Item | Value |
---|---|
geneid | 23151 |
ensemblid | ENSG00000075240.17 |
hgncid | 29113 |
symbol | GRAMD4 |
name | GRAM domain containing 4 |
refseq_nuc | NM_015124.5 |
refseq_prot | NP_055939.1 |
ensembl_nuc | ENST00000406902.6 |
ensembl_prot | ENSP00000385689.1 |
mane_status | MANE Select |
chr | chr22 |
start | 46620386 |
end | 46679785 |
strand | + |
ver | v1.2 |
region | chr22:46620386-46679785 |
region5000 | chr22:46615386-46684785 |
regionname0 | GRAMD4_chr22_46620386_46679785 |
regionname5000 | GRAMD4_chr22_46615386_46684785 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 578 | 326 | 82 | 70 | 120 | 14 | 38 | 84 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | MLRRL others(573): Show |
chr22 | 46615386 | 46684785 |
a0002 | 0/0 | 578 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | MLRRL others(573): Show |
chr22 | 46615386 | 46684785 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1734 | 297 | 69 | 63 | 116 | 14 | 34 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | ATGCT others(1729): Show |
chr22 | 46615386 | 46684785 | ||
a0001c0002 | 0/0 | 1734 | 20 | 9 | 6 | 2 | 0 | 3 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | ATGCT others(1729): Show |
chr22 | 46615386 | 46684785 | ||
a0001c0003 | 0/0 | 1734 | 2 | 2 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | ATGCT others(1729): Show |
chr22 | 46615386 | 46684785 | ||
a0001c0004 | 1/0 | 1734 | 2 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | ATGCT others(1729): Show |
chr22 | 46615386 | 46684785 | ||
a0001c0005 | 0/0 | 1734 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | ATGCT others(1729): Show |
chr22 | 46615386 | 46684785 | ||
a0001c0006 | 0/0 | 1734 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | ATGCT others(1729): Show |
chr22 | 46615386 | 46684785 | ||
a0001c0007 | 0/0 | 1734 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | ATGCT others(1729): Show |
chr22 | 46615386 | 46684785 | ||
a0001c0008 | 0/0 | 1734 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | ATGCT others(1729): Show |
chr22 | 46615386 | 46684785 | ||
a0001c0009 | 0/0 | 1734 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | ATGCT others(1729): Show |
chr22 | 46615386 | 46684785 | ||
a0002c0010 | 0/0 | 1734 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | ATGCT others(1729): Show |
chr22 | 46615386 | 46684785 | ||
a0002c0011 | 0/0 | 1734 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | ATGCT others(1729): Show |
chr22 | 46615386 | 46684785 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4500 | 77 | 0 | 14 | 55 | 0 | 8 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4495): Show |
chr22 | 46615386 | 46684785 |
a0001c0001t0002 | 0/0 | 4500 | 50 | 1 | 16 | 25 | 6 | 2 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4495): Show |
chr22 | 46615386 | 46684785 |
a0001c0001t0003 | 0/1 | 4500 | 41 | 11 | 12 | 4 | 5 | 8 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4495): Show |
chr22 | 46615386 | 46684785 |
a0001c0001t0004 | 0/0 | 4500 | 7 | 6 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4495): Show |
chr22 | 46615386 | 46684785 |
a0001c0001t0005 | 0/0 | 4500 | 16 | 6 | 2 | 0 | 1 | 7 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4495): Show |
chr22 | 46615386 | 46684785 |
a0001c0001t0006 | 0/0 | 4500 | 14 | 0 | 0 | 14 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4495): Show |
chr22 | 46615386 | 46684785 |
a0001c0001t0007 | 0/0 | 4499 | 9 | 7 | 2 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4494): Show |
chr22 | 46615386 | 46684785 |
a0001c0001t0008 | 0/0 | 4501 | 9 | 9 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4496): Show |
chr22 | 46615386 | 46684785 |
a0001c0001t0009 | 0/0 | 4500 | 6 | 1 | 3 | 0 | 0 | 2 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4495): Show |
chr22 | 46615386 | 46684785 |
a0001c0001t0010 | 0/0 | 4500 | 4 | 4 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4495): Show |
chr22 | 46615386 | 46684785 |
a0001c0001t0011 | 0/0 | 4501 | 3 | 3 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4496): Show |
chr22 | 46615386 | 46684785 |
a0001c0001t0012 | 0/0 | 4499 | 3 | 0 | 0 | 2 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4494): Show |
chr22 | 46615386 | 46684785 |
a0001c0001t0013 | 0/0 | 4499 | 2 | 1 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4494): Show |
chr22 | 46615386 | 46684785 |
a0001c0001t0014 | 0/0 | 4500 | 2 | 1 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4495): Show |
chr22 | 46615386 | 46684785 |
a0001c0001t0015 | 0/0 | 4500 | 2 | 2 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4495): Show |
chr22 | 46615386 | 46684785 |
a0001c0001t0016 | 0/0 | 4500 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4495): Show |
chr22 | 46615386 | 46684785 |
a0001c0001t0017 | 0/0 | 4500 | 2 | 1 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4495): Show |
chr22 | 46615386 | 46684785 |
a0001c0001t0018 | 0/0 | 4499 | 2 | 1 | 0 | 0 | 1 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4494): Show |
chr22 | 46615386 | 46684785 |
a0001c0001t0019 | 0/0 | 4499 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4494): Show |
chr22 | 46615386 | 46684785 |
a0001c0001t0020 | 0/0 | 4500 | 2 | 1 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4495): Show |
chr22 | 46615386 | 46684785 |
a0001c0001t0021 | 0/0 | 4500 | 2 | 0 | 0 | 2 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4495): Show |
chr22 | 46615386 | 46684785 |
a0001c0001t0022 | 0/0 | 4500 | 2 | 0 | 0 | 2 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4495): Show |
chr22 | 46615386 | 46684785 |
a0001c0001t0023 | 0/0 | 4500 | 2 | 0 | 2 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4495): Show |
chr22 | 46615386 | 46684785 |
a0001c0001t0024 | 0/0 | 4500 | 2 | 0 | 2 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4495): Show |
chr22 | 46615386 | 46684785 |
a0001c0001t0025 | 0/0 | 4500 | 2 | 1 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4495): Show |
chr22 | 46615386 | 46684785 |
a0001c0001t0026 | 0/0 | 4500 | 2 | 0 | 0 | 2 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4495): Show |
chr22 | 46615386 | 46684785 |
a0001c0001t0027 | 0/0 | 4500 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4495): Show |
chr22 | 46615386 | 46684785 |
a0001c0001t0028 | 0/0 | 4500 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4495): Show |
chr22 | 46615386 | 46684785 |
a0001c0001t0029 | 0/0 | 4500 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4495): Show |
chr22 | 46615386 | 46684785 |
a0001c0001t0030 | 0/0 | 4501 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4496): Show |
chr22 | 46615386 | 46684785 |
a0001c0001t0031 | 0/0 | 4500 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4495): Show |
chr22 | 46615386 | 46684785 |
a0001c0001t0032 | 0/0 | 4500 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4495): Show |
chr22 | 46615386 | 46684785 |
a0001c0001t0033 | 0/0 | 4499 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4494): Show |
chr22 | 46615386 | 46684785 |
a0001c0001t0034 | 0/0 | 4499 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4494): Show |
chr22 | 46615386 | 46684785 |
a0001c0001t0035 | 0/0 | 4499 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4494): Show |
chr22 | 46615386 | 46684785 |
a0001c0001t0036 | 0/0 | 4499 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4494): Show |
chr22 | 46615386 | 46684785 |
a0001c0001t0037 | 0/0 | 4500 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4495): Show |
chr22 | 46615386 | 46684785 |
a0001c0001t0038 | 0/0 | 4500 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4495): Show |
chr22 | 46615386 | 46684785 |
a0001c0001t0039 | 0/0 | 4500 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4495): Show |
chr22 | 46615386 | 46684785 |
a0001c0001t0040 | 0/0 | 4500 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4495): Show |
chr22 | 46615386 | 46684785 |
a0001c0001t0041 | 0/0 | 4501 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4496): Show |
chr22 | 46615386 | 46684785 |
a0001c0001t0043 | 0/0 | 4500 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4495): Show |
chr22 | 46615386 | 46684785 |
a0001c0001t0044 | 0/0 | 4500 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4495): Show |
chr22 | 46615386 | 46684785 |
a0001c0001t0045 | 0/0 | 4500 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4495): Show |
chr22 | 46615386 | 46684785 |
a0001c0001t0048 | 0/0 | 4500 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4495): Show |
chr22 | 46615386 | 46684785 |
a0001c0001t0049 | 0/0 | 4500 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4495): Show |
chr22 | 46615386 | 46684785 |
a0001c0001t0050 | 0/0 | 4500 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4495): Show |
chr22 | 46615386 | 46684785 |
a0001c0001t0051 | 0/0 | 4500 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4495): Show |
chr22 | 46615386 | 46684785 |
a0001c0001t0052 | 0/0 | 4500 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4495): Show |
chr22 | 46615386 | 46684785 |
a0001c0001t0054 | 0/0 | 4500 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4495): Show |
chr22 | 46615386 | 46684785 |
a0001c0001t0056 | 0/0 | 4500 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4495): Show |
chr22 | 46615386 | 46684785 |
a0001c0001t0057 | 0/0 | 4500 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4495): Show |
chr22 | 46615386 | 46684785 |
a0001c0001t0058 | 0/0 | 4500 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4495): Show |
chr22 | 46615386 | 46684785 |
a0001c0001t0059 | 0/0 | 4500 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4495): Show |
chr22 | 46615386 | 46684785 |
a0001c0001t0060 | 0/0 | 4500 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4495): Show |
chr22 | 46615386 | 46684785 |
a0001c0001t0061 | 0/0 | 4500 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4495): Show |
chr22 | 46615386 | 46684785 |
a0001c0001t0063 | 0/0 | 4500 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4495): Show |
chr22 | 46615386 | 46684785 |
a0001c0001t0064 | 0/0 | 4500 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4495): Show |
chr22 | 46615386 | 46684785 |
a0001c0002t0002 | 0/0 | 4500 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4495): Show |
chr22 | 46615386 | 46684785 |
a0001c0002t0004 | 0/0 | 4500 | 18 | 9 | 5 | 2 | 0 | 2 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4495): Show |
chr22 | 46615386 | 46684785 |
a0001c0002t0046 | 0/0 | 4500 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4495): Show |
chr22 | 46615386 | 46684785 |
a0001c0003t0003 | 0/0 | 4500 | 2 | 2 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4495): Show |
chr22 | 46615386 | 46684785 |
a0001c0004t0001 | 0/0 | 4500 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4495): Show |
chr22 | 46615386 | 46684785 |
a0001c0004t0016 | 1/0 | 4500 | 1 | 0 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4495): Show |
chr22 | 46615386 | 46684785 |
a0001c0005t0002 | 0/0 | 4500 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4495): Show |
chr22 | 46615386 | 46684785 |
a0001c0006t0042 | 0/0 | 4500 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4495): Show |
chr22 | 46615386 | 46684785 |
a0001c0007t0019 | 0/0 | 4499 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4494): Show |
chr22 | 46615386 | 46684785 |
a0001c0008t0055 | 0/0 | 4501 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4496): Show |
chr22 | 46615386 | 46684785 |
a0001c0009t0062 | 0/0 | 4500 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4495): Show |
chr22 | 46615386 | 46684785 |
a0002c0010t0047 | 0/0 | 4500 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4495): Show |
chr22 | 46615386 | 46684785 |
a0002c0011t0053 | 0/0 | 4500 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | GCACA others(4495): Show |
chr22 | 46615386 | 46684785 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0002g0007 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0002g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0002g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0002g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0002g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0002g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0003g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0003g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0003g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0003g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0003g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0003g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0003g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0003g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0003g0223 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0003g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0003g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0003g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0003g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0003g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0003g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0004g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0004g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0004g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0005g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0005g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0005g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0005g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0005g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0005g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0005g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0005g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0005g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0005g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0005g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0005g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0005g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0005g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0005g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0006g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0006g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0006g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0006g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0006g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0006g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0006g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0006g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0006g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0006g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0006g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0006g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0006g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0006g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0007g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0007g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0007g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0007g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0007g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0007g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0007g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0007g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0007g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0008g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0008g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0008g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0008g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0008g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0008g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0008g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0008g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0008g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0009g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0009g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0009g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0009g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0009g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0009g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0010g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0010g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0010g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0010g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0011g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0011g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0011g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0012g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0012g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0012g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0013g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0013g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0014g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0014g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0015g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0015g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0016g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0017g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0017g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0018g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0018g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0019g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0020g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0020g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0021g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0021g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0022g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0022g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0023g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0023g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0024g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0025g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0025g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0026g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0026g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0027g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0028g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0029g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0030g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0031g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0032g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0033g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0034g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0035g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0036g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0037g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0038g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0039g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0040g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0041g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0043g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0044g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0045g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0048g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0049g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0050g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0051g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0052g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0054g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0056g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0057g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0058g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0059g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0060g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0061g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0063g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0001t0064g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0002t0004g0002 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0002t0004g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0002t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0002t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0002t0004g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0002t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0002t0004g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0002t0004g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0002t0004g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0002t0004g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0002t0004g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0002t0004g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0002t0004g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0002t0004g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0002t0004g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0002t0004g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0002t0004g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0002t0046g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0003t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0003t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0004t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0004t0016g0051 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0005t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0006t0042g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0007t0019g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0008t0055g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0001c0009t0062g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0002c0010t0047g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
a0002c0011t0053g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0297 | EUR | GBR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG00099 | hp2 | a0001 | c0001 | t0003 | g0208 | EUR | GBR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG00140 | hp1 | a0001 | c0001 | t0003 | g0248 | EUR | GBR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0269 | EUR | GBR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0319 | EUR | FIN | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG00323 | hp2 | a0001 | c0001 | t0005 | g0145 | EUR | FIN | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | CHS | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | CHS | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG00438 | hp2 | a0001 | c0001 | t0006 | g0192 | EAS | CHS | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG00597 | hp1 | a0001 | c0006 | t0042 | g0318 | EAS | CHS | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | CHS | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | CHS | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0281 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0312 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG00642 | hp2 | a0001 | c0001 | t0007 | g0027 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG00673 | hp2 | a0001 | c0001 | t0021 | g0156 | EAS | CHS | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG00733 | hp1 | a0001 | c0001 | t0003 | g0245 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG00733 | hp2 | a0001 | c0001 | t0025 | g0265 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0266 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG00735 | hp2 | a0001 | c0001 | t0056 | g0313 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0315 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG00738 | hp2 | a0001 | c0001 | t0005 | g0258 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG00741 | hp1 | a0001 | c0001 | t0003 | g0206 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG00741 | hp2 | a0001 | c0001 | t0064 | g0306 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG01069 | hp1 | a0001 | c0001 | t0024 | g0004 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0305 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG01070 | hp1 | a0001 | c0001 | t0003 | g0104 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG01070 | hp2 | a0001 | c0001 | t0013 | g0020 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG01071 | hp1 | a0001 | c0001 | t0003 | g0169 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG01071 | hp2 | a0001 | c0001 | t0024 | g0004 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG01081 | hp2 | a0001 | c0001 | t0003 | g0214 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG01106 | hp1 | a0001 | c0001 | t0009 | g0047 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG01106 | hp2 | a0001 | c0009 | t0062 | g0303 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG01109 | hp1 | a0001 | c0002 | t0004 | g0095 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0307 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG01168 | hp1 | a0001 | c0001 | t0009 | g0050 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG01168 | hp2 | a0001 | c0001 | t0005 | g0142 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0259 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG01175 | hp2 | a0001 | c0001 | t0003 | g0225 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0209 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG01243 | hp1 | a0001 | c0001 | t0007 | g0033 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG01243 | hp2 | a0001 | c0001 | t0003 | g0085 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0310 | AMR | CLM | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0226 | AMR | CLM | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | CLM | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG01257 | hp2 | a0001 | c0001 | t0003 | g0212 | AMR | CLM | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0314 | AMR | CLM | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG01261 | hp2 | a0001 | c0001 | t0003 | g0240 | AMR | CLM | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG01361 | hp1 | a0001 | c0001 | t0063 | g0227 | AMR | CLM | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG01361 | hp2 | a0001 | c0002 | t0046 | g0089 | AMR | CLM | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG01433 | hp1 | a0001 | c0001 | t0048 | g0191 | AMR | CLM | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG01433 | hp2 | a0001 | c0001 | t0003 | g0205 | AMR | CLM | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG01496 | hp1 | a0001 | c0001 | t0014 | g0058 | AMR | CLM | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG01496 | hp2 | a0001 | c0002 | t0004 | g0002 | AMR | CLM | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG01515 | hp1 | a0001 | c0001 | t0018 | g0247 | EUR | IBS | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0279 | EUR | IBS | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG01516 | hp1 | a0001 | c0001 | t0003 | g0283 | EUR | IBS | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0241 | EUR | IBS | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0007 | EUR | IBS | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0224 | EUR | IBS | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG01884 | hp1 | a0001 | c0001 | t0004 | g0061 | AFR | ACB | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG01884 | hp2 | a0001 | c0001 | t0010 | g0185 | AFR | ACB | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG01891 | hp1 | a0001 | c0001 | t0003 | g0243 | AFR | ACB | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG01891 | hp2 | a0001 | c0002 | t0004 | g0092 | AFR | ACB | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG01934 | hp2 | a0001 | c0002 | t0004 | g0117 | AMR | PEL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0172 | AMR | PEL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG01943 | hp2 | a0001 | c0001 | t0020 | g0231 | AMR | PEL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG01952 | hp1 | a0001 | c0001 | t0023 | g0122 | AMR | PEL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG01952 | hp2 | a0001 | c0001 | t0017 | g0045 | AMR | PEL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG01975 | hp1 | a0001 | c0002 | t0004 | g0118 | AMR | PEL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0296 | AMR | PEL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG01978 | hp1 | a0001 | c0001 | t0009 | g0056 | AMR | PEL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0308 | AMR | PEL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG01981 | hp2 | a0001 | c0001 | t0043 | g0311 | AMR | PEL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG01993 | hp2 | a0001 | c0002 | t0004 | g0086 | AMR | PEL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02015 | hp1 | a0001 | c0001 | t0006 | g0194 | EAS | KHV | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | KHV | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | KHV | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02027 | hp2 | a0001 | c0001 | t0040 | g0246 | EAS | KHV | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02040 | hp2 | a0001 | c0001 | t0036 | g0173 | EAS | KHV | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | KHV | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02071 | hp1 | a0001 | c0001 | t0006 | g0102 | EAS | KHV | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02071 | hp2 | a0001 | c0001 | t0022 | g0138 | EAS | KHV | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | KHV | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0262 | EAS | KHV | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0300 | EAS | KHV | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | KHV | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02135 | hp2 | a0001 | c0001 | t0006 | g0164 | EAS | KHV | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02145 | hp1 | a0001 | c0001 | t0027 | g0038 | AFR | ACB | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02145 | hp2 | a0001 | c0001 | t0009 | g0049 | AFR | ACB | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0293 | AMR | PEL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0288 | EAS | CDX | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | CDX | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02257 | hp1 | a0001 | c0001 | t0029 | g0053 | AFR | ACB | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02257 | hp2 | a0001 | c0001 | t0017 | g0043 | AFR | ACB | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02258 | hp1 | a0001 | c0001 | t0032 | g0046 | AFR | ACB | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02258 | hp2 | a0001 | c0001 | t0004 | g0021 | AFR | ACB | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0298 | AMR | PEL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0299 | AMR | PEL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02293 | hp2 | a0001 | c0001 | t0023 | g0121 | AMR | PEL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02300 | hp1 | a0001 | c0001 | t0003 | g0221 | AMR | PEL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02451 | hp1 | a0001 | c0002 | t0004 | g0096 | AFR | ACB | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02451 | hp2 | a0001 | c0001 | t0007 | g0025 | AFR | ACB | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02572 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | GWD | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02572 | hp2 | a0002 | c0011 | t0053 | g0019 | AFR | GWD | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02615 | hp1 | a0001 | c0001 | t0007 | g0028 | AFR | GWD | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02615 | hp2 | a0001 | c0001 | t0005 | g0001 | AFR | GWD | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02622 | hp1 | a0001 | c0002 | t0004 | g0091 | AFR | GWD | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02622 | hp2 | a0001 | c0001 | t0004 | g0036 | AFR | GWD | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02630 | hp1 | a0001 | c0001 | t0007 | g0024 | AFR | GWD | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02630 | hp2 | a0001 | c0001 | t0003 | g0084 | AFR | GWD | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02647 | hp1 | a0001 | c0002 | t0004 | g0069 | AFR | GWD | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02647 | hp2 | a0001 | c0001 | t0054 | g0251 | AFR | GWD | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02683 | hp1 | a0001 | c0001 | t0009 | g0048 | SAS | PJL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02683 | hp2 | a0001 | c0001 | t0003 | g0228 | SAS | PJL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0250 | SAS | PJL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02698 | hp2 | a0001 | c0001 | t0035 | g0263 | SAS | PJL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02717 | hp1 | a0001 | c0001 | t0003 | g0083 | AFR | GWD | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02717 | hp2 | a0001 | c0001 | t0004 | g0233 | AFR | GWD | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02723 | hp1 | a0001 | c0001 | t0008 | g0011 | AFR | GWD | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02723 | hp2 | a0001 | c0001 | t0011 | g0183 | AFR | GWD | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02735 | hp1 | a0001 | c0001 | t0050 | g0147 | SAS | PJL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02735 | hp2 | a0001 | c0001 | t0005 | g0213 | SAS | PJL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02738 | hp1 | a0001 | c0001 | t0016 | g0018 | SAS | PJL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02738 | hp2 | a0001 | c0001 | t0009 | g0054 | SAS | PJL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02809 | hp1 | a0001 | c0001 | t0008 | g0010 | AFR | GWD | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02809 | hp2 | a0001 | c0001 | t0018 | g0230 | AFR | GWD | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02818 | hp1 | a0001 | c0001 | t0008 | g0009 | AFR | GWD | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02818 | hp2 | a0001 | c0001 | t0005 | g0001 | AFR | GWD | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02886 | hp1 | a0002 | c0010 | t0047 | g0064 | AFR | GWD | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02886 | hp2 | a0001 | c0002 | t0004 | g0097 | AFR | GWD | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02896 | hp1 | a0001 | c0001 | t0019 | g0062 | AFR | GWD | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02896 | hp2 | a0001 | c0001 | t0005 | g0039 | AFR | GWD | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02922 | hp1 | a0001 | c0001 | t0005 | g0188 | AFR | ESN | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02922 | hp2 | a0001 | c0001 | t0004 | g0035 | AFR | ESN | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02965 | hp1 | a0001 | c0002 | t0004 | g0032 | AFR | ESN | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02965 | hp2 | a0001 | c0001 | t0030 | g0044 | AFR | ESN | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02970 | hp1 | a0001 | c0002 | t0004 | g0094 | AFR | ESN | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02970 | hp2 | a0001 | c0007 | t0019 | g0182 | AFR | ESN | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02976 | hp1 | a0001 | c0001 | t0008 | g0014 | AFR | ESN | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02976 | hp2 | a0001 | c0001 | t0033 | g0037 | AFR | ESN | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG03017 | hp1 | a0001 | c0001 | t0003 | g0216 | SAS | PJL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0237 | SAS | PJL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG03041 | hp1 | a0001 | c0001 | t0028 | g0060 | AFR | GWD | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG03041 | hp2 | a0001 | c0001 | t0049 | g0042 | AFR | GWD | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG03098 | hp1 | a0001 | c0002 | t0004 | g0093 | AFR | MSL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG03098 | hp2 | a0001 | c0001 | t0005 | g0040 | AFR | MSL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG03130 | hp1 | a0001 | c0001 | t0015 | g0190 | AFR | ESN | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG03130 | hp2 | a0001 | c0001 | t0003 | g0030 | AFR | ESN | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG03195 | hp1 | a0001 | c0001 | t0003 | g0218 | AFR | ESN | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG03195 | hp2 | a0001 | c0001 | t0020 | g0232 | AFR | ESN | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG03225 | hp1 | a0001 | c0001 | t0007 | g0023 | AFR | MSL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG03225 | hp2 | a0001 | c0001 | t0008 | g0015 | AFR | MSL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG03239 | hp2 | a0001 | c0001 | t0005 | g0063 | SAS | PJL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG03486 | hp1 | a0001 | c0001 | t0003 | g0234 | AFR | MSL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG03486 | hp2 | a0001 | c0001 | t0060 | g0280 | AFR | MSL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG03491 | hp1 | a0001 | c0001 | t0003 | g0207 | SAS | PJL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG03491 | hp2 | a0001 | c0001 | t0012 | g0005 | SAS | PJL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG03492 | hp2 | a0001 | c0001 | t0031 | g0059 | SAS | PJL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG03516 | hp1 | a0001 | c0001 | t0008 | g0012 | AFR | ESN | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG03516 | hp2 | a0001 | c0001 | t0008 | g0013 | AFR | ESN | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG03540 | hp1 | a0001 | c0001 | t0005 | g0041 | AFR | GWD | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG03540 | hp2 | a0001 | c0001 | t0007 | g0029 | AFR | GWD | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG03579 | hp1 | a0001 | c0001 | t0038 | g0180 | AFR | MSL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG03579 | hp2 | a0001 | c0001 | t0039 | g0077 | AFR | MSL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG03669 | hp2 | a0001 | c0001 | t0005 | g0105 | SAS | PJL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG03688 | hp1 | a0001 | c0002 | t0004 | g0099 | SAS | STU | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG03688 | hp2 | a0001 | c0001 | t0005 | g0143 | SAS | STU | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | BEB | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG03831 | hp2 | a0001 | c0001 | t0003 | g0244 | SAS | BEB | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG03834 | hp1 | a0001 | c0001 | t0003 | g0215 | SAS | BEB | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG03834 | hp2 | a0001 | c0001 | t0005 | g0111 | SAS | BEB | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG03927 | hp1 | a0001 | c0002 | t0004 | g0090 | SAS | BEB | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG03927 | hp2 | a0001 | c0001 | t0003 | g0222 | SAS | BEB | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG03942 | hp1 | a0001 | c0001 | t0005 | g0144 | SAS | BEB | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0274 | SAS | BEB | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG04115 | hp1 | a0001 | c0005 | t0002 | g0294 | SAS | STU | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG04115 | hp2 | a0001 | c0002 | t0002 | g0071 | SAS | STU | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG04199 | hp1 | a0001 | c0001 | t0045 | g0140 | SAS | STU | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG04199 | hp2 | a0001 | c0001 | t0005 | g0211 | SAS | STU | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | STU | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | STU | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0278 | SAS | STU | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | STU | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA18522 | hp1 | a0001 | c0001 | t0015 | g0189 | AFR | YRI | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA18522 | hp2 | a0001 | c0001 | t0003 | g0217 | AFR | YRI | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | CHB | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | CHB | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA18906 | hp1 | a0001 | c0001 | t0008 | g0016 | AFR | YRI | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA18906 | hp2 | a0001 | c0001 | t0008 | g0008 | AFR | YRI | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA18946 | hp1 | a0001 | c0001 | t0003 | g0239 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA18946 | hp2 | a0001 | c0001 | t0006 | g0195 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA18948 | hp1 | a0001 | c0001 | t0006 | g0170 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA18951 | hp1 | a0001 | c0001 | t0012 | g0079 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA18952 | hp1 | a0001 | c0001 | t0003 | g0238 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA18959 | hp2 | a0001 | c0001 | t0006 | g0199 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA18964 | hp1 | a0001 | c0001 | t0012 | g0078 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA18969 | hp2 | a0001 | c0001 | t0006 | g0198 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA18970 | hp1 | a0001 | c0001 | t0059 | g0284 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA18971 | hp2 | a0001 | c0001 | t0037 | g0065 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA18975 | hp1 | a0001 | c0002 | t0004 | g0088 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA18975 | hp2 | a0001 | c0001 | t0026 | g0082 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0320 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA18980 | hp2 | a0001 | c0001 | t0052 | g0136 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA18982 | hp1 | a0001 | c0001 | t0003 | g0210 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA18985 | hp2 | a0001 | c0004 | t0001 | g0321 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA18991 | hp2 | a0001 | c0002 | t0004 | g0070 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA18994 | hp1 | a0001 | c0001 | t0003 | g0101 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA18994 | hp2 | a0001 | c0001 | t0006 | g0076 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0317 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA18995 | hp2 | a0001 | c0001 | t0044 | g0316 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA18998 | hp1 | a0001 | c0001 | t0006 | g0200 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA19002 | hp1 | a0001 | c0001 | t0022 | g0176 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA19030 | hp1 | a0001 | c0008 | t0055 | g0067 | AFR | LWK | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA19030 | hp2 | a0001 | c0001 | t0003 | g0242 | AFR | LWK | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA19043 | hp1 | a0001 | c0001 | t0011 | g0057 | AFR | LWK | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA19043 | hp2 | a0001 | c0001 | t0041 | g0006 | AFR | LWK | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA19056 | hp1 | a0001 | c0001 | t0034 | g0201 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA19057 | hp1 | a0001 | c0001 | t0061 | g0289 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA19059 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA19059 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA19064 | hp1 | a0001 | c0001 | t0021 | g0155 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA19065 | hp1 | a0001 | c0001 | t0058 | g0277 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA19067 | hp1 | a0001 | c0001 | t0026 | g0292 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA19068 | hp2 | a0001 | c0001 | t0051 | g0162 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA19074 | hp2 | a0001 | c0001 | t0006 | g0202 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA19081 | hp2 | a0001 | c0001 | t0006 | g0174 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA19085 | hp2 | a0001 | c0001 | t0006 | g0302 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA19090 | hp1 | a0001 | c0001 | t0006 | g0193 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA19240 | hp1 | a0001 | c0001 | t0010 | g0034 | AFR | YRI | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA19240 | hp2 | a0001 | c0001 | t0010 | g0187 | AFR | YRI | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA20752 | hp1 | a0001 | c0001 | t0057 | g0304 | EUR | TSI | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0268 | EUR | TSI | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | GIH | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA20905 | hp2 | a0001 | c0001 | t0004 | g0295 | SAS | GIH | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02109 | hp1 | a0001 | c0001 | t0025 | g0256 | AFR | ACB | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02109 | hp2 | a0001 | c0003 | t0003 | g0235 | AFR | ACB | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02486 | hp1 | a0001 | c0001 | t0014 | g0052 | AFR | ACB | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02486 | hp2 | a0001 | c0001 | t0013 | g0055 | AFR | ACB | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02559 | hp1 | a0001 | c0001 | t0007 | g0026 | AFR | ACB | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG02559 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | ACB | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG03471 | hp1 | a0001 | c0001 | t0007 | g0022 | AFR | MSL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG03471 | hp2 | a0001 | c0001 | t0010 | g0186 | AFR | MSL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0267 | AFR | USA | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
HG06807 | hp2 | a0001 | c0001 | t0003 | g0031 | AFR | USA | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA20300 | hp1 | a0001 | c0001 | t0011 | g0184 | AFR | USA | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA20300 | hp2 | a0001 | c0002 | t0004 | g0002 | AFR | USA | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA21309 | hp1 | a0001 | c0003 | t0003 | g0236 | AFR | LWK | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
NA21309 | hp2 | a0001 | c0001 | t0003 | g0229 | AFR | LWK | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0223 | REF | REF | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
homoSapiens_grch38 | hp1 | a0001 | c0004 | t0016 | g0051 | REF | REF | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:46626917 | G | T | 1 | a0002 | 2 | HG02572.hp2 HG02886.hp1 |
missense_variant | MODERATE | c.118G>T | p.Val40Leu | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/19 | 347/4500 | 118/1737 | 40/578 | chr22 | 46626917 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:46663095 | T | C | 10 | a0001c0001 a0001c0002 a0001c0003 others(7): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
synonymous_variant | LOW | c.522T>C | p.Phe174Phe | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 6/19 | 751/4500 | 522/1737 | 174/578 | chr22 | 46663095 | |||
chr22:46663104 | C | T | 1 | a0001c0009 | 1 | HG01106.hp2 | synonymous_variant | LOW | c.531C>T | p.Tyr177Tyr | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 6/19 | 760/4500 | 531/1737 | 177/578 | chr22 | 46663104 | |||
chr22:46664030 | C | T | 1 | a0001c0008 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.630C>T | p.Arg210Arg | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 8/19 | 859/4500 | 630/1737 | 210/578 | chr22 | 46664030 | |||
chr22:46664042 | G | A | 2 | a0001c0002 a0002c0010 |
21 | HG01109.hp1 HG01361.hp2 HG01496.hp2 others(18): Show |
synonymous_variant | LOW | c.642G>A | p.Pro214Pro | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 8/19 | 871/4500 | 642/1737 | 214/578 | chr22 | 46664042 | |||
chr22:46668155 | C | T | 1 | a0001c0003 | 2 | HG02109.hp2 NA21309.hp1 |
synonymous_variant | LOW | c.918C>T | p.Ala306Ala | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 11/19 | 1147/4500 | 918/1737 | 306/578 | chr22 | 46668155 | |||
chr22:46674727 | C | T | 1 | a0001c0007 | 1 | HG02970.hp2 | synonymous_variant | LOW | c.1455C>T | p.Asn485Asn | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 16/19 | 1684/4500 | 1455/1737 | 485/578 | chr22 | 46674727 | |||
chr22:46674745 | G | A | 1 | a0001c0005 | 1 | HG04115.hp1 | synonymous_variant | LOW | c.1473G>A | p.Thr491Thr | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 16/19 | 1702/4500 | 1473/1737 | 491/578 | chr22 | 46674745 | |||
chr22:46675507 | G | A | 1 | a0001c0006 | 1 | HG00597.hp1 | synonymous_variant | LOW | c.1518G>A | p.Lys506Lys | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 17/19 | 1747/4500 | 1518/1737 | 506/578 | chr22 | 46675507 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:46620455 | C | T | 57 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(54): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
5_prime_UTR_variant | MODIFIER | c.-160C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/19 | 6345 | chr22 | 46620455 | ||||||
chr22:46620456 | G | A | 1 | a0001c0001t0027 | 1 | HG02145.hp1 | 5_prime_UTR_variant | MODIFIER | c.-159G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/19 | 6344 | chr22 | 46620456 | ||||||
chr22:46677302 | CT | C | 11 | a0001c0001t0007 a0001c0001t0012 a0001c0001t0013 others(8): Show |
23 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*64delT | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 64 | INFO_REALIGN_3_PRIME | chr22 | 46677302 | |||||
chr22:46677357 | T | C | 3 | a0001c0001t0007 a0001c0001t0013 a0001c0001t0029 |
12 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*106T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 106 | chr22 | 46677357 | ||||||
chr22:46677525 | G | A | 1 | a0001c0001t0037 | 1 | NA18971.hp2 | 3_prime_UTR_variant | MODIFIER | c.*274G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 274 | chr22 | 46677525 | ||||||
chr22:46677560 | C | G | 1 | a0001c0001t0064 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*309C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 309 | chr22 | 46677560 | ||||||
chr22:46677631 | C | T | 1 | a0001c0001t0032 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*380C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 380 | chr22 | 46677631 | ||||||
chr22:46677670 | A | G | 1 | a0001c0001t0063 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*419A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 419 | chr22 | 46677670 | ||||||
chr22:46677824 | C | T | 18 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0017 others(15): Show |
83 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*573C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 573 | chr22 | 46677824 | ||||||
chr22:46677831 | C | T | 1 | a0001c0009t0062 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*580C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 580 | chr22 | 46677831 | ||||||
chr22:46677836 | G | A | 1 | a0001c0001t0038 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*585G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 585 | chr22 | 46677836 | ||||||
chr22:46677879 | A | G | 10 | a0001c0001t0007 a0001c0001t0011 a0001c0001t0013 others(7): Show |
21 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*628A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 628 | chr22 | 46677879 | ||||||
chr22:46677904 | G | A | 9 | a0001c0001t0003 a0001c0001t0014 a0001c0001t0018 others(6): Show |
53 | HG00099.hp2 HG00140.hp1 HG00733.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*653G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 653 | chr22 | 46677904 | ||||||
chr22:46677961 | C | G | 1 | a0001c0001t0031 | 1 | HG03492.hp2 | 3_prime_UTR_variant | MODIFIER | c.*710C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 710 | chr22 | 46677961 | ||||||
chr22:46677964 | C | T | 9 | a0001c0001t0003 a0001c0001t0014 a0001c0001t0018 others(6): Show |
53 | HG00099.hp2 HG00140.hp1 HG00733.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*713C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 713 | chr22 | 46677964 | ||||||
chr22:46677978 | T | C | 44 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(41): Show |
172 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(169): Show |
3_prime_UTR_variant | MODIFIER | c.*727T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 727 | chr22 | 46677978 | ||||||
chr22:46678047 | G | A | 1 | a0001c0001t0039 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*796G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 796 | chr22 | 46678047 | ||||||
chr22:46678212 | C | G | 4 | a0001c0001t0005 a0001c0001t0009 a0001c0001t0049 others(1): Show |
24 | HG00323.hp2 HG00738.hp2 HG01106.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*961C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 961 | chr22 | 46678212 | ||||||
chr22:46678240 | C | T | 1 | a0001c0001t0061 | 1 | NA19057.hp1 | 3_prime_UTR_variant | MODIFIER | c.*989C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 989 | chr22 | 46678240 | ||||||
chr22:46678300 | C | T | 2 | a0001c0001t0038 a0001c0001t0048 |
2 | HG01433.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1049C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 1049 | chr22 | 46678300 | ||||||
chr22:46678360 | C | G | 1 | a0001c0001t0060 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1109C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 1109 | chr22 | 46678360 | ||||||
chr22:46678361 | G | A | 19 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0017 others(16): Show |
84 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*1110G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 1110 | chr22 | 46678361 | ||||||
chr22:46678365 | G | A | 1 | a0002c0011t0053 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1114G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 1114 | chr22 | 46678365 | ||||||
chr22:46678373 | G | C | 5 | a0001c0001t0006 a0001c0001t0034 a0001c0001t0036 others(2): Show |
18 | HG00438.hp2 HG00597.hp1 HG02015.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1122G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 1122 | chr22 | 46678373 | ||||||
chr22:46678384 | G | A | 20 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0017 others(17): Show |
85 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*1133G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 1133 | chr22 | 46678384 | ||||||
chr22:46678584 | C | T | 1 | a0002c0010t0047 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1333C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 1333 | chr22 | 46678584 | ||||||
chr22:46678621 | C | T | 1 | a0001c0001t0052 | 1 | NA18980.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1370C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 1370 | chr22 | 46678621 | ||||||
chr22:46678944 | C | T | 1 | a0001c0001t0024 | 2 | HG01069.hp1 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1693C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 1693 | chr22 | 46678944 | ||||||
chr22:46679040 | T | C | 45 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(42): Show |
177 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(174): Show |
3_prime_UTR_variant | MODIFIER | c.*1789T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 1789 | chr22 | 46679040 | ||||||
chr22:46679146 | T | C | 1 | a0001c0001t0054 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1895T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 1895 | chr22 | 46679146 | ||||||
chr22:46679168 | A | C | 1 | a0001c0001t0020 | 2 | HG01943.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1917A>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 1917 | chr22 | 46679168 | ||||||
chr22:46679352 | G | GC | 6 | a0001c0001t0008 a0001c0001t0011 a0001c0001t0028 others(3): Show |
16 | HG02723.hp1 HG02723.hp2 HG02809.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2106dupC | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 2107 | INFO_REALIGN_3_PRIME | chr22 | 46679352 | |||||
chr22:46679381 | G | A | 1 | a0001c0001t0056 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2130G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 2130 | chr22 | 46679381 | ||||||
chr22:46679385 | G | T | 2 | a0001c0001t0019 a0001c0007t0019 |
2 | HG02896.hp1 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2134G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 2134 | chr22 | 46679385 | ||||||
chr22:46679565 | C | T | 47 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(44): Show |
179 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(176): Show |
3_prime_UTR_variant | MODIFIER | c.*2314C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 2314 | chr22 | 46679565 | ||||||
chr22:46679696 | A | T | 1 | a0001c0001t0025 | 2 | HG00733.hp2 HG02109.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2445A>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 2445 | chr22 | 46679696 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:46620567 | T | TAGGGGGC | 133 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0204 others(130): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.-50+23_-50+29dupCA others(5): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 46620567 | ||||||
chr22:46620645 | A | C | 3 | a0001c0001t0015g0189 a0001c0001t0015g0190 a0001c0001t0048g0191 |
3 | HG01433.hp1 HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-50+80A>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46620645 | |||||||
chr22:46620729 | G | A | 3 | a0001c0001t0015g0189 a0001c0001t0015g0190 a0001c0001t0048g0191 |
3 | HG01433.hp1 HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-50+164G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46620729 | |||||||
chr22:46620762 | G | A | 3 | a0001c0001t0015g0189 a0001c0001t0015g0190 a0001c0001t0048g0191 |
3 | HG01433.hp1 HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-50+197G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46620762 | |||||||
chr22:46620985 | A | G | 7 | a0001c0001t0005g0188 a0001c0001t0010g0185 a0001c0001t0010g0186 others(4): Show |
7 | HG01884.hp2 HG02723.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-50+420A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46620985 | |||||||
chr22:46621033 | G | A | 1 | a0001c0007t0019g0182 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-50+468G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46621033 | |||||||
chr22:46621074 | C | T | 2 | a0001c0001t0001g0181 a0001c0001t0038g0180 |
2 | HG03579.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.-50+509C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46621074 | |||||||
chr22:46621086 | G | A | 10 | a0001c0001t0004g0017 a0001c0001t0008g0008 a0001c0001t0008g0009 others(7): Show |
10 | HG02572.hp1 HG02723.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.-50+521G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46621086 | |||||||
chr22:46621139 | C | T | 122 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0066 others(119): Show |
125 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.-50+574C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46621139 | |||||||
chr22:46621153 | A | G | 1 | a0001c0001t0038g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-50+588A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46621153 | |||||||
chr22:46621158 | G | T | 5 | a0001c0001t0005g0188 a0001c0001t0010g0185 a0001c0001t0010g0186 others(2): Show |
5 | HG01884.hp2 HG02922.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-50+593G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46621158 | |||||||
chr22:46621388 | T | C | 1 | a0001c0001t0016g0018 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-50+823T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46621388 | |||||||
chr22:46621441 | TGGAGGGC others(65): Show |
T | 2 | a0001c0001t0013g0020 a0001c0001t0048g0191 |
2 | HG01070.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.-50+1011_-50+1082d others(74): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 46621441 | ||||||
chr22:46621441 | TGGAGGGC others(137): Show |
T | 1 | a0001c0001t0038g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-50+939_-50+1082de others(1): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 46621441 | ||||||
chr22:46621504 | GGTGTGTC others(137): Show |
G | 14 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0204 others(11): Show |
14 | HG00438.hp2 HG00621.hp2 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.-50+976_-50+1119de others(1): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 46621504 | ||||||
chr22:46621514 | G | A | 1 | a0001c0001t0037g0065 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-50+949G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46621514 | |||||||
chr22:46621528 | CCCCGGTG others(64): Show |
C | 1 | a0001c0001t0001g0066 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-50+967_-50+1037de others(72): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 46621528 | ||||||
chr22:46621541 | GCAGGCTG others(137): Show |
G | 1 | a0001c0001t0005g0063 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-50+1002_-50+1145d others(2): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 46621541 | ||||||
chr22:46621551 | GGCGTAGC others(209): Show |
G | 1 | a0002c0010t0047g0064 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-50+988_-50+1203de others(1): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 46621551 | ||||||
chr22:46621567 | A | G | 1 | a0001c0001t0002g0320 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-50+1002A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46621567 | |||||||
chr22:46621576 | G | A | 2 | a0001c0001t0015g0189 a0001c0001t0015g0190 |
2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-50+1011G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46621576 | |||||||
chr22:46621576 | GGTGTGTC others(65): Show |
G | 277 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0068 others(274): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.-50+1048_-50+1119d others(74): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 46621576 | ||||||
chr22:46621586 | G | A | 2 | a0001c0001t0015g0189 a0001c0001t0015g0190 |
2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-50+1021G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46621586 | |||||||
chr22:46621613 | G | A | 2 | a0001c0001t0015g0189 a0001c0001t0015g0190 |
2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-50+1048G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46621613 | |||||||
chr22:46621613 | GCAGGCTG others(65): Show |
G | 1 | a0001c0001t0001g0179 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-50+1074_-50+1145d others(74): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 46621613 | ||||||
chr22:46621639 | A | G | 2 | a0001c0001t0015g0189 a0001c0001t0015g0190 |
2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-50+1074A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46621639 | |||||||
chr22:46621648 | A | G | 5 | a0001c0001t0001g0066 a0001c0001t0004g0061 a0001c0001t0015g0189 others(2): Show |
5 | HG01884.hp1 HG02896.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-50+1083A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46621648 | |||||||
chr22:46621649 | G | C | 2 | a0001c0001t0015g0189 a0001c0001t0015g0190 |
2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-50+1084G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46621649 | |||||||
chr22:46621680 | C | T | 1 | a0001c0001t0028g0060 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-50+1115C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46621680 | |||||||
chr22:46621685 | A | G | 3 | a0001c0001t0015g0189 a0001c0001t0015g0190 a0001c0001t0048g0191 |
3 | HG01433.hp1 HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-50+1120A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46621685 | |||||||
chr22:46621727 | C | T | 2 | a0001c0001t0011g0183 a0001c0001t0011g0184 |
2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-50+1162C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46621727 | |||||||
chr22:46621814 | C | T | 3 | a0001c0001t0015g0189 a0001c0001t0015g0190 a0001c0001t0038g0180 |
3 | HG03130.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-50+1249C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46621814 | |||||||
chr22:46622051 | C | T | 1 | a0001c0001t0004g0017 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-50+1486C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46622051 | |||||||
chr22:46622060 | G | A | 1 | a0001c0008t0055g0067 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-50+1495G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46622060 | |||||||
chr22:46622269 | C | T | 80 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0204 others(77): Show |
81 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.-50+1704C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46622269 | |||||||
chr22:46622334 | C | T | 1 | a0001c0001t0038g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-50+1769C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46622334 | |||||||
chr22:46622370 | C | T | 7 | a0001c0001t0005g0001 a0001c0001t0005g0039 a0001c0001t0005g0040 others(4): Show |
8 | HG02572.hp2 HG02615.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.-50+1805C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46622370 | |||||||
chr22:46622445 | G | C | 1 | a0001c0001t0004g0021 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-50+1880G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46622445 | |||||||
chr22:46622674 | G | A | 1 | a0001c0001t0017g0043 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-50+2109G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46622674 | |||||||
chr22:46622799 | C | T | 3 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG01256.hp2 HG01258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.-50+2234C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46622799 | |||||||
chr22:46622867 | A | G | 3 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0022g0176 |
3 | NA19002.hp1 NA19066.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.-50+2302A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46622867 | |||||||
chr22:46622868 | C | T | 2 | a0001c0001t0004g0061 a0001c0001t0019g0062 |
2 | HG01884.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-50+2303C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46622868 | |||||||
chr22:46622869 | G | A | 4 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0255 others(1): Show |
4 | NA18939.hp2 NA19002.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.-50+2304G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46622869 | |||||||
chr22:46622885 | C | T | 1 | a0001c0001t0054g0251 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-50+2320C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46622885 | |||||||
chr22:46622890 | C | T | 147 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0066 others(144): Show |
150 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.-50+2325C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46622890 | |||||||
chr22:46622899 | A | G | 1 | a0001c0001t0001g0068 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-50+2334A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46622899 | |||||||
chr22:46622912 | T | TA | 16 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0074 others(13): Show |
16 | HG00741.hp1 HG01192.hp2 HG01433.hp2 others(13): Show |
intron_variant | MODIFIER | c.-50+2366dupA | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 46622912 | ||||||
chr22:46622912 | TA | T | 78 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0204 others(75): Show |
79 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.-50+2366delA | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 46622912 | ||||||
chr22:46622913 | A | T | 2 | a0001c0001t0002g0319 a0002c0011t0053g0019 |
2 | HG00323.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-50+2348A>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46622913 | |||||||
chr22:46622922 | A | G | 1 | a0001c0001t0002g0319 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-50+2357A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46622922 | |||||||
chr22:46622971 | C | T | 2 | a0002c0010t0047g0064 a0002c0011t0053g0019 |
2 | HG02572.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-50+2406C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46622971 | |||||||
chr22:46622993 | A | G | 1 | a0001c0001t0011g0057 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-50+2428A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46622993 | |||||||
chr22:46623044 | C | T | 1 | a0001c0001t0038g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-50+2479C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46623044 | |||||||
chr22:46623045 | G | A | 1 | a0001c0001t0039g0077 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-50+2480G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46623045 | |||||||
chr22:46623068 | G | A | 2 | a0001c0001t0002g0259 a0001c0001t0005g0258 |
2 | HG00738.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.-50+2503G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46623068 | |||||||
chr22:46623090 | G | A | 1 | a0001c0001t0038g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-50+2525G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46623090 | |||||||
chr22:46623091 | A | G | 1 | a0001c0001t0038g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-50+2526A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46623091 | |||||||
chr22:46623102 | G | A | 5 | a0001c0001t0001g0080 a0001c0001t0002g0081 a0001c0001t0012g0078 others(2): Show |
5 | HG02074.hp2 NA18951.hp1 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.-50+2537G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46623102 | |||||||
chr22:46623199 | C | T | 142 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0066 others(139): Show |
145 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.-50+2634C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46623199 | |||||||
chr22:46623227 | G | C | 1 | a0001c0001t0048g0191 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-50+2662G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46623227 | |||||||
chr22:46623361 | C | T | 7 | a0001c0001t0003g0083 a0001c0001t0003g0084 a0001c0001t0003g0085 others(4): Show |
7 | HG01243.hp1 HG01243.hp2 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.-50+2796C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46623361 | |||||||
chr22:46623362 | G | A | 1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-50+2797G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46623362 | |||||||
chr22:46623525 | C | T | 1 | a0001c0001t0001g0204 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-50+2960C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46623525 | |||||||
chr22:46623529 | T | G | 2 | a0001c0001t0004g0017 a0001c0001t0007g0022 |
2 | HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-50+2964T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46623529 | |||||||
chr22:46623563 | C | T | 1 | a0002c0011t0053g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-50+2998C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46623563 | |||||||
chr22:46623597 | C | T | 81 | a0001c0001t0001g0197 a0001c0001t0001g0204 a0001c0001t0001g0255 others(78): Show |
82 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.-50+3032C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46623597 | |||||||
chr22:46623639 | G | A | 31 | a0001c0001t0001g0087 a0001c0001t0001g0098 a0001c0001t0001g0177 others(28): Show |
32 | HG00438.hp2 HG01109.hp1 HG01361.hp2 others(29): Show |
intron_variant | MODIFIER | c.-50+3074G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46623639 | |||||||
chr22:46623784 | CT | C | 6 | a0001c0001t0001g0103 a0001c0001t0003g0104 a0001c0001t0003g0207 others(3): Show |
6 | HG00099.hp2 HG01070.hp1 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.-49-2951delT | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 46623784 | ||||||
chr22:46623816 | C | T | 4 | a0001c0001t0004g0035 a0001c0001t0004g0036 a0001c0001t0010g0034 others(1): Show |
4 | HG02622.hp2 HG02922.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49-2935C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46623816 | |||||||
chr22:46623835 | G | A | 1 | a0001c0001t0038g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-49-2916G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46623835 | |||||||
chr22:46623860 | C | T | 3 | a0001c0001t0006g0102 a0001c0001t0036g0173 a0001c0006t0042g0318 |
3 | HG00597.hp1 HG02040.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.-49-2891C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46623860 | |||||||
chr22:46623874 | C | T | 1 | a0002c0011t0053g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-49-2877C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46623874 | |||||||
chr22:46623891 | C | G | 3 | a0001c0001t0005g0188 a0001c0001t0011g0057 a0001c0001t0013g0055 |
3 | HG02486.hp2 HG02922.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-49-2860C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46623891 | |||||||
chr22:46623926 | C | T | 1 | a0001c0001t0001g0178 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-49-2825C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46623926 | |||||||
chr22:46623970 | T | C | 158 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0066 others(155): Show |
162 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.-49-2781T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46623970 | |||||||
chr22:46623973 | A | G | 4 | a0001c0001t0004g0035 a0001c0001t0004g0036 a0001c0001t0010g0034 others(1): Show |
4 | HG02622.hp2 HG02922.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49-2778A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46623973 | |||||||
chr22:46623998 | T | A | 2 | a0002c0010t0047g0064 a0002c0011t0053g0019 |
2 | HG02572.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-49-2753T>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46623998 | |||||||
chr22:46624003 | G | A | 101 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0204 others(98): Show |
102 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.-49-2748G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46624003 | |||||||
chr22:46624039 | C | A | 102 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0066 others(99): Show |
105 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.-49-2712C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46624039 | |||||||
chr22:46624083 | A | G | 2 | a0001c0001t0003g0030 a0001c0001t0003g0031 |
2 | HG03130.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-49-2668A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46624083 | |||||||
chr22:46624158 | G | T | 3 | a0001c0001t0015g0189 a0001c0001t0015g0190 a0001c0001t0048g0191 |
3 | HG01433.hp1 HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-49-2593G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46624158 | |||||||
chr22:46624243 | C | CT | 12 | a0001c0001t0001g0254 a0001c0001t0004g0017 a0001c0001t0008g0008 others(9): Show |
12 | HG01256.hp2 HG01515.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.-49-2497dupT | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 46624243 | ||||||
chr22:46624243 | CT | C | 7 | a0001c0001t0003g0210 a0001c0001t0011g0183 a0001c0001t0011g0184 others(4): Show |
7 | HG02572.hp2 HG02723.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-49-2497delT | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 46624243 | ||||||
chr22:46624274 | C | T | 1 | a0002c0010t0047g0064 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-49-2477C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46624274 | |||||||
chr22:46624291 | C | G | 7 | a0001c0001t0001g0177 a0001c0001t0001g0181 a0001c0001t0002g0100 others(4): Show |
7 | NA18955.hp1 NA18962.hp2 NA18985.hp2 others(4): Show |
intron_variant | MODIFIER | c.-49-2460C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46624291 | |||||||
chr22:46624316 | C | T | 148 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0066 others(145): Show |
152 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.-49-2435C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46624316 | |||||||
chr22:46624324 | C | CT | 19 | a0001c0001t0001g0309 a0001c0001t0002g0203 a0001c0001t0002g0310 others(16): Show |
19 | HG00621.hp2 HG00642.hp1 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.-49-2402dupT | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 46624324 | ||||||
chr22:46624324 | C | CTT | 6 | a0001c0001t0004g0035 a0001c0001t0004g0036 a0001c0001t0010g0034 others(3): Show |
6 | HG02622.hp2 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-49-2403_-49-2402d others(4): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 46624324 | ||||||
chr22:46624324 | C | CTTT | 14 | a0001c0001t0001g0066 a0001c0001t0001g0109 a0001c0001t0001g0110 others(11): Show |
14 | HG00438.hp1 HG02145.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.-49-2404_-49-2402d others(5): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 46624324 | ||||||
chr22:46624324 | C | CTTTT | 91 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0068 others(88): Show |
94 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.-49-2405_-49-2402d others(6): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 46624324 | ||||||
chr22:46624324 | C | CTTTTT | 20 | a0001c0001t0001g0098 a0001c0001t0001g0163 a0001c0001t0001g0165 others(17): Show |
20 | HG00597.hp2 HG02135.hp2 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.-49-2406_-49-2402d others(7): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 46624324 | ||||||
chr22:46624349 | T | TTTC | 10 | a0001c0001t0003g0248 a0001c0001t0004g0021 a0001c0001t0005g0063 others(7): Show |
10 | HG00140.hp1 HG00642.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.-49-2402_-49-2401i others(5): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46624349 | |||||||
chr22:46624448 | T | C | 4 | a0001c0001t0003g0030 a0001c0001t0003g0031 a0001c0001t0027g0038 others(1): Show |
4 | HG02145.hp1 HG03130.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-2303T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46624448 | |||||||
chr22:46624548 | G | A | 1 | a0001c0001t0038g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-49-2203G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46624548 | |||||||
chr22:46624687 | A | G | 60 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0252 others(57): Show |
60 | HG00099.hp2 HG00733.hp1 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.-49-2064A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46624687 | |||||||
chr22:46624783 | C | T | 1 | a0002c0011t0053g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-49-1968C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46624783 | |||||||
chr22:46624858 | A | AT | 18 | a0001c0001t0001g0204 a0001c0001t0001g0255 a0001c0001t0001g0308 others(15): Show |
18 | HG01175.hp1 HG01261.hp2 HG01516.hp2 others(15): Show |
intron_variant | MODIFIER | c.-49-1873dupT | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 46624858 | ||||||
chr22:46624858 | AT | A | 148 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0068 others(145): Show |
152 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.-49-1873delT | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 46624858 | ||||||
chr22:46624883 | C | G | 1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-49-1868C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46624883 | |||||||
chr22:46624892 | G | C | 1 | a0001c0001t0002g0264 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-49-1859G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46624892 | |||||||
chr22:46625006 | G | A | 2 | a0001c0001t0004g0061 a0001c0001t0019g0062 |
2 | HG01884.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-49-1745G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46625006 | |||||||
chr22:46625077 | G | T | 1 | a0001c0001t0002g0307 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-49-1674G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46625077 | |||||||
chr22:46625082 | A | G | 1 | a0001c0001t0003g0245 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-49-1669A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46625082 | |||||||
chr22:46625095 | T | C | 1 | a0001c0001t0003g0245 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-49-1656T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46625095 | |||||||
chr22:46625116 | T | C | 9 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(6): Show |
9 | HG02723.hp1 HG02809.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.-49-1635T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46625116 | |||||||
chr22:46625139 | C | T | 1 | a0001c0001t0003g0210 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-49-1612C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46625139 | |||||||
chr22:46625162 | C | T | 3 | a0001c0001t0005g0188 a0001c0001t0011g0057 a0001c0001t0013g0055 |
3 | HG02486.hp2 HG02922.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-49-1589C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46625162 | |||||||
chr22:46625297 | G | A | 1 | a0001c0001t0025g0256 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-49-1454G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46625297 | |||||||
chr22:46625306 | T | G | 147 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0066 others(144): Show |
151 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.-49-1445T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46625306 | |||||||
chr22:46625327 | C | T | 1 | a0001c0002t0004g0099 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-49-1424C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46625327 | |||||||
chr22:46625329 | A | G | 93 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0204 others(90): Show |
94 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.-49-1422A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46625329 | |||||||
chr22:46625401 | C | T | 7 | a0001c0001t0002g0305 a0001c0001t0002g0314 a0001c0001t0002g0315 others(4): Show |
7 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.-49-1350C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46625401 | |||||||
chr22:46625460 | G | A | 3 | a0001c0001t0006g0102 a0001c0001t0036g0173 a0001c0006t0042g0318 |
3 | HG00597.hp1 HG02040.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.-49-1291G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46625460 | |||||||
chr22:46625546 | C | T | 2 | a0001c0001t0015g0189 a0001c0001t0015g0190 |
2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-49-1205C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46625546 | |||||||
chr22:46625725 | G | A | 1 | a0001c0001t0032g0046 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-49-1026G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46625725 | |||||||
chr22:46625732 | G | A | 1 | a0001c0001t0013g0020 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-49-1019G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46625732 | |||||||
chr22:46625820 | C | T | 1 | a0001c0001t0001g0253 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-49-931C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46625820 | |||||||
chr22:46626099 | G | T | 147 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0066 others(144): Show |
151 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.-49-652G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46626099 | |||||||
chr22:46626219 | A | G | 1 | a0001c0001t0038g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-49-532A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46626219 | |||||||
chr22:46626348 | G | C | 10 | a0001c0001t0004g0017 a0001c0001t0008g0008 a0001c0001t0008g0009 others(7): Show |
10 | HG02572.hp1 HG02723.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.-49-403G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46626348 | |||||||
chr22:46626360 | T | A | 2 | a0001c0001t0004g0061 a0001c0001t0019g0062 |
2 | HG01884.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-49-391T>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46626360 | |||||||
chr22:46626466 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-49-285C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46626466 | |||||||
chr22:46626565 | C | T | 34 | a0001c0001t0001g0098 a0001c0001t0004g0017 a0001c0001t0004g0035 others(31): Show |
35 | HG01109.hp1 HG01361.hp2 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.-49-186C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46626565 | |||||||
chr22:46626565 | CGTGCCCT others(102): Show |
C | 8 | a0001c0001t0003g0234 a0001c0001t0004g0233 a0001c0001t0020g0231 others(5): Show |
8 | HG01943.hp2 HG02109.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.-49-177_-49-69del | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 46626565 | ||||||
chr22:46626607 | T | A | 1 | a0001c0001t0003g0207 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-49-144T>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46626607 | |||||||
chr22:46626620 | C | T | 4 | a0001c0001t0004g0035 a0001c0001t0004g0036 a0001c0001t0010g0034 others(1): Show |
4 | HG02622.hp2 HG02922.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49-131C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46626620 | |||||||
chr22:46626667 | G | T | 1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-49-84G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46626667 | |||||||
chr22:46626992 | G | T | 2 | a0001c0001t0004g0061 a0001c0001t0019g0062 |
2 | HG01884.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.162+31G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46626992 | |||||||
chr22:46627132 | C | T | 1 | a0002c0011t0053g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.162+171C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46627132 | |||||||
chr22:46627135 | G | C | 2 | a0001c0001t0007g0033 a0001c0002t0004g0032 |
2 | HG01243.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.162+174G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46627135 | |||||||
chr22:46627189 | G | C | 5 | a0001c0001t0004g0035 a0001c0001t0004g0036 a0001c0001t0010g0034 others(2): Show |
5 | HG02622.hp2 HG02922.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.162+228G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46627189 | |||||||
chr22:46627232 | G | A | 18 | a0001c0001t0002g0209 a0001c0001t0002g0259 a0001c0001t0002g0266 others(15): Show |
18 | HG00140.hp2 HG00323.hp1 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.162+271G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46627232 | |||||||
chr22:46627237 | T | C | 1 | a0001c0001t0007g0026 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.162+276T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46627237 | |||||||
chr22:46627271 | G | A | 2 | a0001c0001t0004g0061 a0001c0001t0019g0062 |
2 | HG01884.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.162+310G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46627271 | |||||||
chr22:46627353 | G | A | 1 | a0001c0001t0001g0178 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.162+392G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46627353 | |||||||
chr22:46627564 | T | C | 312 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0066 others(309): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.162+603T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46627564 | |||||||
chr22:46627576 | C | T | 4 | a0001c0001t0003g0234 a0001c0001t0004g0233 a0001c0003t0003g0235 others(1): Show |
4 | HG02109.hp2 HG02717.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.162+615C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46627576 | |||||||
chr22:46627628 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.162+667C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46627628 | |||||||
chr22:46627642 | C | T | 1 | a0001c0001t0028g0060 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.162+681C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46627642 | |||||||
chr22:46627819 | G | A | 2 | a0002c0010t0047g0064 a0002c0011t0053g0019 |
2 | HG02572.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.162+858G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46627819 | |||||||
chr22:46627832 | C | T | 4 | a0001c0001t0003g0229 a0001c0001t0003g0245 a0001c0001t0014g0052 others(1): Show |
4 | HG00733.hp1 HG02486.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.162+871C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46627832 | |||||||
chr22:46627876 | G | A | 1 | a0002c0011t0053g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.162+915G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46627876 | |||||||
chr22:46627979 | T | C | 1 | a0001c0001t0001g0114 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.162+1018T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46627979 | |||||||
chr22:46628090 | C | A | 1 | a0001c0001t0002g0270 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.162+1129C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46628090 | |||||||
chr22:46628280 | C | T | 31 | a0001c0001t0001g0098 a0001c0001t0004g0017 a0001c0001t0004g0035 others(28): Show |
32 | HG01109.hp1 HG01361.hp2 HG01496.hp2 others(29): Show |
intron_variant | MODIFIER | c.162+1319C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46628280 | |||||||
chr22:46628295 | G | C | 1 | a0001c0001t0001g0181 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.162+1334G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46628295 | |||||||
chr22:46628336 | G | A | 1 | a0001c0001t0038g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.162+1375G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46628336 | |||||||
chr22:46628453 | TGTGCGTT others(25): Show |
T | 1 | a0001c0001t0038g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.162+1528_162+1559d others(34): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46628453 | ||||||
chr22:46628454 | G | T | 5 | a0001c0001t0006g0102 a0001c0001t0006g0174 a0001c0001t0006g0302 others(2): Show |
5 | HG00597.hp1 HG02040.hp2 HG02071.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+1493G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46628454 | |||||||
chr22:46628475 | GGGTGGAC others(95): Show |
G | 13 | a0001c0001t0003g0248 a0001c0001t0005g0063 a0001c0001t0007g0022 others(10): Show |
13 | HG00140.hp1 HG00642.hp2 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.162+1528_162+1629d others(2): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46628475 | ||||||
chr22:46628489 | C | T | 140 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0066 others(137): Show |
143 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.162+1528C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46628489 | |||||||
chr22:46628491 | T | TGCG | 138 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0066 others(135): Show |
141 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.162+1530_162+1531i others(5): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46628491 | |||||||
chr22:46628491 | T | TGCGTGGT others(67): Show |
1 | a0001c0001t0008g0014 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.162+1530_162+1531i others(76): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46628491 | |||||||
chr22:46628507 | G | GGGTGGAC others(29): Show |
18 | a0001c0001t0001g0098 a0001c0002t0002g0071 a0001c0002t0004g0002 others(15): Show |
19 | HG01109.hp1 HG01361.hp2 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.162+1566_162+1567i others(38): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46628507 | ||||||
chr22:46628507 | G | GGGTGGAC others(64): Show |
7 | a0001c0001t0004g0017 a0001c0001t0008g0008 a0001c0001t0008g0009 others(4): Show |
7 | HG02572.hp1 HG02723.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.162+1566_162+1567i others(73): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46628507 | ||||||
chr22:46628507 | GGGTGGAC others(28): Show |
G | 101 | a0001c0001t0001g0115 a0001c0001t0001g0196 a0001c0001t0001g0197 others(98): Show |
103 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.162+1616_162+1650d others(37): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46628507 | ||||||
chr22:46628521 | T | C | 2 | a0001c0001t0002g0301 a0001c0001t0002g0317 |
2 | NA18995.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.162+1560T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46628521 | |||||||
chr22:46628526 | G | GT | 108 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0066 others(105): Show |
110 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.162+1566dupT | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46628526 | ||||||
chr22:46628526 | G | GTTGGTGT others(206): Show |
4 | a0001c0001t0004g0035 a0001c0001t0004g0036 a0001c0001t0010g0034 others(1): Show |
4 | HG02622.hp2 HG02922.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.162+1566_162+1567i others(215): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46628526 | ||||||
chr22:46628542 | A | G | 6 | a0001c0001t0002g0301 a0001c0001t0002g0317 a0001c0001t0008g0013 others(3): Show |
6 | HG03516.hp2 HG03579.hp1 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.162+1581A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46628542 | |||||||
chr22:46628577 | A | G | 8 | a0001c0001t0001g0166 a0001c0001t0004g0017 a0001c0001t0008g0008 others(5): Show |
8 | HG00597.hp2 HG02572.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.162+1616A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46628577 | |||||||
chr22:46628596 | G | T | 1 | a0001c0001t0011g0057 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.162+1635G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46628596 | |||||||
chr22:46628612 | G | A | 1 | a0001c0001t0038g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.162+1651G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46628612 | |||||||
chr22:46628630 | C | T | 1 | a0001c0001t0003g0244 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.162+1669C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46628630 | |||||||
chr22:46628646 | G | A | 3 | a0001c0001t0009g0047 a0001c0001t0009g0048 a0001c0001t0009g0054 |
3 | HG01106.hp1 HG02683.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.162+1685G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46628646 | |||||||
chr22:46628730 | A | G | 3 | a0001c0001t0004g0035 a0001c0001t0004g0036 a0001c0001t0033g0037 |
3 | HG02622.hp2 HG02922.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.162+1769A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46628730 | |||||||
chr22:46628801 | T | C | 6 | a0001c0001t0011g0183 a0001c0001t0011g0184 a0001c0001t0015g0189 others(3): Show |
6 | HG02723.hp2 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.162+1840T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46628801 | |||||||
chr22:46628901 | G | A | 2 | a0001c0001t0009g0056 a0001c0001t0017g0043 |
2 | HG01978.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.162+1940G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46628901 | |||||||
chr22:46628921 | C | T | 1 | a0001c0001t0038g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.162+1960C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46628921 | |||||||
chr22:46629099 | G | A | 1 | a0001c0001t0013g0055 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.162+2138G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46629099 | |||||||
chr22:46629117 | C | G | 1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.162+2156C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46629117 | |||||||
chr22:46629156 | G | T | 1 | a0001c0001t0001g0157 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.162+2195G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46629156 | |||||||
chr22:46629173 | G | A | 1 | a0002c0010t0047g0064 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.162+2212G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46629173 | |||||||
chr22:46629196 | G | A | 1 | a0001c0001t0008g0008 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.162+2235G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46629196 | |||||||
chr22:46629204 | T | G | 3 | a0001c0001t0008g0013 a0001c0001t0008g0014 a0001c0001t0008g0016 |
3 | HG02976.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.162+2243T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46629204 | |||||||
chr22:46629247 | G | A | 5 | a0001c0001t0003g0083 a0001c0001t0003g0084 a0001c0001t0003g0085 others(2): Show |
5 | HG01243.hp2 HG01496.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.162+2286G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46629247 | |||||||
chr22:46629260 | C | T | 1 | a0001c0001t0002g0300 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.162+2299C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46629260 | |||||||
chr22:46629296 | C | T | 1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.162+2335C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46629296 | |||||||
chr22:46629373 | G | A | 1 | a0001c0001t0003g0242 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.162+2412G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46629373 | |||||||
chr22:46629427 | G | A | 1 | a0001c0001t0002g0314 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.162+2466G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46629427 | |||||||
chr22:46629449 | G | C | 1 | a0001c0001t0006g0198 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.162+2488G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46629449 | |||||||
chr22:46629453 | C | T | 1 | a0001c0001t0003g0228 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.162+2492C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46629453 | |||||||
chr22:46629769 | T | C | 1 | a0001c0001t0004g0021 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.162+2808T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46629769 | |||||||
chr22:46629787 | C | T | 1 | a0001c0001t0004g0021 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.162+2826C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46629787 | |||||||
chr22:46629931 | G | A | 2 | a0001c0001t0004g0061 a0001c0001t0019g0062 |
2 | HG01884.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.162+2970G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46629931 | |||||||
chr22:46629932 | C | T | 6 | a0001c0001t0011g0183 a0001c0001t0011g0184 a0001c0001t0015g0189 others(3): Show |
6 | HG02723.hp2 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.162+2971C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46629932 | |||||||
chr22:46629971 | G | A | 1 | a0001c0002t0046g0089 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.162+3010G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46629971 | |||||||
chr22:46630029 | T | C | 2 | a0001c0001t0004g0061 a0001c0001t0019g0062 |
2 | HG01884.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.162+3068T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46630029 | |||||||
chr22:46630185 | C | T | 1 | a0001c0001t0056g0313 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.162+3224C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46630185 | |||||||
chr22:46630210 | G | A | 1 | a0001c0001t0013g0020 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.162+3249G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46630210 | |||||||
chr22:46630254 | G | C | 1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.162+3293G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46630254 | |||||||
chr22:46630256 | G | A | 4 | a0001c0001t0011g0183 a0001c0001t0011g0184 a0001c0001t0028g0060 others(1): Show |
4 | HG02723.hp2 HG02965.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.162+3295G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46630256 | |||||||
chr22:46630356 | C | T | 92 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0066 others(89): Show |
95 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.162+3395C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46630356 | |||||||
chr22:46630414 | T | G | 1 | a0001c0001t0003g0212 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.162+3453T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46630414 | |||||||
chr22:46630464 | C | T | 2 | a0001c0001t0021g0155 a0001c0001t0021g0156 |
2 | HG00673.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.162+3503C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46630464 | |||||||
chr22:46630545 | T | C | 1 | a0001c0001t0048g0191 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.162+3584T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46630545 | |||||||
chr22:46630570 | C | A | 150 | a0001c0001t0001g0003 a0001c0001t0001g0066 a0001c0001t0001g0068 others(147): Show |
153 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.162+3609C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46630570 | |||||||
chr22:46630638 | G | A | 2 | a0001c0001t0003g0030 a0001c0001t0003g0031 |
2 | HG03130.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.162+3677G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46630638 | |||||||
chr22:46630638 | G | T | 1 | a0001c0001t0004g0233 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.162+3677G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46630638 | |||||||
chr22:46630694 | G | A | 7 | a0001c0001t0004g0233 a0001c0001t0011g0183 a0001c0001t0011g0184 others(4): Show |
7 | HG02486.hp1 HG02717.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.162+3733G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46630694 | |||||||
chr22:46630824 | T | G | 2 | a0001c0001t0004g0061 a0001c0001t0019g0062 |
2 | HG01884.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.162+3863T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46630824 | |||||||
chr22:46630848 | C | T | 1 | a0001c0001t0048g0191 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.162+3887C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46630848 | |||||||
chr22:46630849 | GGTGTGCC others(46): Show |
G | 102 | a0001c0001t0001g0115 a0001c0001t0001g0151 a0001c0001t0001g0152 others(99): Show |
103 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.162+3905_162+3957d others(55): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46630849 | ||||||
chr22:46630869 | C | T | 1 | a0001c0001t0004g0017 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.162+3908C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46630869 | |||||||
chr22:46630871 | G | A | 4 | a0001c0001t0004g0035 a0001c0001t0004g0036 a0001c0001t0010g0034 others(1): Show |
4 | HG02622.hp2 HG02922.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.162+3910G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46630871 | |||||||
chr22:46630899 | C | T | 1 | a0001c0001t0004g0017 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.162+3938C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46630899 | |||||||
chr22:46630900 | G | T | 1 | a0002c0010t0047g0064 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.162+3939G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46630900 | |||||||
chr22:46630931 | C | T | 39 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0003g0006 others(36): Show |
39 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.162+3970C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46630931 | |||||||
chr22:46630946 | C | T | 8 | a0001c0001t0001g0308 a0001c0001t0002g0296 a0001c0001t0002g0297 others(5): Show |
8 | HG00099.hp1 HG00642.hp1 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.162+3985C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46630946 | |||||||
chr22:46630947 | G | A | 4 | a0001c0001t0011g0183 a0001c0001t0011g0184 a0001c0001t0028g0060 others(1): Show |
4 | HG02723.hp2 HG02965.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.162+3986G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46630947 | |||||||
chr22:46630955 | C | T | 93 | a0001c0001t0001g0005 a0001c0001t0001g0066 a0001c0001t0001g0068 others(90): Show |
95 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.162+3994C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46630955 | |||||||
chr22:46631035 | C | T | 1 | a0001c0002t0004g0097 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.162+4074C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46631035 | |||||||
chr22:46631120 | T | C | 121 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0066 others(118): Show |
124 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.162+4159T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46631120 | |||||||
chr22:46631126 | C | T | 1 | a0001c0001t0032g0046 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.162+4165C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46631126 | |||||||
chr22:46631175 | C | T | 1 | a0001c0001t0004g0017 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.162+4214C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46631175 | |||||||
chr22:46631202 | A | G | 1 | a0001c0001t0054g0251 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.162+4241A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46631202 | |||||||
chr22:46631218 | G | A | 1 | a0001c0001t0054g0251 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.162+4257G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46631218 | |||||||
chr22:46631389 | A | ACTCCTGG others(140): Show |
1 | a0001c0001t0005g0188 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.162+4455_162+4456i others(149): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46631389 | ||||||
chr22:46631389 | A | ACTCCTGG others(42): Show |
1 | a0001c0002t0004g0090 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.162+4460_162+4461i others(51): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46631389 | ||||||
chr22:46631389 | A | ACTCCTGG others(91): Show |
1 | a0001c0001t0003g0226 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.162+4460_162+4461i others(100): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46631389 | ||||||
chr22:46631389 | ACTCCTGG others(91): Show |
A | 10 | a0001c0001t0001g0098 a0001c0002t0002g0071 a0001c0002t0004g0002 others(7): Show |
11 | HG01361.hp2 HG01496.hp2 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.162+4461_162+4558d others(100): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46631389 | ||||||
chr22:46631389 | ACTCCTGG others(140): Show |
A | 11 | a0001c0001t0028g0060 a0001c0001t0030g0044 a0001c0002t0004g0032 others(8): Show |
11 | HG01109.hp1 HG01891.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.162+4461_162+4607d others(2): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46631389 | ||||||
chr22:46631389 | ACTCCTGG others(189): Show |
A | 2 | a0001c0001t0011g0183 a0001c0001t0011g0184 |
2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.162+4461_162+4656d others(2): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46631389 | ||||||
chr22:46631389 | ACTCCTGG others(238): Show |
A | 2 | a0001c0001t0013g0055 a0001c0001t0054g0251 |
2 | HG02486.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.162+4461_162+4705d others(2): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46631389 | ||||||
chr22:46631422 | A | AGCCTGTG others(287): Show |
1 | a0001c0001t0001g0196 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.162+4509_162+4510i others(296): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46631422 | ||||||
chr22:46631422 | A | AGCCTGTG others(42): Show |
11 | a0001c0001t0001g0103 a0001c0001t0001g0109 a0001c0001t0003g0030 others(8): Show |
11 | HG01070.hp1 HG01071.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.162+4993_162+5041d others(51): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46631422 | ||||||
chr22:46631422 | A | AGCCTGTG others(238): Show |
1 | a0001c0001t0006g0198 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.162+4558_162+4559i others(247): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46631422 | ||||||
chr22:46631422 | A | AGCCTGTG others(91): Show |
49 | a0001c0001t0003g0006 a0001c0001t0003g0083 a0001c0001t0003g0084 others(46): Show |
49 | HG00099.hp2 HG00733.hp1 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.162+4944_162+5041d others(100): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46631422 | ||||||
chr22:46631422 | A | AGCCTGTG others(140): Show |
3 | a0001c0001t0002g0270 a0001c0005t0002g0294 a0001c0008t0055g0067 |
3 | HG00423.hp2 HG04115.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.162+4895_162+5041d others(149): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46631422 | ||||||
chr22:46631422 | A | AGCCTGTG others(189): Show |
20 | a0001c0001t0002g0172 a0001c0001t0002g0209 a0001c0001t0002g0269 others(17): Show |
20 | HG00140.hp2 HG00738.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.162+4846_162+5041d others(198): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46631422 | ||||||
chr22:46631422 | A | AGCCTGTG others(238): Show |
64 | a0001c0001t0001g0115 a0001c0001t0001g0197 a0001c0001t0001g0255 others(61): Show |
65 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.162+4797_162+5041d others(247): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46631422 | ||||||
chr22:46631422 | A | AGCCTGTG others(287): Show |
9 | a0001c0001t0001g0271 a0001c0001t0001g0309 a0001c0001t0002g0249 others(6): Show |
10 | HG00733.hp2 HG02015.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.162+4748_162+5041d others(296): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46631422 | ||||||
chr22:46631422 | A | AGCCTGTG others(532): Show |
2 | a0001c0001t0015g0189 a0001c0001t0015g0190 |
2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.162+4503_162+5041d others(541): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46631422 | ||||||
chr22:46631422 | A | G | 4 | a0001c0001t0001g0112 a0001c0001t0003g0226 a0001c0001t0005g0188 others(1): Show |
4 | HG00438.hp1 HG01255.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.162+4461A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46631422 | |||||||
chr22:46631422 | AGCCTGTG others(42): Show |
A | 13 | a0001c0001t0001g0146 a0001c0001t0001g0252 a0001c0001t0001g0254 others(10): Show |
13 | HG00741.hp1 HG01175.hp2 HG01256.hp2 others(10): Show |
intron_variant | MODIFIER | c.162+4993_162+5041d others(51): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46631422 | ||||||
chr22:46631422 | AGCCTGTG others(91): Show |
A | 1 | a0001c0004t0001g0321 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.162+4944_162+5041d others(100): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46631422 | ||||||
chr22:46631422 | AGCCTGTG others(140): Show |
A | 3 | a0001c0001t0004g0036 a0001c0001t0010g0034 a0001c0001t0033g0037 |
3 | HG02622.hp2 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.162+4895_162+5041d others(2): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46631422 | ||||||
chr22:46631422 | AGCCTGTG others(189): Show |
A | 1 | a0002c0011t0053g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.162+4846_162+5041d others(2): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46631422 | ||||||
chr22:46631422 | AGCCTGTG others(238): Show |
A | 1 | a0001c0001t0004g0017 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.162+4797_162+5041d others(2): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46631422 | ||||||
chr22:46631422 | AGCCTGTG others(287): Show |
A | 6 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(3): Show |
6 | HG02723.hp1 HG02809.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.162+4748_162+5041d others(2): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46631422 | ||||||
chr22:46631422 | AGCCTGTG others(336): Show |
A | 13 | a0001c0001t0003g0248 a0001c0001t0004g0021 a0001c0001t0005g0063 others(10): Show |
13 | HG00140.hp1 HG00642.hp2 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.162+4699_162+5041d others(2): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46631422 | ||||||
chr22:46631437 | G | GTCTCCTG others(287): Show |
1 | a0001c0001t0048g0191 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.162+4769_162+4770i others(296): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46631437 | ||||||
chr22:46631520 | G | A | 1 | a0001c0001t0003g0229 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.162+4559G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46631520 | |||||||
chr22:46631616 | A | ACGGCCTG others(42): Show |
1 | a0002c0010t0047g0064 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.162+4703_162+4704i others(51): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46631616 | ||||||
chr22:46631647 | G | GGGGATGG others(285): Show |
1 | a0001c0001t0002g0260 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.162+4968_162+4969i others(294): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46631647 | ||||||
chr22:46631661 | C | T | 6 | a0001c0001t0001g0080 a0001c0001t0001g0148 a0001c0001t0001g0149 others(3): Show |
6 | HG00673.hp1 HG02074.hp2 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.162+4700C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46631661 | |||||||
chr22:46631714 | A | G | 1 | a0002c0010t0047g0064 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.162+4753A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46631714 | |||||||
chr22:46631759 | C | CCTCACGG others(91): Show |
1 | a0001c0001t0040g0246 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.162+4895_162+4896i others(100): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46631759 | ||||||
chr22:46631763 | A | G | 1 | a0002c0010t0047g0064 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.162+4802A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46631763 | |||||||
chr22:46631765 | G | A | 1 | a0001c0001t0013g0055 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.162+4804G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46631765 | |||||||
chr22:46631813 | C | CGGCCTGT others(91): Show |
1 | a0001c0001t0001g0220 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.162+4949_162+4950i others(100): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46631813 | ||||||
chr22:46631901 | T | A | 1 | a0001c0002t0004g0097 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.162+4940T>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46631901 | |||||||
chr22:46632009 | C | T | 1 | a0001c0001t0005g0041 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.162+5048C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46632009 | |||||||
chr22:46632010 | G | A | 154 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0066 others(151): Show |
157 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.162+5049G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46632010 | |||||||
chr22:46632033 | C | T | 14 | a0001c0001t0003g0248 a0001c0001t0004g0021 a0001c0001t0005g0063 others(11): Show |
14 | HG00140.hp1 HG00642.hp2 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.162+5072C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46632033 | |||||||
chr22:46632093 | T | C | 100 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0066 others(97): Show |
102 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.162+5132T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46632093 | |||||||
chr22:46632137 | C | T | 1 | a0001c0001t0004g0017 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.162+5176C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46632137 | |||||||
chr22:46632141 | G | C | 1 | a0001c0001t0001g0123 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.162+5180G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46632141 | |||||||
chr22:46632311 | G | A | 1 | a0001c0001t0001g0196 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.162+5350G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46632311 | |||||||
chr22:46632317 | G | A | 2 | a0001c0001t0004g0061 a0001c0001t0019g0062 |
2 | HG01884.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.162+5356G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46632317 | |||||||
chr22:46632417 | A | T | 100 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0066 others(97): Show |
102 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.163-5423A>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46632417 | |||||||
chr22:46632436 | T | G | 7 | a0001c0001t0004g0017 a0001c0001t0008g0008 a0001c0001t0008g0009 others(4): Show |
7 | HG02572.hp1 HG02723.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.163-5404T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46632436 | |||||||
chr22:46632728 | C | G | 1 | a0001c0001t0038g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.163-5112C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46632728 | |||||||
chr22:46632850 | G | A | 1 | a0001c0001t0048g0191 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.163-4990G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46632850 | |||||||
chr22:46633058 | C | T | 1 | a0001c0001t0002g0293 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.163-4782C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46633058 | |||||||
chr22:46633145 | T | C | 1 | a0001c0001t0004g0021 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.163-4695T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46633145 | |||||||
chr22:46633289 | T | C | 1 | a0001c0002t0004g0090 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.163-4551T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46633289 | |||||||
chr22:46633319 | C | T | 2 | a0001c0001t0003g0218 a0001c0001t0003g0242 |
2 | HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.163-4521C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46633319 | |||||||
chr22:46633354 | C | T | 1 | a0001c0001t0038g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.163-4486C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46633354 | |||||||
chr22:46633557 | G | T | 7 | a0001c0001t0004g0035 a0001c0001t0004g0036 a0001c0001t0010g0034 others(4): Show |
7 | HG02622.hp2 HG02723.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.163-4283G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46633557 | |||||||
chr22:46633583 | G | A | 18 | a0001c0001t0004g0017 a0001c0001t0004g0035 a0001c0001t0004g0036 others(15): Show |
18 | HG01884.hp1 HG02572.hp1 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.163-4257G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46633583 | |||||||
chr22:46633586 | G | C | 92 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0066 others(89): Show |
94 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.163-4254G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46633586 | |||||||
chr22:46633596 | C | G | 1 | a0001c0002t0002g0071 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.163-4244C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46633596 | |||||||
chr22:46633657 | G | T | 3 | a0001c0001t0004g0036 a0001c0001t0010g0034 a0001c0001t0033g0037 |
3 | HG02622.hp2 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.163-4183G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46633657 | |||||||
chr22:46633680 | A | T | 1 | a0001c0001t0054g0251 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.163-4160A>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46633680 | |||||||
chr22:46633691 | G | A | 1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.163-4149G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46633691 | |||||||
chr22:46633740 | G | C | 3 | a0001c0001t0011g0183 a0001c0001t0011g0184 a0001c0001t0028g0060 |
3 | HG02723.hp2 HG03041.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.163-4100G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46633740 | |||||||
chr22:46633821 | C | T | 3 | a0001c0001t0008g0013 a0001c0001t0008g0014 a0001c0001t0008g0016 |
3 | HG02976.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.163-4019C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46633821 | |||||||
chr22:46633996 | C | T | 1 | a0001c0001t0054g0251 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.163-3844C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46633996 | |||||||
chr22:46633999 | A | G | 4 | a0001c0001t0004g0035 a0001c0001t0004g0036 a0001c0001t0010g0034 others(1): Show |
4 | HG02622.hp2 HG02922.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.163-3841A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46633999 | |||||||
chr22:46634076 | G | A | 11 | a0001c0001t0004g0017 a0001c0001t0004g0035 a0001c0001t0004g0036 others(8): Show |
11 | HG01884.hp1 HG02572.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.163-3764G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46634076 | |||||||
chr22:46634079 | C | T | 13 | a0001c0001t0004g0021 a0001c0001t0005g0063 a0001c0001t0007g0022 others(10): Show |
13 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.163-3761C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46634079 | |||||||
chr22:46634153 | G | C | 1 | a0001c0001t0040g0246 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.163-3687G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46634153 | |||||||
chr22:46634179 | G | T | 6 | a0001c0001t0002g0285 a0001c0001t0002g0291 a0001c0001t0002g0320 others(3): Show |
6 | NA18970.hp1 NA18980.hp1 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.163-3661G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46634179 | |||||||
chr22:46634180 | G | T | 1 | a0001c0001t0004g0233 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.163-3660G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46634180 | |||||||
chr22:46634190 | A | G | 1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.163-3650A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46634190 | |||||||
chr22:46634254 | G | C | 8 | a0001c0001t0004g0035 a0001c0001t0004g0036 a0001c0001t0010g0034 others(5): Show |
8 | HG02622.hp2 HG02723.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.163-3586G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46634254 | |||||||
chr22:46634304 | G | A | 3 | a0001c0001t0008g0013 a0001c0001t0008g0014 a0001c0001t0008g0016 |
3 | HG02976.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.163-3536G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46634304 | |||||||
chr22:46634343 | A | C | 146 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0066 others(143): Show |
149 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.163-3497A>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46634343 | |||||||
chr22:46634547 | C | T | 1 | a0001c0001t0037g0065 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.163-3293C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46634547 | |||||||
chr22:46634711 | C | T | 93 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0066 others(90): Show |
95 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.163-3129C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46634711 | |||||||
chr22:46634829 | G | A | 1 | a0001c0001t0006g0194 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.163-3011G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46634829 | |||||||
chr22:46634892 | G | A | 1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.163-2948G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46634892 | |||||||
chr22:46634901 | T | G | 1 | a0001c0001t0030g0044 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.163-2939T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46634901 | |||||||
chr22:46634945 | CA | C | 12 | a0001c0001t0003g0212 a0001c0001t0004g0017 a0001c0001t0005g0039 others(9): Show |
12 | HG01257.hp2 HG02572.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.163-2881delA | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46634945 | ||||||
chr22:46634951 | A | T | 1 | a0001c0001t0011g0057 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.163-2889A>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46634951 | |||||||
chr22:46634958 | A | C | 1 | a0001c0001t0001g0177 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.163-2882A>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46634958 | |||||||
chr22:46635013 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.163-2827C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635013 | |||||||
chr22:46635058 | A | ACCACCCC others(39): Show |
20 | a0001c0001t0001g0220 a0001c0001t0003g0006 a0001c0001t0003g0205 others(17): Show |
20 | HG00140.hp1 HG00741.hp1 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.163-2761_163-2760i others(48): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635058 | ||||||
chr22:46635066 | T | TGGCCACT others(593): Show |
1 | a0001c0001t0033g0037 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.163-2761_163-2760i others(602): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635066 | ||||||
chr22:46635066 | T | TGGCCACT others(223): Show |
1 | a0001c0002t0002g0071 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.163-2761_163-2760i others(232): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635066 | ||||||
chr22:46635066 | T | TGGCCACT others(39): Show |
2 | a0001c0001t0003g0104 a0001c0001t0003g0169 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.163-2761_163-2760i others(48): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635066 | ||||||
chr22:46635067 | GGCCACTC others(39): Show |
G | 1 | a0001c0001t0010g0034 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.163-2760_163-2715d others(48): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635067 | ||||||
chr22:46635080 | T | C | 52 | a0001c0001t0001g0098 a0001c0001t0001g0220 a0001c0001t0003g0006 others(49): Show |
53 | HG00140.hp1 HG00741.hp1 HG01070.hp1 others(50): Show |
intron_variant | MODIFIER | c.163-2760T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635080 | |||||||
chr22:46635086 | A | G | 1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.163-2754A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635086 | |||||||
chr22:46635087 | G | A | 51 | a0001c0001t0001g0098 a0001c0001t0001g0220 a0001c0001t0003g0006 others(48): Show |
52 | HG00140.hp1 HG00741.hp1 HG01070.hp1 others(49): Show |
intron_variant | MODIFIER | c.163-2753G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635087 | |||||||
chr22:46635104 | C | T | 3 | a0001c0001t0003g0210 a0001c0001t0003g0238 a0001c0001t0003g0239 |
3 | NA18946.hp1 NA18952.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.163-2736C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635104 | |||||||
chr22:46635107 | G | A | 10 | a0001c0001t0003g0210 a0001c0001t0003g0238 a0001c0001t0003g0239 others(7): Show |
10 | HG01891.hp2 HG02622.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.163-2733G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635107 | |||||||
chr22:46635107 | G | GACCCCGG others(131): Show |
1 | a0001c0001t0002g0317 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.163-2733_163-2732i others(140): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635107 | |||||||
chr22:46635107 | G | GACCCCGG others(177): Show |
2 | a0001c0001t0030g0044 a0001c0001t0048g0191 |
2 | HG01433.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.163-2733_163-2732i others(186): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635107 | |||||||
chr22:46635107 | G | GCCCCCGG others(39): Show |
1 | a0001c0001t0005g0213 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.163-2728_163-2727i others(48): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635107 | ||||||
chr22:46635108 | C | A | 17 | a0001c0001t0001g0098 a0001c0001t0001g0166 a0001c0001t0003g0234 others(14): Show |
18 | HG00597.hp2 HG01109.hp1 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.163-2732C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635108 | |||||||
chr22:46635112 | C | CGGCCACT others(315): Show |
1 | a0001c0001t0054g0251 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.163-2728_163-2727i others(324): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635112 | |||||||
chr22:46635112 | C | T | 12 | a0001c0001t0003g0210 a0001c0001t0003g0238 a0001c0001t0003g0239 others(9): Show |
12 | HG01433.hp1 HG01891.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.163-2728C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635112 | |||||||
chr22:46635113 | A | AGCCACTC others(269): Show |
1 | a0001c0001t0002g0312 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.163-2691_163-2690i others(278): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635113 | ||||||
chr22:46635113 | A | AGCCACTC others(775): Show |
1 | a0001c0001t0043g0311 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.163-2691_163-2690i others(784): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635113 | ||||||
chr22:46635113 | A | AGCCACTC others(407): Show |
1 | a0001c0001t0002g0264 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.163-2691_163-2690i others(416): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635113 | ||||||
chr22:46635113 | A | AGCCACTC others(315): Show |
17 | a0001c0001t0002g0209 a0001c0001t0002g0259 a0001c0001t0002g0266 others(14): Show |
17 | HG00140.hp2 HG00323.hp1 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.163-2691_163-2690i others(324): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635113 | ||||||
chr22:46635113 | A | AGCCACTC others(915): Show |
1 | a0001c0001t0011g0183 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.163-2709_163-2708i others(924): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635113 | ||||||
chr22:46635113 | A | AGCCACTC others(961): Show |
1 | a0001c0001t0011g0184 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.163-2709_163-2708i others(970): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635113 | ||||||
chr22:46635113 | A | AGCCACTC others(1329): Show |
1 | a0001c0001t0028g0060 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.163-2709_163-2708i others(1338): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635113 | ||||||
chr22:46635113 | A | G | 38 | a0001c0001t0001g0220 a0001c0001t0003g0006 a0001c0001t0003g0104 others(35): Show |
38 | HG00140.hp1 HG00741.hp1 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.163-2727A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635113 | |||||||
chr22:46635126 | C | CTGGGGAA others(178): Show |
1 | a0001c0001t0005g0039 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.163-2691_163-2690i others(187): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635126 | ||||||
chr22:46635131 | G | A | 1 | a0001c0002t0002g0071 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.163-2709G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635131 | |||||||
chr22:46635132 | A | AACCGTGT others(177): Show |
1 | a0001c0001t0004g0233 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.163-2691_163-2690i others(186): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635132 | ||||||
chr22:46635132 | A | G | 28 | a0001c0001t0001g0220 a0001c0001t0003g0006 a0001c0001t0003g0104 others(25): Show |
28 | HG00140.hp1 HG00741.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.163-2708A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635132 | |||||||
chr22:46635133 | A | ACCGTGTC others(1695): Show |
1 | a0001c0001t0002g0310 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.163-2691_163-2690i others(1704): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635133 | ||||||
chr22:46635133 | A | G | 2 | a0001c0001t0033g0037 a0001c0002t0002g0071 |
2 | HG02976.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.163-2707A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635133 | |||||||
chr22:46635135 | C | CGTGTCCT others(912): Show |
1 | a0002c0011t0053g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.163-2691_163-2690i others(921): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635135 | ||||||
chr22:46635141 | C | T | 5 | a0001c0002t0004g0032 a0001c0002t0004g0069 a0001c0002t0004g0092 others(2): Show |
5 | HG01891.hp2 HG02647.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.163-2699C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635141 | |||||||
chr22:46635150 | T | C | 144 | a0001c0001t0001g0003 a0001c0001t0001g0098 a0001c0001t0001g0106 others(141): Show |
148 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.163-2690T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635150 | |||||||
chr22:46635150 | T | TCCACCCC others(39): Show |
1 | a0001c0001t0015g0190 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.163-2683_163-2682i others(48): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635150 | ||||||
chr22:46635152 | C | CG | 46 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0002g0007 others(43): Show |
48 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.163-2688_163-2687i others(3): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635152 | |||||||
chr22:46635152 | C | CGACCCCG others(455): Show |
1 | a0001c0001t0006g0076 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.163-2688_163-2687i others(464): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635152 | |||||||
chr22:46635153 | A | G | 47 | a0001c0001t0001g0003 a0001c0001t0001g0106 a0001c0001t0001g0113 others(44): Show |
48 | HG00099.hp1 HG00741.hp2 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.163-2687A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635153 | |||||||
chr22:46635154 | C | A | 33 | a0001c0001t0001g0219 a0001c0001t0001g0308 a0001c0001t0002g0171 others(30): Show |
33 | HG00099.hp1 HG00741.hp2 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.163-2686C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635154 | |||||||
chr22:46635154 | C | CCCCCAGC others(85): Show |
1 | a0001c0001t0015g0189 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.163-2683_163-2682i others(94): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635154 | ||||||
chr22:46635158 | T | C | 73 | a0001c0001t0001g0003 a0001c0001t0001g0106 a0001c0001t0001g0113 others(70): Show |
74 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.163-2682T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635158 | |||||||
chr22:46635158 | T | G | 46 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0002g0007 others(43): Show |
48 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.163-2682T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635158 | |||||||
chr22:46635158 | T | TGGCCACT others(39): Show |
2 | a0001c0001t0010g0186 a0001c0001t0010g0187 |
2 | HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.163-2662_163-2617d others(48): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635158 | ||||||
chr22:46635158 | T | TGGCCACT others(39): Show |
1 | a0001c0001t0010g0185 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.163-2663_163-2662i others(48): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635158 | ||||||
chr22:46635158 | T | TGGCCACT others(223): Show |
1 | a0001c0002t0004g0070 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.163-2663_163-2662i others(232): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635158 | ||||||
chr22:46635159 | G | GCCACTCC others(130): Show |
5 | a0001c0001t0006g0193 a0001c0001t0006g0199 a0001c0001t0006g0200 others(2): Show |
5 | NA18959.hp2 NA18998.hp1 NA19056.hp1 others(2): Show |
intron_variant | MODIFIER | c.163-2681_163-2680i others(139): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635159 | |||||||
chr22:46635159 | G | GCCACTCC others(176): Show |
1 | a0001c0001t0005g0188 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.163-2681_163-2680i others(185): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635159 | |||||||
chr22:46635159 | G | GCCACTCC others(176): Show |
34 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0002g0007 others(31): Show |
36 | HG00423.hp2 HG00597.hp1 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.163-2681_163-2680i others(185): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635159 | |||||||
chr22:46635159 | G | GCCACTCC others(406): Show |
1 | a0001c0001t0006g0170 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.163-2681_163-2680i others(415): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635159 | |||||||
chr22:46635159 | G | GCCACTCC others(130): Show |
1 | a0001c0001t0002g0281 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.163-2681_163-2680i others(139): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635159 | |||||||
chr22:46635159 | G | GCCACTCC others(130): Show |
3 | a0001c0001t0006g0192 a0001c0001t0006g0194 a0001c0001t0006g0195 |
3 | HG00438.hp2 HG02015.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.163-2681_163-2680i others(139): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635159 | |||||||
chr22:46635159 | G | GCCACTCC others(314): Show |
1 | a0001c0001t0002g0282 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.163-2681_163-2680i others(323): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635159 | |||||||
chr22:46635159 | G | GGCCACTC others(223): Show |
1 | a0001c0001t0026g0292 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.163-2641_163-2640i others(232): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635159 | ||||||
chr22:46635159 | G | GGCCACTC others(39): Show |
1 | a0001c0001t0002g0317 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.163-2669_163-2668i others(48): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635159 | ||||||
chr22:46635178 | A | G | 68 | a0001c0001t0001g0098 a0001c0001t0001g0220 a0001c0001t0002g0209 others(65): Show |
69 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.163-2662A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635178 | |||||||
chr22:46635179 | A | ACCGTGTC others(223): Show |
2 | a0001c0002t0004g0090 a0001c0002t0004g0095 |
2 | HG01109.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.163-2654_163-2653i others(232): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635179 | ||||||
chr22:46635187 | C | CTCCCTGC others(39): Show |
1 | a0001c0001t0038g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.163-2642_163-2641i others(48): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635187 | ||||||
chr22:46635187 | C | CTCCCTGC others(775): Show |
3 | a0001c0001t0008g0013 a0001c0001t0008g0014 a0001c0001t0008g0016 |
3 | HG02976.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.163-2641_163-2640i others(784): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635187 | ||||||
chr22:46635187 | C | T | 16 | a0001c0001t0001g0098 a0001c0002t0004g0002 a0001c0002t0004g0032 others(13): Show |
17 | HG01361.hp2 HG01496.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.163-2653C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635187 | |||||||
chr22:46635194 | C | CCCCCACC others(959): Show |
1 | a0001c0001t0004g0295 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.163-2642_163-2641i others(968): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635194 | ||||||
chr22:46635194 | C | CCCCCACC others(821): Show |
1 | a0001c0001t0001g0308 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.163-2642_163-2641i others(830): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635194 | ||||||
chr22:46635194 | C | CCCCCACC others(1097): Show |
1 | a0001c0001t0002g0296 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.163-2642_163-2641i others(1106): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635194 | ||||||
chr22:46635194 | C | CCCCCACC others(913): Show |
3 | a0001c0001t0002g0297 a0001c0001t0002g0298 a0001c0001t0002g0299 |
3 | HG00099.hp1 HG02273.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.163-2642_163-2641i others(922): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635194 | ||||||
chr22:46635194 | C | CCCCCACC others(453): Show |
4 | a0001c0001t0002g0274 a0001c0001t0002g0278 a0001c0001t0017g0045 others(1): Show |
4 | HG01952.hp2 HG03942.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.163-2642_163-2641i others(462): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635194 | ||||||
chr22:46635194 | C | CCCCCGAC others(38): Show |
1 | a0001c0001t0005g0063 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.163-2641_163-2640i others(47): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635194 | ||||||
chr22:46635194 | C | CCCCCGAC others(499): Show |
1 | a0001c0001t0001g0255 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.163-2641_163-2640i others(508): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635194 | ||||||
chr22:46635196 | C | T | 10 | a0001c0001t0001g0072 a0001c0001t0001g0116 a0001c0001t0001g0168 others(7): Show |
10 | HG00741.hp2 HG01433.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.163-2644C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635196 | |||||||
chr22:46635199 | G | A | 21 | a0001c0001t0001g0072 a0001c0001t0001g0116 a0001c0001t0001g0168 others(18): Show |
21 | HG00642.hp1 HG00741.hp2 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.163-2641G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635199 | |||||||
chr22:46635199 | G | GACCCCGG others(681): Show |
1 | a0001c0001t0007g0033 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.163-2641_163-2640i others(690): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635199 | |||||||
chr22:46635199 | G | GACCCCGG others(544): Show |
1 | a0001c0001t0004g0021 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.163-2641_163-2640i others(553): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635199 | |||||||
chr22:46635199 | G | GACCCCGG others(681): Show |
1 | a0001c0001t0007g0027 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.163-2641_163-2640i others(690): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635199 | |||||||
chr22:46635199 | G | GACCCCGG others(727): Show |
6 | a0001c0001t0007g0024 a0001c0001t0007g0025 a0001c0001t0007g0026 others(3): Show |
6 | HG02451.hp2 HG02486.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.163-2641_163-2640i others(736): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635199 | |||||||
chr22:46635200 | C | A | 122 | a0001c0001t0001g0003 a0001c0001t0001g0098 a0001c0001t0001g0106 others(119): Show |
126 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.163-2640C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635200 | |||||||
chr22:46635200 | C | CCCCCGGC others(39): Show |
7 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0154 others(4): Show |
8 | HG01069.hp1 HG01071.hp2 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.163-2617_163-2616i others(48): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635200 | ||||||
chr22:46635200 | C | CCCCCGGC others(269): Show |
1 | a0001c0001t0001g0073 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.163-2617_163-2616i others(278): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635200 | ||||||
chr22:46635200 | C | CCCCCGGC others(39): Show |
1 | a0001c0001t0001g0075 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.163-2617_163-2616i others(48): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635200 | ||||||
chr22:46635204 | C | CGGCCACT others(177): Show |
1 | a0001c0001t0001g0139 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.163-2617_163-2616i others(186): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635204 | ||||||
chr22:46635204 | C | CGGCCACT others(39): Show |
1 | a0001c0001t0003g0212 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.163-2595_163-2550d others(48): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635204 | ||||||
chr22:46635204 | C | T | 18 | a0001c0001t0001g0072 a0001c0001t0001g0116 a0001c0001t0001g0168 others(15): Show |
18 | HG00642.hp1 HG00741.hp2 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.163-2636C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635204 | |||||||
chr22:46635204 | CGGCCACT others(39): Show |
C | 1 | a0001c0001t0031g0059 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.163-2595_163-2550d others(48): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635204 | ||||||
chr22:46635205 | G | A | 1 | a0001c0001t0005g0039 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.163-2635G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635205 | |||||||
chr22:46635223 | G | A | 16 | a0001c0001t0001g0255 a0001c0001t0001g0308 a0001c0001t0002g0274 others(13): Show |
16 | HG00099.hp1 HG01952.hp2 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.163-2617G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635223 | |||||||
chr22:46635223 | G | GAACCGTG others(499): Show |
4 | a0001c0001t0002g0172 a0001c0001t0002g0290 a0001c0001t0002g0293 others(1): Show |
4 | HG01943.hp1 HG02148.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.163-2617_163-2616i others(508): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635223 | |||||||
chr22:46635224 | G | A | 192 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0066 others(189): Show |
196 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.163-2616G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635224 | |||||||
chr22:46635225 | A | ACCGTGTC others(269): Show |
1 | a0001c0001t0004g0017 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.163-2596_163-2595i others(278): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635225 | ||||||
chr22:46635225 | A | G | 21 | a0001c0001t0001g0112 a0001c0001t0001g0255 a0001c0001t0001g0308 others(18): Show |
21 | HG00099.hp1 HG00438.hp1 HG01943.hp1 others(18): Show |
intron_variant | MODIFIER | c.163-2615A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635225 | |||||||
chr22:46635227 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.163-2613C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635227 | |||||||
chr22:46635230 | G | GTCCTCCC others(177): Show |
4 | a0001c0001t0001g0005 a0001c0001t0001g0252 a0001c0001t0001g0254 others(1): Show |
4 | HG01256.hp2 HG01258.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.163-2596_163-2595i others(186): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635230 | ||||||
chr22:46635230 | G | GTCCTCCC others(39): Show |
6 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(3): Show |
6 | HG02723.hp1 HG02809.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.163-2596_163-2595i others(48): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635230 | ||||||
chr22:46635233 | C | T | 27 | a0001c0001t0001g0098 a0001c0001t0004g0061 a0001c0001t0007g0024 others(24): Show |
28 | HG00642.hp2 HG01243.hp1 HG01361.hp2 others(25): Show |
intron_variant | MODIFIER | c.163-2607C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635233 | |||||||
chr22:46635235 | C | G | 1 | a0001c0001t0015g0190 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.163-2605C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635235 | |||||||
chr22:46635242 | C | CCCACCCC others(223): Show |
1 | a0001c0001t0063g0227 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.163-2591_163-2590i others(232): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635242 | ||||||
chr22:46635242 | C | CCCGACCC others(545): Show |
1 | a0001c0001t0001g0153 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.163-2596_163-2595i others(554): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635242 | ||||||
chr22:46635242 | C | T | 66 | a0001c0001t0001g0125 a0001c0001t0001g0160 a0001c0001t0001g0177 others(63): Show |
68 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.163-2598C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635242 | |||||||
chr22:46635244 | C | CG | 3 | a0001c0001t0011g0183 a0001c0001t0011g0184 a0001c0001t0028g0060 |
3 | HG02723.hp2 HG03041.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.163-2596_163-2595i others(3): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635244 | |||||||
chr22:46635244 | C | CGACCCCG others(223): Show |
3 | a0001c0001t0007g0022 a0001c0001t0007g0023 a0001c0001t0013g0020 |
3 | HG01070.hp2 HG03225.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.163-2596_163-2595i others(232): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635244 | |||||||
chr22:46635244 | C | CGACCCCG others(86): Show |
1 | a0001c0001t0001g0074 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.163-2596_163-2595i others(95): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635244 | |||||||
chr22:46635245 | A | ACCCCCAG others(85): Show |
2 | a0001c0001t0002g0171 a0001c0001t0002g0257 |
2 | NA18982.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.163-2591_163-2590i others(94): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635245 | ||||||
chr22:46635245 | A | G | 83 | a0001c0001t0001g0066 a0001c0001t0001g0068 a0001c0001t0001g0072 others(80): Show |
84 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.163-2595A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635245 | |||||||
chr22:46635246 | C | A | 70 | a0001c0001t0001g0066 a0001c0001t0001g0068 a0001c0001t0001g0072 others(67): Show |
71 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.163-2594C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635246 | |||||||
chr22:46635249 | CT | C | 4 | a0001c0001t0001g0074 a0001c0001t0007g0022 a0001c0001t0007g0023 others(1): Show |
4 | HG01070.hp2 HG03225.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.163-2590delT | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635249 | |||||||
chr22:46635250 | T | C | 106 | a0001c0001t0001g0066 a0001c0001t0001g0068 a0001c0001t0001g0072 others(103): Show |
107 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.163-2590T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635250 | |||||||
chr22:46635250 | T | TGGCCACT others(39): Show |
2 | a0001c0001t0002g0317 a0001c0001t0005g0039 |
2 | HG02896.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.163-2571_163-2570i others(48): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635250 | ||||||
chr22:46635251 | G | A | 3 | a0001c0001t0001g0112 a0001c0001t0002g0171 a0001c0001t0002g0257 |
3 | HG00438.hp1 NA18982.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.163-2589G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635251 | |||||||
chr22:46635251 | G | GGCCACTC others(269): Show |
1 | a0001c0001t0002g0312 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.163-2571_163-2570i others(278): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635251 | ||||||
chr22:46635268 | G | GGAACCGT others(224): Show |
1 | a0001c0001t0023g0121 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.163-2571_163-2570i others(233): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635268 | ||||||
chr22:46635269 | G | A | 7 | a0001c0001t0001g0005 a0001c0001t0001g0252 a0001c0001t0001g0254 others(4): Show |
7 | HG01109.hp1 HG01256.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.163-2571G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635269 | |||||||
chr22:46635270 | G | A | 168 | a0001c0001t0001g0003 a0001c0001t0001g0066 a0001c0001t0001g0068 others(165): Show |
172 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.163-2570G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635270 | |||||||
chr22:46635271 | A | ACCGTGTC others(1099): Show |
1 | a0001c0001t0004g0035 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.163-2549_163-2548i others(1108): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635271 | ||||||
chr22:46635271 | A | ACCGTGTC others(131): Show |
10 | a0001c0001t0001g0098 a0001c0002t0004g0002 a0001c0002t0004g0086 others(7): Show |
11 | HG01361.hp2 HG01496.hp2 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.163-2562_163-2561i others(140): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635271 | ||||||
chr22:46635271 | A | G | 8 | a0001c0001t0001g0005 a0001c0001t0001g0252 a0001c0001t0001g0254 others(5): Show |
8 | HG01109.hp1 HG01256.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.163-2569A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635271 | |||||||
chr22:46635273 | C | T | 1 | a0001c0001t0002g0317 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.163-2567C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635273 | |||||||
chr22:46635274 | G | C | 2 | a0001c0001t0001g0252 a0001c0001t0001g0254 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.163-2566G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635274 | |||||||
chr22:46635276 | G | A | 2 | a0001c0001t0001g0252 a0001c0001t0001g0254 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.163-2564G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635276 | |||||||
chr22:46635276 | G | GTCCTCCC others(269): Show |
1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.163-2553_163-2552i others(278): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635276 | ||||||
chr22:46635279 | C | CTCCCTGC others(131): Show |
1 | a0001c0001t0005g0063 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.163-2549_163-2548i others(140): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635279 | ||||||
chr22:46635279 | C | T | 34 | a0001c0001t0002g0209 a0001c0001t0002g0259 a0001c0001t0002g0264 others(31): Show |
34 | HG00140.hp2 HG00323.hp1 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.163-2561C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635279 | |||||||
chr22:46635281 | C | G | 3 | a0001c0001t0005g0213 a0001c0001t0030g0044 a0001c0001t0048g0191 |
3 | HG01433.hp1 HG02735.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.163-2559C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635281 | |||||||
chr22:46635285 | GC | G | 6 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(3): Show |
6 | HG02723.hp1 HG02809.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.163-2550delC | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635285 | ||||||
chr22:46635286 | C | CCCCCACC others(361): Show |
1 | a0001c0007t0019g0182 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.163-2550_163-2549i others(370): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635286 | ||||||
chr22:46635286 | C | T | 3 | a0001c0001t0005g0213 a0001c0001t0030g0044 a0001c0001t0048g0191 |
3 | HG01433.hp1 HG02735.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.163-2554C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635286 | |||||||
chr22:46635288 | C | T | 52 | a0001c0001t0001g0112 a0001c0001t0001g0160 a0001c0001t0001g0196 others(49): Show |
54 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.163-2552C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635288 | |||||||
chr22:46635290 | C | G | 1 | a0001c0001t0015g0190 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.163-2550C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635290 | |||||||
chr22:46635291 | G | A | 129 | a0001c0001t0001g0005 a0001c0001t0001g0066 a0001c0001t0001g0068 others(126): Show |
131 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.163-2549G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635291 | |||||||
chr22:46635291 | G | GACCCCGG others(454): Show |
1 | a0001c0001t0001g0115 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.163-2549_163-2548i others(463): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635291 | |||||||
chr22:46635292 | C | A | 93 | a0001c0001t0001g0003 a0001c0001t0001g0075 a0001c0001t0001g0098 others(90): Show |
96 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.163-2548C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635292 | |||||||
chr22:46635292 | C | CCCCCGGC others(39): Show |
4 | a0001c0001t0001g0177 a0001c0001t0002g0100 a0001c0001t0002g0175 others(1): Show |
4 | NA18955.hp1 NA18962.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.163-2525_163-2524i others(48): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635292 | ||||||
chr22:46635296 | C | CAGCCACT others(315): Show |
1 | a0001c0001t0006g0198 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.163-2544_163-2543i others(324): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635296 | |||||||
chr22:46635296 | C | CAGCCACT others(453): Show |
1 | a0001c0001t0001g0273 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.163-2544_163-2543i others(462): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635296 | |||||||
chr22:46635296 | C | T | 70 | a0001c0001t0001g0005 a0001c0001t0001g0066 a0001c0001t0001g0068 others(67): Show |
70 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.163-2544C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635296 | |||||||
chr22:46635297 | G | A | 3 | a0001c0001t0001g0261 a0001c0001t0001g0271 a0001c0001t0001g0309 |
3 | NA18612.hp1 NA18955.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.163-2543G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635297 | |||||||
chr22:46635314 | G | GA | 3 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0002g0262 |
3 | HG01256.hp2 HG01258.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.163-2526_163-2525i others(3): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635314 | |||||||
chr22:46635315 | G | A | 17 | a0001c0001t0001g0005 a0001c0001t0001g0072 a0001c0001t0001g0074 others(14): Show |
17 | HG01255.hp1 HG01433.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.163-2525G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635315 | |||||||
chr22:46635316 | G | A | 135 | a0001c0001t0001g0066 a0001c0001t0001g0068 a0001c0001t0001g0073 others(132): Show |
136 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.163-2524G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635316 | |||||||
chr22:46635316 | G | GACCGTGT others(85): Show |
1 | a0001c0001t0001g0148 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.163-2504_163-2503i others(94): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635316 | ||||||
chr22:46635316 | G | GACCGTGT others(132): Show |
2 | a0001c0001t0004g0061 a0001c0001t0019g0062 |
2 | HG01884.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.163-2516_163-2515i others(141): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635316 | ||||||
chr22:46635316 | G | GACCGTGT others(39): Show |
1 | a0001c0001t0038g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.163-2516_163-2515i others(48): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635316 | ||||||
chr22:46635317 | A | G | 20 | a0001c0001t0001g0005 a0001c0001t0001g0072 a0001c0001t0001g0074 others(17): Show |
20 | HG01255.hp1 HG01256.hp2 HG01258.hp2 others(17): Show |
intron_variant | MODIFIER | c.163-2523A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635317 | |||||||
chr22:46635322 | G | A | 7 | a0001c0001t0001g0072 a0001c0001t0001g0074 a0001c0001t0001g0116 others(4): Show |
7 | HG03130.hp1 NA18952.hp2 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.163-2518G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635322 | |||||||
chr22:46635322 | G | GTCCTCCC others(85): Show |
1 | a0001c0001t0022g0138 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.163-2504_163-2503i others(94): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635322 | ||||||
chr22:46635322 | G | GTCCTCCC others(223): Show |
1 | a0001c0001t0001g0146 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.163-2504_163-2503i others(232): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635322 | ||||||
chr22:46635325 | C | T | 6 | a0001c0001t0001g0108 a0001c0001t0001g0115 a0001c0001t0003g0250 others(3): Show |
6 | HG02293.hp2 HG02698.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.163-2515C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635325 | |||||||
chr22:46635327 | C | G | 19 | a0001c0001t0002g0209 a0001c0001t0002g0259 a0001c0001t0002g0264 others(16): Show |
19 | HG00140.hp2 HG00323.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.163-2513C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635327 | |||||||
chr22:46635332 | C | T | 19 | a0001c0001t0002g0209 a0001c0001t0002g0259 a0001c0001t0002g0264 others(16): Show |
19 | HG00140.hp2 HG00323.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.163-2508C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635332 | |||||||
chr22:46635334 | C | T | 25 | a0001c0001t0001g0157 a0001c0001t0001g0255 a0001c0001t0001g0261 others(22): Show |
25 | HG00099.hp1 HG00642.hp1 HG01943.hp1 others(22): Show |
intron_variant | MODIFIER | c.163-2506C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635334 | |||||||
chr22:46635337 | A | C | 1 | a0001c0001t0003g0240 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.163-2503A>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635337 | |||||||
chr22:46635337 | A | G | 183 | a0001c0001t0001g0003 a0001c0001t0001g0066 a0001c0001t0001g0068 others(180): Show |
187 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.163-2503A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635337 | |||||||
chr22:46635338 | C | A | 100 | a0001c0001t0001g0066 a0001c0001t0001g0068 a0001c0001t0001g0073 others(97): Show |
102 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.163-2502C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635338 | |||||||
chr22:46635338 | C | CCCCCGGC others(85): Show |
1 | a0001c0001t0001g0103 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.163-2499_163-2498i others(94): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635338 | ||||||
chr22:46635342 | T | C | 199 | a0001c0001t0001g0003 a0001c0001t0001g0066 a0001c0001t0001g0068 others(196): Show |
204 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.163-2498T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635342 | |||||||
chr22:46635342 | T | TGGCCACT others(85): Show |
1 | a0001c0001t0001g0157 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.163-2480_163-2479i others(94): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635342 | ||||||
chr22:46635342 | T | TGGCCACT others(315): Show |
1 | a0001c0001t0003g0229 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.163-2480_163-2479i others(324): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635342 | ||||||
chr22:46635342 | T | TGGCCACT others(85): Show |
8 | a0001c0001t0003g0208 a0001c0001t0003g0214 a0001c0001t0003g0215 others(5): Show |
8 | HG00099.hp2 HG00733.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.163-2480_163-2479i others(94): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635342 | ||||||
chr22:46635342 | T | TGGCCACT others(315): Show |
1 | a0001c0001t0003g0283 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.163-2480_163-2479i others(324): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635342 | ||||||
chr22:46635342 | T | TGGCCACT others(545): Show |
1 | a0001c0001t0001g0261 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.163-2485_163-2484i others(554): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635342 | ||||||
chr22:46635342 | T | TGGCCACT others(361): Show |
2 | a0001c0001t0001g0271 a0001c0001t0001g0309 |
2 | NA18955.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.163-2485_163-2484i others(370): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635342 | ||||||
chr22:46635343 | G | A | 6 | a0001c0002t0004g0032 a0001c0002t0004g0069 a0001c0002t0004g0088 others(3): Show |
6 | HG01891.hp2 HG02647.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.163-2497G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635343 | |||||||
chr22:46635357 | T | TGGGGAAC others(364): Show |
1 | a0001c0001t0004g0036 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.163-2480_163-2479i others(373): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635357 | ||||||
chr22:46635361 | A | AGGCCGTA others(86): Show |
3 | a0001c0001t0001g0127 a0001c0001t0006g0164 a0001c0001t0024g0004 |
4 | HG01069.hp1 HG01071.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.163-2478_163-2477i others(95): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635361 | ||||||
chr22:46635361 | A | AGGCCGTA others(362): Show |
1 | a0001c0001t0001g0126 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.163-2478_163-2477i others(371): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635361 | ||||||
chr22:46635361 | A | AGGCCGTA others(269): Show |
3 | a0001c0001t0002g0278 a0001c0001t0017g0045 a0001c0005t0002g0294 |
3 | HG01952.hp2 HG04115.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.163-2478_163-2477i others(278): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635361 | ||||||
chr22:46635361 | A | G | 232 | a0001c0001t0001g0066 a0001c0001t0001g0068 a0001c0001t0001g0073 others(229): Show |
234 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.163-2479A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635361 | |||||||
chr22:46635362 | G | A | 91 | a0001c0001t0001g0073 a0001c0001t0001g0108 a0001c0001t0001g0112 others(88): Show |
93 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.163-2478G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635362 | |||||||
chr22:46635363 | A | G | 87 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0072 others(84): Show |
90 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.163-2477A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635363 | |||||||
chr22:46635365 | C | T | 3 | a0001c0001t0011g0183 a0001c0001t0011g0184 a0001c0001t0028g0060 |
3 | HG02723.hp2 HG03041.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.163-2475C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635365 | |||||||
chr22:46635366 | G | C | 6 | a0001c0001t0001g0072 a0001c0001t0001g0074 a0001c0001t0001g0116 others(3): Show |
6 | HG02071.hp2 NA18952.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.163-2474G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635366 | |||||||
chr22:46635368 | G | A | 38 | a0001c0001t0001g0003 a0001c0001t0001g0072 a0001c0001t0001g0074 others(35): Show |
39 | HG00099.hp1 HG00642.hp1 HG01255.hp1 others(36): Show |
intron_variant | MODIFIER | c.163-2472G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635368 | |||||||
chr22:46635368 | G | GTCCTCCC others(39): Show |
1 | a0001c0002t0004g0090 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.163-2470_163-2469i others(48): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635368 | ||||||
chr22:46635371 | A | C | 265 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0066 others(262): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.163-2469A>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635371 | |||||||
chr22:46635371 | A | T | 57 | a0001c0001t0001g0115 a0001c0001t0001g0252 a0001c0001t0001g0254 others(54): Show |
57 | HG00323.hp2 HG00738.hp2 HG00741.hp2 others(54): Show |
intron_variant | MODIFIER | c.163-2469A>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635371 | |||||||
chr22:46635373 | C | G | 9 | a0001c0001t0007g0024 a0001c0001t0007g0025 a0001c0001t0007g0026 others(6): Show |
9 | HG00642.hp2 HG01243.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.163-2467C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635373 | |||||||
chr22:46635378 | C | CCCCCGCC others(316): Show |
1 | a0001c0001t0009g0056 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.163-2434_163-2433i others(325): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635378 | ||||||
chr22:46635378 | C | CCCCCGCC others(315): Show |
11 | a0001c0001t0005g0105 a0001c0001t0005g0142 a0001c0001t0005g0144 others(8): Show |
11 | HG00738.hp2 HG01106.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.163-2434_163-2433i others(324): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635378 | ||||||
chr22:46635378 | C | CCCCCGCC others(591): Show |
3 | a0001c0001t0005g0111 a0001c0001t0005g0143 a0001c0001t0050g0147 |
3 | HG02735.hp1 HG03688.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.163-2434_163-2433i others(600): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635378 | ||||||
chr22:46635378 | C | CCCCCGCC others(361): Show |
1 | a0001c0001t0005g0211 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.163-2434_163-2433i others(370): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635378 | ||||||
chr22:46635383 | G | A | 148 | a0001c0001t0001g0003 a0001c0001t0001g0073 a0001c0001t0001g0075 others(145): Show |
153 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.163-2457G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635383 | |||||||
chr22:46635383 | G | GACCCCGG others(85): Show |
2 | a0001c0001t0006g0302 a0001c0001t0032g0046 |
2 | HG02258.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.163-2457_163-2456i others(94): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635383 | |||||||
chr22:46635384 | C | A | 32 | a0001c0001t0001g0112 a0001c0001t0001g0139 a0001c0001t0001g0146 others(29): Show |
32 | HG00438.hp1 HG00673.hp1 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.163-2456C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635384 | |||||||
chr22:46635384 | C | CCCCCGGC others(269): Show |
2 | a0001c0003t0003g0235 a0001c0003t0003g0236 |
2 | HG02109.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.163-2434_163-2433i others(278): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635384 | ||||||
chr22:46635384 | C | CCCCCGGC others(270): Show |
1 | a0001c0001t0014g0058 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.163-2434_163-2433i others(279): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635384 | ||||||
chr22:46635384 | C | CCCCCGGC others(269): Show |
12 | a0001c0001t0003g0030 a0001c0001t0003g0031 a0001c0001t0003g0083 others(9): Show |
12 | HG01243.hp2 HG01891.hp1 HG01943.hp2 others(9): Show |
intron_variant | MODIFIER | c.163-2434_163-2433i others(278): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635384 | ||||||
chr22:46635384 | C | CCCCCGGC others(453): Show |
1 | a0001c0001t0003g0218 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.163-2434_163-2433i others(462): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635384 | ||||||
chr22:46635388 | C | CGGCCACT others(39): Show |
1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.163-2434_163-2433i others(48): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635388 | ||||||
chr22:46635388 | C | CGGCCACT others(39): Show |
2 | a0001c0001t0010g0185 a0001c0001t0020g0232 |
2 | HG01884.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.163-2424_163-2423i others(48): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635388 | ||||||
chr22:46635388 | C | CGGCCACT others(406): Show |
1 | a0001c0001t0003g0212 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.163-2424_163-2423i others(415): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635388 | ||||||
chr22:46635388 | C | T | 138 | a0001c0001t0001g0003 a0001c0001t0001g0073 a0001c0001t0001g0075 others(135): Show |
141 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.163-2452C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635388 | |||||||
chr22:46635389 | G | A | 1 | a0001c0002t0004g0099 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.163-2451G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635389 | |||||||
chr22:46635405 | G | GGAGGCCG others(451): Show |
1 | a0001c0001t0005g0145 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.163-2434_163-2433i others(460): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635405 | ||||||
chr22:46635406 | G | GA | 6 | a0001c0001t0001g0072 a0001c0001t0001g0074 a0001c0001t0001g0116 others(3): Show |
6 | HG02071.hp2 NA18952.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.163-2434_163-2433i others(3): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635406 | |||||||
chr22:46635407 | G | A | 70 | a0001c0001t0001g0003 a0001c0001t0001g0066 a0001c0001t0001g0068 others(67): Show |
71 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.163-2433G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635407 | |||||||
chr22:46635408 | G | A | 54 | a0001c0001t0001g0073 a0001c0001t0001g0075 a0001c0001t0001g0103 others(51): Show |
54 | HG00408.hp1 HG00741.hp2 HG01070.hp2 others(51): Show |
intron_variant | MODIFIER | c.163-2432G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635408 | |||||||
chr22:46635409 | A | G | 77 | a0001c0001t0001g0003 a0001c0001t0001g0066 a0001c0001t0001g0068 others(74): Show |
78 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.163-2431A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635409 | |||||||
chr22:46635412 | G | C | 17 | a0001c0001t0001g0003 a0001c0001t0001g0106 a0001c0001t0001g0113 others(14): Show |
18 | HG01993.hp1 HG02129.hp2 HG02165.hp2 others(15): Show |
intron_variant | MODIFIER | c.163-2428G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635412 | |||||||
chr22:46635414 | G | A | 67 | a0001c0001t0001g0003 a0001c0001t0001g0066 a0001c0001t0001g0068 others(64): Show |
68 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.163-2426G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635414 | |||||||
chr22:46635414 | G | GTCCTCCC others(39): Show |
1 | a0001c0001t0030g0044 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.163-2424_163-2423i others(48): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635414 | ||||||
chr22:46635414 | G | GTCCTCCC others(85): Show |
1 | a0001c0001t0048g0191 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.163-2424_163-2423i others(94): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635414 | ||||||
chr22:46635414 | G | GTCCTCCC others(177): Show |
1 | a0001c0001t0004g0035 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.163-2424_163-2423i others(186): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635414 | ||||||
chr22:46635417 | T | C | 192 | a0001c0001t0001g0003 a0001c0001t0001g0066 a0001c0001t0001g0068 others(189): Show |
194 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.163-2423T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635417 | |||||||
chr22:46635417 | T | TTCCCTGC others(131): Show |
1 | a0001c0001t0005g0041 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.163-2411_163-2410i others(140): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635417 | ||||||
chr22:46635417 | T | TTCCCTGC others(223): Show |
7 | a0001c0001t0002g0286 a0001c0001t0002g0287 a0001c0001t0005g0001 others(4): Show |
8 | HG02615.hp2 HG02818.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.163-2411_163-2410i others(232): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635417 | ||||||
chr22:46635417 | T | TTCCCTGC others(269): Show |
3 | a0001c0001t0002g0007 a0001c0001t0002g0279 a0001c0001t0002g0281 |
4 | HG00639.hp1 HG01256.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.163-2411_163-2410i others(278): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635417 | ||||||
chr22:46635419 | C | G | 19 | a0001c0001t0002g0317 a0001c0001t0003g0030 a0001c0001t0003g0031 others(16): Show |
19 | HG00741.hp2 HG01243.hp2 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.163-2421C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635419 | |||||||
chr22:46635423 | GC | G | 8 | a0001c0001t0007g0024 a0001c0001t0007g0025 a0001c0001t0007g0026 others(5): Show |
8 | HG00642.hp2 HG01243.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.163-2412delC | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635423 | ||||||
chr22:46635424 | C | CCCCCACC others(498): Show |
3 | a0001c0001t0003g0210 a0001c0001t0003g0238 a0001c0001t0003g0239 |
3 | NA18946.hp1 NA18952.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.163-2412_163-2411i others(507): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635424 | ||||||
chr22:46635424 | C | T | 19 | a0001c0001t0002g0317 a0001c0001t0003g0030 a0001c0001t0003g0031 others(16): Show |
19 | HG00741.hp2 HG01243.hp2 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.163-2416C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635424 | |||||||
chr22:46635426 | C | T | 1 | a0001c0001t0001g0273 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.163-2414C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635426 | |||||||
chr22:46635428 | C | G | 1 | a0001c0001t0015g0189 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.163-2412C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635428 | |||||||
chr22:46635429 | G | A | 71 | a0001c0001t0001g0066 a0001c0001t0001g0068 a0001c0001t0001g0072 others(68): Show |
71 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.163-2411G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635429 | |||||||
chr22:46635429 | G | GACCCCGG others(39): Show |
1 | a0001c0002t0046g0089 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.163-2411_163-2410i others(48): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635429 | |||||||
chr22:46635429 | G | GACCCCGG others(177): Show |
1 | a0001c0001t0060g0280 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.163-2411_163-2410i others(186): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635429 | |||||||
chr22:46635429 | G | GACCCCGG others(269): Show |
37 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0002g0081 others(34): Show |
37 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.163-2411_163-2410i others(278): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635429 | |||||||
chr22:46635429 | G | GACCCCGG others(362): Show |
1 | a0001c0001t0006g0195 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.163-2411_163-2410i others(371): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635429 | |||||||
chr22:46635430 | C | A | 21 | a0001c0001t0001g0098 a0001c0001t0001g0103 a0001c0001t0001g0126 others(18): Show |
22 | HG00639.hp2 HG01257.hp2 HG01496.hp2 others(19): Show |
intron_variant | MODIFIER | c.163-2410C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635430 | |||||||
chr22:46635434 | C | CGGCCACT others(315): Show |
1 | a0001c0001t0004g0036 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.163-2388_163-2387i others(324): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635434 | ||||||
chr22:46635434 | C | T | 111 | a0001c0001t0001g0066 a0001c0001t0001g0068 a0001c0001t0001g0080 others(108): Show |
112 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.163-2406C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635434 | |||||||
chr22:46635435 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.163-2405G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635435 | |||||||
chr22:46635449 | T | G | 8 | a0001c0001t0007g0024 a0001c0001t0007g0025 a0001c0001t0007g0026 others(5): Show |
8 | HG00642.hp2 HG01243.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.163-2391T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635449 | |||||||
chr22:46635453 | A | AG | 11 | a0001c0001t0001g0003 a0001c0001t0001g0106 a0001c0001t0001g0113 others(8): Show |
12 | HG01993.hp1 NA18612.hp2 NA18948.hp2 others(9): Show |
intron_variant | MODIFIER | c.163-2385dupG | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635453 | ||||||
chr22:46635453 | A | G | 60 | a0001c0001t0001g0072 a0001c0001t0001g0098 a0001c0001t0001g0116 others(57): Show |
62 | HG00140.hp2 HG00323.hp1 HG00733.hp2 others(59): Show |
intron_variant | MODIFIER | c.163-2387A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635453 | |||||||
chr22:46635454 | G | A | 40 | a0001c0001t0001g0098 a0001c0001t0001g0261 a0001c0001t0001g0271 others(37): Show |
41 | HG00140.hp2 HG00323.hp1 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.163-2386G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635454 | |||||||
chr22:46635454 | G | GACCGTGT others(360): Show |
1 | a0001c0001t0003g0244 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.163-2386_163-2385i others(369): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635454 | |||||||
chr22:46635455 | G | A | 58 | a0001c0001t0001g0072 a0001c0001t0001g0098 a0001c0001t0001g0116 others(55): Show |
60 | HG00140.hp2 HG00323.hp1 HG00733.hp2 others(57): Show |
intron_variant | MODIFIER | c.163-2385G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635455 | |||||||
chr22:46635455 | G | GCCGTGTC others(39): Show |
1 | a0001c0001t0005g0142 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.163-2361_163-2360i others(48): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635455 | ||||||
chr22:46635455 | G | GCTGTATC others(130): Show |
1 | a0001c0002t0004g0090 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.163-2384_163-2383i others(139): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635455 | ||||||
chr22:46635457 | C | T | 5 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0006g0164 others(2): Show |
5 | HG00639.hp2 HG02135.hp2 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.163-2383C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635457 | |||||||
chr22:46635458 | G | C | 38 | a0001c0001t0001g0066 a0001c0001t0001g0068 a0001c0001t0001g0080 others(35): Show |
38 | HG00408.hp2 HG00423.hp1 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.163-2382G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635458 | |||||||
chr22:46635460 | G | A | 123 | a0001c0001t0001g0005 a0001c0001t0001g0066 a0001c0001t0001g0068 others(120): Show |
124 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.163-2380G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635460 | |||||||
chr22:46635463 | C | T | 18 | a0001c0001t0001g0072 a0001c0001t0001g0074 a0001c0001t0001g0116 others(15): Show |
19 | HG01069.hp1 HG01071.hp2 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.163-2377C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635463 | |||||||
chr22:46635465 | C | G | 1 | a0001c0001t0003g0212 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.163-2375C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635465 | |||||||
chr22:46635470 | C | T | 1 | a0001c0001t0003g0212 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.163-2370C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635470 | |||||||
chr22:46635472 | C | CCCACCCC others(85): Show |
1 | a0001c0001t0064g0306 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.163-2342_163-2341i others(94): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635472 | ||||||
chr22:46635472 | C | T | 24 | a0001c0001t0001g0261 a0001c0001t0001g0271 a0001c0001t0001g0309 others(21): Show |
24 | HG00140.hp2 HG00323.hp1 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.163-2368C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635472 | |||||||
chr22:46635474 | C | CG | 3 | a0001c0001t0001g0158 a0001c0001t0015g0190 a0001c0001t0022g0138 |
3 | HG02071.hp2 HG03130.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.163-2366_163-2365i others(3): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635474 | |||||||
chr22:46635475 | A | ACCCCCGG others(315): Show |
1 | a0001c0002t0004g0088 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.163-2361_163-2360i others(324): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635475 | ||||||
chr22:46635475 | A | C | 1 | a0001c0001t0001g0158 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.163-2365A>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635475 | |||||||
chr22:46635475 | A | G | 60 | a0001c0001t0001g0066 a0001c0001t0001g0068 a0001c0001t0001g0072 others(57): Show |
61 | HG00408.hp2 HG00423.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.163-2365A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635475 | |||||||
chr22:46635476 | C | A | 3 | a0001c0001t0001g0074 a0001c0002t0002g0071 a0002c0010t0047g0064 |
3 | HG02886.hp1 HG04115.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.163-2364C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635476 | |||||||
chr22:46635480 | T | C | 164 | a0001c0001t0001g0003 a0001c0001t0001g0066 a0001c0001t0001g0068 others(161): Show |
167 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.163-2360T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635480 | |||||||
chr22:46635480 | T | TGGCCACT others(544): Show |
6 | a0001c0001t0003g0206 a0001c0001t0003g0224 a0001c0001t0003g0225 others(3): Show |
6 | HG00140.hp1 HG00741.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.163-2286_163-2285i others(553): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635480 | ||||||
chr22:46635480 | T | TGGCCACT others(39): Show |
5 | a0001c0001t0001g0098 a0001c0002t0004g0002 a0001c0002t0004g0086 others(2): Show |
6 | HG01496.hp2 HG01934.hp2 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.163-2342_163-2341i others(48): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635480 | ||||||
chr22:46635499 | A | AG | 34 | a0001c0001t0001g0066 a0001c0001t0001g0068 a0001c0001t0001g0080 others(31): Show |
34 | HG00408.hp2 HG00423.hp1 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.163-2339dupG | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635499 | ||||||
chr22:46635499 | A | G | 127 | a0001c0001t0001g0003 a0001c0001t0001g0072 a0001c0001t0001g0106 others(124): Show |
130 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.163-2341A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635499 | |||||||
chr22:46635500 | G | A | 6 | a0001c0001t0004g0036 a0001c0001t0011g0057 a0001c0001t0033g0037 others(3): Show |
6 | HG02622.hp2 HG02886.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.163-2340G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635500 | |||||||
chr22:46635500 | G | GACCGTGT others(85): Show |
1 | a0001c0001t0002g0317 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.163-2340_163-2339i others(94): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635500 | |||||||
chr22:46635501 | G | A | 125 | a0001c0001t0001g0003 a0001c0001t0001g0072 a0001c0001t0001g0106 others(122): Show |
128 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.163-2339G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635501 | |||||||
chr22:46635503 | C | T | 16 | a0001c0001t0001g0074 a0001c0001t0001g0252 a0001c0001t0001g0254 others(13): Show |
16 | HG00140.hp1 HG00741.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.163-2337C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635503 | |||||||
chr22:46635504 | C | G | 223 | a0001c0001t0001g0003 a0001c0001t0001g0066 a0001c0001t0001g0068 others(220): Show |
227 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.163-2336C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635504 | |||||||
chr22:46635506 | A | G | 176 | a0001c0001t0001g0003 a0001c0001t0001g0066 a0001c0001t0001g0068 others(173): Show |
180 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(177): Show |
intron_variant | MODIFIER | c.163-2334A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635506 | |||||||
chr22:46635509 | C | CTCCCTGC others(407): Show |
1 | a0001c0001t0015g0190 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.163-2320_163-2319i others(416): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635509 | ||||||
chr22:46635509 | C | CTCCCTGC others(85): Show |
2 | a0001c0001t0002g0286 a0001c0001t0002g0287 |
2 | NA18964.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.163-2320_163-2319i others(94): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635509 | ||||||
chr22:46635509 | C | CTCCCTGC others(85): Show |
1 | a0001c0001t0033g0037 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.163-2320_163-2319i others(94): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635509 | ||||||
chr22:46635509 | C | CTCCCTGC others(177): Show |
5 | a0001c0002t0004g0032 a0001c0002t0004g0069 a0001c0002t0004g0092 others(2): Show |
5 | HG01891.hp2 HG02647.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.163-2319_163-2318i others(186): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635509 | ||||||
chr22:46635509 | C | CTCCCTGC others(821): Show |
1 | a0001c0001t0015g0189 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.163-2319_163-2318i others(830): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635509 | ||||||
chr22:46635509 | C | CTCCCTGC others(39): Show |
1 | a0001c0002t0004g0099 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.163-2296_163-2295i others(48): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635509 | ||||||
chr22:46635509 | C | CTCCCTGC others(543): Show |
1 | a0001c0001t0003g0205 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.163-2321_163-2320i others(552): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635509 | ||||||
chr22:46635509 | C | CTCCCTGC others(543): Show |
2 | a0001c0001t0003g0104 a0001c0001t0003g0169 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.163-2321_163-2320i others(552): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635509 | ||||||
chr22:46635509 | C | T | 108 | a0001c0001t0001g0003 a0001c0001t0001g0072 a0001c0001t0001g0106 others(105): Show |
111 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.163-2331C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635509 | |||||||
chr22:46635515 | GC | G | 8 | a0001c0001t0007g0024 a0001c0001t0007g0025 a0001c0001t0007g0026 others(5): Show |
8 | HG00642.hp2 HG01243.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.163-2320delC | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635515 | ||||||
chr22:46635516 | C | CCCCCACC others(177): Show |
1 | a0001c0001t0010g0185 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.163-2320_163-2319i others(186): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635516 | ||||||
chr22:46635516 | C | CCCCCACC others(131): Show |
2 | a0001c0001t0010g0186 a0001c0001t0010g0187 |
2 | HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.163-2320_163-2319i others(140): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635516 | ||||||
chr22:46635516 | C | CCCCCGCC others(774): Show |
1 | a0001c0001t0003g0214 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.163-2286_163-2285i others(783): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635516 | ||||||
chr22:46635516 | C | CCCCCGCC others(774): Show |
2 | a0001c0001t0003g0208 a0001c0001t0003g0215 |
2 | HG00099.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.163-2286_163-2285i others(783): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635516 | ||||||
chr22:46635521 | G | A | 84 | a0001c0001t0001g0066 a0001c0001t0001g0068 a0001c0001t0001g0074 others(81): Show |
85 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.163-2319G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635521 | |||||||
chr22:46635522 | C | A | 1 | a0001c0001t0011g0057 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.163-2318C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635522 | |||||||
chr22:46635523 | C | T | 1 | a0001c0001t0054g0251 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.163-2317C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635523 | |||||||
chr22:46635526 | C | CGGCCACT others(498): Show |
4 | a0001c0001t0003g0245 a0001c0001t0014g0052 a0001c0001t0018g0230 others(1): Show |
4 | HG00733.hp1 HG02486.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.163-2286_163-2285i others(507): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635526 | ||||||
chr22:46635526 | C | CGGCCACT others(361): Show |
1 | a0001c0001t0005g0039 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.163-2296_163-2295i others(370): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635526 | ||||||
chr22:46635526 | C | T | 43 | a0001c0001t0001g0123 a0001c0001t0001g0154 a0001c0001t0001g0252 others(40): Show |
44 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.163-2314C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635526 | |||||||
chr22:46635527 | G | A | 1 | a0001c0001t0054g0251 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.163-2313G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635527 | |||||||
chr22:46635533 | T | C | 1 | a0001c0001t0054g0251 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.163-2307T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635533 | |||||||
chr22:46635541 | T | A | 1 | a0001c0001t0054g0251 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.163-2299T>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635541 | |||||||
chr22:46635541 | T | G | 8 | a0001c0001t0007g0024 a0001c0001t0007g0025 a0001c0001t0007g0026 others(5): Show |
8 | HG00642.hp2 HG01243.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.163-2299T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635541 | |||||||
chr22:46635545 | A | AG | 32 | a0001c0001t0001g0005 a0001c0001t0001g0073 a0001c0001t0001g0075 others(29): Show |
32 | HG00438.hp1 HG00673.hp1 HG01192.hp2 others(29): Show |
intron_variant | MODIFIER | c.163-2293dupG | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635545 | ||||||
chr22:46635545 | A | G | 130 | a0001c0001t0001g0003 a0001c0001t0001g0066 a0001c0001t0001g0068 others(127): Show |
134 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.163-2295A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635545 | |||||||
chr22:46635546 | G | A | 3 | a0001c0001t0011g0057 a0001c0001t0054g0251 a0002c0010t0047g0064 |
3 | HG02647.hp2 HG02886.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.163-2294G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635546 | |||||||
chr22:46635547 | G | A | 129 | a0001c0001t0001g0003 a0001c0001t0001g0066 a0001c0001t0001g0068 others(126): Show |
133 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.163-2293G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635547 | |||||||
chr22:46635547 | G | GCCGTATC others(177): Show |
1 | a0001c0001t0043g0311 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.163-2289_163-2288i others(186): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635547 | ||||||
chr22:46635547 | G | GCCGTATC others(131): Show |
2 | a0001c0001t0001g0261 a0001c0001t0006g0302 |
2 | NA18612.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.163-2289_163-2288i others(140): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635547 | ||||||
chr22:46635547 | G | GCTGTATC others(498): Show |
1 | a0001c0002t0004g0088 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.163-2292_163-2291i others(507): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635547 | ||||||
chr22:46635547 | G | GGCCGTGT others(40): Show |
1 | a0001c0001t0023g0121 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.163-2293_163-2292i others(49): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635547 | |||||||
chr22:46635549 | C | CGTATCCT others(85): Show |
1 | a0001c0001t0009g0054 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.163-2289_163-2288i others(94): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635549 | ||||||
chr22:46635549 | C | T | 34 | a0001c0001t0003g0030 a0001c0001t0003g0031 a0001c0001t0003g0083 others(31): Show |
35 | HG01069.hp1 HG01070.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.163-2291C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635549 | |||||||
chr22:46635550 | G | C | 10 | a0001c0001t0001g0074 a0001c0001t0001g0123 a0001c0001t0001g0154 others(7): Show |
10 | HG00408.hp1 HG02451.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.163-2290G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635550 | |||||||
chr22:46635552 | G | A | 43 | a0001c0001t0001g0074 a0001c0001t0001g0123 a0001c0001t0001g0154 others(40): Show |
44 | HG00408.hp1 HG00735.hp2 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.163-2288G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635552 | |||||||
chr22:46635552 | G | GTCCTCCC others(361): Show |
1 | a0001c0007t0019g0182 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.163-2274_163-2273i others(370): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635552 | ||||||
chr22:46635552 | G | GTCTTCCC others(590): Show |
1 | a0001c0001t0003g0221 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.163-2286_163-2285i others(599): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635552 | ||||||
chr22:46635552 | G | GTCTTCCC others(498): Show |
12 | a0001c0001t0001g0220 a0001c0001t0003g0006 a0001c0001t0003g0207 others(9): Show |
12 | HG01255.hp2 HG02027.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.163-2286_163-2285i others(507): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635552 | ||||||
chr22:46635552 | G | GTCTTCCC others(589): Show |
1 | a0001c0001t0003g0244 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.163-2286_163-2285i others(598): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635552 | ||||||
chr22:46635552 | G | GTCTTCCC others(681): Show |
1 | a0001c0001t0003g0283 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.163-2286_163-2285i others(690): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635552 | ||||||
chr22:46635555 | C | CTCCCTGC others(178): Show |
1 | a0001c0001t0002g0274 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.163-2274_163-2273i others(187): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635555 | ||||||
chr22:46635555 | C | CTCCCTGC others(85): Show |
2 | a0001c0001t0001g0271 a0001c0001t0001g0273 |
2 | HG02027.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.163-2274_163-2273i others(94): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635555 | ||||||
chr22:46635555 | C | CTCCCTGC others(85): Show |
1 | a0001c0001t0001g0309 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.163-2250_163-2249i others(94): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635555 | ||||||
chr22:46635555 | C | T | 140 | a0001c0001t0001g0003 a0001c0001t0001g0066 a0001c0001t0001g0068 others(137): Show |
144 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.163-2285C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635555 | |||||||
chr22:46635557 | C | G | 1 | a0001c0001t0005g0063 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.163-2283C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635557 | |||||||
chr22:46635561 | GC | G | 8 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0008g0008 others(5): Show |
8 | HG01256.hp2 HG01258.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.163-2274delC | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635561 | ||||||
chr22:46635562 | C | CCCCCACC others(84): Show |
3 | a0001c0001t0007g0022 a0001c0001t0007g0023 a0001c0001t0013g0020 |
3 | HG01070.hp2 HG03225.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.163-2274_163-2273i others(93): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635562 | ||||||
chr22:46635562 | C | CCCCGCCC others(589): Show |
1 | a0001c0001t0003g0240 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.163-2275_163-2274i others(598): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635562 | ||||||
chr22:46635567 | G | A | 137 | a0001c0001t0001g0005 a0001c0001t0001g0073 a0001c0001t0001g0075 others(134): Show |
138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.163-2273G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635567 | |||||||
chr22:46635567 | GCCCCCGG others(37): Show |
G | 1 | a0001c0001t0010g0034 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.163-2272_163-2229d others(46): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635567 | |||||||
chr22:46635568 | C | A | 1 | a0001c0001t0011g0057 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.163-2272C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635568 | |||||||
chr22:46635572 | C | CCGGCCAC others(40): Show |
1 | a0001c0002t0004g0070 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.163-2268_163-2267i others(49): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635572 | |||||||
chr22:46635572 | C | CGGCCACT others(85): Show |
1 | a0001c0001t0009g0056 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.163-2240_163-2239i others(94): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635572 | ||||||
chr22:46635572 | C | CGGCCACT others(39): Show |
18 | a0001c0001t0001g0098 a0001c0001t0005g0105 a0001c0001t0005g0111 others(15): Show |
19 | HG01106.hp1 HG01168.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.163-2246_163-2245i others(48): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635572 | ||||||
chr22:46635572 | C | CGGCCACT others(269): Show |
1 | a0001c0001t0017g0043 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.163-2246_163-2245i others(278): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635572 | ||||||
chr22:46635572 | C | CGGCCACT others(315): Show |
2 | a0001c0001t0005g0213 a0001c0001t0020g0232 |
2 | HG02735.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.163-2250_163-2249i others(324): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635572 | ||||||
chr22:46635572 | C | CGGCCACT others(85): Show |
4 | a0001c0001t0003g0210 a0001c0001t0003g0238 a0001c0001t0003g0239 others(1): Show |
4 | HG02965.hp2 NA18946.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.163-2250_163-2249i others(94): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635572 | ||||||
chr22:46635572 | C | CGGCCACT others(177): Show |
1 | a0001c0001t0048g0191 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.163-2250_163-2249i others(186): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635572 | ||||||
chr22:46635572 | C | CGGCCACT others(177): Show |
1 | a0001c0001t0001g0115 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.163-2250_163-2249i others(186): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635572 | ||||||
chr22:46635572 | C | CGGCCACT others(131): Show |
1 | a0001c0001t0001g0126 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.163-2250_163-2249i others(140): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635572 | ||||||
chr22:46635572 | C | CGGCCACT others(177): Show |
3 | a0001c0001t0005g0001 a0001c0001t0005g0040 a0001c0001t0049g0042 |
4 | HG02615.hp2 HG02818.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.163-2250_163-2249i others(186): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635572 | ||||||
chr22:46635572 | C | T | 61 | a0001c0001t0001g0072 a0001c0001t0001g0116 a0001c0001t0001g0179 others(58): Show |
62 | HG00733.hp1 HG00735.hp2 HG01069.hp1 others(59): Show |
intron_variant | MODIFIER | c.163-2268C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635572 | |||||||
chr22:46635575 | C | G | 1 | a0001c0001t0038g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.163-2265C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635575 | |||||||
chr22:46635587 | T | G | 3 | a0001c0001t0007g0022 a0001c0001t0007g0023 a0001c0001t0013g0020 |
3 | HG01070.hp2 HG03225.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.163-2253T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635587 | |||||||
chr22:46635589 | G | GGGAACCG others(267): Show |
1 | a0001c0001t0005g0041 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.163-2250_163-2249i others(276): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635589 | ||||||
chr22:46635591 | A | G | 207 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0066 others(204): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.163-2249A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635591 | |||||||
chr22:46635592 | G | A | 4 | a0001c0001t0004g0021 a0001c0001t0011g0057 a0001c0001t0015g0189 others(1): Show |
4 | HG02258.hp2 HG03130.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.163-2248G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635592 | |||||||
chr22:46635593 | G | A | 205 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0066 others(202): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.163-2247G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635593 | |||||||
chr22:46635593 | G | GCCGTATC others(131): Show |
3 | a0001c0001t0008g0013 a0001c0001t0008g0014 a0001c0001t0008g0016 |
3 | HG02976.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.163-2243_163-2242i others(140): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635593 | ||||||
chr22:46635595 | C | T | 4 | a0001c0001t0001g0072 a0001c0001t0001g0116 a0001c0001t0001g0179 others(1): Show |
4 | HG02572.hp2 NA18952.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.163-2245C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635595 | |||||||
chr22:46635598 | G | A | 4 | a0001c0001t0001g0072 a0001c0001t0001g0116 a0001c0001t0001g0179 others(1): Show |
4 | HG02572.hp2 NA18952.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.163-2242G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635598 | |||||||
chr22:46635601 | T | C | 26 | a0001c0001t0001g0072 a0001c0001t0001g0115 a0001c0001t0001g0116 others(23): Show |
27 | HG00408.hp1 HG00639.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.163-2239T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635601 | |||||||
chr22:46635601 | T | TTCCCTGC others(39): Show |
1 | a0001c0001t0004g0233 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.163-2229_163-2228i others(48): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635601 | ||||||
chr22:46635603 | C | G | 1 | a0001c0001t0004g0021 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.163-2237C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635603 | |||||||
chr22:46635607 | G | GC | 123 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0066 others(120): Show |
124 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.163-2229dupC | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635607 | ||||||
chr22:46635607 | G | GCCCCCGA others(224): Show |
1 | a0001c0001t0001g0157 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.163-2229_163-2228i others(233): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635607 | ||||||
chr22:46635607 | G | GCCCCCGA others(178): Show |
2 | a0001c0001t0001g0112 a0001c0001t0001g0146 |
2 | HG00438.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.163-2229_163-2228i others(187): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635607 | ||||||
chr22:46635607 | G | GCCCCCGA others(86): Show |
1 | a0001c0001t0004g0017 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.163-2229_163-2228i others(95): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635607 | ||||||
chr22:46635612 | G | A | 19 | a0001c0001t0001g0072 a0001c0001t0001g0116 a0001c0001t0001g0123 others(16): Show |
19 | HG00408.hp1 HG00735.hp2 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.163-2228G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635612 | |||||||
chr22:46635617 | C | T | 22 | a0001c0001t0001g0003 a0001c0001t0001g0072 a0001c0001t0001g0106 others(19): Show |
24 | HG01993.hp1 HG02615.hp2 HG02818.hp2 others(21): Show |
intron_variant | MODIFIER | c.163-2223C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635617 | |||||||
chr22:46635618 | G | A | 9 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(6): Show |
9 | HG01361.hp1 HG02647.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.163-2222G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635618 | |||||||
chr22:46635618 | G | GGCCACTC others(222): Show |
1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.163-2195_163-2194i others(231): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635618 | ||||||
chr22:46635624 | T | C | 1 | a0001c0001t0054g0251 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.163-2216T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635624 | |||||||
chr22:46635632 | T | G | 9 | a0001c0001t0005g0063 a0001c0001t0007g0024 a0001c0001t0007g0025 others(6): Show |
9 | HG00642.hp2 HG01243.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.163-2208T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635632 | |||||||
chr22:46635635 | G | A | 9 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(6): Show |
9 | HG02572.hp2 HG02647.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.163-2205G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635635 | |||||||
chr22:46635635 | G | GGGCCCGT others(85): Show |
1 | a0001c0002t0004g0086 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.163-2203_163-2202i others(94): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635635 | ||||||
chr22:46635636 | G | A | 32 | a0001c0001t0001g0003 a0001c0001t0001g0072 a0001c0001t0001g0106 others(29): Show |
33 | HG00323.hp2 HG00642.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.163-2204G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635636 | |||||||
chr22:46635637 | G | A | 2 | a0001c0001t0011g0057 a0002c0010t0047g0064 |
2 | HG02886.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.163-2203G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635637 | |||||||
chr22:46635637 | GACCGTGT others(39): Show |
G | 1 | a0001c0001t0031g0059 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.163-2202_163-2157d others(48): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635637 | |||||||
chr22:46635638 | A | G | 31 | a0001c0001t0001g0003 a0001c0001t0001g0072 a0001c0001t0001g0106 others(28): Show |
32 | HG00323.hp2 HG00642.hp2 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.163-2202A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635638 | |||||||
chr22:46635640 | C | CGTGTCCT others(39): Show |
2 | a0001c0001t0004g0035 a0001c0001t0010g0186 |
2 | HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.163-2181_163-2180i others(48): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635640 | ||||||
chr22:46635640 | C | CGTGTCCT others(85): Show |
1 | a0001c0002t0004g0117 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.163-2181_163-2180i others(94): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635640 | ||||||
chr22:46635640 | C | CGTGTCCT others(85): Show |
8 | a0001c0001t0001g0098 a0001c0002t0002g0071 a0001c0002t0004g0002 others(5): Show |
9 | HG01361.hp2 HG01496.hp2 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.163-2181_163-2180i others(94): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635640 | ||||||
chr22:46635640 | C | CGTGTCCT others(268): Show |
1 | a0001c0001t0004g0021 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.163-2181_163-2180i others(277): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635640 | ||||||
chr22:46635640 | C | CGTGTCCT others(40): Show |
2 | a0001c0001t0004g0036 a0001c0001t0033g0037 |
2 | HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.163-2183_163-2182i others(49): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635640 | ||||||
chr22:46635640 | C | CGTGTCTT others(590): Show |
2 | a0001c0001t0004g0061 a0001c0001t0019g0062 |
2 | HG01884.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.163-2195_163-2194i others(599): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635640 | ||||||
chr22:46635640 | C | CGTGTCTT others(130): Show |
1 | a0001c0001t0038g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.163-2195_163-2194i others(139): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635640 | ||||||
chr22:46635640 | C | CT | 77 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0255 others(74): Show |
79 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.163-2200_163-2199i others(3): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635640 | |||||||
chr22:46635640 | C | CTGTGTCC others(132): Show |
1 | a0001c0001t0005g0188 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.163-2200_163-2199i others(141): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635640 | |||||||
chr22:46635640 | C | T | 31 | a0001c0001t0001g0003 a0001c0001t0001g0106 a0001c0001t0001g0113 others(28): Show |
33 | HG00639.hp2 HG01069.hp1 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.163-2200C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635640 | |||||||
chr22:46635643 | G | A | 15 | a0001c0001t0001g0003 a0001c0001t0001g0106 a0001c0001t0001g0113 others(12): Show |
16 | HG01993.hp1 HG02451.hp1 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.163-2197G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635643 | |||||||
chr22:46635646 | C | T | 96 | a0001c0001t0001g0005 a0001c0001t0001g0066 a0001c0001t0001g0068 others(93): Show |
96 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.163-2194C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635646 | |||||||
chr22:46635652 | GC | G | 5 | a0001c0001t0001g0072 a0001c0001t0001g0116 a0001c0001t0001g0179 others(2): Show |
5 | HG01109.hp1 HG02293.hp2 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.163-2183delC | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635652 | ||||||
chr22:46635655 | C | T | 1 | a0001c0001t0011g0057 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.163-2185C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635655 | |||||||
chr22:46635658 | A | G | 99 | a0001c0001t0001g0005 a0001c0001t0001g0066 a0001c0001t0001g0068 others(96): Show |
99 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.163-2182A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635658 | |||||||
chr22:46635660 | T | C | 133 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0066 others(130): Show |
134 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.163-2180T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635660 | |||||||
chr22:46635663 | C | T | 62 | a0001c0001t0001g0003 a0001c0001t0001g0066 a0001c0001t0001g0068 others(59): Show |
63 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.163-2177C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635663 | |||||||
chr22:46635664 | A | G | 127 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0066 others(124): Show |
128 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.163-2176A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635664 | |||||||
chr22:46635670 | C | T | 133 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0066 others(130): Show |
134 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.163-2170C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635670 | |||||||
chr22:46635678 | A | G | 1 | a0001c0001t0002g0264 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.163-2162A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635678 | |||||||
chr22:46635678 | A | T | 130 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0066 others(127): Show |
131 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.163-2162A>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635678 | |||||||
chr22:46635681 | G | A | 1 | a0001c0001t0004g0233 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.163-2159G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635681 | |||||||
chr22:46635682 | G | A | 64 | a0001c0001t0001g0003 a0001c0001t0001g0066 a0001c0001t0001g0068 others(61): Show |
65 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.163-2158G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635682 | |||||||
chr22:46635683 | A | G | 117 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0066 others(114): Show |
118 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.163-2157A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635683 | |||||||
chr22:46635684 | G | A | 66 | a0001c0001t0001g0005 a0001c0001t0001g0073 a0001c0001t0001g0075 others(63): Show |
66 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.163-2156G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635684 | |||||||
chr22:46635684 | G | C | 1 | a0001c0001t0002g0264 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.163-2156G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635684 | |||||||
chr22:46635686 | T | C | 79 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0073 others(76): Show |
80 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.163-2154T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635686 | |||||||
chr22:46635689 | G | A | 50 | a0001c0001t0001g0005 a0001c0001t0001g0066 a0001c0001t0001g0068 others(47): Show |
50 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.163-2151G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635689 | |||||||
chr22:46635692 | C | T | 47 | a0001c0001t0001g0073 a0001c0001t0001g0075 a0001c0001t0001g0103 others(44): Show |
47 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.163-2148C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635692 | |||||||
chr22:46635698 | GCT | G | 34 | a0001c0001t0001g0003 a0001c0001t0001g0106 a0001c0001t0001g0113 others(31): Show |
35 | HG00140.hp2 HG00323.hp1 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.163-2140_163-2139d others(4): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635698 | ||||||
chr22:46635699 | C | CCCCCGCC others(905): Show |
1 | a0001c0001t0005g0063 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.163-2141_163-2140i others(914): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635699 | |||||||
chr22:46635699 | C | CCCCCGCC others(676): Show |
1 | a0001c0001t0007g0022 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.163-2141_163-2140i others(685): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635699 | |||||||
chr22:46635699 | C | CCCCCGCC others(905): Show |
1 | a0001c0001t0013g0020 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.163-2141_163-2140i others(914): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635699 | |||||||
chr22:46635699 | C | CCCCCGCC others(265): Show |
8 | a0001c0001t0007g0024 a0001c0001t0007g0025 a0001c0001t0007g0026 others(5): Show |
8 | HG00642.hp2 HG01243.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.163-2141_163-2140i others(274): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635699 | |||||||
chr22:46635699 | C | CCCCCGCC others(38): Show |
1 | a0001c0001t0038g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.163-2141_163-2140i others(47): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635699 | |||||||
chr22:46635699 | CT | C | 92 | a0001c0001t0001g0005 a0001c0001t0001g0066 a0001c0001t0001g0068 others(89): Show |
92 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.163-2140delT | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635699 | |||||||
chr22:46635700 | T | C | 2 | a0001c0001t0003g0226 a0001c0001t0038g0180 |
2 | HG01255.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.163-2140T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635700 | |||||||
chr22:46635700 | T | G | 11 | a0001c0001t0005g0063 a0001c0001t0007g0022 a0001c0001t0007g0024 others(8): Show |
11 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.163-2140T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635700 | |||||||
chr22:46635702 | C | T | 1 | a0001c0001t0011g0057 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.163-2138C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635702 | |||||||
chr22:46635705 | A | G | 72 | a0001c0001t0001g0003 a0001c0001t0001g0073 a0001c0001t0001g0075 others(69): Show |
73 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.163-2135A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635705 | |||||||
chr22:46635707 | C | T | 5 | a0001c0001t0001g0179 a0001c0001t0002g0264 a0001c0001t0004g0233 others(2): Show |
5 | HG01109.hp1 HG02056.hp2 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.163-2133C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635707 | |||||||
chr22:46635710 | T | C | 51 | a0001c0001t0001g0003 a0001c0001t0001g0106 a0001c0001t0001g0113 others(48): Show |
52 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.163-2130T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635710 | |||||||
chr22:46635711 | G | A | 10 | a0001c0001t0001g0179 a0001c0001t0002g0264 a0001c0001t0004g0233 others(7): Show |
10 | HG01109.hp1 HG01891.hp2 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.163-2129G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635711 | |||||||
chr22:46635712 | A | G | 124 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0066 others(121): Show |
125 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.163-2128A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635712 | |||||||
chr22:46635717 | T | C | 5 | a0001c0001t0001g0179 a0001c0001t0002g0264 a0001c0001t0004g0233 others(2): Show |
5 | HG01109.hp1 HG02056.hp2 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.163-2123T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635717 | |||||||
chr22:46635725 | T | A | 5 | a0001c0001t0001g0179 a0001c0001t0002g0264 a0001c0001t0004g0233 others(2): Show |
5 | HG01109.hp1 HG02056.hp2 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.163-2115T>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635725 | |||||||
chr22:46635728 | G | A | 5 | a0001c0002t0004g0032 a0001c0002t0004g0069 a0001c0002t0004g0092 others(2): Show |
5 | HG01891.hp2 HG02647.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.163-2112G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635728 | |||||||
chr22:46635728 | G | GA | 24 | a0001c0001t0001g0005 a0001c0001t0001g0073 a0001c0001t0001g0075 others(21): Show |
24 | HG00673.hp1 HG01192.hp2 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.163-2112_163-2111i others(3): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635728 | |||||||
chr22:46635729 | G | A | 53 | a0001c0001t0001g0066 a0001c0001t0001g0068 a0001c0001t0001g0074 others(50): Show |
53 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.163-2111G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635729 | |||||||
chr22:46635730 | G | A | 7 | a0001c0001t0001g0179 a0001c0001t0002g0264 a0001c0001t0004g0233 others(4): Show |
7 | HG01109.hp1 HG02056.hp2 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.163-2110G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635730 | |||||||
chr22:46635731 | C | A | 40 | a0001c0001t0001g0003 a0001c0001t0001g0106 a0001c0001t0001g0113 others(37): Show |
41 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(38): Show |
intron_variant | MODIFIER | c.163-2109C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635731 | |||||||
chr22:46635731 | C | CTGTATCC others(313): Show |
1 | a0001c0001t0023g0122 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.163-2109_163-2108i others(322): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635731 | |||||||
chr22:46635731 | C | CTGTATCC others(129): Show |
1 | a0001c0001t0001g0149 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.163-2109_163-2108i others(138): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635731 | |||||||
chr22:46635731 | C | CTGTATCC others(130): Show |
1 | a0001c0001t0001g0073 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.163-2109_163-2108i others(139): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635731 | |||||||
chr22:46635731 | C | CTGTATCC others(129): Show |
16 | a0001c0001t0001g0075 a0001c0001t0001g0103 a0001c0001t0001g0148 others(13): Show |
16 | HG00673.hp1 HG01361.hp1 HG02071.hp2 others(13): Show |
intron_variant | MODIFIER | c.163-2109_163-2108i others(138): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635731 | |||||||
chr22:46635731 | C | CTGTATCC others(358): Show |
1 | a0001c0001t0001g0150 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.163-2109_163-2108i others(367): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635731 | |||||||
chr22:46635731 | C | G | 60 | a0001c0001t0001g0066 a0001c0001t0001g0068 a0001c0001t0001g0074 others(57): Show |
60 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.163-2109C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635731 | |||||||
chr22:46635733 | C | CGTGTCTT others(222): Show |
1 | a0001c0001t0001g0123 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.163-2102_163-2101i others(231): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635733 | ||||||
chr22:46635733 | C | CGTGTCTT others(175): Show |
2 | a0001c0002t0004g0091 a0001c0002t0004g0096 |
2 | HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.163-2102_163-2101i others(184): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635733 | ||||||
chr22:46635733 | C | CGTGTCTT others(84): Show |
3 | a0001c0001t0008g0013 a0001c0001t0008g0014 a0001c0001t0008g0016 |
3 | HG02976.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.163-2102_163-2101i others(93): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635733 | ||||||
chr22:46635733 | C | CGTGTCTT others(85): Show |
2 | a0001c0001t0056g0313 a0001c0009t0062g0303 |
2 | HG00735.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.163-2102_163-2101i others(94): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635733 | ||||||
chr22:46635733 | C | CGTGTCTT others(84): Show |
3 | a0001c0001t0011g0183 a0001c0001t0011g0184 a0001c0001t0028g0060 |
3 | HG02723.hp2 HG03041.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.163-2102_163-2101i others(93): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635733 | ||||||
chr22:46635733 | C | CTATCCTC others(683): Show |
2 | a0001c0001t0001g0005 a0001c0001t0012g0005 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.163-2107_163-2106i others(692): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635733 | |||||||
chr22:46635733 | C | CTGTGTCC others(40): Show |
16 | a0001c0001t0002g0209 a0001c0001t0002g0259 a0001c0001t0002g0266 others(13): Show |
16 | HG00140.hp2 HG00323.hp1 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.163-2107_163-2106i others(49): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635733 | |||||||
chr22:46635733 | C | T | 42 | a0001c0001t0001g0003 a0001c0001t0001g0073 a0001c0001t0001g0075 others(39): Show |
43 | HG00673.hp1 HG01109.hp1 HG01192.hp2 others(40): Show |
intron_variant | MODIFIER | c.163-2107C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635733 | |||||||
chr22:46635736 | G | A | 1 | a0001c0001t0003g0250 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.163-2104G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635736 | |||||||
chr22:46635739 | C | T | 1 | a0001c0001t0001g0154 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.163-2101C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635739 | |||||||
chr22:46635746 | C | CCCCCCGC others(39): Show |
1 | a0001c0001t0002g0282 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.163-2088_163-2043d others(48): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635746 | ||||||
chr22:46635747 | C | CCCCACTC others(590): Show |
1 | a0001c0001t0004g0017 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.163-2090_163-2089i others(599): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635747 | ||||||
chr22:46635747 | C | CCCCACTC others(39): Show |
18 | a0001c0001t0001g0003 a0001c0001t0001g0106 a0001c0001t0001g0113 others(15): Show |
19 | HG01891.hp2 HG01993.hp1 HG02647.hp1 others(16): Show |
intron_variant | MODIFIER | c.163-2090_163-2089i others(48): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635747 | ||||||
chr22:46635747 | C | CCCCCGCC others(642): Show |
1 | a0001c0001t0058g0277 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.163-2068_163-2067i others(651): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635747 | ||||||
chr22:46635747 | C | CCCCGACC others(683): Show |
1 | a0001c0001t0011g0057 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.163-2090_163-2089i others(692): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635747 | ||||||
chr22:46635747 | C | CCCCGACC others(630): Show |
1 | a0001c0001t0007g0023 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.163-2090_163-2089i others(639): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635747 | ||||||
chr22:46635747 | C | CCCCGCCC others(683): Show |
1 | a0002c0010t0047g0064 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.163-2090_163-2089i others(692): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635747 | ||||||
chr22:46635747 | C | CCCCGCCC others(131): Show |
1 | a0001c0001t0054g0251 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.163-2090_163-2089i others(140): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635747 | ||||||
chr22:46635747 | C | CCCGCCCC others(85): Show |
8 | a0001c0001t0001g0087 a0001c0001t0001g0129 a0001c0001t0001g0130 others(5): Show |
8 | HG01081.hp1 HG01257.hp1 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.163-2091_163-2090i others(94): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635747 | ||||||
chr22:46635747 | C | CCCGCCCC others(84): Show |
34 | a0001c0001t0001g0066 a0001c0001t0001g0068 a0001c0001t0001g0074 others(31): Show |
34 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(31): Show |
intron_variant | MODIFIER | c.163-2091_163-2090i others(93): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635747 | ||||||
chr22:46635747 | C | CCCGCCCC others(85): Show |
1 | a0001c0001t0001g0137 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.163-2091_163-2090i others(94): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635747 | ||||||
chr22:46635747 | C | T | 52 | a0001c0001t0001g0005 a0001c0001t0001g0073 a0001c0001t0001g0075 others(49): Show |
52 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.163-2093C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635747 | |||||||
chr22:46635752 | G | A | 119 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0066 others(116): Show |
120 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.163-2088G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635752 | |||||||
chr22:46635752 | GCCCCTGG others(40): Show |
G | 2 | a0001c0001t0001g0072 a0001c0001t0001g0116 |
2 | NA18952.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.163-2083_163-2037d others(49): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635752 | ||||||
chr22:46635757 | T | C | 1 | a0001c0001t0031g0059 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.163-2083T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635757 | |||||||
chr22:46635759 | G | A | 119 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0066 others(116): Show |
121 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.163-2081G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635759 | |||||||
chr22:46635773 | A | G | 121 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0066 others(118): Show |
123 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.163-2067A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635773 | |||||||
chr22:46635776 | T | A | 2 | a0001c0001t0001g0154 a0001c0001t0003g0250 |
2 | HG02698.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.163-2064T>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635776 | |||||||
chr22:46635776 | T | G | 119 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0066 others(116): Show |
121 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.163-2064T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635776 | |||||||
chr22:46635778 | G | C | 119 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0066 others(116): Show |
121 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.163-2062G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635778 | |||||||
chr22:46635778 | G | GCCGTGTC others(131): Show |
1 | a0001c0001t0003g0250 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.163-2044_163-2043i others(140): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635778 | ||||||
chr22:46635778 | G | GCTGTATC others(177): Show |
1 | a0001c0001t0001g0154 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.163-2061_163-2060i others(186): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635778 | ||||||
chr22:46635798 | C | A | 1 | a0001c0001t0001g0253 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.163-2042C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635798 | |||||||
chr22:46635798 | C | CG | 7 | a0001c0001t0001g0075 a0001c0001t0001g0115 a0001c0001t0001g0127 others(4): Show |
7 | HG02622.hp1 HG03831.hp1 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.163-2042_163-2041i others(3): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635798 | |||||||
chr22:46635799 | A | C | 8 | a0001c0001t0001g0075 a0001c0001t0001g0115 a0001c0001t0001g0127 others(5): Show |
8 | HG02622.hp1 HG03831.hp1 HG04204.hp2 others(5): Show |
intron_variant | MODIFIER | c.163-2041A>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635799 | |||||||
chr22:46635799 | A | G | 95 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0066 others(92): Show |
97 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.163-2041A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635799 | |||||||
chr22:46635815 | G | A | 12 | a0001c0001t0005g0063 a0001c0001t0007g0022 a0001c0001t0007g0023 others(9): Show |
12 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.163-2025G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635815 | |||||||
chr22:46635841 | C | T | 1 | a0001c0001t0056g0313 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.163-1999C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635841 | |||||||
chr22:46635922 | G | A | 1 | a0001c0001t0002g0266 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.163-1918G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635922 | |||||||
chr22:46635943 | G | A | 1 | a0001c0001t0009g0056 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.163-1897G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635943 | |||||||
chr22:46635962 | C | T | 2 | a0001c0001t0008g0013 a0001c0001t0008g0016 |
2 | HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.163-1878C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635962 | |||||||
chr22:46636070 | C | T | 156 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0220 others(153): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.163-1770C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46636070 | |||||||
chr22:46636151 | G | A | 3 | a0001c0001t0010g0185 a0001c0001t0010g0186 a0001c0001t0010g0187 |
3 | HG01884.hp2 HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.163-1689G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46636151 | |||||||
chr22:46636189 | A | G | 304 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0066 others(301): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.163-1651A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46636189 | |||||||
chr22:46636532 | G | A | 92 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0066 others(89): Show |
94 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.163-1308G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46636532 | |||||||
chr22:46636718 | A | G | 4 | a0001c0001t0005g0001 a0001c0001t0005g0039 a0001c0001t0005g0040 others(1): Show |
5 | HG02615.hp2 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.163-1122A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46636718 | |||||||
chr22:46636750 | G | T | 13 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0006g0076 others(10): Show |
13 | HG00438.hp2 HG02015.hp1 HG02083.hp2 others(10): Show |
intron_variant | MODIFIER | c.163-1090G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46636750 | |||||||
chr22:46637029 | G | C | 3 | a0001c0001t0008g0013 a0001c0001t0008g0014 a0001c0001t0008g0016 |
3 | HG02976.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.163-811G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46637029 | |||||||
chr22:46637062 | G | A | 1 | a0001c0001t0004g0017 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.163-778G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46637062 | |||||||
chr22:46637068 | A | G | 15 | a0001c0001t0004g0021 a0001c0001t0005g0063 a0001c0001t0007g0022 others(12): Show |
15 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.163-772A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46637068 | |||||||
chr22:46637120 | G | C | 250 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0066 others(247): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.163-720G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46637120 | |||||||
chr22:46637145 | C | T | 7 | a0001c0001t0004g0035 a0001c0001t0004g0036 a0001c0001t0010g0034 others(4): Show |
7 | HG02622.hp2 HG02723.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.163-695C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46637145 | |||||||
chr22:46637256 | C | CT | 182 | a0001c0001t0001g0074 a0001c0001t0001g0098 a0001c0001t0001g0196 others(179): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.163-570dupT | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46637256 | ||||||
chr22:46637256 | C | CTT | 15 | a0001c0001t0002g0278 a0001c0001t0004g0021 a0001c0001t0005g0063 others(12): Show |
15 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.163-571_163-570dup others(2): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46637256 | ||||||
chr22:46637313 | C | T | 3 | a0001c0001t0008g0013 a0001c0001t0008g0014 a0001c0001t0008g0016 |
3 | HG02976.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.163-527C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46637313 | |||||||
chr22:46637543 | T | G | 3 | a0001c0001t0010g0185 a0001c0001t0010g0186 a0001c0001t0010g0187 |
3 | HG01884.hp2 HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.163-297T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46637543 | |||||||
chr22:46637554 | T | C | 1 | a0001c0001t0054g0251 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.163-286T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46637554 | |||||||
chr22:46637637 | G | A | 95 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0066 others(92): Show |
97 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.163-203G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46637637 | |||||||
chr22:46637731 | A | AT | 95 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0066 others(92): Show |
97 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.163-108dupT | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46637731 | ||||||
chr22:46637796 | G | A | 2 | a0001c0001t0015g0189 a0001c0001t0015g0190 |
2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.163-44G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46637796 | |||||||
chr22:46638085 | C | T | 1 | a0001c0001t0001g0219 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.283+125C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46638085 | |||||||
chr22:46638108 | C | T | 1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.283+148C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46638108 | |||||||
chr22:46638149 | G | C | 4 | a0001c0001t0004g0035 a0001c0001t0004g0036 a0001c0001t0010g0034 others(1): Show |
4 | HG02622.hp2 HG02922.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+189G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46638149 | |||||||
chr22:46638245 | A | G | 3 | a0001c0001t0038g0180 a0001c0001t0054g0251 a0002c0011t0053g0019 |
3 | HG02572.hp2 HG02647.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.283+285A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46638245 | |||||||
chr22:46638522 | G | A | 2 | a0001c0001t0004g0061 a0001c0001t0019g0062 |
2 | HG01884.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.283+562G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46638522 | |||||||
chr22:46638825 | C | T | 96 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0255 others(93): Show |
98 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.283+865C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46638825 | |||||||
chr22:46638830 | G | A | 7 | a0001c0001t0011g0183 a0001c0001t0011g0184 a0001c0001t0028g0060 others(4): Show |
7 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.283+870G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46638830 | |||||||
chr22:46638932 | G | A | 58 | a0001c0001t0001g0220 a0001c0001t0003g0006 a0001c0001t0003g0030 others(55): Show |
58 | HG00099.hp2 HG00140.hp1 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.283+972G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46638932 | |||||||
chr22:46638941 | T | C | 96 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0255 others(93): Show |
98 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.283+981T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46638941 | |||||||
chr22:46639026 | C | A | 1 | a0001c0001t0011g0184 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.283+1066C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46639026 | |||||||
chr22:46639031 | A | G | 1 | a0001c0001t0004g0233 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.283+1071A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46639031 | |||||||
chr22:46639078 | T | G | 1 | a0001c0001t0005g0143 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.283+1118T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46639078 | |||||||
chr22:46639118 | A | G | 6 | a0001c0001t0005g0001 a0001c0001t0005g0039 a0001c0001t0005g0040 others(3): Show |
7 | HG02615.hp2 HG02818.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.283+1158A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46639118 | |||||||
chr22:46639153 | A | AGT | 24 | a0001c0001t0003g0208 a0001c0001t0003g0214 a0001c0001t0003g0215 others(21): Show |
24 | HG00099.hp2 HG00733.hp1 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.283+1220_283+1221d others(4): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46639153 | ||||||
chr22:46639153 | A | AGTGT | 74 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0066 others(71): Show |
76 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.283+1218_283+1221d others(6): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46639153 | ||||||
chr22:46639153 | A | AGTGTGT | 4 | a0001c0001t0001g0179 a0001c0001t0019g0062 a0001c0001t0023g0121 others(1): Show |
4 | HG01952.hp1 HG02293.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.283+1216_283+1221d others(8): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46639153 | ||||||
chr22:46639153 | AGT | A | 124 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0255 others(121): Show |
125 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.283+1220_283+1221d others(4): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46639153 | ||||||
chr22:46639153 | AGTGT | A | 8 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 others(5): Show |
8 | HG01175.hp2 HG01433.hp1 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.283+1218_283+1221d others(6): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46639153 | ||||||
chr22:46639153 | AGTGTGT | A | 4 | a0001c0001t0002g0007 a0001c0001t0002g0279 a0001c0001t0016g0018 others(1): Show |
5 | HG01256.hp1 HG01515.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.283+1216_283+1221d others(8): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46639153 | ||||||
chr22:46639153 | AGTGTGTG others(5): Show |
A | 2 | a0001c0001t0015g0189 a0001c0001t0015g0190 |
2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.283+1210_283+1221d others(14): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46639153 | ||||||
chr22:46639182 | A | G | 3 | a0001c0001t0008g0013 a0001c0001t0008g0014 a0001c0001t0008g0016 |
3 | HG02976.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.283+1222A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46639182 | |||||||
chr22:46639292 | G | GCCTGTGT others(15): Show |
65 | a0001c0001t0001g0220 a0001c0001t0003g0006 a0001c0001t0003g0030 others(62): Show |
65 | HG00099.hp2 HG00140.hp1 HG00733.hp1 others(62): Show |
intron_variant | MODIFIER | c.283+1341_283+1362d others(24): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46639292 | ||||||
chr22:46639473 | C | G | 3 | a0001c0001t0011g0183 a0001c0001t0011g0184 a0001c0001t0028g0060 |
3 | HG02723.hp2 HG03041.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.283+1513C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46639473 | |||||||
chr22:46639480 | G | A | 16 | a0001c0001t0001g0098 a0001c0002t0002g0071 a0001c0002t0004g0002 others(13): Show |
17 | HG01361.hp2 HG01496.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.283+1520G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46639480 | |||||||
chr22:46639614 | G | C | 1 | a0001c0007t0019g0182 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.283+1654G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46639614 | |||||||
chr22:46639627 | G | A | 5 | a0001c0001t0002g0262 a0001c0001t0002g0264 a0001c0001t0002g0270 others(2): Show |
5 | HG00423.hp2 HG02056.hp2 HG02129.hp1 others(2): Show |
intron_variant | MODIFIER | c.283+1667G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46639627 | |||||||
chr22:46639632 | CTG | C | 16 | a0001c0001t0001g0098 a0001c0002t0002g0071 a0001c0002t0004g0002 others(13): Show |
17 | HG01361.hp2 HG01496.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.283+1679_283+1680d others(4): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46639632 | ||||||
chr22:46639653 | C | G | 1 | a0001c0001t0007g0022 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.283+1693C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46639653 | |||||||
chr22:46639717 | G | T | 60 | a0001c0001t0001g0220 a0001c0001t0003g0006 a0001c0001t0003g0030 others(57): Show |
60 | HG00099.hp2 HG00140.hp1 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.283+1757G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46639717 | |||||||
chr22:46639826 | G | C | 1 | a0001c0001t0048g0191 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.283+1866G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46639826 | |||||||
chr22:46640043 | G | A | 1 | a0001c0001t0011g0057 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.283+2083G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46640043 | |||||||
chr22:46640125 | G | A | 1 | a0001c0005t0002g0294 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.283+2165G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46640125 | |||||||
chr22:46640162 | C | T | 16 | a0001c0001t0001g0098 a0001c0002t0002g0071 a0001c0002t0004g0002 others(13): Show |
17 | HG01361.hp2 HG01496.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.283+2202C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46640162 | |||||||
chr22:46640199 | T | C | 65 | a0001c0001t0001g0220 a0001c0001t0003g0006 a0001c0001t0003g0030 others(62): Show |
65 | HG00099.hp2 HG00140.hp1 HG00733.hp1 others(62): Show |
intron_variant | MODIFIER | c.283+2239T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46640199 | |||||||
chr22:46640214 | G | A | 2 | a0001c0001t0001g0149 a0001c0001t0001g0150 |
2 | HG02129.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.283+2254G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46640214 | |||||||
chr22:46640281 | C | G | 320 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0066 others(317): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.283+2321C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46640281 | |||||||
chr22:46640398 | T | C | 1 | a0001c0007t0019g0182 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.283+2438T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46640398 | |||||||
chr22:46640554 | G | A | 61 | a0001c0001t0001g0220 a0001c0001t0003g0006 a0001c0001t0003g0030 others(58): Show |
61 | HG00099.hp2 HG00140.hp1 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.283+2594G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46640554 | |||||||
chr22:46640596 | G | A | 1 | a0001c0001t0030g0044 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.283+2636G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46640596 | |||||||
chr22:46640637 | G | A | 1 | a0001c0001t0003g0205 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.283+2677G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46640637 | |||||||
chr22:46640786 | G | A | 1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.283+2826G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46640786 | |||||||
chr22:46640787 | A | G | 1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.283+2827A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46640787 | |||||||
chr22:46640820 | C | T | 104 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0066 others(101): Show |
107 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.283+2860C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46640820 | |||||||
chr22:46640978 | C | A | 1 | a0001c0002t0004g0097 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.283+3018C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46640978 | |||||||
chr22:46641025 | C | T | 1 | a0002c0010t0047g0064 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.283+3065C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46641025 | |||||||
chr22:46641157 | T | C | 187 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0220 others(184): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.283+3197T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46641157 | |||||||
chr22:46641176 | G | A | 1 | a0001c0001t0054g0251 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.283+3216G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46641176 | |||||||
chr22:46641265 | G | A | 1 | a0001c0001t0003g0221 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.283+3305G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46641265 | |||||||
chr22:46641292 | C | T | 1 | a0002c0011t0053g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.283+3332C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46641292 | |||||||
chr22:46641392 | TAAGG | T | 301 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0066 others(298): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.283+3459_283+3462d others(6): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46641392 | ||||||
chr22:46641424 | C | G | 1 | a0001c0001t0004g0021 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.283+3464C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46641424 | |||||||
chr22:46641466 | C | T | 1 | a0001c0001t0009g0048 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.283+3506C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46641466 | |||||||
chr22:46641471 | T | G | 1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.283+3511T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46641471 | |||||||
chr22:46641560 | T | C | 2 | a0001c0001t0008g0013 a0001c0001t0008g0016 |
2 | HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.283+3600T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46641560 | |||||||
chr22:46641621 | G | A | 1 | a0002c0011t0053g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.283+3661G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46641621 | |||||||
chr22:46641810 | G | A | 10 | a0001c0001t0007g0022 a0001c0001t0007g0023 a0001c0001t0007g0024 others(7): Show |
10 | HG00642.hp2 HG01243.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.283+3850G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46641810 | |||||||
chr22:46641871 | G | A | 1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.283+3911G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46641871 | |||||||
chr22:46641881 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.283+3921G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46641881 | |||||||
chr22:46641929 | C | T | 1 | a0001c0001t0002g0288 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.283+3969C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46641929 | |||||||
chr22:46641952 | A | T | 1 | a0001c0001t0001g0177 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.283+3992A>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46641952 | |||||||
chr22:46641962 | G | A | 13 | a0001c0001t0004g0021 a0001c0001t0005g0063 a0001c0001t0007g0022 others(10): Show |
13 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.283+4002G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46641962 | |||||||
chr22:46642069 | T | A | 1 | a0001c0001t0006g0199 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.283+4109T>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46642069 | |||||||
chr22:46642162 | C | T | 1 | a0001c0001t0003g0208 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.283+4202C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46642162 | |||||||
chr22:46642184 | G | A | 57 | a0001c0001t0001g0220 a0001c0001t0003g0006 a0001c0001t0003g0030 others(54): Show |
57 | HG00099.hp2 HG00140.hp1 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.283+4224G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46642184 | |||||||
chr22:46642210 | G | A | 2 | a0001c0001t0003g0083 a0001c0001t0003g0084 |
2 | HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.283+4250G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46642210 | |||||||
chr22:46642390 | A | G | 5 | a0001c0001t0008g0008 a0001c0001t0008g0010 a0001c0001t0008g0011 others(2): Show |
5 | HG02723.hp1 HG02809.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.283+4430A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46642390 | |||||||
chr22:46642444 | G | C | 3 | a0001c0001t0008g0013 a0001c0001t0008g0014 a0001c0001t0008g0016 |
3 | HG02976.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.283+4484G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46642444 | |||||||
chr22:46642862 | G | A | 1 | a0001c0001t0003g0085 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.283+4902G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46642862 | |||||||
chr22:46642964 | T | TATCC | 15 | a0001c0001t0002g0259 a0001c0001t0002g0266 a0001c0001t0002g0267 others(12): Show |
15 | HG00733.hp2 HG00735.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.283+5031_283+5034d others(6): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46642964 | ||||||
chr22:46642973 | A | T | 2 | a0001c0001t0006g0174 a0001c0001t0006g0302 |
2 | NA19081.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.283+5013A>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46642973 | |||||||
chr22:46643084 | T | TATCC | 150 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0066 others(147): Show |
153 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.283+5159_283+5162d others(6): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643084 | ||||||
chr22:46643084 | T | TATCCATC others(1): Show |
17 | a0001c0001t0001g0110 a0001c0001t0001g0158 a0001c0001t0001g0219 others(14): Show |
17 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.283+5155_283+5162d others(10): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643084 | ||||||
chr22:46643084 | T | TATCCATC others(5): Show |
1 | a0001c0001t0007g0026 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.283+5151_283+5162d others(14): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643084 | ||||||
chr22:46643084 | TATCCATC others(1): Show |
T | 8 | a0001c0001t0002g0257 a0001c0001t0002g0264 a0001c0001t0002g0278 others(5): Show |
8 | HG01952.hp2 HG02056.hp2 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.283+5155_283+5162d others(10): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643084 | ||||||
chr22:46643088 | C | CATCCATC others(505): Show |
1 | a0001c0001t0064g0306 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.283+5154_283+5155i others(514): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643088 | ||||||
chr22:46643092 | C | CATCCATC others(505): Show |
1 | a0001c0001t0006g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.283+5154_283+5155i others(514): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643092 | ||||||
chr22:46643092 | C | CATCCATC others(501): Show |
1 | a0001c0001t0002g0267 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.283+5154_283+5155i others(510): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643092 | ||||||
chr22:46643092 | C | CATCCATC others(497): Show |
9 | a0001c0001t0001g0197 a0001c0001t0001g0255 a0001c0001t0002g0301 others(6): Show |
9 | HG00438.hp2 HG02083.hp2 NA18939.hp2 others(6): Show |
intron_variant | MODIFIER | c.283+5154_283+5155i others(506): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643092 | ||||||
chr22:46643092 | C | CATCCATC others(493): Show |
1 | a0001c0001t0006g0194 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.283+5154_283+5155i others(502): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643092 | ||||||
chr22:46643092 | C | CATCCATC others(493): Show |
1 | a0001c0001t0002g0310 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.283+5154_283+5155i others(502): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643092 | ||||||
chr22:46643092 | C | CATCCATC others(493): Show |
1 | a0001c0001t0004g0061 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.283+5150_283+5151i others(502): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643092 | ||||||
chr22:46643092 | C | CATCCATC others(493): Show |
2 | a0001c0001t0008g0013 a0001c0001t0008g0016 |
2 | HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.283+5150_283+5151i others(502): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643092 | ||||||
chr22:46643111 | C | CCATG | 73 | a0001c0001t0001g0261 a0001c0001t0001g0271 a0001c0001t0001g0273 others(70): Show |
75 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.283+5154_283+5155i others(6): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643111 | ||||||
chr22:46643111 | C | G | 3 | a0001c0001t0004g0233 a0001c0001t0008g0014 a0001c0001t0019g0062 |
3 | HG02717.hp2 HG02896.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.283+5151C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46643111 | |||||||
chr22:46643123 | G | C | 17 | a0001c0001t0001g0197 a0001c0001t0001g0255 a0001c0001t0002g0267 others(14): Show |
17 | HG00438.hp2 HG00741.hp2 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.283+5163G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46643123 | |||||||
chr22:46643129 | A | T | 76 | a0001c0001t0001g0261 a0001c0001t0001g0271 a0001c0001t0001g0273 others(73): Show |
78 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.283+5169A>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46643129 | |||||||
chr22:46643135 | G | C | 77 | a0001c0001t0001g0261 a0001c0001t0001g0271 a0001c0001t0001g0273 others(74): Show |
79 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.283+5175G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46643135 | |||||||
chr22:46643141 | T | A | 94 | a0001c0001t0001g0197 a0001c0001t0001g0255 a0001c0001t0001g0261 others(91): Show |
96 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.283+5181T>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46643141 | |||||||
chr22:46643147 | C | CCATCCAT others(509): Show |
1 | a0001c0001t0004g0035 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.283+5218_283+5219i others(518): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643147 | ||||||
chr22:46643147 | C | CCATCCAT others(497): Show |
1 | a0001c0001t0019g0062 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.283+5214_283+5215i others(506): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643147 | ||||||
chr22:46643147 | C | CCATCCAT others(493): Show |
1 | a0001c0001t0008g0014 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.283+5214_283+5215i others(502): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643147 | ||||||
chr22:46643147 | C | G | 17 | a0001c0001t0001g0197 a0001c0001t0001g0255 a0001c0001t0002g0267 others(14): Show |
17 | HG00438.hp2 HG00741.hp2 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.283+5187C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46643147 | |||||||
chr22:46643151 | C | CCATCCAT others(505): Show |
1 | a0001c0001t0003g0222 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.283+5230_283+5231i others(514): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643151 | ||||||
chr22:46643151 | C | CCATCCAT others(501): Show |
1 | a0001c0001t0003g0212 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.283+5226_283+5227i others(510): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643151 | ||||||
chr22:46643151 | C | CCATCCAT others(497): Show |
1 | a0001c0001t0003g0239 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.283+5226_283+5227i others(506): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643151 | ||||||
chr22:46643151 | C | CCATCCAT others(489): Show |
2 | a0001c0001t0003g0030 a0001c0001t0003g0031 |
2 | HG03130.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.283+5222_283+5223i others(498): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643151 | ||||||
chr22:46643151 | C | CCATCCAT others(517): Show |
1 | a0001c0001t0007g0026 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.283+5222_283+5223i others(526): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643151 | ||||||
chr22:46643151 | C | CCATCCAT others(513): Show |
2 | a0001c0001t0004g0036 a0001c0001t0033g0037 |
2 | HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.283+5222_283+5223i others(522): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643151 | ||||||
chr22:46643151 | C | CCATCCAT others(509): Show |
1 | a0001c0001t0010g0034 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.283+5222_283+5223i others(518): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643151 | ||||||
chr22:46643151 | C | CCATCCAT others(501): Show |
1 | a0001c0001t0048g0191 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.283+5218_283+5219i others(510): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643151 | ||||||
chr22:46643151 | C | CCATCCAT others(509): Show |
1 | a0001c0001t0005g0063 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.283+5218_283+5219i others(518): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643151 | ||||||
chr22:46643151 | C | CCATCCAT others(497): Show |
2 | a0001c0001t0006g0198 a0001c0001t0034g0201 |
2 | NA18969.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.283+5214_283+5215i others(506): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643151 | ||||||
chr22:46643151 | C | CCATCCAT others(513): Show |
1 | a0001c0001t0054g0251 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.283+5214_283+5215i others(522): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643151 | ||||||
chr22:46643151 | C | G | 17 | a0001c0001t0001g0197 a0001c0001t0001g0255 a0001c0001t0002g0267 others(14): Show |
17 | HG00438.hp2 HG00741.hp2 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.283+5191C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46643151 | |||||||
chr22:46643155 | C | CCATCCAT others(501): Show |
1 | a0001c0001t0001g0220 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.283+5230_283+5231i others(510): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | ||||||
chr22:46643155 | C | CCATCCAT others(497): Show |
1 | a0001c0001t0003g0238 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.283+5226_283+5227i others(506): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | ||||||
chr22:46643155 | C | CCATCCAT others(509): Show |
1 | a0001c0001t0006g0202 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.283+5226_283+5227i others(518): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | ||||||
chr22:46643155 | C | CCATCCAT others(501): Show |
1 | a0001c0008t0055g0067 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.283+5226_283+5227i others(510): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | ||||||
chr22:46643155 | C | CCATCCAT others(501): Show |
1 | a0001c0001t0003g0241 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.283+5226_283+5227i others(510): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | ||||||
chr22:46643155 | C | CCATCCAT others(505): Show |
1 | a0001c0001t0018g0247 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.283+5226_283+5227i others(514): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | ||||||
chr22:46643155 | C | CCATCCAT others(501): Show |
5 | a0001c0001t0003g0206 a0001c0001t0003g0224 a0001c0001t0003g0225 others(2): Show |
5 | HG00140.hp1 HG00741.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.283+5226_283+5227i others(510): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | ||||||
chr22:46643155 | C | CCATCCAT others(497): Show |
3 | a0001c0001t0003g0207 a0001c0001t0003g0228 a0001c0001t0003g0229 |
3 | HG02683.hp2 HG03491.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.283+5226_283+5227i others(506): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | ||||||
chr22:46643155 | C | CCATCCAT others(497): Show |
1 | a0001c0001t0003g0223 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.283+5226_283+5227i others(506): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | ||||||
chr22:46643155 | C | CCATCCAT others(493): Show |
4 | a0001c0001t0003g0208 a0001c0001t0003g0214 a0001c0001t0003g0215 others(1): Show |
4 | HG00099.hp2 HG01081.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.283+5226_283+5227i others(502): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | ||||||
chr22:46643155 | C | CCATCCAT others(493): Show |
5 | a0001c0001t0003g0210 a0001c0001t0003g0245 a0001c0001t0014g0052 others(2): Show |
5 | HG00733.hp1 HG02027.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.283+5226_283+5227i others(502): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | ||||||
chr22:46643155 | C | CCATCCAT others(509): Show |
1 | a0001c0001t0003g0250 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.283+5226_283+5227i others(518): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | ||||||
chr22:46643155 | C | CCATCCAT others(505): Show |
7 | a0001c0001t0001g0005 a0001c0001t0001g0151 a0001c0001t0002g0100 others(4): Show |
7 | HG01952.hp1 HG02040.hp1 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.283+5226_283+5227i others(514): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | ||||||
chr22:46643155 | C | CCATCCAT others(513): Show |
1 | a0001c0001t0015g0189 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.283+5222_283+5223i others(522): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | ||||||
chr22:46643155 | C | CCATCCAT others(529): Show |
1 | a0001c0001t0028g0060 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.283+5222_283+5223i others(538): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | ||||||
chr22:46643155 | C | CCATCCAT others(505): Show |
1 | a0001c0002t0004g0092 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.283+5222_283+5223i others(514): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | ||||||
chr22:46643155 | C | CCATCCAT others(505): Show |
3 | a0001c0002t0004g0032 a0001c0002t0004g0093 a0001c0002t0004g0094 |
3 | HG02965.hp1 HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.283+5222_283+5223i others(514): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | ||||||
chr22:46643155 | C | CCATCCAT others(501): Show |
1 | a0001c0002t0004g0069 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.283+5222_283+5223i others(510): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | ||||||
chr22:46643155 | C | CCATCCAT others(525): Show |
1 | a0001c0001t0005g0105 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.283+5222_283+5223i others(534): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | ||||||
chr22:46643155 | C | CCATCCAT others(497): Show |
1 | a0001c0001t0003g0218 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.283+5222_283+5223i others(506): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | ||||||
chr22:46643155 | C | CCATCCAT others(493): Show |
3 | a0001c0001t0003g0217 a0001c0001t0003g0242 a0001c0001t0003g0243 |
3 | HG01891.hp1 NA18522.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.283+5222_283+5223i others(502): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | ||||||
chr22:46643155 | C | CCATCCAT others(517): Show |
2 | a0001c0002t0002g0071 a0001c0002t0004g0070 |
2 | HG04115.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.283+5222_283+5223i others(526): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | ||||||
chr22:46643155 | C | CCATCCAT others(513): Show |
8 | a0001c0001t0001g0098 a0001c0002t0004g0002 a0001c0002t0004g0086 others(5): Show |
9 | HG01361.hp2 HG01496.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.283+5222_283+5223i others(522): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | ||||||
chr22:46643155 | C | CCATCCAT others(513): Show |
1 | a0001c0002t0004g0097 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.283+5222_283+5223i others(522): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | ||||||
chr22:46643155 | C | CCATCCAT others(497): Show |
1 | a0001c0001t0030g0044 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.283+5218_283+5219i others(506): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | ||||||
chr22:46643155 | C | CCATCCAT others(505): Show |
1 | a0001c0001t0038g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.283+5218_283+5219i others(514): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | ||||||
chr22:46643155 | C | CCATCCAT others(513): Show |
1 | a0001c0001t0004g0021 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.283+5218_283+5219i others(522): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | ||||||
chr22:46643155 | C | CCATCCAT others(513): Show |
1 | a0001c0001t0007g0033 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.283+5218_283+5219i others(522): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | ||||||
chr22:46643155 | C | CCATCCAT others(509): Show |
9 | a0001c0001t0007g0022 a0001c0001t0007g0023 a0001c0001t0007g0024 others(6): Show |
9 | HG00642.hp2 HG01070.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.283+5218_283+5219i others(518): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | ||||||
chr22:46643155 | C | CCATCCAT others(501): Show |
1 | a0002c0011t0053g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.283+5218_283+5219i others(510): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | ||||||
chr22:46643155 | C | CCATCCAT others(513): Show |
1 | a0001c0001t0004g0017 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.283+5218_283+5219i others(522): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | ||||||
chr22:46643155 | C | CCATCCAT others(509): Show |
1 | a0001c0001t0032g0046 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.283+5218_283+5219i others(518): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | ||||||
chr22:46643155 | C | G | 14 | a0001c0001t0001g0197 a0001c0001t0001g0255 a0001c0001t0002g0267 others(11): Show |
14 | HG00438.hp2 HG00741.hp2 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.283+5195C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46643155 | |||||||
chr22:46643159 | C | CCATCCAT others(490): Show |
1 | a0001c0001t0001g0179 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.283+5215_283+5216i others(499): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | ||||||
chr22:46643159 | C | CCATCCAT others(529): Show |
1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.283+5230_283+5231i others(538): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | ||||||
chr22:46643159 | C | CCATCCAT others(505): Show |
11 | a0001c0001t0001g0072 a0001c0001t0001g0080 a0001c0001t0001g0107 others(8): Show |
12 | HG00423.hp1 HG00673.hp2 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.283+5230_283+5231i others(514): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | ||||||
chr22:46643159 | C | CCATCCAT others(509): Show |
1 | a0001c0001t0001g0165 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.283+5230_283+5231i others(518): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | ||||||
chr22:46643159 | C | CCATCCAT others(505): Show |
1 | a0001c0001t0010g0186 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.283+5226_283+5227i others(514): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | ||||||
chr22:46643159 | C | CCATCCAT others(489): Show |
1 | a0001c0001t0020g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.283+5226_283+5227i others(498): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | ||||||
chr22:46643159 | C | CCATCCAT others(505): Show |
3 | a0001c0001t0002g0264 a0001c0001t0002g0278 a0001c0005t0002g0294 |
3 | HG02056.hp2 HG04115.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.283+5226_283+5227i others(514): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | ||||||
chr22:46643159 | C | CCATCCAT others(501): Show |
2 | a0001c0001t0002g0257 a0001c0001t0002g0300 |
2 | HG02132.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.283+5226_283+5227i others(510): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | ||||||
chr22:46643159 | C | CCATCCAT others(497): Show |
3 | a0001c0001t0003g0244 a0001c0001t0003g0283 a0001c0001t0058g0277 |
3 | HG01516.hp1 HG03831.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.283+5226_283+5227i others(506): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | ||||||
chr22:46643159 | C | CCATCCAT others(493): Show |
7 | a0001c0001t0003g0006 a0001c0001t0003g0104 a0001c0001t0003g0169 others(4): Show |
7 | HG01070.hp1 HG01071.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.283+5226_283+5227i others(502): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | ||||||
chr22:46643159 | C | CCATCCAT others(497): Show |
1 | a0001c0001t0003g0226 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.283+5226_283+5227i others(506): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | ||||||
chr22:46643159 | C | CCATCCAT others(497): Show |
1 | a0001c0001t0017g0045 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.283+5226_283+5227i others(506): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | ||||||
chr22:46643159 | C | CCATCCAT others(505): Show |
4 | a0001c0001t0001g0115 a0001c0001t0001g0119 a0001c0001t0001g0120 others(1): Show |
4 | HG00621.hp1 HG02083.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.283+5226_283+5227i others(514): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | ||||||
chr22:46643159 | C | CCATCCAT others(505): Show |
1 | a0001c0001t0001g0163 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.283+5226_283+5227i others(514): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | ||||||
chr22:46643159 | C | CCATCCAT others(509): Show |
1 | a0001c0001t0001g0178 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.283+5226_283+5227i others(518): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | ||||||
chr22:46643159 | C | CCATCCAT others(505): Show |
2 | a0001c0001t0001g0134 a0001c0001t0001g0154 |
2 | NA19065.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.283+5226_283+5227i others(514): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | ||||||
chr22:46643159 | C | CCATCCAT others(501): Show |
50 | a0001c0001t0001g0003 a0001c0001t0001g0066 a0001c0001t0001g0068 others(47): Show |
51 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.283+5226_283+5227i others(510): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | ||||||
chr22:46643159 | C | CCATCCAT others(497): Show |
1 | a0001c0001t0001g0141 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.283+5226_283+5227i others(506): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | ||||||
chr22:46643159 | C | CCATCCAT others(489): Show |
4 | a0001c0001t0001g0112 a0001c0001t0001g0125 a0001c0001t0001g0127 others(1): Show |
4 | HG00438.hp1 HG02135.hp2 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.283+5226_283+5227i others(498): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | ||||||
chr22:46643159 | C | CCATCCAT others(501): Show |
1 | a0001c0001t0001g0177 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.283+5226_283+5227i others(510): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | ||||||
chr22:46643159 | C | CCATCCAT others(493): Show |
1 | a0001c0003t0003g0235 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.283+5226_283+5227i others(502): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | ||||||
chr22:46643159 | C | CCATCCAT others(489): Show |
1 | a0001c0003t0003g0236 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.283+5226_283+5227i others(498): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | ||||||
chr22:46643159 | C | CCATCCAT others(493): Show |
1 | a0001c0001t0063g0227 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.283+5226_283+5227i others(502): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | ||||||
chr22:46643159 | C | CCATCCAT others(513): Show |
1 | a0001c0001t0015g0190 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.283+5222_283+5223i others(522): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | ||||||
chr22:46643159 | C | CCATCCAT others(501): Show |
1 | a0001c0001t0010g0185 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.283+5222_283+5223i others(510): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | ||||||
chr22:46643159 | C | CCATCCAT others(497): Show |
1 | a0001c0001t0010g0187 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.283+5222_283+5223i others(506): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | ||||||
chr22:46643159 | C | CCATCCAT others(485): Show |
1 | a0001c0001t0020g0231 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.283+5222_283+5223i others(494): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | ||||||
chr22:46643159 | C | CCATCCAT others(525): Show |
7 | a0001c0001t0005g0142 a0001c0001t0005g0143 a0001c0001t0005g0144 others(4): Show |
7 | HG00323.hp2 HG01168.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.283+5222_283+5223i others(534): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | ||||||
chr22:46643159 | C | CCATCCAT others(521): Show |
1 | a0001c0001t0005g0111 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.283+5222_283+5223i others(530): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | ||||||
chr22:46643159 | C | CCATCCAT others(489): Show |
6 | a0001c0001t0003g0083 a0001c0001t0003g0084 a0001c0001t0003g0085 others(3): Show |
6 | HG01243.hp2 HG01496.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.283+5222_283+5223i others(498): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | ||||||
chr22:46643159 | C | CCATCCAT others(517): Show |
1 | a0001c0002t0004g0095 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.283+5222_283+5223i others(526): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | ||||||
chr22:46643159 | C | CCATCCAT others(517): Show |
1 | a0001c0001t0011g0184 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.283+5222_283+5223i others(526): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | ||||||
chr22:46643159 | C | CCATCCAT others(513): Show |
1 | a0001c0001t0011g0183 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.283+5222_283+5223i others(522): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | ||||||
chr22:46643159 | C | CCATCCAT others(485): Show |
1 | a0001c0001t0003g0234 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.283+5222_283+5223i others(494): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | ||||||
chr22:46643159 | C | CCATCCAT others(497): Show |
1 | a0001c0007t0019g0182 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.283+5218_283+5219i others(506): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | ||||||
chr22:46643159 | C | CCATCCAT others(493): Show |
2 | a0001c0001t0004g0233 a0001c0001t0052g0136 |
2 | HG02717.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.283+5218_283+5219i others(502): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | ||||||
chr22:46643159 | C | CCATCCAT others(505): Show |
6 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(3): Show |
6 | HG02723.hp1 HG02809.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.283+5218_283+5219i others(514): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | ||||||
chr22:46643159 | C | CCATCCAT others(501): Show |
1 | a0001c0001t0002g0270 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.283+5214_283+5215i others(510): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | ||||||
chr22:46643159 | C | CCATCCAT others(493): Show |
1 | a0001c0001t0056g0313 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.283+5214_283+5215i others(502): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | ||||||
chr22:46643159 | C | CCATCCAT others(497): Show |
1 | a0001c0001t0002g0282 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.283+5214_283+5215i others(506): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | ||||||
chr22:46643159 | C | CCATCCAT others(497): Show |
1 | a0001c0001t0044g0316 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.283+5214_283+5215i others(506): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | ||||||
chr22:46643159 | C | CCATCCAT others(497): Show |
1 | a0001c0001t0060g0280 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.283+5214_283+5215i others(506): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | ||||||
chr22:46643159 | C | CCATCCAT others(493): Show |
15 | a0001c0001t0002g0081 a0001c0001t0002g0259 a0001c0001t0002g0266 others(12): Show |
15 | HG00140.hp2 HG00323.hp1 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.283+5214_283+5215i others(502): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | ||||||
chr22:46643159 | C | CCATCCAT others(489): Show |
4 | a0001c0001t0005g0001 a0001c0001t0005g0039 a0001c0001t0005g0040 others(1): Show |
5 | HG02615.hp2 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.283+5214_283+5215i others(498): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | ||||||
chr22:46643159 | C | CCATCCAT others(493): Show |
1 | a0001c0001t0001g0261 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.283+5214_283+5215i others(502): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | ||||||
chr22:46643159 | C | CCATCCAT others(489): Show |
1 | a0001c0001t0002g0172 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.283+5214_283+5215i others(498): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | ||||||
chr22:46643159 | C | CCATCCAT others(489): Show |
26 | a0001c0001t0001g0271 a0001c0001t0001g0273 a0001c0001t0001g0309 others(23): Show |
26 | HG00597.hp1 HG00639.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.283+5214_283+5215i others(498): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | ||||||
chr22:46643159 | C | CCATCCAT others(477): Show |
7 | a0001c0001t0002g0296 a0001c0001t0002g0297 a0001c0001t0002g0298 others(4): Show |
7 | HG00099.hp1 HG00642.hp1 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.283+5214_283+5215i others(486): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | ||||||
chr22:46643159 | C | CCATCCAT others(485): Show |
2 | a0001c0001t0005g0041 a0001c0001t0005g0188 |
2 | HG02922.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.283+5214_283+5215i others(494): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | ||||||
chr22:46643159 | C | CCATCCAT others(485): Show |
6 | a0001c0001t0002g0007 a0001c0001t0002g0171 a0001c0001t0002g0275 others(3): Show |
7 | HG01109.hp2 HG01256.hp1 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.283+5214_283+5215i others(494): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | ||||||
chr22:46643159 | C | CCATCCAT others(473): Show |
1 | a0001c0001t0001g0308 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.283+5214_283+5215i others(482): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | ||||||
chr22:46643159 | C | CCATCCAT others(493): Show |
1 | a0001c0001t0002g0203 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.283+5214_283+5215i others(502): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | ||||||
chr22:46643159 | C | CCATCCAT others(489): Show |
1 | a0001c0001t0002g0274 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.283+5214_283+5215i others(498): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | ||||||
chr22:46643163 | C | CCATCCAT others(497): Show |
2 | a0001c0001t0001g0073 a0001c0001t0023g0121 |
2 | HG01192.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.283+5226_283+5227i others(506): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643163 | ||||||
chr22:46643163 | C | CCATCCAT others(525): Show |
1 | a0001c0001t0005g0213 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.283+5222_283+5223i others(534): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643163 | ||||||
chr22:46643163 | C | CCATCCAT others(521): Show |
1 | a0001c0001t0009g0048 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.283+5222_283+5223i others(530): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643163 | ||||||
chr22:46643163 | C | CCATCCAT others(521): Show |
4 | a0001c0001t0005g0258 a0001c0001t0009g0047 a0001c0001t0009g0054 others(1): Show |
4 | HG00738.hp2 HG01106.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+5222_283+5223i others(530): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643163 | ||||||
chr22:46643163 | C | CCATCCAT others(517): Show |
1 | a0001c0001t0009g0050 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.283+5222_283+5223i others(526): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643163 | ||||||
chr22:46643163 | C | CCATCCAT others(517): Show |
1 | a0001c0001t0009g0056 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.283+5222_283+5223i others(526): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643163 | ||||||
chr22:46643163 | C | CCATCCAT others(517): Show |
1 | a0001c0002t0004g0091 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.283+5222_283+5223i others(526): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643163 | ||||||
chr22:46643163 | C | CCATCCAT others(513): Show |
1 | a0001c0001t0009g0049 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.283+5218_283+5219i others(522): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643163 | ||||||
chr22:46643163 | C | CCATCCAT others(485): Show |
1 | a0002c0010t0047g0064 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.283+5214_283+5215i others(494): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643163 | ||||||
chr22:46643167 | C | CCATCCAT others(513): Show |
1 | a0001c0002t0004g0096 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.283+5222_283+5223i others(522): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643167 | ||||||
chr22:46643171 | C | CCATCCAT others(477): Show |
1 | a0001c0001t0011g0057 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.283+5218_283+5219i others(486): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643171 | ||||||
chr22:46643180 | C | CATTTATC others(245): Show |
1 | a0001c0002t0004g0088 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.283+5222_283+5223i others(254): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643180 | ||||||
chr22:46643204 | T | C | 5 | a0001c0001t0011g0057 a0001c0002t0004g0088 a0001c0002t0004g0091 others(2): Show |
5 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.283+5244T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46643204 | |||||||
chr22:46643211 | C | T | 1 | a0001c0002t0004g0088 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.283+5251C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46643211 | |||||||
chr22:46643237 | A | ATCCCTGG others(326): Show |
1 | a0001c0002t0004g0088 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.283+5279_283+5280i others(335): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643237 | ||||||
chr22:46643249 | A | T | 1 | a0001c0001t0038g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.283+5289A>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46643249 | |||||||
chr22:46643327 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.283+5367G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46643327 | |||||||
chr22:46643327 | G | C | 67 | a0001c0001t0001g0220 a0001c0001t0002g0209 a0001c0001t0003g0030 others(64): Show |
67 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.283+5367G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46643327 | |||||||
chr22:46643331 | C | CCATG | 3 | a0001c0001t0003g0104 a0001c0001t0003g0169 a0001c0001t0005g0063 |
3 | HG01070.hp1 HG01071.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.283+5371_283+5372i others(6): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46643331 | |||||||
chr22:46643331 | C | G | 64 | a0001c0001t0001g0220 a0001c0001t0002g0209 a0001c0001t0003g0030 others(61): Show |
64 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.283+5371C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46643331 | |||||||
chr22:46643332 | T | C | 67 | a0001c0001t0001g0220 a0001c0001t0002g0209 a0001c0001t0003g0030 others(64): Show |
67 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.283+5372T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46643332 | |||||||
chr22:46643332 | TATCC | T | 237 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0066 others(234): Show |
242 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.283+5392_283+5395d others(6): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643332 | ||||||
chr22:46643336 | C | T | 67 | a0001c0001t0001g0220 a0001c0001t0002g0209 a0001c0001t0003g0030 others(64): Show |
67 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.283+5376C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46643336 | |||||||
chr22:46643394 | T | C | 1 | a0002c0011t0053g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.283+5434T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46643394 | |||||||
chr22:46643869 | G | A | 304 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0066 others(301): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.283+5909G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46643869 | |||||||
chr22:46643984 | G | A | 3 | a0001c0001t0008g0013 a0001c0001t0008g0014 a0001c0001t0008g0016 |
3 | HG02976.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.283+6024G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46643984 | |||||||
chr22:46644201 | C | T | 1 | a0001c0001t0001g0179 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.283+6241C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46644201 | |||||||
chr22:46644207 | C | T | 3 | a0001c0001t0011g0183 a0001c0001t0011g0184 a0001c0001t0028g0060 |
3 | HG02723.hp2 HG03041.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.283+6247C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46644207 | |||||||
chr22:46644236 | C | T | 1 | a0001c0001t0002g0317 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.283+6276C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46644236 | |||||||
chr22:46644303 | G | A | 5 | a0001c0001t0004g0061 a0001c0001t0008g0013 a0001c0001t0008g0014 others(2): Show |
5 | HG01884.hp1 HG02896.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.283+6343G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46644303 | |||||||
chr22:46644326 | T | G | 1 | a0002c0011t0053g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.283+6366T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46644326 | |||||||
chr22:46644339 | T | C | 304 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0066 others(301): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.283+6379T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46644339 | |||||||
chr22:46644444 | C | A | 1 | a0001c0001t0002g0272 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.283+6484C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46644444 | |||||||
chr22:46644513 | C | T | 1 | a0001c0001t0038g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.283+6553C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46644513 | |||||||
chr22:46644583 | T | C | 1 | a0002c0011t0053g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.283+6623T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46644583 | |||||||
chr22:46644587 | C | T | 2 | a0001c0001t0015g0189 a0001c0001t0015g0190 |
2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.283+6627C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46644587 | |||||||
chr22:46644679 | C | G | 20 | a0001c0001t0001g0098 a0001c0002t0002g0071 a0001c0002t0004g0002 others(17): Show |
21 | HG01109.hp1 HG01361.hp2 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.283+6719C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46644679 | |||||||
chr22:46644697 | G | GTT | 12 | a0001c0001t0005g0111 a0001c0001t0005g0143 a0001c0001t0005g0144 others(9): Show |
13 | HG00323.hp2 HG01106.hp1 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.283+6773_283+6774d others(4): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46644697 | ||||||
chr22:46644697 | G | GTTT | 6 | a0001c0001t0005g0213 a0001c0001t0008g0014 a0001c0001t0009g0048 others(3): Show |
6 | HG01975.hp1 HG02683.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.283+6772_283+6774d others(5): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46644697 | ||||||
chr22:46644697 | G | GTTTTTTT others(4): Show |
1 | a0001c0002t0004g0069 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.283+6764_283+6774d others(13): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46644697 | ||||||
chr22:46644697 | G | GTTTTTTT others(6): Show |
2 | a0001c0002t0004g0093 a0001c0002t0004g0094 |
2 | HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.283+6762_283+6774d others(15): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46644697 | ||||||
chr22:46644697 | G | GTTTTTTT others(10): Show |
2 | a0001c0001t0001g0098 a0001c0002t0004g0092 |
2 | HG01891.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.283+6758_283+6774d others(19): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46644697 | ||||||
chr22:46644697 | G | GTTTTTTT others(16): Show |
1 | a0001c0002t0004g0090 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.283+6752_283+6774d others(25): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46644697 | ||||||
chr22:46644697 | G | GTTTTTTT others(27): Show |
1 | a0001c0002t0004g0095 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.283+6741_283+6774d others(36): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46644697 | ||||||
chr22:46644697 | GTTT | G | 11 | a0001c0001t0001g0080 a0001c0001t0001g0158 a0001c0001t0001g0253 others(8): Show |
11 | HG00738.hp2 HG02074.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.283+6772_283+6774d others(5): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46644697 | ||||||
chr22:46644697 | GTTTT | G | 43 | a0001c0001t0001g0005 a0001c0001t0001g0066 a0001c0001t0001g0072 others(40): Show |
44 | HG00423.hp1 HG00597.hp2 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.283+6771_283+6774d others(6): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46644697 | ||||||
chr22:46644697 | GTTTTT | G | 34 | a0001c0001t0001g0003 a0001c0001t0001g0068 a0001c0001t0001g0073 others(31): Show |
35 | HG00408.hp1 HG00408.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.283+6770_283+6774d others(7): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46644697 | ||||||
chr22:46644697 | GTTTTTT | G | 15 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0134 others(12): Show |
15 | HG00741.hp1 HG01175.hp2 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.283+6769_283+6774d others(8): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46644697 | ||||||
chr22:46644697 | GTTTTTTT | G | 48 | a0001c0001t0001g0220 a0001c0001t0003g0006 a0001c0001t0003g0030 others(45): Show |
48 | HG00099.hp2 HG00140.hp1 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.283+6768_283+6774d others(9): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46644697 | ||||||
chr22:46644697 | GTTTTTTT others(5): Show |
G | 3 | a0001c0001t0004g0061 a0001c0001t0004g0233 a0001c0001t0019g0062 |
3 | HG01884.hp1 HG02717.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.283+6763_283+6774d others(14): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46644697 | ||||||
chr22:46644697 | GTTTTTTT others(6): Show |
G | 1 | a0001c0001t0015g0190 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.283+6762_283+6774d others(15): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46644697 | ||||||
chr22:46644697 | GTTTTTTT others(7): Show |
G | 3 | a0001c0001t0011g0183 a0001c0001t0011g0184 a0001c0001t0015g0189 |
3 | HG02723.hp2 NA18522.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.283+6761_283+6774d others(16): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46644697 | ||||||
chr22:46644697 | GTTTTTTT others(8): Show |
G | 1 | a0001c0001t0013g0055 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.283+6760_283+6774d others(17): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46644697 | ||||||
chr22:46644697 | GTTTTTTT others(9): Show |
G | 12 | a0001c0001t0004g0021 a0001c0001t0005g0063 a0001c0001t0007g0022 others(9): Show |
12 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.283+6759_283+6774d others(18): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46644697 | ||||||
chr22:46644697 | GTTTTTTT others(10): Show |
G | 1 | a0001c0001t0001g0125 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.283+6758_283+6774d others(19): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46644697 | ||||||
chr22:46644697 | GTTTTTTT others(11): Show |
G | 11 | a0001c0001t0001g0103 a0001c0001t0001g0109 a0001c0001t0001g0112 others(8): Show |
11 | HG00423.hp2 HG00438.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.283+6757_283+6774d others(20): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46644697 | ||||||
chr22:46644697 | GTTTTTTT others(12): Show |
G | 91 | a0001c0001t0001g0197 a0001c0001t0001g0255 a0001c0001t0001g0261 others(88): Show |
93 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.283+6756_283+6774d others(21): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46644697 | ||||||
chr22:46644697 | GTTTTTTT others(13): Show |
G | 1 | a0001c0001t0002g0172 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.283+6755_283+6774d others(22): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46644697 | ||||||
chr22:46644707 | T | G | 1 | a0001c0001t0001g0253 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.283+6747T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46644707 | |||||||
chr22:46644710 | T | G | 1 | a0001c0001t0003g0223 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.283+6750T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46644710 | |||||||
chr22:46644711 | T | G | 6 | a0001c0001t0003g0206 a0001c0001t0003g0210 a0001c0001t0003g0225 others(3): Show |
6 | HG00741.hp1 HG01175.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.283+6751T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46644711 | |||||||
chr22:46644712 | T | G | 46 | a0001c0001t0001g0220 a0001c0001t0003g0006 a0001c0001t0003g0030 others(43): Show |
46 | HG00099.hp2 HG00140.hp1 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.283+6752T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46644712 | |||||||
chr22:46644713 | T | G | 2 | a0001c0001t0003g0242 a0001c0001t0040g0246 |
2 | HG02027.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.283+6753T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46644713 | |||||||
chr22:46644720 | T | G | 5 | a0001c0001t0003g0208 a0001c0001t0003g0214 a0001c0001t0003g0215 others(2): Show |
5 | HG00099.hp2 HG01081.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.283+6760T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46644720 | |||||||
chr22:46644721 | T | G | 9 | a0001c0001t0007g0022 a0001c0001t0007g0023 a0001c0001t0007g0024 others(6): Show |
9 | HG00642.hp2 HG01243.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.283+6761T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46644721 | |||||||
chr22:46644757 | G | A | 2 | a0001c0001t0004g0061 a0001c0001t0019g0062 |
2 | HG01884.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.283+6797G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46644757 | |||||||
chr22:46644780 | C | T | 13 | a0001c0001t0004g0021 a0001c0001t0005g0063 a0001c0001t0007g0022 others(10): Show |
13 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.283+6820C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46644780 | |||||||
chr22:46644843 | C | T | 1 | a0001c0001t0003g0217 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.283+6883C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46644843 | |||||||
chr22:46644845 | A | C | 1 | a0001c0001t0001g0179 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.283+6885A>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46644845 | |||||||
chr22:46644897 | C | CTT | 15 | a0001c0001t0002g0171 a0001c0001t0002g0260 a0001c0001t0002g0272 others(12): Show |
16 | HG02015.hp2 HG02132.hp2 HG02135.hp1 others(13): Show |
intron_variant | MODIFIER | c.283+6969_283+6970d others(4): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46644897 | ||||||
chr22:46644897 | C | CTTT | 24 | a0001c0001t0002g0081 a0001c0001t0002g0203 a0001c0001t0002g0249 others(21): Show |
24 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(21): Show |
intron_variant | MODIFIER | c.283+6968_283+6970d others(5): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46644897 | ||||||
chr22:46644897 | C | CTTTT | 30 | a0001c0001t0001g0197 a0001c0001t0001g0308 a0001c0001t0002g0007 others(27): Show |
31 | HG00438.hp2 HG00597.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.283+6967_283+6970d others(6): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46644897 | ||||||
chr22:46644897 | C | CTTTTT | 10 | a0001c0001t0002g0269 a0001c0001t0002g0293 a0001c0001t0002g0317 others(7): Show |
10 | HG00140.hp2 HG01106.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.283+6966_283+6970d others(7): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46644897 | ||||||
chr22:46644897 | CT | C | 60 | a0001c0001t0001g0005 a0001c0001t0001g0074 a0001c0001t0001g0146 others(57): Show |
61 | HG01070.hp1 HG01071.hp1 HG01109.hp1 others(58): Show |
intron_variant | MODIFIER | c.283+6970delT | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46644897 | ||||||
chr22:46644897 | CTT | C | 90 | a0001c0001t0001g0080 a0001c0001t0001g0087 a0001c0001t0001g0098 others(87): Show |
90 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.283+6969_283+6970d others(4): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46644897 | ||||||
chr22:46644897 | CTTT | C | 54 | a0001c0001t0001g0003 a0001c0001t0001g0066 a0001c0001t0001g0068 others(51): Show |
56 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.283+6968_283+6970d others(5): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46644897 | ||||||
chr22:46644897 | CTTTTTTT others(11): Show |
C | 2 | a0001c0001t0002g0259 a0001c0001t0002g0266 |
2 | HG00735.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.283+6953_283+6970d others(20): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46644897 | ||||||
chr22:46644897 | CTTTTTTT others(12): Show |
C | 6 | a0001c0001t0002g0267 a0001c0001t0002g0268 a0001c0001t0002g0307 others(3): Show |
6 | HG00733.hp2 HG01109.hp2 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.283+6952_283+6970d others(21): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46644897 | ||||||
chr22:46645001 | C | T | 156 | a0001c0001t0001g0197 a0001c0001t0001g0220 a0001c0001t0001g0255 others(153): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.283+7041C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46645001 | |||||||
chr22:46645018 | T | A | 1 | a0001c0002t0004g0097 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.283+7058T>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46645018 | |||||||
chr22:46645169 | A | C | 1 | a0001c0001t0028g0060 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.283+7209A>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46645169 | |||||||
chr22:46645231 | G | T | 1 | a0001c0001t0001g0179 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.283+7271G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46645231 | |||||||
chr22:46645320 | G | A | 1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.283+7360G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46645320 | |||||||
chr22:46645366 | G | A | 1 | a0001c0001t0002g0315 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.283+7406G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46645366 | |||||||
chr22:46645402 | A | G | 1 | a0001c0001t0054g0251 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.283+7442A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46645402 | |||||||
chr22:46645439 | C | G | 1 | a0001c0001t0048g0191 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.283+7479C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46645439 | |||||||
chr22:46645595 | A | C | 1 | a0002c0011t0053g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.283+7635A>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46645595 | |||||||
chr22:46645795 | A | G | 4 | a0001c0001t0003g0208 a0001c0001t0003g0214 a0001c0001t0003g0215 others(1): Show |
4 | HG00099.hp2 HG01081.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.283+7835A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46645795 | |||||||
chr22:46645804 | C | G | 1 | a0001c0001t0001g0179 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.283+7844C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46645804 | |||||||
chr22:46645805 | G | C | 1 | a0001c0001t0001g0179 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.283+7845G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46645805 | |||||||
chr22:46645806 | T | G | 1 | a0001c0001t0001g0179 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.283+7846T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46645806 | |||||||
chr22:46645902 | G | A | 2 | a0001c0001t0015g0189 a0001c0001t0015g0190 |
2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.283+7942G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46645902 | |||||||
chr22:46645979 | G | A | 2 | a0001c0001t0015g0189 a0001c0001t0015g0190 |
2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.283+8019G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46645979 | |||||||
chr22:46646049 | C | T | 1 | a0001c0001t0020g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.283+8089C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46646049 | |||||||
chr22:46646065 | T | G | 1 | a0001c0001t0001g0134 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.283+8105T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46646065 | |||||||
chr22:46646186 | G | A | 1 | a0001c0001t0002g0081 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.283+8226G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46646186 | |||||||
chr22:46646277 | A | G | 1 | a0001c0001t0001g0066 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.283+8317A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46646277 | |||||||
chr22:46646321 | C | T | 1 | a0001c0001t0001g0179 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.283+8361C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46646321 | |||||||
chr22:46646324 | T | C | 1 | a0001c0001t0001g0179 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.283+8364T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46646324 | |||||||
chr22:46646473 | C | T | 3 | a0001c0001t0008g0013 a0001c0001t0008g0014 a0001c0001t0008g0016 |
3 | HG02976.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.283+8513C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46646473 | |||||||
chr22:46646571 | T | C | 1 | a0002c0011t0053g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.283+8611T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46646571 | |||||||
chr22:46646657 | G | T | 2 | a0001c0001t0008g0010 a0001c0001t0008g0011 |
2 | HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.283+8697G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46646657 | |||||||
chr22:46646742 | C | A | 1 | a0001c0001t0005g0144 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.283+8782C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46646742 | |||||||
chr22:46646769 | G | A | 1 | a0001c0001t0005g0040 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.283+8809G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46646769 | |||||||
chr22:46646798 | C | T | 1 | a0001c0001t0038g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.283+8838C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46646798 | |||||||
chr22:46646799 | G | A | 1 | a0001c0001t0002g0281 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.283+8839G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46646799 | |||||||
chr22:46646868 | G | A | 11 | a0001c0001t0004g0021 a0001c0001t0007g0022 a0001c0001t0007g0023 others(8): Show |
11 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.283+8908G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46646868 | |||||||
chr22:46646897 | A | AC | 4 | a0001c0001t0001g0112 a0001c0001t0001g0125 a0001c0001t0001g0127 others(1): Show |
4 | HG00438.hp1 HG02135.hp2 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.283+8939dupC | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46646897 | ||||||
chr22:46646900 | A | G | 4 | a0001c0001t0001g0112 a0001c0001t0001g0125 a0001c0001t0001g0127 others(1): Show |
4 | HG00438.hp1 HG02135.hp2 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.283+8940A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46646900 | |||||||
chr22:46646904 | A | G | 4 | a0001c0001t0001g0112 a0001c0001t0001g0125 a0001c0001t0001g0127 others(1): Show |
4 | HG00438.hp1 HG02135.hp2 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.283+8944A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46646904 | |||||||
chr22:46647016 | C | T | 1 | a0001c0001t0011g0057 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.283+9056C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46647016 | |||||||
chr22:46647263 | T | C | 1 | a0002c0011t0053g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.283+9303T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46647263 | |||||||
chr22:46647284 | T | A | 1 | a0001c0001t0001g0074 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.283+9324T>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46647284 | |||||||
chr22:46647285 | G | T | 1 | a0001c0001t0001g0074 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.283+9325G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46647285 | |||||||
chr22:46647286 | A | G | 1 | a0001c0001t0001g0074 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.283+9326A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46647286 | |||||||
chr22:46647293 | C | A | 2 | a0001c0001t0011g0183 a0001c0001t0011g0184 |
2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.283+9333C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46647293 | |||||||
chr22:46647308 | T | G | 2 | a0001c0001t0001g0114 a0001c0001t0001g0135 |
2 | NA19088.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.283+9348T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46647308 | |||||||
chr22:46647313 | A | G | 1 | a0001c0001t0001g0220 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.283+9353A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46647313 | |||||||
chr22:46647383 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.283+9423A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46647383 | |||||||
chr22:46647438 | C | T | 1 | a0001c0001t0006g0193 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.283+9478C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46647438 | |||||||
chr22:46647439 | G | A | 1 | a0001c0001t0001g0179 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.283+9479G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46647439 | |||||||
chr22:46647503 | TG | T | 10 | a0001c0001t0004g0035 a0001c0001t0004g0036 a0001c0001t0004g0061 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.283+9549delG | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46647503 | ||||||
chr22:46647578 | G | C | 1 | a0001c0001t0058g0277 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.283+9618G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46647578 | |||||||
chr22:46647616 | G | A | 3 | a0001c0003t0003g0235 a0001c0003t0003g0236 a0002c0011t0053g0019 |
3 | HG02109.hp2 HG02572.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.283+9656G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46647616 | |||||||
chr22:46647658 | G | A | 1 | a0001c0001t0024g0004 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.283+9698G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46647658 | |||||||
chr22:46647669 | G | A | 13 | a0001c0001t0004g0021 a0001c0001t0005g0063 a0001c0001t0007g0022 others(10): Show |
13 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.283+9709G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46647669 | |||||||
chr22:46647707 | A | G | 303 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0066 others(300): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.283+9747A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46647707 | |||||||
chr22:46647707 | A | T | 2 | a0001c0001t0015g0189 a0001c0001t0015g0190 |
2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.283+9747A>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46647707 | |||||||
chr22:46647785 | C | G | 1 | a0002c0011t0053g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.283+9825C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46647785 | |||||||
chr22:46647798 | A | G | 3 | a0001c0002t0004g0091 a0001c0002t0004g0095 a0001c0002t0004g0096 |
3 | HG01109.hp1 HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.283+9838A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46647798 | |||||||
chr22:46647846 | A | G | 1 | a0001c0001t0038g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.283+9886A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46647846 | |||||||
chr22:46647928 | T | C | 11 | a0001c0001t0001g0073 a0001c0001t0001g0087 a0001c0001t0001g0119 others(8): Show |
11 | HG00621.hp1 HG01081.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.283+9968T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46647928 | |||||||
chr22:46647966 | A | G | 1 | a0001c0001t0001g0179 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.283+10006A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46647966 | |||||||
chr22:46647967 | G | A | 1 | a0001c0001t0001g0179 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.283+10007G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46647967 | |||||||
chr22:46648099 | T | C | 2 | a0001c0001t0004g0017 a0001c0001t0032g0046 |
2 | HG02258.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.284-10088T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648099 | |||||||
chr22:46648318 | G | GTGGA | 40 | a0001c0001t0001g0068 a0001c0001t0001g0087 a0001c0001t0001g0115 others(37): Show |
40 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.284-9830_284-9827d others(6): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648318 | ||||||
chr22:46648318 | GTGGA | G | 49 | a0001c0001t0001g0137 a0001c0001t0003g0006 a0001c0001t0003g0221 others(46): Show |
50 | HG00642.hp2 HG00738.hp2 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.284-9830_284-9827d others(6): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648318 | ||||||
chr22:46648318 | GTGGATGG others(1): Show |
G | 6 | a0001c0001t0008g0013 a0001c0001t0008g0014 a0001c0001t0008g0016 others(3): Show |
6 | HG02647.hp2 HG02723.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.284-9834_284-9827d others(10): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648318 | ||||||
chr22:46648318 | GTGGATGG others(5): Show |
G | 8 | a0001c0001t0001g0163 a0001c0001t0010g0185 a0001c0001t0010g0186 others(5): Show |
8 | HG01433.hp1 HG01884.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.284-9838_284-9827d others(14): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648318 | ||||||
chr22:46648357 | GATGA | G | 4 | a0001c0002t0004g0032 a0001c0002t0004g0069 a0001c0002t0004g0092 others(1): Show |
4 | HG01891.hp2 HG02647.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284-9826_284-9823d others(6): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648357 | ||||||
chr22:46648361 | A | G | 1 | a0001c0002t0004g0093 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.284-9826A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648361 | |||||||
chr22:46648686 | T | G | 1 | a0002c0011t0053g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.284-9501T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648686 | |||||||
chr22:46648686 | T | TGATGGAT others(21): Show |
2 | a0001c0001t0030g0044 a0001c0001t0048g0191 |
2 | HG01433.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.284-9468_284-9441d others(30): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648686 | ||||||
chr22:46648699 | C | CATGG | 12 | a0001c0001t0004g0021 a0001c0001t0005g0063 a0001c0001t0007g0022 others(9): Show |
12 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.284-9464_284-9461d others(6): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648699 | ||||||
chr22:46648699 | C | G | 1 | a0002c0011t0053g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.284-9488C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648699 | |||||||
chr22:46648715 | G | GATGGATG others(141): Show |
1 | a0002c0011t0053g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.284-9465_284-9464i others(150): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648715 | ||||||
chr22:46648727 | C | CATGGATG others(1): Show |
4 | a0001c0001t0010g0185 a0001c0001t0010g0186 a0001c0001t0010g0187 others(1): Show |
4 | HG01884.hp2 HG03471.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.284-9448_284-9441d others(10): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648727 | ||||||
chr22:46648727 | C | G | 1 | a0002c0011t0053g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.284-9460C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648727 | |||||||
chr22:46648767 | C | CATGG | 15 | a0001c0001t0002g0259 a0001c0001t0002g0266 a0001c0001t0002g0267 others(12): Show |
15 | HG00639.hp1 HG00733.hp2 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.284-9388_284-9385d others(6): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648767 | ||||||
chr22:46648767 | C | G | 1 | a0002c0011t0053g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.284-9420C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648767 | |||||||
chr22:46648767 | CATGG | C | 18 | a0001c0001t0005g0105 a0001c0001t0005g0111 a0001c0001t0005g0142 others(15): Show |
18 | HG00738.hp2 HG01106.hp1 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.284-9388_284-9385d others(6): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648767 | ||||||
chr22:46648767 | CATGGATG others(53): Show |
C | 6 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(3): Show |
6 | HG02723.hp1 HG02809.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.284-9400_284-9341d others(62): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648767 | ||||||
chr22:46648787 | G | C | 4 | a0001c0001t0010g0185 a0001c0001t0010g0186 a0001c0001t0010g0187 others(1): Show |
4 | HG01884.hp2 HG02572.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-9400G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648787 | |||||||
chr22:46648795 | G | GATGGATG others(5): Show |
1 | a0001c0001t0003g0223 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.284-9385_284-9384i others(14): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648795 | ||||||
chr22:46648799 | G | C | 2 | a0001c0001t0004g0021 a0001c0001t0027g0038 |
2 | HG02145.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.284-9388G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648799 | |||||||
chr22:46648799 | GATGC | G | 5 | a0001c0001t0002g0172 a0001c0001t0002g0293 a0001c0001t0030g0044 others(2): Show |
5 | HG01433.hp1 HG01943.hp1 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.284-9384_284-9381d others(6): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648799 | ||||||
chr22:46648803 | C | CATGG | 107 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0068 others(104): Show |
109 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.284-9344_284-9341d others(6): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648803 | ||||||
chr22:46648803 | C | CATGGATG others(1): Show |
6 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0003g0218 others(3): Show |
6 | HG01255.hp2 HG02129.hp2 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.284-9348_284-9341d others(10): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648803 | ||||||
chr22:46648803 | C | CATGGATG others(5): Show |
1 | a0001c0001t0001g0154 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.284-9352_284-9341d others(14): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648803 | ||||||
chr22:46648803 | C | G | 86 | a0001c0001t0001g0197 a0001c0001t0001g0255 a0001c0001t0001g0261 others(83): Show |
88 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.284-9384C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648803 | |||||||
chr22:46648803 | CATGG | C | 12 | a0001c0001t0002g0259 a0001c0001t0002g0266 a0001c0001t0002g0267 others(9): Show |
12 | HG00733.hp2 HG00735.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.284-9344_284-9341d others(6): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648803 | ||||||
chr22:46648803 | CATGGATG others(9): Show |
C | 1 | a0001c0001t0001g0080 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.284-9356_284-9341d others(18): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648803 | ||||||
chr22:46648807 | G | C | 65 | a0001c0001t0001g0197 a0001c0001t0001g0255 a0001c0001t0001g0261 others(62): Show |
67 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.284-9380G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648807 | |||||||
chr22:46648807 | G | GATGC | 9 | a0001c0001t0002g0203 a0001c0001t0002g0288 a0001c0001t0006g0102 others(6): Show |
9 | HG00597.hp1 HG00621.hp2 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.284-9377_284-9376i others(6): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648807 | ||||||
chr22:46648808 | A | G | 1 | a0001c0001t0002g0270 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.284-9379A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648808 | |||||||
chr22:46648811 | G | C | 5 | a0001c0001t0002g0172 a0001c0001t0002g0293 a0001c0001t0030g0044 others(2): Show |
5 | HG01433.hp1 HG01943.hp1 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.284-9376G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648811 | |||||||
chr22:46648823 | G | C | 1 | a0001c0001t0011g0057 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.284-9364G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648823 | |||||||
chr22:46648827 | G | C | 3 | a0001c0001t0010g0185 a0001c0001t0010g0186 a0001c0001t0010g0187 |
3 | HG01884.hp2 HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.284-9360G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648827 | |||||||
chr22:46648831 | G | C | 8 | a0001c0001t0005g0145 a0001c0001t0008g0013 a0001c0001t0008g0014 others(5): Show |
8 | HG00323.hp2 HG02145.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.284-9356G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648831 | |||||||
chr22:46648847 | C | CATGGATG others(5): Show |
1 | a0001c0001t0011g0183 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.284-9336_284-9325d others(14): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648847 | ||||||
chr22:46648847 | C | CATGGATG others(41): Show |
1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.284-9325_284-9324i others(50): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648847 | ||||||
chr22:46648847 | C | G | 17 | a0001c0001t0005g0063 a0001c0001t0007g0022 a0001c0001t0007g0023 others(14): Show |
17 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.284-9340C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648847 | |||||||
chr22:46648851 | G | C | 3 | a0001c0001t0007g0022 a0001c0001t0007g0029 a0001c0001t0013g0055 |
3 | HG02486.hp2 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.284-9336G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648851 | |||||||
chr22:46648851 | G | GATGC | 7 | a0001c0001t0005g0063 a0001c0001t0007g0023 a0001c0001t0007g0024 others(4): Show |
7 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.284-9333_284-9332i others(6): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648851 | ||||||
chr22:46648855 | G | C | 2 | a0001c0001t0003g0215 a0001c0001t0038g0180 |
2 | HG03579.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.284-9332G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648855 | |||||||
chr22:46648859 | G | GATGGATG others(29): Show |
3 | a0001c0001t0008g0013 a0001c0001t0008g0014 a0001c0001t0008g0016 |
3 | HG02976.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.284-9325_284-9324i others(38): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648859 | ||||||
chr22:46648863 | C | CATGG | 4 | a0001c0001t0001g0219 a0001c0001t0015g0190 a0001c0003t0003g0235 others(1): Show |
4 | HG02109.hp2 HG03130.hp1 NA20905.hp1 others(1): Show |
intron_variant | MODIFIER | c.284-9292_284-9289d others(6): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648863 | ||||||
chr22:46648863 | C | G | 22 | a0001c0001t0003g0215 a0001c0001t0005g0063 a0001c0001t0005g0145 others(19): Show |
22 | HG00323.hp2 HG00642.hp2 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.284-9324C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648863 | |||||||
chr22:46648867 | G | C | 13 | a0001c0001t0005g0063 a0001c0001t0007g0022 a0001c0001t0007g0023 others(10): Show |
13 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.284-9320G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648867 | |||||||
chr22:46648867 | G | GATGGATG others(5): Show |
1 | a0001c0001t0011g0057 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.284-9309_284-9308i others(14): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648867 | ||||||
chr22:46648871 | G | C | 1 | a0001c0001t0003g0215 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.284-9316G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648871 | |||||||
chr22:46648871 | G | GATGGATG others(5): Show |
1 | a0001c0001t0005g0145 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.284-9305_284-9304i others(14): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648871 | ||||||
chr22:46648875 | G | C | 1 | a0002c0011t0053g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.284-9312G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648875 | |||||||
chr22:46648875 | G | GATGC | 3 | a0001c0001t0010g0185 a0001c0001t0010g0186 a0001c0001t0010g0187 |
3 | HG01884.hp2 HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.284-9309_284-9308i others(6): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648875 | ||||||
chr22:46648879 | G | GATGGATG others(9): Show |
1 | a0001c0001t0006g0199 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.284-9293_284-9292i others(18): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648879 | ||||||
chr22:46648895 | G | C | 2 | a0001c0001t0004g0021 a0001c0001t0030g0044 |
2 | HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.284-9292G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648895 | |||||||
chr22:46648899 | C | CATGG | 6 | a0001c0001t0005g0211 a0001c0001t0005g0258 a0001c0001t0009g0047 others(3): Show |
6 | HG00738.hp2 HG01106.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.284-9256_284-9253d others(6): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648899 | ||||||
chr22:46648899 | C | G | 17 | a0001c0001t0001g0168 a0001c0001t0003g0208 a0001c0001t0003g0214 others(14): Show |
17 | HG00099.hp2 HG00323.hp2 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.284-9288C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648899 | |||||||
chr22:46648903 | G | C | 6 | a0001c0001t0001g0168 a0001c0001t0003g0208 a0001c0001t0003g0214 others(3): Show |
6 | HG00099.hp2 HG01081.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.284-9284G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648903 | |||||||
chr22:46648907 | G | C | 5 | a0001c0001t0010g0185 a0001c0001t0010g0186 a0001c0001t0010g0187 others(2): Show |
5 | HG01884.hp2 HG03041.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.284-9280G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648907 | |||||||
chr22:46648907 | G | GATGGATG others(17): Show |
1 | a0001c0001t0054g0251 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.284-9257_284-9256i others(26): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648907 | ||||||
chr22:46648907 | G | GATGGATG others(161): Show |
1 | a0002c0011t0053g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.284-9257_284-9256i others(170): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648907 | ||||||
chr22:46648911 | G | C | 2 | a0001c0001t0003g0215 a0001c0001t0005g0145 |
2 | HG00323.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.284-9276G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648911 | |||||||
chr22:46648911 | G | GATGGATG others(21): Show |
9 | a0001c0001t0005g0105 a0001c0001t0005g0111 a0001c0001t0005g0142 others(6): Show |
9 | HG01168.hp2 HG02257.hp2 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.284-9253_284-9252i others(30): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648911 | ||||||
chr22:46648911 | G | GATGGATG others(25): Show |
1 | a0001c0001t0009g0049 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.284-9253_284-9252i others(34): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648911 | ||||||
chr22:46648915 | G | C | 2 | a0001c0001t0006g0199 a0001c0001t0027g0038 |
2 | HG02145.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.284-9272G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648915 | |||||||
chr22:46648915 | G | GATGGATG others(17): Show |
2 | a0001c0001t0002g0281 a0001c0001t0002g0290 |
2 | HG00639.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.284-9253_284-9252i others(26): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648915 | ||||||
chr22:46648919 | GATGGATG others(9): Show |
G | 1 | a0001c0001t0048g0191 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.284-9252_284-9237d others(18): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648919 | ||||||
chr22:46648923 | G | C | 1 | a0001c0001t0004g0021 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.284-9264G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648923 | |||||||
chr22:46648931 | GATGC | G | 5 | a0001c0002t0004g0032 a0001c0002t0004g0069 a0001c0002t0004g0092 others(2): Show |
5 | HG01891.hp2 HG02647.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.284-9252_284-9249d others(6): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648931 | ||||||
chr22:46648935 | C | CATGG | 4 | a0001c0001t0001g0087 a0001c0001t0001g0109 a0001c0001t0018g0230 others(1): Show |
4 | HG01981.hp1 HG02809.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-9205_284-9202d others(6): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648935 | ||||||
chr22:46648935 | C | G | 35 | a0001c0001t0001g0168 a0001c0001t0002g0281 a0001c0001t0002g0290 others(32): Show |
35 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.284-9252C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648935 | |||||||
chr22:46648935 | CATGG | C | 51 | a0001c0001t0001g0005 a0001c0001t0001g0112 a0001c0001t0001g0125 others(48): Show |
52 | HG00140.hp1 HG00438.hp1 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.284-9205_284-9202d others(6): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648935 | ||||||
chr22:46648935 | CATGGATG others(1): Show |
C | 17 | a0001c0001t0001g0098 a0001c0001t0011g0183 a0001c0002t0002g0071 others(14): Show |
18 | HG01109.hp1 HG01361.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.284-9209_284-9202d others(10): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648935 | ||||||
chr22:46648935 | CATGGATG others(5): Show |
C | 1 | a0001c0001t0003g0239 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.284-9213_284-9202d others(14): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648935 | ||||||
chr22:46648939 | G | C | 7 | a0001c0001t0001g0168 a0001c0001t0003g0208 a0001c0001t0003g0214 others(4): Show |
7 | HG00099.hp2 HG01081.hp2 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.284-9248G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648939 | |||||||
chr22:46648943 | G | C | 12 | a0001c0001t0008g0013 a0001c0001t0008g0014 a0001c0001t0008g0016 others(9): Show |
12 | HG01433.hp1 HG01891.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.284-9244G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648943 | |||||||
chr22:46648943 | G | GATGGATG others(21): Show |
2 | a0001c0001t0004g0061 a0001c0001t0019g0062 |
2 | HG01884.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.284-9217_284-9216i others(30): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648943 | ||||||
chr22:46648947 | G | C | 16 | a0001c0001t0003g0215 a0001c0001t0005g0105 a0001c0001t0005g0111 others(13): Show |
16 | HG00323.hp2 HG01168.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.284-9240G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648947 | |||||||
chr22:46648947 | G | GATGGATG others(9): Show |
1 | a0001c0001t0004g0021 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.284-9233_284-9232i others(18): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648947 | ||||||
chr22:46648947 | G | GATGGATG others(21): Show |
12 | a0001c0001t0005g0063 a0001c0001t0007g0022 a0001c0001t0007g0023 others(9): Show |
12 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.284-9221_284-9220i others(30): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648947 | ||||||
chr22:46648947 | G | GATGGATG others(17): Show |
7 | a0001c0001t0005g0144 a0001c0001t0005g0211 a0001c0001t0005g0258 others(4): Show |
7 | HG00738.hp2 HG01106.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.284-9217_284-9216i others(26): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648947 | ||||||
chr22:46648951 | G | C | 5 | a0001c0001t0002g0281 a0001c0001t0002g0290 a0001c0001t0006g0199 others(2): Show |
5 | HG00639.hp1 HG02145.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.284-9236G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648951 | |||||||
chr22:46648951 | G | GATGGATG others(13): Show |
91 | a0001c0001t0001g0197 a0001c0001t0001g0255 a0001c0001t0001g0261 others(88): Show |
93 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.284-9217_284-9216i others(22): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648951 | ||||||
chr22:46648951 | G | GATGGATG others(33): Show |
1 | a0001c0001t0002g0312 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.284-9217_284-9216i others(42): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648951 | ||||||
chr22:46648967 | G | GATGCATG others(17): Show |
4 | a0001c0001t0004g0035 a0001c0001t0004g0036 a0001c0001t0010g0034 others(1): Show |
4 | HG02622.hp2 HG02922.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-9217_284-9216i others(26): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648967 | ||||||
chr22:46648986 | A | G | 1 | a0002c0011t0053g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.284-9201A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648986 | |||||||
chr22:46649127 | G | A | 4 | a0001c0001t0003g0229 a0001c0001t0003g0245 a0001c0001t0014g0052 others(1): Show |
4 | HG00733.hp1 HG02486.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-9060G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46649127 | |||||||
chr22:46649272 | G | C | 2 | a0001c0001t0002g0171 a0001c0001t0002g0257 |
2 | NA18982.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.284-8915G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46649272 | |||||||
chr22:46649383 | C | T | 1 | a0001c0001t0014g0058 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.284-8804C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46649383 | |||||||
chr22:46649384 | G | A | 1 | a0001c0001t0009g0056 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.284-8803G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46649384 | |||||||
chr22:46649659 | T | A | 94 | a0001c0001t0001g0197 a0001c0001t0001g0255 a0001c0001t0001g0261 others(91): Show |
96 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.284-8528T>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46649659 | |||||||
chr22:46649685 | C | T | 1 | a0001c0001t0003g0212 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.284-8502C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46649685 | |||||||
chr22:46649858 | A | T | 1 | a0001c0001t0001g0179 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.284-8329A>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46649858 | |||||||
chr22:46649896 | C | T | 1 | a0001c0001t0056g0313 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.284-8291C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46649896 | |||||||
chr22:46649941 | G | T | 1 | a0001c0002t0004g0099 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.284-8246G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46649941 | |||||||
chr22:46650058 | G | A | 1 | a0002c0011t0053g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.284-8129G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46650058 | |||||||
chr22:46650208 | C | T | 1 | a0001c0001t0003g0245 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.284-7979C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46650208 | |||||||
chr22:46650308 | A | AGTGTCGA others(18): Show |
1 | a0002c0011t0053g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.284-7829_284-7805d others(27): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46650308 | ||||||
chr22:46650308 | AGTGTCGA others(18): Show |
A | 15 | a0001c0001t0001g0273 a0001c0001t0004g0021 a0001c0001t0005g0063 others(12): Show |
15 | HG00642.hp2 HG01070.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.284-7829_284-7805d others(27): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46650308 | ||||||
chr22:46650349 | G | A | 1 | a0001c0001t0003g0207 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.284-7838G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46650349 | |||||||
chr22:46650379 | G | T | 12 | a0001c0001t0005g0063 a0001c0001t0007g0022 a0001c0001t0007g0023 others(9): Show |
12 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.284-7808G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46650379 | |||||||
chr22:46650430 | C | G | 1 | a0001c0001t0002g0266 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.284-7757C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46650430 | |||||||
chr22:46650433 | AGCATTGA others(6): Show |
A | 13 | a0001c0001t0004g0021 a0001c0001t0005g0063 a0001c0001t0007g0022 others(10): Show |
13 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.284-7752_284-7740d others(15): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46650433 | ||||||
chr22:46650495 | G | A | 1 | a0001c0001t0064g0306 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.284-7692G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46650495 | |||||||
chr22:46650497 | C | G | 2 | a0001c0001t0015g0189 a0001c0001t0015g0190 |
2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.284-7690C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46650497 | |||||||
chr22:46650498 | G | A | 1 | a0001c0001t0003g0240 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.284-7689G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46650498 | |||||||
chr22:46650500 | T | C | 232 | a0001c0001t0001g0098 a0001c0001t0001g0197 a0001c0001t0001g0220 others(229): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.284-7687T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46650500 | |||||||
chr22:46650529 | C | G | 22 | a0001c0001t0004g0021 a0001c0001t0005g0063 a0001c0001t0007g0022 others(19): Show |
22 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.284-7658C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46650529 | |||||||
chr22:46650615 | T | C | 117 | a0001c0001t0001g0197 a0001c0001t0001g0255 a0001c0001t0001g0261 others(114): Show |
119 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.284-7572T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46650615 | |||||||
chr22:46650671 | A | G | 3 | a0001c0001t0003g0234 a0001c0003t0003g0235 a0001c0003t0003g0236 |
3 | HG02109.hp2 HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.284-7516A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46650671 | |||||||
chr22:46650718 | C | T | 2 | a0001c0001t0001g0110 a0001c0001t0038g0180 |
2 | HG03579.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.284-7469C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46650718 | |||||||
chr22:46650926 | G | A | 17 | a0001c0001t0003g0030 a0001c0001t0003g0031 a0001c0001t0003g0083 others(14): Show |
17 | HG01243.hp2 HG01496.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.284-7261G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46650926 | |||||||
chr22:46650931 | G | A | 2 | a0001c0001t0030g0044 a0001c0001t0048g0191 |
2 | HG01433.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.284-7256G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46650931 | |||||||
chr22:46651039 | T | G | 1 | a0001c0001t0001g0167 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.284-7148T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46651039 | |||||||
chr22:46651040 | G | A | 8 | a0001c0001t0010g0185 a0001c0001t0010g0186 a0001c0001t0010g0187 others(5): Show |
8 | HG01433.hp1 HG01884.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.284-7147G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46651040 | |||||||
chr22:46651138 | AG | A | 21 | a0001c0001t0001g0098 a0001c0002t0002g0071 a0001c0002t0004g0002 others(18): Show |
22 | HG01109.hp1 HG01361.hp2 HG01496.hp2 others(19): Show |
intron_variant | MODIFIER | c.284-7048delG | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46651138 | |||||||
chr22:46651214 | T | G | 12 | a0001c0001t0004g0035 a0001c0001t0004g0036 a0001c0001t0010g0034 others(9): Show |
12 | HG01433.hp1 HG01884.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.284-6973T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46651214 | |||||||
chr22:46651454 | C | T | 4 | a0001c0001t0010g0185 a0001c0001t0010g0186 a0001c0001t0010g0187 others(1): Show |
4 | HG01884.hp2 HG02572.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-6733C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46651454 | |||||||
chr22:46651512 | T | C | 3 | a0001c0001t0011g0183 a0001c0001t0011g0184 a0001c0001t0028g0060 |
3 | HG02723.hp2 HG03041.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.284-6675T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46651512 | |||||||
chr22:46651527 | G | T | 1 | a0001c0001t0008g0014 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.284-6660G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46651527 | |||||||
chr22:46651557 | C | T | 1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.284-6630C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46651557 | |||||||
chr22:46651571 | G | C | 1 | a0001c0001t0001g0074 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.284-6616G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46651571 | |||||||
chr22:46651640 | A | C | 1 | a0001c0001t0058g0277 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.284-6547A>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46651640 | |||||||
chr22:46651650 | C | G | 2 | a0001c0001t0030g0044 a0001c0001t0054g0251 |
2 | HG02647.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.284-6537C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46651650 | |||||||
chr22:46651737 | G | T | 3 | a0001c0001t0002g0172 a0001c0001t0002g0293 a0001c0001t0061g0289 |
3 | HG01943.hp1 HG02148.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.284-6450G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46651737 | |||||||
chr22:46651850 | G | C | 1 | a0001c0002t0002g0071 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.284-6337G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46651850 | |||||||
chr22:46651850 | G | T | 1 | a0001c0001t0006g0198 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.284-6337G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46651850 | |||||||
chr22:46651852 | G | A | 41 | a0001c0001t0001g0003 a0001c0001t0001g0072 a0001c0001t0001g0106 others(38): Show |
42 | HG00423.hp1 HG00642.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.284-6335G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46651852 | |||||||
chr22:46651977 | G | C | 10 | a0001c0002t0002g0071 a0001c0002t0004g0002 a0001c0002t0004g0070 others(7): Show |
11 | HG01361.hp2 HG01496.hp2 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.284-6210G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46651977 | |||||||
chr22:46652045 | G | T | 2 | a0001c0001t0005g0258 a0001c0001t0009g0050 |
2 | HG00738.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.284-6142G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46652045 | |||||||
chr22:46652159 | G | A | 4 | a0001c0001t0005g0111 a0001c0001t0005g0142 a0001c0001t0005g0143 others(1): Show |
4 | HG01168.hp2 HG02735.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-6028G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46652159 | |||||||
chr22:46652227 | G | A | 13 | a0001c0001t0004g0021 a0001c0001t0005g0063 a0001c0001t0007g0022 others(10): Show |
13 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.284-5960G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46652227 | |||||||
chr22:46652283 | A | G | 2 | a0001c0001t0027g0038 a0002c0011t0053g0019 |
2 | HG02145.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.284-5904A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46652283 | |||||||
chr22:46652305 | G | A | 10 | a0001c0001t0004g0035 a0001c0001t0004g0036 a0001c0001t0010g0034 others(7): Show |
10 | HG01433.hp1 HG01884.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.284-5882G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46652305 | |||||||
chr22:46652368 | C | T | 6 | a0001c0001t0003g0030 a0001c0001t0003g0031 a0001c0001t0003g0083 others(3): Show |
6 | HG01243.hp2 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.284-5819C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46652368 | |||||||
chr22:46652403 | T | C | 2 | a0001c0001t0030g0044 a0001c0001t0048g0191 |
2 | HG01433.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.284-5784T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46652403 | |||||||
chr22:46652481 | A | G | 140 | a0001c0001t0001g0197 a0001c0001t0001g0308 a0001c0001t0002g0007 others(137): Show |
142 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.284-5706A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46652481 | |||||||
chr22:46652579 | G | A | 7 | a0001c0001t0003g0206 a0001c0001t0003g0224 a0001c0001t0003g0225 others(4): Show |
7 | HG00140.hp1 HG00741.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.284-5608G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46652579 | |||||||
chr22:46652632 | G | A | 1 | a0002c0011t0053g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.284-5555G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46652632 | |||||||
chr22:46652659 | G | A | 1 | a0001c0001t0038g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.284-5528G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46652659 | |||||||
chr22:46652736 | C | T | 1 | a0001c0001t0038g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.284-5451C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46652736 | |||||||
chr22:46652737 | A | G | 322 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0066 others(319): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.284-5450A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46652737 | |||||||
chr22:46652768 | G | A | 1 | a0001c0001t0012g0079 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.284-5419G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46652768 | |||||||
chr22:46652874 | T | A | 1 | a0001c0001t0010g0034 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.284-5313T>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46652874 | |||||||
chr22:46652874 | T | G | 133 | a0001c0001t0001g0197 a0001c0001t0001g0308 a0001c0001t0002g0007 others(130): Show |
134 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.284-5313T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46652874 | |||||||
chr22:46652895 | A | G | 84 | a0001c0001t0001g0197 a0001c0001t0001g0308 a0001c0001t0002g0007 others(81): Show |
85 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.284-5292A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46652895 | |||||||
chr22:46653189 | C | T | 92 | a0001c0001t0001g0168 a0001c0001t0001g0197 a0001c0001t0001g0308 others(89): Show |
93 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.284-4998C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46653189 | |||||||
chr22:46653207 | G | C | 1 | a0001c0001t0001g0152 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.284-4980G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46653207 | |||||||
chr22:46653227 | C | T | 1 | a0001c0001t0038g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.284-4960C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46653227 | |||||||
chr22:46653241 | C | A | 107 | a0001c0001t0001g0197 a0001c0001t0001g0308 a0001c0001t0002g0007 others(104): Show |
108 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.284-4946C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46653241 | |||||||
chr22:46653244 | C | G | 8 | a0001c0001t0001g0074 a0001c0001t0001g0112 a0001c0001t0001g0125 others(5): Show |
8 | HG00438.hp1 HG00639.hp2 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.284-4943C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46653244 | |||||||
chr22:46653254 | G | C | 2 | a0001c0001t0023g0121 a0001c0001t0023g0122 |
2 | HG01952.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.284-4933G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46653254 | |||||||
chr22:46653328 | T | C | 26 | a0001c0001t0004g0021 a0001c0001t0004g0035 a0001c0001t0004g0036 others(23): Show |
26 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.284-4859T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46653328 | |||||||
chr22:46653366 | C | T | 1 | a0002c0011t0053g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.284-4821C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46653366 | |||||||
chr22:46653413 | G | A | 1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.284-4774G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46653413 | |||||||
chr22:46653577 | G | A | 227 | a0001c0001t0001g0197 a0001c0001t0001g0220 a0001c0001t0001g0308 others(224): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.284-4610G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46653577 | |||||||
chr22:46653588 | C | G | 1 | a0001c0001t0011g0057 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.284-4599C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46653588 | |||||||
chr22:46653607 | C | T | 2 | a0001c0001t0004g0061 a0001c0001t0019g0062 |
2 | HG01884.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.284-4580C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46653607 | |||||||
chr22:46653619 | C | T | 1 | a0001c0001t0002g0276 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.284-4568C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46653619 | |||||||
chr22:46653776 | G | A | 14 | a0001c0001t0004g0021 a0001c0001t0005g0063 a0001c0001t0007g0022 others(11): Show |
14 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.284-4411G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46653776 | |||||||
chr22:46653859 | C | T | 1 | a0001c0001t0006g0202 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.284-4328C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46653859 | |||||||
chr22:46653910 | A | G | 1 | a0001c0002t0004g0091 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.284-4277A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46653910 | |||||||
chr22:46653961 | G | A | 10 | a0001c0001t0004g0035 a0001c0001t0004g0036 a0001c0001t0010g0034 others(7): Show |
10 | HG01433.hp1 HG01884.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.284-4226G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46653961 | |||||||
chr22:46654044 | T | G | 1 | a0001c0001t0009g0054 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.284-4143T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46654044 | |||||||
chr22:46654069 | C | G | 1 | a0001c0001t0002g0310 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.284-4118C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46654069 | |||||||
chr22:46654070 | G | A | 13 | a0001c0001t0004g0021 a0001c0001t0005g0063 a0001c0001t0007g0022 others(10): Show |
13 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.284-4117G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46654070 | |||||||
chr22:46654179 | G | A | 2 | a0001c0001t0015g0189 a0001c0001t0015g0190 |
2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.284-4008G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46654179 | |||||||
chr22:46654313 | G | A | 85 | a0001c0001t0001g0197 a0001c0001t0001g0308 a0001c0001t0002g0007 others(82): Show |
86 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.284-3874G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46654313 | |||||||
chr22:46654400 | C | G | 1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.284-3787C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46654400 | |||||||
chr22:46654423 | C | T | 2 | a0001c0001t0002g0171 a0001c0001t0002g0257 |
2 | NA18982.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.284-3764C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46654423 | |||||||
chr22:46654439 | C | T | 99 | a0001c0001t0001g0197 a0001c0001t0001g0308 a0001c0001t0002g0007 others(96): Show |
100 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.284-3748C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46654439 | |||||||
chr22:46654490 | G | A | 84 | a0001c0001t0001g0197 a0001c0001t0001g0308 a0001c0001t0002g0007 others(81): Show |
85 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.284-3697G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46654490 | |||||||
chr22:46654637 | C | T | 20 | a0001c0002t0002g0071 a0001c0002t0004g0002 a0001c0002t0004g0032 others(17): Show |
21 | HG01109.hp1 HG01361.hp2 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.284-3550C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46654637 | |||||||
chr22:46654726 | C | T | 1 | a0001c0001t0001g0179 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.284-3461C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46654726 | |||||||
chr22:46654736 | C | G | 1 | a0001c0001t0001g0134 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.284-3451C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46654736 | |||||||
chr22:46654847 | G | A | 85 | a0001c0001t0001g0197 a0001c0001t0001g0308 a0001c0001t0002g0007 others(82): Show |
86 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.284-3340G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46654847 | |||||||
chr22:46654956 | A | G | 2 | a0001c0001t0004g0061 a0001c0001t0019g0062 |
2 | HG01884.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.284-3231A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46654956 | |||||||
chr22:46655008 | C | T | 1 | a0001c0001t0054g0251 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.284-3179C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46655008 | |||||||
chr22:46655052 | A | G | 1 | a0001c0002t0004g0099 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.284-3135A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46655052 | |||||||
chr22:46655081 | G | C | 2 | a0001c0001t0003g0006 a0001c0001t0041g0006 |
2 | HG02559.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.284-3106G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46655081 | |||||||
chr22:46655137 | A | C | 1 | a0001c0001t0001g0204 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.284-3050A>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46655137 | |||||||
chr22:46655141 | C | T | 1 | a0001c0001t0029g0053 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.284-3046C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46655141 | |||||||
chr22:46655144 | G | A | 1 | a0001c0001t0001g0204 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.284-3043G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46655144 | |||||||
chr22:46655150 | G | A | 1 | a0001c0001t0001g0204 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.284-3037G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46655150 | |||||||
chr22:46655151 | G | T | 1 | a0001c0001t0001g0204 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.284-3036G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46655151 | |||||||
chr22:46655153 | C | G | 1 | a0001c0001t0001g0204 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.284-3034C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46655153 | |||||||
chr22:46655156 | A | G | 1 | a0001c0001t0001g0204 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.284-3031A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46655156 | |||||||
chr22:46655157 | C | T | 1 | a0001c0001t0001g0204 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.284-3030C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46655157 | |||||||
chr22:46655158 | C | G | 1 | a0001c0001t0001g0204 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.284-3029C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46655158 | |||||||
chr22:46655159 | C | T | 1 | a0001c0001t0001g0204 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.284-3028C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46655159 | |||||||
chr22:46655242 | G | A | 2 | a0001c0001t0030g0044 a0001c0001t0048g0191 |
2 | HG01433.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.284-2945G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46655242 | |||||||
chr22:46655303 | A | C | 1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.284-2884A>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46655303 | |||||||
chr22:46655342 | T | C | 7 | a0001c0001t0010g0185 a0001c0001t0010g0186 a0001c0001t0010g0187 others(4): Show |
7 | HG01433.hp1 HG01884.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.284-2845T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46655342 | |||||||
chr22:46655441 | G | A | 3 | a0001c0001t0010g0185 a0001c0001t0010g0186 a0001c0001t0010g0187 |
3 | HG01884.hp2 HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.284-2746G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46655441 | |||||||
chr22:46655451 | A | G | 4 | a0001c0001t0003g0208 a0001c0001t0003g0214 a0001c0001t0003g0215 others(1): Show |
4 | HG00099.hp2 HG01081.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.284-2736A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46655451 | |||||||
chr22:46655600 | C | T | 98 | a0001c0001t0001g0197 a0001c0001t0001g0308 a0001c0001t0002g0007 others(95): Show |
99 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.284-2587C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46655600 | |||||||
chr22:46655735 | G | C | 1 | a0001c0001t0003g0229 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.284-2452G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46655735 | |||||||
chr22:46655866 | G | A | 13 | a0001c0001t0004g0021 a0001c0001t0005g0063 a0001c0001t0007g0022 others(10): Show |
13 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.284-2321G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46655866 | |||||||
chr22:46655890 | G | GCCAGGTG others(6): Show |
112 | a0001c0001t0001g0197 a0001c0001t0001g0308 a0001c0001t0002g0007 others(109): Show |
114 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.284-2295_284-2294i others(15): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46655890 | ||||||
chr22:46655927 | G | A | 4 | a0001c0001t0001g0112 a0001c0001t0001g0125 a0001c0001t0001g0127 others(1): Show |
4 | HG00438.hp1 HG02135.hp2 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.284-2260G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46655927 | |||||||
chr22:46655955 | C | T | 6 | a0001c0001t0002g0285 a0001c0001t0002g0291 a0001c0001t0002g0320 others(3): Show |
6 | NA18970.hp1 NA18980.hp1 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.284-2232C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46655955 | |||||||
chr22:46655976 | C | T | 10 | a0001c0001t0007g0022 a0001c0001t0007g0023 a0001c0001t0007g0024 others(7): Show |
10 | HG00642.hp2 HG01243.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.284-2211C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46655976 | |||||||
chr22:46656010 | C | A | 1 | a0001c0001t0010g0185 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.284-2177C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46656010 | |||||||
chr22:46656021 | T | C | 112 | a0001c0001t0001g0197 a0001c0001t0001g0308 a0001c0001t0002g0007 others(109): Show |
114 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.284-2166T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46656021 | |||||||
chr22:46656022 | G | A | 1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.284-2165G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46656022 | |||||||
chr22:46656031 | G | A | 1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.284-2156G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46656031 | |||||||
chr22:46656178 | G | A | 2 | a0001c0001t0002g0305 a0001c0001t0057g0304 |
2 | HG01069.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.284-2009G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46656178 | |||||||
chr22:46656380 | G | A | 1 | a0001c0001t0022g0138 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.284-1807G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46656380 | |||||||
chr22:46656796 | T | G | 107 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0308 others(104): Show |
109 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.284-1391T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46656796 | |||||||
chr22:46656844 | C | T | 2 | a0001c0001t0003g0218 a0001c0001t0003g0242 |
2 | HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.284-1343C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46656844 | |||||||
chr22:46656949 | C | T | 1 | a0001c0001t0011g0057 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.284-1238C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46656949 | |||||||
chr22:46656950 | C | G | 2 | a0001c0001t0001g0271 a0001c0001t0001g0309 |
2 | NA18955.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.284-1237C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46656950 | |||||||
chr22:46656961 | T | C | 13 | a0001c0001t0004g0021 a0001c0001t0005g0063 a0001c0001t0007g0022 others(10): Show |
13 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.284-1226T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46656961 | |||||||
chr22:46657162 | G | A | 2 | a0001c0001t0015g0189 a0001c0001t0015g0190 |
2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.284-1025G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46657162 | |||||||
chr22:46657225 | A | T | 3 | a0001c0001t0010g0185 a0001c0001t0010g0186 a0001c0001t0010g0187 |
3 | HG01884.hp2 HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.284-962A>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46657225 | |||||||
chr22:46657231 | T | C | 2 | a0001c0001t0001g0129 a0001c0001t0001g0132 |
2 | HG02148.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.284-956T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46657231 | |||||||
chr22:46657268 | G | A | 26 | a0001c0001t0001g0220 a0001c0001t0003g0006 a0001c0001t0003g0104 others(23): Show |
26 | HG00140.hp1 HG00741.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.284-919G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46657268 | |||||||
chr22:46657336 | A | G | 135 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0308 others(132): Show |
137 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.284-851A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46657336 | |||||||
chr22:46657368 | C | T | 1 | a0001c0001t0007g0025 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.284-819C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46657368 | |||||||
chr22:46657406 | G | A | 1 | a0001c0001t0001g0204 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.284-781G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46657406 | |||||||
chr22:46657407 | A | C | 1 | a0001c0001t0001g0204 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.284-780A>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46657407 | |||||||
chr22:46657408 | G | A | 1 | a0001c0001t0001g0204 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.284-779G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46657408 | |||||||
chr22:46657409 | G | C | 1 | a0001c0001t0001g0204 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.284-778G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46657409 | |||||||
chr22:46657410 | A | T | 1 | a0001c0001t0001g0204 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.284-777A>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46657410 | |||||||
chr22:46657413 | C | A | 1 | a0001c0001t0001g0204 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.284-774C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46657413 | |||||||
chr22:46657414 | G | T | 1 | a0001c0001t0001g0204 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.284-773G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46657414 | |||||||
chr22:46657415 | G | C | 1 | a0001c0001t0001g0204 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.284-772G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46657415 | |||||||
chr22:46657417 | A | C | 1 | a0001c0001t0001g0204 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.284-770A>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46657417 | |||||||
chr22:46657419 | A | T | 1 | a0001c0001t0001g0204 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.284-768A>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46657419 | |||||||
chr22:46657421 | A | T | 1 | a0001c0001t0001g0204 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.284-766A>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46657421 | |||||||
chr22:46657422 | G | T | 1 | a0001c0001t0001g0204 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.284-765G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46657422 | |||||||
chr22:46657425 | C | G | 1 | a0001c0001t0003g0207 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.284-762C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46657425 | |||||||
chr22:46657512 | T | C | 4 | a0001c0001t0004g0035 a0001c0001t0004g0036 a0001c0001t0010g0034 others(1): Show |
4 | HG02622.hp2 HG02922.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-675T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46657512 | |||||||
chr22:46657821 | T | C | 173 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0308 others(170): Show |
176 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.284-366T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46657821 | |||||||
chr22:46657829 | G | A | 1 | a0001c0001t0004g0035 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.284-358G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46657829 | |||||||
chr22:46657836 | C | T | 1 | a0001c0001t0029g0053 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.284-351C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46657836 | |||||||
chr22:46657852 | C | T | 2 | a0001c0001t0003g0210 a0001c0001t0003g0239 |
2 | NA18946.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.284-335C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46657852 | |||||||
chr22:46658019 | G | A | 3 | a0001c0001t0007g0024 a0001c0001t0007g0025 a0001c0001t0007g0029 |
3 | HG02451.hp2 HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.284-168G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46658019 | |||||||
chr22:46658033 | G | A | 1 | a0002c0010t0047g0064 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.284-154G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46658033 | |||||||
chr22:46658064 | A | G | 3 | a0001c0001t0015g0189 a0001c0001t0015g0190 a0001c0001t0054g0251 |
3 | HG02647.hp2 HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.284-123A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46658064 | |||||||
chr22:46658119 | C | T | 8 | a0001c0001t0010g0185 a0001c0001t0010g0186 a0001c0001t0010g0187 others(5): Show |
8 | HG01433.hp1 HG01884.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.284-68C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46658119 | |||||||
chr22:46658161 | T | C | 10 | a0001c0001t0003g0243 a0001c0001t0008g0008 a0001c0001t0008g0009 others(7): Show |
10 | HG01891.hp1 HG02723.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.284-26T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46658161 | |||||||
chr22:46658451 | C | T | 1 | a0001c0001t0001g0255 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.404+144C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46658451 | |||||||
chr22:46658517 | A | G | 18 | a0001c0001t0005g0105 a0001c0001t0005g0111 a0001c0001t0005g0142 others(15): Show |
18 | HG00323.hp2 HG00738.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.404+210A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46658517 | |||||||
chr22:46658535 | C | T | 1 | a0001c0007t0019g0182 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.404+228C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46658535 | |||||||
chr22:46658612 | T | C | 4 | a0001c0001t0004g0035 a0001c0001t0004g0036 a0001c0001t0010g0034 others(1): Show |
4 | HG02622.hp2 HG02922.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.404+305T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46658612 | |||||||
chr22:46658774 | C | T | 190 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0220 others(187): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.404+467C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46658774 | |||||||
chr22:46658782 | TGCCCCAG others(16): Show |
T | 1 | a0001c0001t0054g0251 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.404+481_404+503del others(23): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr22 | 46658782 | ||||||
chr22:46658786 | C | CCAGCCGC others(19): Show |
1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.404+484_404+485ins others(26): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr22 | 46658786 | ||||||
chr22:46658792 | A | G | 91 | a0001c0001t0001g0220 a0001c0001t0003g0006 a0001c0001t0003g0030 others(88): Show |
93 | HG00099.hp2 HG00140.hp1 HG00733.hp1 others(90): Show |
intron_variant | MODIFIER | c.404+485A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46658792 | |||||||
chr22:46658798 | T | C | 32 | a0001c0001t0003g0243 a0001c0001t0004g0017 a0001c0001t0008g0008 others(29): Show |
33 | HG01109.hp1 HG01361.hp2 HG01496.hp2 others(30): Show |
intron_variant | MODIFIER | c.404+491T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46658798 | |||||||
chr22:46658799 | G | A | 32 | a0001c0001t0003g0243 a0001c0001t0004g0017 a0001c0001t0008g0008 others(29): Show |
33 | HG01109.hp1 HG01361.hp2 HG01496.hp2 others(30): Show |
intron_variant | MODIFIER | c.404+492G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46658799 | |||||||
chr22:46658806 | G | A | 13 | a0001c0001t0004g0021 a0001c0001t0005g0063 a0001c0001t0007g0022 others(10): Show |
13 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.404+499G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46658806 | |||||||
chr22:46658845 | G | A | 2 | a0001c0001t0006g0174 a0001c0001t0006g0302 |
2 | NA19081.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.404+538G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46658845 | |||||||
chr22:46658915 | T | C | 1 | a0001c0001t0004g0233 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.404+608T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46658915 | |||||||
chr22:46659082 | G | A | 5 | a0001c0002t0004g0032 a0001c0002t0004g0069 a0001c0002t0004g0092 others(2): Show |
5 | HG01891.hp2 HG02647.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.404+775G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46659082 | |||||||
chr22:46659141 | C | T | 1 | a0001c0007t0019g0182 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.404+834C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46659141 | |||||||
chr22:46659235 | TCCCTCAG others(6): Show |
T | 13 | a0001c0001t0004g0021 a0001c0001t0005g0063 a0001c0001t0007g0022 others(10): Show |
13 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.404+936_404+948del others(13): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr22 | 46659235 | ||||||
chr22:46659245 | T | G | 4 | a0001c0001t0010g0185 a0001c0001t0010g0186 a0001c0001t0010g0187 others(1): Show |
4 | HG01884.hp2 HG03471.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.404+938T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46659245 | |||||||
chr22:46659254 | A | G | 1 | a0001c0001t0013g0055 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.404+947A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46659254 | |||||||
chr22:46659276 | C | T | 1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.404+969C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46659276 | |||||||
chr22:46659308 | G | A | 3 | a0001c0001t0001g0003 a0001c0001t0001g0113 a0001c0001t0001g0163 |
4 | NA18969.hp1 NA18970.hp2 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.404+1001G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46659308 | |||||||
chr22:46659316 | A | C | 2 | a0001c0001t0003g0006 a0001c0001t0041g0006 |
2 | HG02559.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.404+1009A>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46659316 | |||||||
chr22:46659482 | C | T | 1 | a0001c0005t0002g0294 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.404+1175C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46659482 | |||||||
chr22:46659668 | C | T | 7 | a0001c0001t0003g0243 a0001c0001t0008g0008 a0001c0001t0008g0009 others(4): Show |
7 | HG01891.hp1 HG02723.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.404+1361C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46659668 | |||||||
chr22:46659707 | GGGGGGCT others(5): Show |
G | 2 | a0001c0001t0027g0038 a0002c0011t0053g0019 |
2 | HG02145.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.404+1419_404+1430d others(14): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr22 | 46659707 | ||||||
chr22:46659739 | T | C | 15 | a0001c0001t0004g0021 a0001c0001t0005g0063 a0001c0001t0007g0022 others(12): Show |
15 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.404+1432T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46659739 | |||||||
chr22:46659761 | G | A | 11 | a0001c0001t0003g0243 a0001c0001t0004g0017 a0001c0001t0008g0008 others(8): Show |
11 | HG01891.hp1 HG02572.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.404+1454G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46659761 | |||||||
chr22:46659782 | G | A | 1 | a0001c0001t0002g0300 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.404+1475G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46659782 | |||||||
chr22:46659978 | A | G | 5 | a0001c0001t0006g0102 a0001c0001t0006g0174 a0001c0001t0006g0302 others(2): Show |
5 | HG00597.hp1 HG02040.hp2 HG02071.hp1 others(2): Show |
intron_variant | MODIFIER | c.405-1403A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46659978 | |||||||
chr22:46659990 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.405-1391G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46659990 | |||||||
chr22:46660000 | G | T | 1 | a0001c0001t0002g0278 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.405-1381G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46660000 | |||||||
chr22:46660042 | C | T | 2 | a0001c0001t0002g0286 a0001c0001t0002g0287 |
2 | NA18964.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.405-1339C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46660042 | |||||||
chr22:46660183 | C | T | 18 | a0001c0001t0005g0105 a0001c0001t0005g0111 a0001c0001t0005g0142 others(15): Show |
18 | HG00323.hp2 HG00738.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.405-1198C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46660183 | |||||||
chr22:46660317 | G | A | 11 | a0001c0001t0004g0035 a0001c0001t0004g0036 a0001c0001t0010g0034 others(8): Show |
11 | HG01433.hp1 HG01884.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.405-1064G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46660317 | |||||||
chr22:46660454 | A | G | 4 | a0001c0001t0004g0035 a0001c0001t0004g0036 a0001c0001t0010g0034 others(1): Show |
4 | HG02622.hp2 HG02922.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.405-927A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46660454 | |||||||
chr22:46660478 | A | C | 13 | a0001c0001t0004g0021 a0001c0001t0005g0063 a0001c0001t0007g0022 others(10): Show |
13 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.405-903A>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46660478 | |||||||
chr22:46660493 | C | T | 5 | a0001c0002t0004g0032 a0001c0002t0004g0069 a0001c0002t0004g0092 others(2): Show |
5 | HG01891.hp2 HG02647.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.405-888C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46660493 | |||||||
chr22:46660505 | A | G | 1 | a0001c0001t0002g0298 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.405-876A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46660505 | |||||||
chr22:46660632 | G | A | 10 | a0001c0001t0007g0022 a0001c0001t0007g0023 a0001c0001t0007g0024 others(7): Show |
10 | HG00642.hp2 HG01243.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.405-749G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46660632 | |||||||
chr22:46660659 | A | G | 11 | a0001c0001t0004g0035 a0001c0001t0004g0036 a0001c0001t0010g0034 others(8): Show |
11 | HG01433.hp1 HG01884.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.405-722A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46660659 | |||||||
chr22:46660715 | C | T | 1 | a0001c0007t0019g0182 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.405-666C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46660715 | |||||||
chr22:46660809 | A | C | 1 | a0001c0001t0004g0233 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.405-572A>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46660809 | |||||||
chr22:46660904 | C | T | 1 | a0001c0001t0012g0079 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.405-477C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46660904 | |||||||
chr22:46660934 | T | A | 5 | a0001c0001t0004g0035 a0001c0001t0004g0036 a0001c0001t0010g0034 others(2): Show |
5 | HG02622.hp2 HG02922.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.405-447T>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46660934 | |||||||
chr22:46660940 | C | T | 5 | a0001c0001t0004g0035 a0001c0001t0004g0036 a0001c0001t0010g0034 others(2): Show |
5 | HG02622.hp2 HG02922.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.405-441C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46660940 | |||||||
chr22:46660945 | C | T | 2 | a0001c0001t0001g0141 a0001c0001t0037g0065 |
2 | NA18948.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.405-436C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46660945 | |||||||
chr22:46661027 | AAC | A | 13 | a0001c0001t0004g0021 a0001c0001t0005g0063 a0001c0001t0007g0022 others(10): Show |
13 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.405-350_405-349del others(2): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr22 | 46661027 | ||||||
chr22:46661028 | A | G | 8 | a0001c0001t0010g0185 a0001c0001t0010g0186 a0001c0001t0010g0187 others(5): Show |
8 | HG01433.hp1 HG01884.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.405-353A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46661028 | |||||||
chr22:46661050 | C | A | 1 | a0001c0001t0054g0251 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.405-331C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46661050 | |||||||
chr22:46661178 | C | T | 11 | a0001c0001t0003g0243 a0001c0001t0004g0017 a0001c0001t0008g0008 others(8): Show |
11 | HG01891.hp1 HG02572.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.405-203C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46661178 | |||||||
chr22:46661179 | G | A | 31 | a0001c0001t0004g0021 a0001c0001t0005g0063 a0001c0001t0005g0105 others(28): Show |
31 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.405-202G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46661179 | |||||||
chr22:46661224 | G | A | 1 | a0001c0001t0063g0227 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.405-157G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46661224 | |||||||
chr22:46661294 | C | T | 101 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0308 others(98): Show |
103 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.405-87C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46661294 | |||||||
chr22:46661300 | C | T | 104 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0308 others(101): Show |
106 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.405-81C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46661300 | |||||||
chr22:46661315 | G | C | 4 | a0001c0001t0004g0035 a0001c0001t0004g0036 a0001c0001t0010g0034 others(1): Show |
4 | HG02622.hp2 HG02922.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.405-66G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46661315 | |||||||
chr22:46661321 | G | T | 3 | a0001c0001t0004g0036 a0001c0001t0010g0034 a0001c0001t0033g0037 |
3 | HG02622.hp2 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.405-60G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46661321 | |||||||
chr22:46661542 | C | T | 1 | a0001c0001t0031g0059 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.466+100C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46661542 | |||||||
chr22:46661546 | C | A | 1 | a0001c0007t0019g0182 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.466+104C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46661546 | |||||||
chr22:46661565 | C | T | 16 | a0001c0001t0004g0061 a0001c0001t0010g0185 a0001c0001t0010g0186 others(13): Show |
16 | HG01433.hp1 HG01884.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.466+123C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46661565 | |||||||
chr22:46661594 | C | G | 2 | a0001c0001t0001g0271 a0001c0001t0001g0309 |
2 | NA18955.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.466+152C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46661594 | |||||||
chr22:46661630 | G | A | 7 | a0001c0001t0001g0115 a0001c0001t0001g0139 a0001c0001t0001g0255 others(4): Show |
7 | HG02027.hp1 NA18612.hp1 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.466+188G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46661630 | |||||||
chr22:46661648 | G | A | 2 | a0001c0001t0003g0218 a0001c0001t0003g0242 |
2 | HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.466+206G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46661648 | |||||||
chr22:46661676 | A | G | 164 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0308 others(161): Show |
167 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.466+234A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46661676 | |||||||
chr22:46661676 | A | T | 1 | a0001c0002t0004g0093 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.466+234A>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46661676 | |||||||
chr22:46661748 | C | A | 1 | a0001c0001t0004g0233 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.466+306C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46661748 | |||||||
chr22:46661795 | T | C | 1 | a0001c0007t0019g0182 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.466+353T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46661795 | |||||||
chr22:46661811 | C | T | 1 | a0001c0001t0009g0049 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.466+369C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46661811 | |||||||
chr22:46661849 | G | C | 4 | a0001c0001t0001g0112 a0001c0001t0001g0125 a0001c0001t0001g0127 others(1): Show |
4 | HG00438.hp1 HG02135.hp2 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.466+407G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46661849 | |||||||
chr22:46661883 | A | T | 8 | a0001c0001t0001g0308 a0001c0001t0002g0296 a0001c0001t0002g0297 others(5): Show |
8 | HG00099.hp1 HG00642.hp1 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.466+441A>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46661883 | |||||||
chr22:46661959 | C | T | 1 | a0001c0001t0004g0021 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.466+517C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46661959 | |||||||
chr22:46661979 | A | C | 18 | a0001c0001t0005g0105 a0001c0001t0005g0111 a0001c0001t0005g0142 others(15): Show |
18 | HG00323.hp2 HG00738.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.466+537A>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46661979 | |||||||
chr22:46662103 | C | G | 1 | a0001c0001t0001g0167 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.466+661C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46662103 | |||||||
chr22:46662273 | G | A | 18 | a0001c0001t0005g0105 a0001c0001t0005g0111 a0001c0001t0005g0142 others(15): Show |
18 | HG00323.hp2 HG00738.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.467-767G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46662273 | |||||||
chr22:46662348 | G | A | 4 | a0001c0001t0010g0185 a0001c0001t0010g0186 a0001c0001t0010g0187 others(1): Show |
4 | HG01884.hp2 HG03471.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.467-692G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46662348 | |||||||
chr22:46662360 | G | A | 1 | a0001c0001t0007g0033 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.467-680G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46662360 | |||||||
chr22:46662368 | C | T | 6 | a0001c0001t0002g0285 a0001c0001t0002g0291 a0001c0001t0002g0320 others(3): Show |
6 | NA18970.hp1 NA18980.hp1 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.467-672C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46662368 | |||||||
chr22:46662477 | G | A | 2 | a0001c0001t0004g0061 a0001c0001t0019g0062 |
2 | HG01884.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.467-563G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46662477 | |||||||
chr22:46662497 | G | A | 1 | a0001c0001t0005g0188 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.467-543G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46662497 | |||||||
chr22:46662507 | C | G | 3 | a0001c0001t0003g0210 a0001c0001t0003g0238 a0001c0001t0003g0239 |
3 | NA18946.hp1 NA18952.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.467-533C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46662507 | |||||||
chr22:46662517 | G | A | 1 | a0001c0001t0002g0257 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.467-523G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46662517 | |||||||
chr22:46662520 | C | A | 3 | a0001c0002t0004g0032 a0001c0002t0004g0093 a0001c0002t0004g0094 |
3 | HG02965.hp1 HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.467-520C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46662520 | |||||||
chr22:46662636 | A | C | 18 | a0001c0001t0005g0105 a0001c0001t0005g0111 a0001c0001t0005g0142 others(15): Show |
18 | HG00323.hp2 HG00738.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.467-404A>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46662636 | |||||||
chr22:46662658 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.467-382G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46662658 | |||||||
chr22:46662696 | C | T | 7 | a0001c0001t0010g0185 a0001c0001t0010g0186 a0001c0001t0010g0187 others(4): Show |
7 | HG01433.hp1 HG01884.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.467-344C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46662696 | |||||||
chr22:46662744 | G | A | 1 | a0001c0001t0004g0233 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.467-296G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46662744 | |||||||
chr22:46662760 | A | G | 5 | a0001c0002t0004g0002 a0001c0002t0004g0086 a0001c0002t0004g0117 others(2): Show |
6 | HG01361.hp2 HG01496.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.467-280A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46662760 | |||||||
chr22:46662787 | C | T | 1 | a0002c0011t0053g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.467-253C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46662787 | |||||||
chr22:46662974 | C | T | 2 | a0001c0001t0021g0155 a0001c0001t0021g0156 |
2 | HG00673.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.467-66C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46662974 | |||||||
chr22:46662981 | G | A | 7 | a0001c0001t0003g0243 a0001c0001t0008g0008 a0001c0001t0008g0009 others(4): Show |
7 | HG01891.hp1 HG02723.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.467-59G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46662981 | |||||||
chr22:46663000 | C | T | 2 | a0001c0001t0005g0105 a0001c0001t0005g0211 |
2 | HG03669.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.467-40C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46663000 | |||||||
chr22:46663182 | C | T | 1 | a0001c0001t0002g0262 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.599+10C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 6/18 | chr22 | 46663182 | |||||||
chr22:46663246 | G | A | 4 | a0001c0001t0004g0035 a0001c0001t0004g0036 a0001c0001t0010g0034 others(1): Show |
4 | HG02622.hp2 HG02922.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.599+74G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 6/18 | chr22 | 46663246 | |||||||
chr22:46663313 | T | C | 1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.599+141T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 6/18 | chr22 | 46663313 | |||||||
chr22:46663385 | C | T | 136 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0308 others(133): Show |
138 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.599+213C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 6/18 | chr22 | 46663385 | |||||||
chr22:46663475 | C | A | 149 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0308 others(146): Show |
151 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.599+303C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 6/18 | chr22 | 46663475 | |||||||
chr22:46663574 | C | A | 1 | a0001c0001t0043g0311 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.600-264C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 6/18 | chr22 | 46663574 | |||||||
chr22:46663642 | G | T | 4 | a0001c0001t0004g0035 a0001c0001t0004g0036 a0001c0001t0010g0034 others(1): Show |
4 | HG02622.hp2 HG02922.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.600-196G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 6/18 | chr22 | 46663642 | |||||||
chr22:46663700 | A | G | 175 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0308 others(172): Show |
178 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.600-138A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 6/18 | chr22 | 46663700 | |||||||
chr22:46663736 | G | A | 7 | a0001c0001t0010g0185 a0001c0001t0010g0186 a0001c0001t0010g0187 others(4): Show |
7 | HG01433.hp1 HG01884.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.600-102G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 6/18 | chr22 | 46663736 | |||||||
chr22:46663769 | G | A | 1 | a0001c0001t0052g0136 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.600-69G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 6/18 | chr22 | 46663769 | |||||||
chr22:46664128 | C | A | 1 | a0001c0001t0001g0134 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.717+11C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 8/18 | chr22 | 46664128 | |||||||
chr22:46664311 | G | A | 2 | a0001c0001t0015g0189 a0001c0001t0015g0190 |
2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.717+194G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 8/18 | chr22 | 46664311 | |||||||
chr22:46664380 | T | C | 166 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0308 others(163): Show |
168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.717+263T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 8/18 | chr22 | 46664380 | |||||||
chr22:46664449 | G | A | 3 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG01256.hp2 HG01258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.717+332G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 8/18 | chr22 | 46664449 | |||||||
chr22:46664487 | C | CA | 230 | a0001c0001t0001g0161 a0001c0001t0001g0196 a0001c0001t0001g0197 others(227): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.717+370_717+371ins others(1): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 8/18 | chr22 | 46664487 | |||||||
chr22:46664496 | T | C | 154 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0308 others(151): Show |
156 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.717+379T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 8/18 | chr22 | 46664496 | |||||||
chr22:46664550 | G | A | 1 | a0001c0002t0002g0071 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.717+433G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 8/18 | chr22 | 46664550 | |||||||
chr22:46664646 | G | T | 6 | a0001c0001t0003g0206 a0001c0001t0003g0224 a0001c0001t0003g0225 others(3): Show |
6 | HG00140.hp1 HG00741.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.717+529G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 8/18 | chr22 | 46664646 | |||||||
chr22:46664650 | C | T | 2 | a0001c0001t0001g0129 a0001c0001t0001g0132 |
2 | HG02148.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.717+533C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 8/18 | chr22 | 46664650 | |||||||
chr22:46664693 | C | G | 9 | a0001c0001t0002g0249 a0001c0001t0002g0260 a0001c0001t0002g0272 others(6): Show |
9 | HG02015.hp2 NA18951.hp2 NA18970.hp1 others(6): Show |
intron_variant | MODIFIER | c.717+576C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 8/18 | chr22 | 46664693 | |||||||
chr22:46664717 | T | C | 1 | a0001c0001t0054g0251 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.717+600T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 8/18 | chr22 | 46664717 | |||||||
chr22:46664728 | G | A | 4 | a0001c0001t0010g0185 a0001c0001t0010g0186 a0001c0001t0010g0187 others(1): Show |
4 | HG01884.hp2 HG03471.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.717+611G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 8/18 | chr22 | 46664728 | |||||||
chr22:46665019 | C | T | 38 | a0001c0001t0003g0243 a0001c0001t0004g0017 a0001c0001t0004g0021 others(35): Show |
39 | HG01109.hp1 HG01361.hp2 HG01496.hp2 others(36): Show |
intron_variant | MODIFIER | c.718-596C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 8/18 | chr22 | 46665019 | |||||||
chr22:46665052 | G | A | 1 | a0001c0001t0003g0217 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.718-563G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 8/18 | chr22 | 46665052 | |||||||
chr22:46665056 | G | A | 1 | a0001c0001t0050g0147 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.718-559G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 8/18 | chr22 | 46665056 | |||||||
chr22:46665079 | C | T | 131 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0308 others(128): Show |
133 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.718-536C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 8/18 | chr22 | 46665079 | |||||||
chr22:46665092 | T | C | 1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.718-523T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 8/18 | chr22 | 46665092 | |||||||
chr22:46665246 | C | G | 1 | a0001c0007t0019g0182 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.718-369C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 8/18 | chr22 | 46665246 | |||||||
chr22:46665362 | C | T | 22 | a0001c0001t0003g0030 a0001c0001t0003g0031 a0001c0001t0003g0083 others(19): Show |
23 | HG01243.hp2 HG01496.hp1 HG01943.hp2 others(20): Show |
intron_variant | MODIFIER | c.718-253C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 8/18 | chr22 | 46665362 | |||||||
chr22:46665367 | G | A | 1 | a0001c0001t0011g0183 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.718-248G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 8/18 | chr22 | 46665367 | |||||||
chr22:46665744 | C | T | 20 | a0001c0002t0002g0071 a0001c0002t0004g0002 a0001c0002t0004g0032 others(17): Show |
21 | HG01109.hp1 HG01361.hp2 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.809+38C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 9/18 | chr22 | 46665744 | |||||||
chr22:46665762 | G | A | 2 | a0001c0001t0005g0258 a0001c0001t0009g0050 |
2 | HG00738.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.809+56G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 9/18 | chr22 | 46665762 | |||||||
chr22:46665782 | C | T | 2 | a0001c0001t0030g0044 a0001c0001t0048g0191 |
2 | HG01433.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.809+76C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 9/18 | chr22 | 46665782 | |||||||
chr22:46665797 | G | A | 4 | a0001c0001t0010g0185 a0001c0001t0010g0186 a0001c0001t0010g0187 others(1): Show |
4 | HG01884.hp2 HG03471.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.809+91G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 9/18 | chr22 | 46665797 | |||||||
chr22:46665862 | C | T | 5 | a0001c0001t0004g0061 a0001c0001t0011g0183 a0001c0001t0011g0184 others(2): Show |
5 | HG01884.hp1 HG02723.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.809+156C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 9/18 | chr22 | 46665862 | |||||||
chr22:46665894 | C | T | 135 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0308 others(132): Show |
137 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.809+188C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 9/18 | chr22 | 46665894 | |||||||
chr22:46665937 | G | A | 4 | a0001c0001t0004g0035 a0001c0001t0004g0036 a0001c0001t0010g0034 others(1): Show |
4 | HG02622.hp2 HG02922.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.809+231G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 9/18 | chr22 | 46665937 | |||||||
chr22:46666019 | A | T | 123 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0308 others(120): Show |
125 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.809+313A>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 9/18 | chr22 | 46666019 | |||||||
chr22:46666089 | G | T | 1 | a0001c0001t0009g0054 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.809+383G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 9/18 | chr22 | 46666089 | |||||||
chr22:46666179 | C | T | 5 | a0001c0001t0010g0034 a0001c0001t0010g0185 a0001c0001t0010g0186 others(2): Show |
5 | HG01884.hp2 HG03471.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.809+473C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 9/18 | chr22 | 46666179 | |||||||
chr22:46666294 | A | G | 2 | a0001c0001t0003g0006 a0001c0001t0041g0006 |
2 | HG02559.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.810-531A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 9/18 | chr22 | 46666294 | |||||||
chr22:46666389 | C | G | 2 | a0001c0001t0030g0044 a0001c0001t0048g0191 |
2 | HG01433.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.810-436C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 9/18 | chr22 | 46666389 | |||||||
chr22:46666492 | C | T | 1 | a0001c0001t0001g0157 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.810-333C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 9/18 | chr22 | 46666492 | |||||||
chr22:46666493 | G | C | 3 | a0001c0002t0004g0091 a0001c0002t0004g0095 a0001c0002t0004g0096 |
3 | HG01109.hp1 HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.810-332G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 9/18 | chr22 | 46666493 | |||||||
chr22:46666494 | TTGGTACC others(33): Show |
T | 1 | a0001c0001t0003g0283 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.810-328_810-289del others(40): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr22 | 46666494 | ||||||
chr22:46666676 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.810-149G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 9/18 | chr22 | 46666676 | |||||||
chr22:46666683 | C | A | 1 | a0001c0001t0001g0168 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.810-142C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 9/18 | chr22 | 46666683 | |||||||
chr22:46666737 | C | T | 1 | a0001c0001t0001g0219 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.810-88C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 9/18 | chr22 | 46666737 | |||||||
chr22:46666745 | C | G | 3 | a0001c0001t0004g0035 a0001c0001t0004g0036 a0001c0001t0033g0037 |
3 | HG02622.hp2 HG02922.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.810-80C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 9/18 | chr22 | 46666745 | |||||||
chr22:46666746 | G | A | 1 | a0001c0001t0003g0283 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.810-79G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 9/18 | chr22 | 46666746 | |||||||
chr22:46666805 | G | A | 1 | a0001c0001t0005g0041 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.810-20G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 9/18 | chr22 | 46666805 | |||||||
chr22:46666904 | C | T | 1 | a0001c0001t0012g0079 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.858+31C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 10/18 | chr22 | 46666904 | |||||||
chr22:46666997 | G | T | 31 | a0001c0001t0005g0063 a0001c0001t0005g0105 a0001c0001t0005g0111 others(28): Show |
31 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.858+124G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 10/18 | chr22 | 46666997 | |||||||
chr22:46667241 | T | G | 1 | a0001c0002t0004g0069 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.858+368T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 10/18 | chr22 | 46667241 | |||||||
chr22:46667433 | A | G | 91 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0308 others(88): Show |
93 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.858+560A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 10/18 | chr22 | 46667433 | |||||||
chr22:46667462 | T | C | 175 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0308 others(172): Show |
178 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.858+589T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 10/18 | chr22 | 46667462 | |||||||
chr22:46667478 | G | A | 5 | a0001c0002t0004g0002 a0001c0002t0004g0086 a0001c0002t0004g0117 others(2): Show |
6 | HG01361.hp2 HG01496.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.858+605G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 10/18 | chr22 | 46667478 | |||||||
chr22:46667515 | T | C | 1 | a0001c0002t0004g0099 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.859-581T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 10/18 | chr22 | 46667515 | |||||||
chr22:46667595 | G | A | 11 | a0001c0001t0004g0035 a0001c0001t0004g0036 a0001c0001t0010g0034 others(8): Show |
11 | HG01433.hp1 HG01884.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.859-501G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 10/18 | chr22 | 46667595 | |||||||
chr22:46667600 | C | T | 1 | a0001c0009t0062g0303 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.859-496C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 10/18 | chr22 | 46667600 | |||||||
chr22:46667611 | C | T | 1 | a0001c0001t0002g0269 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.859-485C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 10/18 | chr22 | 46667611 | |||||||
chr22:46667677 | G | A | 12 | a0001c0001t0005g0063 a0001c0001t0007g0022 a0001c0001t0007g0023 others(9): Show |
12 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.859-419G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 10/18 | chr22 | 46667677 | |||||||
chr22:46667712 | C | T | 1 | a0001c0002t0002g0071 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.859-384C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 10/18 | chr22 | 46667712 | |||||||
chr22:46667784 | G | C | 2 | a0001c0001t0002g0305 a0001c0001t0057g0304 |
2 | HG01069.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.859-312G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 10/18 | chr22 | 46667784 | |||||||
chr22:46667985 | G | A | 1 | a0002c0010t0047g0064 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.859-111G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 10/18 | chr22 | 46667985 | |||||||
chr22:46668178 | G | A | 1 | a0001c0001t0003g0212 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.930+11G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 11/18 | chr22 | 46668178 | |||||||
chr22:46668267 | C | A | 168 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0308 others(165): Show |
170 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.930+100C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 11/18 | chr22 | 46668267 | |||||||
chr22:46668288 | G | A | 12 | a0001c0001t0005g0063 a0001c0001t0007g0022 a0001c0001t0007g0023 others(9): Show |
12 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.930+121G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 11/18 | chr22 | 46668288 | |||||||
chr22:46668417 | G | A | 5 | a0001c0001t0010g0034 a0001c0001t0010g0185 a0001c0001t0010g0186 others(2): Show |
5 | HG01884.hp2 HG03471.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.930+250G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 11/18 | chr22 | 46668417 | |||||||
chr22:46668419 | G | A | 1 | a0001c0001t0028g0060 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.930+252G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 11/18 | chr22 | 46668419 | |||||||
chr22:46668430 | T | C | 317 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0066 others(314): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.931-259T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 11/18 | chr22 | 46668430 | |||||||
chr22:46668489 | C | T | 1 | a0001c0001t0004g0233 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.931-200C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 11/18 | chr22 | 46668489 | |||||||
chr22:46668768 | C | T | 99 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0253 others(96): Show |
100 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.975-31C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 12/18 | chr22 | 46668768 | |||||||
chr22:46668937 | T | G | 1 | a0001c0001t0007g0027 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1084+29T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46668937 | |||||||
chr22:46668940 | A | C | 87 | a0001c0001t0001g0163 a0001c0001t0001g0196 a0001c0001t0001g0197 others(84): Show |
88 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.1084+32A>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46668940 | |||||||
chr22:46668953 | C | T | 6 | a0001c0001t0004g0061 a0001c0001t0009g0049 a0001c0001t0011g0183 others(3): Show |
6 | HG01884.hp1 HG02145.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1084+45C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46668953 | |||||||
chr22:46669048 | A | G | 1 | a0001c0007t0019g0182 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1084+140A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46669048 | |||||||
chr22:46669073 | G | A | 3 | a0001c0001t0003g0083 a0001c0001t0003g0084 a0001c0001t0003g0085 |
3 | HG01243.hp2 HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1084+165G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46669073 | |||||||
chr22:46669187 | A | C | 38 | a0001c0001t0003g0243 a0001c0001t0004g0035 a0001c0001t0004g0036 others(35): Show |
38 | HG00738.hp2 HG01106.hp1 HG01168.hp1 others(35): Show |
intron_variant | MODIFIER | c.1084+279A>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46669187 | |||||||
chr22:46669413 | G | A | 1 | a0001c0001t0052g0136 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1084+505G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46669413 | |||||||
chr22:46669443 | GC | G | 24 | a0001c0001t0003g0083 a0001c0001t0003g0084 a0001c0001t0003g0226 others(21): Show |
24 | HG00642.hp2 HG01243.hp1 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.1084+542delC | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr22 | 46669443 | ||||||
chr22:46669464 | C | T | 1 | a0001c0001t0003g0240 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1084+556C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46669464 | |||||||
chr22:46669553 | T | C | 80 | a0001c0001t0003g0226 a0001c0001t0003g0243 a0001c0001t0003g0250 others(77): Show |
82 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(79): Show |
intron_variant | MODIFIER | c.1084+645T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46669553 | |||||||
chr22:46669577 | C | G | 86 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0002g0007 others(83): Show |
87 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.1084+669C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46669577 | |||||||
chr22:46669579 | CT | C | 11 | a0001c0001t0004g0035 a0001c0001t0004g0036 a0001c0001t0004g0061 others(8): Show |
11 | HG01884.hp1 HG02572.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1084+684delT | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr22 | 46669579 | ||||||
chr22:46669713 | C | T | 1 | a0001c0001t0007g0029 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1084+805C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46669713 | |||||||
chr22:46669725 | G | A | 5 | a0001c0001t0004g0035 a0001c0001t0004g0036 a0001c0001t0027g0038 others(2): Show |
5 | HG02145.hp1 HG02572.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1084+817G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46669725 | |||||||
chr22:46669733 | G | A | 1 | a0001c0001t0002g0281 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1084+825G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46669733 | |||||||
chr22:46669767 | C | T | 157 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0002g0007 others(154): Show |
160 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.1084+859C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46669767 | |||||||
chr22:46669787 | T | C | 179 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0002g0007 others(176): Show |
182 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.1084+879T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46669787 | |||||||
chr22:46669816 | C | T | 12 | a0001c0001t0005g0063 a0001c0001t0007g0022 a0001c0001t0007g0023 others(9): Show |
12 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.1084+908C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46669816 | |||||||
chr22:46669851 | T | C | 1 | a0001c0001t0001g0179 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1084+943T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46669851 | |||||||
chr22:46669858 | C | T | 117 | a0001c0001t0002g0007 a0001c0001t0002g0081 a0001c0001t0002g0100 others(114): Show |
119 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.1084+950C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46669858 | |||||||
chr22:46669959 | T | C | 1 | a0001c0001t0004g0295 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1084+1051T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46669959 | |||||||
chr22:46669990 | C | T | 2 | a0001c0001t0004g0061 a0001c0001t0019g0062 |
2 | HG01884.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1084+1082C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46669990 | |||||||
chr22:46669991 | G | A | 1 | a0001c0001t0002g0257 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1084+1083G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46669991 | |||||||
chr22:46669993 | C | T | 8 | a0001c0001t0004g0035 a0001c0001t0004g0036 a0001c0001t0011g0183 others(5): Show |
8 | HG02572.hp2 HG02622.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1084+1085C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46669993 | |||||||
chr22:46670050 | G | A | 2 | a0001c0001t0004g0061 a0001c0001t0019g0062 |
2 | HG01884.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1084+1142G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46670050 | |||||||
chr22:46670150 | C | G | 1 | a0001c0001t0002g0301 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1084+1242C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46670150 | |||||||
chr22:46670151 | G | A | 1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1084+1243G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46670151 | |||||||
chr22:46670229 | C | T | 2 | a0001c0001t0002g0305 a0001c0001t0057g0304 |
2 | HG01069.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1084+1321C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46670229 | |||||||
chr22:46670397 | T | C | 86 | a0001c0001t0002g0007 a0001c0001t0002g0081 a0001c0001t0002g0100 others(83): Show |
87 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.1084+1489T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46670397 | |||||||
chr22:46670450 | C | G | 3 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 |
3 | HG02040.hp1 HG02074.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.1084+1542C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46670450 | |||||||
chr22:46670460 | C | T | 1 | a0001c0007t0019g0182 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1084+1552C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46670460 | |||||||
chr22:46670525 | C | G | 2 | a0001c0001t0015g0189 a0001c0001t0015g0190 |
2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1084+1617C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46670525 | |||||||
chr22:46670629 | C | T | 1 | a0001c0001t0001g0220 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1084+1721C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46670629 | |||||||
chr22:46670729 | G | A | 1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1084+1821G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46670729 | |||||||
chr22:46670733 | G | A | 4 | a0001c0001t0003g0208 a0001c0001t0003g0214 a0001c0001t0003g0215 others(1): Show |
4 | HG00099.hp2 HG01081.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.1084+1825G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46670733 | |||||||
chr22:46670899 | G | A | 11 | a0001c0001t0007g0022 a0001c0001t0007g0023 a0001c0001t0007g0024 others(8): Show |
11 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.1085-1944G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46670899 | |||||||
chr22:46670907 | C | CT | 26 | a0001c0001t0005g0001 a0001c0001t0005g0039 a0001c0001t0005g0040 others(23): Show |
27 | HG00323.hp2 HG00738.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.1085-1935dupT | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr22 | 46670907 | ||||||
chr22:46671018 | T | C | 3 | a0001c0001t0011g0057 a0001c0001t0038g0180 a0001c0001t0054g0251 |
3 | HG02647.hp2 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1085-1825T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46671018 | |||||||
chr22:46671023 | T | C | 29 | a0001c0001t0004g0061 a0001c0001t0005g0001 a0001c0001t0005g0039 others(26): Show |
30 | HG00323.hp2 HG00738.hp2 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.1085-1820T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46671023 | |||||||
chr22:46671026 | C | T | 2 | a0001c0001t0004g0061 a0001c0001t0019g0062 |
2 | HG01884.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1085-1817C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46671026 | |||||||
chr22:46671264 | C | T | 11 | a0001c0001t0007g0022 a0001c0001t0007g0023 a0001c0001t0007g0024 others(8): Show |
11 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.1085-1579C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46671264 | |||||||
chr22:46671267 | A | G | 29 | a0001c0001t0004g0061 a0001c0001t0005g0001 a0001c0001t0005g0039 others(26): Show |
30 | HG00323.hp2 HG00738.hp2 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.1085-1576A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46671267 | |||||||
chr22:46671271 | G | A | 1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1085-1572G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46671271 | |||||||
chr22:46671328 | A | G | 29 | a0001c0001t0004g0061 a0001c0001t0005g0001 a0001c0001t0005g0039 others(26): Show |
30 | HG00323.hp2 HG00738.hp2 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.1085-1515A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46671328 | |||||||
chr22:46671362 | G | A | 29 | a0001c0001t0004g0061 a0001c0001t0005g0001 a0001c0001t0005g0039 others(26): Show |
30 | HG00323.hp2 HG00738.hp2 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.1085-1481G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46671362 | |||||||
chr22:46671371 | C | T | 8 | a0001c0001t0004g0035 a0001c0001t0004g0036 a0001c0001t0011g0183 others(5): Show |
8 | HG02572.hp2 HG02622.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1085-1472C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46671371 | |||||||
chr22:46671399 | C | T | 1 | a0001c0001t0048g0191 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1085-1444C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46671399 | |||||||
chr22:46671424 | A | T | 1 | a0002c0011t0053g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1085-1419A>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46671424 | |||||||
chr22:46671615 | T | C | 157 | a0001c0001t0002g0007 a0001c0001t0002g0081 a0001c0001t0002g0100 others(154): Show |
160 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.1085-1228T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46671615 | |||||||
chr22:46671634 | C | T | 1 | a0001c0001t0021g0156 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1085-1209C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46671634 | |||||||
chr22:46671650 | C | T | 11 | a0001c0001t0007g0022 a0001c0001t0007g0023 a0001c0001t0007g0024 others(8): Show |
11 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.1085-1193C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46671650 | |||||||
chr22:46671651 | G | A | 5 | a0001c0001t0004g0061 a0001c0001t0015g0189 a0001c0001t0015g0190 others(2): Show |
5 | HG01884.hp1 HG02896.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1085-1192G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46671651 | |||||||
chr22:46671656 | AAAAATAA others(3): Show |
A | 226 | a0001c0001t0002g0007 a0001c0001t0002g0081 a0001c0001t0002g0100 others(223): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1085-1157_1085-114 others(14): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr22 | 46671656 | ||||||
chr22:46671762 | C | T | 3 | a0001c0001t0011g0057 a0001c0001t0038g0180 a0001c0001t0054g0251 |
3 | HG02647.hp2 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1085-1081C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46671762 | |||||||
chr22:46671861 | T | C | 1 | a0001c0001t0003g0248 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1085-982T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46671861 | |||||||
chr22:46672083 | C | T | 1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1085-760C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46672083 | |||||||
chr22:46672084 | G | A | 9 | a0001c0001t0002g0171 a0001c0001t0002g0257 a0001c0001t0002g0262 others(6): Show |
9 | HG00423.hp2 HG02056.hp2 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.1085-759G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46672084 | |||||||
chr22:46672111 | T | C | 29 | a0001c0001t0004g0061 a0001c0001t0005g0001 a0001c0001t0005g0039 others(26): Show |
30 | HG00323.hp2 HG00738.hp2 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.1085-732T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46672111 | |||||||
chr22:46672243 | G | A | 28 | a0001c0001t0004g0061 a0001c0001t0005g0001 a0001c0001t0005g0039 others(25): Show |
29 | HG00323.hp2 HG00738.hp2 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.1085-600G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46672243 | |||||||
chr22:46672301 | T | C | 29 | a0001c0001t0004g0061 a0001c0001t0005g0001 a0001c0001t0005g0039 others(26): Show |
30 | HG00323.hp2 HG00738.hp2 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.1085-542T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46672301 | |||||||
chr22:46672340 | A | G | 12 | a0001c0001t0001g0003 a0001c0001t0001g0072 a0001c0001t0001g0106 others(9): Show |
13 | HG00673.hp2 HG02056.hp1 NA18612.hp2 others(10): Show |
intron_variant | MODIFIER | c.1085-503A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46672340 | |||||||
chr22:46672355 | G | T | 1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1085-488G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46672355 | |||||||
chr22:46672359 | G | T | 21 | a0001c0001t0004g0233 a0001c0001t0064g0306 a0001c0002t0004g0002 others(18): Show |
22 | HG00741.hp2 HG01109.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.1085-484G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46672359 | |||||||
chr22:46672394 | A | G | 28 | a0001c0001t0004g0061 a0001c0001t0005g0001 a0001c0001t0005g0039 others(25): Show |
29 | HG00323.hp2 HG00738.hp2 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.1085-449A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46672394 | |||||||
chr22:46672468 | T | C | 25 | a0001c0001t0002g0266 a0001c0001t0005g0001 a0001c0001t0005g0039 others(22): Show |
26 | HG00323.hp2 HG00735.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.1085-375T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46672468 | |||||||
chr22:46673025 | G | C | 1 | a0001c0001t0048g0191 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1239+28G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 14/18 | chr22 | 46673025 | |||||||
chr22:46673032 | TG | T | 88 | a0001c0001t0001g0005 a0001c0001t0001g0080 a0001c0001t0001g0098 others(85): Show |
89 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(86): Show |
intron_variant | MODIFIER | c.1239+41delG | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr22 | 46673032 | ||||||
chr22:46673038 | G | T | 88 | a0001c0001t0001g0005 a0001c0001t0001g0080 a0001c0001t0001g0098 others(85): Show |
89 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(86): Show |
intron_variant | MODIFIER | c.1239+41G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 14/18 | chr22 | 46673038 | |||||||
chr22:46673129 | C | A | 20 | a0001c0001t0005g0001 a0001c0001t0005g0039 a0001c0001t0005g0040 others(17): Show |
21 | HG00323.hp2 HG00738.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.1239+132C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 14/18 | chr22 | 46673129 | |||||||
chr22:46673130 | T | TA | 20 | a0001c0001t0005g0001 a0001c0001t0005g0039 a0001c0001t0005g0040 others(17): Show |
21 | HG00323.hp2 HG00738.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.1239+133_1239+134i others(3): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 14/18 | chr22 | 46673130 | |||||||
chr22:46673136 | G | GT | 6 | a0001c0001t0001g0074 a0001c0001t0001g0120 a0001c0001t0001g0131 others(3): Show |
6 | HG01257.hp1 HG01981.hp2 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.1239+149dupT | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr22 | 46673136 | ||||||
chr22:46673137 | T | G | 18 | a0001c0001t0005g0001 a0001c0001t0005g0039 a0001c0001t0005g0041 others(15): Show |
19 | HG00323.hp2 HG00738.hp2 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.1239+140T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 14/18 | chr22 | 46673137 | |||||||
chr22:46673304 | G | A | 21 | a0001c0001t0003g0030 a0001c0001t0003g0031 a0001c0001t0003g0083 others(18): Show |
21 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.1239+307G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 14/18 | chr22 | 46673304 | |||||||
chr22:46673326 | A | G | 93 | a0001c0001t0001g0072 a0001c0001t0001g0115 a0001c0001t0001g0116 others(90): Show |
94 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.1239+329A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 14/18 | chr22 | 46673326 | |||||||
chr22:46673422 | G | C | 1 | a0001c0001t0002g0264 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1240-248G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 14/18 | chr22 | 46673422 | |||||||
chr22:46673439 | C | G | 6 | a0001c0001t0002g0259 a0001c0001t0002g0266 a0001c0001t0002g0267 others(3): Show |
6 | HG00735.hp1 HG01109.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.1240-231C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 14/18 | chr22 | 46673439 | |||||||
chr22:46673451 | C | T | 3 | a0001c0001t0005g0111 a0001c0001t0005g0143 a0001c0001t0050g0147 |
3 | HG02735.hp1 HG03688.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1240-219C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 14/18 | chr22 | 46673451 | |||||||
chr22:46673452 | G | A | 10 | a0001c0001t0007g0022 a0001c0001t0007g0023 a0001c0001t0007g0024 others(7): Show |
10 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.1240-218G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 14/18 | chr22 | 46673452 | |||||||
chr22:46673874 | G | A | 3 | a0001c0001t0006g0192 a0001c0001t0006g0194 a0001c0007t0019g0182 |
3 | HG00438.hp2 HG02015.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1384+60G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 15/18 | chr22 | 46673874 | |||||||
chr22:46673896 | C | T | 1 | a0001c0001t0019g0062 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1384+82C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 15/18 | chr22 | 46673896 | |||||||
chr22:46673943 | C | T | 1 | a0001c0001t0022g0138 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1384+129C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 15/18 | chr22 | 46673943 | |||||||
chr22:46673994 | C | T | 1 | a0001c0001t0005g0213 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1384+180C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 15/18 | chr22 | 46673994 | |||||||
chr22:46674003 | G | C | 2 | a0001c0001t0001g0005 a0001c0001t0012g0005 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1384+189G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 15/18 | chr22 | 46674003 | |||||||
chr22:46674015 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1384+201G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 15/18 | chr22 | 46674015 | |||||||
chr22:46674065 | G | T | 3 | a0001c0001t0007g0024 a0001c0001t0007g0025 a0001c0001t0007g0029 |
3 | HG02451.hp2 HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1384+251G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 15/18 | chr22 | 46674065 | |||||||
chr22:46674093 | C | T | 5 | a0001c0001t0002g0285 a0001c0001t0002g0320 a0001c0001t0026g0292 others(2): Show |
5 | NA18970.hp1 NA18980.hp1 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.1384+279C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 15/18 | chr22 | 46674093 | |||||||
chr22:46674108 | G | A | 2 | a0001c0001t0015g0189 a0001c0001t0015g0190 |
2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1384+294G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 15/18 | chr22 | 46674108 | |||||||
chr22:46674121 | G | A | 23 | a0001c0001t0005g0001 a0001c0001t0005g0039 a0001c0001t0005g0040 others(20): Show |
24 | HG00323.hp2 HG00738.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.1384+307G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 15/18 | chr22 | 46674121 | |||||||
chr22:46674182 | A | C | 1 | a0001c0001t0005g0142 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1384+368A>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 15/18 | chr22 | 46674182 | |||||||
chr22:46674305 | C | T | 1 | a0001c0001t0014g0058 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1385-352C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 15/18 | chr22 | 46674305 | |||||||
chr22:46674327 | C | T | 2 | a0001c0001t0030g0044 a0001c0001t0048g0191 |
2 | HG01433.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1385-330C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 15/18 | chr22 | 46674327 | |||||||
chr22:46674349 | C | T | 1 | a0001c0001t0011g0057 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1385-308C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 15/18 | chr22 | 46674349 | |||||||
chr22:46674511 | C | T | 1 | a0001c0001t0003g0223 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1385-146C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 15/18 | chr22 | 46674511 | |||||||
chr22:46674516 | C | T | 1 | a0001c0001t0008g0009 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1385-141C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 15/18 | chr22 | 46674516 | |||||||
chr22:46674535 | G | C | 84 | a0001c0001t0002g0007 a0001c0001t0002g0081 a0001c0001t0002g0100 others(81): Show |
85 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.1385-122G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 15/18 | chr22 | 46674535 | |||||||
chr22:46674551 | G | A | 1 | a0001c0001t0002g0298 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1385-106G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 15/18 | chr22 | 46674551 | |||||||
chr22:46674563 | C | T | 21 | a0001c0001t0004g0061 a0001c0001t0004g0295 a0001c0002t0004g0002 others(18): Show |
22 | HG01109.hp1 HG01361.hp2 HG01496.hp2 others(19): Show |
intron_variant | MODIFIER | c.1385-94C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 15/18 | chr22 | 46674563 | |||||||
chr22:46674653 | T | A | 1 | a0001c0001t0011g0057 | 1 | NA19043.hp1 | splice_region_variant&intron_variant | LOW | c.1385-4T>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 15/18 | chr22 | 46674653 | |||||||
chr22:46674850 | G | T | 52 | a0001c0001t0003g0006 a0001c0001t0003g0030 a0001c0001t0003g0031 others(49): Show |
52 | HG00099.hp2 HG00140.hp1 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.1478+100G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 16/18 | chr22 | 46674850 | |||||||
chr22:46674856 | T | A | 1 | a0001c0002t0004g0069 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1478+106T>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 16/18 | chr22 | 46674856 | |||||||
chr22:46675013 | C | T | 2 | a0001c0001t0019g0062 a0001c0007t0019g0182 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1478+263C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 16/18 | chr22 | 46675013 | |||||||
chr22:46675113 | G | A | 1 | a0001c0001t0001g0135 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1479-355G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 16/18 | chr22 | 46675113 | |||||||
chr22:46675153 | GCAGAGCA others(20): Show |
G | 1 | a0001c0001t0005g0145 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1479-289_1479-263d others(29): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr22 | 46675153 | ||||||
chr22:46675262 | TGTGA | T | 33 | a0001c0001t0003g0243 a0001c0001t0004g0021 a0001c0001t0004g0061 others(30): Show |
34 | HG01109.hp1 HG01361.hp2 HG01496.hp2 others(31): Show |
intron_variant | MODIFIER | c.1479-202_1479-199d others(6): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr22 | 46675262 | ||||||
chr22:46675343 | G | C | 5 | a0001c0001t0011g0057 a0001c0001t0011g0183 a0001c0001t0011g0184 others(2): Show |
5 | HG02723.hp2 HG03041.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.1479-125G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 16/18 | chr22 | 46675343 | |||||||
chr22:46675444 | C | T | 2 | a0001c0001t0003g0218 a0001c0001t0003g0242 |
2 | HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1479-24C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 16/18 | chr22 | 46675444 | |||||||
chr22:46675570 | C | T | 3 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG01256.hp2 HG01258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1563+18C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 17/18 | chr22 | 46675570 | |||||||
chr22:46675615 | C | T | 2 | a0001c0001t0019g0062 a0001c0007t0019g0182 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1563+63C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 17/18 | chr22 | 46675615 | |||||||
chr22:46675634 | T | C | 106 | a0001c0001t0002g0007 a0001c0001t0002g0081 a0001c0001t0002g0100 others(103): Show |
107 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.1563+82T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 17/18 | chr22 | 46675634 | |||||||
chr22:46675741 | G | C | 23 | a0001c0001t0005g0001 a0001c0001t0005g0039 a0001c0001t0005g0040 others(20): Show |
24 | HG00323.hp2 HG00738.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.1563+189G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 17/18 | chr22 | 46675741 | |||||||
chr22:46675839 | G | A | 1 | a0001c0001t0002g0310 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1563+287G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 17/18 | chr22 | 46675839 | |||||||
chr22:46675963 | A | C | 136 | a0001c0001t0002g0007 a0001c0001t0002g0081 a0001c0001t0002g0100 others(133): Show |
138 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.1563+411A>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 17/18 | chr22 | 46675963 | |||||||
chr22:46676159 | T | A | 1 | a0001c0001t0019g0062 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1564-441T>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 17/18 | chr22 | 46676159 | |||||||
chr22:46676173 | C | T | 89 | a0001c0001t0002g0007 a0001c0001t0002g0081 a0001c0001t0002g0100 others(86): Show |
90 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1564-427C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 17/18 | chr22 | 46676173 | |||||||
chr22:46676276 | C | T | 2 | a0001c0003t0003g0235 a0001c0003t0003g0236 |
2 | HG02109.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1564-324C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 17/18 | chr22 | 46676276 | |||||||
chr22:46676299 | C | T | 11 | a0001c0001t0007g0022 a0001c0001t0007g0023 a0001c0001t0007g0024 others(8): Show |
11 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.1564-301C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 17/18 | chr22 | 46676299 | |||||||
chr22:46676423 | G | A | 1 | a0001c0001t0001g0178 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1564-177G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 17/18 | chr22 | 46676423 | |||||||
chr22:46676423 | G | C | 1 | a0001c0007t0019g0182 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1564-177G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 17/18 | chr22 | 46676423 | |||||||
chr22:46676580 | G | A | 122 | a0001c0001t0001g0115 a0001c0001t0001g0139 a0001c0001t0001g0255 others(119): Show |
124 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.1564-20G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 17/18 | chr22 | 46676580 | |||||||
chr22:46676716 | G | C | 1 | a0001c0001t0019g0062 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1632+48G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 18/18 | chr22 | 46676716 | |||||||
chr22:46676723 | T | C | 32 | a0001c0001t0004g0021 a0001c0001t0004g0061 a0001c0001t0004g0233 others(29): Show |
33 | HG01109.hp1 HG01361.hp2 HG01496.hp2 others(30): Show |
intron_variant | MODIFIER | c.1632+55T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 18/18 | chr22 | 46676723 | |||||||
chr22:46676741 | C | T | 1 | a0001c0001t0005g0143 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1632+73C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 18/18 | chr22 | 46676741 | |||||||
chr22:46676823 | G | A | 2 | a0001c0001t0019g0062 a0001c0007t0019g0182 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1632+155G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 18/18 | chr22 | 46676823 | |||||||
chr22:46676830 | G | A | 11 | a0001c0001t0007g0022 a0001c0001t0007g0023 a0001c0001t0007g0024 others(8): Show |
11 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.1632+162G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 18/18 | chr22 | 46676830 | |||||||
chr22:46676873 | G | A | 2 | a0001c0001t0001g0129 a0001c0001t0001g0132 |
2 | HG02148.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.1632+205G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 18/18 | chr22 | 46676873 | |||||||
chr22:46676889 | T | C | 9 | a0001c0001t0009g0049 a0001c0001t0011g0057 a0001c0001t0011g0183 others(6): Show |
9 | HG02145.hp2 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1632+221T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 18/18 | chr22 | 46676889 | |||||||
chr22:46676890 | G | A | 1 | a0001c0001t0038g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1632+222G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 18/18 | chr22 | 46676890 |