Item | Value |
---|---|
geneid | 23161 |
ensemblid | ENSG00000071189.21 |
hgncid | 21335 |
symbol | SNX13 |
name | sorting nexin 13 |
refseq_nuc | NM_015132.5 |
refseq_prot | NP_055947.1 |
ensembl_nuc | ENST00000428135.7 |
ensembl_prot | ENSP00000398789.2 |
mane_status | MANE Select |
chr | chr7 |
start | 17790761 |
end | 17940494 |
strand | - |
ver | v1.2 |
region | chr7:17790761-17940494 |
region5000 | chr7:17785761-17945494 |
regionname0 | SNX13_chr7_17790761_17940494 |
regionname5000 | SNX13_chr7_17785761_17945494 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 957 | 336 | 73 | 68 | 144 | 14 | 35 | 112 | SNX13_chr7_17785761_17945494 | SNX13 | MLTEA others(952): Show |
chr7 | 17785761 | 17945494 |
a0002 | 0/0 | 957 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | MLTEA others(952): Show |
chr7 | 17785761 | 17945494 |
a0003 | 0/0 | 957 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | MLTEA others(952): Show |
chr7 | 17785761 | 17945494 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 2871 | 228 | 58 | 43 | 90 | 10 | 26 | SNX13_chr7_17785761_17945494 | SNX13 | ATGTT others(2866): Show |
chr7 | 17785761 | 17945494 | ||
a0001c0002 | 1/0 | 2871 | 94 | 9 | 21 | 50 | 4 | 9 | SNX13_chr7_17785761_17945494 | SNX13 | ATGTT others(2866): Show |
chr7 | 17785761 | 17945494 | ||
a0001c0003 | 0/0 | 2871 | 4 | 0 | 0 | 4 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | ATGTT others(2866): Show |
chr7 | 17785761 | 17945494 | ||
a0001c0004 | 0/0 | 2871 | 3 | 3 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | ATGTT others(2866): Show |
chr7 | 17785761 | 17945494 | ||
a0001c0005 | 0/0 | 2871 | 2 | 0 | 2 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | ATGTT others(2866): Show |
chr7 | 17785761 | 17945494 | ||
a0001c0006 | 0/0 | 2871 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | ATGTT others(2866): Show |
chr7 | 17785761 | 17945494 | ||
a0001c0007 | 0/0 | 2871 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | ATGTT others(2866): Show |
chr7 | 17785761 | 17945494 | ||
a0001c0008 | 0/0 | 2871 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | ATGTT others(2866): Show |
chr7 | 17785761 | 17945494 | ||
a0001c0010 | 0/0 | 2871 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | ATGTT others(2866): Show |
chr7 | 17785761 | 17945494 | ||
a0001c0011 | 0/0 | 2871 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | ATGTT others(2866): Show |
chr7 | 17785761 | 17945494 | ||
a0002c0009 | 0/0 | 2871 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | ATGTT others(2866): Show |
chr7 | 17785761 | 17945494 | ||
a0003c0012 | 0/0 | 2871 | 1 | 0 | 0 | 0 | 0 | 1 | SNX13_chr7_17785761_17945494 | SNX13 | ATGTT others(2866): Show |
chr7 | 17785761 | 17945494 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 6357 | 166 | 40 | 31 | 64 | 10 | 20 | SNX13_chr7_17785761_17945494 | SNX13 | GCTCT others(6352): Show |
chr7 | 17785761 | 17945494 |
a0001c0001t0002 | 0/0 | 6357 | 2 | 1 | 0 | 0 | 0 | 1 | SNX13_chr7_17785761_17945494 | SNX13 | GCTCT others(6352): Show |
chr7 | 17785761 | 17945494 |
a0001c0001t0003 | 0/0 | 6357 | 13 | 0 | 0 | 13 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | GCTCT others(6352): Show |
chr7 | 17785761 | 17945494 |
a0001c0001t0004 | 0/0 | 6357 | 12 | 0 | 2 | 7 | 0 | 3 | SNX13_chr7_17785761_17945494 | SNX13 | GCTCT others(6352): Show |
chr7 | 17785761 | 17945494 |
a0001c0001t0005 | 0/0 | 6357 | 9 | 3 | 2 | 3 | 0 | 1 | SNX13_chr7_17785761_17945494 | SNX13 | GCTCT others(6352): Show |
chr7 | 17785761 | 17945494 |
a0001c0001t0008 | 0/0 | 6357 | 6 | 5 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | GCTCT others(6352): Show |
chr7 | 17785761 | 17945494 |
a0001c0001t0010 | 0/0 | 6356 | 3 | 3 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | GCTCT others(6351): Show |
chr7 | 17785761 | 17945494 |
a0001c0001t0012 | 0/0 | 6357 | 3 | 3 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | GCTCT others(6352): Show |
chr7 | 17785761 | 17945494 |
a0001c0001t0013 | 0/0 | 6357 | 2 | 0 | 2 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | GCTCT others(6352): Show |
chr7 | 17785761 | 17945494 |
a0001c0001t0014 | 0/0 | 6357 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | GCTCT others(6352): Show |
chr7 | 17785761 | 17945494 |
a0001c0001t0016 | 0/0 | 6357 | 2 | 0 | 0 | 2 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | GCTCT others(6352): Show |
chr7 | 17785761 | 17945494 |
a0001c0001t0018 | 0/0 | 6357 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | GCTCT others(6352): Show |
chr7 | 17785761 | 17945494 |
a0001c0001t0019 | 0/0 | 6357 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | GCTCT others(6352): Show |
chr7 | 17785761 | 17945494 |
a0001c0001t0020 | 0/0 | 6357 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | GCTCT others(6352): Show |
chr7 | 17785761 | 17945494 |
a0001c0001t0021 | 0/0 | 6357 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | GCTCT others(6352): Show |
chr7 | 17785761 | 17945494 |
a0001c0001t0022 | 0/0 | 6357 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | GCTCT others(6352): Show |
chr7 | 17785761 | 17945494 |
a0001c0001t0026 | 0/0 | 6357 | 1 | 0 | 0 | 0 | 0 | 1 | SNX13_chr7_17785761_17945494 | SNX13 | GCTCT others(6352): Show |
chr7 | 17785761 | 17945494 |
a0001c0001t0028 | 0/0 | 6357 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | GCTCT others(6352): Show |
chr7 | 17785761 | 17945494 |
a0001c0001t0029 | 0/0 | 6357 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | GCTCT others(6352): Show |
chr7 | 17785761 | 17945494 |
a0001c0001t0031 | 0/0 | 6357 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | GCTCT others(6352): Show |
chr7 | 17785761 | 17945494 |
a0001c0002t0001 | 0/0 | 6357 | 20 | 0 | 1 | 18 | 0 | 1 | SNX13_chr7_17785761_17945494 | SNX13 | GCTCT others(6352): Show |
chr7 | 17785761 | 17945494 |
a0001c0002t0002 | 1/0 | 6357 | 48 | 6 | 12 | 18 | 3 | 8 | SNX13_chr7_17785761_17945494 | SNX13 | GCTCT others(6352): Show |
chr7 | 17785761 | 17945494 |
a0001c0002t0006 | 0/0 | 6357 | 6 | 0 | 6 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | GCTCT others(6352): Show |
chr7 | 17785761 | 17945494 |
a0001c0002t0007 | 0/0 | 6357 | 7 | 0 | 0 | 6 | 1 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | GCTCT others(6352): Show |
chr7 | 17785761 | 17945494 |
a0001c0002t0009 | 0/0 | 6357 | 5 | 0 | 1 | 4 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | GCTCT others(6352): Show |
chr7 | 17785761 | 17945494 |
a0001c0002t0015 | 0/0 | 6357 | 2 | 0 | 0 | 2 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | GCTCT others(6352): Show |
chr7 | 17785761 | 17945494 |
a0001c0002t0017 | 0/0 | 6357 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | GCTCT others(6352): Show |
chr7 | 17785761 | 17945494 |
a0001c0002t0023 | 0/0 | 6357 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | GCTCT others(6352): Show |
chr7 | 17785761 | 17945494 |
a0001c0002t0024 | 0/0 | 6357 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | GCTCT others(6352): Show |
chr7 | 17785761 | 17945494 |
a0001c0002t0027 | 0/0 | 6357 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | GCTCT others(6352): Show |
chr7 | 17785761 | 17945494 |
a0001c0002t0030 | 0/0 | 6357 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | GCTCT others(6352): Show |
chr7 | 17785761 | 17945494 |
a0001c0002t0032 | 0/0 | 6357 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | GCTCT others(6352): Show |
chr7 | 17785761 | 17945494 |
a0001c0003t0001 | 0/0 | 6357 | 3 | 0 | 0 | 3 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | GCTCT others(6352): Show |
chr7 | 17785761 | 17945494 |
a0001c0003t0003 | 0/0 | 6357 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | GCTCT others(6352): Show |
chr7 | 17785761 | 17945494 |
a0001c0004t0011 | 0/0 | 6357 | 3 | 3 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | GCTCT others(6352): Show |
chr7 | 17785761 | 17945494 |
a0001c0005t0002 | 0/0 | 6357 | 2 | 0 | 2 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | GCTCT others(6352): Show |
chr7 | 17785761 | 17945494 |
a0001c0006t0025 | 0/0 | 6357 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | GCTCT others(6352): Show |
chr7 | 17785761 | 17945494 |
a0001c0007t0001 | 0/0 | 6357 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | GCTCT others(6352): Show |
chr7 | 17785761 | 17945494 |
a0001c0008t0002 | 0/0 | 6357 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | GCTCT others(6352): Show |
chr7 | 17785761 | 17945494 |
a0001c0010t0014 | 0/0 | 6357 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | GCTCT others(6352): Show |
chr7 | 17785761 | 17945494 |
a0001c0011t0006 | 0/0 | 6357 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | GCTCT others(6352): Show |
chr7 | 17785761 | 17945494 |
a0002c0009t0001 | 0/0 | 6357 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | GCTCT others(6352): Show |
chr7 | 17785761 | 17945494 |
a0003c0012t0001 | 0/0 | 6357 | 1 | 0 | 0 | 0 | 0 | 1 | SNX13_chr7_17785761_17945494 | SNX13 | GCTCT others(6352): Show |
chr7 | 17785761 | 17945494 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0165 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0004g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0004g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0004g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0004g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0004g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0004g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0004g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0004g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0004g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0004g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0004g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0005g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0005g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0005g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0005g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0005g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0005g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0005g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0005g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0005g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0008g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0008g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0008g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0008g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0008g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0008g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0010g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0010g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0010g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0012g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0012g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0012g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0013g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0013g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0014g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0016g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0016g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0018g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0019g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0020g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0021g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0022g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0026g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0028g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0029g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0001t0031g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0002g0168 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0002g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0002g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0002g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0002g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0002g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0002g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0002g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0002g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0002g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0006g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0006g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0006g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0006g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0006g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0006g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0007g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0007g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0007g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0007g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0007g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0007g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0007g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0009g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0009g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0009g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0009g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0009g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0015g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0015g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0017g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0023g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0024g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0027g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0030g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0002t0032g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0003t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0003t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0003t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0003t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0004t0011g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0004t0011g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0004t0011g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0005t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0005t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0006t0025g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0007t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0008t0002g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0010t0014g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0001c0011t0006g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0002c0009t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
a0003c0012t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0149 | EUR | GBR | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG00140 | hp2 | a0001 | c0002 | t0002 | g0281 | EUR | GBR | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0243 | EUR | FIN | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0054 | EUR | FIN | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0036 | EUR | FIN | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG00323 | hp2 | a0001 | c0002 | t0007 | g0299 | EUR | FIN | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG00408 | hp2 | a0001 | c0002 | t0002 | g0247 | EAS | CHS | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG00423 | hp2 | a0001 | c0001 | t0003 | g0182 | EAS | CHS | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG00544 | hp1 | a0001 | c0001 | t0004 | g0184 | EAS | CHS | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG00558 | hp1 | a0001 | c0002 | t0001 | g0322 | EAS | CHS | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG00609 | hp2 | a0001 | c0001 | t0003 | g0200 | EAS | CHS | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG00639 | hp1 | a0001 | c0001 | t0019 | g0143 | AMR | PUR | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG00639 | hp2 | a0001 | c0001 | t0014 | g0019 | AMR | PUR | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0315 | AMR | PUR | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG00642 | hp2 | a0001 | c0002 | t0006 | g0333 | AMR | PUR | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | CHS | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | CHS | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG00735 | hp1 | a0001 | c0001 | t0004 | g0116 | AMR | PUR | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG00738 | hp1 | a0001 | c0001 | t0018 | g0216 | AMR | PUR | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG00741 | hp2 | a0001 | c0002 | t0006 | g0296 | AMR | PUR | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0314 | AMR | PUR | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG01069 | hp2 | a0001 | c0002 | t0002 | g0209 | AMR | PUR | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG01074 | hp1 | a0001 | c0001 | t0008 | g0006 | AMR | PUR | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG01081 | hp2 | a0001 | c0001 | t0005 | g0151 | AMR | PUR | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG01099 | hp2 | a0001 | c0002 | t0002 | g0278 | AMR | PUR | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG01109 | hp2 | a0001 | c0002 | t0002 | g0308 | AMR | PUR | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG01169 | hp2 | a0001 | c0002 | t0002 | g0311 | AMR | PUR | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG01175 | hp1 | a0001 | c0002 | t0001 | g0034 | AMR | PUR | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG01175 | hp2 | a0001 | c0002 | t0002 | g0305 | AMR | PUR | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG01243 | hp1 | a0001 | c0002 | t0002 | g0059 | AMR | PUR | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG01255 | hp1 | a0001 | c0001 | t0005 | g0136 | AMR | CLM | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG01255 | hp2 | a0001 | c0001 | t0004 | g0115 | AMR | CLM | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG01256 | hp1 | a0001 | c0002 | t0006 | g0284 | AMR | CLM | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG01256 | hp2 | a0001 | c0005 | t0002 | g0206 | AMR | CLM | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG01257 | hp1 | a0001 | c0002 | t0002 | g0285 | AMR | CLM | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG01258 | hp1 | a0001 | c0005 | t0002 | g0279 | AMR | CLM | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG01261 | hp2 | a0001 | c0002 | t0024 | g0257 | AMR | CLM | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG01346 | hp1 | a0001 | c0007 | t0001 | g0179 | AMR | CLM | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG01346 | hp2 | a0001 | c0002 | t0006 | g0253 | AMR | CLM | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG01358 | hp1 | a0001 | c0002 | t0002 | g0264 | AMR | CLM | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG01496 | hp2 | a0001 | c0002 | t0006 | g0294 | AMR | CLM | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG01516 | hp1 | a0001 | c0002 | t0002 | g0204 | EUR | IBS | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG01517 | hp1 | a0001 | c0002 | t0002 | g0286 | EUR | IBS | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG01884 | hp1 | a0001 | c0002 | t0002 | g0201 | AFR | ACB | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG01884 | hp2 | a0001 | c0002 | t0002 | g0223 | AFR | ACB | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG01891 | hp1 | a0002 | c0009 | t0001 | g0053 | AFR | ACB | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG01891 | hp2 | a0001 | c0002 | t0002 | g0202 | AFR | ACB | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG01928 | hp2 | a0001 | c0002 | t0006 | g0295 | AMR | PEL | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PEL | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG01943 | hp1 | a0001 | c0002 | t0002 | g0255 | AMR | PEL | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG01952 | hp1 | a0001 | c0001 | t0013 | g0239 | AMR | PEL | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG01952 | hp2 | a0001 | c0002 | t0002 | g0263 | AMR | PEL | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0319 | AMR | PEL | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG01978 | hp2 | a0001 | c0001 | t0029 | g0037 | AMR | PEL | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG01993 | hp1 | a0001 | c0008 | t0002 | g0324 | AMR | PEL | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0320 | AMR | PEL | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02015 | hp1 | a0001 | c0002 | t0001 | g0282 | EAS | KHV | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02040 | hp1 | a0001 | c0002 | t0002 | g0212 | EAS | KHV | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02055 | hp1 | a0001 | c0001 | t0012 | g0188 | AFR | ACB | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | ACB | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02056 | hp1 | a0001 | c0002 | t0002 | g0321 | EAS | KHV | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02129 | hp2 | a0001 | c0002 | t0001 | g0276 | EAS | KHV | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02132 | hp1 | a0001 | c0002 | t0001 | g0258 | EAS | KHV | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02132 | hp2 | a0001 | c0001 | t0005 | g0073 | EAS | KHV | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02135 | hp2 | a0001 | c0002 | t0001 | g0269 | EAS | KHV | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02148 | hp1 | a0001 | c0002 | t0002 | g0218 | AMR | PEL | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0316 | AMR | PEL | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | ACB | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02258 | hp2 | a0001 | c0002 | t0032 | g0335 | AFR | ACB | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02273 | hp1 | a0001 | c0001 | t0022 | g0210 | AMR | PEL | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02273 | hp2 | a0001 | c0002 | t0009 | g0293 | AMR | PEL | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02280 | hp1 | a0001 | c0001 | t0020 | g0191 | AFR | ACB | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02280 | hp2 | a0001 | c0006 | t0025 | g0005 | AFR | ACB | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02293 | hp1 | a0001 | c0001 | t0013 | g0015 | AMR | PEL | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02293 | hp2 | a0001 | c0002 | t0002 | g0310 | AMR | PEL | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0317 | AMR | PEL | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | ACB | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02523 | hp2 | a0001 | c0002 | t0001 | g0277 | EAS | KHV | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02572 | hp1 | a0001 | c0010 | t0014 | g0020 | AFR | GWD | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0334 | SAS | PJL | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02602 | hp2 | a0001 | c0002 | t0002 | g0303 | SAS | PJL | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02622 | hp1 | a0001 | c0001 | t0008 | g0234 | AFR | GWD | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02622 | hp2 | a0001 | c0004 | t0011 | g0067 | AFR | GWD | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02647 | hp1 | a0001 | c0001 | t0008 | g0060 | AFR | GWD | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02647 | hp2 | a0001 | c0001 | t0021 | g0134 | AFR | GWD | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02698 | hp1 | a0001 | c0002 | t0002 | g0213 | SAS | PJL | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02723 | hp1 | a0001 | c0011 | t0006 | g0017 | AFR | GWD | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02895 | hp1 | a0001 | c0001 | t0005 | g0012 | AFR | GWD | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02896 | hp1 | a0001 | c0001 | t0010 | g0138 | AFR | GWD | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | GWD | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02897 | hp1 | a0001 | c0001 | t0005 | g0013 | AFR | GWD | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02897 | hp2 | a0001 | c0001 | t0010 | g0139 | AFR | GWD | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02922 | hp1 | a0001 | c0002 | t0030 | g0056 | AFR | ESN | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ESN | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02970 | hp1 | a0001 | c0001 | t0012 | g0190 | AFR | ESN | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ESN | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02976 | hp1 | a0001 | c0001 | t0012 | g0189 | AFR | ESN | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ESN | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG03017 | hp1 | a0001 | c0002 | t0002 | g0298 | SAS | PJL | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG03041 | hp1 | a0001 | c0002 | t0002 | g0221 | AFR | GWD | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG03098 | hp1 | a0001 | c0002 | t0002 | g0220 | AFR | MSL | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG03098 | hp2 | a0001 | c0001 | t0010 | g0233 | AFR | MSL | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | ESN | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | MSL | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | MSL | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | MSL | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | MSL | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG03486 | hp1 | a0001 | c0002 | t0002 | g0222 | AFR | MSL | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | MSL | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG03516 | hp2 | a0001 | c0002 | t0023 | g0055 | AFR | ESN | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | GWD | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG03540 | hp2 | a0001 | c0001 | t0031 | g0242 | AFR | GWD | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG03579 | hp1 | a0001 | c0001 | t0008 | g0009 | AFR | MSL | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | MSL | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG03669 | hp1 | a0001 | c0001 | t0004 | g0113 | SAS | PJL | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | STU | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG03688 | hp2 | a0001 | c0001 | t0005 | g0010 | SAS | STU | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG03710 | hp1 | a0001 | c0002 | t0002 | g0302 | SAS | PJL | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | BEB | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG03831 | hp2 | a0001 | c0001 | t0026 | g0249 | SAS | BEB | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG03834 | hp1 | a0001 | c0002 | t0002 | g0057 | SAS | BEB | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG03834 | hp2 | a0003 | c0012 | t0001 | g0180 | SAS | BEB | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | BEB | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG03942 | hp2 | a0001 | c0002 | t0002 | g0309 | SAS | BEB | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG04184 | hp1 | a0001 | c0001 | t0004 | g0117 | SAS | BEB | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG04184 | hp2 | a0001 | c0002 | t0001 | g0214 | SAS | BEB | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | STU | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | STU | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG04204 | hp1 | a0001 | c0002 | t0002 | g0105 | SAS | STU | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | STU | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG04228 | hp1 | a0001 | c0002 | t0002 | g0304 | SAS | STU | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG04228 | hp2 | a0001 | c0001 | t0004 | g0147 | SAS | STU | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18612 | hp1 | a0001 | c0001 | t0003 | g0244 | EAS | CHB | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | CHB | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | CHB | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18747 | hp2 | a0001 | c0002 | t0015 | g0287 | EAS | CHB | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | YRI | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | YRI | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18942 | hp2 | a0001 | c0002 | t0001 | g0325 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18943 | hp2 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18944 | hp1 | a0001 | c0002 | t0007 | g0208 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18945 | hp1 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18945 | hp2 | a0001 | c0002 | t0009 | g0328 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18946 | hp2 | a0001 | c0002 | t0002 | g0256 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18948 | hp2 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18949 | hp1 | a0001 | c0001 | t0005 | g0197 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18949 | hp2 | a0001 | c0001 | t0003 | g0262 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18952 | hp1 | a0001 | c0002 | t0002 | g0323 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18954 | hp1 | a0001 | c0002 | t0027 | g0300 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18957 | hp2 | a0001 | c0002 | t0002 | g0327 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18961 | hp1 | a0001 | c0002 | t0001 | g0267 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18962 | hp2 | a0001 | c0001 | t0016 | g0250 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18963 | hp1 | a0001 | c0001 | t0003 | g0199 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18965 | hp1 | a0001 | c0002 | t0001 | g0301 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18969 | hp1 | a0001 | c0001 | t0004 | g0112 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18969 | hp2 | a0001 | c0003 | t0001 | g0272 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18971 | hp2 | a0001 | c0002 | t0002 | g0248 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18972 | hp1 | a0001 | c0002 | t0001 | g0259 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18974 | hp1 | a0001 | c0002 | t0002 | g0332 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18974 | hp2 | a0001 | c0001 | t0004 | g0186 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18978 | hp2 | a0001 | c0002 | t0002 | g0326 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18979 | hp1 | a0001 | c0001 | t0005 | g0274 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18979 | hp2 | a0001 | c0001 | t0004 | g0114 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18980 | hp1 | a0001 | c0002 | t0001 | g0203 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18981 | hp1 | a0001 | c0002 | t0009 | g0331 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18981 | hp2 | a0001 | c0001 | t0028 | g0078 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18983 | hp1 | a0001 | c0001 | t0004 | g0185 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18983 | hp2 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18984 | hp1 | a0001 | c0002 | t0007 | g0292 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18985 | hp1 | a0001 | c0001 | t0004 | g0187 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18986 | hp1 | a0001 | c0002 | t0007 | g0207 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18987 | hp2 | a0001 | c0002 | t0002 | g0289 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18993 | hp1 | a0001 | c0001 | t0003 | g0194 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18995 | hp2 | a0001 | c0002 | t0001 | g0266 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA18998 | hp2 | a0001 | c0002 | t0009 | g0329 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA19001 | hp2 | a0001 | c0003 | t0003 | g0270 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA19002 | hp2 | a0001 | c0002 | t0002 | g0307 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA19004 | hp1 | a0001 | c0002 | t0001 | g0198 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA19004 | hp2 | a0001 | c0001 | t0003 | g0261 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA19007 | hp1 | a0001 | c0002 | t0002 | g0312 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA19010 | hp2 | a0001 | c0002 | t0002 | g0290 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA19012 | hp2 | a0001 | c0002 | t0001 | g0254 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA19030 | hp1 | a0001 | c0004 | t0011 | g0016 | AFR | LWK | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | LWK | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA19056 | hp1 | a0001 | c0003 | t0001 | g0271 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA19056 | hp2 | a0001 | c0001 | t0003 | g0252 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA19057 | hp1 | a0001 | c0001 | t0003 | g0193 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA19058 | hp2 | a0001 | c0002 | t0002 | g0280 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA19060 | hp2 | a0001 | c0002 | t0001 | g0260 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA19062 | hp1 | a0001 | c0001 | t0004 | g0118 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA19062 | hp2 | a0001 | c0002 | t0002 | g0306 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA19070 | hp1 | a0001 | c0002 | t0001 | g0268 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA19072 | hp2 | a0001 | c0002 | t0007 | g0205 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA19076 | hp2 | a0001 | c0002 | t0009 | g0330 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA19078 | hp1 | a0001 | c0002 | t0007 | g0058 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA19079 | hp2 | a0001 | c0002 | t0001 | g0275 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA19081 | hp2 | a0001 | c0002 | t0001 | g0283 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA19083 | hp2 | a0001 | c0003 | t0001 | g0273 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA19084 | hp1 | a0001 | c0002 | t0015 | g0291 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA19085 | hp1 | a0001 | c0002 | t0002 | g0313 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA19087 | hp1 | a0001 | c0002 | t0002 | g0288 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA19088 | hp1 | a0001 | c0002 | t0017 | g0004 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA19090 | hp1 | a0001 | c0001 | t0016 | g0251 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA19090 | hp2 | a0001 | c0002 | t0007 | g0297 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA19091 | hp1 | a0001 | c0002 | t0002 | g0241 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | YRI | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA19240 | hp2 | a0001 | c0001 | t0008 | g0007 | AFR | YRI | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | ASW | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ASW | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0043 | EUR | TSI | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0170 | EUR | TSI | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0148 | EUR | TSI | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0032 | EUR | TSI | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | ACB | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02109 | hp2 | a0001 | c0001 | t0005 | g0142 | AFR | ACB | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG03471 | hp1 | a0001 | c0001 | t0008 | g0008 | AFR | MSL | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | MSL | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA20300 | hp1 | a0001 | c0004 | t0011 | g0014 | AFR | USA | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0318 | AFR | USA | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | LWK | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | LWK | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0165 | REF | REF | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
homoSapiens | grch38p0 | a0001 | c0002 | t0002 | g0168 | REF | REF | SNX13_chr7_17785761_17945494 | SNX13 | chr7 | 17785761 | 17945494 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:17850348 | T | C | 1 | a0002 | 1 | HG01891.hp1 | missense_variant&splice_region_variant | MODERATE | c.1064A>G | p.Lys355Arg | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 11/26 | 1263/6357 | 1064/2874 | 355/957 | chr7 | 17850348 | |||
chr7:17873572 | G | A | 1 | a0003 | 1 | HG03834.hp2 | missense_variant | MODERATE | c.709C>T | p.Pro237Ser | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/26 | 908/6357 | 709/2874 | 237/957 | chr7 | 17873572 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:17814909 | G | T | 7 | a0001c0001 a0001c0004 a0001c0006 others(4): Show |
235 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(232): Show |
synonymous_variant | LOW | c.1989C>A | p.Pro663Pro | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/26 | 2188/6357 | 1989/2874 | 663/957 | chr7 | 17814909 | |||
chr7:17821584 | T | C | 1 | a0001c0006 | 1 | HG02280.hp2 | synonymous_variant | LOW | c.1770A>G | p.Leu590Leu | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 18/26 | 1969/6357 | 1770/2874 | 590/957 | chr7 | 17821584 | |||
chr7:17826065 | A | T | 1 | a0001c0005 | 2 | HG01256.hp2 HG01258.hp1 |
synonymous_variant | LOW | c.1662T>A | p.Ser554Ser | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 17/26 | 1861/6357 | 1662/2874 | 554/957 | chr7 | 17826065 | |||
chr7:17839861 | T | C | 1 | a0001c0007 | 1 | HG01346.hp1 | synonymous_variant | LOW | c.1305A>G | p.Lys435Lys | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 13/26 | 1504/6357 | 1305/2874 | 435/957 | chr7 | 17839861 | |||
chr7:17839912 | T | C | 1 | a0001c0004 | 3 | HG02622.hp2 NA19030.hp1 NA20300.hp1 |
synonymous_variant | LOW | c.1254A>G | p.Glu418Glu | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 13/26 | 1453/6357 | 1254/2874 | 418/957 | chr7 | 17839912 | |||
chr7:17839930 | G | A | 1 | a0001c0008 | 1 | HG01993.hp1 | synonymous_variant | LOW | c.1236C>T | p.Thr412Thr | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 13/26 | 1435/6357 | 1236/2874 | 412/957 | chr7 | 17839930 | |||
chr7:17850869 | T | C | 2 | a0001c0010 a0001c0011 |
2 | HG02572.hp1 HG02723.hp1 |
synonymous_variant | LOW | c.933A>G | p.Ala311Ala | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 10/26 | 1132/6357 | 933/2874 | 311/957 | chr7 | 17850869 | |||
chr7:17875556 | G | C | 1 | a0001c0003 | 4 | NA18969.hp2 NA19001.hp2 NA19056.hp1 others(1): Show |
synonymous_variant | LOW | c.588C>G | p.Thr196Thr | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 7/26 | 787/6357 | 588/2874 | 196/957 | chr7 | 17875556 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:17790832 | G | C | 1 | a0001c0001t0021 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3213C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 26/26 | 3213 | chr7 | 17790832 | ||||||
chr7:17791113 | C | T | 1 | a0001c0006t0025 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2932G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 26/26 | 2932 | chr7 | 17791113 | ||||||
chr7:17791143 | G | C | 1 | a0001c0002t0024 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2902C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 26/26 | 2902 | chr7 | 17791143 | ||||||
chr7:17791354 | A | C | 1 | a0001c0001t0008 | 6 | HG01074.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2691T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 26/26 | 2691 | chr7 | 17791354 | ||||||
chr7:17791364 | A | G | 3 | a0001c0002t0023 a0001c0002t0030 a0001c0002t0032 |
3 | HG02258.hp2 HG02922.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2681T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 26/26 | 2681 | chr7 | 17791364 | ||||||
chr7:17791380 | G | T | 1 | a0001c0001t0013 | 2 | HG01952.hp1 HG02293.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2665C>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 26/26 | 2665 | chr7 | 17791380 | ||||||
chr7:17791393 | T | A | 1 | a0001c0001t0022 | 1 | HG02273.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2652A>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 26/26 | 2652 | chr7 | 17791393 | ||||||
chr7:17791394 | T | A | 27 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(24): Show |
248 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(245): Show |
3_prime_UTR_variant | MODIFIER | c.*2651A>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 26/26 | 2651 | chr7 | 17791394 | ||||||
chr7:17791395 | A | T | 6 | a0001c0002t0006 a0001c0002t0009 a0001c0002t0023 others(3): Show |
15 | HG00642.hp2 HG00741.hp2 HG01256.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2650T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 26/26 | 2650 | chr7 | 17791395 | ||||||
chr7:17791396 | A | T | 1 | a0001c0002t0009 | 5 | HG02273.hp2 NA18945.hp2 NA18981.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2649T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 26/26 | 2649 | chr7 | 17791396 | ||||||
chr7:17791518 | AT | A | 1 | a0001c0001t0010 | 3 | HG02896.hp1 HG02897.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2526delA | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 26/26 | 2526 | chr7 | 17791518 | ||||||
chr7:17791605 | G | T | 1 | a0001c0001t0020 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2440C>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 26/26 | 2440 | chr7 | 17791605 | ||||||
chr7:17791772 | C | T | 1 | a0001c0001t0013 | 2 | HG01952.hp1 HG02293.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2273G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 26/26 | 2273 | chr7 | 17791772 | ||||||
chr7:17792086 | T | C | 1 | a0001c0001t0026 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1959A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 26/26 | 1959 | chr7 | 17792086 | ||||||
chr7:17792182 | C | T | 21 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(18): Show |
230 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(227): Show |
3_prime_UTR_variant | MODIFIER | c.*1863G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 26/26 | 1863 | chr7 | 17792182 | ||||||
chr7:17792301 | A | G | 1 | a0001c0001t0019 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1744T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 26/26 | 1744 | chr7 | 17792301 | ||||||
chr7:17792329 | G | C | 2 | a0001c0001t0014 a0001c0010t0014 |
2 | HG00639.hp2 HG02572.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1716C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 26/26 | 1716 | chr7 | 17792329 | ||||||
chr7:17792495 | C | T | 2 | a0001c0001t0004 a0001c0001t0018 |
13 | HG00544.hp1 HG00735.hp1 HG00738.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1550G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 26/26 | 1550 | chr7 | 17792495 | ||||||
chr7:17792504 | T | C | 1 | a0001c0002t0015 | 2 | NA18747.hp2 NA19084.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1541A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 26/26 | 1541 | chr7 | 17792504 | ||||||
chr7:17792731 | T | C | 1 | a0001c0002t0027 | 1 | NA18954.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1314A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 26/26 | 1314 | chr7 | 17792731 | ||||||
chr7:17792817 | T | C | 1 | a0001c0001t0028 | 1 | NA18981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1228A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 26/26 | 1228 | chr7 | 17792817 | ||||||
chr7:17793042 | T | C | 1 | a0001c0001t0016 | 2 | NA18962.hp2 NA19090.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1003A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 26/26 | 1003 | chr7 | 17793042 | ||||||
chr7:17793051 | T | C | 1 | a0001c0004t0011 | 3 | HG02622.hp2 NA19030.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*994A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 26/26 | 994 | chr7 | 17793051 | ||||||
chr7:17793399 | T | C | 1 | a0001c0004t0011 | 3 | HG02622.hp2 NA19030.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*646A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 26/26 | 646 | chr7 | 17793399 | ||||||
chr7:17793438 | T | C | 1 | a0001c0001t0012 | 3 | HG02055.hp1 HG02970.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*607A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 26/26 | 607 | chr7 | 17793438 | ||||||
chr7:17793566 | C | T | 1 | a0001c0001t0018 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*479G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 26/26 | 479 | chr7 | 17793566 | ||||||
chr7:17793720 | T | C | 1 | a0001c0002t0007 | 7 | HG00323.hp2 NA18944.hp1 NA18984.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*325A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 26/26 | 325 | chr7 | 17793720 | ||||||
chr7:17793810 | T | C | 1 | a0001c0001t0029 | 1 | HG01978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*235A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 26/26 | 235 | chr7 | 17793810 | ||||||
chr7:17793871 | T | C | 1 | a0001c0002t0030 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*174A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 26/26 | 174 | chr7 | 17793871 | ||||||
chr7:17793958 | C | A | 1 | a0001c0001t0031 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*87G>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 26/26 | 87 | chr7 | 17793958 | ||||||
chr7:17940437 | C | G | 1 | a0001c0002t0017 | 1 | NA19088.hp1 | 5_prime_UTR_variant | MODIFIER | c.-142G>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/26 | 142 | chr7 | 17940437 | ||||||
chr7:17940445 | T | G | 1 | a0001c0002t0032 | 1 | HG02258.hp2 | 5_prime_UTR_variant | MODIFIER | c.-150A>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/26 | 150 | chr7 | 17940445 | ||||||
chr7:17940468 | A | G | 1 | a0001c0002t0017 | 1 | NA19088.hp1 | 5_prime_UTR_variant | MODIFIER | c.-173T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/26 | 173 | chr7 | 17940468 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:17794355 | A | G | 3 | a0001c0001t0012g0188 a0001c0001t0012g0189 a0001c0001t0012g0190 |
3 | HG02055.hp1 HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2627-63T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 25/25 | chr7 | 17794355 | |||||||
chr7:17794436 | G | C | 2 | a0001c0001t0005g0012 a0001c0001t0005g0013 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2627-144C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 25/25 | chr7 | 17794436 | |||||||
chr7:17794465 | A | G | 3 | a0001c0001t0012g0188 a0001c0001t0012g0189 a0001c0001t0012g0190 |
3 | HG02055.hp1 HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2627-173T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 25/25 | chr7 | 17794465 | |||||||
chr7:17795065 | T | A | 33 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(30): Show |
36 | HG00609.hp1 HG00741.hp1 HG01168.hp1 others(33): Show |
intron_variant | MODIFIER | c.2627-773A>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 25/25 | chr7 | 17795065 | |||||||
chr7:17795103 | G | T | 85 | a0001c0001t0001g0031 a0001c0001t0008g0006 a0001c0001t0008g0007 others(82): Show |
85 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.2627-811C>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 25/25 | chr7 | 17795103 | |||||||
chr7:17795145 | A | T | 1 | a0001c0001t0001g0123 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2627-853T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 25/25 | chr7 | 17795145 | |||||||
chr7:17795156 | G | A | 1 | a0001c0011t0006g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2627-864C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 25/25 | chr7 | 17795156 | |||||||
chr7:17795212 | G | A | 7 | a0001c0001t0001g0033 a0001c0001t0001g0040 a0001c0001t0001g0042 others(4): Show |
7 | HG00735.hp2 HG00738.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.2627-920C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 25/25 | chr7 | 17795212 | |||||||
chr7:17795232 | G | C | 1 | a0001c0001t0031g0242 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2627-940C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 25/25 | chr7 | 17795232 | |||||||
chr7:17795328 | C | A | 1 | a0001c0001t0001g0243 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2627-1036G>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 25/25 | chr7 | 17795328 | |||||||
chr7:17795362 | A | C | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(217): Show |
223 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.2627-1070T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 25/25 | chr7 | 17795362 | |||||||
chr7:17795363 | G | A | 1 | a0001c0001t0020g0191 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2627-1071C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 25/25 | chr7 | 17795363 | |||||||
chr7:17795417 | T | C | 1 | a0001c0001t0004g0116 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2627-1125A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 25/25 | chr7 | 17795417 | |||||||
chr7:17795744 | C | T | 1 | a0001c0006t0025g0005 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2626+1083G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 25/25 | chr7 | 17795744 | |||||||
chr7:17795760 | G | A | 1 | a0001c0001t0001g0170 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2626+1067C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 25/25 | chr7 | 17795760 | |||||||
chr7:17795870 | A | T | 9 | a0001c0001t0001g0072 a0001c0001t0001g0087 a0001c0001t0001g0109 others(6): Show |
9 | HG02109.hp1 HG02451.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.2626+957T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 25/25 | chr7 | 17795870 | |||||||
chr7:17795881 | C | T | 2 | a0001c0001t0001g0035 a0001c0001t0001g0129 |
2 | HG01361.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.2626+946G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 25/25 | chr7 | 17795881 | |||||||
chr7:17795947 | C | G | 1 | a0001c0001t0022g0210 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2626+880G>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 25/25 | chr7 | 17795947 | |||||||
chr7:17795972 | G | A | 1 | a0001c0001t0014g0019 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2626+855C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 25/25 | chr7 | 17795972 | |||||||
chr7:17796334 | C | A | 1 | a0001c0001t0004g0147 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2626+493G>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 25/25 | chr7 | 17796334 | |||||||
chr7:17796565 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2626+262T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 25/25 | chr7 | 17796565 | |||||||
chr7:17796631 | C | T | 3 | a0001c0004t0011g0014 a0001c0004t0011g0016 a0001c0004t0011g0067 |
3 | HG02622.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2626+196G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 25/25 | chr7 | 17796631 | |||||||
chr7:17796639 | A | T | 7 | a0001c0002t0006g0253 a0001c0002t0006g0284 a0001c0002t0006g0294 others(4): Show |
7 | HG00642.hp2 HG00741.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.2626+188T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 25/25 | chr7 | 17796639 | |||||||
chr7:17796665 | G | A | 1 | a0001c0001t0001g0031 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2626+162C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 25/25 | chr7 | 17796665 | |||||||
chr7:17796706 | T | C | 1 | a0001c0001t0004g0185 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2626+121A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 25/25 | chr7 | 17796706 | |||||||
chr7:17796764 | G | A | 1 | a0001c0006t0025g0005 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2626+63C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 25/25 | chr7 | 17796764 | |||||||
chr7:17797070 | T | G | 3 | a0001c0001t0012g0188 a0001c0001t0012g0189 a0001c0001t0012g0190 |
3 | HG02055.hp1 HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2514-131A>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 24/25 | chr7 | 17797070 | |||||||
chr7:17797280 | A | G | 2 | a0001c0001t0010g0138 a0001c0001t0010g0139 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2514-341T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 24/25 | chr7 | 17797280 | |||||||
chr7:17797286 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2514-347G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 24/25 | chr7 | 17797286 | |||||||
chr7:17797299 | T | C | 1 | a0001c0002t0002g0310 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2514-360A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 24/25 | chr7 | 17797299 | |||||||
chr7:17797324 | T | C | 2 | a0001c0001t0005g0012 a0001c0001t0005g0013 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2514-385A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 24/25 | chr7 | 17797324 | |||||||
chr7:17797368 | A | C | 1 | a0001c0001t0001g0226 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2514-429T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 24/25 | chr7 | 17797368 | |||||||
chr7:17797428 | T | C | 7 | a0001c0001t0001g0031 a0001c0001t0008g0006 a0001c0001t0008g0007 others(4): Show |
7 | HG01074.hp1 HG02572.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2514-489A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 24/25 | chr7 | 17797428 | |||||||
chr7:17797498 | T | C | 3 | a0001c0001t0001g0135 a0001c0001t0020g0191 a0001c0001t0021g0134 |
3 | HG02280.hp1 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2514-559A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 24/25 | chr7 | 17797498 | |||||||
chr7:17797920 | A | G | 6 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0008 others(3): Show |
6 | HG01074.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.2513+770T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 24/25 | chr7 | 17797920 | |||||||
chr7:17797952 | A | C | 1 | a0001c0001t0001g0100 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2513+738T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 24/25 | chr7 | 17797952 | |||||||
chr7:17798032 | C | T | 3 | a0001c0001t0001g0167 a0001c0001t0005g0136 a0001c0001t0005g0142 |
3 | HG01255.hp1 HG02109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2513+658G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 24/25 | chr7 | 17798032 | |||||||
chr7:17798064 | A | G | 222 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(219): Show |
225 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.2513+626T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 24/25 | chr7 | 17798064 | |||||||
chr7:17798114 | G | T | 1 | a0001c0001t0001g0021 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2513+576C>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 24/25 | chr7 | 17798114 | |||||||
chr7:17798236 | C | T | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(236): Show |
242 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.2513+454G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 24/25 | chr7 | 17798236 | |||||||
chr7:17798346 | C | T | 1 | a0001c0001t0008g0060 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2513+344G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 24/25 | chr7 | 17798346 | |||||||
chr7:17798895 | T | A | 3 | a0001c0004t0011g0014 a0001c0004t0011g0016 a0001c0004t0011g0067 |
3 | HG02622.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2444+114A>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 23/25 | chr7 | 17798895 | |||||||
chr7:17798963 | A | T | 5 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0010g0138 others(2): Show |
5 | HG02896.hp1 HG02897.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.2444+46T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 23/25 | chr7 | 17798963 | |||||||
chr7:17799194 | T | C | 10 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0008 others(7): Show |
10 | HG01074.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.2299-40A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 22/25 | chr7 | 17799194 | |||||||
chr7:17799228 | C | T | 20 | a0001c0001t0001g0066 a0001c0001t0001g0068 a0001c0001t0001g0074 others(17): Show |
20 | HG00408.hp1 HG00544.hp2 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.2299-74G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 22/25 | chr7 | 17799228 | |||||||
chr7:17799242 | T | C | 2 | a0001c0001t0005g0012 a0001c0001t0005g0013 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2299-88A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 22/25 | chr7 | 17799242 | |||||||
chr7:17799301 | T | C | 1 | a0001c0001t0001g0032 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2299-147A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 22/25 | chr7 | 17799301 | |||||||
chr7:17799375 | T | G | 2 | a0001c0001t0001g0132 a0001c0001t0001g0243 |
2 | HG00280.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.2299-221A>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 22/25 | chr7 | 17799375 | |||||||
chr7:17799383 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2299-229A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 22/25 | chr7 | 17799383 | |||||||
chr7:17799451 | T | C | 1 | a0001c0011t0006g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2299-297A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 22/25 | chr7 | 17799451 | |||||||
chr7:17799514 | T | A | 5 | a0001c0002t0002g0059 a0001c0002t0002g0220 a0001c0002t0002g0221 others(2): Show |
5 | HG01243.hp1 HG01884.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2299-360A>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 22/25 | chr7 | 17799514 | |||||||
chr7:17799611 | T | C | 2 | a0001c0001t0001g0042 a0001c0001t0001g0043 |
2 | HG01074.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.2299-457A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 22/25 | chr7 | 17799611 | |||||||
chr7:17799680 | T | G | 3 | a0001c0001t0002g0018 a0001c0001t0014g0019 a0001c0010t0014g0020 |
3 | HG00639.hp2 HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.2299-526A>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 22/25 | chr7 | 17799680 | |||||||
chr7:17799687 | G | C | 1 | a0001c0001t0001g0028 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2299-533C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 22/25 | chr7 | 17799687 | |||||||
chr7:17799715 | T | C | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(208): Show |
214 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.2299-561A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 22/25 | chr7 | 17799715 | |||||||
chr7:17799986 | C | T | 223 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(220): Show |
226 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.2299-832G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 22/25 | chr7 | 17799986 | |||||||
chr7:17800120 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2299-966T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 22/25 | chr7 | 17800120 | |||||||
chr7:17800328 | T | C | 1 | a0001c0001t0002g0018 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2299-1174A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 22/25 | chr7 | 17800328 | |||||||
chr7:17800330 | AC | A | 8 | a0001c0002t0002g0213 a0001c0002t0006g0253 a0001c0002t0006g0284 others(5): Show |
8 | HG00642.hp2 HG00741.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.2299-1177delG | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 22/25 | chr7 | 17800330 | |||||||
chr7:17800741 | C | G | 3 | a0001c0004t0011g0014 a0001c0004t0011g0016 a0001c0004t0011g0067 |
3 | HG02622.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2298+847G>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 22/25 | chr7 | 17800741 | |||||||
chr7:17800898 | T | C | 1 | a0001c0001t0020g0191 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2298+690A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 22/25 | chr7 | 17800898 | |||||||
chr7:17801007 | A | ATCATATA others(3): Show |
1 | a0001c0002t0001g0301 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2298+580_2298+581i others(12): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 22/25 | chr7 | 17801007 | |||||||
chr7:17801009 | C | CAT | 11 | a0001c0002t0002g0201 a0001c0002t0002g0213 a0001c0002t0002g0248 others(8): Show |
11 | HG01099.hp2 HG01261.hp2 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.2298+577_2298+578d others(4): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 22/25 | chr7 | 17801009 | |||||||
chr7:17801009 | C | CATAT | 7 | a0001c0002t0001g0203 a0001c0002t0002g0202 a0001c0002t0002g0263 others(4): Show |
7 | HG00741.hp2 HG01891.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.2298+575_2298+578d others(6): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 22/25 | chr7 | 17801009 | |||||||
chr7:17801009 | C | CATATAT | 10 | a0001c0001t0005g0197 a0001c0002t0001g0282 a0001c0002t0002g0241 others(7): Show |
10 | HG00140.hp2 HG02015.hp1 HG03942.hp2 others(7): Show |
intron_variant | MODIFIER | c.2298+573_2298+578d others(8): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 22/25 | chr7 | 17801009 | |||||||
chr7:17801009 | C | CATATATA others(1): Show |
8 | a0001c0001t0001g0265 a0001c0002t0001g0267 a0001c0002t0001g0277 others(5): Show |
8 | HG02148.hp1 HG02523.hp2 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.2298+571_2298+578d others(10): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 22/25 | chr7 | 17801009 | |||||||
chr7:17801009 | C | CATATATA others(3): Show |
10 | a0001c0001t0003g0252 a0001c0001t0004g0117 a0001c0001t0005g0274 others(7): Show |
10 | HG04184.hp1 HG04204.hp1 NA18942.hp2 others(7): Show |
intron_variant | MODIFIER | c.2298+569_2298+578d others(12): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 22/25 | chr7 | 17801009 | |||||||
chr7:17801009 | C | CATATATA others(5): Show |
5 | a0001c0002t0001g0214 a0001c0002t0002g0212 a0001c0002t0002g0312 others(2): Show |
5 | HG02040.hp1 HG04184.hp2 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.2298+567_2298+578d others(14): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 22/25 | chr7 | 17801009 | |||||||
chr7:17801009 | C | CATATATA others(7): Show |
6 | a0001c0002t0001g0260 a0001c0002t0001g0266 a0001c0002t0001g0275 others(3): Show |
6 | HG01109.hp2 HG01169.hp2 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.2298+565_2298+578d others(16): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 22/25 | chr7 | 17801009 | |||||||
chr7:17801009 | C | CATATATA others(9): Show |
5 | a0001c0002t0001g0259 a0001c0002t0001g0269 a0001c0002t0002g0304 others(2): Show |
5 | HG02135.hp2 HG04228.hp1 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.2298+563_2298+578d others(18): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 22/25 | chr7 | 17801009 | |||||||
chr7:17801009 | C | CATATATA others(11): Show |
1 | a0001c0002t0001g0198 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2298+561_2298+578d others(20): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 22/25 | chr7 | 17801009 | |||||||
chr7:17801009 | C | CATATATA others(13): Show |
1 | a0001c0001t0005g0151 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2298+559_2298+578d others(22): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 22/25 | chr7 | 17801009 | |||||||
chr7:17801009 | C | T | 2 | a0001c0002t0001g0258 a0001c0002t0001g0301 |
2 | HG02132.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.2298+579G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 22/25 | chr7 | 17801009 | |||||||
chr7:17801009 | CAT | C | 11 | a0001c0002t0001g0322 a0001c0002t0002g0209 a0001c0002t0002g0289 others(8): Show |
11 | HG00558.hp1 HG01069.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.2298+577_2298+578d others(4): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 22/25 | chr7 | 17801009 | |||||||
chr7:17801009 | CATAT | C | 6 | a0001c0002t0002g0264 a0001c0002t0007g0297 a0001c0002t0007g0299 others(3): Show |
6 | HG00323.hp2 HG01358.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2298+575_2298+578d others(6): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 22/25 | chr7 | 17801009 | |||||||
chr7:17801009 | CATATAT | C | 4 | a0001c0001t0008g0008 a0001c0001t0008g0060 a0001c0001t0008g0234 others(1): Show |
4 | HG02622.hp1 HG02647.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2298+573_2298+578d others(8): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 22/25 | chr7 | 17801009 | |||||||
chr7:17801009 | CATATATA others(3): Show |
C | 8 | a0001c0001t0001g0070 a0001c0001t0001g0097 a0001c0001t0002g0018 others(5): Show |
8 | HG01081.hp1 HG01243.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.2298+569_2298+578d others(12): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 22/25 | chr7 | 17801009 | |||||||
chr7:17801009 | CATATATA others(5): Show |
C | 4 | a0001c0001t0001g0031 a0001c0001t0001g0119 a0001c0001t0014g0019 others(1): Show |
4 | HG00639.hp2 HG01993.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.2298+567_2298+578d others(14): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 22/25 | chr7 | 17801009 | |||||||
chr7:17801009 | CATATATA others(7): Show |
C | 2 | a0001c0002t0002g0057 a0001c0002t0002g0247 |
2 | HG00408.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.2298+565_2298+578d others(16): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 22/25 | chr7 | 17801009 | |||||||
chr7:17801009 | CATATATA others(9): Show |
C | 3 | a0001c0002t0002g0204 a0001c0002t0015g0287 a0001c0002t0015g0291 |
3 | HG01516.hp1 NA18747.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.2298+563_2298+578d others(18): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 22/25 | chr7 | 17801009 | |||||||
chr7:17801009 | CATATATA others(13): Show |
C | 3 | a0001c0001t0029g0037 a0001c0002t0002g0285 a0001c0002t0002g0286 |
3 | HG01257.hp1 HG01517.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.2298+559_2298+578d others(22): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 22/25 | chr7 | 17801009 | |||||||
chr7:17801009 | CATATATA others(15): Show |
C | 2 | a0001c0001t0013g0015 a0001c0001t0013g0239 |
2 | HG01952.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.2298+557_2298+578d others(24): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 22/25 | chr7 | 17801009 | |||||||
chr7:17801009 | CATATATA others(19): Show |
C | 1 | a0001c0002t0001g0254 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.2298+553_2298+578d others(28): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 22/25 | chr7 | 17801009 | |||||||
chr7:17801009 | CATATATA others(23): Show |
C | 2 | a0001c0001t0005g0012 a0001c0001t0005g0013 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2298+549_2298+578d others(32): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 22/25 | chr7 | 17801009 | |||||||
chr7:17801009 | CATATATA others(31): Show |
C | 204 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(201): Show |
207 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.2298+541_2298+578d others(40): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 22/25 | chr7 | 17801009 | |||||||
chr7:17801010 | A | T | 2 | a0001c0001t0008g0006 a0001c0001t0008g0009 |
2 | HG01074.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2298+578T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 22/25 | chr7 | 17801010 | |||||||
chr7:17801014 | A | T | 1 | a0001c0001t0008g0007 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2298+574T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 22/25 | chr7 | 17801014 | |||||||
chr7:17801016 | A | ATATATAT others(13): Show |
1 | a0001c0001t0012g0188 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2298+571_2298+572i others(22): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 22/25 | chr7 | 17801016 | |||||||
chr7:17801016 | A | T | 3 | a0001c0001t0008g0008 a0001c0001t0008g0060 a0001c0001t0008g0234 |
3 | HG02622.hp1 HG02647.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2298+572T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 22/25 | chr7 | 17801016 | |||||||
chr7:17801018 | A | ATATATAT others(11): Show |
1 | a0001c0001t0012g0190 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2298+569_2298+570i others(20): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 22/25 | chr7 | 17801018 | |||||||
chr7:17801018 | A | T | 3 | a0001c0001t0008g0008 a0001c0001t0008g0060 a0001c0001t0008g0234 |
3 | HG02622.hp1 HG02647.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2298+570T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 22/25 | chr7 | 17801018 | |||||||
chr7:17801020 | A | T | 8 | a0001c0001t0001g0070 a0001c0001t0001g0097 a0001c0001t0002g0018 others(5): Show |
8 | HG01081.hp1 HG01243.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.2298+568T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 22/25 | chr7 | 17801020 | |||||||
chr7:17801022 | A | ATATATAT others(13): Show |
1 | a0001c0001t0012g0189 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2298+565_2298+566i others(22): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 22/25 | chr7 | 17801022 | |||||||
chr7:17801022 | A | T | 2 | a0001c0001t0001g0031 a0001c0001t0014g0019 |
2 | HG00639.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.2298+566T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 22/25 | chr7 | 17801022 | |||||||
chr7:17801024 | A | T | 1 | a0001c0001t0001g0031 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2298+564T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 22/25 | chr7 | 17801024 | |||||||
chr7:17801032 | A | T | 2 | a0001c0001t0013g0015 a0001c0001t0013g0239 |
2 | HG01952.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.2298+556T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 22/25 | chr7 | 17801032 | |||||||
chr7:17801277 | T | C | 1 | a0001c0001t0014g0019 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2298+311A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 22/25 | chr7 | 17801277 | |||||||
chr7:17801284 | C | T | 2 | a0001c0001t0008g0008 a0001c0001t0008g0234 |
2 | HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2298+304G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 22/25 | chr7 | 17801284 | |||||||
chr7:17801459 | A | C | 1 | a0001c0001t0002g0018 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2298+129T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 22/25 | chr7 | 17801459 | |||||||
chr7:17801808 | C | T | 5 | a0001c0002t0002g0059 a0001c0002t0002g0220 a0001c0002t0002g0221 others(2): Show |
5 | HG01243.hp1 HG01884.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2227-149G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 21/25 | chr7 | 17801808 | |||||||
chr7:17801832 | T | C | 22 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0137 others(19): Show |
23 | HG00609.hp1 HG00741.hp1 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.2227-173A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 21/25 | chr7 | 17801832 | |||||||
chr7:17802029 | C | T | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(223): Show |
229 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.2227-370G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 21/25 | chr7 | 17802029 | |||||||
chr7:17802110 | G | C | 2 | a0001c0001t0013g0015 a0001c0001t0013g0239 |
2 | HG01952.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.2227-451C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 21/25 | chr7 | 17802110 | |||||||
chr7:17802129 | A | C | 1 | a0001c0001t0001g0316 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2227-470T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 21/25 | chr7 | 17802129 | |||||||
chr7:17802171 | G | C | 1 | a0001c0002t0006g0296 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2227-512C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 21/25 | chr7 | 17802171 | |||||||
chr7:17802220 | A | T | 1 | a0001c0001t0001g0011 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2227-561T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 21/25 | chr7 | 17802220 | |||||||
chr7:17802258 | G | A | 7 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 others(4): Show |
7 | HG00673.hp1 HG02056.hp2 NA18952.hp2 others(4): Show |
intron_variant | MODIFIER | c.2227-599C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 21/25 | chr7 | 17802258 | |||||||
chr7:17802279 | T | C | 1 | a0001c0001t0001g0245 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2227-620A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 21/25 | chr7 | 17802279 | |||||||
chr7:17802555 | T | G | 2 | a0001c0001t0001g0042 a0001c0001t0001g0043 |
2 | HG01074.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.2226+864A>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 21/25 | chr7 | 17802555 | |||||||
chr7:17802740 | A | G | 2 | a0001c0001t0013g0015 a0001c0001t0013g0239 |
2 | HG01952.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.2226+679T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 21/25 | chr7 | 17802740 | |||||||
chr7:17802886 | TA | T | 37 | a0001c0001t0001g0062 a0001c0001t0001g0069 a0001c0001t0001g0076 others(34): Show |
37 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.2226+532delT | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 21/25 | chr7 | 17802886 | |||||||
chr7:17802924 | G | A | 1 | a0001c0001t0020g0191 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2226+495C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 21/25 | chr7 | 17802924 | |||||||
chr7:17803017 | A | G | 3 | a0001c0004t0011g0014 a0001c0004t0011g0016 a0001c0004t0011g0067 |
3 | HG02622.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2226+402T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 21/25 | chr7 | 17803017 | |||||||
chr7:17803266 | T | C | 1 | a0001c0001t0001g0070 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2226+153A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 21/25 | chr7 | 17803266 | |||||||
chr7:17803334 | A | C | 1 | a0001c0001t0001g0152 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2226+85T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 21/25 | chr7 | 17803334 | |||||||
chr7:17803597 | T | C | 2 | a0001c0001t0003g0192 a0001c0001t0003g0193 |
2 | NA18943.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.2065-17A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17803597 | |||||||
chr7:17803703 | T | C | 1 | a0001c0002t0002g0288 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.2065-123A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17803703 | |||||||
chr7:17803707 | G | A | 2 | a0001c0001t0010g0138 a0001c0001t0010g0139 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2065-127C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17803707 | |||||||
chr7:17803746 | T | C | 2 | a0001c0001t0005g0012 a0001c0001t0005g0013 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2065-166A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17803746 | |||||||
chr7:17803787 | T | A | 2 | a0001c0001t0013g0015 a0001c0001t0013g0239 |
2 | HG01952.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.2065-207A>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17803787 | |||||||
chr7:17803792 | T | C | 2 | a0001c0001t0001g0035 a0001c0001t0001g0036 |
2 | HG00323.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.2065-212A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17803792 | |||||||
chr7:17803874 | C | T | 4 | a0001c0002t0009g0328 a0001c0002t0009g0329 a0001c0002t0009g0330 others(1): Show |
4 | NA18945.hp2 NA18981.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.2065-294G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17803874 | |||||||
chr7:17803880 | T | TA | 15 | a0001c0001t0001g0024 a0001c0001t0001g0028 a0001c0001t0001g0052 others(12): Show |
15 | HG00735.hp2 HG01943.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.2065-301dupT | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17803880 | |||||||
chr7:17803880 | T | TAA | 7 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0008 others(4): Show |
7 | HG01074.hp1 HG02622.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.2065-302_2065-301d others(4): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17803880 | |||||||
chr7:17803880 | TA | T | 9 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0132 others(6): Show |
9 | HG01993.hp1 HG02451.hp1 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.2065-301delT | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17803880 | |||||||
chr7:17804128 | T | C | 2 | a0001c0001t0014g0019 a0001c0010t0014g0020 |
2 | HG00639.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.2065-548A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17804128 | |||||||
chr7:17804234 | G | A | 4 | a0001c0001t0001g0137 a0001c0001t0001g0167 a0001c0001t0005g0136 others(1): Show |
4 | HG01255.hp1 HG02109.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2065-654C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17804234 | |||||||
chr7:17804242 | T | C | 1 | a0001c0002t0002g0298 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2065-662A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17804242 | |||||||
chr7:17804356 | A | G | 3 | a0001c0002t0023g0055 a0001c0002t0030g0056 a0001c0002t0032g0335 |
3 | HG02258.hp2 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2065-776T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17804356 | |||||||
chr7:17804689 | A | G | 3 | a0001c0002t0023g0055 a0001c0002t0030g0056 a0001c0002t0032g0335 |
3 | HG02258.hp2 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2065-1109T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17804689 | |||||||
chr7:17804947 | A | G | 2 | a0001c0001t0005g0012 a0001c0001t0005g0013 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2065-1367T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17804947 | |||||||
chr7:17805198 | G | C | 6 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0008 others(3): Show |
6 | HG01074.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.2065-1618C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805198 | |||||||
chr7:17805211 | T | G | 3 | a0001c0004t0011g0014 a0001c0004t0011g0016 a0001c0004t0011g0067 |
3 | HG02622.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2065-1631A>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805211 | |||||||
chr7:17805211 | T | TGTG | 3 | a0001c0001t0001g0041 a0001c0001t0001g0155 a0001c0001t0005g0013 |
3 | HG01258.hp2 HG02897.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.2065-1632_2065-163 others(7): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805211 | |||||||
chr7:17805211 | T | TGTGTG | 3 | a0001c0001t0001g0108 a0001c0001t0004g0185 a0001c0002t0002g0321 |
3 | HG02056.hp1 NA18946.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.2065-1632_2065-163 others(9): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805211 | |||||||
chr7:17805211 | T | TTG | 32 | a0001c0001t0001g0003 a0001c0001t0001g0038 a0001c0001t0001g0039 others(29): Show |
33 | HG00558.hp1 HG00642.hp1 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.2065-1633_2065-163 others(6): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805211 | |||||||
chr7:17805211 | T | TTGTG | 40 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0061 others(37): Show |
40 | HG00140.hp1 HG00544.hp2 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.2065-1635_2065-163 others(8): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805211 | |||||||
chr7:17805211 | T | TTGTGTG | 18 | a0001c0001t0001g0042 a0001c0001t0001g0074 a0001c0001t0001g0084 others(15): Show |
18 | HG00558.hp2 HG00673.hp1 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.2065-1637_2065-163 others(10): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805211 | |||||||
chr7:17805211 | T | TTGTGTGT others(1): Show |
11 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0066 others(8): Show |
11 | HG00639.hp2 HG01496.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.2065-1639_2065-163 others(12): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805211 | |||||||
chr7:17805211 | T | TTGTGTGT others(3): Show |
1 | a0001c0001t0001g0106 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2065-1641_2065-163 others(14): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805211 | |||||||
chr7:17805211 | T | TTGTGTGT others(5): Show |
8 | a0001c0001t0001g0049 a0001c0001t0001g0051 a0001c0001t0001g0081 others(5): Show |
8 | HG00741.hp1 HG02523.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2065-1643_2065-163 others(16): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805211 | |||||||
chr7:17805211 | T | TTGTGTGT others(7): Show |
2 | a0001c0001t0001g0178 a0001c0001t0008g0060 |
2 | HG02647.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.2065-1645_2065-163 others(18): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805211 | |||||||
chr7:17805211 | T | TTGTGTGT others(9): Show |
2 | a0001c0001t0001g0047 a0001c0001t0001g0050 |
2 | HG02451.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2065-1647_2065-163 others(20): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805211 | |||||||
chr7:17805211 | T | TTGTGTGT others(11): Show |
3 | a0001c0001t0001g0227 a0001c0001t0008g0006 a0001c0006t0025g0005 |
3 | HG01074.hp1 HG02280.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2065-1649_2065-163 others(22): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805211 | |||||||
chr7:17805211 | T | TTGTGTGT others(13): Show |
1 | a0001c0001t0001g0048 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2065-1651_2065-163 others(24): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805211 | |||||||
chr7:17805238 | T | C | 1 | a0001c0002t0002g0286 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.2065-1658A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805238 | |||||||
chr7:17805240 | TGTGTGTG others(5): Show |
T | 1 | a0001c0001t0001g0091 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2065-1672_2065-166 others(16): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805240 | |||||||
chr7:17805242 | T | C | 1 | a0001c0001t0020g0191 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2065-1662A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805242 | |||||||
chr7:17805242 | TGTGTGTG others(3): Show |
T | 2 | a0001c0001t0001g0040 a0001c0001t0001g0126 |
2 | HG02683.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.2065-1672_2065-166 others(14): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805242 | |||||||
chr7:17805244 | T | C | 3 | a0001c0002t0002g0285 a0001c0002t0002g0286 a0001c0004t0011g0016 |
3 | HG01257.hp1 HG01517.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2065-1664A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805244 | |||||||
chr7:17805246 | T | C | 4 | a0001c0001t0001g0002 a0001c0001t0020g0191 a0001c0004t0011g0014 others(1): Show |
4 | HG02280.hp1 HG03492.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.2065-1666A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805246 | |||||||
chr7:17805248 | T | C | 7 | a0001c0001t0001g0002 a0001c0001t0020g0191 a0001c0002t0002g0285 others(4): Show |
8 | HG01257.hp1 HG01517.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.2065-1668A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805248 | |||||||
chr7:17805248 | T | TGTGTGTG others(3): Show |
2 | a0001c0002t0007g0292 a0001c0002t0009g0331 |
2 | NA18981.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.2065-1669_2065-166 others(14): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805248 | |||||||
chr7:17805248 | T | TGTGTGTG others(5): Show |
2 | a0001c0002t0007g0058 a0001c0002t0007g0299 |
2 | HG00323.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.2065-1669_2065-166 others(16): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805248 | |||||||
chr7:17805248 | TGTGC | T | 4 | a0001c0001t0001g0063 a0001c0001t0001g0068 a0001c0001t0004g0117 others(1): Show |
4 | HG01109.hp1 HG02080.hp2 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.2065-1672_2065-166 others(8): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805248 | |||||||
chr7:17805250 | T | C | 8 | a0001c0001t0001g0002 a0001c0001t0001g0052 a0001c0001t0002g0018 others(5): Show |
9 | HG01257.hp1 HG01517.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.2065-1670A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805250 | |||||||
chr7:17805250 | T | TGTGCGTG others(7): Show |
1 | a0001c0002t0002g0309 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2065-1671_2065-167 others(18): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805250 | |||||||
chr7:17805250 | T | TGTGCGTG others(11): Show |
3 | a0001c0002t0006g0296 a0001c0002t0009g0293 a0001c0002t0009g0328 |
3 | HG00741.hp2 HG02273.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.2065-1671_2065-167 others(22): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805250 | |||||||
chr7:17805250 | T | TGTGCGTG others(18): Show |
1 | a0001c0002t0002g0307 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2065-1671_2065-167 others(29): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805250 | |||||||
chr7:17805250 | T | TGTGCGTG others(17): Show |
1 | a0001c0002t0027g0300 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.2065-1671_2065-167 others(28): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805250 | |||||||
chr7:17805250 | T | TGTGTGCG others(3): Show |
3 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0025 |
3 | HG01433.hp2 HG01934.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.2065-1671_2065-167 others(14): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805250 | |||||||
chr7:17805250 | T | TGTGTGCG others(7): Show |
1 | a0001c0001t0001g0024 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2065-1671_2065-167 others(18): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805250 | |||||||
chr7:17805250 | T | TGTGTGCG others(9): Show |
1 | a0001c0002t0002g0255 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2065-1671_2065-167 others(20): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805250 | |||||||
chr7:17805250 | T | TGTGTGCG others(13): Show |
2 | a0001c0002t0002g0263 a0001c0002t0002g0311 |
2 | HG01169.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.2065-1671_2065-167 others(24): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805250 | |||||||
chr7:17805250 | T | TGTGTGTG others(3): Show |
2 | a0001c0001t0001g0022 a0001c0001t0001g0026 |
2 | HG02257.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.2065-1671_2065-167 others(14): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805250 | |||||||
chr7:17805250 | T | TGTGTGTG others(7): Show |
2 | a0001c0001t0001g0001 a0001c0002t0002g0222 |
2 | HG01169.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2065-1671_2065-167 others(18): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805250 | |||||||
chr7:17805250 | T | TGTGTGTG others(13): Show |
1 | a0001c0001t0021g0134 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2065-1671_2065-167 others(24): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805250 | |||||||
chr7:17805250 | T | TGTGTGTG others(5): Show |
2 | a0001c0002t0007g0297 a0001c0002t0015g0287 |
2 | NA18747.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.2065-1671_2065-167 others(16): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805250 | |||||||
chr7:17805250 | T | TGTGTGTG others(7): Show |
1 | a0001c0002t0015g0291 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2065-1671_2065-167 others(18): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805250 | |||||||
chr7:17805250 | T | TGTGTGTG others(15): Show |
2 | a0001c0002t0002g0308 a0001c0002t0006g0333 |
2 | HG00642.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.2065-1671_2065-167 others(26): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805250 | |||||||
chr7:17805250 | T | TGTGTGTG others(17): Show |
1 | a0001c0002t0002g0204 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2065-1671_2065-167 others(28): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805250 | |||||||
chr7:17805250 | T | TGTGTGTG others(7): Show |
1 | a0001c0001t0001g0028 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2065-1671_2065-167 others(18): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805250 | |||||||
chr7:17805250 | T | TGTGTGTG others(9): Show |
3 | a0001c0001t0001g0023 a0001c0001t0001g0030 a0001c0001t0004g0187 |
3 | HG01168.hp2 HG01361.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.2065-1671_2065-167 others(20): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805250 | |||||||
chr7:17805250 | T | TGTGTGTG others(13): Show |
1 | a0001c0001t0004g0116 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2065-1671_2065-167 others(24): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805250 | |||||||
chr7:17805250 | T | TGTGTGTG others(15): Show |
1 | a0001c0001t0004g0118 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2065-1671_2065-167 others(26): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805250 | |||||||
chr7:17805250 | T | TGTGTGTG others(9): Show |
1 | a0001c0002t0002g0241 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2065-1671_2065-167 others(20): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805250 | |||||||
chr7:17805250 | T | TGTGTGTG others(19): Show |
1 | a0001c0002t0002g0305 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2065-1671_2065-167 others(30): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805250 | |||||||
chr7:17805250 | T | TGTGTGTG others(7): Show |
1 | a0001c0002t0002g0288 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.2065-1671_2065-167 others(18): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805250 | |||||||
chr7:17805250 | T | TGTGTGTG others(17): Show |
1 | a0001c0002t0002g0209 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2065-1671_2065-167 others(28): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805250 | |||||||
chr7:17805250 | T | TGTGTGTG others(19): Show |
1 | a0001c0008t0002g0324 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2065-1671_2065-167 others(30): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805250 | |||||||
chr7:17805250 | T | TGTGTGTG others(9): Show |
2 | a0001c0001t0001g0029 a0001c0001t0001g0145 |
2 | HG00609.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.2065-1671_2065-167 others(20): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805250 | |||||||
chr7:17805250 | T | TGTGTGTG others(15): Show |
1 | a0001c0001t0004g0113 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2065-1671_2065-167 others(26): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805250 | |||||||
chr7:17805250 | T | TGTGTGTG others(17): Show |
2 | a0001c0001t0001g0146 a0001c0001t0004g0186 |
2 | HG03225.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.2065-1671_2065-167 others(28): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805250 | |||||||
chr7:17805250 | T | TGTGTGTG others(15): Show |
1 | a0001c0002t0002g0218 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2065-1671_2065-167 others(26): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805250 | |||||||
chr7:17805250 | T | TGTGTGTG others(17): Show |
1 | a0001c0002t0002g0290 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2065-1671_2065-167 others(28): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805250 | |||||||
chr7:17805250 | T | TGTGTGTG others(19): Show |
1 | a0001c0002t0024g0257 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2065-1671_2065-167 others(30): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805250 | |||||||
chr7:17805250 | T | TGTGTGTG others(18): Show |
1 | a0001c0002t0002g0289 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.2065-1671_2065-167 others(29): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805250 | |||||||
chr7:17805250 | T | TGTGTGTG others(7): Show |
1 | a0002c0009t0001g0053 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2065-1671_2065-167 others(18): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805250 | |||||||
chr7:17805250 | T | TGTGTGTG others(13): Show |
1 | a0001c0001t0001g0027 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2065-1671_2065-167 others(24): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805250 | |||||||
chr7:17805250 | T | TGTGTGTG others(17): Show |
1 | a0001c0002t0002g0213 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2065-1671_2065-167 others(28): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805250 | |||||||
chr7:17805250 | T | TGTGTGTG others(19): Show |
1 | a0001c0001t0001g0135 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2065-1671_2065-167 others(30): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805250 | |||||||
chr7:17805250 | T | TGTGTGTG others(21): Show |
2 | a0001c0002t0006g0253 a0001c0002t0006g0284 |
2 | HG01256.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.2065-1671_2065-167 others(32): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805250 | |||||||
chr7:17805250 | T | TGTGTGTG others(23): Show |
1 | a0001c0002t0006g0294 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2065-1671_2065-167 others(34): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805250 | |||||||
chr7:17805250 | T | TGTGTGTG others(9): Show |
1 | a0001c0001t0008g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2065-1671_2065-167 others(20): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805250 | |||||||
chr7:17805250 | T | TGTGTGTG others(13): Show |
1 | a0001c0001t0001g0226 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2065-1671_2065-167 others(24): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805250 | |||||||
chr7:17805250 | T | TGTGTGTG others(11): Show |
1 | a0001c0001t0019g0143 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2065-1671_2065-167 others(22): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805250 | |||||||
chr7:17805250 | T | TGTGTGTG others(15): Show |
1 | a0001c0002t0002g0223 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2065-1671_2065-167 others(26): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805250 | |||||||
chr7:17805250 | T | TGTGTGTG others(17): Show |
2 | a0001c0001t0004g0114 a0001c0002t0002g0059 |
2 | HG01243.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.2065-1671_2065-167 others(28): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805250 | |||||||
chr7:17805250 | T | TGTGTGTG others(23): Show |
1 | a0001c0002t0002g0220 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2065-1671_2065-167 others(34): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805250 | |||||||
chr7:17805250 | T | TGTGTGTG others(21): Show |
1 | a0001c0002t0002g0221 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2065-1671_2065-167 others(32): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805250 | |||||||
chr7:17805250 | T | TGTGTGTG others(25): Show |
1 | a0001c0001t0004g0115 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2065-1671_2065-167 others(36): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805250 | |||||||
chr7:17805250 | T | TGTGTGTG others(29): Show |
1 | a0001c0001t0004g0112 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2065-1671_2065-167 others(40): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805250 | |||||||
chr7:17805250 | TGC | T | 4 | a0001c0001t0001g0011 a0001c0001t0001g0035 a0001c0001t0001g0036 others(1): Show |
4 | HG00323.hp1 HG01361.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.2065-1672_2065-167 others(6): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805250 | |||||||
chr7:17805250 | TGCGTGC | T | 3 | a0001c0002t0023g0055 a0001c0002t0030g0056 a0001c0002t0032g0335 |
3 | HG02258.hp2 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2065-1676_2065-167 others(10): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805250 | |||||||
chr7:17805251 | GCGTGCGC others(9): Show |
G | 1 | a0001c0002t0002g0304 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2065-1687_2065-167 others(20): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805251 | |||||||
chr7:17805252 | C | T | 152 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0038 others(149): Show |
152 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.2065-1672G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805252 | |||||||
chr7:17805253 | GTGCGCGC others(11): Show |
G | 2 | a0001c0001t0001g0046 a0001c0002t0002g0306 |
2 | HG03041.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.2065-1691_2065-167 others(22): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805253 | |||||||
chr7:17805254 | T | C | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(115): Show |
121 | HG00323.hp2 HG00609.hp1 HG00639.hp1 others(118): Show |
intron_variant | MODIFIER | c.2065-1674A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805254 | |||||||
chr7:17805254 | T | TGC | 4 | a0001c0001t0001g0099 a0001c0001t0001g0243 a0001c0001t0003g0196 others(1): Show |
4 | HG00280.hp1 HG02486.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.2065-1676_2065-167 others(6): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805254 | |||||||
chr7:17805254 | T | TGCGCGCG others(14): Show |
1 | a0001c0001t0001g0119 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2065-1675_2065-167 others(25): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805254 | |||||||
chr7:17805254 | T | TGCGCGCG others(9): Show |
1 | a0001c0002t0002g0310 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2065-1675_2065-167 others(20): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805254 | |||||||
chr7:17805254 | T | TGCGTGCG others(15): Show |
2 | a0001c0002t0002g0247 a0001c0002t0002g0321 |
2 | HG00408.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.2065-1675_2065-167 others(26): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805254 | |||||||
chr7:17805254 | T | TGTGC | 9 | a0001c0001t0001g0054 a0001c0001t0001g0088 a0001c0001t0001g0217 others(6): Show |
9 | HG00280.hp2 HG01952.hp1 HG04199.hp1 others(6): Show |
intron_variant | MODIFIER | c.2065-1675_2065-167 others(8): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805254 | |||||||
chr7:17805254 | T | TGTGCGTG others(13): Show |
1 | a0001c0001t0029g0037 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2065-1675_2065-167 others(24): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805254 | |||||||
chr7:17805254 | T | TGTGCGTG others(20): Show |
1 | a0001c0002t0002g0264 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2065-1675_2065-167 others(31): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805254 | |||||||
chr7:17805254 | T | TGTGTGC | 10 | a0001c0001t0001g0071 a0001c0001t0001g0121 a0001c0001t0001g0123 others(7): Show |
10 | HG01243.hp2 HG02129.hp1 HG03688.hp1 others(7): Show |
intron_variant | MODIFIER | c.2065-1675_2065-167 others(10): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805254 | |||||||
chr7:17805254 | T | TGTGTGTG others(1): Show |
9 | a0001c0001t0001g0082 a0001c0001t0001g0101 a0001c0001t0001g0111 others(6): Show |
9 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(6): Show |
intron_variant | MODIFIER | c.2065-1675_2065-167 others(12): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805254 | |||||||
chr7:17805254 | T | TGTGTGTG others(3): Show |
2 | a0001c0001t0001g0064 a0001c0001t0001g0124 |
2 | HG02723.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.2065-1675_2065-167 others(14): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805254 | |||||||
chr7:17805254 | T | TGTGTGTG others(8): Show |
1 | a0001c0001t0001g0219 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2065-1675_2065-167 others(19): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805254 | |||||||
chr7:17805254 | T | TGTGTGTG others(7): Show |
1 | a0001c0001t0001g0120 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2065-1675_2065-167 others(18): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805254 | |||||||
chr7:17805254 | T | TGTGTGTG others(13): Show |
1 | a0001c0001t0001g0110 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2065-1675_2065-167 others(24): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805254 | |||||||
chr7:17805255 | GCGCGCGC others(5): Show |
G | 1 | a0001c0002t0002g0302 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2065-1687_2065-167 others(16): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805255 | |||||||
chr7:17805256 | C | T | 7 | a0001c0001t0001g0066 a0001c0001t0004g0147 a0001c0001t0012g0188 others(4): Show |
7 | HG02055.hp1 HG02970.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.2065-1676G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805256 | |||||||
chr7:17805257 | GCGCGCGC others(3): Show |
G | 3 | a0001c0001t0004g0147 a0001c0001t0012g0189 a0001c0001t0012g0190 |
3 | HG02970.hp1 HG02976.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2065-1687_2065-167 others(14): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805257 | |||||||
chr7:17805258 | C | T | 3 | a0001c0001t0012g0188 a0001c0002t0009g0329 a0001c0002t0009g0330 |
3 | HG02055.hp1 NA18998.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.2065-1678G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805258 | |||||||
chr7:17805259 | G | T | 1 | a0001c0002t0002g0264 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2065-1679C>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805259 | |||||||
chr7:17805260 | C | T | 1 | a0001c0001t0012g0188 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2065-1680G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805260 | |||||||
chr7:17805261 | G | A | 3 | a0001c0002t0023g0055 a0001c0002t0030g0056 a0001c0002t0032g0335 |
3 | HG02258.hp2 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2065-1681C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805261 | |||||||
chr7:17805261 | GCGCGCA | G | 3 | a0001c0001t0012g0188 a0001c0002t0009g0329 a0001c0002t0009g0330 |
3 | HG02055.hp1 NA18998.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.2065-1687_2065-168 others(10): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805261 | |||||||
chr7:17805263 | G | A | 6 | a0001c0001t0001g0033 a0001c0001t0001g0040 a0001c0001t0001g0042 others(3): Show |
6 | HG00735.hp2 HG00738.hp2 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.2065-1683C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805263 | |||||||
chr7:17805265 | G | A | 10 | a0001c0001t0001g0135 a0001c0001t0004g0112 a0001c0001t0004g0113 others(7): Show |
10 | HG00735.hp1 HG01255.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.2065-1685C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805265 | |||||||
chr7:17805265 | G | GCGCGCGC others(5): Show |
1 | a0001c0001t0018g0216 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2065-1686_2065-168 others(16): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805265 | |||||||
chr7:17805265 | G | GTGCGCGC others(7): Show |
2 | a0001c0001t0004g0184 a0001c0001t0004g0185 |
2 | HG00544.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.2065-1686_2065-168 others(18): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805265 | |||||||
chr7:17805270 | C | T | 1 | a0001c0001t0004g0147 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2065-1690G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805270 | |||||||
chr7:17805271 | A | G | 6 | a0001c0001t0004g0147 a0001c0001t0012g0188 a0001c0001t0012g0189 others(3): Show |
6 | HG02055.hp1 HG02970.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.2065-1691T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805271 | |||||||
chr7:17805275 | A | G | 4 | a0001c0001t0004g0147 a0001c0001t0012g0188 a0001c0001t0012g0189 others(1): Show |
4 | HG02055.hp1 HG02970.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.2065-1695T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805275 | |||||||
chr7:17805281 | G | A | 4 | a0001c0001t0012g0188 a0001c0001t0012g0189 a0001c0001t0012g0190 others(1): Show |
4 | HG02055.hp1 HG02280.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2065-1701C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805281 | |||||||
chr7:17805532 | A | G | 1 | a0001c0001t0001g0040 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2065-1952T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805532 | |||||||
chr7:17805540 | A | C | 1 | a0001c0011t0006g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2065-1960T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805540 | |||||||
chr7:17805821 | GT | G | 3 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0031g0242 |
3 | HG02257.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2065-2242delA | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805821 | |||||||
chr7:17805940 | A | G | 6 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(3): Show |
6 | HG02602.hp1 HG03017.hp2 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.2065-2360T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805940 | |||||||
chr7:17805965 | T | C | 1 | a0001c0001t0001g0044 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2065-2385A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17805965 | |||||||
chr7:17806057 | C | T | 1 | a0001c0006t0025g0005 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2065-2477G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17806057 | |||||||
chr7:17806058 | G | A | 1 | a0001c0011t0006g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2065-2478C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17806058 | |||||||
chr7:17806074 | G | A | 37 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(34): Show |
40 | HG00609.hp1 HG00741.hp1 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.2065-2494C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17806074 | |||||||
chr7:17806181 | T | G | 3 | a0001c0001t0012g0188 a0001c0001t0012g0189 a0001c0001t0012g0190 |
3 | HG02055.hp1 HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2065-2601A>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17806181 | |||||||
chr7:17806219 | TA | T | 331 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(328): Show |
334 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.2065-2640delT | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17806219 | |||||||
chr7:17806221 | A | C | 1 | a0001c0002t0009g0330 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.2065-2641T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17806221 | |||||||
chr7:17806222 | C | A | 1 | a0001c0002t0009g0330 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.2065-2642G>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17806222 | |||||||
chr7:17806225 | A | G | 1 | a0001c0002t0009g0330 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.2065-2645T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17806225 | |||||||
chr7:17806324 | T | A | 144 | a0001c0001t0001g0011 a0001c0001t0001g0033 a0001c0001t0001g0035 others(141): Show |
144 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.2065-2744A>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17806324 | |||||||
chr7:17806486 | T | G | 1 | a0001c0002t0009g0330 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.2065-2906A>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17806486 | |||||||
chr7:17806488 | G | A | 1 | a0001c0002t0009g0330 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.2065-2908C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17806488 | |||||||
chr7:17806491 | A | C | 1 | a0001c0002t0009g0330 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.2065-2911T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17806491 | |||||||
chr7:17806640 | T | A | 1 | a0001c0001t0028g0078 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2065-3060A>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17806640 | |||||||
chr7:17806642 | A | T | 1 | a0001c0001t0001g0245 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2065-3062T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17806642 | |||||||
chr7:17806691 | G | A | 3 | a0001c0001t0003g0215 a0001c0001t0003g0261 a0001c0001t0003g0262 |
3 | NA18945.hp1 NA18949.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.2065-3111C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17806691 | |||||||
chr7:17806990 | G | A | 2 | a0001c0001t0013g0015 a0001c0001t0013g0239 |
2 | HG01952.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.2065-3410C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17806990 | |||||||
chr7:17806997 | C | G | 230 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(227): Show |
233 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.2065-3417G>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17806997 | |||||||
chr7:17807109 | G | C | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2065-3529C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17807109 | |||||||
chr7:17807194 | A | G | 1 | a0001c0002t0002g0310 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2065-3614T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17807194 | |||||||
chr7:17807200 | T | C | 1 | a0001c0002t0009g0330 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.2065-3620A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17807200 | |||||||
chr7:17807280 | G | A | 2 | a0001c0001t0005g0012 a0001c0001t0005g0013 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2065-3700C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17807280 | |||||||
chr7:17807512 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2065-3932C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17807512 | |||||||
chr7:17807582 | A | C | 236 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(233): Show |
239 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.2065-4002T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17807582 | |||||||
chr7:17807602 | C | A | 2 | a0001c0001t0005g0012 a0001c0001t0005g0013 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2065-4022G>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17807602 | |||||||
chr7:17807607 | G | A | 2 | a0001c0001t0005g0012 a0001c0001t0005g0013 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2065-4027C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17807607 | |||||||
chr7:17807659 | C | T | 10 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0008 others(7): Show |
10 | HG01074.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.2065-4079G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17807659 | |||||||
chr7:17807770 | A | T | 1 | a0001c0002t0007g0058 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.2065-4190T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17807770 | |||||||
chr7:17807839 | C | CCTCCAGC others(3): Show |
240 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(237): Show |
243 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.2065-4269_2065-426 others(14): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17807839 | |||||||
chr7:17807839 | C | CCTCCAGC others(3): Show |
1 | a0001c0001t0001g0226 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2065-4260_2065-425 others(14): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17807839 | |||||||
chr7:17807940 | A | G | 2 | a0001c0001t0001g0042 a0001c0001t0001g0043 |
2 | HG01074.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.2065-4360T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17807940 | |||||||
chr7:17807969 | C | A | 2 | a0001c0005t0002g0206 a0001c0005t0002g0279 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.2065-4389G>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17807969 | |||||||
chr7:17808040 | C | T | 1 | a0001c0001t0001g0121 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.2065-4460G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17808040 | |||||||
chr7:17808059 | G | C | 14 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0021 others(11): Show |
16 | HG01168.hp2 HG01169.hp1 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.2065-4479C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17808059 | |||||||
chr7:17808215 | C | A | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(213): Show |
219 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.2065-4635G>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17808215 | |||||||
chr7:17808367 | C | G | 6 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0008 others(3): Show |
6 | HG01074.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.2065-4787G>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17808367 | |||||||
chr7:17808472 | A | C | 1 | a0001c0001t0001g0031 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2065-4892T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17808472 | |||||||
chr7:17808499 | G | A | 1 | a0001c0001t0002g0018 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2065-4919C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17808499 | |||||||
chr7:17808624 | A | G | 1 | a0001c0001t0001g0243 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2065-5044T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17808624 | |||||||
chr7:17808627 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2065-5047C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17808627 | |||||||
chr7:17808713 | A | T | 1 | a0001c0001t0001g0164 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2065-5133T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17808713 | |||||||
chr7:17808863 | A | C | 1 | a0001c0002t0002g0326 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2065-5283T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17808863 | |||||||
chr7:17808979 | C | T | 3 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0245 |
3 | HG00673.hp1 NA19057.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.2065-5399G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17808979 | |||||||
chr7:17809030 | A | G | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | NA19002.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.2065-5450T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17809030 | |||||||
chr7:17809053 | G | A | 1 | a0001c0001t0001g0075 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2065-5473C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17809053 | |||||||
chr7:17809174 | T | G | 1 | a0001c0002t0027g0300 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.2065-5594A>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17809174 | |||||||
chr7:17809217 | C | T | 1 | a0001c0001t0002g0334 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2064+5617G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17809217 | |||||||
chr7:17809282 | C | CA | 27 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0001g0097 others(24): Show |
27 | HG00741.hp2 HG01081.hp1 HG01256.hp1 others(24): Show |
intron_variant | MODIFIER | c.2064+5551dupT | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17809282 | |||||||
chr7:17809282 | CA | C | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
159 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.2064+5551delT | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17809282 | |||||||
chr7:17809282 | CAAAAAAA others(7): Show |
C | 3 | a0001c0001t0010g0138 a0001c0001t0010g0139 a0001c0001t0010g0233 |
3 | HG02896.hp1 HG02897.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2064+5538_2064+555 others(18): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17809282 | |||||||
chr7:17809319 | A | C | 8 | a0001c0002t0002g0213 a0001c0002t0006g0253 a0001c0002t0006g0284 others(5): Show |
8 | HG00642.hp2 HG00741.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.2064+5515T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17809319 | |||||||
chr7:17809339 | C | CAGACTTT others(10): Show |
6 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0008 others(3): Show |
6 | HG01074.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.2064+5478_2064+549 others(21): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17809339 | |||||||
chr7:17809360 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2064+5474G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17809360 | |||||||
chr7:17809500 | G | C | 3 | a0001c0002t0023g0055 a0001c0002t0030g0056 a0001c0002t0032g0335 |
3 | HG02258.hp2 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2064+5334C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17809500 | |||||||
chr7:17809507 | A | G | 2 | a0001c0001t0001g0070 a0001c0001t0001g0097 |
2 | HG01081.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2064+5327T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17809507 | |||||||
chr7:17809614 | G | A | 2 | a0001c0001t0013g0015 a0001c0001t0013g0239 |
2 | HG01952.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.2064+5220C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17809614 | |||||||
chr7:17809616 | G | A | 4 | a0001c0002t0002g0241 a0001c0004t0011g0014 a0001c0004t0011g0016 others(1): Show |
4 | HG02622.hp2 NA19030.hp1 NA19091.hp1 others(1): Show |
intron_variant | MODIFIER | c.2064+5218C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17809616 | |||||||
chr7:17809906 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2064+4928G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17809906 | |||||||
chr7:17810035 | C | T | 1 | a0001c0001t0001g0086 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2064+4799G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17810035 | |||||||
chr7:17810130 | T | C | 1 | a0001c0001t0002g0018 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2064+4704A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17810130 | |||||||
chr7:17810137 | G | C | 2 | a0001c0002t0002g0285 a0001c0002t0002g0286 |
2 | HG01257.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.2064+4697C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17810137 | |||||||
chr7:17810378 | A | G | 1 | a0001c0001t0013g0015 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2064+4456T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17810378 | |||||||
chr7:17810503 | G | A | 3 | a0001c0004t0011g0014 a0001c0004t0011g0016 a0001c0004t0011g0067 |
3 | HG02622.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2064+4331C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17810503 | |||||||
chr7:17810787 | T | G | 2 | a0001c0001t0005g0136 a0001c0001t0005g0142 |
2 | HG01255.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2064+4047A>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17810787 | |||||||
chr7:17810991 | A | G | 1 | a0001c0002t0001g0322 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2064+3843T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17810991 | |||||||
chr7:17810998 | G | A | 1 | a0001c0002t0007g0207 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2064+3836C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17810998 | |||||||
chr7:17811054 | A | G | 2 | a0001c0001t0001g0035 a0001c0001t0001g0036 |
2 | HG00323.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.2064+3780T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17811054 | |||||||
chr7:17811152 | G | C | 6 | a0001c0001t0001g0087 a0001c0001t0001g0228 a0001c0001t0001g0229 others(3): Show |
6 | HG02257.hp1 HG02451.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.2064+3682C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17811152 | |||||||
chr7:17811158 | C | T | 3 | a0001c0001t0012g0188 a0001c0001t0012g0189 a0001c0001t0012g0190 |
3 | HG02055.hp1 HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2064+3676G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17811158 | |||||||
chr7:17811305 | C | T | 2 | a0001c0001t0013g0015 a0001c0001t0013g0239 |
2 | HG01952.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.2064+3529G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17811305 | |||||||
chr7:17811585 | C | T | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(222): Show |
228 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.2064+3249G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17811585 | |||||||
chr7:17811595 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2064+3239C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17811595 | |||||||
chr7:17811737 | C | G | 4 | a0001c0001t0012g0188 a0001c0001t0012g0189 a0001c0001t0012g0190 others(1): Show |
4 | HG02055.hp1 HG02280.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2064+3097G>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17811737 | |||||||
chr7:17811762 | G | A | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(190): Show |
196 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.2064+3072C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17811762 | |||||||
chr7:17811777 | T | C | 1 | a0001c0011t0006g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2064+3057A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17811777 | |||||||
chr7:17811782 | C | G | 4 | a0001c0001t0012g0188 a0001c0001t0012g0189 a0001c0001t0012g0190 others(1): Show |
4 | HG02055.hp1 HG02280.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2064+3052G>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17811782 | |||||||
chr7:17811838 | C | T | 1 | a0001c0001t0001g0024 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2064+2996G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17811838 | |||||||
chr7:17811904 | T | C | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(223): Show |
229 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.2064+2930A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17811904 | |||||||
chr7:17811905 | T | C | 228 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(225): Show |
231 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.2064+2929A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17811905 | |||||||
chr7:17811974 | T | C | 2 | a0001c0001t0005g0012 a0001c0001t0005g0013 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2064+2860A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17811974 | |||||||
chr7:17812041 | A | C | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(206): Show |
212 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.2064+2793T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17812041 | |||||||
chr7:17812313 | C | A | 2 | a0001c0001t0005g0012 a0001c0001t0005g0013 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2064+2521G>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17812313 | |||||||
chr7:17812337 | C | T | 1 | a0001c0001t0001g0101 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.2064+2497G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17812337 | |||||||
chr7:17812462 | T | C | 2 | a0001c0001t0005g0012 a0001c0001t0005g0013 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2064+2372A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17812462 | |||||||
chr7:17812982 | G | C | 6 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0008 others(3): Show |
6 | HG01074.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.2064+1852C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17812982 | |||||||
chr7:17812984 | G | A | 1 | a0001c0001t0004g0113 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2064+1850C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17812984 | |||||||
chr7:17813109 | G | C | 2 | a0001c0001t0012g0189 a0001c0001t0012g0190 |
2 | HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2064+1725C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17813109 | |||||||
chr7:17813447 | G | T | 318 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(315): Show |
321 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(318): Show |
intron_variant | MODIFIER | c.2064+1387C>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17813447 | |||||||
chr7:17813492 | T | G | 3 | a0001c0001t0002g0018 a0001c0001t0014g0019 a0001c0010t0014g0020 |
3 | HG00639.hp2 HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.2064+1342A>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17813492 | |||||||
chr7:17813552 | T | C | 3 | a0001c0002t0001g0254 a0001c0002t0001g0259 a0001c0002t0001g0260 |
3 | NA18972.hp1 NA19012.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.2064+1282A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17813552 | |||||||
chr7:17813587 | C | CT | 13 | a0001c0001t0001g0046 a0001c0001t0001g0229 a0001c0001t0005g0012 others(10): Show |
13 | HG01099.hp2 HG01175.hp1 HG01516.hp1 others(10): Show |
intron_variant | MODIFIER | c.2064+1246dupA | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17813587 | |||||||
chr7:17813992 | T | C | 1 | a0001c0002t0001g0267 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2064+842A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17813992 | |||||||
chr7:17814181 | C | T | 2 | a0001c0001t0005g0012 a0001c0001t0005g0013 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2064+653G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17814181 | |||||||
chr7:17814360 | C | T | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(228): Show |
234 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.2064+474G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17814360 | |||||||
chr7:17814432 | A | G | 2 | a0001c0001t0005g0012 a0001c0001t0005g0013 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2064+402T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17814432 | |||||||
chr7:17814486 | T | A | 1 | a0001c0001t0001g0135 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2064+348A>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17814486 | |||||||
chr7:17814557 | C | T | 1 | a0001c0006t0025g0005 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2064+277G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17814557 | |||||||
chr7:17814590 | T | C | 2 | a0001c0001t0005g0012 a0001c0001t0005g0013 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2064+244A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17814590 | |||||||
chr7:17814601 | C | T | 1 | a0001c0001t0014g0019 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2064+233G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17814601 | |||||||
chr7:17814606 | C | T | 1 | a0001c0006t0025g0005 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2064+228G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17814606 | |||||||
chr7:17814816 | A | T | 4 | a0001c0001t0004g0184 a0001c0001t0004g0185 a0001c0001t0004g0186 others(1): Show |
4 | HG00544.hp1 NA18974.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.2064+18T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | 17814816 | |||||||
chr7:17814952 | G | GAA | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(222): Show |
228 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.1954-10_1954-9dupT others(1): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 19/25 | chr7 | 17814952 | |||||||
chr7:17814993 | T | C | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(212): Show |
218 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.1954-49A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 19/25 | chr7 | 17814993 | |||||||
chr7:17815210 | T | A | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
235 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.1954-266A>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 19/25 | chr7 | 17815210 | |||||||
chr7:17815226 | C | T | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
235 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.1954-282G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 19/25 | chr7 | 17815226 | |||||||
chr7:17815279 | A | G | 9 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0008 others(6): Show |
9 | HG01074.hp1 HG02055.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1954-335T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 19/25 | chr7 | 17815279 | |||||||
chr7:17815337 | A | G | 2 | a0001c0001t0001g0135 a0001c0001t0021g0134 |
2 | HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1954-393T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 19/25 | chr7 | 17815337 | |||||||
chr7:17815541 | C | T | 1 | a0001c0006t0025g0005 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1954-597G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 19/25 | chr7 | 17815541 | |||||||
chr7:17815665 | T | C | 3 | a0001c0001t0001g0132 a0001c0001t0004g0115 a0001c0001t0018g0216 |
3 | HG00738.hp1 HG01255.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1953+517A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 19/25 | chr7 | 17815665 | |||||||
chr7:17815811 | T | G | 1 | a0001c0001t0001g0178 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1953+371A>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 19/25 | chr7 | 17815811 | |||||||
chr7:17815843 | A | G | 234 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(231): Show |
237 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.1953+339T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 19/25 | chr7 | 17815843 | |||||||
chr7:17815864 | C | A | 3 | a0001c0004t0011g0014 a0001c0004t0011g0016 a0001c0004t0011g0067 |
3 | HG02622.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1953+318G>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 19/25 | chr7 | 17815864 | |||||||
chr7:17815978 | CT | C | 3 | a0001c0004t0011g0014 a0001c0004t0011g0016 a0001c0004t0011g0067 |
3 | HG02622.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1953+203delA | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 19/25 | chr7 | 17815978 | |||||||
chr7:17816036 | C | T | 10 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0008 others(7): Show |
10 | HG01074.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1953+146G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 19/25 | chr7 | 17816036 | |||||||
chr7:17816037 | G | A | 1 | a0001c0001t0016g0250 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1953+145C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 19/25 | chr7 | 17816037 | |||||||
chr7:17816667 | A | AAAC | 8 | a0001c0001t0001g0032 a0001c0001t0004g0116 a0001c0001t0008g0006 others(5): Show |
8 | HG00735.hp1 HG01074.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1846-381_1846-379d others(5): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 18/25 | chr7 | 17816667 | |||||||
chr7:17816919 | G | A | 17 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0008g0006 others(14): Show |
17 | HG01074.hp1 HG01952.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1846-630C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 18/25 | chr7 | 17816919 | |||||||
chr7:17817129 | T | C | 2 | a0001c0004t0011g0014 a0001c0004t0011g0067 |
2 | HG02622.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1846-840A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 18/25 | chr7 | 17817129 | |||||||
chr7:17817262 | A | G | 1 | a0001c0002t0002g0223 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1846-973T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 18/25 | chr7 | 17817262 | |||||||
chr7:17817307 | G | A | 1 | a0001c0001t0004g0116 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1846-1018C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 18/25 | chr7 | 17817307 | |||||||
chr7:17817309 | C | A | 1 | a0001c0001t0004g0116 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1846-1020G>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 18/25 | chr7 | 17817309 | |||||||
chr7:17817379 | T | C | 1 | a0001c0001t0001g0070 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1846-1090A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 18/25 | chr7 | 17817379 | |||||||
chr7:17817384 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1846-1095G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 18/25 | chr7 | 17817384 | |||||||
chr7:17817472 | T | G | 1 | a0001c0001t0001g0044 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1846-1183A>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 18/25 | chr7 | 17817472 | |||||||
chr7:17817746 | A | T | 1 | a0001c0002t0002g0298 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1846-1457T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 18/25 | chr7 | 17817746 | |||||||
chr7:17817753 | A | C | 1 | a0001c0002t0007g0205 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1846-1464T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 18/25 | chr7 | 17817753 | |||||||
chr7:17817797 | T | A | 1 | a0001c0001t0001g0086 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1846-1508A>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 18/25 | chr7 | 17817797 | |||||||
chr7:17817885 | T | C | 3 | a0001c0002t0023g0055 a0001c0002t0030g0056 a0001c0002t0032g0335 |
3 | HG02258.hp2 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1846-1596A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 18/25 | chr7 | 17817885 | |||||||
chr7:17817933 | G | A | 2 | a0001c0001t0013g0015 a0001c0001t0013g0239 |
2 | HG01952.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.1846-1644C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 18/25 | chr7 | 17817933 | |||||||
chr7:17818036 | G | C | 1 | a0001c0001t0008g0009 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1846-1747C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 18/25 | chr7 | 17818036 | |||||||
chr7:17818082 | T | C | 12 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0008g0006 others(9): Show |
12 | HG01074.hp1 HG02055.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1846-1793A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 18/25 | chr7 | 17818082 | |||||||
chr7:17818117 | C | G | 14 | a0001c0001t0001g0032 a0001c0001t0001g0045 a0001c0001t0001g0046 others(11): Show |
14 | HG01891.hp1 HG02451.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.1846-1828G>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 18/25 | chr7 | 17818117 | |||||||
chr7:17818119 | A | G | 3 | a0001c0002t0023g0055 a0001c0002t0030g0056 a0001c0002t0032g0335 |
3 | HG02258.hp2 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1846-1830T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 18/25 | chr7 | 17818119 | |||||||
chr7:17818506 | T | C | 5 | a0001c0002t0002g0241 a0001c0002t0002g0256 a0001c0002t0002g0288 others(2): Show |
5 | NA18747.hp2 NA18946.hp2 NA19084.hp1 others(2): Show |
intron_variant | MODIFIER | c.1846-2217A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 18/25 | chr7 | 17818506 | |||||||
chr7:17818523 | T | C | 14 | a0001c0001t0001g0032 a0001c0001t0001g0045 a0001c0001t0001g0046 others(11): Show |
14 | HG01891.hp1 HG02451.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.1846-2234A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 18/25 | chr7 | 17818523 | |||||||
chr7:17818595 | T | C | 2 | a0001c0001t0003g0199 a0001c0001t0003g0200 |
2 | HG00609.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.1846-2306A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 18/25 | chr7 | 17818595 | |||||||
chr7:17818596 | C | A | 1 | a0001c0001t0001g0227 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1846-2307G>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 18/25 | chr7 | 17818596 | |||||||
chr7:17818762 | T | C | 1 | a0001c0001t0004g0113 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1846-2473A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 18/25 | chr7 | 17818762 | |||||||
chr7:17818930 | T | A | 1 | a0001c0001t0019g0143 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1845+2579A>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 18/25 | chr7 | 17818930 | |||||||
chr7:17818931 | A | G | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(215): Show |
221 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.1845+2578T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 18/25 | chr7 | 17818931 | |||||||
chr7:17819007 | T | C | 2 | a0001c0001t0005g0012 a0001c0001t0005g0013 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1845+2502A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 18/25 | chr7 | 17819007 | |||||||
chr7:17819094 | A | G | 12 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0021 others(9): Show |
14 | HG01168.hp2 HG01169.hp1 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.1845+2415T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 18/25 | chr7 | 17819094 | |||||||
chr7:17819291 | G | C | 10 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0008 others(7): Show |
10 | HG01074.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1845+2218C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 18/25 | chr7 | 17819291 | |||||||
chr7:17819384 | G | C | 1 | a0001c0001t0029g0037 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1845+2125C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 18/25 | chr7 | 17819384 | |||||||
chr7:17819509 | G | C | 1 | a0001c0006t0025g0005 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1845+2000C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 18/25 | chr7 | 17819509 | |||||||
chr7:17819516 | C | T | 1 | a0001c0006t0025g0005 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1845+1993G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 18/25 | chr7 | 17819516 | |||||||
chr7:17819636 | T | C | 1 | a0001c0002t0001g0277 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1845+1873A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 18/25 | chr7 | 17819636 | |||||||
chr7:17819890 | G | GTTTTATA others(18): Show |
1 | a0001c0001t0001g0172 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1845+1618_1845+161 others(29): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 18/25 | chr7 | 17819890 | |||||||
chr7:17819892 | A | G | 1 | a0001c0001t0001g0172 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1845+1617T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 18/25 | chr7 | 17819892 | |||||||
chr7:17819892 | AAC | A | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(212): Show |
218 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.1845+1615_1845+161 others(6): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 18/25 | chr7 | 17819892 | |||||||
chr7:17819894 | C | A | 1 | a0001c0001t0001g0172 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1845+1615G>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 18/25 | chr7 | 17819894 | |||||||
chr7:17820068 | C | A | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(211): Show |
217 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1845+1441G>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 18/25 | chr7 | 17820068 | |||||||
chr7:17820229 | T | C | 2 | a0001c0001t0013g0015 a0001c0001t0013g0239 |
2 | HG01952.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.1845+1280A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 18/25 | chr7 | 17820229 | |||||||
chr7:17820362 | CAG | C | 3 | a0001c0001t0012g0188 a0001c0001t0012g0189 a0001c0001t0012g0190 |
3 | HG02055.hp1 HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1845+1145_1845+114 others(6): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 18/25 | chr7 | 17820362 | |||||||
chr7:17820363 | A | G | 3 | a0001c0002t0023g0055 a0001c0002t0030g0056 a0001c0002t0032g0335 |
3 | HG02258.hp2 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1845+1146T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 18/25 | chr7 | 17820363 | |||||||
chr7:17820655 | A | C | 1 | a0001c0001t0001g0011 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1845+854T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 18/25 | chr7 | 17820655 | |||||||
chr7:17820757 | C | A | 1 | a0001c0001t0001g0122 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1845+752G>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 18/25 | chr7 | 17820757 | |||||||
chr7:17820903 | T | G | 1 | a0001c0001t0001g0235 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1845+606A>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 18/25 | chr7 | 17820903 | |||||||
chr7:17821038 | T | G | 240 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(237): Show |
243 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.1845+471A>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 18/25 | chr7 | 17821038 | |||||||
chr7:17821039 | G | T | 1 | a0001c0001t0020g0191 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1845+470C>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 18/25 | chr7 | 17821039 | |||||||
chr7:17821187 | T | C | 3 | a0001c0004t0011g0014 a0001c0004t0011g0016 a0001c0004t0011g0067 |
3 | HG02622.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1845+322A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 18/25 | chr7 | 17821187 | |||||||
chr7:17821189 | C | T | 3 | a0001c0004t0011g0014 a0001c0004t0011g0016 a0001c0004t0011g0067 |
3 | HG02622.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1845+320G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 18/25 | chr7 | 17821189 | |||||||
chr7:17821234 | G | T | 1 | a0001c0011t0006g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1845+275C>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 18/25 | chr7 | 17821234 | |||||||
chr7:17821302 | T | C | 3 | a0001c0004t0011g0014 a0001c0004t0011g0016 a0001c0004t0011g0067 |
3 | HG02622.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1845+207A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 18/25 | chr7 | 17821302 | |||||||
chr7:17821327 | A | G | 3 | a0001c0002t0023g0055 a0001c0002t0030g0056 a0001c0002t0032g0335 |
3 | HG02258.hp2 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1845+182T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 18/25 | chr7 | 17821327 | |||||||
chr7:17821340 | T | C | 1 | a0001c0001t0001g0041 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1845+169A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 18/25 | chr7 | 17821340 | |||||||
chr7:17821411 | T | C | 1 | a0001c0001t0019g0143 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1845+98A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 18/25 | chr7 | 17821411 | |||||||
chr7:17821470 | A | C | 1 | a0001c0001t0001g0217 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1845+39T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 18/25 | chr7 | 17821470 | |||||||
chr7:17822186 | G | A | 9 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(6): Show |
9 | HG02451.hp1 HG02630.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1706-538C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 17/25 | chr7 | 17822186 | |||||||
chr7:17822330 | C | T | 1 | a0001c0001t0001g0041 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1706-682G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 17/25 | chr7 | 17822330 | |||||||
chr7:17822335 | T | G | 13 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0021 others(10): Show |
15 | HG01168.hp2 HG01169.hp1 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.1706-687A>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 17/25 | chr7 | 17822335 | |||||||
chr7:17822402 | G | C | 238 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(235): Show |
241 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.1706-754C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 17/25 | chr7 | 17822402 | |||||||
chr7:17822961 | G | A | 5 | a0001c0001t0001g0183 a0001c0001t0004g0184 a0001c0001t0004g0185 others(2): Show |
5 | HG00544.hp1 HG02129.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.1706-1313C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 17/25 | chr7 | 17822961 | |||||||
chr7:17823108 | T | C | 3 | a0001c0004t0011g0014 a0001c0004t0011g0016 a0001c0004t0011g0067 |
3 | HG02622.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1706-1460A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 17/25 | chr7 | 17823108 | |||||||
chr7:17823136 | T | C | 2 | a0001c0001t0001g0064 a0001c0001t0001g0232 |
2 | HG01243.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1706-1488A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 17/25 | chr7 | 17823136 | |||||||
chr7:17823344 | G | A | 1 | a0001c0001t0004g0113 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1706-1696C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 17/25 | chr7 | 17823344 | |||||||
chr7:17823377 | T | C | 10 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(7): Show |
10 | HG00609.hp2 NA18943.hp2 NA18945.hp1 others(7): Show |
intron_variant | MODIFIER | c.1706-1729A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 17/25 | chr7 | 17823377 | |||||||
chr7:17823699 | T | C | 1 | a0001c0001t0004g0115 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1706-2051A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 17/25 | chr7 | 17823699 | |||||||
chr7:17823835 | G | A | 1 | a0001c0001t0020g0191 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1705+2187C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 17/25 | chr7 | 17823835 | |||||||
chr7:17823903 | A | C | 2 | a0001c0001t0001g0076 a0001c0001t0001g0225 |
2 | NA18973.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.1705+2119T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 17/25 | chr7 | 17823903 | |||||||
chr7:17824007 | AT | A | 3 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 |
3 | NA18971.hp1 NA19010.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.1705+2014delA | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 17/25 | chr7 | 17824007 | |||||||
chr7:17824010 | T | A | 229 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(226): Show |
232 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.1705+2012A>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 17/25 | chr7 | 17824010 | |||||||
chr7:17824447 | C | T | 3 | a0001c0002t0023g0055 a0001c0002t0030g0056 a0001c0002t0032g0335 |
3 | HG02258.hp2 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1705+1575G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 17/25 | chr7 | 17824447 | |||||||
chr7:17824468 | C | T | 2 | a0001c0001t0005g0012 a0001c0001t0005g0013 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1705+1554G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 17/25 | chr7 | 17824468 | |||||||
chr7:17824492 | A | G | 1 | a0001c0001t0001g0224 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1705+1530T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 17/25 | chr7 | 17824492 | |||||||
chr7:17824774 | C | CT | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(213): Show |
219 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1705+1247dupA | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 17/25 | chr7 | 17824774 | |||||||
chr7:17824863 | G | A | 9 | a0001c0001t0001g0064 a0001c0001t0001g0173 a0001c0001t0001g0174 others(6): Show |
9 | HG00673.hp1 HG02056.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1705+1159C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 17/25 | chr7 | 17824863 | |||||||
chr7:17824915 | G | A | 1 | a0001c0001t0001g0103 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1705+1107C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 17/25 | chr7 | 17824915 | |||||||
chr7:17825011 | G | A | 1 | a0001c0001t0001g0085 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1705+1011C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 17/25 | chr7 | 17825011 | |||||||
chr7:17825021 | G | C | 2 | a0001c0001t0005g0012 a0001c0001t0005g0013 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1705+1001C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 17/25 | chr7 | 17825021 | |||||||
chr7:17825039 | G | T | 2 | a0001c0001t0013g0015 a0001c0001t0013g0239 |
2 | HG01952.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.1705+983C>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 17/25 | chr7 | 17825039 | |||||||
chr7:17825193 | C | G | 233 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(230): Show |
236 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.1705+829G>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 17/25 | chr7 | 17825193 | |||||||
chr7:17825254 | T | TTACTAGA others(6): Show |
1 | a0001c0001t0001g0099 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1705+767_1705+768i others(15): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 17/25 | chr7 | 17825254 | |||||||
chr7:17825257 | A | AACTAG | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(114): Show |
119 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.1705+760_1705+764d others(7): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 17/25 | chr7 | 17825257 | |||||||
chr7:17825257 | A | AACTAGAC others(3): Show |
57 | a0001c0001t0001g0032 a0001c0001t0001g0036 a0001c0001t0001g0045 others(54): Show |
57 | HG00323.hp1 HG00544.hp1 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.1705+755_1705+764d others(12): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 17/25 | chr7 | 17825257 | |||||||
chr7:17825257 | A | AACTAGAC others(8): Show |
11 | a0001c0001t0001g0071 a0001c0001t0001g0087 a0001c0001t0001g0088 others(8): Show |
11 | HG00673.hp1 HG01891.hp1 HG02015.hp2 others(8): Show |
intron_variant | MODIFIER | c.1705+750_1705+764d others(17): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 17/25 | chr7 | 17825257 | |||||||
chr7:17825257 | A | AACTAGAC others(13): Show |
1 | a0001c0001t0004g0186 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1705+745_1705+764d others(22): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 17/25 | chr7 | 17825257 | |||||||
chr7:17825257 | A | AACTAGAC others(18): Show |
1 | a0001c0002t0002g0280 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1705+740_1705+764d others(27): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 17/25 | chr7 | 17825257 | |||||||
chr7:17825257 | A | AACTAGAC others(28): Show |
1 | a0001c0002t0002g0332 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1705+730_1705+764d others(37): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 17/25 | chr7 | 17825257 | |||||||
chr7:17825257 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1705+765T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 17/25 | chr7 | 17825257 | |||||||
chr7:17825257 | AACTAG | A | 12 | a0001c0001t0001g0062 a0001c0001t0001g0173 a0001c0001t0002g0018 others(9): Show |
12 | HG01109.hp2 HG01169.hp2 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.1705+760_1705+764d others(7): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 17/25 | chr7 | 17825257 | |||||||
chr7:17825257 | AACTAGAC others(3): Show |
A | 29 | a0001c0001t0005g0197 a0001c0001t0005g0274 a0001c0002t0001g0198 others(26): Show |
29 | HG00558.hp1 HG02015.hp1 HG02129.hp2 others(26): Show |
intron_variant | MODIFIER | c.1705+755_1705+764d others(12): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 17/25 | chr7 | 17825257 | |||||||
chr7:17825257 | AACTAGAC others(8): Show |
A | 1 | a0003c0012t0001g0180 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1705+750_1705+764d others(17): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 17/25 | chr7 | 17825257 | |||||||
chr7:17825257 | AACTAGAC others(13): Show |
A | 1 | a0001c0001t0014g0019 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1705+745_1705+764d others(22): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 17/25 | chr7 | 17825257 | |||||||
chr7:17825364 | A | G | 2 | a0001c0001t0001g0069 a0001c0001t0001g0126 |
2 | NA18985.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.1705+658T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 17/25 | chr7 | 17825364 | |||||||
chr7:17825672 | C | A | 1 | a0001c0001t0001g0140 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1705+350G>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 17/25 | chr7 | 17825672 | |||||||
chr7:17825789 | G | C | 12 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0021 others(9): Show |
14 | HG01168.hp2 HG01169.hp1 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.1705+233C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 17/25 | chr7 | 17825789 | |||||||
chr7:17826199 | A | G | 1 | a0001c0002t0002g0264 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1636-108T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 16/25 | chr7 | 17826199 | |||||||
chr7:17826203 | T | G | 1 | a0001c0003t0003g0270 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1636-112A>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 16/25 | chr7 | 17826203 | |||||||
chr7:17826292 | A | G | 2 | a0001c0001t0013g0015 a0001c0001t0013g0239 |
2 | HG01952.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.1636-201T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 16/25 | chr7 | 17826292 | |||||||
chr7:17826645 | T | C | 1 | a0001c0001t0001g0069 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1636-554A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 16/25 | chr7 | 17826645 | |||||||
chr7:17826764 | C | T | 210 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(207): Show |
213 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.1636-673G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 16/25 | chr7 | 17826764 | |||||||
chr7:17827273 | C | T | 1 | a0001c0010t0014g0020 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1636-1182G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 16/25 | chr7 | 17827273 | |||||||
chr7:17827352 | A | G | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(209): Show |
215 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.1636-1261T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 16/25 | chr7 | 17827352 | |||||||
chr7:17827764 | T | C | 3 | a0001c0001t0001g0061 a0001c0001t0001g0107 a0001c0001t0001g0108 |
3 | NA18946.hp1 NA18957.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1636-1673A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 16/25 | chr7 | 17827764 | |||||||
chr7:17827911 | A | G | 1 | a0001c0001t0001g0031 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1636-1820T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 16/25 | chr7 | 17827911 | |||||||
chr7:17827972 | A | G | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(210): Show |
216 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.1636-1881T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 16/25 | chr7 | 17827972 | |||||||
chr7:17827976 | C | G | 3 | a0001c0001t0001g0135 a0001c0001t0020g0191 a0001c0001t0021g0134 |
3 | HG02280.hp1 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1636-1885G>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 16/25 | chr7 | 17827976 | |||||||
chr7:17828008 | T | C | 1 | a0001c0006t0025g0005 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1636-1917A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 16/25 | chr7 | 17828008 | |||||||
chr7:17828174 | A | G | 3 | a0001c0002t0023g0055 a0001c0002t0030g0056 a0001c0002t0032g0335 |
3 | HG02258.hp2 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1635+1836T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 16/25 | chr7 | 17828174 | |||||||
chr7:17828256 | C | G | 2 | a0001c0001t0001g0101 a0001c0001t0001g0110 |
2 | HG02135.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.1635+1754G>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 16/25 | chr7 | 17828256 | |||||||
chr7:17828343 | T | C | 1 | a0001c0011t0006g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1635+1667A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 16/25 | chr7 | 17828343 | |||||||
chr7:17828490 | T | G | 1 | a0001c0001t0001g0093 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1635+1520A>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 16/25 | chr7 | 17828490 | |||||||
chr7:17828528 | A | G | 1 | a0001c0001t0001g0104 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1635+1482T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 16/25 | chr7 | 17828528 | |||||||
chr7:17828539 | G | T | 1 | a0001c0010t0014g0020 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1635+1471C>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 16/25 | chr7 | 17828539 | |||||||
chr7:17828659 | G | A | 2 | a0001c0001t0013g0015 a0001c0001t0013g0239 |
2 | HG01952.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.1635+1351C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 16/25 | chr7 | 17828659 | |||||||
chr7:17828708 | T | C | 235 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(232): Show |
238 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.1635+1302A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 16/25 | chr7 | 17828708 | |||||||
chr7:17828752 | C | T | 1 | a0001c0002t0009g0329 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1635+1258G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 16/25 | chr7 | 17828752 | |||||||
chr7:17828877 | C | T | 2 | a0001c0001t0001g0072 a0001c0001t0001g0230 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1635+1133G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 16/25 | chr7 | 17828877 | |||||||
chr7:17829017 | T | C | 3 | a0001c0001t0001g0160 a0001c0001t0001g0162 a0001c0001t0001g0166 |
3 | NA18986.hp2 NA19080.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.1635+993A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 16/25 | chr7 | 17829017 | |||||||
chr7:17829167 | C | T | 3 | a0001c0002t0007g0208 a0001c0002t0007g0292 a0001c0002t0007g0297 |
3 | NA18944.hp1 NA18984.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1635+843G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 16/25 | chr7 | 17829167 | |||||||
chr7:17829196 | C | T | 12 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0021 others(9): Show |
14 | HG01168.hp2 HG01169.hp1 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.1635+814G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 16/25 | chr7 | 17829196 | |||||||
chr7:17829197 | G | A | 1 | a0001c0001t0001g0124 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1635+813C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 16/25 | chr7 | 17829197 | |||||||
chr7:17829266 | C | T | 1 | a0001c0010t0014g0020 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1635+744G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 16/25 | chr7 | 17829266 | |||||||
chr7:17829508 | A | C | 1 | a0001c0010t0014g0020 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1635+502T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 16/25 | chr7 | 17829508 | |||||||
chr7:17829518 | A | T | 7 | a0001c0002t0006g0253 a0001c0002t0006g0284 a0001c0002t0006g0294 others(4): Show |
7 | HG00642.hp2 HG00741.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.1635+492T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 16/25 | chr7 | 17829518 | |||||||
chr7:17829524 | T | G | 14 | a0001c0001t0001g0033 a0001c0001t0001g0035 a0001c0001t0001g0036 others(11): Show |
14 | HG00280.hp2 HG00323.hp1 HG00673.hp2 others(11): Show |
intron_variant | MODIFIER | c.1635+486A>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 16/25 | chr7 | 17829524 | |||||||
chr7:17829560 | T | TA | 13 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0021 others(10): Show |
15 | HG01168.hp2 HG01169.hp1 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.1635+449dupT | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 16/25 | chr7 | 17829560 | |||||||
chr7:17829625 | G | A | 2 | a0001c0001t0001g0162 a0001c0001t0001g0166 |
2 | NA19080.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.1635+385C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 16/25 | chr7 | 17829625 | |||||||
chr7:17829761 | G | A | 1 | a0001c0001t0001g0170 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1635+249C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 16/25 | chr7 | 17829761 | |||||||
chr7:17829775 | A | G | 10 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0008 others(7): Show |
10 | HG01074.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1635+235T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 16/25 | chr7 | 17829775 | |||||||
chr7:17829944 | T | C | 1 | a0001c0001t0001g0054 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1635+66A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 16/25 | chr7 | 17829944 | |||||||
chr7:17829980 | C | T | 1 | a0001c0002t0002g0212 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1635+30G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 16/25 | chr7 | 17829980 | |||||||
chr7:17830118 | C | T | 3 | a0001c0004t0011g0014 a0001c0004t0011g0016 a0001c0004t0011g0067 |
3 | HG02622.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1598-71G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 15/25 | chr7 | 17830118 | |||||||
chr7:17830161 | T | TA | 20 | a0001c0001t0001g0011 a0001c0001t0001g0036 a0001c0001t0001g0130 others(17): Show |
20 | HG00323.hp1 HG00741.hp2 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1598-115dupT | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 15/25 | chr7 | 17830161 | |||||||
chr7:17830161 | T | TAA | 187 | a0001c0001t0001g0003 a0001c0001t0001g0031 a0001c0001t0001g0032 others(184): Show |
188 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.1598-116_1598-115d others(4): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 15/25 | chr7 | 17830161 | |||||||
chr7:17830161 | T | TAAA | 23 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0024 others(20): Show |
24 | HG00639.hp1 HG00735.hp1 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.1598-117_1598-115d others(5): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 15/25 | chr7 | 17830161 | |||||||
chr7:17830161 | T | TAAAA | 5 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0023 others(2): Show |
6 | HG01168.hp2 HG01169.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.1598-118_1598-115d others(6): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 15/25 | chr7 | 17830161 | |||||||
chr7:17830161 | TA | T | 7 | a0001c0002t0001g0254 a0001c0002t0002g0213 a0001c0002t0002g0278 others(4): Show |
7 | HG01099.hp2 HG01256.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1598-115delT | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 15/25 | chr7 | 17830161 | |||||||
chr7:17830161 | TAAAAAAA others(3): Show |
T | 2 | a0001c0001t0001g0084 a0001c0001t0001g0238 |
2 | HG02683.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1598-124_1598-115d others(12): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 15/25 | chr7 | 17830161 | |||||||
chr7:17830231 | C | G | 25 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0045 others(22): Show |
26 | HG00609.hp1 HG00741.hp1 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.1598-184G>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 15/25 | chr7 | 17830231 | |||||||
chr7:17830316 | T | A | 1 | a0001c0001t0001g0120 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1598-269A>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 15/25 | chr7 | 17830316 | |||||||
chr7:17830685 | A | C | 1 | a0001c0001t0001g0240 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1598-638T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 15/25 | chr7 | 17830685 | |||||||
chr7:17830717 | C | T | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
235 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.1598-670G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 15/25 | chr7 | 17830717 | |||||||
chr7:17830760 | C | T | 1 | a0001c0001t0014g0019 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1598-713G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 15/25 | chr7 | 17830760 | |||||||
chr7:17831045 | T | C | 12 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0021 others(9): Show |
14 | HG01168.hp2 HG01169.hp1 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.1598-998A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 15/25 | chr7 | 17831045 | |||||||
chr7:17831273 | A | T | 1 | a0001c0001t0001g0171 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1598-1226T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 15/25 | chr7 | 17831273 | |||||||
chr7:17831277 | C | T | 2 | a0001c0001t0001g0088 a0001c0001t0001g0224 |
2 | HG02015.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.1598-1230G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 15/25 | chr7 | 17831277 | |||||||
chr7:17831278 | T | C | 1 | a0001c0006t0025g0005 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1598-1231A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 15/25 | chr7 | 17831278 | |||||||
chr7:17831304 | T | C | 1 | a0001c0001t0001g0041 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1598-1257A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 15/25 | chr7 | 17831304 | |||||||
chr7:17831457 | G | A | 12 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0021 others(9): Show |
14 | HG01168.hp2 HG01169.hp1 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.1598-1410C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 15/25 | chr7 | 17831457 | |||||||
chr7:17831470 | G | A | 12 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0021 others(9): Show |
14 | HG01168.hp2 HG01169.hp1 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.1598-1423C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 15/25 | chr7 | 17831470 | |||||||
chr7:17831531 | G | A | 2 | a0001c0005t0002g0206 a0001c0005t0002g0279 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1598-1484C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 15/25 | chr7 | 17831531 | |||||||
chr7:17831741 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1598-1694C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 15/25 | chr7 | 17831741 | |||||||
chr7:17831994 | G | C | 1 | a0001c0001t0002g0018 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1598-1947C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 15/25 | chr7 | 17831994 | |||||||
chr7:17832096 | T | A | 12 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0021 others(9): Show |
14 | HG01168.hp2 HG01169.hp1 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.1597+1956A>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 15/25 | chr7 | 17832096 | |||||||
chr7:17832200 | G | A | 1 | a0001c0001t0001g0178 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1597+1852C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 15/25 | chr7 | 17832200 | |||||||
chr7:17832290 | C | T | 1 | a0001c0001t0001g0040 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1597+1762G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 15/25 | chr7 | 17832290 | |||||||
chr7:17832347 | G | A | 12 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0021 others(9): Show |
14 | HG01168.hp2 HG01169.hp1 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.1597+1705C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 15/25 | chr7 | 17832347 | |||||||
chr7:17832383 | G | A | 1 | a0001c0002t0001g0203 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1597+1669C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 15/25 | chr7 | 17832383 | |||||||
chr7:17832470 | C | A | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(210): Show |
216 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.1597+1582G>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 15/25 | chr7 | 17832470 | |||||||
chr7:17832529 | C | T | 7 | a0001c0001t0002g0018 a0001c0001t0008g0006 a0001c0001t0008g0007 others(4): Show |
7 | HG01074.hp1 HG02622.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1597+1523G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 15/25 | chr7 | 17832529 | |||||||
chr7:17832556 | T | A | 1 | a0001c0002t0002g0290 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1597+1496A>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 15/25 | chr7 | 17832556 | |||||||
chr7:17832685 | G | C | 1 | a0001c0011t0006g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1597+1367C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 15/25 | chr7 | 17832685 | |||||||
chr7:17832693 | C | A | 1 | a0001c0001t0026g0249 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1597+1359G>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 15/25 | chr7 | 17832693 | |||||||
chr7:17832705 | A | T | 2 | a0001c0002t0009g0329 a0001c0002t0009g0330 |
2 | NA18998.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.1597+1347T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 15/25 | chr7 | 17832705 | |||||||
chr7:17832745 | C | G | 11 | a0001c0001t0004g0112 a0001c0001t0004g0113 a0001c0001t0004g0114 others(8): Show |
11 | HG00544.hp1 HG00738.hp1 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.1597+1307G>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 15/25 | chr7 | 17832745 | |||||||
chr7:17832871 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1597+1181T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 15/25 | chr7 | 17832871 | |||||||
chr7:17833361 | G | C | 14 | a0001c0001t0001g0032 a0001c0001t0001g0045 a0001c0001t0001g0046 others(11): Show |
14 | HG01891.hp1 HG02451.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.1597+691C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 15/25 | chr7 | 17833361 | |||||||
chr7:17833542 | C | T | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(210): Show |
216 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.1597+510G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 15/25 | chr7 | 17833542 | |||||||
chr7:17833731 | T | C | 2 | a0001c0001t0005g0012 a0001c0001t0005g0013 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1597+321A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 15/25 | chr7 | 17833731 | |||||||
chr7:17833751 | T | C | 1 | a0001c0001t0002g0334 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1597+301A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 15/25 | chr7 | 17833751 | |||||||
chr7:17833846 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1597+206A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 15/25 | chr7 | 17833846 | |||||||
chr7:17833852 | C | T | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(199): Show |
205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.1597+200G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 15/25 | chr7 | 17833852 | |||||||
chr7:17834038 | G | A | 3 | a0001c0004t0011g0014 a0001c0004t0011g0016 a0001c0004t0011g0067 |
3 | HG02622.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1597+14C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 15/25 | chr7 | 17834038 | |||||||
chr7:17834188 | G | T | 6 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0008 others(3): Show |
6 | HG01074.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.1465-4C>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 14/25 | chr7 | 17834188 | |||||||
chr7:17834242 | A | G | 1 | a0001c0001t0031g0242 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1465-58T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 14/25 | chr7 | 17834242 | |||||||
chr7:17834300 | A | G | 1 | a0001c0001t0001g0228 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1465-116T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 14/25 | chr7 | 17834300 | |||||||
chr7:17834441 | G | A | 1 | a0001c0002t0002g0281 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1465-257C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 14/25 | chr7 | 17834441 | |||||||
chr7:17834469 | A | C | 2 | a0001c0001t0005g0197 a0001c0001t0005g0274 |
2 | NA18949.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.1465-285T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 14/25 | chr7 | 17834469 | |||||||
chr7:17834592 | A | G | 3 | a0001c0004t0011g0014 a0001c0004t0011g0016 a0001c0004t0011g0067 |
3 | HG02622.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1464+169T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 14/25 | chr7 | 17834592 | |||||||
chr7:17834607 | C | T | 1 | a0001c0001t0001g0181 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1464+154G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 14/25 | chr7 | 17834607 | |||||||
chr7:17834648 | T | C | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(273): Show |
279 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.1464+113A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 14/25 | chr7 | 17834648 | |||||||
chr7:17834677 | G | A | 223 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(220): Show |
226 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.1464+84C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 14/25 | chr7 | 17834677 | |||||||
chr7:17834881 | A | G | 2 | a0001c0001t0013g0015 a0001c0001t0013g0239 |
2 | HG01952.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.1360-16T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 13/25 | chr7 | 17834881 | |||||||
chr7:17835099 | T | C | 2 | a0001c0001t0013g0015 a0001c0001t0013g0239 |
2 | HG01952.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.1360-234A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 13/25 | chr7 | 17835099 | |||||||
chr7:17835224 | A | G | 1 | a0001c0001t0001g0088 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1360-359T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 13/25 | chr7 | 17835224 | |||||||
chr7:17835281 | A | C | 1 | a0001c0001t0012g0188 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1360-416T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 13/25 | chr7 | 17835281 | |||||||
chr7:17835289 | T | C | 1 | a0001c0002t0006g0253 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1360-424A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 13/25 | chr7 | 17835289 | |||||||
chr7:17835356 | A | C | 28 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(25): Show |
28 | HG00280.hp2 HG00323.hp1 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.1360-491T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 13/25 | chr7 | 17835356 | |||||||
chr7:17835445 | G | T | 1 | a0001c0011t0006g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1360-580C>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 13/25 | chr7 | 17835445 | |||||||
chr7:17835560 | A | T | 1 | a0001c0004t0011g0014 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1360-695T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 13/25 | chr7 | 17835560 | |||||||
chr7:17835628 | A | G | 9 | a0001c0001t0001g0072 a0001c0001t0001g0087 a0001c0001t0001g0109 others(6): Show |
9 | HG02109.hp1 HG02451.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1360-763T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 13/25 | chr7 | 17835628 | |||||||
chr7:17835629 | A | T | 2 | a0001c0001t0005g0012 a0001c0001t0005g0013 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1360-764T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 13/25 | chr7 | 17835629 | |||||||
chr7:17835808 | C | T | 228 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(225): Show |
231 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.1360-943G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 13/25 | chr7 | 17835808 | |||||||
chr7:17836153 | A | G | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(208): Show |
214 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.1360-1288T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 13/25 | chr7 | 17836153 | |||||||
chr7:17836334 | T | C | 2 | a0001c0001t0001g0050 a0001c0001t0001g0227 |
2 | HG02451.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1360-1469A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 13/25 | chr7 | 17836334 | |||||||
chr7:17836430 | T | C | 3 | a0001c0004t0011g0014 a0001c0004t0011g0016 a0001c0004t0011g0067 |
3 | HG02622.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1360-1565A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 13/25 | chr7 | 17836430 | |||||||
chr7:17836452 | G | C | 3 | a0001c0004t0011g0014 a0001c0004t0011g0016 a0001c0004t0011g0067 |
3 | HG02622.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1360-1587C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 13/25 | chr7 | 17836452 | |||||||
chr7:17836486 | A | G | 2 | a0001c0001t0005g0012 a0001c0001t0005g0013 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1360-1621T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 13/25 | chr7 | 17836486 | |||||||
chr7:17836554 | T | C | 17 | a0001c0001t0001g0061 a0001c0001t0001g0065 a0001c0001t0001g0070 others(14): Show |
17 | HG01081.hp1 HG02015.hp2 HG02135.hp1 others(14): Show |
intron_variant | MODIFIER | c.1360-1689A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 13/25 | chr7 | 17836554 | |||||||
chr7:17836942 | G | T | 2 | a0001c0001t0005g0012 a0001c0001t0005g0013 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1360-2077C>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 13/25 | chr7 | 17836942 | |||||||
chr7:17836943 | C | T | 2 | a0001c0001t0005g0012 a0001c0001t0005g0013 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1360-2078G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 13/25 | chr7 | 17836943 | |||||||
chr7:17837014 | A | G | 1 | a0001c0001t0014g0019 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1360-2149T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 13/25 | chr7 | 17837014 | |||||||
chr7:17837145 | A | T | 6 | a0001c0001t0001g0122 a0001c0001t0012g0188 a0001c0001t0012g0189 others(3): Show |
6 | HG02055.hp1 HG02280.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1360-2280T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 13/25 | chr7 | 17837145 | |||||||
chr7:17837176 | C | T | 2 | a0001c0010t0014g0020 a0001c0011t0006g0017 |
2 | HG02572.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1360-2311G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 13/25 | chr7 | 17837176 | |||||||
chr7:17837188 | C | T | 1 | a0001c0001t0001g0011 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1360-2323G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 13/25 | chr7 | 17837188 | |||||||
chr7:17837333 | T | C | 2 | a0001c0001t0010g0138 a0001c0001t0010g0139 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1360-2468A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 13/25 | chr7 | 17837333 | |||||||
chr7:17837476 | T | A | 2 | a0001c0001t0001g0089 a0001c0001t0001g0090 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1359+2331A>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 13/25 | chr7 | 17837476 | |||||||
chr7:17837602 | A | G | 3 | a0001c0001t0008g0006 a0001c0001t0008g0009 a0001c0001t0008g0060 |
3 | HG01074.hp1 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1359+2205T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 13/25 | chr7 | 17837602 | |||||||
chr7:17837825 | T | C | 235 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(232): Show |
238 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.1359+1982A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 13/25 | chr7 | 17837825 | |||||||
chr7:17837995 | A | C | 1 | a0001c0002t0002g0305 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1359+1812T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 13/25 | chr7 | 17837995 | |||||||
chr7:17838170 | T | C | 3 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0025 |
4 | HG01168.hp2 HG01169.hp1 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.1359+1637A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 13/25 | chr7 | 17838170 | |||||||
chr7:17838249 | G | C | 1 | a0001c0011t0006g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1359+1558C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 13/25 | chr7 | 17838249 | |||||||
chr7:17838407 | T | C | 1 | a0001c0002t0009g0293 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1359+1400A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 13/25 | chr7 | 17838407 | |||||||
chr7:17838510 | T | C | 1 | a0001c0001t0004g0186 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1359+1297A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 13/25 | chr7 | 17838510 | |||||||
chr7:17838567 | T | C | 1 | a0001c0001t0001g0021 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1359+1240A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 13/25 | chr7 | 17838567 | |||||||
chr7:17838642 | T | C | 6 | a0001c0001t0001g0032 a0001c0001t0001g0045 a0001c0001t0001g0046 others(3): Show |
6 | HG01891.hp1 HG03041.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1359+1165A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 13/25 | chr7 | 17838642 | |||||||
chr7:17838703 | T | C | 2 | a0001c0001t0005g0012 a0001c0001t0005g0013 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1359+1104A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 13/25 | chr7 | 17838703 | |||||||
chr7:17839053 | T | C | 24 | a0001c0001t0001g0135 a0001c0001t0001g0173 a0001c0001t0001g0174 others(21): Show |
24 | HG00544.hp1 HG00673.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.1359+754A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 13/25 | chr7 | 17839053 | |||||||
chr7:17839071 | T | G | 1 | a0001c0001t0001g0144 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1359+736A>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 13/25 | chr7 | 17839071 | |||||||
chr7:17839174 | A | G | 15 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0021 others(12): Show |
17 | HG01081.hp1 HG01168.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.1359+633T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 13/25 | chr7 | 17839174 | |||||||
chr7:17839193 | T | G | 2 | a0001c0001t0013g0015 a0001c0001t0013g0239 |
2 | HG01952.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.1359+614A>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 13/25 | chr7 | 17839193 | |||||||
chr7:17839213 | T | A | 1 | a0001c0001t0001g0068 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1359+594A>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 13/25 | chr7 | 17839213 | |||||||
chr7:17839311 | T | G | 2 | a0001c0001t0001g0135 a0001c0001t0021g0134 |
2 | HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1359+496A>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 13/25 | chr7 | 17839311 | |||||||
chr7:17839347 | G | T | 122 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0032 others(119): Show |
123 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.1359+460C>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 13/25 | chr7 | 17839347 | |||||||
chr7:17839480 | G | A | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(212): Show |
218 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.1359+327C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 13/25 | chr7 | 17839480 | |||||||
chr7:17840008 | T | C | 1 | a0001c0002t0002g0241 | 1 | NA19091.hp1 | splice_region_variant&intron_variant | LOW | c.1166-8A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17840008 | |||||||
chr7:17840169 | C | T | 1 | a0001c0006t0025g0005 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1166-169G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17840169 | |||||||
chr7:17840207 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1166-207G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17840207 | |||||||
chr7:17840220 | A | AT | 4 | a0001c0001t0001g0061 a0001c0001t0001g0096 a0001c0001t0001g0107 others(1): Show |
4 | NA18946.hp1 NA18957.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.1166-221dupA | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17840220 | |||||||
chr7:17841015 | C | T | 2 | a0001c0001t0001g0314 a0001c0001t0001g0315 |
2 | HG00642.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.1166-1015G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17841015 | |||||||
chr7:17841123 | T | C | 2 | a0001c0001t0001g0035 a0001c0001t0001g0036 |
2 | HG00323.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.1166-1123A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17841123 | |||||||
chr7:17841127 | T | G | 11 | a0001c0001t0001g0062 a0001c0001t0001g0069 a0001c0001t0001g0076 others(8): Show |
11 | HG01496.hp1 HG02040.hp2 NA18942.hp1 others(8): Show |
intron_variant | MODIFIER | c.1166-1127A>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17841127 | |||||||
chr7:17841171 | A | AT | 11 | a0001c0001t0002g0018 a0001c0001t0008g0006 a0001c0001t0008g0007 others(8): Show |
11 | HG01074.hp1 HG02055.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1166-1172dupA | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17841171 | |||||||
chr7:17841265 | G | C | 1 | a0001c0001t0001g0028 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1166-1265C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17841265 | |||||||
chr7:17841288 | G | A | 2 | a0001c0002t0001g0283 a0001c0002t0001g0322 |
2 | HG00558.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1166-1288C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17841288 | |||||||
chr7:17841356 | G | C | 1 | a0001c0001t0001g0106 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1166-1356C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17841356 | |||||||
chr7:17841512 | CAG | C | 6 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0008 others(3): Show |
6 | HG01074.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1166-1514_1166-151 others(6): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17841512 | |||||||
chr7:17841539 | C | T | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(212): Show |
218 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.1166-1539G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17841539 | |||||||
chr7:17841553 | T | TAC | 12 | a0001c0001t0001g0030 a0001c0001t0001g0148 a0001c0001t0001g0159 others(9): Show |
12 | HG01255.hp1 HG01361.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1166-1555_1166-155 others(6): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17841553 | |||||||
chr7:17841553 | T | TACAC | 73 | a0001c0001t0001g0062 a0001c0001t0001g0069 a0001c0001t0001g0075 others(70): Show |
73 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.1166-1557_1166-155 others(8): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17841553 | |||||||
chr7:17841553 | T | TACACAC | 91 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0035 others(88): Show |
92 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.1166-1559_1166-155 others(10): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17841553 | |||||||
chr7:17841553 | T | TACACACA others(1): Show |
74 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0001g0041 others(71): Show |
74 | HG00140.hp2 HG00280.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.1166-1561_1166-155 others(12): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17841553 | |||||||
chr7:17841553 | T | TACACACA others(3): Show |
43 | a0001c0001t0001g0028 a0001c0001t0001g0033 a0001c0001t0001g0042 others(40): Show |
43 | HG00408.hp1 HG00544.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.1166-1563_1166-155 others(14): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17841553 | |||||||
chr7:17841553 | T | TACACACA others(5): Show |
20 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0022 others(17): Show |
21 | HG01074.hp1 HG01168.hp2 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.1166-1565_1166-155 others(16): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17841553 | |||||||
chr7:17841553 | T | TACACACA others(7): Show |
3 | a0001c0001t0001g0081 a0001c0001t0001g0227 a0001c0001t0008g0007 |
3 | HG02523.hp1 HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1166-1567_1166-155 others(18): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17841553 | |||||||
chr7:17841553 | T | TACACACA others(9): Show |
2 | a0001c0001t0001g0031 a0001c0001t0001g0032 |
2 | HG02572.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1166-1569_1166-155 others(20): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17841553 | |||||||
chr7:17841553 | T | TACACACA others(11): Show |
1 | a0001c0001t0001g0002 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1166-1571_1166-155 others(22): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17841553 | |||||||
chr7:17841584 | G | A | 6 | a0001c0001t0001g0093 a0001c0001t0001g0101 a0001c0001t0002g0018 others(3): Show |
6 | HG02258.hp2 HG02896.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1166-1584C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17841584 | |||||||
chr7:17841586 | A | ACACACAC others(7): Show |
1 | a0001c0002t0023g0055 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1166-1587_1166-158 others(18): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17841586 | |||||||
chr7:17841586 | A | ACACACAC others(3): Show |
2 | a0001c0002t0030g0056 a0001c0002t0032g0335 |
2 | HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1166-1587_1166-158 others(14): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17841586 | |||||||
chr7:17841706 | G | A | 2 | a0001c0001t0001g0064 a0001c0001t0001g0232 |
2 | HG01243.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1166-1706C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17841706 | |||||||
chr7:17841758 | T | G | 1 | a0001c0002t0001g0034 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1166-1758A>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17841758 | |||||||
chr7:17841881 | G | A | 13 | a0001c0001t0004g0112 a0001c0001t0004g0113 a0001c0001t0004g0114 others(10): Show |
13 | HG00544.hp1 HG00735.hp1 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.1166-1881C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17841881 | |||||||
chr7:17841926 | A | C | 1 | a0001c0001t0001g0045 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1166-1926T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17841926 | |||||||
chr7:17842039 | G | C | 1 | a0001c0001t0021g0134 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1166-2039C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17842039 | |||||||
chr7:17842299 | G | A | 1 | a0001c0006t0025g0005 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1166-2299C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17842299 | |||||||
chr7:17842380 | G | C | 1 | a0001c0001t0001g0159 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1166-2380C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17842380 | |||||||
chr7:17842622 | C | T | 1 | a0001c0004t0011g0014 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1166-2622G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17842622 | |||||||
chr7:17842634 | T | A | 1 | a0001c0001t0001g0240 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1166-2634A>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17842634 | |||||||
chr7:17842841 | T | G | 2 | a0001c0001t0001g0127 a0001c0001t0001g0130 |
2 | NA18942.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.1165+2754A>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17842841 | |||||||
chr7:17842885 | T | C | 1 | a0001c0001t0019g0143 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1165+2710A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17842885 | |||||||
chr7:17842979 | C | T | 3 | a0001c0001t0001g0031 a0001c0001t0001g0097 a0001c0001t0001g0226 |
3 | HG01081.hp1 HG02572.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1165+2616G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17842979 | |||||||
chr7:17843304 | G | T | 2 | a0001c0001t0001g0135 a0001c0001t0021g0134 |
2 | HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1165+2291C>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17843304 | |||||||
chr7:17843343 | T | C | 1 | a0001c0001t0001g0173 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1165+2252A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17843343 | |||||||
chr7:17843719 | T | C | 2 | a0001c0001t0013g0015 a0001c0001t0013g0239 |
2 | HG01952.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.1165+1876A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17843719 | |||||||
chr7:17843757 | C | G | 1 | a0001c0001t0014g0019 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1165+1838G>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17843757 | |||||||
chr7:17843796 | A | G | 2 | a0001c0001t0005g0136 a0001c0001t0005g0142 |
2 | HG01255.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1165+1799T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17843796 | |||||||
chr7:17843804 | C | T | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(192): Show |
198 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.1165+1791G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17843804 | |||||||
chr7:17843937 | T | C | 1 | a0001c0001t0001g0119 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1165+1658A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17843937 | |||||||
chr7:17844018 | T | C | 1 | a0001c0001t0001g0022 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1165+1577A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17844018 | |||||||
chr7:17844022 | A | G | 2 | a0001c0001t0002g0334 a0001c0002t0002g0302 |
2 | HG02602.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1165+1573T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17844022 | |||||||
chr7:17844136 | T | G | 1 | a0001c0001t0001g0137 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1165+1459A>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17844136 | |||||||
chr7:17844233 | G | A | 2 | a0001c0001t0005g0012 a0001c0001t0005g0013 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1165+1362C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17844233 | |||||||
chr7:17844234 | A | G | 1 | a0001c0001t0001g0100 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1165+1361T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17844234 | |||||||
chr7:17844293 | G | A | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(194): Show |
200 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.1165+1302C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17844293 | |||||||
chr7:17844358 | G | A | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(211): Show |
217 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1165+1237C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17844358 | |||||||
chr7:17844383 | A | C | 2 | a0001c0001t0013g0015 a0001c0001t0013g0239 |
2 | HG01952.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.1165+1212T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17844383 | |||||||
chr7:17844400 | G | C | 1 | a0001c0001t0001g0226 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1165+1195C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17844400 | |||||||
chr7:17844475 | T | C | 3 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0232 |
3 | HG01109.hp1 HG01243.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1165+1120A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17844475 | |||||||
chr7:17844495 | A | G | 3 | a0001c0004t0011g0014 a0001c0004t0011g0016 a0001c0004t0011g0067 |
3 | HG02622.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1165+1100T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17844495 | |||||||
chr7:17844643 | C | G | 6 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0008 others(3): Show |
6 | HG01074.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1165+952G>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17844643 | |||||||
chr7:17844746 | C | CA | 42 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(39): Show |
44 | HG00408.hp1 HG01081.hp1 HG01168.hp2 others(41): Show |
intron_variant | MODIFIER | c.1165+848dupT | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17844746 | |||||||
chr7:17844851 | G | A | 2 | a0001c0001t0005g0012 a0001c0001t0005g0013 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1165+744C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17844851 | |||||||
chr7:17845069 | T | C | 1 | a0001c0001t0001g0164 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1165+526A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17845069 | |||||||
chr7:17845145 | C | T | 3 | a0001c0001t0004g0184 a0001c0001t0004g0185 a0001c0001t0004g0187 |
3 | HG00544.hp1 NA18983.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.1165+450G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17845145 | |||||||
chr7:17845153 | T | TAC | 157 | a0001c0001t0001g0062 a0001c0001t0001g0069 a0001c0001t0001g0076 others(154): Show |
157 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.1165+440_1165+441d others(4): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17845153 | |||||||
chr7:17845153 | T | TACAC | 5 | a0001c0001t0001g0104 a0001c0001t0001g0171 a0001c0001t0001g0183 others(2): Show |
5 | HG02129.hp1 HG02630.hp1 HG04204.hp2 others(2): Show |
intron_variant | MODIFIER | c.1165+438_1165+441d others(6): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17845153 | |||||||
chr7:17845153 | TAC | T | 4 | a0001c0001t0001g0159 a0001c0001t0005g0012 a0001c0001t0005g0013 others(1): Show |
4 | HG02280.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1165+440_1165+441d others(4): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17845153 | |||||||
chr7:17845153 | TACAC | T | 15 | a0001c0001t0001g0031 a0001c0001t0004g0112 a0001c0001t0004g0113 others(12): Show |
15 | HG00544.hp1 HG00735.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.1165+438_1165+441d others(6): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17845153 | |||||||
chr7:17845189 | A | G | 2 | a0001c0001t0012g0189 a0001c0001t0012g0190 |
2 | HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1165+406T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17845189 | |||||||
chr7:17845217 | T | C | 13 | a0001c0001t0004g0112 a0001c0001t0004g0113 a0001c0001t0004g0114 others(10): Show |
13 | HG00544.hp1 HG00735.hp1 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.1165+378A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17845217 | |||||||
chr7:17845427 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1165+168T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17845427 | |||||||
chr7:17845577 | T | C | 1 | a0001c0001t0001g0033 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1165+18A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | 17845577 | |||||||
chr7:17845845 | T | C | 65 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(62): Show |
67 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.1066-151A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 11/25 | chr7 | 17845845 | |||||||
chr7:17846088 | C | T | 1 | a0001c0006t0025g0005 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1066-394G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 11/25 | chr7 | 17846088 | |||||||
chr7:17846159 | A | G | 1 | a0001c0001t0001g0064 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1066-465T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 11/25 | chr7 | 17846159 | |||||||
chr7:17846198 | T | C | 1 | a0001c0001t0014g0019 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1066-504A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 11/25 | chr7 | 17846198 | |||||||
chr7:17846409 | A | T | 1 | a0001c0001t0001g0144 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1066-715T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 11/25 | chr7 | 17846409 | |||||||
chr7:17846552 | C | A | 11 | a0001c0001t0002g0018 a0001c0001t0008g0006 a0001c0001t0008g0007 others(8): Show |
11 | HG01074.hp1 HG02055.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1066-858G>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 11/25 | chr7 | 17846552 | |||||||
chr7:17846754 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1066-1060C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 11/25 | chr7 | 17846754 | |||||||
chr7:17846818 | C | T | 1 | a0001c0004t0011g0016 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1066-1124G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 11/25 | chr7 | 17846818 | |||||||
chr7:17846901 | A | G | 1 | a0001c0001t0002g0018 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1066-1207T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 11/25 | chr7 | 17846901 | |||||||
chr7:17846992 | TA | T | 12 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0021 others(9): Show |
14 | HG01168.hp2 HG01169.hp1 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.1066-1299delT | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 11/25 | chr7 | 17846992 | |||||||
chr7:17847126 | G | C | 1 | a0001c0001t0001g0226 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1066-1432C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 11/25 | chr7 | 17847126 | |||||||
chr7:17847156 | T | C | 1 | a0001c0002t0002g0304 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1066-1462A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 11/25 | chr7 | 17847156 | |||||||
chr7:17847168 | T | C | 1 | a0001c0001t0004g0113 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1066-1474A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 11/25 | chr7 | 17847168 | |||||||
chr7:17847235 | GCA | G | 201 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0031 others(198): Show |
202 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.1066-1543_1066-154 others(6): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 11/25 | chr7 | 17847235 | |||||||
chr7:17847254 | C | T | 1 | a0001c0002t0030g0056 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1066-1560G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 11/25 | chr7 | 17847254 | |||||||
chr7:17847292 | A | G | 1 | a0001c0001t0029g0037 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1066-1598T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 11/25 | chr7 | 17847292 | |||||||
chr7:17847325 | TTTTG | T | 7 | a0001c0001t0002g0018 a0001c0001t0008g0006 a0001c0001t0008g0007 others(4): Show |
7 | HG01074.hp1 HG02622.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1066-1635_1066-163 others(8): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 11/25 | chr7 | 17847325 | |||||||
chr7:17847366 | T | A | 1 | a0001c0002t0007g0058 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1066-1672A>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 11/25 | chr7 | 17847366 | |||||||
chr7:17847381 | G | C | 13 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0021 others(10): Show |
15 | HG01168.hp2 HG01169.hp1 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.1066-1687C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 11/25 | chr7 | 17847381 | |||||||
chr7:17847557 | C | G | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(211): Show |
217 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1066-1863G>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 11/25 | chr7 | 17847557 | |||||||
chr7:17847566 | A | G | 14 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0002g0018 others(11): Show |
14 | HG01074.hp1 HG02055.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1066-1872T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 11/25 | chr7 | 17847566 | |||||||
chr7:17847980 | C | T | 1 | a0001c0001t0004g0113 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1066-2286G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 11/25 | chr7 | 17847980 | |||||||
chr7:17848023 | T | C | 6 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0008 others(3): Show |
6 | HG01074.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1065+2324A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 11/25 | chr7 | 17848023 | |||||||
chr7:17848226 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1065+2121G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 11/25 | chr7 | 17848226 | |||||||
chr7:17848276 | C | T | 91 | a0001c0001t0001g0011 a0001c0001t0001g0061 a0001c0001t0001g0062 others(88): Show |
91 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.1065+2071G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 11/25 | chr7 | 17848276 | |||||||
chr7:17848294 | C | T | 2 | a0001c0001t0004g0115 a0001c0001t0018g0216 |
2 | HG00738.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.1065+2053G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 11/25 | chr7 | 17848294 | |||||||
chr7:17848302 | G | A | 1 | a0001c0001t0003g0192 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1065+2045C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 11/25 | chr7 | 17848302 | |||||||
chr7:17848369 | G | T | 4 | a0001c0002t0002g0281 a0001c0002t0002g0303 a0001c0005t0002g0206 others(1): Show |
4 | HG00140.hp2 HG01256.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1065+1978C>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 11/25 | chr7 | 17848369 | |||||||
chr7:17848455 | T | C | 2 | a0001c0001t0001g0152 a0001c0001t0001g0169 |
2 | HG01358.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.1065+1892A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 11/25 | chr7 | 17848455 | |||||||
chr7:17848593 | C | A | 6 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0008 others(3): Show |
6 | HG01074.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1065+1754G>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 11/25 | chr7 | 17848593 | |||||||
chr7:17848663 | G | A | 3 | a0001c0003t0001g0271 a0001c0003t0001g0272 a0001c0003t0001g0273 |
3 | NA18969.hp2 NA19056.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.1065+1684C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 11/25 | chr7 | 17848663 | |||||||
chr7:17848672 | G | A | 7 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0012g0188 others(4): Show |
7 | HG02055.hp1 HG02257.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1065+1675C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 11/25 | chr7 | 17848672 | |||||||
chr7:17848964 | T | C | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(228): Show |
234 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.1065+1383A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 11/25 | chr7 | 17848964 | |||||||
chr7:17849618 | A | C | 14 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0002g0018 others(11): Show |
14 | HG01074.hp1 HG02055.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1065+729T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 11/25 | chr7 | 17849618 | |||||||
chr7:17850060 | G | A | 1 | a0001c0001t0004g0113 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1065+287C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 11/25 | chr7 | 17850060 | |||||||
chr7:17850270 | T | C | 6 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0008 others(3): Show |
6 | HG01074.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1065+77A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 11/25 | chr7 | 17850270 | |||||||
chr7:17850544 | T | C | 11 | a0001c0001t0001g0169 a0001c0001t0001g0173 a0001c0001t0001g0174 others(8): Show |
11 | HG00673.hp1 HG01346.hp1 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.977-109A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 10/25 | chr7 | 17850544 | |||||||
chr7:17850572 | T | C | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(208): Show |
214 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.977-137A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 10/25 | chr7 | 17850572 | |||||||
chr7:17850574 | T | C | 6 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(3): Show |
6 | HG02451.hp1 HG02717.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.977-139A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 10/25 | chr7 | 17850574 | |||||||
chr7:17850770 | T | C | 1 | a0001c0001t0001g0070 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.976+56A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 10/25 | chr7 | 17850770 | |||||||
chr7:17850790 | CA | C | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(210): Show |
216 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.976+35delT | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 10/25 | chr7 | 17850790 | |||||||
chr7:17851018 | A | G | 2 | a0001c0001t0001g0031 a0001c0001t0001g0097 |
2 | HG01081.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.838-54T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17851018 | |||||||
chr7:17851145 | T | C | 1 | a0001c0002t0024g0257 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.838-181A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17851145 | |||||||
chr7:17851213 | A | C | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(206): Show |
212 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.838-249T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17851213 | |||||||
chr7:17851276 | T | C | 10 | a0001c0001t0002g0018 a0001c0001t0008g0006 a0001c0001t0008g0007 others(7): Show |
10 | HG01074.hp1 HG02055.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.838-312A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17851276 | |||||||
chr7:17851281 | G | A | 3 | a0001c0004t0011g0014 a0001c0004t0011g0016 a0001c0004t0011g0067 |
3 | HG02622.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.838-317C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17851281 | |||||||
chr7:17851343 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.838-379T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17851343 | |||||||
chr7:17851423 | T | A | 2 | a0001c0002t0002g0289 a0001c0002t0002g0290 |
2 | NA18987.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.838-459A>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17851423 | |||||||
chr7:17851443 | G | A | 1 | a0001c0002t0002g0223 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.838-479C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17851443 | |||||||
chr7:17851553 | G | A | 14 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0002g0018 others(11): Show |
14 | HG01074.hp1 HG02055.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.838-589C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17851553 | |||||||
chr7:17851591 | A | C | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(206): Show |
212 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.838-627T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17851591 | |||||||
chr7:17851643 | G | T | 1 | a0001c0001t0001g0217 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.838-679C>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17851643 | |||||||
chr7:17851719 | C | CG | 41 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0044 others(38): Show |
41 | HG00673.hp1 HG00673.hp2 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.838-756dupC | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17851719 | |||||||
chr7:17851719 | C | T | 1 | a0001c0002t0001g0277 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.838-755G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17851719 | |||||||
chr7:17851722 | G | A | 4 | a0001c0001t0001g0137 a0001c0001t0001g0167 a0001c0001t0005g0136 others(1): Show |
4 | HG01255.hp1 HG02109.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.838-758C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17851722 | |||||||
chr7:17851722 | G | T | 4 | a0001c0001t0012g0188 a0001c0001t0012g0189 a0001c0001t0012g0190 others(1): Show |
4 | HG02055.hp1 HG02280.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.838-758C>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17851722 | |||||||
chr7:17851726 | G | C | 1 | a0001c0001t0001g0075 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.838-762C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17851726 | |||||||
chr7:17852094 | A | G | 4 | a0001c0001t0012g0188 a0001c0001t0012g0189 a0001c0001t0012g0190 others(1): Show |
4 | HG02055.hp1 HG02280.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.838-1130T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17852094 | |||||||
chr7:17852201 | C | G | 7 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0012g0188 others(4): Show |
7 | HG02055.hp1 HG02257.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.838-1237G>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17852201 | |||||||
chr7:17852279 | G | A | 1 | a0001c0001t0001g0122 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.838-1315C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17852279 | |||||||
chr7:17852334 | C | A | 4 | a0001c0001t0012g0188 a0001c0001t0012g0189 a0001c0001t0012g0190 others(1): Show |
4 | HG02055.hp1 HG02280.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.838-1370G>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17852334 | |||||||
chr7:17852356 | G | C | 2 | a0001c0001t0001g0163 a0001c0001t0001g0231 |
2 | HG02055.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.838-1392C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17852356 | |||||||
chr7:17852365 | T | G | 2 | a0001c0001t0013g0015 a0001c0001t0013g0239 |
2 | HG01952.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.838-1401A>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17852365 | |||||||
chr7:17852732 | A | G | 1 | a0001c0001t0001g0226 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.838-1768T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17852732 | |||||||
chr7:17853004 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.838-2040C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17853004 | |||||||
chr7:17853079 | A | G | 1 | a0001c0001t0014g0019 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.838-2115T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17853079 | |||||||
chr7:17853353 | T | A | 2 | a0001c0002t0002g0247 a0001c0002t0002g0321 |
2 | HG00408.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.838-2389A>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17853353 | |||||||
chr7:17853454 | T | A | 6 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(3): Show |
6 | HG01168.hp1 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.838-2490A>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17853454 | |||||||
chr7:17853465 | G | A | 1 | a0001c0001t0001g0075 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.838-2501C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17853465 | |||||||
chr7:17853533 | T | A | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(199): Show |
205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.838-2569A>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17853533 | |||||||
chr7:17853575 | T | C | 7 | a0001c0001t0002g0018 a0001c0001t0008g0006 a0001c0001t0008g0007 others(4): Show |
7 | HG01074.hp1 HG02622.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.838-2611A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17853575 | |||||||
chr7:17853681 | C | A | 3 | a0001c0004t0011g0014 a0001c0004t0011g0016 a0001c0004t0011g0067 |
3 | HG02622.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.838-2717G>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17853681 | |||||||
chr7:17853714 | C | T | 2 | a0001c0010t0014g0020 a0001c0011t0006g0017 |
2 | HG02572.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.838-2750G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17853714 | |||||||
chr7:17853747 | G | A | 1 | a0001c0007t0001g0179 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.838-2783C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17853747 | |||||||
chr7:17853810 | T | C | 275 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(272): Show |
278 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.838-2846A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17853810 | |||||||
chr7:17853811 | G | A | 4 | a0001c0001t0012g0188 a0001c0001t0012g0189 a0001c0001t0012g0190 others(1): Show |
4 | HG02055.hp1 HG02280.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.838-2847C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17853811 | |||||||
chr7:17853920 | G | A | 1 | a0001c0002t0002g0247 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.838-2956C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17853920 | |||||||
chr7:17853927 | C | T | 1 | a0001c0006t0025g0005 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.838-2963G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17853927 | |||||||
chr7:17853935 | C | T | 1 | a0001c0001t0026g0249 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.838-2971G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17853935 | |||||||
chr7:17853953 | A | G | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(191): Show |
197 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.838-2989T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17853953 | |||||||
chr7:17854034 | G | A | 1 | a0001c0006t0025g0005 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.838-3070C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17854034 | |||||||
chr7:17854048 | A | T | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(191): Show |
197 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.838-3084T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17854048 | |||||||
chr7:17854050 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.838-3086A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17854050 | |||||||
chr7:17854101 | T | G | 5 | a0001c0001t0001g0032 a0001c0001t0001g0045 a0001c0001t0001g0046 others(2): Show |
5 | HG01891.hp1 HG03041.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.838-3137A>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17854101 | |||||||
chr7:17854248 | T | C | 3 | a0001c0001t0012g0188 a0001c0001t0012g0189 a0001c0001t0012g0190 |
3 | HG02055.hp1 HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.838-3284A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17854248 | |||||||
chr7:17854293 | C | G | 1 | a0001c0001t0001g0156 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.838-3329G>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17854293 | |||||||
chr7:17854451 | A | G | 1 | a0001c0001t0001g0011 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.838-3487T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17854451 | |||||||
chr7:17854560 | T | C | 1 | a0001c0006t0025g0005 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.838-3596A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17854560 | |||||||
chr7:17854643 | T | C | 3 | a0001c0002t0023g0055 a0001c0002t0030g0056 a0001c0002t0032g0335 |
3 | HG02258.hp2 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.838-3679A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17854643 | |||||||
chr7:17854735 | A | G | 14 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0002g0018 others(11): Show |
14 | HG01074.hp1 HG02055.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.838-3771T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17854735 | |||||||
chr7:17854856 | G | T | 2 | a0001c0002t0002g0247 a0001c0002t0002g0321 |
2 | HG00408.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.838-3892C>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17854856 | |||||||
chr7:17854947 | T | A | 1 | a0001c0001t0004g0118 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.838-3983A>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17854947 | |||||||
chr7:17854990 | A | T | 1 | a0001c0002t0007g0299 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.838-4026T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17854990 | |||||||
chr7:17855156 | C | T | 2 | a0001c0010t0014g0020 a0001c0011t0006g0017 |
2 | HG02572.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.838-4192G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17855156 | |||||||
chr7:17855310 | G | A | 106 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(103): Show |
106 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.838-4346C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17855310 | |||||||
chr7:17855443 | A | G | 1 | a0001c0001t0001g0044 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.838-4479T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17855443 | |||||||
chr7:17855555 | A | C | 1 | a0001c0001t0001g0100 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.838-4591T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17855555 | |||||||
chr7:17855609 | T | G | 13 | a0001c0001t0002g0018 a0001c0001t0008g0006 a0001c0001t0008g0007 others(10): Show |
13 | HG01074.hp1 HG02055.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.838-4645A>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17855609 | |||||||
chr7:17855867 | A | G | 1 | a0001c0002t0002g0304 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.838-4903T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17855867 | |||||||
chr7:17855921 | G | C | 1 | a0001c0001t0001g0217 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.838-4957C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17855921 | |||||||
chr7:17855952 | G | C | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(196): Show |
202 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.838-4988C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17855952 | |||||||
chr7:17856293 | G | A | 1 | a0001c0003t0001g0272 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.838-5329C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17856293 | |||||||
chr7:17856637 | A | G | 3 | a0001c0004t0011g0014 a0001c0004t0011g0016 a0001c0004t0011g0067 |
3 | HG02622.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.838-5673T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17856637 | |||||||
chr7:17856785 | TA | T | 121 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0023 others(118): Show |
123 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.838-5822delT | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17856785 | |||||||
chr7:17856799 | AAAAAG | A | 9 | a0001c0001t0001g0069 a0001c0001t0001g0076 a0001c0001t0001g0126 others(6): Show |
9 | HG01496.hp1 HG02040.hp2 NA18942.hp1 others(6): Show |
intron_variant | MODIFIER | c.838-5840_838-5836d others(7): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17856799 | |||||||
chr7:17856800 | A | G | 2 | a0001c0001t0001g0046 a0001c0001t0001g0119 |
2 | HG03041.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.838-5836T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17856800 | |||||||
chr7:17856816 | G | A | 2 | a0001c0001t0001g0050 a0001c0003t0001g0272 |
2 | HG02451.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.838-5852C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17856816 | |||||||
chr7:17856816 | G | GAAAAGA | 12 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(9): Show |
12 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.838-5858_838-5853d others(8): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17856816 | |||||||
chr7:17857067 | T | C | 2 | a0001c0001t0005g0012 a0001c0001t0005g0013 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.838-6103A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17857067 | |||||||
chr7:17857164 | A | T | 1 | a0001c0001t0001g0032 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.838-6200T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17857164 | |||||||
chr7:17857189 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.838-6225C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17857189 | |||||||
chr7:17857244 | A | C | 1 | a0001c0002t0002g0278 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.838-6280T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17857244 | |||||||
chr7:17857356 | A | C | 3 | a0001c0002t0023g0055 a0001c0002t0030g0056 a0001c0002t0032g0335 |
3 | HG02258.hp2 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.838-6392T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17857356 | |||||||
chr7:17857690 | A | G | 1 | a0001c0001t0001g0178 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.838-6726T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17857690 | |||||||
chr7:17857742 | G | A | 1 | a0001c0001t0001g0033 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.838-6778C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17857742 | |||||||
chr7:17857877 | T | C | 1 | a0001c0001t0019g0143 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.838-6913A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17857877 | |||||||
chr7:17858444 | A | C | 21 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 others(18): Show |
21 | HG00544.hp1 HG00673.hp1 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.838-7480T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17858444 | |||||||
chr7:17858766 | C | T | 1 | a0001c0002t0002g0218 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.838-7802G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17858766 | |||||||
chr7:17858780 | C | A | 2 | a0001c0002t0002g0201 a0001c0002t0002g0202 |
2 | HG01884.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.838-7816G>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17858780 | |||||||
chr7:17858838 | A | G | 1 | a0001c0001t0001g0231 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.838-7874T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17858838 | |||||||
chr7:17858856 | A | C | 238 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(235): Show |
241 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.838-7892T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17858856 | |||||||
chr7:17858860 | T | C | 69 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0062 others(66): Show |
69 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.838-7896A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17858860 | |||||||
chr7:17858861 | A | G | 2 | a0001c0001t0013g0015 a0001c0001t0013g0239 |
2 | HG01952.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.838-7897T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17858861 | |||||||
chr7:17858995 | T | C | 1 | a0001c0001t0001g0226 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.838-8031A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17858995 | |||||||
chr7:17859018 | C | T | 1 | a0001c0006t0025g0005 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.838-8054G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17859018 | |||||||
chr7:17859205 | A | C | 2 | a0001c0001t0005g0012 a0001c0001t0005g0013 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.838-8241T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17859205 | |||||||
chr7:17859251 | A | C | 1 | a0001c0001t0019g0143 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.838-8287T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17859251 | |||||||
chr7:17859262 | G | A | 2 | a0001c0001t0014g0019 a0001c0010t0014g0020 |
2 | HG00639.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.838-8298C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17859262 | |||||||
chr7:17859294 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.838-8330T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17859294 | |||||||
chr7:17859325 | C | T | 4 | a0001c0002t0023g0055 a0001c0002t0030g0056 a0001c0002t0032g0335 others(1): Show |
4 | HG02258.hp2 HG02723.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.838-8361G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17859325 | |||||||
chr7:17859407 | T | C | 3 | a0001c0001t0012g0188 a0001c0001t0012g0189 a0001c0001t0012g0190 |
3 | HG02055.hp1 HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.838-8443A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17859407 | |||||||
chr7:17859761 | T | C | 3 | a0001c0001t0004g0112 a0001c0001t0004g0114 a0001c0001t0004g0118 |
3 | NA18969.hp1 NA18979.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.837+8646A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17859761 | |||||||
chr7:17859779 | C | G | 1 | a0001c0006t0025g0005 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.837+8628G>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17859779 | |||||||
chr7:17859863 | A | G | 23 | a0001c0001t0001g0132 a0001c0001t0001g0173 a0001c0001t0001g0174 others(20): Show |
23 | HG00544.hp1 HG00673.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.837+8544T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17859863 | |||||||
chr7:17859899 | T | C | 3 | a0001c0004t0011g0014 a0001c0004t0011g0016 a0001c0004t0011g0067 |
3 | HG02622.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.837+8508A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17859899 | |||||||
chr7:17859929 | C | G | 2 | a0001c0001t0014g0019 a0001c0010t0014g0020 |
2 | HG00639.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.837+8478G>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17859929 | |||||||
chr7:17860004 | A | G | 1 | a0001c0002t0007g0205 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.837+8403T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17860004 | |||||||
chr7:17860104 | G | A | 3 | a0001c0004t0011g0014 a0001c0004t0011g0016 a0001c0004t0011g0067 |
3 | HG02622.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.837+8303C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17860104 | |||||||
chr7:17860179 | G | A | 2 | a0001c0001t0001g0148 a0001c0001t0001g0150 |
2 | HG02258.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.837+8228C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17860179 | |||||||
chr7:17860618 | T | C | 1 | a0001c0001t0001g0011 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.837+7789A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17860618 | |||||||
chr7:17860619 | T | C | 3 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0031g0242 |
3 | HG02257.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.837+7788A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17860619 | |||||||
chr7:17860776 | G | A | 2 | a0001c0001t0013g0015 a0001c0001t0013g0239 |
2 | HG01952.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.837+7631C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17860776 | |||||||
chr7:17860886 | G | A | 2 | a0001c0001t0014g0019 a0001c0010t0014g0020 |
2 | HG00639.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.837+7521C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17860886 | |||||||
chr7:17860949 | T | C | 1 | a0001c0001t0001g0148 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.837+7458A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17860949 | |||||||
chr7:17861018 | T | C | 4 | a0001c0001t0001g0137 a0001c0001t0001g0167 a0001c0001t0005g0136 others(1): Show |
4 | HG01255.hp1 HG02109.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.837+7389A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17861018 | |||||||
chr7:17861052 | G | C | 2 | a0001c0002t0007g0208 a0001c0002t0007g0292 |
2 | NA18944.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.837+7355C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17861052 | |||||||
chr7:17861342 | T | TCA | 7 | a0001c0001t0001g0070 a0001c0001t0001g0095 a0001c0001t0001g0144 others(4): Show |
7 | HG02602.hp2 HG02895.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.837+7063_837+7064d others(4): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17861342 | |||||||
chr7:17861342 | T | TCACA | 3 | a0001c0001t0001g0318 a0001c0002t0030g0056 a0001c0002t0032g0335 |
3 | HG02258.hp2 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.837+7061_837+7064d others(6): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17861342 | |||||||
chr7:17861342 | T | TCTCACAC others(3): Show |
2 | a0001c0001t0013g0015 a0001c0001t0013g0239 |
2 | HG01952.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.837+7064_837+7065i others(12): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17861342 | |||||||
chr7:17861342 | TCA | T | 146 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(143): Show |
149 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.837+7063_837+7064d others(4): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17861342 | |||||||
chr7:17861342 | TCACA | T | 50 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0035 others(47): Show |
50 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.837+7061_837+7064d others(6): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17861342 | |||||||
chr7:17861342 | TCACACA | T | 86 | a0001c0001t0001g0128 a0001c0001t0001g0226 a0001c0001t0005g0197 others(83): Show |
86 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.837+7059_837+7064d others(8): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17861342 | |||||||
chr7:17861342 | TCACACAC others(5): Show |
T | 3 | a0001c0001t0001g0181 a0001c0001t0003g0182 a0001c0001t0012g0189 |
3 | HG00423.hp2 HG02976.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.837+7053_837+7064d others(14): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17861342 | |||||||
chr7:17861517 | C | G | 2 | a0001c0001t0001g0314 a0001c0001t0001g0315 |
2 | HG00642.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.837+6890G>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17861517 | |||||||
chr7:17861578 | G | A | 2 | a0001c0001t0014g0019 a0001c0010t0014g0020 |
2 | HG00639.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.837+6829C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17861578 | |||||||
chr7:17861949 | T | C | 11 | a0001c0001t0002g0018 a0001c0001t0008g0006 a0001c0001t0008g0007 others(8): Show |
11 | HG01074.hp1 HG02055.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.837+6458A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17861949 | |||||||
chr7:17861964 | C | T | 1 | a0001c0001t0004g0116 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.837+6443G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17861964 | |||||||
chr7:17861981 | G | C | 3 | a0001c0002t0002g0204 a0001c0002t0002g0264 a0001c0002t0024g0257 |
3 | HG01261.hp2 HG01358.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.837+6426C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17861981 | |||||||
chr7:17862016 | C | A | 1 | a0001c0001t0001g0135 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.837+6391G>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17862016 | |||||||
chr7:17862079 | T | A | 1 | a0001c0001t0029g0037 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.837+6328A>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17862079 | |||||||
chr7:17862218 | A | T | 2 | a0001c0001t0001g0148 a0001c0001t0001g0150 |
2 | HG02258.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.837+6189T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17862218 | |||||||
chr7:17862230 | T | C | 6 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0008 others(3): Show |
6 | HG01074.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.837+6177A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17862230 | |||||||
chr7:17862295 | C | T | 2 | a0001c0001t0014g0019 a0001c0010t0014g0020 |
2 | HG00639.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.837+6112G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17862295 | |||||||
chr7:17862491 | T | C | 4 | a0001c0001t0012g0188 a0001c0001t0012g0189 a0001c0001t0012g0190 others(1): Show |
4 | HG02055.hp1 HG02280.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.837+5916A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17862491 | |||||||
chr7:17862754 | C | T | 3 | a0001c0002t0023g0055 a0001c0002t0030g0056 a0001c0002t0032g0335 |
3 | HG02258.hp2 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.837+5653G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17862754 | |||||||
chr7:17862903 | C | T | 3 | a0001c0004t0011g0014 a0001c0004t0011g0016 a0001c0004t0011g0067 |
3 | HG02622.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.837+5504G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17862903 | |||||||
chr7:17863198 | T | TA | 224 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(221): Show |
227 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.837+5208_837+5209i others(3): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17863198 | |||||||
chr7:17863283 | G | A | 1 | a0001c0001t0021g0134 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.837+5124C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17863283 | |||||||
chr7:17863306 | G | A | 1 | a0001c0001t0001g0027 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.837+5101C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17863306 | |||||||
chr7:17863360 | A | G | 2 | a0001c0001t0013g0015 a0001c0001t0013g0239 |
2 | HG01952.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.837+5047T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17863360 | |||||||
chr7:17863552 | T | C | 3 | a0001c0002t0023g0055 a0001c0002t0030g0056 a0001c0002t0032g0335 |
3 | HG02258.hp2 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.837+4855A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17863552 | |||||||
chr7:17863563 | A | G | 1 | a0001c0001t0004g0186 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.837+4844T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17863563 | |||||||
chr7:17863675 | C | CAGA | 4 | a0001c0001t0003g0252 a0001c0002t0002g0312 a0001c0002t0002g0313 others(1): Show |
4 | NA18974.hp1 NA19007.hp1 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.837+4731_837+4732i others(5): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17863675 | |||||||
chr7:17863697 | G | A | 4 | a0001c0001t0012g0188 a0001c0001t0012g0189 a0001c0001t0012g0190 others(1): Show |
4 | HG02055.hp1 HG02280.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.837+4710C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17863697 | |||||||
chr7:17863757 | C | G | 7 | a0001c0001t0001g0072 a0001c0001t0001g0087 a0001c0001t0001g0109 others(4): Show |
7 | HG02109.hp1 HG02451.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.837+4650G>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17863757 | |||||||
chr7:17863823 | A | G | 3 | a0001c0004t0011g0014 a0001c0004t0011g0016 a0001c0004t0011g0067 |
3 | HG02622.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.837+4584T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17863823 | |||||||
chr7:17863845 | G | A | 8 | a0001c0001t0001g0145 a0001c0001t0001g0156 a0001c0001t0001g0157 others(5): Show |
8 | HG00609.hp1 HG00741.hp1 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.837+4562C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17863845 | |||||||
chr7:17863915 | C | T | 1 | a0001c0001t0026g0249 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.837+4492G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17863915 | |||||||
chr7:17864016 | C | G | 1 | a0001c0002t0001g0267 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.837+4391G>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17864016 | |||||||
chr7:17864047 | G | T | 124 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0061 others(121): Show |
125 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.837+4360C>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17864047 | |||||||
chr7:17864284 | T | C | 2 | a0001c0001t0001g0135 a0001c0001t0021g0134 |
2 | HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.837+4123A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17864284 | |||||||
chr7:17864433 | C | T | 4 | a0001c0001t0001g0032 a0001c0001t0004g0112 a0001c0001t0004g0114 others(1): Show |
4 | NA18969.hp1 NA18979.hp2 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.837+3974G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17864433 | |||||||
chr7:17864696 | A | C | 1 | a0001c0002t0001g0266 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.837+3711T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17864696 | |||||||
chr7:17864696 | A | G | 2 | a0001c0001t0013g0015 a0001c0001t0013g0239 |
2 | HG01952.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.837+3711T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17864696 | |||||||
chr7:17864829 | AGAG | A | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(200): Show |
206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.837+3575_837+3577d others(5): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17864829 | |||||||
chr7:17864839 | G | A | 2 | a0001c0001t0001g0089 a0001c0001t0001g0090 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.837+3568C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17864839 | |||||||
chr7:17864869 | C | T | 1 | a0001c0002t0002g0306 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.837+3538G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17864869 | |||||||
chr7:17864933 | C | T | 11 | a0001c0001t0002g0018 a0001c0001t0008g0006 a0001c0001t0008g0007 others(8): Show |
11 | HG01074.hp1 HG02055.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.837+3474G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17864933 | |||||||
chr7:17864974 | T | C | 2 | a0001c0001t0014g0019 a0001c0010t0014g0020 |
2 | HG00639.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.837+3433A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17864974 | |||||||
chr7:17865081 | G | A | 1 | a0001c0002t0001g0034 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.837+3326C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17865081 | |||||||
chr7:17865104 | G | A | 1 | a0001c0001t0020g0191 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.837+3303C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17865104 | |||||||
chr7:17865181 | A | C | 2 | a0001c0001t0013g0015 a0001c0001t0013g0239 |
2 | HG01952.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.837+3226T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17865181 | |||||||
chr7:17865315 | C | T | 2 | a0001c0002t0007g0208 a0001c0002t0007g0292 |
2 | NA18944.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.837+3092G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17865315 | |||||||
chr7:17865465 | T | C | 1 | a0001c0002t0001g0282 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.837+2942A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17865465 | |||||||
chr7:17865677 | C | T | 1 | a0001c0001t0004g0117 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.837+2730G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17865677 | |||||||
chr7:17865797 | A | T | 2 | a0001c0001t0013g0015 a0001c0001t0013g0239 |
2 | HG01952.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.837+2610T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17865797 | |||||||
chr7:17865815 | A | C | 2 | a0001c0001t0001g0135 a0001c0001t0021g0134 |
2 | HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.837+2592T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17865815 | |||||||
chr7:17866067 | G | T | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(195): Show |
201 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.837+2340C>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17866067 | |||||||
chr7:17866102 | C | T | 2 | a0001c0001t0013g0015 a0001c0001t0013g0239 |
2 | HG01952.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.837+2305G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17866102 | |||||||
chr7:17866288 | C | G | 1 | a0001c0002t0002g0280 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.837+2119G>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17866288 | |||||||
chr7:17866404 | C | A | 13 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0021 others(10): Show |
15 | HG01168.hp2 HG01169.hp1 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.837+2003G>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17866404 | |||||||
chr7:17866531 | T | A | 2 | a0001c0001t0005g0012 a0001c0001t0005g0013 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.837+1876A>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17866531 | |||||||
chr7:17866535 | T | C | 5 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(2): Show |
5 | HG02602.hp1 HG03017.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.837+1872A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17866535 | |||||||
chr7:17866537 | C | T | 1 | a0001c0001t0001g0066 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.837+1870G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17866537 | |||||||
chr7:17866662 | A | C | 3 | a0001c0004t0011g0014 a0001c0004t0011g0016 a0001c0004t0011g0067 |
3 | HG02622.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.837+1745T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17866662 | |||||||
chr7:17866772 | A | G | 2 | a0001c0001t0001g0064 a0001c0001t0001g0232 |
2 | HG01243.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.837+1635T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17866772 | |||||||
chr7:17866859 | T | A | 1 | a0001c0011t0006g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.837+1548A>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17866859 | |||||||
chr7:17866997 | C | G | 2 | a0001c0001t0005g0197 a0001c0001t0005g0274 |
2 | NA18949.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.837+1410G>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17866997 | |||||||
chr7:17867253 | C | T | 3 | a0001c0004t0011g0014 a0001c0004t0011g0016 a0001c0004t0011g0067 |
3 | HG02622.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.837+1154G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17867253 | |||||||
chr7:17867365 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.837+1042C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17867365 | |||||||
chr7:17867375 | G | A | 1 | a0001c0001t0001g0045 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.837+1032C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17867375 | |||||||
chr7:17867387 | G | A | 2 | a0001c0001t0005g0012 a0001c0001t0005g0013 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.837+1020C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17867387 | |||||||
chr7:17867513 | G | A | 2 | a0001c0001t0001g0093 a0001c0001t0001g0102 |
2 | HG03491.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.837+894C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17867513 | |||||||
chr7:17867539 | G | A | 3 | a0001c0004t0011g0014 a0001c0004t0011g0016 a0001c0004t0011g0067 |
3 | HG02622.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.837+868C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17867539 | |||||||
chr7:17867591 | T | A | 1 | a0001c0001t0001g0094 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.837+816A>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17867591 | |||||||
chr7:17867629 | TA | T | 14 | a0001c0001t0002g0018 a0001c0001t0008g0006 a0001c0001t0008g0007 others(11): Show |
14 | HG01074.hp1 HG02055.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.837+777delT | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17867629 | |||||||
chr7:17867691 | A | C | 3 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0031g0242 |
3 | HG02257.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.837+716T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17867691 | |||||||
chr7:17867731 | G | A | 1 | a0001c0002t0001g0282 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.837+676C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17867731 | |||||||
chr7:17867804 | C | G | 1 | a0001c0001t0001g0226 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.837+603G>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17867804 | |||||||
chr7:17867815 | C | G | 1 | a0001c0002t0001g0267 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.837+592G>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17867815 | |||||||
chr7:17867917 | T | C | 11 | a0001c0001t0002g0018 a0001c0001t0008g0006 a0001c0001t0008g0007 others(8): Show |
11 | HG01074.hp1 HG02055.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.837+490A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17867917 | |||||||
chr7:17868120 | A | G | 1 | a0001c0002t0001g0267 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.837+287T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17868120 | |||||||
chr7:17868160 | T | G | 2 | a0001c0001t0013g0015 a0001c0001t0013g0239 |
2 | HG01952.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.837+247A>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17868160 | |||||||
chr7:17868210 | A | G | 1 | a0001c0001t0002g0334 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.837+197T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 9/25 | chr7 | 17868210 | |||||||
chr7:17868507 | T | A | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(211): Show |
217 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.754-17A>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17868507 | |||||||
chr7:17868684 | G | A | 11 | a0001c0001t0002g0018 a0001c0001t0008g0006 a0001c0001t0008g0007 others(8): Show |
11 | HG01074.hp1 HG02055.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.754-194C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17868684 | |||||||
chr7:17868721 | G | C | 1 | a0001c0002t0009g0293 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.754-231C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17868721 | |||||||
chr7:17868725 | G | A | 2 | a0001c0002t0001g0258 a0001c0002t0001g0301 |
2 | HG02132.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.754-235C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17868725 | |||||||
chr7:17868803 | T | A | 11 | a0001c0001t0002g0018 a0001c0001t0008g0006 a0001c0001t0008g0007 others(8): Show |
11 | HG01074.hp1 HG02055.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.754-313A>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17868803 | |||||||
chr7:17868893 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.754-403C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17868893 | |||||||
chr7:17868923 | T | C | 52 | a0001c0001t0002g0334 a0001c0001t0029g0037 a0001c0002t0002g0204 others(49): Show |
52 | HG00323.hp2 HG00408.hp2 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.754-433A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17868923 | |||||||
chr7:17868958 | C | A | 1 | a0001c0001t0001g0137 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.754-468G>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17868958 | |||||||
chr7:17869007 | A | G | 3 | a0001c0002t0023g0055 a0001c0002t0030g0056 a0001c0002t0032g0335 |
3 | HG02258.hp2 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.754-517T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17869007 | |||||||
chr7:17869167 | C | T | 7 | a0001c0001t0002g0018 a0001c0001t0008g0006 a0001c0001t0008g0007 others(4): Show |
7 | HG01074.hp1 HG02622.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.754-677G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17869167 | |||||||
chr7:17869194 | C | A | 1 | a0001c0001t0019g0143 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.754-704G>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17869194 | |||||||
chr7:17869217 | A | T | 1 | a0001c0001t0001g0211 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.754-727T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17869217 | |||||||
chr7:17869276 | T | C | 17 | a0001c0001t0001g0132 a0001c0001t0001g0183 a0001c0001t0001g0319 others(14): Show |
17 | HG00544.hp1 HG00735.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.754-786A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17869276 | |||||||
chr7:17869555 | T | C | 1 | a0001c0001t0001g0159 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.754-1065A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17869555 | |||||||
chr7:17869577 | T | C | 2 | a0001c0001t0013g0015 a0001c0001t0013g0239 |
2 | HG01952.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.754-1087A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17869577 | |||||||
chr7:17869651 | T | C | 1 | a0001c0001t0002g0018 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.754-1161A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17869651 | |||||||
chr7:17869688 | T | C | 2 | a0001c0001t0014g0019 a0001c0010t0014g0020 |
2 | HG00639.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.754-1198A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17869688 | |||||||
chr7:17869879 | G | GACAC | 3 | a0001c0004t0011g0014 a0001c0004t0011g0016 a0001c0004t0011g0067 |
3 | HG02622.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.754-1393_754-1390d others(6): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17869879 | |||||||
chr7:17869879 | GAC | G | 160 | a0001c0001t0001g0003 a0001c0001t0001g0031 a0001c0001t0001g0032 others(157): Show |
161 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.754-1391_754-1390d others(4): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17869879 | |||||||
chr7:17869883 | C | G | 1 | a0001c0002t0002g0248 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.754-1393G>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17869883 | |||||||
chr7:17869889 | C | G | 1 | a0001c0001t0001g0121 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.754-1399G>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17869889 | |||||||
chr7:17869891 | C | G | 160 | a0001c0001t0001g0003 a0001c0001t0001g0031 a0001c0001t0001g0032 others(157): Show |
161 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.754-1401G>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17869891 | |||||||
chr7:17869918 | C | G | 2 | a0001c0001t0001g0084 a0001c0001t0001g0238 |
2 | HG02683.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.754-1428G>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17869918 | |||||||
chr7:17869952 | T | A | 1 | a0001c0001t0001g0174 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.754-1462A>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17869952 | |||||||
chr7:17869993 | A | T | 2 | a0001c0001t0005g0197 a0001c0001t0005g0274 |
2 | NA18949.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.754-1503T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17869993 | |||||||
chr7:17870117 | A | G | 1 | a0001c0001t0002g0018 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.754-1627T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17870117 | |||||||
chr7:17870194 | C | A | 4 | a0001c0001t0012g0188 a0001c0001t0012g0189 a0001c0001t0012g0190 others(1): Show |
4 | HG02055.hp1 HG02280.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.754-1704G>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17870194 | |||||||
chr7:17870233 | G | A | 1 | a0001c0001t0004g0118 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.754-1743C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17870233 | |||||||
chr7:17870331 | G | A | 1 | a0001c0001t0014g0019 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.754-1841C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17870331 | |||||||
chr7:17870491 | C | T | 4 | a0001c0001t0001g0137 a0001c0001t0001g0167 a0001c0001t0005g0136 others(1): Show |
4 | HG01255.hp1 HG02109.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.754-2001G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17870491 | |||||||
chr7:17870537 | C | A | 4 | a0001c0001t0001g0137 a0001c0001t0001g0167 a0001c0001t0005g0136 others(1): Show |
4 | HG01255.hp1 HG02109.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.754-2047G>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17870537 | |||||||
chr7:17870657 | G | C | 1 | a0001c0001t0001g0031 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.754-2167C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17870657 | |||||||
chr7:17870696 | G | C | 1 | a0001c0001t0001g0049 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.754-2206C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17870696 | |||||||
chr7:17870873 | T | A | 7 | a0001c0001t0005g0197 a0001c0001t0005g0274 a0001c0002t0001g0198 others(4): Show |
7 | NA18949.hp1 NA18972.hp1 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.754-2383A>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17870873 | |||||||
chr7:17871036 | G | T | 1 | a0001c0001t0001g0101 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.753+2492C>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17871036 | |||||||
chr7:17871066 | C | T | 7 | a0001c0001t0001g0046 a0001c0001t0008g0006 a0001c0001t0008g0007 others(4): Show |
7 | HG01074.hp1 HG02622.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.753+2462G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17871066 | |||||||
chr7:17871075 | A | G | 7 | a0001c0001t0001g0046 a0001c0001t0008g0006 a0001c0001t0008g0007 others(4): Show |
7 | HG01074.hp1 HG02622.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.753+2453T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17871075 | |||||||
chr7:17871097 | C | T | 2 | a0001c0001t0001g0176 a0001c0001t0001g0177 |
2 | NA18962.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.753+2431G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17871097 | |||||||
chr7:17871098 | C | T | 2 | a0001c0001t0001g0176 a0001c0001t0001g0177 |
2 | NA18962.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.753+2430G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17871098 | |||||||
chr7:17871106 | T | C | 2 | a0001c0001t0001g0176 a0001c0001t0001g0177 |
2 | NA18962.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.753+2422A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17871106 | |||||||
chr7:17871119 | C | T | 1 | a0001c0002t0001g0283 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.753+2409G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17871119 | |||||||
chr7:17871162 | T | C | 1 | a0001c0002t0001g0322 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.753+2366A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17871162 | |||||||
chr7:17871167 | A | G | 1 | a0001c0002t0001g0322 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.753+2361T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17871167 | |||||||
chr7:17871198 | C | G | 3 | a0001c0001t0012g0188 a0001c0001t0012g0189 a0001c0001t0012g0190 |
3 | HG02055.hp1 HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.753+2330G>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17871198 | |||||||
chr7:17871206 | C | T | 2 | a0001c0001t0001g0228 a0001c0001t0031g0242 |
2 | HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.753+2322G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17871206 | |||||||
chr7:17871278 | C | T | 2 | a0001c0002t0002g0201 a0001c0002t0002g0202 |
2 | HG01884.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.753+2250G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17871278 | |||||||
chr7:17871296 | C | T | 6 | a0001c0002t0023g0055 a0001c0002t0030g0056 a0001c0002t0032g0335 others(3): Show |
6 | HG02258.hp2 HG02622.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.753+2232G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17871296 | |||||||
chr7:17871415 | C | T | 193 | a0001c0001t0001g0003 a0001c0001t0001g0031 a0001c0001t0001g0032 others(190): Show |
194 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.753+2113G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17871415 | |||||||
chr7:17871677 | C | A | 7 | a0001c0001t0001g0072 a0001c0001t0001g0087 a0001c0001t0001g0109 others(4): Show |
7 | HG02109.hp1 HG02451.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.753+1851G>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17871677 | |||||||
chr7:17871904 | T | C | 1 | a0001c0001t0008g0234 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.753+1624A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17871904 | |||||||
chr7:17871975 | G | A | 4 | a0001c0001t0012g0188 a0001c0001t0012g0189 a0001c0001t0012g0190 others(1): Show |
4 | HG02055.hp1 HG02280.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.753+1553C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17871975 | |||||||
chr7:17872071 | G | C | 1 | a0001c0002t0009g0293 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.753+1457C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17872071 | |||||||
chr7:17872129 | G | T | 184 | a0001c0001t0001g0003 a0001c0001t0001g0031 a0001c0001t0001g0032 others(181): Show |
185 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.753+1399C>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17872129 | |||||||
chr7:17872219 | A | G | 3 | a0001c0002t0023g0055 a0001c0002t0030g0056 a0001c0002t0032g0335 |
3 | HG02258.hp2 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.753+1309T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17872219 | |||||||
chr7:17872290 | G | C | 6 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0008 others(3): Show |
6 | HG01074.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.753+1238C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17872290 | |||||||
chr7:17872504 | T | C | 1 | a0001c0001t0001g0076 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.753+1024A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17872504 | |||||||
chr7:17872536 | T | C | 5 | a0001c0002t0002g0059 a0001c0002t0002g0220 a0001c0002t0002g0221 others(2): Show |
5 | HG01243.hp1 HG01884.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.753+992A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17872536 | |||||||
chr7:17872553 | C | T | 1 | a0001c0002t0002g0213 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.753+975G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17872553 | |||||||
chr7:17872598 | T | C | 1 | a0002c0009t0001g0053 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.753+930A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17872598 | |||||||
chr7:17872713 | A | G | 29 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(26): Show |
29 | HG00280.hp2 HG00323.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.753+815T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17872713 | |||||||
chr7:17872744 | A | G | 3 | a0001c0004t0011g0014 a0001c0004t0011g0016 a0001c0004t0011g0067 |
3 | HG02622.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.753+784T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17872744 | |||||||
chr7:17872824 | T | C | 9 | a0001c0001t0001g0072 a0001c0001t0001g0087 a0001c0001t0001g0109 others(6): Show |
9 | HG02109.hp1 HG02451.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.753+704A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17872824 | |||||||
chr7:17872889 | C | T | 2 | a0001c0001t0013g0015 a0001c0001t0013g0239 |
2 | HG01952.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.753+639G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17872889 | |||||||
chr7:17873169 | T | A | 4 | a0001c0001t0001g0137 a0001c0001t0001g0167 a0001c0001t0005g0136 others(1): Show |
4 | HG01255.hp1 HG02109.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.753+359A>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17873169 | |||||||
chr7:17873239 | A | C | 1 | a0001c0001t0001g0099 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.753+289T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17873239 | |||||||
chr7:17873518 | T | G | 2 | a0001c0002t0001g0283 a0001c0002t0001g0322 |
2 | HG00558.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.753+10A>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 8/25 | chr7 | 17873518 | |||||||
chr7:17873677 | G | C | 1 | a0001c0001t0004g0112 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.665-61C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 7/25 | chr7 | 17873677 | |||||||
chr7:17874139 | G | A | 1 | a0001c0001t0002g0018 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.665-523C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 7/25 | chr7 | 17874139 | |||||||
chr7:17874176 | G | A | 3 | a0001c0001t0010g0138 a0001c0001t0010g0139 a0001c0001t0010g0233 |
3 | HG02896.hp1 HG02897.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.665-560C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 7/25 | chr7 | 17874176 | |||||||
chr7:17874261 | A | C | 1 | a0001c0001t0001g0033 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.665-645T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 7/25 | chr7 | 17874261 | |||||||
chr7:17874287 | C | CA | 4 | a0001c0001t0012g0188 a0001c0001t0012g0189 a0001c0001t0012g0190 others(1): Show |
4 | HG02055.hp1 HG02280.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.665-672dupT | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 7/25 | chr7 | 17874287 | |||||||
chr7:17874654 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.664+826C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 7/25 | chr7 | 17874654 | |||||||
chr7:17874832 | G | C | 4 | a0001c0002t0023g0055 a0001c0002t0030g0056 a0001c0002t0032g0335 others(1): Show |
4 | HG02258.hp2 HG02280.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.664+648C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 7/25 | chr7 | 17874832 | |||||||
chr7:17874936 | G | A | 8 | a0001c0002t0001g0214 a0001c0002t0001g0258 a0001c0002t0001g0269 others(5): Show |
8 | HG02015.hp1 HG02129.hp2 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.664+544C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 7/25 | chr7 | 17874936 | |||||||
chr7:17874977 | C | T | 199 | a0001c0001t0001g0003 a0001c0001t0001g0031 a0001c0001t0001g0032 others(196): Show |
200 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.664+503G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 7/25 | chr7 | 17874977 | |||||||
chr7:17875016 | CTTTTT | C | 6 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0008 others(3): Show |
6 | HG01074.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.664+459_664+463del others(5): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 7/25 | chr7 | 17875016 | |||||||
chr7:17875031 | G | T | 8 | a0001c0002t0001g0214 a0001c0002t0001g0258 a0001c0002t0001g0269 others(5): Show |
8 | HG02015.hp1 HG02129.hp2 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.664+449C>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 7/25 | chr7 | 17875031 | |||||||
chr7:17875042 | C | T | 1 | a0001c0002t0002g0263 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.664+438G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 7/25 | chr7 | 17875042 | |||||||
chr7:17875245 | G | A | 8 | a0001c0002t0001g0214 a0001c0002t0001g0258 a0001c0002t0001g0269 others(5): Show |
8 | HG02015.hp1 HG02129.hp2 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.664+235C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 7/25 | chr7 | 17875245 | |||||||
chr7:17875393 | T | G | 1 | a0001c0001t0001g0106 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.664+87A>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 7/25 | chr7 | 17875393 | |||||||
chr7:17875464 | T | A | 5 | a0001c0002t0002g0059 a0001c0002t0002g0220 a0001c0002t0002g0221 others(2): Show |
5 | HG01243.hp1 HG01884.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.664+16A>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 7/25 | chr7 | 17875464 | |||||||
chr7:17875892 | T | C | 1 | a0003c0012t0001g0180 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.441-102A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17875892 | |||||||
chr7:17876038 | G | T | 1 | a0001c0001t0008g0007 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.441-248C>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17876038 | |||||||
chr7:17876186 | T | C | 2 | a0001c0001t0013g0015 a0001c0001t0013g0239 |
2 | HG01952.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.441-396A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17876186 | |||||||
chr7:17876238 | C | A | 1 | a0001c0002t0027g0300 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.441-448G>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17876238 | |||||||
chr7:17876267 | T | C | 1 | a0001c0001t0001g0063 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.441-477A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17876267 | |||||||
chr7:17876447 | G | A | 1 | a0001c0001t0003g0182 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.441-657C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17876447 | |||||||
chr7:17876501 | G | C | 4 | a0001c0001t0001g0145 a0001c0001t0001g0156 a0001c0001t0001g0158 others(1): Show |
4 | HG00609.hp1 HG00741.hp1 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.441-711C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17876501 | |||||||
chr7:17876516 | G | A | 1 | a0001c0001t0003g0244 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.441-726C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17876516 | |||||||
chr7:17876549 | G | A | 4 | a0001c0001t0012g0188 a0001c0001t0012g0189 a0001c0001t0012g0190 others(1): Show |
4 | HG02055.hp1 HG02280.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.441-759C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17876549 | |||||||
chr7:17876573 | T | C | 236 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(233): Show |
239 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.441-783A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17876573 | |||||||
chr7:17876574 | C | CA | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(206): Show |
212 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.441-785dupT | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17876574 | |||||||
chr7:17876574 | C | CAA | 14 | a0001c0001t0001g0046 a0001c0001t0001g0050 a0001c0001t0001g0076 others(11): Show |
14 | HG00741.hp1 HG01346.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.441-786_441-785dup others(2): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17876574 | |||||||
chr7:17876696 | T | C | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(211): Show |
217 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.441-906A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17876696 | |||||||
chr7:17876723 | A | G | 1 | a0001c0001t0001g0035 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.441-933T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17876723 | |||||||
chr7:17876793 | T | C | 1 | a0001c0001t0013g0239 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.441-1003A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17876793 | |||||||
chr7:17876816 | A | C | 1 | a0001c0001t0001g0171 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.441-1026T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17876816 | |||||||
chr7:17876870 | C | T | 3 | a0001c0002t0023g0055 a0001c0002t0030g0056 a0001c0002t0032g0335 |
3 | HG02258.hp2 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.441-1080G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17876870 | |||||||
chr7:17876916 | AAG | A | 8 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(5): Show |
8 | HG02451.hp1 HG02630.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.441-1128_441-1127d others(4): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17876916 | |||||||
chr7:17877039 | CT | C | 134 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0032 others(131): Show |
135 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.441-1250delA | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17877039 | |||||||
chr7:17877044 | T | G | 85 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0021 others(82): Show |
87 | HG00323.hp1 HG00544.hp1 HG00639.hp1 others(84): Show |
intron_variant | MODIFIER | c.441-1254A>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17877044 | |||||||
chr7:17877045 | G | GA | 11 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0002g0018 others(8): Show |
11 | HG00323.hp1 HG01074.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.441-1256dupT | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17877045 | |||||||
chr7:17877045 | GAA | G | 10 | a0001c0001t0001g0065 a0001c0001t0001g0070 a0001c0001t0001g0086 others(7): Show |
10 | HG01081.hp1 HG02273.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.441-1257_441-1256d others(4): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17877045 | |||||||
chr7:17877046 | A | G | 134 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0032 others(131): Show |
135 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.441-1256T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17877046 | |||||||
chr7:17877145 | T | G | 1 | a0001c0010t0014g0020 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.441-1355A>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17877145 | |||||||
chr7:17877247 | T | C | 18 | a0001c0001t0001g0003 a0001c0001t0001g0030 a0001c0001t0001g0145 others(15): Show |
19 | HG00609.hp1 HG00741.hp1 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.441-1457A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17877247 | |||||||
chr7:17877327 | A | C | 1 | a0001c0002t0006g0333 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.441-1537T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17877327 | |||||||
chr7:17877567 | G | C | 7 | a0001c0001t0005g0197 a0001c0001t0005g0274 a0001c0002t0001g0198 others(4): Show |
7 | NA18949.hp1 NA18972.hp1 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.441-1777C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17877567 | |||||||
chr7:17877704 | C | A | 2 | a0001c0001t0013g0015 a0001c0001t0013g0239 |
2 | HG01952.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.441-1914G>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17877704 | |||||||
chr7:17877704 | C | T | 1 | a0001c0001t0001g0011 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.441-1914G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17877704 | |||||||
chr7:17877705 | G | A | 2 | a0001c0001t0013g0015 a0001c0001t0013g0239 |
2 | HG01952.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.441-1915C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17877705 | |||||||
chr7:17877721 | C | T | 1 | a0001c0002t0002g0306 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.441-1931G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17877721 | |||||||
chr7:17877736 | CA | C | 209 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(206): Show |
211 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.441-1947delT | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17877736 | |||||||
chr7:17877808 | G | A | 7 | a0001c0001t0002g0018 a0001c0001t0008g0006 a0001c0001t0008g0007 others(4): Show |
7 | HG01074.hp1 HG02622.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.441-2018C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17877808 | |||||||
chr7:17877896 | A | C | 1 | a0001c0002t0006g0284 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.441-2106T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17877896 | |||||||
chr7:17877906 | G | C | 1 | a0001c0001t0001g0002 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.441-2116C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17877906 | |||||||
chr7:17878050 | GATAA | G | 3 | a0001c0002t0023g0055 a0001c0002t0030g0056 a0001c0002t0032g0335 |
3 | HG02258.hp2 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.441-2264_441-2261d others(6): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17878050 | |||||||
chr7:17878239 | A | C | 1 | a0001c0001t0019g0143 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.441-2449T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17878239 | |||||||
chr7:17878255 | A | T | 2 | a0001c0001t0005g0012 a0001c0001t0005g0013 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.441-2465T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17878255 | |||||||
chr7:17878359 | A | C | 1 | a0001c0001t0029g0037 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.441-2569T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17878359 | |||||||
chr7:17878571 | C | A | 6 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0008 others(3): Show |
6 | HG01074.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.441-2781G>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17878571 | |||||||
chr7:17878615 | C | T | 1 | a0001c0011t0006g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.441-2825G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17878615 | |||||||
chr7:17878801 | C | T | 3 | a0001c0004t0011g0014 a0001c0004t0011g0016 a0001c0004t0011g0067 |
3 | HG02622.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.441-3011G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17878801 | |||||||
chr7:17878973 | C | G | 6 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0008 others(3): Show |
6 | HG01074.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.441-3183G>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17878973 | |||||||
chr7:17879038 | T | G | 1 | a0001c0001t0001g0086 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.441-3248A>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17879038 | |||||||
chr7:17879172 | T | C | 18 | a0001c0001t0001g0135 a0001c0001t0001g0183 a0001c0001t0001g0319 others(15): Show |
18 | HG00544.hp1 HG00735.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.441-3382A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17879172 | |||||||
chr7:17879231 | C | T | 5 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0008 others(2): Show |
5 | HG01074.hp1 HG02622.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.441-3441G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17879231 | |||||||
chr7:17879446 | C | T | 2 | a0001c0001t0012g0189 a0001c0001t0012g0190 |
2 | HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.441-3656G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17879446 | |||||||
chr7:17879570 | T | G | 2 | a0001c0001t0013g0015 a0001c0001t0013g0239 |
2 | HG01952.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.441-3780A>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17879570 | |||||||
chr7:17879635 | G | T | 193 | a0001c0001t0001g0003 a0001c0001t0001g0031 a0001c0001t0001g0032 others(190): Show |
194 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.441-3845C>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17879635 | |||||||
chr7:17879661 | T | C | 1 | a0001c0002t0007g0058 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.441-3871A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17879661 | |||||||
chr7:17879870 | C | T | 10 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0008 others(7): Show |
10 | HG01074.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.441-4080G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17879870 | |||||||
chr7:17879937 | C | T | 3 | a0001c0002t0002g0306 a0001c0002t0002g0307 a0001c0002t0002g0326 |
3 | NA18978.hp2 NA19002.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.441-4147G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17879937 | |||||||
chr7:17879998 | T | C | 2 | a0001c0001t0005g0012 a0001c0001t0005g0013 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.441-4208A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17879998 | |||||||
chr7:17880101 | G | T | 1 | a0001c0002t0001g0276 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.441-4311C>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17880101 | |||||||
chr7:17880105 | A | C | 4 | a0001c0001t0012g0188 a0001c0001t0012g0189 a0001c0001t0012g0190 others(1): Show |
4 | HG02055.hp1 HG02280.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.441-4315T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17880105 | |||||||
chr7:17880278 | C | T | 1 | a0001c0001t0004g0117 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.441-4488G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17880278 | |||||||
chr7:17880307 | C | G | 14 | a0001c0001t0001g0319 a0001c0001t0004g0112 a0001c0001t0004g0113 others(11): Show |
14 | HG00544.hp1 HG00735.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.441-4517G>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17880307 | |||||||
chr7:17880349 | G | A | 1 | a0001c0001t0001g0095 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.441-4559C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17880349 | |||||||
chr7:17880403 | C | T | 1 | a0001c0001t0020g0191 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.441-4613G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17880403 | |||||||
chr7:17880472 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.441-4682G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17880472 | |||||||
chr7:17880513 | G | T | 4 | a0001c0001t0012g0188 a0001c0001t0012g0189 a0001c0001t0012g0190 others(1): Show |
4 | HG02055.hp1 HG02280.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.441-4723C>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17880513 | |||||||
chr7:17880630 | G | C | 173 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0033 others(170): Show |
174 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.441-4840C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17880630 | |||||||
chr7:17880722 | C | T | 1 | a0001c0002t0009g0328 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.441-4932G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17880722 | |||||||
chr7:17880990 | C | T | 195 | a0001c0001t0001g0003 a0001c0001t0001g0031 a0001c0001t0001g0032 others(192): Show |
196 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.441-5200G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17880990 | |||||||
chr7:17881109 | G | A | 1 | a0001c0001t0004g0112 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.441-5319C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17881109 | |||||||
chr7:17881237 | A | AAC | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(167): Show |
173 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.441-5449_441-5448d others(4): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17881237 | |||||||
chr7:17881237 | A | AACAC | 5 | a0001c0001t0001g0098 a0001c0001t0005g0012 a0001c0001t0005g0013 others(2): Show |
5 | HG00558.hp2 HG01952.hp1 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.441-5451_441-5448d others(6): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17881237 | |||||||
chr7:17881237 | A | AACACACA others(5): Show |
3 | a0001c0004t0011g0014 a0001c0004t0011g0016 a0001c0004t0011g0067 |
3 | HG02622.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.441-5459_441-5448d others(14): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17881237 | |||||||
chr7:17881237 | AAC | A | 27 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(24): Show |
27 | HG00280.hp2 HG00323.hp1 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.441-5449_441-5448d others(4): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17881237 | |||||||
chr7:17881287 | T | G | 3 | a0001c0002t0023g0055 a0001c0002t0030g0056 a0001c0002t0032g0335 |
3 | HG02258.hp2 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.441-5497A>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17881287 | |||||||
chr7:17881355 | C | A | 1 | a0001c0001t0001g0102 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.441-5565G>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17881355 | |||||||
chr7:17881582 | G | C | 1 | a0001c0001t0002g0018 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.441-5792C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17881582 | |||||||
chr7:17881630 | C | T | 6 | a0001c0002t0002g0218 a0001c0002t0002g0255 a0001c0002t0002g0308 others(3): Show |
6 | HG01109.hp2 HG01169.hp2 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.441-5840G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17881630 | |||||||
chr7:17881740 | TCTAAATA others(7): Show |
T | 3 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0031g0242 |
3 | HG02257.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.441-5964_441-5951d others(16): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17881740 | |||||||
chr7:17881814 | A | T | 1 | a0001c0001t0001g0163 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.441-6024T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17881814 | |||||||
chr7:17881895 | C | T | 3 | a0001c0001t0001g0156 a0001c0001t0013g0015 a0001c0001t0013g0239 |
3 | HG00741.hp1 HG01952.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.441-6105G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17881895 | |||||||
chr7:17881915 | A | G | 12 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0021 others(9): Show |
14 | HG01168.hp2 HG01169.hp1 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.441-6125T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17881915 | |||||||
chr7:17882088 | C | T | 12 | a0001c0001t0004g0112 a0001c0001t0004g0113 a0001c0001t0004g0114 others(9): Show |
12 | HG00544.hp1 HG00735.hp1 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.441-6298G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17882088 | |||||||
chr7:17882219 | C | G | 1 | a0001c0001t0001g0102 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.441-6429G>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17882219 | |||||||
chr7:17882425 | T | C | 1 | a0001c0001t0001g0063 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.441-6635A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17882425 | |||||||
chr7:17882436 | G | A | 1 | a0001c0006t0025g0005 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.441-6646C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17882436 | |||||||
chr7:17882524 | T | C | 1 | a0001c0001t0001g0159 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.441-6734A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17882524 | |||||||
chr7:17882614 | A | G | 3 | a0001c0001t0012g0188 a0001c0001t0012g0189 a0001c0001t0012g0190 |
3 | HG02055.hp1 HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.441-6824T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17882614 | |||||||
chr7:17882745 | C | T | 1 | a0001c0002t0009g0293 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.441-6955G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17882745 | |||||||
chr7:17882922 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.441-7132C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17882922 | |||||||
chr7:17882932 | C | G | 1 | a0001c0010t0014g0020 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.441-7142G>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17882932 | |||||||
chr7:17883000 | A | T | 11 | a0001c0001t0001g0062 a0001c0001t0001g0069 a0001c0001t0001g0076 others(8): Show |
11 | HG01496.hp1 HG02040.hp2 NA18942.hp1 others(8): Show |
intron_variant | MODIFIER | c.441-7210T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17883000 | |||||||
chr7:17883176 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.440+7187T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17883176 | |||||||
chr7:17883616 | G | A | 1 | a0001c0006t0025g0005 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.440+6747C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17883616 | |||||||
chr7:17883626 | C | G | 1 | a0001c0002t0002g0306 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.440+6737G>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17883626 | |||||||
chr7:17883777 | G | A | 13 | a0001c0001t0001g0132 a0001c0001t0001g0319 a0001c0001t0004g0112 others(10): Show |
13 | HG00544.hp1 HG01255.hp2 HG01978.hp1 others(10): Show |
intron_variant | MODIFIER | c.440+6586C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17883777 | |||||||
chr7:17883798 | T | A | 2 | a0001c0001t0001g0052 a0002c0009t0001g0053 |
2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.440+6565A>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17883798 | |||||||
chr7:17883892 | C | T | 1 | a0001c0002t0002g0306 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.440+6471G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17883892 | |||||||
chr7:17884066 | T | C | 1 | a0001c0002t0002g0303 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.440+6297A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17884066 | |||||||
chr7:17884121 | T | C | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(236): Show |
242 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.440+6242A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17884121 | |||||||
chr7:17884221 | T | C | 4 | a0001c0001t0012g0188 a0001c0001t0012g0189 a0001c0001t0012g0190 others(1): Show |
4 | HG02055.hp1 HG02280.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.440+6142A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17884221 | |||||||
chr7:17884254 | C | T | 3 | a0001c0004t0011g0014 a0001c0004t0011g0016 a0001c0004t0011g0067 |
3 | HG02622.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.440+6109G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17884254 | |||||||
chr7:17884349 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.440+6014G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17884349 | |||||||
chr7:17884391 | G | C | 1 | a0001c0001t0001g0140 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.440+5972C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17884391 | |||||||
chr7:17884400 | T | C | 21 | a0001c0001t0001g0132 a0001c0001t0001g0173 a0001c0001t0001g0174 others(18): Show |
21 | HG00544.hp1 HG00673.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.440+5963A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17884400 | |||||||
chr7:17884470 | T | C | 1 | a0001c0001t0001g0135 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.440+5893A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17884470 | |||||||
chr7:17884539 | G | T | 1 | a0001c0001t0001g0160 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.440+5824C>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17884539 | |||||||
chr7:17884810 | C | T | 1 | a0001c0002t0024g0257 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.440+5553G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17884810 | |||||||
chr7:17884876 | T | C | 21 | a0001c0001t0001g0132 a0001c0001t0001g0173 a0001c0001t0001g0174 others(18): Show |
21 | HG00544.hp1 HG00673.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.440+5487A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17884876 | |||||||
chr7:17884916 | C | T | 1 | a0001c0002t0001g0203 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.440+5447G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17884916 | |||||||
chr7:17885001 | T | C | 14 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0021 others(11): Show |
16 | HG01168.hp2 HG01169.hp1 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.440+5362A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17885001 | |||||||
chr7:17885023 | T | C | 1 | a0001c0001t0014g0019 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.440+5340A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17885023 | |||||||
chr7:17885025 | G | C | 1 | a0001c0002t0001g0034 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.440+5338C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17885025 | |||||||
chr7:17885043 | C | T | 1 | a0001c0001t0008g0009 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.440+5320G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17885043 | |||||||
chr7:17885055 | T | C | 2 | a0001c0001t0003g0200 a0001c0001t0004g0116 |
2 | HG00609.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.440+5308A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17885055 | |||||||
chr7:17885058 | T | C | 3 | a0001c0001t0001g0132 a0001c0001t0004g0115 a0001c0001t0018g0216 |
3 | HG00738.hp1 HG01255.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.440+5305A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17885058 | |||||||
chr7:17885297 | C | CA | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(212): Show |
218 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.440+5065dupT | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17885297 | |||||||
chr7:17885439 | T | C | 3 | a0001c0002t0023g0055 a0001c0002t0030g0056 a0001c0002t0032g0335 |
3 | HG02258.hp2 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.440+4924A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17885439 | |||||||
chr7:17885550 | G | C | 2 | a0001c0001t0013g0015 a0001c0001t0013g0239 |
2 | HG01952.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.440+4813C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17885550 | |||||||
chr7:17885576 | C | T | 1 | a0001c0001t0001g0022 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.440+4787G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17885576 | |||||||
chr7:17885653 | C | T | 6 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0008 others(3): Show |
6 | HG01074.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.440+4710G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17885653 | |||||||
chr7:17885717 | A | C | 11 | a0001c0001t0002g0018 a0001c0001t0008g0006 a0001c0001t0008g0007 others(8): Show |
11 | HG01074.hp1 HG02055.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.440+4646T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17885717 | |||||||
chr7:17885777 | G | A | 1 | a0001c0001t0019g0143 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.440+4586C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17885777 | |||||||
chr7:17885919 | T | C | 1 | a0001c0002t0002g0256 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.440+4444A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17885919 | |||||||
chr7:17885994 | T | C | 1 | a0001c0001t0001g0235 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.440+4369A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17885994 | |||||||
chr7:17886020 | A | G | 1 | a0001c0001t0004g0186 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.440+4343T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17886020 | |||||||
chr7:17886115 | G | A | 3 | a0001c0004t0011g0014 a0001c0004t0011g0016 a0001c0004t0011g0067 |
3 | HG02622.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.440+4248C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17886115 | |||||||
chr7:17886224 | C | T | 1 | a0001c0001t0003g0244 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.440+4139G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17886224 | |||||||
chr7:17886306 | A | G | 5 | a0001c0002t0002g0059 a0001c0002t0002g0220 a0001c0002t0002g0221 others(2): Show |
5 | HG01243.hp1 HG01884.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.440+4057T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17886306 | |||||||
chr7:17886339 | G | A | 1 | a0001c0001t0001g0041 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.440+4024C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17886339 | |||||||
chr7:17886344 | C | T | 8 | a0001c0001t0001g0062 a0001c0001t0001g0076 a0001c0001t0001g0103 others(5): Show |
8 | HG02040.hp2 NA18942.hp1 NA18954.hp2 others(5): Show |
intron_variant | MODIFIER | c.440+4019G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17886344 | |||||||
chr7:17886351 | C | T | 145 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0031 others(142): Show |
146 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.440+4012G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17886351 | |||||||
chr7:17886352 | A | G | 236 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(233): Show |
239 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.440+4011T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17886352 | |||||||
chr7:17886584 | C | T | 1 | a0001c0001t0001g0103 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.440+3779G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17886584 | |||||||
chr7:17886604 | T | C | 1 | a0001c0001t0001g0021 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.440+3759A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17886604 | |||||||
chr7:17886612 | G | A | 11 | a0001c0001t0002g0018 a0001c0001t0008g0006 a0001c0001t0008g0007 others(8): Show |
11 | HG01074.hp1 HG02055.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.440+3751C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17886612 | |||||||
chr7:17886798 | A | G | 1 | a0001c0001t0002g0018 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.440+3565T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17886798 | |||||||
chr7:17886835 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.440+3528G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17886835 | |||||||
chr7:17887410 | C | G | 1 | a0001c0001t0012g0188 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.440+2953G>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17887410 | |||||||
chr7:17887471 | G | T | 1 | a0001c0001t0001g0126 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.440+2892C>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17887471 | |||||||
chr7:17887559 | A | G | 1 | a0001c0001t0003g0182 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.440+2804T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17887559 | |||||||
chr7:17887569 | G | A | 6 | a0001c0002t0002g0218 a0001c0002t0002g0255 a0001c0002t0002g0308 others(3): Show |
6 | HG01109.hp2 HG01169.hp2 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.440+2794C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17887569 | |||||||
chr7:17887604 | T | A | 1 | a0001c0002t0001g0034 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.440+2759A>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17887604 | |||||||
chr7:17887782 | A | T | 1 | a0001c0001t0004g0113 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.440+2581T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17887782 | |||||||
chr7:17887846 | T | C | 2 | a0001c0002t0002g0204 a0001c0002t0024g0257 |
2 | HG01261.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.440+2517A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17887846 | |||||||
chr7:17887853 | G | GA | 207 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(204): Show |
210 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.440+2509dupT | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17887853 | |||||||
chr7:17887853 | G | GAA | 7 | a0001c0001t0001g0038 a0001c0001t0001g0141 a0001c0001t0001g0175 others(4): Show |
7 | HG02055.hp2 HG02647.hp2 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.440+2508_440+2509d others(4): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17887853 | |||||||
chr7:17887853 | GA | G | 11 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0008g0006 others(8): Show |
11 | HG01074.hp1 HG02055.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.440+2509delT | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17887853 | |||||||
chr7:17887983 | C | A | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(209): Show |
215 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.440+2380G>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17887983 | |||||||
chr7:17888009 | A | G | 2 | a0001c0001t0005g0012 a0001c0001t0005g0013 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.440+2354T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17888009 | |||||||
chr7:17888027 | A | C | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(209): Show |
215 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.440+2336T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17888027 | |||||||
chr7:17888084 | T | C | 4 | a0001c0001t0001g0061 a0001c0001t0001g0096 a0001c0001t0001g0107 others(1): Show |
4 | NA18946.hp1 NA18957.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.440+2279A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17888084 | |||||||
chr7:17888134 | G | A | 2 | a0001c0001t0005g0012 a0001c0001t0005g0013 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.440+2229C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17888134 | |||||||
chr7:17888166 | C | T | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
193 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.440+2197G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17888166 | |||||||
chr7:17888215 | A | G | 1 | a0001c0011t0006g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.440+2148T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17888215 | |||||||
chr7:17888255 | T | G | 1 | a0001c0002t0002g0302 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.440+2108A>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17888255 | |||||||
chr7:17888311 | C | A | 1 | a0001c0001t0002g0018 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.440+2052G>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17888311 | |||||||
chr7:17888838 | T | C | 1 | a0001c0001t0001g0121 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.440+1525A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17888838 | |||||||
chr7:17888886 | T | C | 2 | a0001c0001t0004g0115 a0001c0001t0018g0216 |
2 | HG00738.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.440+1477A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17888886 | |||||||
chr7:17888900 | G | A | 3 | a0001c0004t0011g0014 a0001c0004t0011g0016 a0001c0004t0011g0067 |
3 | HG02622.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.440+1463C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17888900 | |||||||
chr7:17889053 | G | C | 1 | a0001c0001t0014g0019 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.440+1310C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17889053 | |||||||
chr7:17889058 | G | A | 1 | a0001c0010t0014g0020 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.440+1305C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17889058 | |||||||
chr7:17889067 | T | A | 2 | a0001c0001t0005g0012 a0001c0001t0005g0013 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.440+1296A>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17889067 | |||||||
chr7:17889150 | T | C | 11 | a0001c0001t0002g0018 a0001c0001t0008g0006 a0001c0001t0008g0007 others(8): Show |
11 | HG01074.hp1 HG02055.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.440+1213A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17889150 | |||||||
chr7:17889162 | C | T | 1 | a0001c0001t0004g0116 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.440+1201G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17889162 | |||||||
chr7:17889350 | C | T | 1 | a0001c0001t0001g0123 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.440+1013G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17889350 | |||||||
chr7:17889682 | A | G | 1 | a0001c0001t0004g0186 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.440+681T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17889682 | |||||||
chr7:17889707 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.440+656G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17889707 | |||||||
chr7:17889795 | A | C | 1 | a0001c0001t0001g0135 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.440+568T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17889795 | |||||||
chr7:17889890 | G | A | 3 | a0001c0004t0011g0014 a0001c0004t0011g0016 a0001c0004t0011g0067 |
3 | HG02622.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.440+473C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17889890 | |||||||
chr7:17889952 | AGGAGAAG | A | 3 | a0001c0002t0007g0208 a0001c0002t0007g0292 a0001c0002t0007g0297 |
3 | NA18944.hp1 NA18984.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.440+404_440+410del others(7): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17889952 | |||||||
chr7:17890032 | C | T | 167 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0032 others(164): Show |
168 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.440+331G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17890032 | |||||||
chr7:17890320 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.440+43A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17890320 | |||||||
chr7:17890353 | G | A | 4 | a0001c0002t0001g0214 a0001c0004t0011g0014 a0001c0004t0011g0016 others(1): Show |
4 | HG02622.hp2 HG04184.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.440+10C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 5/25 | chr7 | 17890353 | |||||||
chr7:17890531 | A | C | 3 | a0001c0001t0001g0135 a0001c0001t0020g0191 a0001c0001t0021g0134 |
3 | HG02280.hp1 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.319-47T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 4/25 | chr7 | 17890531 | |||||||
chr7:17890715 | A | AT | 3 | a0001c0004t0011g0014 a0001c0004t0011g0016 a0001c0004t0011g0067 |
3 | HG02622.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.319-232_319-231ins others(1): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 4/25 | chr7 | 17890715 | |||||||
chr7:17890715 | A | T | 8 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(5): Show |
8 | HG02055.hp1 HG02451.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.319-231T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 4/25 | chr7 | 17890715 | |||||||
chr7:17890773 | G | T | 1 | a0001c0001t0001g0075 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.319-289C>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 4/25 | chr7 | 17890773 | |||||||
chr7:17890918 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.319-434G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 4/25 | chr7 | 17890918 | |||||||
chr7:17891179 | G | A | 2 | a0001c0001t0001g0101 a0001c0001t0001g0110 |
2 | HG02135.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.318+367C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 4/25 | chr7 | 17891179 | |||||||
chr7:17891282 | T | C | 2 | a0001c0001t0001g0110 a0001c0002t0001g0276 |
2 | HG02129.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.318+264A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 4/25 | chr7 | 17891282 | |||||||
chr7:17891497 | T | C | 1 | a0001c0011t0006g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.318+49A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 4/25 | chr7 | 17891497 | |||||||
chr7:17891515 | T | C | 2 | a0001c0001t0010g0138 a0001c0001t0010g0139 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.318+31A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 4/25 | chr7 | 17891515 | |||||||
chr7:17891660 | C | T | 3 | a0001c0001t0012g0188 a0001c0001t0012g0189 a0001c0001t0012g0190 |
3 | HG02055.hp1 HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.229-25G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 3/25 | chr7 | 17891660 | |||||||
chr7:17891674 | G | C | 3 | a0001c0001t0012g0188 a0001c0001t0012g0189 a0001c0001t0012g0190 |
3 | HG02055.hp1 HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.229-39C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 3/25 | chr7 | 17891674 | |||||||
chr7:17891945 | G | A | 6 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0008 others(3): Show |
6 | HG01074.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.229-310C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 3/25 | chr7 | 17891945 | |||||||
chr7:17891949 | G | C | 2 | a0001c0001t0010g0138 a0001c0001t0010g0139 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.229-314C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 3/25 | chr7 | 17891949 | |||||||
chr7:17891966 | G | A | 1 | a0001c0001t0008g0060 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.229-331C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 3/25 | chr7 | 17891966 | |||||||
chr7:17892153 | T | TA | 6 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0008 others(3): Show |
6 | HG01074.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.229-519dupT | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 3/25 | chr7 | 17892153 | |||||||
chr7:17892196 | T | C | 2 | a0001c0001t0005g0012 a0001c0001t0005g0013 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.229-561A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 3/25 | chr7 | 17892196 | |||||||
chr7:17892494 | T | G | 4 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0155 others(1): Show |
4 | HG01168.hp1 HG01257.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.228+838A>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 3/25 | chr7 | 17892494 | |||||||
chr7:17892812 | T | C | 7 | a0001c0002t0006g0253 a0001c0002t0006g0284 a0001c0002t0006g0294 others(4): Show |
7 | HG00642.hp2 HG00741.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.228+520A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 3/25 | chr7 | 17892812 | |||||||
chr7:17892847 | C | T | 2 | a0001c0001t0013g0015 a0001c0001t0013g0239 |
2 | HG01952.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.228+485G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 3/25 | chr7 | 17892847 | |||||||
chr7:17892897 | T | C | 3 | a0001c0001t0012g0188 a0001c0001t0012g0189 a0001c0001t0012g0190 |
3 | HG02055.hp1 HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.228+435A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 3/25 | chr7 | 17892897 | |||||||
chr7:17892928 | C | T | 1 | a0001c0010t0014g0020 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.228+404G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 3/25 | chr7 | 17892928 | |||||||
chr7:17893056 | A | G | 3 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0232 |
3 | HG01109.hp1 HG01243.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.228+276T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 3/25 | chr7 | 17893056 | |||||||
chr7:17893164 | G | A | 2 | a0001c0001t0005g0012 a0001c0001t0005g0013 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.228+168C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 3/25 | chr7 | 17893164 | |||||||
chr7:17893253 | G | A | 1 | a0001c0002t0001g0277 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.228+79C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 3/25 | chr7 | 17893253 | |||||||
chr7:17893302 | T | C | 1 | a0001c0002t0001g0214 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.228+30A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 3/25 | chr7 | 17893302 | |||||||
chr7:17893309 | T | C | 31 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(28): Show |
31 | HG00280.hp2 HG00323.hp1 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.228+23A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 3/25 | chr7 | 17893309 | |||||||
chr7:17893554 | T | C | 1 | a0001c0001t0001g0033 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.126-120A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 2/25 | chr7 | 17893554 | |||||||
chr7:17893642 | A | G | 1 | a0001c0002t0001g0282 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.126-208T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 2/25 | chr7 | 17893642 | |||||||
chr7:17893643 | T | C | 1 | a0001c0001t0001g0085 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.126-209A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 2/25 | chr7 | 17893643 | |||||||
chr7:17893716 | T | C | 1 | a0001c0001t0004g0117 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.126-282A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 2/25 | chr7 | 17893716 | |||||||
chr7:17893850 | T | C | 1 | a0001c0011t0006g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.126-416A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 2/25 | chr7 | 17893850 | |||||||
chr7:17893970 | G | GA | 9 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0008 others(6): Show |
9 | HG01074.hp1 HG02055.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.126-537dupT | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 2/25 | chr7 | 17893970 | |||||||
chr7:17893970 | GA | G | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(163): Show |
169 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.126-537delT | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 2/25 | chr7 | 17893970 | |||||||
chr7:17893971 | A | G | 7 | a0001c0002t0006g0253 a0001c0002t0006g0284 a0001c0002t0006g0294 others(4): Show |
7 | HG00642.hp2 HG00741.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.126-537T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 2/25 | chr7 | 17893971 | |||||||
chr7:17894063 | G | A | 2 | a0001c0001t0001g0171 a0001c0001t0001g0172 |
2 | HG02630.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.126-629C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 2/25 | chr7 | 17894063 | |||||||
chr7:17894100 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.126-666G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 2/25 | chr7 | 17894100 | |||||||
chr7:17894163 | T | G | 2 | a0001c0001t0005g0012 a0001c0001t0005g0013 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.126-729A>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 2/25 | chr7 | 17894163 | |||||||
chr7:17894260 | G | A | 2 | a0001c0001t0013g0015 a0001c0001t0013g0239 |
2 | HG01952.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.126-826C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 2/25 | chr7 | 17894260 | |||||||
chr7:17894264 | C | G | 2 | a0001c0001t0013g0015 a0001c0001t0013g0239 |
2 | HG01952.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.126-830G>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 2/25 | chr7 | 17894264 | |||||||
chr7:17894274 | G | A | 12 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0021 others(9): Show |
14 | HG01168.hp2 HG01169.hp1 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.126-840C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 2/25 | chr7 | 17894274 | |||||||
chr7:17894369 | T | C | 3 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0245 |
3 | HG00673.hp1 NA19057.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.126-935A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 2/25 | chr7 | 17894369 | |||||||
chr7:17894391 | T | G | 32 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(29): Show |
32 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.126-957A>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 2/25 | chr7 | 17894391 | |||||||
chr7:17894472 | T | C | 1 | a0001c0001t0003g0252 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.126-1038A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 2/25 | chr7 | 17894472 | |||||||
chr7:17894543 | A | T | 1 | a0001c0001t0001g0228 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.126-1109T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 2/25 | chr7 | 17894543 | |||||||
chr7:17894690 | T | C | 184 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(181): Show |
187 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.126-1256A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 2/25 | chr7 | 17894690 | |||||||
chr7:17894707 | A | C | 3 | a0001c0001t0001g0065 a0001c0001t0001g0101 a0001c0001t0001g0110 |
3 | HG02135.hp1 NA18948.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.126-1273T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 2/25 | chr7 | 17894707 | |||||||
chr7:17894750 | T | C | 1 | a0001c0001t0019g0143 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.126-1316A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 2/25 | chr7 | 17894750 | |||||||
chr7:17895088 | A | G | 18 | a0001c0001t0001g0003 a0001c0001t0001g0030 a0001c0001t0001g0145 others(15): Show |
19 | HG00609.hp1 HG00741.hp1 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.126-1654T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 2/25 | chr7 | 17895088 | |||||||
chr7:17895181 | G | A | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
170 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.126-1747C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 2/25 | chr7 | 17895181 | |||||||
chr7:17895469 | A | C | 1 | a0001c0001t0003g0244 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.125+1865T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 2/25 | chr7 | 17895469 | |||||||
chr7:17895649 | G | A | 6 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0008 others(3): Show |
6 | HG01074.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.125+1685C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 2/25 | chr7 | 17895649 | |||||||
chr7:17895754 | T | G | 2 | a0001c0002t0001g0258 a0001c0002t0001g0301 |
2 | HG02132.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.125+1580A>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 2/25 | chr7 | 17895754 | |||||||
chr7:17895879 | T | C | 4 | a0001c0001t0012g0188 a0001c0001t0012g0189 a0001c0001t0012g0190 others(1): Show |
4 | HG02055.hp1 HG02280.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.125+1455A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 2/25 | chr7 | 17895879 | |||||||
chr7:17896042 | G | A | 134 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0031 others(131): Show |
135 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.125+1292C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 2/25 | chr7 | 17896042 | |||||||
chr7:17896046 | C | T | 1 | a0001c0001t0004g0117 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.125+1288G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 2/25 | chr7 | 17896046 | |||||||
chr7:17896102 | G | C | 31 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(28): Show |
31 | HG00280.hp2 HG00323.hp1 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.125+1232C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 2/25 | chr7 | 17896102 | |||||||
chr7:17896255 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.125+1079G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 2/25 | chr7 | 17896255 | |||||||
chr7:17896391 | T | A | 15 | a0001c0001t0001g0132 a0001c0001t0001g0183 a0001c0001t0001g0226 others(12): Show |
15 | HG00544.hp1 HG00735.hp1 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.125+943A>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 2/25 | chr7 | 17896391 | |||||||
chr7:17896423 | A | G | 1 | a0001c0011t0006g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.125+911T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 2/25 | chr7 | 17896423 | |||||||
chr7:17896617 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.125+717C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 2/25 | chr7 | 17896617 | |||||||
chr7:17896742 | G | A | 224 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(221): Show |
227 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.125+592C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 2/25 | chr7 | 17896742 | |||||||
chr7:17896832 | T | C | 4 | a0001c0001t0012g0188 a0001c0001t0012g0189 a0001c0001t0012g0190 others(1): Show |
4 | HG02055.hp1 HG02280.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.125+502A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 2/25 | chr7 | 17896832 | |||||||
chr7:17896938 | G | T | 1 | a0001c0001t0001g0265 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.125+396C>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 2/25 | chr7 | 17896938 | |||||||
chr7:17897003 | A | G | 1 | a0001c0001t0014g0019 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.125+331T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 2/25 | chr7 | 17897003 | |||||||
chr7:17897192 | T | C | 1 | a0001c0001t0014g0019 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.125+142A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 2/25 | chr7 | 17897192 | |||||||
chr7:17897225 | A | C | 1 | a0001c0006t0025g0005 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.125+109T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 2/25 | chr7 | 17897225 | |||||||
chr7:17897547 | A | G | 3 | a0001c0004t0011g0014 a0001c0004t0011g0016 a0001c0004t0011g0067 |
3 | HG02622.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.13-101T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17897547 | |||||||
chr7:17897664 | C | T | 43 | a0001c0001t0001g0265 a0001c0001t0003g0192 a0001c0001t0003g0193 others(40): Show |
43 | HG00558.hp1 HG00609.hp2 HG02015.hp1 others(40): Show |
intron_variant | MODIFIER | c.13-218G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17897664 | |||||||
chr7:17897685 | C | A | 11 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0021 others(8): Show |
13 | HG01168.hp2 HG01169.hp1 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.13-239G>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17897685 | |||||||
chr7:17897935 | A | ATTC | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(214): Show |
220 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.13-490_13-489insGA others(1): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17897935 | |||||||
chr7:17897956 | A | G | 172 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(169): Show |
175 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.13-510T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17897956 | |||||||
chr7:17898027 | C | T | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
174 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.13-581G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17898027 | |||||||
chr7:17898140 | T | C | 4 | a0001c0001t0001g0003 a0001c0001t0001g0026 a0001c0001t0001g0161 others(1): Show |
5 | HG01261.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.13-694A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17898140 | |||||||
chr7:17898231 | C | T | 5 | a0001c0002t0002g0059 a0001c0002t0002g0220 a0001c0002t0002g0221 others(2): Show |
5 | HG01243.hp1 HG01884.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.13-785G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17898231 | |||||||
chr7:17898424 | T | C | 1 | a0001c0011t0006g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.13-978A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17898424 | |||||||
chr7:17898623 | G | A | 2 | a0001c0001t0001g0149 a0001c0001t0005g0151 |
2 | HG00140.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.13-1177C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17898623 | |||||||
chr7:17898660 | C | T | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(210): Show |
216 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.13-1214G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17898660 | |||||||
chr7:17898868 | T | C | 147 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(144): Show |
150 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.13-1422A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17898868 | |||||||
chr7:17898974 | C | G | 2 | a0001c0001t0005g0012 a0001c0001t0005g0013 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.13-1528G>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17898974 | |||||||
chr7:17899225 | C | T | 1 | a0001c0001t0001g0074 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.13-1779G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17899225 | |||||||
chr7:17899266 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.13-1820A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17899266 | |||||||
chr7:17899445 | A | T | 5 | a0001c0002t0002g0059 a0001c0002t0002g0220 a0001c0002t0002g0221 others(2): Show |
5 | HG01243.hp1 HG01884.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.13-1999T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17899445 | |||||||
chr7:17899496 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.13-2050G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17899496 | |||||||
chr7:17899500 | T | C | 3 | a0001c0001t0001g0032 a0001c0001t0001g0045 a0001c0001t0001g0046 |
3 | HG03041.hp2 NA20805.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.13-2054A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17899500 | |||||||
chr7:17899732 | C | T | 2 | a0001c0001t0001g0107 a0001c0001t0001g0108 |
2 | NA18946.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.13-2286G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17899732 | |||||||
chr7:17899895 | T | C | 3 | a0001c0004t0011g0014 a0001c0004t0011g0016 a0001c0004t0011g0067 |
3 | HG02622.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.13-2449A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17899895 | |||||||
chr7:17900114 | T | C | 1 | a0001c0001t0001g0178 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.13-2668A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17900114 | |||||||
chr7:17900187 | T | C | 11 | a0001c0001t0001g0062 a0001c0001t0001g0069 a0001c0001t0001g0103 others(8): Show |
11 | HG01496.hp1 HG02040.hp2 NA18942.hp1 others(8): Show |
intron_variant | MODIFIER | c.13-2741A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17900187 | |||||||
chr7:17900278 | T | G | 4 | a0001c0001t0001g0032 a0001c0001t0001g0045 a0001c0001t0001g0046 others(1): Show |
4 | HG03041.hp2 HG03486.hp2 NA20805.hp2 others(1): Show |
intron_variant | MODIFIER | c.13-2832A>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17900278 | |||||||
chr7:17900423 | G | A | 1 | a0001c0001t0001g0045 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.13-2977C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17900423 | |||||||
chr7:17900529 | T | C | 222 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(219): Show |
225 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.13-3083A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17900529 | |||||||
chr7:17901030 | G | A | 4 | a0001c0001t0012g0188 a0001c0001t0012g0189 a0001c0001t0012g0190 others(1): Show |
4 | HG02055.hp1 HG02280.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.13-3584C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17901030 | |||||||
chr7:17901095 | G | A | 1 | a0001c0001t0001g0027 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.13-3649C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17901095 | |||||||
chr7:17901121 | A | G | 4 | a0001c0001t0012g0188 a0001c0001t0012g0189 a0001c0001t0012g0190 others(1): Show |
4 | HG02055.hp1 HG02280.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.13-3675T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17901121 | |||||||
chr7:17901242 | G | A | 2 | a0001c0001t0001g0314 a0001c0001t0001g0315 |
2 | HG00642.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.13-3796C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17901242 | |||||||
chr7:17901256 | C | T | 2 | a0001c0002t0002g0201 a0001c0002t0002g0202 |
2 | HG01884.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.13-3810G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17901256 | |||||||
chr7:17901681 | G | A | 93 | a0001c0001t0001g0011 a0001c0001t0001g0061 a0001c0001t0001g0062 others(90): Show |
93 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.13-4235C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17901681 | |||||||
chr7:17901713 | T | C | 2 | a0001c0001t0013g0015 a0001c0001t0013g0239 |
2 | HG01952.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.13-4267A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17901713 | |||||||
chr7:17902092 | T | C | 1 | a0001c0002t0007g0297 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.13-4646A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17902092 | |||||||
chr7:17902218 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.13-4772C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17902218 | |||||||
chr7:17902242 | G | GT | 34 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0021 others(31): Show |
36 | HG00408.hp1 HG01168.hp2 HG01169.hp1 others(33): Show |
intron_variant | MODIFIER | c.13-4797dupA | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17902242 | |||||||
chr7:17902242 | GT | G | 135 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0031 others(132): Show |
136 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.13-4797delA | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17902242 | |||||||
chr7:17902242 | GTT | G | 37 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(34): Show |
37 | HG00280.hp2 HG00323.hp1 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.13-4798_13-4797del others(2): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17902242 | |||||||
chr7:17902242 | GTTT | G | 11 | a0001c0001t0001g0042 a0001c0001t0005g0012 a0001c0001t0005g0013 others(8): Show |
11 | HG01074.hp2 HG01256.hp1 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.13-4799_13-4797del others(3): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17902242 | |||||||
chr7:17902242 | GTTTT | G | 42 | a0001c0002t0002g0209 a0001c0002t0002g0213 a0001c0002t0002g0218 others(39): Show |
42 | HG00323.hp2 HG00408.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.13-4800_13-4797del others(4): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17902242 | |||||||
chr7:17902420 | T | C | 5 | a0001c0001t0001g0066 a0001c0001t0001g0080 a0001c0001t0001g0081 others(2): Show |
5 | HG00408.hp1 HG02523.hp1 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.13-4974A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17902420 | |||||||
chr7:17902573 | T | A | 2 | a0001c0001t0001g0135 a0001c0001t0021g0134 |
2 | HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.13-5127A>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17902573 | |||||||
chr7:17902592 | G | T | 1 | a0001c0001t0001g0031 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.13-5146C>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17902592 | |||||||
chr7:17902783 | C | T | 31 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(28): Show |
31 | HG00280.hp2 HG00323.hp1 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.13-5337G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17902783 | |||||||
chr7:17902974 | T | C | 224 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(221): Show |
227 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.13-5528A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17902974 | |||||||
chr7:17903094 | T | G | 1 | a0001c0002t0006g0253 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.13-5648A>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17903094 | |||||||
chr7:17903135 | G | C | 6 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0008 others(3): Show |
6 | HG01074.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.13-5689C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17903135 | |||||||
chr7:17903185 | A | T | 32 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(29): Show |
32 | HG00280.hp2 HG00323.hp1 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.13-5739T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17903185 | |||||||
chr7:17903412 | G | A | 1 | a0001c0001t0001g0181 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.13-5966C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17903412 | |||||||
chr7:17903429 | G | GT | 3 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0219 |
3 | HG02717.hp1 HG02922.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.13-5984dupA | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17903429 | |||||||
chr7:17903485 | G | C | 1 | a0001c0001t0002g0018 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.13-6039C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17903485 | |||||||
chr7:17903562 | T | C | 2 | a0001c0001t0001g0314 a0001c0001t0001g0315 |
2 | HG00642.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.13-6116A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17903562 | |||||||
chr7:17903722 | A | C | 172 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(169): Show |
175 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.13-6276T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17903722 | |||||||
chr7:17903750 | G | C | 1 | a0001c0001t0001g0069 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.13-6304C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17903750 | |||||||
chr7:17903846 | G | A | 2 | a0001c0001t0001g0162 a0001c0001t0001g0166 |
2 | NA19080.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.13-6400C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17903846 | |||||||
chr7:17903873 | G | A | 1 | a0001c0002t0002g0298 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.13-6427C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17903873 | |||||||
chr7:17904094 | T | A | 1 | a0001c0001t0001g0102 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.13-6648A>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17904094 | |||||||
chr7:17904178 | T | C | 1 | a0001c0001t0019g0143 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.13-6732A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17904178 | |||||||
chr7:17904236 | G | A | 173 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(170): Show |
176 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.13-6790C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17904236 | |||||||
chr7:17904238 | T | C | 10 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0008 others(7): Show |
10 | HG01074.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.13-6792A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17904238 | |||||||
chr7:17904325 | A | G | 1 | a0001c0011t0006g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.13-6879T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17904325 | |||||||
chr7:17904434 | A | C | 9 | a0001c0001t0001g0072 a0001c0001t0001g0087 a0001c0001t0001g0109 others(6): Show |
9 | HG02109.hp1 HG02451.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.13-6988T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17904434 | |||||||
chr7:17904438 | T | A | 1 | a0001c0002t0002g0248 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.13-6992A>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17904438 | |||||||
chr7:17904797 | T | A | 1 | a0001c0001t0001g0099 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.13-7351A>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17904797 | |||||||
chr7:17904939 | G | T | 1 | a0001c0001t0001g0086 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.13-7493C>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17904939 | |||||||
chr7:17905406 | A | G | 6 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0008 others(3): Show |
6 | HG01074.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.13-7960T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17905406 | |||||||
chr7:17905448 | G | A | 3 | a0001c0002t0023g0055 a0001c0002t0030g0056 a0001c0002t0032g0335 |
3 | HG02258.hp2 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.13-8002C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17905448 | |||||||
chr7:17905460 | G | T | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(166): Show |
172 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.13-8014C>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17905460 | |||||||
chr7:17905516 | G | C | 10 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0008 others(7): Show |
10 | HG01074.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.13-8070C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17905516 | |||||||
chr7:17905537 | T | C | 1 | a0001c0001t0001g0173 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.13-8091A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17905537 | |||||||
chr7:17905636 | A | T | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(214): Show |
220 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.13-8190T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17905636 | |||||||
chr7:17905641 | A | T | 1 | a0001c0002t0002g0263 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.13-8195T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17905641 | |||||||
chr7:17905696 | T | C | 1 | a0001c0010t0014g0020 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.13-8250A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17905696 | |||||||
chr7:17905800 | T | C | 2 | a0001c0001t0001g0135 a0001c0001t0021g0134 |
2 | HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.13-8354A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17905800 | |||||||
chr7:17905950 | C | T | 1 | a0001c0006t0025g0005 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.13-8504G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17905950 | |||||||
chr7:17906016 | TAAAG | T | 9 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0008 others(6): Show |
9 | HG01074.hp1 HG02055.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.13-8574_13-8571del others(4): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17906016 | |||||||
chr7:17906021 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.13-8575T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17906021 | |||||||
chr7:17906058 | G | C | 1 | a0001c0006t0025g0005 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.13-8612C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17906058 | |||||||
chr7:17906133 | T | A | 1 | a0001c0001t0001g0217 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.13-8687A>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17906133 | |||||||
chr7:17906232 | T | C | 1 | a0001c0001t0020g0191 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.13-8786A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17906232 | |||||||
chr7:17906285 | T | C | 1 | a0001c0006t0025g0005 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.13-8839A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17906285 | |||||||
chr7:17906341 | C | A | 1 | a0001c0001t0001g0135 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.13-8895G>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17906341 | |||||||
chr7:17906564 | A | G | 15 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(12): Show |
15 | HG00609.hp2 HG03831.hp2 NA18612.hp1 others(12): Show |
intron_variant | MODIFIER | c.13-9118T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17906564 | |||||||
chr7:17906951 | G | C | 1 | a0001c0001t0001g0102 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.13-9505C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17906951 | |||||||
chr7:17906957 | G | A | 2 | a0001c0001t0001g0176 a0001c0001t0001g0177 |
2 | NA18962.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.13-9511C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17906957 | |||||||
chr7:17906981 | A | G | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(214): Show |
220 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.13-9535T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17906981 | |||||||
chr7:17907025 | C | G | 1 | a0001c0001t0010g0233 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.13-9579G>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17907025 | |||||||
chr7:17907026 | G | A | 2 | a0001c0001t0003g0199 a0001c0001t0003g0200 |
2 | HG00609.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.13-9580C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17907026 | |||||||
chr7:17907172 | G | A | 14 | a0001c0001t0001g0033 a0001c0001t0001g0035 a0001c0001t0001g0036 others(11): Show |
14 | HG00280.hp2 HG00323.hp1 HG00673.hp2 others(11): Show |
intron_variant | MODIFIER | c.13-9726C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17907172 | |||||||
chr7:17907205 | A | C | 168 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(165): Show |
171 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.13-9759T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17907205 | |||||||
chr7:17907619 | C | A | 1 | a0001c0001t0014g0019 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.13-10173G>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17907619 | |||||||
chr7:17907691 | G | T | 2 | a0001c0001t0005g0012 a0001c0001t0005g0013 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.13-10245C>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17907691 | |||||||
chr7:17907758 | C | T | 1 | a0001c0006t0025g0005 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.13-10312G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17907758 | |||||||
chr7:17908012 | C | T | 1 | a0001c0001t0001g0107 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.13-10566G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17908012 | |||||||
chr7:17908129 | C | T | 1 | a0001c0001t0002g0018 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.13-10683G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17908129 | |||||||
chr7:17908136 | A | G | 2 | a0001c0001t0001g0103 a0001c0001t0005g0073 |
2 | HG02132.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.13-10690T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17908136 | |||||||
chr7:17908181 | G | A | 12 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0021 others(9): Show |
14 | HG01168.hp2 HG01169.hp1 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.13-10735C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17908181 | |||||||
chr7:17908303 | C | G | 1 | a0001c0001t0001g0031 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.13-10857G>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17908303 | |||||||
chr7:17908358 | T | G | 168 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(165): Show |
171 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.13-10912A>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17908358 | |||||||
chr7:17908422 | C | G | 1 | a0001c0001t0001g0149 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.13-10976G>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17908422 | |||||||
chr7:17908464 | A | G | 9 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0008 others(6): Show |
9 | HG01074.hp1 HG02055.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.13-11018T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17908464 | |||||||
chr7:17908517 | C | A | 129 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0031 others(126): Show |
130 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.13-11071G>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17908517 | |||||||
chr7:17908596 | A | G | 168 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(165): Show |
171 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.13-11150T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17908596 | |||||||
chr7:17908651 | A | T | 3 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0031g0242 |
3 | HG02257.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.13-11205T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17908651 | |||||||
chr7:17908967 | T | A | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
170 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.13-11521A>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17908967 | |||||||
chr7:17909367 | T | C | 1 | a0001c0006t0025g0005 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.13-11921A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17909367 | |||||||
chr7:17909439 | T | C | 1 | a0001c0001t0001g0137 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.13-11993A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17909439 | |||||||
chr7:17909498 | C | T | 3 | a0001c0002t0001g0254 a0001c0002t0001g0259 a0001c0002t0001g0260 |
3 | NA18972.hp1 NA19012.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.13-12052G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17909498 | |||||||
chr7:17909572 | C | T | 4 | a0001c0001t0001g0003 a0001c0001t0001g0153 a0001c0001t0001g0161 others(1): Show |
5 | HG01168.hp1 HG01261.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.13-12126G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17909572 | |||||||
chr7:17909573 | G | A | 1 | a0001c0001t0001g0031 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.13-12127C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17909573 | |||||||
chr7:17909659 | TGATGAGA others(15): Show |
T | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
151 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.13-12235_13-12214d others(24): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17909659 | |||||||
chr7:17909734 | G | A | 2 | a0001c0001t0005g0012 a0001c0001t0005g0013 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.13-12288C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17909734 | |||||||
chr7:17909807 | C | T | 1 | a0001c0001t0005g0010 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.13-12361G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17909807 | |||||||
chr7:17909811 | A | G | 168 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(165): Show |
171 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.13-12365T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17909811 | |||||||
chr7:17909857 | T | C | 2 | a0001c0001t0001g0042 a0001c0001t0001g0043 |
2 | HG01074.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.13-12411A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17909857 | |||||||
chr7:17910153 | A | T | 2 | a0001c0001t0001g0045 a0001c0001t0001g0046 |
2 | HG03041.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.13-12707T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17910153 | |||||||
chr7:17910162 | C | T | 1 | a0001c0001t0004g0147 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.13-12716G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17910162 | |||||||
chr7:17910184 | G | A | 153 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0061 others(150): Show |
154 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.13-12738C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17910184 | |||||||
chr7:17910222 | G | A | 10 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0008 others(7): Show |
10 | HG01074.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.13-12776C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17910222 | |||||||
chr7:17910343 | T | C | 1 | a0001c0001t0001g0131 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.13-12897A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17910343 | |||||||
chr7:17910363 | G | A | 1 | a0001c0002t0007g0299 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.13-12917C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17910363 | |||||||
chr7:17910443 | A | G | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
170 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.13-12997T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17910443 | |||||||
chr7:17910516 | A | C | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
170 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.13-13070T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17910516 | |||||||
chr7:17910585 | C | A | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
170 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.13-13139G>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17910585 | |||||||
chr7:17910882 | C | A | 2 | a0001c0001t0001g0101 a0001c0001t0001g0110 |
2 | HG02135.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.13-13436G>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17910882 | |||||||
chr7:17910943 | A | T | 2 | a0001c0001t0003g0192 a0001c0001t0003g0193 |
2 | NA18943.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.13-13497T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17910943 | |||||||
chr7:17910948 | T | C | 33 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(30): Show |
33 | HG00280.hp2 HG00323.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.13-13502A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17910948 | |||||||
chr7:17910994 | T | A | 2 | a0001c0001t0001g0140 a0001c0001t0001g0141 |
2 | HG03516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.13-13548A>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17910994 | |||||||
chr7:17911214 | C | A | 8 | a0001c0001t0002g0018 a0001c0001t0014g0019 a0001c0002t0002g0059 others(5): Show |
8 | HG00639.hp2 HG01243.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.13-13768G>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17911214 | |||||||
chr7:17911301 | C | G | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
170 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.13-13855G>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17911301 | |||||||
chr7:17911358 | C | T | 2 | a0001c0001t0002g0334 a0001c0002t0002g0302 |
2 | HG02602.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.13-13912G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17911358 | |||||||
chr7:17911359 | C | T | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
170 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.13-13913G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17911359 | |||||||
chr7:17911371 | A | G | 1 | a0001c0001t0008g0007 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.13-13925T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17911371 | |||||||
chr7:17911411 | G | C | 16 | a0001c0001t0001g0033 a0001c0001t0001g0035 a0001c0001t0001g0036 others(13): Show |
16 | HG00280.hp2 HG00323.hp1 HG00673.hp2 others(13): Show |
intron_variant | MODIFIER | c.13-13965C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17911411 | |||||||
chr7:17911435 | T | A | 33 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(30): Show |
33 | HG00280.hp2 HG00323.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.13-13989A>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17911435 | |||||||
chr7:17911500 | G | A | 2 | a0001c0002t0002g0209 a0001c0002t0002g0305 |
2 | HG01069.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.13-14054C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17911500 | |||||||
chr7:17911613 | C | G | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
170 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.13-14167G>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17911613 | |||||||
chr7:17911637 | CA | C | 47 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(44): Show |
47 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.13-14192delT | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17911637 | |||||||
chr7:17911637 | CAA | C | 172 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(169): Show |
175 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.13-14193_13-14192d others(4): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17911637 | |||||||
chr7:17911681 | G | A | 3 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0002t0027g0300 |
3 | HG02895.hp1 HG02897.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.13-14235C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17911681 | |||||||
chr7:17911695 | A | T | 1 | a0001c0001t0001g0068 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.13-14249T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17911695 | |||||||
chr7:17911823 | T | C | 6 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0008 others(3): Show |
6 | HG01074.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.13-14377A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17911823 | |||||||
chr7:17912095 | T | G | 1 | a0001c0002t0002g0212 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.13-14649A>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17912095 | |||||||
chr7:17912232 | C | T | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(163): Show |
169 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.13-14786G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17912232 | |||||||
chr7:17912298 | G | A | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
170 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.13-14852C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17912298 | |||||||
chr7:17912396 | T | C | 1 | a0001c0001t0001g0043 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.13-14950A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17912396 | |||||||
chr7:17912415 | C | CT | 154 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0061 others(151): Show |
155 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.13-14970dupA | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17912415 | |||||||
chr7:17912415 | C | CTT | 13 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0021 others(10): Show |
15 | HG01168.hp2 HG01169.hp1 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.13-14971_13-14970d others(4): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17912415 | |||||||
chr7:17912545 | G | C | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
170 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.13-15099C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17912545 | |||||||
chr7:17912613 | T | C | 1 | a0001c0002t0027g0300 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.13-15167A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17912613 | |||||||
chr7:17912767 | T | A | 2 | a0001c0001t0012g0189 a0001c0001t0012g0190 |
2 | HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.13-15321A>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17912767 | |||||||
chr7:17912780 | C | G | 1 | a0001c0001t0020g0191 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.13-15334G>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17912780 | |||||||
chr7:17912811 | C | T | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
170 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.13-15365G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17912811 | |||||||
chr7:17912882 | C | T | 1 | a0001c0001t0014g0019 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.13-15436G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17912882 | |||||||
chr7:17912974 | C | T | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(163): Show |
169 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.13-15528G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17912974 | |||||||
chr7:17912995 | A | G | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
170 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.13-15549T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17912995 | |||||||
chr7:17912998 | C | T | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
170 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.13-15552G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17912998 | |||||||
chr7:17913065 | T | G | 5 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0010g0138 others(2): Show |
5 | HG02896.hp1 HG02897.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.13-15619A>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17913065 | |||||||
chr7:17913087 | G | A | 2 | a0001c0001t0013g0015 a0001c0001t0013g0239 |
2 | HG01952.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.13-15641C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17913087 | |||||||
chr7:17913109 | C | T | 10 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0008 others(7): Show |
10 | HG01074.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.13-15663G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17913109 | |||||||
chr7:17913204 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.13-15758C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17913204 | |||||||
chr7:17913441 | C | T | 2 | a0001c0001t0016g0250 a0001c0001t0016g0251 |
2 | NA18962.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.13-15995G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17913441 | |||||||
chr7:17913483 | G | C | 1 | a0001c0011t0006g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.13-16037C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17913483 | |||||||
chr7:17913488 | C | T | 1 | a0001c0006t0025g0005 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.13-16042G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17913488 | |||||||
chr7:17913595 | T | C | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
170 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.13-16149A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17913595 | |||||||
chr7:17913628 | G | A | 2 | a0001c0001t0001g0101 a0001c0001t0001g0110 |
2 | HG02135.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.13-16182C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17913628 | |||||||
chr7:17913713 | A | T | 157 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(154): Show |
160 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.13-16267T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17913713 | |||||||
chr7:17913754 | CAAAAACA others(3): Show |
C | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(148): Show |
154 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.13-16318_13-16309d others(12): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17913754 | |||||||
chr7:17913754 | CAAAAACA others(4): Show |
C | 1 | a0001c0001t0001g0061 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.13-16319_13-16309d others(13): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17913754 | |||||||
chr7:17913760 | C | A | 2 | a0001c0001t0005g0012 a0001c0001t0014g0019 |
2 | HG00639.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.13-16314G>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17913760 | |||||||
chr7:17913760 | CA | C | 54 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0178 others(51): Show |
54 | HG00408.hp2 HG00642.hp2 HG00741.hp2 others(51): Show |
intron_variant | MODIFIER | c.13-16315delT | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17913760 | |||||||
chr7:17913760 | CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0001g0176 a0001c0001t0001g0177 |
2 | NA18962.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.13-16325_13-16315d others(13): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17913760 | |||||||
chr7:17913767 | A | C | 1 | a0001c0001t0019g0143 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.13-16321T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17913767 | |||||||
chr7:17913784 | A | C | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(156): Show |
162 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.13-16338T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17913784 | |||||||
chr7:17913794 | G | A | 1 | a0001c0002t0002g0105 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.13-16348C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17913794 | |||||||
chr7:17913896 | C | T | 9 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0008 others(6): Show |
9 | HG01074.hp1 HG02055.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.13-16450G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17913896 | |||||||
chr7:17913921 | G | A | 1 | a0001c0001t0001g0178 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.13-16475C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17913921 | |||||||
chr7:17913998 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.13-16552C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17913998 | |||||||
chr7:17914032 | A | G | 30 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(27): Show |
30 | HG00280.hp2 HG00323.hp1 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.13-16586T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17914032 | |||||||
chr7:17914127 | G | GAA | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
170 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.13-16682_13-16681i others(4): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17914127 | |||||||
chr7:17914205 | G | GA | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
170 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.13-16760dupT | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17914205 | |||||||
chr7:17914211 | A | C | 2 | a0001c0001t0001g0035 a0001c0001t0001g0036 |
2 | HG00323.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.13-16765T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17914211 | |||||||
chr7:17914245 | G | C | 6 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0008 others(3): Show |
6 | HG01074.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.13-16799C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17914245 | |||||||
chr7:17914327 | G | A | 1 | a0001c0010t0014g0020 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.13-16881C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17914327 | |||||||
chr7:17914650 | A | T | 3 | a0001c0001t0001g0122 a0001c0001t0001g0181 a0001c0001t0003g0182 |
3 | HG00423.hp2 NA19076.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.13-17204T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17914650 | |||||||
chr7:17914721 | G | A | 1 | a0001c0001t0014g0019 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.13-17275C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17914721 | |||||||
chr7:17914722 | G | A | 1 | a0001c0001t0002g0334 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.13-17276C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17914722 | |||||||
chr7:17914933 | T | C | 1 | a0001c0001t0001g0044 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.13-17487A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17914933 | |||||||
chr7:17914952 | T | C | 9 | a0001c0001t0001g0211 a0001c0001t0001g0314 a0001c0001t0001g0315 others(6): Show |
9 | HG00642.hp1 HG01069.hp1 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.13-17506A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17914952 | |||||||
chr7:17914964 | C | T | 1 | a0001c0002t0001g0258 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.13-17518G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17914964 | |||||||
chr7:17915028 | T | C | 1 | a0001c0001t0020g0191 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.13-17582A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17915028 | |||||||
chr7:17915274 | C | T | 2 | a0001c0001t0013g0015 a0001c0001t0013g0239 |
2 | HG01952.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.13-17828G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17915274 | |||||||
chr7:17915402 | T | C | 157 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(154): Show |
160 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.13-17956A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17915402 | |||||||
chr7:17915403 | G | C | 157 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(154): Show |
160 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.13-17957C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17915403 | |||||||
chr7:17915453 | G | A | 157 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(154): Show |
160 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.13-18007C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17915453 | |||||||
chr7:17915456 | A | T | 1 | a0001c0010t0014g0020 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.13-18010T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17915456 | |||||||
chr7:17915460 | A | G | 157 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(154): Show |
160 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.13-18014T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17915460 | |||||||
chr7:17915609 | CTCTG | C | 157 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(154): Show |
160 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.13-18167_13-18164d others(6): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17915609 | |||||||
chr7:17915627 | CTG | C | 9 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0008 others(6): Show |
9 | HG01074.hp1 HG02055.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.13-18183_13-18182d others(4): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17915627 | |||||||
chr7:17915629 | G | C | 2 | a0001c0006t0025g0005 a0001c0011t0006g0017 |
2 | HG02280.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.13-18183C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17915629 | |||||||
chr7:17915671 | C | T | 157 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(154): Show |
160 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.13-18225G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17915671 | |||||||
chr7:17915687 | G | C | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(161): Show |
167 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.13-18241C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17915687 | |||||||
chr7:17915778 | A | C | 1 | a0001c0006t0025g0005 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.13-18332T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17915778 | |||||||
chr7:17915800 | T | C | 2 | a0001c0001t0013g0015 a0001c0001t0013g0239 |
2 | HG01952.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.13-18354A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17915800 | |||||||
chr7:17915975 | C | A | 173 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(170): Show |
176 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.13-18529G>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17915975 | |||||||
chr7:17916191 | T | TAGAC | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(161): Show |
167 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.13-18749_13-18746d others(6): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17916191 | |||||||
chr7:17916252 | C | T | 1 | a0001c0001t0026g0249 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.13-18806G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17916252 | |||||||
chr7:17916538 | C | T | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(161): Show |
167 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.13-19092G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17916538 | |||||||
chr7:17916648 | T | C | 1 | a0001c0001t0001g0225 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.13-19202A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17916648 | |||||||
chr7:17916680 | C | CA | 7 | a0001c0001t0001g0085 a0001c0001t0001g0145 a0001c0001t0004g0117 others(4): Show |
7 | HG00609.hp1 HG01993.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.13-19235dupT | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17916680 | |||||||
chr7:17916836 | C | T | 7 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0013g0015 others(4): Show |
7 | HG01952.hp1 HG02293.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.13-19390G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17916836 | |||||||
chr7:17916878 | C | T | 7 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0013g0015 others(4): Show |
7 | HG01952.hp1 HG02293.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.13-19432G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17916878 | |||||||
chr7:17916896 | C | G | 1 | a0001c0001t0001g0174 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.13-19450G>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17916896 | |||||||
chr7:17916900 | T | C | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
168 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.13-19454A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17916900 | |||||||
chr7:17917012 | T | G | 2 | a0001c0001t0013g0015 a0001c0001t0013g0239 |
2 | HG01952.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.13-19566A>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17917012 | |||||||
chr7:17917044 | C | T | 2 | a0001c0002t0002g0323 a0001c0002t0002g0327 |
2 | NA18952.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.13-19598G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17917044 | |||||||
chr7:17917065 | T | C | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(163): Show |
169 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.13-19619A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17917065 | |||||||
chr7:17917081 | T | C | 6 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0008 others(3): Show |
6 | HG01074.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.13-19635A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17917081 | |||||||
chr7:17917339 | G | A | 12 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0021 others(9): Show |
14 | HG01168.hp2 HG01169.hp1 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.13-19893C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17917339 | |||||||
chr7:17917410 | T | G | 1 | a0001c0002t0002g0248 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.13-19964A>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17917410 | |||||||
chr7:17917417 | A | G | 17 | a0001c0001t0001g0066 a0001c0001t0001g0068 a0001c0001t0001g0074 others(14): Show |
17 | HG00408.hp1 HG00544.hp2 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.13-19971T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17917417 | |||||||
chr7:17917631 | C | T | 1 | a0001c0001t0008g0006 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.13-20185G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17917631 | |||||||
chr7:17917710 | C | T | 1 | a0001c0002t0002g0305 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.13-20264G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17917710 | |||||||
chr7:17917847 | C | T | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(155): Show |
161 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.13-20401G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17917847 | |||||||
chr7:17917864 | G | C | 1 | a0001c0011t0006g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.13-20418C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17917864 | |||||||
chr7:17917925 | C | G | 1 | a0001c0001t0001g0021 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.13-20479G>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17917925 | |||||||
chr7:17918435 | GA | G | 158 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(155): Show |
158 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.13-20990delT | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17918435 | |||||||
chr7:17918435 | GAA | G | 10 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0008 others(7): Show |
10 | HG01074.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.13-20991_13-20990d others(4): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17918435 | |||||||
chr7:17918509 | T | C | 4 | a0001c0001t0001g0032 a0001c0001t0001g0045 a0001c0001t0001g0046 others(1): Show |
4 | HG03041.hp2 HG03486.hp2 NA20805.hp2 others(1): Show |
intron_variant | MODIFIER | c.13-21063A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17918509 | |||||||
chr7:17918662 | T | A | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(166): Show |
172 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.13-21216A>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17918662 | |||||||
chr7:17918804 | T | C | 1 | a0001c0001t0001g0225 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.13-21358A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17918804 | |||||||
chr7:17919305 | T | A | 1 | a0001c0001t0001g0122 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.12+20979A>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17919305 | |||||||
chr7:17919437 | A | G | 1 | a0001c0002t0002g0241 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.12+20847T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17919437 | |||||||
chr7:17919457 | A | G | 1 | a0001c0002t0002g0057 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.12+20827T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17919457 | |||||||
chr7:17919511 | C | A | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(161): Show |
167 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.12+20773G>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17919511 | |||||||
chr7:17919767 | C | T | 1 | a0001c0002t0024g0257 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.12+20517G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17919767 | |||||||
chr7:17919880 | C | G | 1 | a0001c0006t0025g0005 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.12+20404G>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17919880 | |||||||
chr7:17919894 | G | A | 1 | a0001c0010t0014g0020 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.12+20390C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17919894 | |||||||
chr7:17919982 | A | G | 2 | a0001c0001t0005g0012 a0001c0001t0005g0013 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.12+20302T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17919982 | |||||||
chr7:17920067 | G | C | 1 | a0001c0001t0001g0243 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.12+20217C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17920067 | |||||||
chr7:17920078 | C | T | 2 | a0001c0001t0001g0072 a0001c0001t0001g0230 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.12+20206G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17920078 | |||||||
chr7:17920227 | A | T | 1 | a0001c0001t0001g0122 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.12+20057T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17920227 | |||||||
chr7:17920538 | A | T | 18 | a0001c0001t0001g0132 a0001c0001t0001g0135 a0001c0001t0001g0183 others(15): Show |
18 | HG00544.hp1 HG00735.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.12+19746T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17920538 | |||||||
chr7:17920733 | T | C | 1 | a0001c0008t0002g0324 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.12+19551A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17920733 | |||||||
chr7:17920887 | C | T | 1 | a0001c0001t0001g0122 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.12+19397G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17920887 | |||||||
chr7:17920954 | T | C | 1 | a0001c0001t0001g0102 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.12+19330A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17920954 | |||||||
chr7:17921051 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.12+19233G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17921051 | |||||||
chr7:17921181 | C | A | 1 | a0001c0001t0001g0235 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.12+19103G>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17921181 | |||||||
chr7:17921204 | T | A | 133 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0031 others(130): Show |
134 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.12+19080A>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17921204 | |||||||
chr7:17921247 | T | G | 2 | a0001c0001t0005g0012 a0001c0001t0005g0013 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.12+19037A>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17921247 | |||||||
chr7:17921381 | A | G | 1 | a0001c0001t0001g0174 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.12+18903T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17921381 | |||||||
chr7:17921622 | T | C | 1 | a0001c0002t0001g0301 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.12+18662A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17921622 | |||||||
chr7:17922053 | C | T | 18 | a0001c0001t0001g0135 a0001c0001t0001g0183 a0001c0001t0001g0226 others(15): Show |
18 | HG00544.hp1 HG00735.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.12+18231G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17922053 | |||||||
chr7:17922072 | T | C | 3 | a0001c0001t0001g0135 a0001c0001t0020g0191 a0001c0001t0021g0134 |
3 | HG02280.hp1 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.12+18212A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17922072 | |||||||
chr7:17922227 | C | T | 3 | a0001c0004t0011g0014 a0001c0004t0011g0016 a0001c0004t0011g0067 |
3 | HG02622.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.12+18057G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17922227 | |||||||
chr7:17922432 | C | G | 2 | a0001c0001t0001g0240 a0001c0002t0001g0034 |
2 | HG00735.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.12+17852G>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17922432 | |||||||
chr7:17922759 | G | GA | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(217): Show |
223 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.12+17524dupT | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17922759 | |||||||
chr7:17923225 | A | G | 6 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0008 others(3): Show |
6 | HG01074.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.12+17059T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17923225 | |||||||
chr7:17923245 | T | C | 23 | a0001c0001t0001g0132 a0001c0001t0001g0173 a0001c0001t0001g0174 others(20): Show |
23 | HG00544.hp1 HG00673.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.12+17039A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17923245 | |||||||
chr7:17923416 | G | A | 1 | a0001c0002t0002g0303 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.12+16868C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17923416 | |||||||
chr7:17923550 | G | A | 1 | a0001c0002t0002g0213 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.12+16734C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17923550 | |||||||
chr7:17923732 | G | A | 3 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0170 |
4 | HG01261.hp1 HG01516.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.12+16552C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17923732 | |||||||
chr7:17923780 | G | A | 10 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0008 others(7): Show |
10 | HG01074.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.12+16504C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17923780 | |||||||
chr7:17923909 | T | G | 3 | a0001c0001t0012g0188 a0001c0001t0012g0189 a0001c0001t0012g0190 |
3 | HG02055.hp1 HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.12+16375A>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17923909 | |||||||
chr7:17923964 | T | C | 5 | a0001c0002t0002g0059 a0001c0002t0002g0220 a0001c0002t0002g0221 others(2): Show |
5 | HG01243.hp1 HG01884.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.12+16320A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17923964 | |||||||
chr7:17924211 | A | G | 1 | a0001c0001t0001g0148 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.12+16073T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17924211 | |||||||
chr7:17924241 | T | G | 6 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0008 others(3): Show |
6 | HG01074.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.12+16043A>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17924241 | |||||||
chr7:17924379 | T | C | 1 | a0001c0001t0001g0211 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.12+15905A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17924379 | |||||||
chr7:17924493 | A | G | 2 | a0001c0002t0002g0218 a0001c0002t0002g0255 |
2 | HG01943.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.12+15791T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17924493 | |||||||
chr7:17924737 | G | A | 6 | a0001c0002t0002g0218 a0001c0002t0002g0255 a0001c0002t0002g0308 others(3): Show |
6 | HG01109.hp2 HG01169.hp2 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.12+15547C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17924737 | |||||||
chr7:17925057 | A | G | 3 | a0001c0004t0011g0014 a0001c0004t0011g0016 a0001c0004t0011g0067 |
3 | HG02622.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.12+15227T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17925057 | |||||||
chr7:17925133 | G | C | 1 | a0001c0001t0019g0143 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.12+15151C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17925133 | |||||||
chr7:17925189 | G | A | 1 | a0001c0001t0014g0019 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.12+15095C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17925189 | |||||||
chr7:17925217 | A | T | 1 | a0001c0001t0001g0178 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.12+15067T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17925217 | |||||||
chr7:17925221 | A | T | 5 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(2): Show |
5 | HG02451.hp1 HG02717.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.12+15063T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17925221 | |||||||
chr7:17925329 | A | C | 169 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(166): Show |
169 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.12+14955T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17925329 | |||||||
chr7:17925343 | C | T | 1 | a0001c0001t0005g0010 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.12+14941G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17925343 | |||||||
chr7:17925778 | A | G | 1 | a0001c0001t0001g0217 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.12+14506T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17925778 | |||||||
chr7:17925783 | G | GA | 10 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0008 others(7): Show |
10 | HG01074.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.12+14500dupT | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17925783 | |||||||
chr7:17925917 | T | C | 4 | a0001c0001t0001g0135 a0001c0001t0005g0012 a0001c0001t0005g0013 others(1): Show |
4 | HG02647.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.12+14367A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17925917 | |||||||
chr7:17925956 | G | A | 112 | a0001c0001t0001g0265 a0001c0001t0003g0192 a0001c0001t0003g0193 others(109): Show |
112 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.12+14328C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17925956 | |||||||
chr7:17925983 | G | A | 1 | a0001c0002t0002g0304 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.12+14301C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17925983 | |||||||
chr7:17926136 | A | AG | 169 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(166): Show |
169 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.12+14147dupC | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17926136 | |||||||
chr7:17926163 | G | C | 1 | a0001c0001t0001g0031 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.12+14121C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17926163 | |||||||
chr7:17926215 | G | A | 65 | a0001c0001t0001g0062 a0001c0001t0001g0069 a0001c0001t0001g0104 others(62): Show |
65 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.12+14069C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17926215 | |||||||
chr7:17926350 | C | A | 4 | a0001c0001t0004g0184 a0001c0001t0004g0185 a0001c0001t0004g0186 others(1): Show |
4 | HG00544.hp1 NA18974.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.12+13934G>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17926350 | |||||||
chr7:17926529 | C | A | 107 | a0001c0001t0001g0265 a0001c0001t0003g0192 a0001c0001t0003g0193 others(104): Show |
107 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.12+13755G>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17926529 | |||||||
chr7:17926677 | G | T | 1 | a0001c0011t0006g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.12+13607C>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17926677 | |||||||
chr7:17926678 | G | A | 4 | a0001c0001t0004g0184 a0001c0001t0004g0185 a0001c0001t0004g0186 others(1): Show |
4 | HG00544.hp1 NA18974.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.12+13606C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17926678 | |||||||
chr7:17926761 | C | T | 2 | a0001c0001t0001g0120 a0001c0001t0001g0121 |
2 | NA18943.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.12+13523G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17926761 | |||||||
chr7:17926783 | G | A | 1 | a0001c0001t0001g0031 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.12+13501C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17926783 | |||||||
chr7:17926841 | G | A | 3 | a0001c0001t0012g0188 a0001c0001t0012g0189 a0001c0001t0012g0190 |
3 | HG02055.hp1 HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.12+13443C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17926841 | |||||||
chr7:17926849 | G | A | 3 | a0001c0001t0012g0188 a0001c0001t0012g0189 a0001c0001t0012g0190 |
3 | HG02055.hp1 HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.12+13435C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17926849 | |||||||
chr7:17926919 | G | A | 1 | a0001c0006t0025g0005 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.12+13365C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17926919 | |||||||
chr7:17926929 | G | A | 165 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(162): Show |
165 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.12+13355C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17926929 | |||||||
chr7:17926995 | T | C | 6 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0008 others(3): Show |
6 | HG01074.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.12+13289A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17926995 | |||||||
chr7:17927029 | A | T | 2 | a0001c0001t0005g0012 a0001c0001t0005g0013 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.12+13255T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17927029 | |||||||
chr7:17927135 | C | T | 2 | a0001c0001t0001g0135 a0001c0001t0021g0134 |
2 | HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.12+13149G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17927135 | |||||||
chr7:17927181 | G | A | 3 | a0001c0001t0012g0188 a0001c0001t0012g0189 a0001c0001t0012g0190 |
3 | HG02055.hp1 HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.12+13103C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17927181 | |||||||
chr7:17927217 | A | G | 1 | a0001c0001t0001g0119 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.12+13067T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17927217 | |||||||
chr7:17927231 | G | GTA | 4 | a0001c0001t0001g0167 a0001c0004t0011g0014 a0001c0004t0011g0016 others(1): Show |
4 | HG02622.hp2 HG03139.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.12+13051_12+13052d others(4): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17927231 | |||||||
chr7:17927233 | A | G | 7 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0008 others(4): Show |
7 | HG01074.hp1 HG02622.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.12+13051T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17927233 | |||||||
chr7:17927246 | T | C | 1 | a0001c0008t0002g0324 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.12+13038A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17927246 | |||||||
chr7:17927305 | C | T | 3 | a0001c0001t0012g0188 a0001c0001t0012g0189 a0001c0001t0012g0190 |
3 | HG02055.hp1 HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.12+12979G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17927305 | |||||||
chr7:17927354 | C | T | 2 | a0001c0001t0001g0135 a0001c0001t0021g0134 |
2 | HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.12+12930G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17927354 | |||||||
chr7:17927784 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.12+12500T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17927784 | |||||||
chr7:17927825 | T | C | 63 | a0001c0001t0001g0062 a0001c0001t0001g0069 a0001c0001t0001g0103 others(60): Show |
63 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.12+12459A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17927825 | |||||||
chr7:17927935 | G | T | 1 | a0001c0002t0002g0248 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.12+12349C>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17927935 | |||||||
chr7:17928008 | A | C | 1 | a0001c0006t0025g0005 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.12+12276T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17928008 | |||||||
chr7:17928168 | C | T | 111 | a0001c0001t0001g0265 a0001c0001t0003g0192 a0001c0001t0003g0193 others(108): Show |
111 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.12+12116G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17928168 | |||||||
chr7:17928191 | G | GC | 3 | a0001c0001t0001g0061 a0001c0001t0001g0107 a0001c0001t0001g0108 |
3 | NA18946.hp1 NA18957.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.12+12092dupG | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17928191 | |||||||
chr7:17928233 | C | T | 1 | a0001c0001t0001g0033 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.12+12051G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17928233 | |||||||
chr7:17928418 | G | A | 3 | a0001c0001t0012g0188 a0001c0001t0012g0189 a0001c0001t0012g0190 |
3 | HG02055.hp1 HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.12+11866C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17928418 | |||||||
chr7:17928537 | C | G | 6 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0008 others(3): Show |
6 | HG01074.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.12+11747G>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17928537 | |||||||
chr7:17928582 | T | C | 43 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(40): Show |
43 | HG00280.hp2 HG00323.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.12+11702A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17928582 | |||||||
chr7:17928670 | C | T | 3 | a0001c0001t0012g0188 a0001c0001t0012g0189 a0001c0001t0012g0190 |
3 | HG02055.hp1 HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.12+11614G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17928670 | |||||||
chr7:17928713 | T | A | 1 | a0001c0001t0004g0112 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.12+11571A>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17928713 | |||||||
chr7:17928717 | T | C | 43 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(40): Show |
43 | HG00280.hp2 HG00323.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.12+11567A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17928717 | |||||||
chr7:17928972 | A | G | 12 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0021 others(9): Show |
14 | HG01168.hp2 HG01169.hp1 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.12+11312T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17928972 | |||||||
chr7:17928984 | C | T | 177 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(174): Show |
177 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.12+11300G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17928984 | |||||||
chr7:17928991 | C | T | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0021 others(243): Show |
248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.12+11293G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17928991 | |||||||
chr7:17928997 | T | TATAA | 177 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(174): Show |
177 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.12+11283_12+11286d others(6): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17928997 | |||||||
chr7:17929193 | A | C | 3 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0031g0242 |
3 | HG02257.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.12+11091T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17929193 | |||||||
chr7:17929226 | A | G | 2 | a0001c0001t0013g0015 a0001c0001t0013g0239 |
2 | HG01952.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.12+11058T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17929226 | |||||||
chr7:17929237 | G | C | 1 | a0001c0001t0001g0144 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.12+11047C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17929237 | |||||||
chr7:17929245 | T | G | 2 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
2 | HG03490.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.12+11039A>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17929245 | |||||||
chr7:17929493 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.12+10791G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17929493 | |||||||
chr7:17929526 | T | A | 12 | a0001c0002t0002g0209 a0001c0002t0002g0218 a0001c0002t0002g0255 others(9): Show |
12 | HG01069.hp2 HG01109.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.12+10758A>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17929526 | |||||||
chr7:17929527 | A | T | 13 | a0001c0001t0001g0068 a0001c0001t0001g0314 a0001c0001t0001g0315 others(10): Show |
13 | HG00642.hp1 HG01069.hp1 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.12+10757T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17929527 | |||||||
chr7:17929583 | G | A | 10 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0008 others(7): Show |
10 | HG01074.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.12+10701C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17929583 | |||||||
chr7:17929721 | T | C | 2 | a0001c0001t0016g0250 a0001c0001t0016g0251 |
2 | NA18962.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.12+10563A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17929721 | |||||||
chr7:17929914 | C | A | 166 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(163): Show |
166 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.12+10370G>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17929914 | |||||||
chr7:17929932 | G | C | 1 | a0001c0001t0001g0011 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.12+10352C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17929932 | |||||||
chr7:17929946 | T | C | 176 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(173): Show |
176 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.12+10338A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17929946 | |||||||
chr7:17930058 | GGAAATAA others(65): Show |
G | 1 | a0001c0004t0011g0067 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.12+10154_12+10225d others(74): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17930058 | |||||||
chr7:17930062 | A | G | 1 | a0001c0011t0006g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.12+10222T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17930062 | |||||||
chr7:17930074 | A | C | 164 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(161): Show |
164 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.12+10210T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17930074 | |||||||
chr7:17930075 | A | C | 164 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(161): Show |
164 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.12+10209T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17930075 | |||||||
chr7:17930076 | TAAGAAAA others(59): Show |
T | 164 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(161): Show |
164 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.12+10142_12+10207d others(68): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17930076 | |||||||
chr7:17930125 | A | T | 1 | a0001c0001t0001g0100 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.12+10159T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17930125 | |||||||
chr7:17930143 | A | C | 164 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(161): Show |
164 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.12+10141T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17930143 | |||||||
chr7:17930147 | T | G | 1 | a0001c0002t0002g0332 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.12+10137A>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17930147 | |||||||
chr7:17930151 | T | C | 1 | a0001c0001t0001g0133 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.12+10133A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17930151 | |||||||
chr7:17930277 | G | A | 111 | a0001c0001t0001g0265 a0001c0001t0003g0192 a0001c0001t0003g0193 others(108): Show |
111 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.12+10007C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17930277 | |||||||
chr7:17930423 | T | C | 17 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0008g0006 others(14): Show |
17 | HG01074.hp1 HG01952.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.12+9861A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17930423 | |||||||
chr7:17930580 | T | C | 6 | a0001c0001t0003g0252 a0001c0002t0002g0312 a0001c0002t0002g0313 others(3): Show |
6 | NA18952.hp1 NA18957.hp2 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.12+9704A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17930580 | |||||||
chr7:17930711 | G | T | 1 | a0001c0001t0004g0112 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.12+9573C>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17930711 | |||||||
chr7:17930913 | G | A | 2 | a0001c0001t0001g0162 a0001c0001t0001g0166 |
2 | NA19080.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.12+9371C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17930913 | |||||||
chr7:17930970 | C | A | 1 | a0001c0001t0005g0010 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.12+9314G>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17930970 | |||||||
chr7:17931087 | C | G | 160 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(157): Show |
160 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.12+9197G>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17931087 | |||||||
chr7:17931353 | TC | T | 144 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(141): Show |
144 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.12+8930delG | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17931353 | |||||||
chr7:17931355 | C | G | 144 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(141): Show |
144 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.12+8929G>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17931355 | |||||||
chr7:17931455 | C | A | 6 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0008 others(3): Show |
6 | HG01074.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.12+8829G>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17931455 | |||||||
chr7:17931596 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.12+8688G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17931596 | |||||||
chr7:17931601 | T | C | 108 | a0001c0001t0001g0265 a0001c0001t0002g0334 a0001c0001t0003g0192 others(105): Show |
108 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.12+8683A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17931601 | |||||||
chr7:17931641 | G | A | 17 | a0001c0001t0001g0003 a0001c0001t0001g0145 a0001c0001t0001g0146 others(14): Show |
18 | HG00609.hp1 HG00741.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.12+8643C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17931641 | |||||||
chr7:17931652 | G | C | 3 | a0001c0002t0023g0055 a0001c0002t0030g0056 a0001c0002t0032g0335 |
3 | HG02258.hp2 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.12+8632C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17931652 | |||||||
chr7:17931700 | A | G | 1 | a0001c0001t0005g0010 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.12+8584T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17931700 | |||||||
chr7:17931813 | G | T | 144 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(141): Show |
144 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.12+8471C>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17931813 | |||||||
chr7:17931940 | C | G | 1 | a0001c0002t0002g0241 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.12+8344G>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17931940 | |||||||
chr7:17932215 | C | T | 174 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(171): Show |
174 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.12+8069G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17932215 | |||||||
chr7:17932229 | C | T | 170 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(167): Show |
170 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.12+8055G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17932229 | |||||||
chr7:17932244 | T | C | 1 | a0001c0006t0025g0005 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.12+8040A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17932244 | |||||||
chr7:17932403 | A | G | 165 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(162): Show |
165 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.12+7881T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17932403 | |||||||
chr7:17932438 | T | C | 12 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0021 others(9): Show |
14 | HG01168.hp2 HG01169.hp1 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.12+7846A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17932438 | |||||||
chr7:17932442 | A | T | 14 | a0001c0001t0001g0183 a0001c0001t0004g0112 a0001c0001t0004g0113 others(11): Show |
14 | HG00544.hp1 HG00735.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.12+7842T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17932442 | |||||||
chr7:17932474 | T | C | 12 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0021 others(9): Show |
14 | HG01168.hp2 HG01169.hp1 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.12+7810A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17932474 | |||||||
chr7:17932479 | G | A | 12 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0021 others(9): Show |
14 | HG01168.hp2 HG01169.hp1 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.12+7805C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17932479 | |||||||
chr7:17932550 | T | C | 12 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0021 others(9): Show |
14 | HG01168.hp2 HG01169.hp1 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.12+7734A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17932550 | |||||||
chr7:17932610 | C | T | 1 | a0001c0002t0002g0241 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.12+7674G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17932610 | |||||||
chr7:17932648 | A | C | 2 | a0001c0001t0001g0171 a0001c0001t0001g0172 |
2 | HG02630.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.12+7636T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17932648 | |||||||
chr7:17932686 | A | C | 16 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0008g0006 others(13): Show |
16 | HG01074.hp1 HG01952.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.12+7598T>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17932686 | |||||||
chr7:17932689 | A | G | 2 | a0001c0001t0005g0012 a0001c0001t0005g0013 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.12+7595T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17932689 | |||||||
chr7:17932884 | A | G | 2 | a0001c0001t0005g0012 a0001c0001t0005g0013 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.12+7400T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17932884 | |||||||
chr7:17933104 | T | C | 2 | a0001c0002t0002g0247 a0001c0002t0002g0321 |
2 | HG00408.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.12+7180A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17933104 | |||||||
chr7:17933139 | G | A | 2 | a0001c0001t0001g0163 a0001c0001t0001g0231 |
2 | HG02055.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.12+7145C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17933139 | |||||||
chr7:17933262 | G | A | 17 | a0001c0001t0001g0003 a0001c0001t0001g0145 a0001c0001t0001g0146 others(14): Show |
18 | HG00609.hp1 HG00741.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.12+7022C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17933262 | |||||||
chr7:17933328 | C | G | 173 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(170): Show |
173 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.12+6956G>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17933328 | |||||||
chr7:17933362 | T | C | 184 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(181): Show |
184 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.12+6922A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17933362 | |||||||
chr7:17933393 | A | G | 1 | a0001c0001t0014g0019 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.12+6891T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17933393 | |||||||
chr7:17933458 | G | A | 1 | a0001c0002t0001g0322 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.12+6826C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17933458 | |||||||
chr7:17933468 | G | C | 1 | a0001c0001t0001g0164 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.12+6816C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17933468 | |||||||
chr7:17933479 | C | G | 177 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(174): Show |
177 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.12+6805G>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17933479 | |||||||
chr7:17933529 | C | G | 10 | a0001c0001t0001g0235 a0001c0001t0008g0006 a0001c0001t0008g0007 others(7): Show |
10 | HG01074.hp1 HG02055.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.12+6755G>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17933529 | |||||||
chr7:17933534 | C | A | 2 | a0001c0001t0005g0012 a0001c0001t0005g0013 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.12+6750G>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17933534 | |||||||
chr7:17933619 | C | G | 1 | a0001c0001t0001g0063 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.12+6665G>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17933619 | |||||||
chr7:17933652 | C | T | 1 | a0001c0001t0001g0070 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.12+6632G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17933652 | |||||||
chr7:17933716 | C | T | 2 | a0001c0001t0013g0015 a0001c0001t0013g0239 |
2 | HG01952.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.12+6568G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17933716 | |||||||
chr7:17933800 | G | GA | 159 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(156): Show |
159 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.12+6483dupT | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17933800 | |||||||
chr7:17933800 | GA | G | 43 | a0001c0001t0001g0062 a0001c0001t0001g0068 a0001c0001t0001g0069 others(40): Show |
43 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(40): Show |
intron_variant | MODIFIER | c.12+6483delT | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17933800 | |||||||
chr7:17934057 | T | G | 1 | a0001c0001t0004g0147 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.12+6227A>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17934057 | |||||||
chr7:17934085 | T | C | 5 | a0001c0001t0001g0106 a0001c0001t0001g0148 a0001c0001t0001g0149 others(2): Show |
5 | HG00140.hp1 HG01081.hp2 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.12+6199A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17934085 | |||||||
chr7:17934147 | A | G | 17 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0008g0006 others(14): Show |
17 | HG01074.hp1 HG01952.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.12+6137T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17934147 | |||||||
chr7:17934175 | G | A | 8 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(5): Show |
8 | HG01891.hp1 HG02451.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.12+6109C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17934175 | |||||||
chr7:17934280 | T | C | 170 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(167): Show |
170 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.12+6004A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17934280 | |||||||
chr7:17934467 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.12+5817T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17934467 | |||||||
chr7:17934475 | T | A | 2 | a0001c0002t0002g0323 a0001c0002t0002g0327 |
2 | NA18952.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.12+5809A>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17934475 | |||||||
chr7:17934518 | T | C | 42 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(39): Show |
42 | HG00280.hp2 HG00323.hp1 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.12+5766A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17934518 | |||||||
chr7:17934553 | G | C | 3 | a0001c0001t0001g0061 a0001c0001t0001g0107 a0001c0001t0001g0108 |
3 | NA18946.hp1 NA18957.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.12+5731C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17934553 | |||||||
chr7:17935029 | C | T | 2 | a0001c0004t0011g0014 a0001c0004t0011g0016 |
2 | NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.12+5255G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17935029 | |||||||
chr7:17935037 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.12+5247C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17935037 | |||||||
chr7:17935233 | G | A | 1 | a0001c0010t0014g0020 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.12+5051C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17935233 | |||||||
chr7:17935243 | T | C | 42 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(39): Show |
42 | HG00280.hp2 HG00323.hp1 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.12+5041A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17935243 | |||||||
chr7:17935474 | T | A | 1 | a0001c0011t0006g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.12+4810A>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17935474 | |||||||
chr7:17935503 | T | C | 183 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(180): Show |
183 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.12+4781A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17935503 | |||||||
chr7:17935780 | A | T | 1 | a0001c0001t0001g0111 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.12+4504T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17935780 | |||||||
chr7:17935898 | T | C | 1 | a0001c0010t0014g0020 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.12+4386A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17935898 | |||||||
chr7:17935960 | G | C | 3 | a0001c0002t0023g0055 a0001c0002t0030g0056 a0001c0002t0032g0335 |
3 | HG02258.hp2 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.12+4324C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17935960 | |||||||
chr7:17936092 | G | C | 1 | a0001c0001t0001g0110 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.12+4192C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17936092 | |||||||
chr7:17936490 | TTTA | T | 6 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0013g0015 others(3): Show |
6 | HG01952.hp1 HG02293.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.12+3791_12+3793del others(3): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17936490 | |||||||
chr7:17936726 | C | A | 1 | a0001c0001t0020g0191 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.12+3558G>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17936726 | |||||||
chr7:17936794 | A | G | 1 | a0001c0002t0006g0253 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.12+3490T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17936794 | |||||||
chr7:17936823 | GAAAAGAA others(5): Show |
G | 16 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0008g0006 others(13): Show |
16 | HG01074.hp1 HG01952.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.12+3449_12+3460del others(12): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17936823 | |||||||
chr7:17936899 | T | G | 1 | a0001c0011t0006g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.12+3385A>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17936899 | |||||||
chr7:17936930 | A | G | 1 | a0001c0001t0001g0066 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.12+3354T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17936930 | |||||||
chr7:17936994 | C | T | 1 | a0001c0001t0001g0065 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.12+3290G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17936994 | |||||||
chr7:17937009 | AT | A | 32 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(29): Show |
32 | HG00280.hp2 HG00323.hp1 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.12+3274delA | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17937009 | |||||||
chr7:17937010 | T | A | 18 | a0001c0001t0002g0018 a0001c0001t0005g0012 a0001c0001t0005g0013 others(15): Show |
18 | HG01074.hp1 HG01952.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.12+3274A>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17937010 | |||||||
chr7:17937011 | A | T | 17 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0008g0006 others(14): Show |
17 | HG01074.hp1 HG01952.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.12+3273T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17937011 | |||||||
chr7:17937020 | T | TA | 23 | a0001c0001t0001g0003 a0001c0001t0001g0030 a0001c0001t0001g0152 others(20): Show |
24 | HG00741.hp1 HG01168.hp1 HG01257.hp2 others(21): Show |
intron_variant | MODIFIER | c.12+3263dupT | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17937020 | |||||||
chr7:17937025 | A | T | 88 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(85): Show |
90 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.12+3259T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17937025 | |||||||
chr7:17937030 | A | T | 1 | a0001c0001t0001g0226 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.12+3254T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17937030 | |||||||
chr7:17937040 | A | G | 2 | a0001c0001t0005g0012 a0001c0001t0005g0013 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.12+3244T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17937040 | |||||||
chr7:17937076 | C | CA | 13 | a0001c0001t0001g0031 a0001c0001t0001g0054 a0001c0001t0001g0166 others(10): Show |
13 | HG00280.hp2 HG02040.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.12+3207dupT | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17937076 | |||||||
chr7:17937094 | A | G | 10 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0008 others(7): Show |
10 | HG01074.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.12+3190T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17937094 | |||||||
chr7:17937197 | C | A | 1 | a0001c0002t0002g0327 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.12+3087G>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17937197 | |||||||
chr7:17937243 | C | G | 16 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0008g0006 others(13): Show |
16 | HG01074.hp1 HG01952.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.12+3041G>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17937243 | |||||||
chr7:17937272 | T | C | 167 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(164): Show |
167 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.12+3012A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17937272 | |||||||
chr7:17937273 | G | A | 4 | a0001c0002t0009g0328 a0001c0002t0009g0329 a0001c0002t0009g0330 others(1): Show |
4 | NA18945.hp2 NA18981.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.12+3011C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17937273 | |||||||
chr7:17937285 | T | C | 1 | a0001c0001t0001g0167 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.12+2999A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17937285 | |||||||
chr7:17937431 | T | C | 123 | a0001c0001t0001g0211 a0001c0001t0001g0217 a0001c0001t0001g0265 others(120): Show |
123 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.12+2853A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17937431 | |||||||
chr7:17937513 | CA | C | 268 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(265): Show |
271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.12+2770delT | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17937513 | |||||||
chr7:17937513 | CAA | C | 23 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(20): Show |
23 | HG00408.hp2 HG01074.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.12+2769_12+2770del others(2): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17937513 | |||||||
chr7:17938122 | G | A | 1 | a0001c0002t0001g0214 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.12+2162C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17938122 | |||||||
chr7:17938326 | T | C | 3 | a0001c0002t0023g0055 a0001c0002t0030g0056 a0001c0002t0032g0335 |
3 | HG02258.hp2 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.12+1958A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17938326 | |||||||
chr7:17938372 | T | A | 2 | a0001c0001t0001g0181 a0001c0001t0003g0182 |
2 | HG00423.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.12+1912A>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17938372 | |||||||
chr7:17938384 | C | T | 6 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0008 others(3): Show |
6 | HG01074.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.12+1900G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17938384 | |||||||
chr7:17938401 | T | C | 1 | a0001c0001t0014g0019 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.12+1883A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17938401 | |||||||
chr7:17938506 | C | T | 142 | a0001c0001t0001g0211 a0001c0001t0001g0217 a0001c0001t0001g0265 others(139): Show |
142 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.12+1778G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17938506 | |||||||
chr7:17938585 | G | A | 1 | a0001c0001t0003g0215 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.12+1699C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17938585 | |||||||
chr7:17938589 | T | C | 123 | a0001c0001t0001g0211 a0001c0001t0001g0217 a0001c0001t0001g0265 others(120): Show |
123 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.12+1695A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17938589 | |||||||
chr7:17938625 | T | C | 5 | a0001c0001t0001g0183 a0001c0001t0004g0184 a0001c0001t0004g0185 others(2): Show |
5 | HG00544.hp1 HG02129.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.12+1659A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17938625 | |||||||
chr7:17938677 | G | A | 1 | a0001c0002t0006g0333 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.12+1607C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17938677 | |||||||
chr7:17938720 | G | C | 6 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0008 others(3): Show |
6 | HG01074.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.12+1564C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17938720 | |||||||
chr7:17938897 | C | G | 184 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0021 others(181): Show |
186 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.12+1387G>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17938897 | |||||||
chr7:17939036 | G | A | 5 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0008 others(2): Show |
5 | HG01074.hp1 HG02622.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.12+1248C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17939036 | |||||||
chr7:17939205 | T | C | 120 | a0001c0001t0001g0211 a0001c0001t0001g0217 a0001c0001t0001g0265 others(117): Show |
120 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.12+1079A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17939205 | |||||||
chr7:17939233 | C | T | 1 | a0001c0001t0001g0011 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.12+1051G>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17939233 | |||||||
chr7:17939433 | T | A | 5 | a0001c0001t0001g0219 a0001c0002t0002g0220 a0001c0002t0002g0221 others(2): Show |
5 | HG01884.hp2 HG02717.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.12+851A>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17939433 | |||||||
chr7:17939586 | A | G | 1 | a0001c0001t0005g0010 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.12+698T>C | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17939586 | |||||||
chr7:17939617 | A | T | 5 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0008 others(2): Show |
5 | HG01074.hp1 HG02280.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.12+667T>A | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17939617 | |||||||
chr7:17939919 | T | C | 2 | a0001c0001t0001g0224 a0001c0001t0001g0225 |
2 | HG02015.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.12+365A>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17939919 | |||||||
chr7:17939951 | G | A | 6 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(3): Show |
6 | HG02055.hp2 HG02257.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.12+333C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17939951 | |||||||
chr7:17939988 | G | A | 3 | a0001c0001t0001g0232 a0001c0001t0008g0234 a0001c0001t0010g0233 |
3 | HG01243.hp2 HG02622.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.12+296C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17939988 | |||||||
chr7:17940028 | G | C | 3 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0001g0237 |
3 | HG02109.hp1 HG02451.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.12+256C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17940028 | |||||||
chr7:17940053 | G | C | 1 | a0001c0001t0001g0238 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.12+231C>G | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17940053 | |||||||
chr7:17940170 | G | A | 98 | a0001c0001t0001g0003 a0001c0001t0001g0240 a0001c0001t0001g0243 others(95): Show |
99 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.12+114C>T | SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 1/25 | chr7 | 17940170 |