(23): Show |
27 | HG00099.hp1 HG00639.hp2 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.457+9253G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49098341 | |||||||
chr10:49098353 | T | C | 1 | a0004c0011t0037g0259 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.457+9241A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49098353 | |||||||
chr10:49098409 | A | G | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG01192.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.457+9185T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49098409 | |||||||
chr10:49098445 | T | C | 1 | a0001c0001t0034g0194 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.457+9149A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49098445 | |||||||
chr10:49098603 | G | A | 13 | a0001c0001t0003g0014 a0001c0001t0003g0244 a0001c0001t0003g0245 others(10): Show |
14 | HG01069.hp1 HG02258.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.457+8991C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49098603 | |||||||
chr10:49098703 | T | C | 1 | a0001c0001t0026g0174 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.457+8891A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49098703 | |||||||
chr10:49098778 | C | T | 5 | a0001c0003t0004g0207 a0001c0003t0004g0208 a0001c0003t0004g0209 others(2): Show |
5 | HG01123.hp1 HG02109.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.457+8816G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49098778 | |||||||
chr10:49098889 | A | G | 1 | a0004c0011t0037g0259 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.457+8705T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49098889 | |||||||
chr10:49099072 | C | G | 30 | a0001c0001t0001g0003 a0001c0001t0001g0256 a0001c0001t0001g0257 others(27): Show |
34 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.457+8522G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49099072 | |||||||
chr10:49099202 | A | C | 14 | a0001c0001t0007g0185 a0001c0001t0007g0186 a0001c0001t0007g0187 others(11): Show |
14 | HG00099.hp1 HG01070.hp1 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.457+8392T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49099202 | |||||||
chr10:49099229 | G | A | 1 | a0002c0002t0001g0086 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.457+8365C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49099229 | |||||||
chr10:49099241 | C | T | 26 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(23): Show |
27 | HG00099.hp1 HG00639.hp2 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.457+8353G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49099241 | |||||||
chr10:49099257 | A | G | 43 | a0001c0001t0001g0037 a0001c0001t0001g0217 a0001c0001t0001g0226 others(40): Show |
48 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.457+8337T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49099257 | |||||||
chr10:49099264 | C | T | 1 | a0001c0001t0001g0016 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.457+8330G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49099264 | |||||||
chr10:49099314 | A | G | 4 | a0001c0001t0001g0217 a0001c0001t0002g0216 a0001c0001t0002g0239 others(1): Show |
4 | HG02615.hp1 HG02738.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.457+8280T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49099314 | |||||||
chr10:49099397 | G | A | 1 | a0001c0001t0027g0028 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.457+8197C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49099397 | |||||||
chr10:49099415 | T | C | 1 | a0001c0001t0002g0231 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.457+8179A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49099415 | |||||||
chr10:49099416 | C | T | 101 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0217 others(98): Show |
113 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.457+8178G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49099416 | |||||||
chr10:49099431 | A | G | 87 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0217 others(84): Show |
98 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.457+8163T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49099431 | |||||||
chr10:49099738 | A | G | 1 | a0001c0001t0023g0175 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.457+7856T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49099738 | |||||||
chr10:49099898 | C | T | 1 | a0002c0002t0002g0108 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.457+7696G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49099898 | |||||||
chr10:49099971 | A | G | 58 | a0001c0001t0001g0003 a0001c0001t0001g0256 a0001c0001t0001g0257 others(55): Show |
65 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.457+7623T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49099971 | |||||||
chr10:49100024 | A | G | 1 | a0001c0001t0016g0177 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.457+7570T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49100024 | |||||||
chr10:49100072 | AAGAGATA others(5): Show |
A | 19 | a0001c0001t0003g0203 a0001c0001t0010g0201 a0001c0003t0004g0168 others(16): Show |
19 | HG01109.hp1 HG01123.hp1 HG01981.hp1 others(16): Show |
intron_variant | MODIFIER | c.457+7510_457+7521d others(14): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49100072 | |||||||
chr10:49100142 | C | T | 101 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0217 others(98): Show |
113 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.457+7452G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49100142 | |||||||
chr10:49100446 | C | T | 58 | a0001c0001t0001g0003 a0001c0001t0001g0256 a0001c0001t0001g0257 others(55): Show |
65 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.457+7148G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49100446 | |||||||
chr10:49100475 | G | A | 43 | a0001c0001t0001g0037 a0001c0001t0001g0217 a0001c0001t0001g0226 others(40): Show |
48 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.457+7119C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49100475 | |||||||
chr10:49100569 | A | T | 13 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0051 others(10): Show |
15 | HG00423.hp2 NA18941.hp2 NA18947.hp1 others(12): Show |
intron_variant | MODIFIER | c.457+7025T>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49100569 | |||||||
chr10:49100578 | C | T | 1 | a0001c0001t0005g0006 | 2 | NA18966.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.457+7016G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49100578 | |||||||
chr10:49100796 | G | GAC | 101 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0217 others(98): Show |
113 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.457+6797_457+6798i others(4): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49100796 | |||||||
chr10:49100833 | T | C | 1 | a0001c0001t0003g0249 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.457+6761A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49100833 | |||||||
chr10:49100855 | T | C | 1 | a0001c0001t0002g0232 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.457+6739A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49100855 | |||||||
chr10:49101021 | A | G | 1 | a0001c0001t0014g0169 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.457+6573T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49101021 | |||||||
chr10:49101069 | A | G | 1 | a0002c0002t0001g0107 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.457+6525T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49101069 | |||||||
chr10:49101097 | T | C | 1 | a0001c0001t0034g0194 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.457+6497A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49101097 | |||||||
chr10:49101183 | C | A | 5 | a0001c0001t0001g0003 a0001c0001t0001g0256 a0001c0001t0001g0257 others(2): Show |
8 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(5): Show |
intron_variant | MODIFIER | c.457+6411G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49101183 | |||||||
chr10:49101285 | T | C | 101 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0217 others(98): Show |
113 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.457+6309A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49101285 | |||||||
chr10:49101339 | G | A | 1 | a0001c0001t0001g0016 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.457+6255C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49101339 | |||||||
chr10:49101653 | A | C | 4 | a0001c0001t0001g0003 a0001c0001t0001g0256 a0001c0001t0001g0257 others(1): Show |
7 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(4): Show |
intron_variant | MODIFIER | c.457+5941T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49101653 | |||||||
chr10:49101804 | A | G | 14 | a0001c0001t0007g0185 a0001c0001t0007g0186 a0001c0001t0007g0187 others(11): Show |
14 | HG00099.hp1 HG01070.hp1 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.457+5790T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49101804 | |||||||
chr10:49101824 | G | T | 1 | a0004c0011t0037g0259 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.457+5770C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49101824 | |||||||
chr10:49101860 | T | C | 43 | a0001c0001t0001g0037 a0001c0001t0001g0217 a0001c0001t0001g0226 others(40): Show |
48 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.457+5734A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49101860 | |||||||
chr10:49101930 | T | A | 19 | a0001c0001t0003g0203 a0001c0001t0010g0201 a0001c0003t0004g0168 others(16): Show |
19 | HG01109.hp1 HG01123.hp1 HG01981.hp1 others(16): Show |
intron_variant | MODIFIER | c.457+5664A>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49101930 | |||||||
chr10:49101968 | T | C | 1 | a0001c0001t0001g0016 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.457+5626A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49101968 | |||||||
chr10:49101972 | CGT | C | 102 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0037 others(99): Show |
114 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.457+5620_457+5621d others(4): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49101972 | |||||||
chr10:49101975 | G | C | 13 | a0001c0001t0003g0014 a0001c0001t0003g0244 a0001c0001t0003g0245 others(10): Show |
14 | HG01069.hp1 HG02258.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.457+5619C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49101975 | |||||||
chr10:49101983 | GTGTGTT | G | 28 | a0001c0001t0007g0185 a0001c0001t0007g0186 a0001c0001t0007g0187 others(25): Show |
28 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.457+5605_457+5610d others(8): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49101983 | |||||||
chr10:49101985 | GTGTT | G | 6 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(3): Show |
6 | HG01192.hp2 HG02717.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.457+5605_457+5608d others(6): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49101985 | |||||||
chr10:49101987 | GTT | G | 7 | a0001c0001t0003g0021 a0001c0004t0006g0019 a0001c0004t0006g0020 others(4): Show |
8 | HG00639.hp2 HG03041.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.457+5605_457+5606d others(4): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49101987 | |||||||
chr10:49102160 | GT | G | 187 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0025 others(184): Show |
202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.457+5433delA | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49102160 | |||||||
chr10:49102175 | AG | A | 57 | a0001c0001t0001g0003 a0001c0001t0001g0256 a0001c0001t0001g0257 others(54): Show |
64 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.457+5418delC | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49102175 | |||||||
chr10:49102178 | G | A | 1 | a0002c0002t0040g0149 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.457+5416C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49102178 | |||||||
chr10:49102182 | T | TCTCGCTC others(10): Show |
57 | a0001c0001t0001g0003 a0001c0001t0001g0256 a0001c0001t0001g0257 others(54): Show |
64 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.457+5411_457+5412i others(19): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49102182 | |||||||
chr10:49102206 | T | C | 158 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0024 others(155): Show |
172 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.457+5388A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49102206 | |||||||
chr10:49102359 | C | G | 1 | a0001c0001t0014g0169 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.457+5235G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49102359 | |||||||
chr10:49102385 | C | T | 1 | a0002c0002t0001g0106 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.457+5209G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49102385 | |||||||
chr10:49102386 | G | A | 1 | a0001c0001t0002g0233 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.457+5208C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49102386 | |||||||
chr10:49102727 | C | A | 12 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0052 others(9): Show |
14 | HG00423.hp2 NA18941.hp2 NA18947.hp1 others(11): Show |
intron_variant | MODIFIER | c.457+4867G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49102727 | |||||||
chr10:49102736 | C | T | 1 | a0001c0005t0008g0173 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.457+4858G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49102736 | |||||||
chr10:49102896 | G | A | 1 | a0002c0002t0006g0102 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.457+4698C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49102896 | |||||||
chr10:49102929 | C | G | 2 | a0002c0002t0002g0154 a0002c0002t0002g0155 |
2 | NA18984.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.457+4665G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49102929 | |||||||
chr10:49102996 | G | A | 5 | a0001c0001t0002g0215 a0001c0005t0001g0172 a0001c0005t0008g0170 others(2): Show |
5 | HG02572.hp1 HG02615.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.457+4598C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49102996 | |||||||
chr10:49103005 | A | T | 4 | a0001c0005t0001g0172 a0001c0005t0008g0170 a0001c0005t0008g0171 others(1): Show |
4 | HG02572.hp1 HG02615.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.457+4589T>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49103005 | |||||||
chr10:49103091 | T | G | 7 | a0001c0001t0003g0021 a0001c0004t0006g0019 a0001c0004t0006g0020 others(4): Show |
8 | HG00639.hp2 HG03041.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.457+4503A>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49103091 | |||||||
chr10:49103296 | A | G | 48 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0217 others(45): Show |
56 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.457+4298T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49103296 | |||||||
chr10:49103328 | G | A | 2 | a0002c0002t0001g0060 a0002c0002t0001g0061 |
2 | HG00642.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.457+4266C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49103328 | |||||||
chr10:49103856 | G | T | 1 | a0001c0001t0001g0016 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.457+3738C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49103856 | |||||||
chr10:49103895 | G | C | 1 | a0001c0001t0027g0028 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.457+3699C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49103895 | |||||||
chr10:49103963 | A | G | 1 | a0001c0001t0016g0177 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.457+3631T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49103963 | |||||||
chr10:49103974 | C | T | 1 | a0005c0009t0001g0041 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.457+3620G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49103974 | |||||||
chr10:49103983 | G | C | 14 | a0001c0001t0010g0015 a0001c0001t0010g0179 a0001c0001t0010g0182 others(11): Show |
14 | HG00642.hp1 HG01106.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.457+3611C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49103983 | |||||||
chr10:49104053 | C | T | 1 | a0001c0001t0020g0036 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.457+3541G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49104053 | |||||||
chr10:49104064 | C | G | 1 | a0001c0003t0004g0195 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.457+3530G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49104064 | |||||||
chr10:49104065 | G | A | 1 | a0001c0001t0023g0175 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.457+3529C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49104065 | |||||||
chr10:49104277 | A | T | 143 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0024 others(140): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.457+3317T>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49104277 | |||||||
chr10:49104304 | A | AAAC | 48 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0217 others(45): Show |
56 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.457+3287_457+3289d others(5): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49104304 | |||||||
chr10:49104327 | A | T | 1 | a0001c0001t0034g0194 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.457+3267T>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49104327 | |||||||
chr10:49104338 | A | G | 1 | a0002c0002t0001g0089 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.457+3256T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49104338 | |||||||
chr10:49104415 | C | T | 13 | a0001c0001t0003g0014 a0001c0001t0003g0244 a0001c0001t0003g0245 others(10): Show |
14 | HG01069.hp1 HG02258.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.457+3179G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49104415 | |||||||
chr10:49104416 | G | A | 1 | a0002c0002t0001g0087 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.457+3178C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49104416 | |||||||
chr10:49104464 | A | G | 1 | a0001c0001t0001g0016 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.457+3130T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49104464 | |||||||
chr10:49104466 | C | A | 1 | a0001c0001t0017g0240 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.457+3128G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49104466 | |||||||
chr10:49104522 | T | A | 48 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0217 others(45): Show |
56 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.457+3072A>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49104522 | |||||||
chr10:49104531 | G | A | 6 | a0001c0001t0002g0178 a0001c0001t0015g0013 a0001c0001t0015g0167 others(3): Show |
7 | HG01069.hp2 HG01071.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.457+3063C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49104531 | |||||||
chr10:49104685 | G | A | 19 | a0001c0001t0003g0203 a0001c0001t0010g0201 a0001c0003t0004g0168 others(16): Show |
19 | HG01109.hp1 HG01123.hp1 HG01981.hp1 others(16): Show |
intron_variant | MODIFIER | c.457+2909C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49104685 | |||||||
chr10:49104726 | G | A | 1 | a0001c0001t0003g0248 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.457+2868C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49104726 | |||||||
chr10:49104761 | A | T | 1 | a0001c0001t0002g0215 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.457+2833T>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49104761 | |||||||
chr10:49104792 | C | G | 1 | a0001c0001t0016g0176 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.457+2802G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49104792 | |||||||
chr10:49104804 | TAGAG | T | 52 | a0001c0001t0002g0178 a0001c0001t0003g0014 a0001c0001t0003g0203 others(49): Show |
56 | HG00423.hp2 HG01069.hp1 HG01069.hp2 others(53): Show |
intron_variant | MODIFIER | c.457+2786_457+2789d others(6): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49104804 | |||||||
chr10:49104830 | CAG | C | 8 | a0001c0001t0007g0185 a0001c0001t0007g0186 a0001c0001t0007g0187 others(5): Show |
8 | HG00099.hp1 HG01070.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.457+2762_457+2763d others(4): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49104830 | |||||||
chr10:49104859 | A | T | 1 | a0002c0002t0002g0154 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.457+2735T>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49104859 | |||||||
chr10:49104860 | C | T | 26 | a0001c0001t0003g0014 a0001c0001t0003g0244 a0001c0001t0003g0245 others(23): Show |
29 | HG00423.hp2 HG01069.hp1 HG02258.hp2 others(26): Show |
intron_variant | MODIFIER | c.457+2734G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49104860 | |||||||
chr10:49104886 | AAG | A | 99 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0217 others(96): Show |
111 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.457+2706_457+2707d others(4): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49104886 | |||||||
chr10:49104957 | AGAGACAG others(13): Show |
A | 1 | a0001c0001t0002g0238 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.457+2617_457+2636d others(22): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49104957 | |||||||
chr10:49104962 | CAG | C | 42 | a0001c0001t0001g0037 a0001c0001t0001g0217 a0001c0001t0001g0226 others(39): Show |
47 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.457+2630_457+2631d others(4): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49104962 | |||||||
chr10:49104966 | G | C | 1 | a0001c0003t0004g0168 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.457+2628C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49104966 | |||||||
chr10:49104998 | CAG | C | 5 | a0001c0001t0001g0003 a0001c0001t0001g0256 a0001c0001t0001g0257 others(2): Show |
8 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(5): Show |
intron_variant | MODIFIER | c.457+2594_457+2595d others(4): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49104998 | |||||||
chr10:49105010 | C | G | 25 | a0001c0001t0002g0178 a0001c0001t0003g0203 a0001c0001t0010g0201 others(22): Show |
26 | HG01069.hp2 HG01071.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.457+2584G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49105010 | |||||||
chr10:49105067 | G | A | 5 | a0001c0001t0001g0003 a0001c0001t0001g0256 a0001c0001t0001g0257 others(2): Show |
8 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(5): Show |
intron_variant | MODIFIER | c.457+2527C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49105067 | |||||||
chr10:49105159 | AAGAG | A | 6 | a0001c0001t0002g0178 a0001c0001t0015g0013 a0001c0001t0015g0167 others(3): Show |
7 | HG01069.hp2 HG01071.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.457+2431_457+2434d others(6): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49105159 | |||||||
chr10:49105213 | C | CAG | 75 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(72): Show |
77 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.457+2379_457+2380d others(4): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49105213 | |||||||
chr10:49105213 | C | CAGAG | 49 | a0001c0001t0001g0037 a0001c0001t0001g0217 a0001c0001t0001g0226 others(46): Show |
55 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.457+2377_457+2380d others(6): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49105213 | |||||||
chr10:49105213 | CAG | C | 14 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0052 others(11): Show |
16 | HG00423.hp2 HG02970.hp1 HG03540.hp1 others(13): Show |
intron_variant | MODIFIER | c.457+2379_457+2380d others(4): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49105213 | |||||||
chr10:49105260 | C | A | 100 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0217 others(97): Show |
112 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.457+2334G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49105260 | |||||||
chr10:49105292 | A | G | 1 | a0001c0001t0035g0165 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.457+2302T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49105292 | |||||||
chr10:49105329 | C | CAG | 18 | a0001c0001t0003g0213 a0001c0001t0007g0185 a0001c0001t0007g0186 others(15): Show |
18 | HG00099.hp1 HG00558.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.457+2264_457+2265i others(4): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49105329 | |||||||
chr10:49105329 | C | CAGA | 65 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(62): Show |
71 | HG00438.hp1 HG00597.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.457+2264_457+2265i others(5): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49105329 | |||||||
chr10:49105329 | C | CAGAG | 13 | a0001c0001t0003g0014 a0001c0001t0003g0244 a0001c0001t0003g0245 others(10): Show |
14 | HG01069.hp1 HG02258.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.457+2264_457+2265i others(6): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49105329 | |||||||
chr10:49105329 | C | CAGAGA | 44 | a0001c0001t0001g0003 a0001c0001t0001g0256 a0001c0001t0001g0257 others(41): Show |
50 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.457+2264_457+2265i others(7): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49105329 | |||||||
chr10:49105330 | G | A | 27 | a0001c0001t0003g0014 a0001c0001t0003g0244 a0001c0001t0003g0245 others(24): Show |
28 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.457+2264C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49105330 | |||||||
chr10:49105331 | G | A | 44 | a0001c0001t0001g0003 a0001c0001t0001g0256 a0001c0001t0001g0257 others(41): Show |
50 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.457+2263C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49105331 | |||||||
chr10:49105331 | G | T | 1 | a0001c0004t0006g0019 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.457+2263C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49105331 | |||||||
chr10:49105332 | G | A | 13 | a0001c0001t0003g0014 a0001c0001t0003g0244 a0001c0001t0003g0245 others(10): Show |
14 | HG01069.hp1 HG02258.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.457+2262C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49105332 | |||||||
chr10:49105392 | G | C | 5 | a0001c0001t0001g0003 a0001c0001t0001g0256 a0001c0001t0001g0257 others(2): Show |
8 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(5): Show |
intron_variant | MODIFIER | c.457+2202C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49105392 | |||||||
chr10:49105576 | G | A | 142 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0024 others(139): Show |
155 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.457+2018C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49105576 | |||||||
chr10:49105656 | T | C | 13 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0051 others(10): Show |
15 | HG00423.hp2 NA18941.hp2 NA18947.hp1 others(12): Show |
intron_variant | MODIFIER | c.457+1938A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49105656 | |||||||
chr10:49105699 | G | A | 43 | a0001c0001t0001g0037 a0001c0001t0001g0217 a0001c0001t0001g0226 others(40): Show |
48 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.457+1895C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49105699 | |||||||
chr10:49105807 | A | C | 7 | a0001c0001t0010g0015 a0001c0001t0010g0179 a0001c0001t0010g0182 others(4): Show |
7 | HG00642.hp1 HG01243.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.457+1787T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49105807 | |||||||
chr10:49105822 | A | G | 1 | a0001c0001t0021g0017 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.457+1772T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49105822 | |||||||
chr10:49105828 | CAT | C | 42 | a0001c0001t0001g0037 a0001c0001t0001g0217 a0001c0001t0001g0226 others(39): Show |
47 | HG00438.hp1 HG00558.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.457+1764_457+1765d others(4): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49105828 | |||||||
chr10:49105835 | G | A | 1 | a0004c0011t0037g0259 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.457+1759C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49105835 | |||||||
chr10:49105841 | G | GTA | 34 | a0001c0001t0003g0021 a0001c0001t0007g0188 a0001c0001t0007g0189 others(31): Show |
35 | HG00099.hp1 HG00639.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.457+1751_457+1752d others(4): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49105841 | |||||||
chr10:49105841 | G | GTATA | 5 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(2): Show |
5 | HG01192.hp2 HG02717.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.457+1749_457+1752d others(6): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49105841 | |||||||
chr10:49105841 | GTA | G | 17 | a0002c0002t0001g0060 a0002c0002t0001g0061 a0002c0002t0001g0090 others(14): Show |
17 | HG00323.hp1 HG00642.hp2 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.457+1751_457+1752d others(4): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49105841 | |||||||
chr10:49105843 | A | G | 1 | a0001c0001t0003g0035 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.457+1751T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49105843 | |||||||
chr10:49106133 | G | T | 1 | a0001c0001t0038g0243 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.457+1461C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49106133 | |||||||
chr10:49106582 | G | A | 1 | a0004c0011t0037g0259 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.457+1012C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49106582 | |||||||
chr10:49106696 | A | G | 27 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(24): Show |
28 | HG00099.hp1 HG00639.hp2 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.457+898T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49106696 | |||||||
chr10:49106742 | C | G | 13 | a0001c0001t0003g0014 a0001c0001t0003g0244 a0001c0001t0003g0245 others(10): Show |
14 | HG01069.hp1 HG02258.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.457+852G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49106742 | |||||||
chr10:49106976 | C | G | 1 | a0002c0002t0001g0089 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.457+618G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49106976 | |||||||
chr10:49107035 | C | G | 95 | a0001c0001t0001g0037 a0001c0001t0001g0217 a0001c0001t0001g0226 others(92): Show |
104 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.457+559G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49107035 | |||||||
chr10:49107050 | T | C | 28 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(25): Show |
29 | HG00099.hp1 HG00639.hp2 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.457+544A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49107050 | |||||||
chr10:49107189 | G | A | 1 | a0001c0003t0004g0206 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.457+405C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49107189 | |||||||
chr10:49107301 | G | A | 27 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(24): Show |
28 | HG00099.hp1 HG00639.hp2 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.457+293C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49107301 | |||||||
chr10:49107323 | G | A | 1 | a0004c0011t0037g0259 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.457+271C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49107323 | |||||||
chr10:49107358 | G | A | 2 | a0001c0001t0001g0016 a0001c0001t0021g0017 |
2 | HG02145.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.457+236C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49107358 | |||||||
chr10:49107390 | G | A | 1 | a0001c0001t0027g0028 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.457+204C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49107390 | |||||||
chr10:49107487 | T | C | 1 | a0002c0002t0001g0150 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.457+107A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49107487 | |||||||
chr10:49107541 | G | T | 1 | a0002c0002t0001g0062 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.457+53C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49107541 | |||||||
chr10:49108182 | C | T | 1 | a0001c0003t0004g0168 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.56-187G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49108182 | |||||||
chr10:49108471 | G | C | 1 | a0001c0001t0002g0235 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.56-476C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49108471 | |||||||
chr10:49108538 | C | G | 2 | a0002c0002t0014g0008 a0002c0002t0014g0073 |
3 | HG02622.hp1 HG03516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.56-543G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49108538 | |||||||
chr10:49108541 | C | T | 1 | a0001c0001t0035g0165 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.56-546G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49108541 | |||||||
chr10:49108573 | A | T | 1 | a0001c0001t0035g0165 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.56-578T>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49108573 | |||||||
chr10:49108636 | G | A | 2 | a0001c0001t0018g0236 a0001c0001t0018g0237 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.56-641C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49108636 | |||||||
chr10:49108948 | C | T | 4 | a0002c0002t0001g0076 a0002c0002t0012g0009 a0002c0002t0012g0074 others(1): Show |
5 | HG02486.hp2 HG02622.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.56-953G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49108948 | |||||||
chr10:49109106 | C | T | 10 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0051 others(7): Show |
12 | NA18941.hp2 NA18947.hp1 NA18948.hp1 others(9): Show |
intron_variant | MODIFIER | c.56-1111G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49109106 | |||||||
chr10:49109269 | G | A | 1 | a0002c0002t0001g0047 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.56-1274C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49109269 | |||||||
chr10:49109348 | G | A | 1 | a0004c0011t0037g0259 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.56-1353C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49109348 | |||||||
chr10:49109356 | G | A | 1 | a0002c0002t0013g0151 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.56-1361C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49109356 | |||||||
chr10:49109364 | G | C | 1 | a0001c0001t0002g0238 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.56-1369C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49109364 | |||||||
chr10:49109474 | A | ATG | 115 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0217 others(112): Show |
125 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.56-1481_56-1480dup others(2): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49109474 | |||||||
chr10:49109488 | A | AT | 78 | a0001c0001t0001g0037 a0001c0001t0001g0217 a0001c0001t0001g0226 others(75): Show |
84 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.56-1494dupA | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49109488 | |||||||
chr10:49109601 | A | T | 1 | a0001c0001t0001g0256 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.56-1606T>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49109601 | |||||||
chr10:49109604 | T | C | 146 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0024 others(143): Show |
159 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.56-1609A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49109604 | |||||||
chr10:49109606 | A | G | 115 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0217 others(112): Show |
125 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.56-1611T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49109606 | |||||||
chr10:49109618 | C | G | 4 | a0001c0005t0001g0172 a0001c0005t0008g0170 a0001c0005t0008g0171 others(1): Show |
4 | HG02572.hp1 HG02615.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.56-1623G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49109618 | |||||||
chr10:49109695 | G | T | 1 | a0001c0001t0017g0240 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.56-1700C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49109695 | |||||||
chr10:49109733 | C | T | 146 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0024 others(143): Show |
159 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.56-1738G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49109733 | |||||||
chr10:49109793 | C | G | 1 | a0001c0001t0005g0064 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.56-1798G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49109793 | |||||||
chr10:49109795 | C | T | 1 | a0001c0001t0003g0035 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.56-1800G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49109795 | |||||||
chr10:49109980 | C | T | 1 | a0001c0001t0035g0165 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.56-1985G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49109980 | |||||||
chr10:49110046 | G | C | 13 | a0002c0002t0001g0158 a0002c0002t0002g0153 a0002c0002t0002g0154 others(10): Show |
13 | HG00558.hp1 HG03704.hp1 HG04199.hp1 others(10): Show |
intron_variant | MODIFIER | c.56-2051C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49110046 | |||||||
chr10:49110064 | C | G | 161 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0024 others(158): Show |
175 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.56-2069G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49110064 | |||||||
chr10:49110096 | C | T | 110 | a0001c0001t0001g0037 a0001c0001t0001g0217 a0001c0001t0001g0226 others(107): Show |
117 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.56-2101G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49110096 | |||||||
chr10:49110401 | T | C | 1 | a0001c0001t0002g0239 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.56-2406A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49110401 | |||||||
chr10:49110439 | G | A | 115 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0217 others(112): Show |
125 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.56-2444C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49110439 | |||||||
chr10:49110455 | AT | A | 4 | a0001c0001t0003g0252 a0001c0001t0003g0254 a0001c0001t0017g0251 others(1): Show |
4 | HG02258.hp2 HG02647.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.56-2461delA | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49110455 | |||||||
chr10:49110479 | A | G | 2 | a0002c0002t0014g0008 a0002c0002t0014g0073 |
3 | HG02622.hp1 HG03516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.56-2484T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49110479 | |||||||
chr10:49110567 | G | A | 5 | a0001c0003t0004g0207 a0001c0003t0004g0208 a0001c0003t0004g0209 others(2): Show |
5 | HG01123.hp1 HG02109.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.56-2572C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49110567 | |||||||
chr10:49110673 | G | T | 7 | a0001c0001t0010g0179 a0001c0001t0010g0182 a0001c0001t0010g0184 others(4): Show |
7 | HG00642.hp1 HG01243.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.56-2678C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49110673 | |||||||
chr10:49111278 | C | T | 9 | a0001c0001t0005g0064 a0001c0001t0005g0065 a0001c0001t0005g0066 others(6): Show |
9 | HG00423.hp2 HG01346.hp2 HG01993.hp2 others(6): Show |
intron_variant | MODIFIER | c.56-3283G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49111278 | |||||||
chr10:49111342 | G | A | 145 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0024 others(142): Show |
158 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.56-3347C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49111342 | |||||||
chr10:49111583 | G | A | 50 | a0001c0001t0001g0037 a0001c0001t0001g0217 a0001c0001t0001g0226 others(47): Show |
55 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.56-3588C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49111583 | |||||||
chr10:49111654 | C | A | 3 | a0001c0001t0001g0016 a0001c0001t0010g0015 a0001c0001t0021g0017 |
3 | HG02145.hp2 HG02257.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.56-3659G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49111654 | |||||||
chr10:49111740 | C | A | 4 | a0001c0001t0001g0003 a0001c0001t0001g0256 a0001c0001t0001g0257 others(1): Show |
7 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(4): Show |
intron_variant | MODIFIER | c.55+3691G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49111740 | |||||||
chr10:49111831 | C | T | 4 | a0001c0001t0001g0003 a0001c0001t0001g0256 a0001c0001t0001g0257 others(1): Show |
7 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(4): Show |
intron_variant | MODIFIER | c.55+3600G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49111831 | |||||||
chr10:49111883 | C | T | 18 | a0001c0001t0003g0203 a0001c0001t0010g0201 a0001c0001t0034g0194 others(15): Show |
18 | HG01109.hp1 HG01123.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.55+3548G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49111883 | |||||||
chr10:49111919 | GTGAGCT | G | 6 | a0001c0001t0008g0029 a0001c0001t0008g0030 a0001c0001t0008g0031 others(3): Show |
6 | HG01884.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.55+3506_55+3511del others(6): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49111919 | |||||||
chr10:49111920 | T | G | 6 | a0001c0001t0002g0178 a0001c0001t0015g0013 a0001c0001t0015g0167 others(3): Show |
7 | HG01069.hp2 HG01071.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.55+3511A>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49111920 | |||||||
chr10:49111995 | G | A | 13 | a0001c0001t0003g0014 a0001c0001t0003g0244 a0001c0001t0003g0245 others(10): Show |
14 | HG01069.hp1 HG02258.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.55+3436C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49111995 | |||||||
chr10:49112096 | C | G | 1 | a0002c0002t0001g0063 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.55+3335G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49112096 | |||||||
chr10:49112210 | A | C | 1 | a0001c0001t0034g0194 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.55+3221T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49112210 | |||||||
chr10:49112236 | C | T | 17 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(14): Show |
18 | HG00639.hp2 HG01192.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.55+3195G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49112236 | |||||||
chr10:49112466 | T | C | 73 | a0001c0001t0001g0037 a0001c0001t0001g0217 a0001c0001t0001g0226 others(70): Show |
78 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.55+2965A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49112466 | |||||||
chr10:49112678 | T | G | 146 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0024 others(143): Show |
159 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.55+2753A>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49112678 | |||||||
chr10:49112842 | T | C | 17 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(14): Show |
18 | HG00639.hp2 HG01192.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.55+2589A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49112842 | |||||||
chr10:49112990 | C | G | 1 | a0001c0001t0035g0165 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.55+2441G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49112990 | |||||||
chr10:49113422 | G | A | 8 | a0001c0001t0007g0185 a0001c0001t0007g0186 a0001c0001t0007g0187 others(5): Show |
8 | HG00099.hp1 HG01070.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.55+2009C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49113422 | |||||||
chr10:49113602 | C | T | 1 | a0002c0002t0001g0062 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.55+1829G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49113602 | |||||||
chr10:49113629 | C | T | 1 | a0001c0001t0003g0213 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.55+1802G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49113629 | |||||||
chr10:49113787 | A | G | 47 | a0001c0001t0001g0037 a0001c0001t0001g0217 a0001c0001t0001g0226 others(44): Show |
52 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.55+1644T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49113787 | |||||||
chr10:49113873 | C | T | 146 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0024 others(143): Show |
159 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.55+1558G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49113873 | |||||||
chr10:49113949 | G | A | 71 | a0001c0001t0001g0037 a0001c0001t0001g0217 a0001c0001t0001g0226 others(68): Show |
76 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.55+1482C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49113949 | |||||||
chr10:49114072 | T | C | 1 | a0001c0001t0023g0175 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.55+1359A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49114072 | |||||||
chr10:49114143 | A | G | 1 | a0001c0001t0023g0175 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.55+1288T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49114143 | |||||||
chr10:49114207 | A | C | 1 | a0004c0011t0037g0259 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.55+1224T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49114207 | |||||||
chr10:49114238 | A | G | 146 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0024 others(143): Show |
159 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.55+1193T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49114238 | |||||||
chr10:49114274 | T | C | 3 | a0001c0001t0019g0048 a0001c0001t0019g0050 a0001c0001t0020g0049 |
3 | HG02056.hp2 NA19002.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.55+1157A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49114274 | |||||||
chr10:49114398 | A | G | 1 | a0001c0001t0002g0212 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.55+1033T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49114398 | |||||||
chr10:49114413 | G | T | 31 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(28): Show |
34 | HG00639.hp2 HG01192.hp2 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.55+1018C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49114413 | |||||||
chr10:49114434 | A | T | 146 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0024 others(143): Show |
159 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.55+997T>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49114434 | |||||||
chr10:49114435 | A | C | 146 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0024 others(143): Show |
159 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.55+996T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49114435 | |||||||
chr10:49114482 | G | A | 1 | a0002c0002t0003g0164 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.55+949C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49114482 | |||||||
chr10:49114503 | G | A | 18 | a0001c0001t0003g0203 a0001c0001t0010g0201 a0001c0001t0034g0194 others(15): Show |
18 | HG01109.hp1 HG01123.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.55+928C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49114503 | |||||||
chr10:49114512 | T | A | 115 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0217 others(112): Show |
125 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.55+919A>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49114512 | |||||||
chr10:49114585 | G | GT | 16 | a0001c0001t0001g0016 a0001c0001t0005g0006 a0001c0001t0005g0007 others(13): Show |
18 | HG00642.hp2 HG00741.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.55+845dupA | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49114585 | |||||||
chr10:49114585 | G | GTT | 37 | a0001c0001t0002g0178 a0001c0001t0003g0203 a0001c0001t0007g0185 others(34): Show |
37 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.55+844_55+845dupAA | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49114585 | |||||||
chr10:49114585 | G | GTTT | 15 | a0001c0001t0001g0003 a0001c0001t0001g0256 a0001c0001t0001g0257 others(12): Show |
19 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(16): Show |
intron_variant | MODIFIER | c.55+843_55+845dupAA others(1): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49114585 | |||||||
chr10:49114585 | G | GTTTTT | 11 | a0001c0001t0003g0014 a0001c0001t0003g0244 a0001c0001t0003g0245 others(8): Show |
12 | HG01069.hp1 HG02258.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.55+841_55+845dupAA others(3): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49114585 | |||||||
chr10:49114585 | GTT | G | 6 | a0001c0001t0003g0021 a0001c0004t0006g0019 a0001c0004t0006g0020 others(3): Show |
7 | HG00639.hp2 HG03041.hp2 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.55+844_55+845delAA | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49114585 | |||||||
chr10:49114587 | T | TTTG | 50 | a0001c0001t0001g0037 a0001c0001t0001g0217 a0001c0001t0001g0226 others(47): Show |
55 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.55+843_55+844insCA others(1): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49114587 | |||||||
chr10:49114639 | G | A | 13 | a0001c0001t0003g0014 a0001c0001t0003g0244 a0001c0001t0003g0245 others(10): Show |
14 | HG01069.hp1 HG02258.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.55+792C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49114639 | |||||||
chr10:49114657 | G | A | 115 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0217 others(112): Show |
125 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.55+774C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49114657 | |||||||
chr10:49114730 | C | T | 16 | a0001c0001t0001g0037 a0001c0001t0002g0038 a0001c0001t0002g0040 others(13): Show |
16 | HG00597.hp1 HG00621.hp2 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.55+701G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49114730 | |||||||
chr10:49114734 | C | CCCTGCTG others(11): Show |
6 | a0001c0001t0003g0021 a0001c0004t0006g0019 a0001c0004t0006g0020 others(3): Show |
7 | HG00639.hp2 HG03041.hp2 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.55+679_55+696dupCT others(16): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49114734 | |||||||
chr10:49114888 | C | T | 6 | a0001c0001t0003g0021 a0001c0004t0006g0019 a0001c0004t0006g0020 others(3): Show |
7 | HG00639.hp2 HG03041.hp2 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.55+543G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49114888 | |||||||
chr10:49115007 | G | A | 1 | a0002c0002t0001g0255 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.55+424C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49115007 | |||||||
chr10:49115167 | C | G | 17 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(14): Show |
18 | HG00639.hp2 HG01192.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.55+264G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49115167 | |||||||
chr10:49115266 | A | G | 1 | a0001c0001t0002g0018 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.55+165T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49115266 | |||||||
chr10:49115303 | G | A | 4 | a0001c0001t0001g0003 a0001c0001t0001g0256 a0001c0001t0001g0257 others(1): Show |
7 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(4): Show |
intron_variant | MODIFIER | c.55+128C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49115303 | |||||||
chr10:49115393 | C | G | 3 | a0001c0001t0001g0016 a0001c0001t0010g0015 a0001c0001t0021g0017 |
3 | HG02145.hp2 HG02257.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+38G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49115393 |