Item | Value |
---|---|
geneid | 343578 |
ensemblid | ENSG00000124143.11 |
hgncid | 16226 |
symbol | ARHGAP40 |
name | Rho GTPase activating protein 40 |
refseq_nuc | NM_001164431.3 |
refseq_prot | NP_001157903.2 |
ensembl_nuc | ENST00000373345.9 |
ensembl_prot | ENSP00000362442.5 |
mane_status | MANE Select |
chr | chr20 |
start | 38601809 |
end | 38650653 |
strand | + |
ver | v1.2 |
region | chr20:38601809-38650653 |
region5000 | chr20:38596809-38655653 |
regionname0 | ARHGAP40_chr20_38601809_38650653 |
regionname5000 | ARHGAP40_chr20_38596809_38655653 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 675 | 278 | 48 | 61 | 125 | 12 | 30 | 88 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | MAEPA others(670): Show |
chr20 | 38596809 | 38655653 |
a0002 | 0/0 | 675 | 16 | 6 | 3 | 0 | 2 | 5 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | MAEPA others(670): Show |
chr20 | 38596809 | 38655653 |
a0003 | 0/0 | 675 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | MAEPA others(670): Show |
chr20 | 38596809 | 38655653 |
a0004 | 0/0 | 675 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | MAEPA others(670): Show |
chr20 | 38596809 | 38655653 |
a0005 | 0/0 | 675 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | MAEPA others(670): Show |
chr20 | 38596809 | 38655653 |
a0006 | 0/0 | 675 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | MAEPA others(670): Show |
chr20 | 38596809 | 38655653 |
a0007 | 0/0 | 675 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | MAEPA others(670): Show |
chr20 | 38596809 | 38655653 |
a0008 | 0/0 | 675 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | MAEPA others(670): Show |
chr20 | 38596809 | 38655653 |
a0009 | 0/0 | 675 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | MAEPA others(670): Show |
chr20 | 38596809 | 38655653 |
a0010 | 0/0 | 675 | 3 | 0 | 0 | 0 | 0 | 3 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | MAEPA others(670): Show |
chr20 | 38596809 | 38655653 |
a0011 | 0/0 | 675 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | MAEPA others(670): Show |
chr20 | 38596809 | 38655653 |
a0012 | 0/0 | 675 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | MAEPA others(670): Show |
chr20 | 38596809 | 38655653 |
a0013 | 0/0 | 675 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | MAEPA others(670): Show |
chr20 | 38596809 | 38655653 |
a0014 | 0/0 | 675 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | MAEPA others(670): Show |
chr20 | 38596809 | 38655653 |
a0015 | 0/0 | 675 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | MAEPA others(670): Show |
chr20 | 38596809 | 38655653 |
a0016 | 0/0 | 675 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | MAEPA others(670): Show |
chr20 | 38596809 | 38655653 |
a0017 | 0/0 | 675 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | MAEPA others(670): Show |
chr20 | 38596809 | 38655653 |
a0018 | 0/0 | 675 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | MAESA others(670): Show |
chr20 | 38596809 | 38655653 |
a0019 | 0/0 | 675 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | MAEPA others(670): Show |
chr20 | 38596809 | 38655653 |
a0020 | 0/0 | 675 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | MAEPA others(670): Show |
chr20 | 38596809 | 38655653 |
a0021 | 0/0 | 675 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | MAEPA others(670): Show |
chr20 | 38596809 | 38655653 |
a0022 | 0/0 | 675 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | MAEPA others(670): Show |
chr20 | 38596809 | 38655653 |
a0023 | 0/0 | 675 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | MAEPA others(670): Show |
chr20 | 38596809 | 38655653 |
a0024 | 0/0 | 675 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | MAEPA others(670): Show |
chr20 | 38596809 | 38655653 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2025 | 196 | 21 | 38 | 99 | 10 | 26 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | ATGGC others(2020): Show |
chr20 | 38596809 | 38655653 | ||
a0001c0002 | 0/0 | 2025 | 59 | 6 | 21 | 26 | 2 | 4 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | ATGGC others(2020): Show |
chr20 | 38596809 | 38655653 | ||
a0001c0004 | 0/0 | 2025 | 6 | 6 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | ATGGC others(2020): Show |
chr20 | 38596809 | 38655653 | ||
a0001c0007 | 0/0 | 2025 | 5 | 5 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | ATGGC others(2020): Show |
chr20 | 38596809 | 38655653 | ||
a0001c0008 | 0/0 | 2025 | 5 | 5 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | ATGGC others(2020): Show |
chr20 | 38596809 | 38655653 | ||
a0001c0020 | 0/0 | 2025 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | ATGGC others(2020): Show |
chr20 | 38596809 | 38655653 | ||
a0001c0021 | 0/0 | 2025 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | ATGGC others(2020): Show |
chr20 | 38596809 | 38655653 | ||
a0001c0029 | 0/0 | 2025 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | ATGGC others(2020): Show |
chr20 | 38596809 | 38655653 | ||
a0001c0030 | 0/0 | 2025 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | ATGGC others(2020): Show |
chr20 | 38596809 | 38655653 | ||
a0001c0038 | 0/0 | 2025 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | ATGGC others(2020): Show |
chr20 | 38596809 | 38655653 | ||
a0002c0003 | 0/0 | 2025 | 15 | 5 | 3 | 0 | 2 | 5 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | ATGGC others(2020): Show |
chr20 | 38596809 | 38655653 | ||
a0002c0024 | 0/0 | 2025 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | ATGGC others(2020): Show |
chr20 | 38596809 | 38655653 | ||
a0003c0005 | 0/0 | 2025 | 6 | 6 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | ATGGC others(2020): Show |
chr20 | 38596809 | 38655653 | ||
a0003c0036 | 0/0 | 2025 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | ATGGC others(2020): Show |
chr20 | 38596809 | 38655653 | ||
a0004c0011 | 0/0 | 2025 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | ATGGC others(2020): Show |
chr20 | 38596809 | 38655653 | ||
a0004c0014 | 0/0 | 2025 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | ATGGC others(2020): Show |
chr20 | 38596809 | 38655653 | ||
a0005c0010 | 0/0 | 2025 | 4 | 3 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | ATGGC others(2020): Show |
chr20 | 38596809 | 38655653 | ||
a0005c0040 | 0/0 | 2025 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | ATGGC others(2020): Show |
chr20 | 38596809 | 38655653 | ||
a0006c0013 | 0/0 | 2025 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | ATGGC others(2020): Show |
chr20 | 38596809 | 38655653 | ||
a0006c0017 | 0/0 | 2025 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | ATGGC others(2020): Show |
chr20 | 38596809 | 38655653 | ||
a0007c0009 | 0/0 | 2025 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | ATGGC others(2020): Show |
chr20 | 38596809 | 38655653 | ||
a0007c0026 | 0/0 | 2025 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | ATGGC others(2020): Show |
chr20 | 38596809 | 38655653 | ||
a0008c0006 | 0/0 | 2025 | 5 | 5 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | ATGGC others(2020): Show |
chr20 | 38596809 | 38655653 | ||
a0009c0019 | 0/0 | 2025 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | ATGGC others(2020): Show |
chr20 | 38596809 | 38655653 | ||
a0009c0035 | 0/0 | 2025 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | ATGGC others(2020): Show |
chr20 | 38596809 | 38655653 | ||
a0010c0012 | 0/0 | 2025 | 3 | 0 | 0 | 0 | 0 | 3 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | ATGGC others(2020): Show |
chr20 | 38596809 | 38655653 | ||
a0011c0016 | 0/0 | 2025 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | ATGGC others(2020): Show |
chr20 | 38596809 | 38655653 | ||
a0012c0018 | 0/0 | 2025 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | ATGGC others(2020): Show |
chr20 | 38596809 | 38655653 | ||
a0013c0015 | 0/0 | 2025 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | ATGGC others(2020): Show |
chr20 | 38596809 | 38655653 | ||
a0014c0022 | 0/0 | 2025 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | ATGGC others(2020): Show |
chr20 | 38596809 | 38655653 | ||
a0015c0033 | 0/0 | 2025 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | ATGGC others(2020): Show |
chr20 | 38596809 | 38655653 | ||
a0016c0025 | 0/0 | 2025 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | ATGGC others(2020): Show |
chr20 | 38596809 | 38655653 | ||
a0017c0027 | 0/0 | 2025 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | ATGGC others(2020): Show |
chr20 | 38596809 | 38655653 | ||
a0018c0037 | 0/0 | 2025 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | ATGGC others(2020): Show |
chr20 | 38596809 | 38655653 | ||
a0019c0034 | 0/0 | 2025 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | ATGGC others(2020): Show |
chr20 | 38596809 | 38655653 | ||
a0020c0023 | 0/0 | 2025 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | ATGGC others(2020): Show |
chr20 | 38596809 | 38655653 | ||
a0021c0039 | 0/0 | 2025 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | ATGGC others(2020): Show |
chr20 | 38596809 | 38655653 | ||
a0022c0031 | 0/0 | 2025 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | ATGGC others(2020): Show |
chr20 | 38596809 | 38655653 | ||
a0023c0032 | 0/0 | 2025 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | ATGGC others(2020): Show |
chr20 | 38596809 | 38655653 | ||
a0024c0028 | 0/0 | 2025 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | ATGGC others(2020): Show |
chr20 | 38596809 | 38655653 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2967 | 68 | 5 | 11 | 38 | 5 | 9 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0001c0001t0002 | 0/0 | 2967 | 39 | 11 | 6 | 14 | 3 | 5 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0001c0001t0003 | 0/1 | 2967 | 62 | 3 | 15 | 33 | 2 | 8 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0001c0001t0004 | 0/0 | 2967 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0001c0001t0005 | 0/0 | 2967 | 5 | 0 | 0 | 2 | 0 | 3 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0001c0001t0006 | 1/0 | 2967 | 19 | 1 | 4 | 12 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0001c0001t0009 | 0/0 | 2967 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0001c0001t0014 | 0/0 | 2967 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0001c0002t0001 | 0/0 | 2967 | 11 | 0 | 0 | 10 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0001c0002t0002 | 0/0 | 2967 | 6 | 0 | 3 | 3 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0001c0002t0003 | 0/0 | 2967 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0001c0002t0004 | 0/0 | 2967 | 10 | 2 | 1 | 6 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0001c0002t0005 | 0/0 | 2967 | 18 | 0 | 11 | 4 | 2 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0001c0002t0007 | 0/0 | 2967 | 8 | 2 | 5 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0001c0002t0008 | 0/0 | 2965 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2960): Show |
chr20 | 38596809 | 38655653 |
a0001c0002t0009 | 0/0 | 2967 | 2 | 0 | 1 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0001c0002t0010 | 0/0 | 2967 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0001c0002t0015 | 0/0 | 2967 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0001c0004t0002 | 0/0 | 2967 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0001c0004t0004 | 0/0 | 2967 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0001c0004t0007 | 0/0 | 2967 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0001c0004t0016 | 0/0 | 2967 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0001c0007t0001 | 0/0 | 2967 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0001c0007t0002 | 0/0 | 2967 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0001c0008t0004 | 0/0 | 2967 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0001c0008t0006 | 0/0 | 2967 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0001c0008t0007 | 0/0 | 2967 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0001c0020t0003 | 0/0 | 2967 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0001c0021t0002 | 0/0 | 2967 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0001c0029t0003 | 0/0 | 2967 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0001c0030t0001 | 0/0 | 2967 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0001c0038t0002 | 0/0 | 2967 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0002c0003t0003 | 0/0 | 2967 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0002c0003t0004 | 0/0 | 2967 | 10 | 2 | 1 | 0 | 2 | 5 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0002c0003t0005 | 0/0 | 2967 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0002c0003t0006 | 0/0 | 2967 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0002c0024t0002 | 0/0 | 2967 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0003c0005t0001 | 0/0 | 2967 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0003c0005t0002 | 0/0 | 2967 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0003c0036t0002 | 0/0 | 2967 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0004c0011t0004 | 0/0 | 2967 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0004c0011t0007 | 0/0 | 2967 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0004c0014t0005 | 0/0 | 2967 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0005c0010t0010 | 0/0 | 2967 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0005c0010t0012 | 0/0 | 2967 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0005c0040t0004 | 0/0 | 2967 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0006c0013t0008 | 0/0 | 2965 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2960): Show |
chr20 | 38596809 | 38655653 |
a0006c0017t0008 | 0/0 | 2965 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2960): Show |
chr20 | 38596809 | 38655653 |
a0007c0009t0006 | 0/0 | 2967 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0007c0009t0013 | 0/0 | 2967 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0007c0026t0002 | 0/0 | 2967 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0008c0006t0002 | 0/0 | 2967 | 5 | 5 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0009c0019t0002 | 0/0 | 2967 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0009c0019t0007 | 0/0 | 2967 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0009c0035t0011 | 0/0 | 2965 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2960): Show |
chr20 | 38596809 | 38655653 |
a0010c0012t0007 | 0/0 | 2967 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0010c0012t0009 | 0/0 | 2967 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0011c0016t0004 | 0/0 | 2967 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0012c0018t0004 | 0/0 | 2967 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0013c0015t0005 | 0/0 | 2967 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0014c0022t0007 | 0/0 | 2967 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0015c0033t0002 | 0/0 | 2967 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0016c0025t0004 | 0/0 | 2967 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0017c0027t0001 | 0/0 | 2967 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0018c0037t0001 | 0/0 | 2967 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0019c0034t0007 | 0/0 | 2967 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0020c0023t0011 | 0/0 | 2965 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2960): Show |
chr20 | 38596809 | 38655653 |
a0021c0039t0013 | 0/0 | 2967 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0022c0031t0002 | 0/0 | 2967 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0023c0032t0005 | 0/0 | 2967 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
a0024c0028t0001 | 0/0 | 2967 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | AGTCC others(2962): Show |
chr20 | 38596809 | 38655653 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0004 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0001 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0002 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0003 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0019 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0211 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0005g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0005g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0005g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0005g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0005g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0006g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0006g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0006g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0006g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0006g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0006g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0006g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0006g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0006g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0006g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0006g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0006g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0006g0284 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0006g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0006g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0006g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0006g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0006g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0009g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0014g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0004g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0004g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0004g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0004g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0004g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0004g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0004g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0004g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0004g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0005g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0005g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0005g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0005g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0005g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0005g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0005g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0005g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0005g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0005g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0005g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0005g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0005g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0005g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0005g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0005g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0005g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0005g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0007g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0007g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0007g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0007g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0007g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0007g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0008g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0009g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0009g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0010g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0015g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0004t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0004t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0004t0004g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0004t0007g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0004t0007g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0004t0016g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0007t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0007t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0007t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0007t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0007t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0008t0004g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0008t0004g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0008t0006g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0008t0007g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0020t0003g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0020t0003g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0021t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0021t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0029t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0030t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0038t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0002c0003t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0002c0003t0004g0012 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0002c0003t0004g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0002c0003t0004g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0002c0003t0004g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0002c0003t0004g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0002c0003t0004g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0002c0003t0004g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0002c0003t0004g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0002c0003t0005g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0002c0003t0005g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0002c0003t0005g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0002c0003t0006g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0002c0024t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0003c0005t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0003c0005t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0003c0005t0002g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0003c0005t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0003c0005t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0003c0036t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0004c0011t0004g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0004c0011t0004g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0004c0011t0004g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0004c0011t0007g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0004c0014t0005g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0005c0010t0010g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0005c0010t0010g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0005c0010t0012g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0005c0010t0012g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0005c0040t0004g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0006c0013t0008g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0006c0013t0008g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0006c0017t0008g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0006c0017t0008g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0007c0009t0006g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0007c0009t0006g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0007c0009t0006g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0007c0009t0013g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0007c0026t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0008c0006t0002g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0008c0006t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0008c0006t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0008c0006t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0009c0019t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0009c0019t0007g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0009c0035t0011g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0010c0012t0007g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0010c0012t0007g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0010c0012t0009g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0011c0016t0004g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0011c0016t0004g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0012c0018t0004g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0012c0018t0004g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0013c0015t0005g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0013c0015t0005g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0014c0022t0007g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0015c0033t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0016c0025t0004g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0017c0027t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0018c0037t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0019c0034t0007g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0020c0023t0011g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0021c0039t0013g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0022c0031t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0023c0032t0005g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0024c0028t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | GBR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0139 | EUR | GBR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG00323 | hp1 | a0001 | c0001 | t0003 | g0193 | EUR | FIN | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0143 | EUR | FIN | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG00408 | hp1 | a0001 | c0001 | t0003 | g0144 | EAS | CHS | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG00408 | hp2 | a0001 | c0001 | t0003 | g0274 | EAS | CHS | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG00423 | hp1 | a0001 | c0001 | t0003 | g0152 | EAS | CHS | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | CHS | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | CHS | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | CHS | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG00544 | hp1 | a0001 | c0001 | t0003 | g0199 | EAS | CHS | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG00544 | hp2 | a0001 | c0001 | t0003 | g0253 | EAS | CHS | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG00558 | hp1 | a0001 | c0002 | t0003 | g0272 | EAS | CHS | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG00639 | hp1 | a0001 | c0001 | t0006 | g0029 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG00639 | hp2 | a0001 | c0002 | t0005 | g0219 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG00642 | hp1 | a0001 | c0001 | t0003 | g0230 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG00642 | hp2 | a0002 | c0003 | t0004 | g0300 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG00673 | hp1 | a0001 | c0002 | t0001 | g0164 | EAS | CHS | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG00673 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | CHS | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG00738 | hp2 | a0001 | c0001 | t0006 | g0091 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG00741 | hp1 | a0001 | c0002 | t0005 | g0127 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0071 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01069 | hp1 | a0001 | c0002 | t0005 | g0201 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01069 | hp2 | a0001 | c0002 | t0007 | g0009 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01070 | hp1 | a0001 | c0002 | t0005 | g0120 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01070 | hp2 | a0001 | c0001 | t0003 | g0019 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01071 | hp1 | a0001 | c0002 | t0005 | g0205 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01071 | hp2 | a0001 | c0002 | t0005 | g0204 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01074 | hp2 | a0001 | c0001 | t0003 | g0231 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01106 | hp1 | a0001 | c0002 | t0002 | g0062 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01106 | hp2 | a0001 | c0002 | t0005 | g0212 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01109 | hp1 | a0005 | c0010 | t0012 | g0128 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0208 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0106 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01167 | hp2 | a0001 | c0001 | t0006 | g0082 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01168 | hp1 | a0001 | c0002 | t0007 | g0009 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01168 | hp2 | a0001 | c0002 | t0005 | g0154 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01169 | hp1 | a0001 | c0001 | t0006 | g0090 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01169 | hp2 | a0001 | c0002 | t0007 | g0043 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01192 | hp1 | a0001 | c0001 | t0014 | g0258 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0060 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01243 | hp1 | a0001 | c0001 | t0003 | g0304 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01243 | hp2 | a0014 | c0022 | t0007 | g0100 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01256 | hp1 | a0001 | c0002 | t0005 | g0269 | AMR | CLM | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01256 | hp2 | a0015 | c0033 | t0002 | g0055 | AMR | CLM | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01261 | hp1 | a0006 | c0017 | t0008 | g0104 | AMR | CLM | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01261 | hp2 | a0001 | c0001 | t0003 | g0171 | AMR | CLM | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01346 | hp1 | a0001 | c0002 | t0005 | g0195 | AMR | CLM | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01346 | hp2 | a0001 | c0002 | t0005 | g0182 | AMR | CLM | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | CLM | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01361 | hp2 | a0009 | c0019 | t0002 | g0031 | AMR | CLM | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01433 | hp2 | a0002 | c0003 | t0003 | g0167 | AMR | CLM | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0249 | AMR | CLM | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01496 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0108 | EUR | IBS | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01515 | hp2 | a0001 | c0001 | t0003 | g0256 | EUR | IBS | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01516 | hp1 | a0001 | c0002 | t0005 | g0156 | EUR | IBS | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01516 | hp2 | a0002 | c0003 | t0004 | g0012 | EUR | IBS | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01517 | hp1 | a0002 | c0003 | t0004 | g0012 | EUR | IBS | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0109 | EUR | IBS | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01884 | hp1 | a0006 | c0013 | t0008 | g0027 | AFR | ACB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01884 | hp2 | a0016 | c0025 | t0004 | g0053 | AFR | ACB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01891 | hp1 | a0009 | c0019 | t0007 | g0307 | AFR | ACB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01891 | hp2 | a0006 | c0013 | t0008 | g0299 | AFR | ACB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01928 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01934 | hp1 | a0001 | c0002 | t0004 | g0089 | AMR | PEL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01934 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01943 | hp1 | a0001 | c0001 | t0003 | g0122 | AMR | PEL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01952 | hp1 | a0001 | c0001 | t0009 | g0114 | AMR | PEL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01952 | hp2 | a0017 | c0027 | t0001 | g0006 | AMR | PEL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01975 | hp2 | a0001 | c0001 | t0003 | g0241 | AMR | PEL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01978 | hp1 | a0001 | c0002 | t0002 | g0038 | AMR | PEL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01978 | hp2 | a0001 | c0002 | t0002 | g0033 | AMR | PEL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01993 | hp1 | a0002 | c0003 | t0006 | g0042 | AMR | PEL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02004 | hp1 | a0001 | c0002 | t0007 | g0013 | AMR | PEL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02004 | hp2 | a0001 | c0020 | t0003 | g0202 | AMR | PEL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | KHV | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02015 | hp2 | a0001 | c0001 | t0006 | g0292 | EAS | KHV | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02027 | hp2 | a0001 | c0001 | t0006 | g0061 | EAS | KHV | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02055 | hp1 | a0002 | c0003 | t0004 | g0079 | AFR | ACB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02055 | hp2 | a0001 | c0001 | t0004 | g0049 | AFR | ACB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02056 | hp1 | a0001 | c0002 | t0002 | g0093 | EAS | KHV | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02056 | hp2 | a0018 | c0037 | t0001 | g0183 | EAS | KHV | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02071 | hp1 | a0001 | c0002 | t0004 | g0302 | EAS | KHV | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02071 | hp2 | a0001 | c0001 | t0006 | g0210 | EAS | KHV | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02074 | hp1 | a0001 | c0001 | t0003 | g0248 | EAS | KHV | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02083 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02129 | hp2 | a0001 | c0002 | t0004 | g0088 | EAS | KHV | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02132 | hp1 | a0001 | c0001 | t0006 | g0160 | EAS | KHV | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0252 | EAS | KHV | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02145 | hp1 | a0019 | c0034 | t0007 | g0099 | AFR | ACB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | ACB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02148 | hp2 | a0001 | c0001 | t0003 | g0263 | AMR | PEL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02155 | hp1 | a0001 | c0001 | t0003 | g0176 | EAS | CDX | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | CDX | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02165 | hp1 | a0001 | c0001 | t0006 | g0001 | EAS | CDX | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02165 | hp2 | a0001 | c0002 | t0015 | g0270 | EAS | CDX | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02257 | hp1 | a0011 | c0016 | t0004 | g0084 | AFR | ACB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0174 | AFR | ACB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02258 | hp1 | a0001 | c0002 | t0004 | g0072 | AFR | ACB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02258 | hp2 | a0001 | c0002 | t0007 | g0080 | AFR | ACB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02273 | hp1 | a0001 | c0020 | t0003 | g0273 | AMR | PEL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02273 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02280 | hp1 | a0001 | c0001 | t0003 | g0220 | AFR | ACB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | ACB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02293 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02293 | hp2 | a0001 | c0002 | t0007 | g0013 | AMR | PEL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02300 | hp2 | a0001 | c0002 | t0009 | g0148 | AMR | PEL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02451 | hp1 | a0002 | c0003 | t0005 | g0177 | AFR | ACB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02451 | hp2 | a0001 | c0007 | t0001 | g0187 | AFR | ACB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02572 | hp1 | a0001 | c0008 | t0004 | g0305 | AFR | GWD | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02572 | hp2 | a0003 | c0005 | t0001 | g0137 | AFR | GWD | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02602 | hp1 | a0002 | c0003 | t0004 | g0291 | SAS | PJL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0083 | SAS | PJL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02622 | hp1 | a0020 | c0023 | t0011 | g0116 | AFR | GWD | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02622 | hp2 | a0001 | c0007 | t0002 | g0276 | AFR | GWD | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02630 | hp1 | a0004 | c0011 | t0004 | g0308 | AFR | GWD | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02630 | hp2 | a0007 | c0026 | t0002 | g0085 | AFR | GWD | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02647 | hp1 | a0001 | c0004 | t0007 | g0283 | AFR | GWD | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02647 | hp2 | a0012 | c0018 | t0004 | g0077 | AFR | GWD | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02683 | hp2 | a0001 | c0001 | t0003 | g0310 | SAS | PJL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02698 | hp1 | a0010 | c0012 | t0007 | g0097 | SAS | PJL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0102 | AFR | GWD | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02717 | hp2 | a0001 | c0007 | t0002 | g0036 | AFR | GWD | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02723 | hp1 | a0001 | c0007 | t0001 | g0240 | AFR | GWD | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02723 | hp2 | a0001 | c0008 | t0006 | g0282 | AFR | GWD | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02809 | hp1 | a0003 | c0036 | t0002 | g0076 | AFR | GWD | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02809 | hp2 | a0004 | c0011 | t0004 | g0309 | AFR | GWD | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02818 | hp1 | a0004 | c0014 | t0005 | g0023 | AFR | GWD | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0078 | AFR | GWD | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02886 | hp1 | a0001 | c0004 | t0007 | g0112 | AFR | GWD | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02886 | hp2 | a0008 | c0006 | t0002 | g0028 | AFR | GWD | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02895 | hp1 | a0007 | c0009 | t0006 | g0069 | AFR | GWD | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02895 | hp2 | a0008 | c0006 | t0002 | g0028 | AFR | GWD | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02896 | hp1 | a0008 | c0006 | t0002 | g0105 | AFR | GWD | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02896 | hp2 | a0005 | c0010 | t0012 | g0223 | AFR | GWD | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02897 | hp1 | a0008 | c0006 | t0002 | g0107 | AFR | GWD | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02897 | hp2 | a0007 | c0009 | t0006 | g0068 | AFR | GWD | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02922 | hp1 | a0003 | c0005 | t0002 | g0010 | AFR | ESN | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | ESN | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0101 | AFR | ESN | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02965 | hp2 | a0007 | c0009 | t0006 | g0067 | AFR | ESN | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02970 | hp1 | a0001 | c0004 | t0004 | g0044 | AFR | ESN | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02970 | hp2 | a0001 | c0030 | t0001 | g0225 | AFR | ESN | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02976 | hp1 | a0001 | c0002 | t0010 | g0081 | AFR | ESN | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02976 | hp2 | a0001 | c0021 | t0002 | g0281 | AFR | ESN | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03017 | hp1 | a0001 | c0001 | t0003 | g0017 | SAS | PJL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0135 | SAS | PJL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03041 | hp1 | a0013 | c0015 | t0005 | g0162 | AFR | GWD | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03041 | hp2 | a0001 | c0008 | t0004 | g0025 | AFR | GWD | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03098 | hp1 | a0001 | c0021 | t0002 | g0278 | AFR | MSL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03098 | hp2 | a0011 | c0016 | t0004 | g0039 | AFR | MSL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03130 | hp1 | a0003 | c0005 | t0002 | g0010 | AFR | ESN | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03130 | hp2 | a0009 | c0035 | t0011 | g0123 | AFR | ESN | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03139 | hp2 | a0002 | c0024 | t0002 | g0050 | AFR | ESN | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03195 | hp1 | a0002 | c0003 | t0005 | g0132 | AFR | ESN | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | ESN | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | MSL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03209 | hp2 | a0005 | c0010 | t0010 | g0303 | AFR | MSL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03225 | hp1 | a0001 | c0007 | t0002 | g0092 | AFR | MSL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03225 | hp2 | a0001 | c0001 | t0006 | g0034 | AFR | MSL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03239 | hp2 | a0002 | c0003 | t0004 | g0293 | SAS | PJL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03453 | hp1 | a0012 | c0018 | t0004 | g0087 | AFR | MSL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03453 | hp2 | a0001 | c0008 | t0007 | g0277 | AFR | MSL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03486 | hp1 | a0004 | c0014 | t0005 | g0023 | AFR | MSL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03486 | hp2 | a0001 | c0008 | t0004 | g0025 | AFR | MSL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03491 | hp1 | a0002 | c0003 | t0004 | g0035 | SAS | PJL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03516 | hp1 | a0001 | c0002 | t0004 | g0070 | AFR | ESN | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03516 | hp2 | a0003 | c0005 | t0002 | g0046 | AFR | ESN | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03540 | hp1 | a0001 | c0038 | t0002 | g0306 | AFR | GWD | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03540 | hp2 | a0021 | c0039 | t0013 | g0280 | AFR | GWD | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03579 | hp1 | a0004 | c0011 | t0007 | g0288 | AFR | MSL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03579 | hp2 | a0005 | c0010 | t0010 | g0224 | AFR | MSL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03654 | hp1 | a0010 | c0012 | t0007 | g0059 | SAS | PJL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03654 | hp2 | a0001 | c0001 | t0003 | g0017 | SAS | PJL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03669 | hp1 | a0010 | c0012 | t0009 | g0236 | SAS | PJL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03669 | hp2 | a0001 | c0001 | t0003 | g0181 | SAS | PJL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03688 | hp1 | a0002 | c0003 | t0004 | g0026 | SAS | STU | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | STU | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03704 | hp2 | a0001 | c0001 | t0003 | g0173 | SAS | PJL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0040 | SAS | PJL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03831 | hp1 | a0001 | c0002 | t0007 | g0066 | SAS | BEB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03831 | hp2 | a0001 | c0002 | t0005 | g0264 | SAS | BEB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03834 | hp1 | a0001 | c0002 | t0004 | g0094 | SAS | BEB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03834 | hp2 | a0001 | c0001 | t0005 | g0251 | SAS | BEB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03927 | hp1 | a0001 | c0001 | t0006 | g0002 | SAS | BEB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03927 | hp2 | a0001 | c0002 | t0001 | g0215 | SAS | BEB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03942 | hp1 | a0001 | c0001 | t0005 | g0185 | SAS | BEB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03942 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | BEB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0175 | SAS | BEB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG04184 | hp2 | a0002 | c0003 | t0004 | g0026 | SAS | BEB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18522 | hp1 | a0002 | c0003 | t0005 | g0119 | AFR | YRI | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | YRI | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18612 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | CHB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | CHB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | CHB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18747 | hp2 | a0001 | c0001 | t0006 | g0001 | EAS | CHB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18906 | hp1 | a0008 | c0006 | t0002 | g0086 | AFR | YRI | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18906 | hp2 | a0001 | c0004 | t0002 | g0074 | AFR | YRI | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18941 | hp1 | a0001 | c0001 | t0006 | g0295 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18941 | hp2 | a0001 | c0002 | t0001 | g0184 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18945 | hp1 | a0001 | c0001 | t0003 | g0209 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18949 | hp2 | a0001 | c0001 | t0003 | g0262 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18950 | hp1 | a0001 | c0001 | t0003 | g0142 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18950 | hp2 | a0001 | c0001 | t0003 | g0133 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18951 | hp1 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18951 | hp2 | a0001 | c0001 | t0003 | g0157 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18954 | hp2 | a0001 | c0002 | t0001 | g0265 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18963 | hp2 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18964 | hp2 | a0001 | c0001 | t0003 | g0247 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18966 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18966 | hp2 | a0001 | c0002 | t0002 | g0111 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18967 | hp1 | a0001 | c0001 | t0003 | g0268 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18967 | hp2 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18968 | hp1 | a0001 | c0002 | t0001 | g0166 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18968 | hp2 | a0001 | c0001 | t0003 | g0189 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18969 | hp2 | a0001 | c0001 | t0005 | g0250 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18973 | hp1 | a0001 | c0002 | t0004 | g0056 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18975 | hp2 | a0001 | c0001 | t0006 | g0161 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18977 | hp1 | a0022 | c0031 | t0002 | g0286 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18977 | hp2 | a0001 | c0002 | t0005 | g0192 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18979 | hp2 | a0001 | c0001 | t0003 | g0261 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18981 | hp2 | a0001 | c0001 | t0006 | g0301 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18984 | hp1 | a0001 | c0001 | t0003 | g0229 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18995 | hp2 | a0001 | c0002 | t0009 | g0134 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18998 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18999 | hp1 | a0001 | c0002 | t0005 | g0163 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18999 | hp2 | a0001 | c0001 | t0006 | g0285 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19002 | hp1 | a0001 | c0002 | t0001 | g0125 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19012 | hp2 | a0001 | c0002 | t0004 | g0054 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19030 | hp1 | a0007 | c0009 | t0013 | g0041 | AFR | LWK | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19030 | hp2 | a0023 | c0032 | t0005 | g0227 | AFR | LWK | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19043 | hp1 | a0006 | c0017 | t0008 | g0045 | AFR | LWK | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | LWK | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19057 | hp1 | a0001 | c0002 | t0004 | g0032 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19057 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19058 | hp1 | a0001 | c0002 | t0005 | g0213 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19058 | hp2 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19060 | hp1 | a0001 | c0001 | t0003 | g0246 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19060 | hp2 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19063 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19063 | hp2 | a0001 | c0002 | t0004 | g0057 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19065 | hp1 | a0001 | c0001 | t0006 | g0298 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19068 | hp1 | a0001 | c0002 | t0001 | g0165 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19068 | hp2 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19070 | hp1 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19074 | hp1 | a0024 | c0028 | t0001 | g0115 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19074 | hp2 | a0001 | c0001 | t0003 | g0257 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19081 | hp1 | a0001 | c0001 | t0003 | g0191 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19086 | hp1 | a0001 | c0001 | t0005 | g0216 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19087 | hp2 | a0001 | c0002 | t0005 | g0214 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19089 | hp1 | a0001 | c0002 | t0002 | g0052 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19089 | hp2 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19090 | hp2 | a0001 | c0002 | t0001 | g0131 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19091 | hp1 | a0001 | c0001 | t0006 | g0058 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0103 | AFR | YRI | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | YRI | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0203 | AFR | ASW | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA20129 | hp2 | a0013 | c0015 | t0005 | g0245 | AFR | ASW | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0290 | EUR | TSI | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0169 | EUR | TSI | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0138 | EUR | TSI | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA20805 | hp2 | a0001 | c0002 | t0005 | g0200 | EUR | TSI | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | GIH | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA20905 | hp2 | a0001 | c0001 | t0005 | g0233 | SAS | GIH | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02109 | hp1 | a0001 | c0029 | t0003 | g0136 | AFR | ACB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02109 | hp2 | a0003 | c0005 | t0001 | g0194 | AFR | ACB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02486 | hp1 | a0001 | c0004 | t0016 | g0228 | AFR | ACB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02486 | hp2 | a0001 | c0002 | t0007 | g0051 | AFR | ACB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02559 | hp1 | a0004 | c0011 | t0004 | g0113 | AFR | ACB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02559 | hp2 | a0001 | c0002 | t0008 | g0073 | AFR | ACB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03471 | hp1 | a0001 | c0004 | t0002 | g0047 | AFR | MSL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03471 | hp2 | a0005 | c0040 | t0004 | g0279 | AFR | MSL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG06807 | hp1 | a0002 | c0003 | t0004 | g0030 | AFR | USA | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0048 | AFR | USA | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18955 | hp2 | a0001 | c0002 | t0001 | g0124 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | USA | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA20300 | hp2 | a0006 | c0013 | t0008 | g0027 | AFR | USA | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | LWK | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA21309 | hp2 | a0003 | c0005 | t0002 | g0075 | AFR | LWK | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0211 | REF | REF | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
homoSapiens | grch38p0 | a0001 | c0001 | t0006 | g0284 | REF | REF | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:38601952 | C | T | 1 | a0018 | 1 | HG02056.hp2 | missense_variant | MODERATE | c.10C>T | p.Pro4Ser | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/15 | 144/2967 | 10/2028 | 4/675 | chr20 | 38601952 | |||
chr20:38602019 | G | A | 1 | a0014 | 1 | HG01243.hp2 | missense_variant | MODERATE | c.77G>A | p.Arg26Gln | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/15 | 211/2967 | 77/2028 | 26/675 | chr20 | 38602019 | |||
chr20:38623364 | G | A | 1 | a0008 | 5 | HG02886.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
missense_variant | MODERATE | c.143G>A | p.Gly48Asp | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/15 | 277/2967 | 143/2028 | 48/675 | chr20 | 38623364 | |||
chr20:38623375 | G | A | 2 | a0002 a0013 |
18 | HG00642.hp2 HG01433.hp2 HG01516.hp2 others(15): Show |
missense_variant | MODERATE | c.154G>A | p.Gly52Ser | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/15 | 288/2967 | 154/2028 | 52/675 | chr20 | 38623375 | |||
chr20:38623379 | G | A | 3 | a0007 a0011 a0016 |
8 | HG01884.hp2 HG02257.hp1 HG02630.hp2 others(5): Show |
missense_variant | MODERATE | c.158G>A | p.Arg53Gln | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/15 | 292/2967 | 158/2028 | 53/675 | chr20 | 38623379 | |||
chr20:38623540 | G | A | 1 | a0010 | 3 | HG02698.hp1 HG03654.hp1 HG03669.hp1 |
missense_variant | MODERATE | c.319G>A | p.Glu107Lys | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/15 | 453/2967 | 319/2028 | 107/675 | chr20 | 38623540 | |||
chr20:38627126 | C | T | 2 | a0003 a0009 |
10 | HG01361.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
missense_variant | MODERATE | c.469C>T | p.Arg157Trp | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/15 | 603/2967 | 469/2028 | 157/675 | chr20 | 38627126 | |||
chr20:38628933 | T | A | 1 | a0017 | 1 | HG01952.hp2 | missense_variant | MODERATE | c.565T>A | p.Ser189Thr | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 4/15 | 699/2967 | 565/2028 | 189/675 | chr20 | 38628933 | |||
chr20:38629553 | A | G | 2 | a0004 a0020 |
7 | HG02559.hp1 HG02622.hp1 HG02630.hp1 others(4): Show |
missense_variant | MODERATE | c.686A>G | p.Asn229Ser | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/15 | 820/2967 | 686/2028 | 229/675 | chr20 | 38629553 | |||
chr20:38629619 | G | A | 1 | a0024 | 1 | NA19074.hp1 | missense_variant | MODERATE | c.752G>A | p.Gly251Asp | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/15 | 886/2967 | 752/2028 | 251/675 | chr20 | 38629619 | |||
chr20:38634765 | C | T | 3 | a0004 a0020 a0023 |
8 | HG02559.hp1 HG02622.hp1 HG02630.hp1 others(5): Show |
missense_variant | MODERATE | c.929C>T | p.Ala310Val | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/15 | 1063/2967 | 929/2028 | 310/675 | chr20 | 38634765 | |||
chr20:38639281 | G | A | 1 | a0015 | 1 | HG01256.hp2 | missense_variant | MODERATE | c.1174G>A | p.Glu392Lys | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/15 | 1308/2967 | 1174/2028 | 392/675 | chr20 | 38639281 | |||
chr20:38639303 | C | G | 1 | a0012 | 2 | HG02647.hp2 HG03453.hp1 |
missense_variant | MODERATE | c.1196C>G | p.Ser399Cys | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/15 | 1330/2967 | 1196/2028 | 399/675 | chr20 | 38639303 | |||
chr20:38639336 | C | T | 1 | a0013 | 2 | HG03041.hp1 NA20129.hp2 |
missense_variant | MODERATE | c.1229C>T | p.Pro410Leu | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/15 | 1363/2967 | 1229/2028 | 410/675 | chr20 | 38639336 | |||
chr20:38643737 | C | T | 2 | a0006 a0020 |
6 | HG01261.hp1 HG01884.hp1 HG01891.hp2 others(3): Show |
missense_variant | MODERATE | c.1396C>T | p.Arg466Trp | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/15 | 1530/2967 | 1396/2028 | 466/675 | chr20 | 38643737 | |||
chr20:38643747 | A | T | 2 | a0005 a0011 |
7 | HG01109.hp1 HG02257.hp1 HG02896.hp2 others(4): Show |
missense_variant | MODERATE | c.1406A>T | p.His469Leu | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/15 | 1540/2967 | 1406/2028 | 469/675 | chr20 | 38643747 | |||
chr20:38643813 | G | A | 1 | a0019 | 1 | HG02145.hp1 | missense_variant | MODERATE | c.1472G>A | p.Arg491Gln | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/15 | 1606/2967 | 1472/2028 | 491/675 | chr20 | 38643813 | |||
chr20:38643825 | T | C | 1 | a0016 | 1 | HG01884.hp2 | missense_variant | MODERATE | c.1484T>C | p.Leu495Pro | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/15 | 1618/2967 | 1484/2028 | 495/675 | chr20 | 38643825 | |||
chr20:38643887 | C | A | 2 | a0005 a0011 |
7 | HG01109.hp1 HG02257.hp1 HG02896.hp2 others(4): Show |
missense_variant | MODERATE | c.1546C>A | p.His516Asn | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/15 | 1680/2967 | 1546/2028 | 516/675 | chr20 | 38643887 | |||
chr20:38646065 | G | T | 1 | a0021 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.1588G>T | p.Ala530Ser | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 12/15 | 1722/2967 | 1588/2028 | 530/675 | chr20 | 38646065 | |||
chr20:38646101 | C | G | 1 | a0003 | 7 | HG02109.hp2 HG02572.hp2 HG02809.hp1 others(4): Show |
missense_variant | MODERATE | c.1624C>G | p.Arg542Gly | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 12/15 | 1758/2967 | 1624/2028 | 542/675 | chr20 | 38646101 | |||
chr20:38646146 | A | C | 1 | a0022 | 1 | NA18977.hp1 | missense_variant | MODERATE | c.1669A>C | p.Met557Leu | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 12/15 | 1803/2967 | 1669/2028 | 557/675 | chr20 | 38646146 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:38601948 | C | T | 5 | a0001c0008 a0001c0021 a0001c0038 others(2): Show |
10 | HG02572.hp1 HG02723.hp2 HG02976.hp2 others(7): Show |
synonymous_variant | LOW | c.6C>T | p.Ala2Ala | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/15 | 140/2967 | 6/2028 | 2/675 | chr20 | 38601948 | |||
chr20:38601957 | C | T | 5 | a0001c0008 a0001c0021 a0001c0038 others(2): Show |
10 | HG02572.hp1 HG02723.hp2 HG02976.hp2 others(7): Show |
synonymous_variant | LOW | c.15C>T | p.Ala5Ala | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/15 | 149/2967 | 15/2028 | 5/675 | chr20 | 38601957 | |||
chr20:38601969 | C | T | 1 | a0001c0020 | 2 | HG02004.hp2 HG02273.hp1 |
synonymous_variant | LOW | c.27C>T | p.Ala9Ala | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/15 | 161/2967 | 27/2028 | 9/675 | chr20 | 38601969 | |||
chr20:38601990 | C | T | 5 | a0001c0008 a0001c0021 a0001c0038 others(2): Show |
10 | HG02572.hp1 HG02723.hp2 HG02976.hp2 others(7): Show |
synonymous_variant | LOW | c.48C>T | p.Ala16Ala | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/15 | 182/2967 | 48/2028 | 16/675 | chr20 | 38601990 | |||
chr20:38623362 | T | G | 5 | a0001c0004 a0001c0021 a0004c0014 others(2): Show |
12 | HG01243.hp2 HG02486.hp1 HG02622.hp1 others(9): Show |
synonymous_variant | LOW | c.141T>G | p.Ser47Ser | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/15 | 275/2967 | 141/2028 | 47/675 | chr20 | 38623362 | |||
chr20:38628947 | C | G | 26 | a0001c0002 a0001c0004 a0001c0007 others(23): Show |
122 | HG00558.hp1 HG00639.hp2 HG00673.hp1 others(119): Show |
synonymous_variant | LOW | c.579C>G | p.Gly193Gly | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 4/15 | 713/2967 | 579/2028 | 193/675 | chr20 | 38628947 | |||
chr20:38634664 | A | C | 1 | a0006c0013 | 3 | HG01884.hp1 HG01891.hp2 NA20300.hp2 |
synonymous_variant | LOW | c.828A>C | p.Gly276Gly | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/15 | 962/2967 | 828/2028 | 276/675 | chr20 | 38634664 | |||
chr20:38637784 | G | A | 1 | a0001c0029 | 1 | HG02109.hp1 | synonymous_variant | LOW | c.1026G>A | p.Pro342Pro | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 7/15 | 1160/2967 | 1026/2028 | 342/675 | chr20 | 38637784 | |||
chr20:38643910 | G | A | 1 | a0003c0036 | 1 | HG02809.hp1 | splice_region_variant&synonymous_variant | LOW | c.1569G>A | p.Thr523Thr | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/15 | 1703/2967 | 1569/2028 | 523/675 | chr20 | 38643910 | |||
chr20:38647043 | C | T | 1 | a0016c0025 | 1 | HG01884.hp2 | synonymous_variant | LOW | c.1797C>T | p.His599His | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 13/15 | 1931/2967 | 1797/2028 | 599/675 | chr20 | 38647043 | |||
chr20:38648658 | G | A | 2 | a0001c0007 a0001c0030 |
6 | HG02451.hp2 HG02622.hp2 HG02717.hp2 others(3): Show |
synonymous_variant | LOW | c.1896G>A | p.Glu632Glu | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 14/15 | 2030/2967 | 1896/2028 | 632/675 | chr20 | 38648658 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:38601843 | C | A | 28 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(25): Show |
195 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(192): Show |
5_prime_UTR_variant | MODIFIER | c.-100C>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/15 | 100 | chr20 | 38601843 | ||||||
chr20:38649915 | C | T | 18 | a0001c0001t0004 a0001c0001t0005 a0001c0002t0004 others(15): Show |
67 | HG00639.hp2 HG00642.hp2 HG00741.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*67C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 15/15 | 67 | chr20 | 38649915 | ||||||
chr20:38649926 | A | C | 18 | a0001c0001t0004 a0001c0001t0005 a0001c0002t0004 others(15): Show |
67 | HG00639.hp2 HG00642.hp2 HG00741.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*78A>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 15/15 | 78 | chr20 | 38649926 | ||||||
chr20:38649948 | G | C | 7 | a0001c0002t0008 a0006c0013t0008 a0006c0017t0008 others(4): Show |
10 | HG01261.hp1 HG01884.hp1 HG01891.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*100G>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 15/15 | 100 | chr20 | 38649948 | ||||||
chr20:38649969 | T | A | 50 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(47): Show |
237 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(234): Show |
3_prime_UTR_variant | MODIFIER | c.*121T>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 15/15 | 121 | chr20 | 38649969 | ||||||
chr20:38650011 | CAG | C | 5 | a0001c0002t0008 a0006c0013t0008 a0006c0017t0008 others(2): Show |
8 | HG01261.hp1 HG01884.hp1 HG01891.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*164_*165delAG | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 15/15 | 164 | chr20 | 38650011 | ||||||
chr20:38650180 | T | C | 47 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(44): Show |
232 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(229): Show |
3_prime_UTR_variant | MODIFIER | c.*332T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 15/15 | 332 | chr20 | 38650180 | ||||||
chr20:38650303 | T | C | 61 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(58): Show |
258 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(255): Show |
3_prime_UTR_variant | MODIFIER | c.*455T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 15/15 | 455 | chr20 | 38650303 | ||||||
chr20:38650316 | A | C | 1 | a0001c0004t0016 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*468A>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 15/15 | 468 | chr20 | 38650316 | ||||||
chr20:38650456 | G | A | 1 | a0001c0002t0015 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*608G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 15/15 | 608 | chr20 | 38650456 | ||||||
chr20:38650612 | C | T | 62 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(59): Show |
259 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(256): Show |
3_prime_UTR_variant | MODIFIER | c.*764C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 15/15 | 764 | chr20 | 38650612 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:38602118 | C | T | 1 | a0001c0001t0003g0310 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.137+39C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38602118 | |||||||
chr20:38602124 | A | G | 2 | a0004c0011t0004g0308 a0004c0011t0004g0309 |
2 | HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.137+45A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38602124 | |||||||
chr20:38602185 | G | T | 1 | a0009c0019t0007g0307 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.137+106G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38602185 | |||||||
chr20:38602235 | G | T | 2 | a0001c0008t0004g0305 a0001c0038t0002g0306 |
2 | HG02572.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.137+156G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38602235 | |||||||
chr20:38602403 | G | T | 1 | a0001c0001t0003g0304 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.137+324G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38602403 | |||||||
chr20:38602407 | T | TAG | 288 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(285): Show |
322 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(319): Show |
intron_variant | MODIFIER | c.137+331_137+332dup others(2): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 38602407 | ||||||
chr20:38602439 | C | T | 9 | a0001c0008t0004g0025 a0001c0008t0004g0305 a0001c0008t0006g0282 others(6): Show |
10 | HG02572.hp1 HG02723.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.137+360C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38602439 | |||||||
chr20:38602442 | G | C | 3 | a0001c0001t0006g0029 a0004c0011t0004g0308 a0004c0011t0004g0309 |
3 | HG00639.hp1 HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.137+363G>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38602442 | |||||||
chr20:38602470 | T | A | 9 | a0001c0008t0004g0025 a0001c0008t0004g0305 a0001c0008t0006g0282 others(6): Show |
10 | HG02572.hp1 HG02723.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.137+391T>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38602470 | |||||||
chr20:38602740 | C | T | 2 | a0004c0011t0004g0308 a0004c0011t0004g0309 |
2 | HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.137+661C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38602740 | |||||||
chr20:38602918 | G | T | 1 | a0001c0007t0002g0276 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.137+839G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38602918 | |||||||
chr20:38603229 | G | A | 2 | a0004c0011t0004g0308 a0004c0011t0004g0309 |
2 | HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.137+1150G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38603229 | |||||||
chr20:38603333 | A | C | 182 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(179): Show |
204 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.137+1254A>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38603333 | |||||||
chr20:38603366 | A | G | 182 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(179): Show |
204 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.137+1287A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38603366 | |||||||
chr20:38603407 | GTCTA | G | 56 | a0001c0001t0001g0275 a0001c0001t0002g0011 a0001c0001t0002g0048 others(53): Show |
62 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.137+1382_137+1385d others(6): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 38603407 | ||||||
chr20:38603407 | GTCTATCT others(1): Show |
G | 39 | a0001c0001t0001g0098 a0001c0001t0002g0004 a0001c0001t0002g0078 others(36): Show |
43 | HG00642.hp2 HG00738.hp2 HG01167.hp2 others(40): Show |
intron_variant | MODIFIER | c.137+1378_137+1385d others(10): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 38603407 | ||||||
chr20:38603407 | GTCTATCT others(5): Show |
G | 19 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(16): Show |
22 | HG01167.hp1 HG01243.hp2 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.137+1374_137+1385d others(14): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 38603407 | ||||||
chr20:38603407 | GTCTATCT others(9): Show |
G | 1 | a0004c0011t0004g0113 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.137+1370_137+1385d others(18): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 38603407 | ||||||
chr20:38603451 | A | ATCTATCT others(9): Show |
1 | a0001c0001t0009g0114 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.137+1385_137+1386i others(18): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 38603451 | ||||||
chr20:38603451 | A | ATCTATCT others(5): Show |
31 | a0001c0001t0001g0018 a0001c0001t0001g0117 a0001c0001t0001g0118 others(28): Show |
34 | HG00140.hp2 HG00741.hp1 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.137+1383_137+1384i others(14): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 38603451 | ||||||
chr20:38603451 | A | ATCTATCT others(1): Show |
49 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0143 others(46): Show |
55 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(52): Show |
intron_variant | MODIFIER | c.137+1379_137+1380i others(10): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 38603451 | ||||||
chr20:38603451 | A | ATCTG | 59 | a0001c0001t0001g0006 a0001c0001t0001g0022 a0001c0001t0001g0190 others(56): Show |
65 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.137+1375_137+1376i others(6): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 38603451 | ||||||
chr20:38603451 | A | G | 41 | a0001c0001t0001g0007 a0001c0001t0001g0242 a0001c0001t0001g0243 others(38): Show |
48 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.137+1372A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38603451 | |||||||
chr20:38603517 | CCATCTAT others(5): Show |
C | 4 | a0004c0011t0007g0288 a0006c0013t0008g0027 a0006c0013t0008g0299 others(1): Show |
6 | HG01884.hp1 HG01891.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.137+1450_137+1461d others(14): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 38603517 | ||||||
chr20:38603584 | ATCTC | A | 87 | a0001c0001t0001g0098 a0001c0001t0002g0004 a0001c0001t0002g0008 others(84): Show |
97 | HG00438.hp2 HG00738.hp2 HG00741.hp2 others(94): Show |
intron_variant | MODIFIER | c.137+1513_137+1516d others(6): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 38603584 | ||||||
chr20:38603596 | GTCTC | G | 9 | a0001c0008t0004g0025 a0001c0008t0004g0305 a0001c0008t0006g0282 others(6): Show |
10 | HG02572.hp1 HG02723.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.137+1526_137+1529d others(6): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 38603596 | ||||||
chr20:38603877 | A | G | 9 | a0001c0008t0004g0025 a0001c0008t0004g0305 a0001c0008t0006g0282 others(6): Show |
10 | HG02572.hp1 HG02723.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.137+1798A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38603877 | |||||||
chr20:38603965 | A | G | 2 | a0001c0002t0008g0073 a0001c0004t0002g0074 |
2 | HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.137+1886A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38603965 | |||||||
chr20:38604068 | G | A | 2 | a0001c0001t0003g0142 a0001c0001t0003g0189 |
2 | NA18950.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.137+1989G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38604068 | |||||||
chr20:38604238 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.137+2159G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38604238 | |||||||
chr20:38604291 | G | A | 1 | a0001c0001t0001g0190 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.137+2212G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38604291 | |||||||
chr20:38604296 | A | G | 15 | a0001c0001t0001g0022 a0001c0001t0001g0139 a0001c0001t0001g0140 others(12): Show |
17 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(14): Show |
intron_variant | MODIFIER | c.137+2217A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38604296 | |||||||
chr20:38604397 | G | GT | 73 | a0001c0001t0001g0098 a0001c0001t0002g0004 a0001c0001t0002g0008 others(70): Show |
80 | HG00438.hp2 HG00738.hp2 HG00741.hp2 others(77): Show |
intron_variant | MODIFIER | c.137+2334dupT | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 38604397 | ||||||
chr20:38604533 | T | A | 3 | a0001c0001t0003g0144 a0001c0001t0003g0191 a0024c0028t0001g0115 |
3 | HG00408.hp1 NA19074.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.137+2454T>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38604533 | |||||||
chr20:38604540 | C | T | 9 | a0001c0008t0004g0025 a0001c0008t0004g0305 a0001c0008t0006g0282 others(6): Show |
10 | HG02572.hp1 HG02723.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.137+2461C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38604540 | |||||||
chr20:38604549 | C | T | 16 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(13): Show |
19 | HG01261.hp1 HG02055.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.137+2470C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38604549 | |||||||
chr20:38604615 | C | T | 1 | a0001c0002t0004g0302 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.137+2536C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38604615 | |||||||
chr20:38604976 | A | G | 66 | a0001c0001t0001g0098 a0001c0001t0002g0004 a0001c0001t0002g0008 others(63): Show |
71 | HG00438.hp2 HG00738.hp2 HG00741.hp2 others(68): Show |
intron_variant | MODIFIER | c.137+2897A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38604976 | |||||||
chr20:38605432 | A | T | 3 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0018c0037t0001g0183 |
3 | HG02056.hp2 NA18954.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.137+3353A>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38605432 | |||||||
chr20:38605517 | C | G | 1 | a0006c0017t0008g0045 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.137+3438C>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38605517 | |||||||
chr20:38605531 | T | C | 1 | a0001c0002t0005g0192 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.137+3452T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38605531 | |||||||
chr20:38605643 | C | T | 1 | a0001c0002t0001g0265 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.137+3564C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38605643 | |||||||
chr20:38605702 | T | A | 1 | a0001c0001t0003g0017 | 2 | HG03017.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.137+3623T>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38605702 | |||||||
chr20:38605718 | G | C | 1 | a0001c0001t0003g0193 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.137+3639G>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38605718 | |||||||
chr20:38605889 | C | CT | 9 | a0001c0008t0004g0025 a0001c0008t0004g0305 a0001c0008t0006g0282 others(6): Show |
10 | HG02572.hp1 HG02723.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.137+3819dupT | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 38605889 | ||||||
chr20:38605893 | T | C | 2 | a0001c0002t0007g0051 a0001c0002t0007g0080 |
2 | HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.137+3814T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38605893 | |||||||
chr20:38605955 | G | A | 4 | a0004c0011t0007g0288 a0006c0013t0008g0027 a0006c0013t0008g0299 others(1): Show |
6 | HG01884.hp1 HG01891.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.137+3876G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38605955 | |||||||
chr20:38606204 | A | G | 7 | a0001c0004t0004g0044 a0003c0005t0002g0010 a0003c0005t0002g0046 others(4): Show |
8 | HG01243.hp2 HG01361.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.137+4125A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38606204 | |||||||
chr20:38606385 | A | G | 2 | a0004c0011t0004g0308 a0004c0011t0004g0309 |
2 | HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.137+4306A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38606385 | |||||||
chr20:38606495 | A | G | 197 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(194): Show |
222 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.137+4416A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38606495 | |||||||
chr20:38606662 | C | A | 70 | a0001c0001t0001g0098 a0001c0001t0002g0004 a0001c0001t0002g0008 others(67): Show |
77 | HG00438.hp2 HG00738.hp2 HG00741.hp2 others(74): Show |
intron_variant | MODIFIER | c.137+4583C>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38606662 | |||||||
chr20:38606842 | C | T | 1 | a0001c0001t0001g0237 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.137+4763C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38606842 | |||||||
chr20:38606888 | G | C | 197 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(194): Show |
222 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.137+4809G>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38606888 | |||||||
chr20:38607050 | T | G | 21 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(18): Show |
25 | HG00639.hp1 HG01261.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.137+4971T>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38607050 | |||||||
chr20:38607097 | C | A | 70 | a0001c0001t0001g0098 a0001c0001t0002g0004 a0001c0001t0002g0008 others(67): Show |
77 | HG00438.hp2 HG00738.hp2 HG00741.hp2 others(74): Show |
intron_variant | MODIFIER | c.137+5018C>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38607097 | |||||||
chr20:38607098 | A | G | 2 | a0001c0001t0003g0263 a0001c0002t0005g0264 |
2 | HG02148.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.137+5019A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38607098 | |||||||
chr20:38607174 | G | A | 5 | a0001c0001t0006g0029 a0001c0007t0001g0240 a0003c0005t0001g0194 others(2): Show |
6 | HG00639.hp1 HG02109.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.137+5095G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38607174 | |||||||
chr20:38607183 | A | T | 1 | a0001c0001t0001g0275 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.137+5104A>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38607183 | |||||||
chr20:38607316 | A | G | 1 | a0010c0012t0009g0236 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.137+5237A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38607316 | |||||||
chr20:38607352 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.137+5273C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38607352 | |||||||
chr20:38607364 | C | A | 1 | a0004c0011t0004g0308 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.137+5285C>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38607364 | |||||||
chr20:38607442 | G | A | 1 | a0006c0017t0008g0045 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.137+5363G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38607442 | |||||||
chr20:38607507 | C | T | 1 | a0001c0007t0001g0187 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.137+5428C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38607507 | |||||||
chr20:38607552 | T | C | 7 | a0001c0002t0007g0009 a0001c0002t0007g0043 a0001c0004t0007g0283 others(4): Show |
9 | HG00642.hp2 HG01069.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.137+5473T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38607552 | |||||||
chr20:38607858 | A | G | 66 | a0001c0001t0001g0098 a0001c0001t0002g0004 a0001c0001t0002g0008 others(63): Show |
71 | HG00438.hp2 HG00738.hp2 HG00741.hp2 others(68): Show |
intron_variant | MODIFIER | c.137+5779A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38607858 | |||||||
chr20:38607939 | T | A | 1 | a0001c0001t0003g0241 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.137+5860T>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38607939 | |||||||
chr20:38608046 | AT | A | 5 | a0001c0001t0006g0029 a0001c0007t0001g0240 a0003c0005t0001g0194 others(2): Show |
6 | HG00639.hp1 HG02109.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.137+5973delT | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 38608046 | ||||||
chr20:38608163 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.137+6084T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38608163 | |||||||
chr20:38608226 | A | ACTC | 288 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(285): Show |
322 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(319): Show |
intron_variant | MODIFIER | c.137+6149_137+6150i others(5): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 38608226 | ||||||
chr20:38608262 | C | T | 16 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(13): Show |
19 | HG01261.hp1 HG02055.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.137+6183C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38608262 | |||||||
chr20:38608311 | T | G | 9 | a0001c0002t0008g0073 a0001c0004t0002g0074 a0001c0004t0004g0044 others(6): Show |
10 | HG01243.hp2 HG01361.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.137+6232T>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38608311 | |||||||
chr20:38608333 | A | G | 1 | a0003c0005t0001g0137 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.137+6254A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38608333 | |||||||
chr20:38608348 | A | G | 3 | a0002c0003t0004g0079 a0002c0024t0002g0050 a0004c0011t0004g0113 |
3 | HG02055.hp1 HG02559.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.137+6269A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38608348 | |||||||
chr20:38608370 | C | T | 1 | a0001c0002t0004g0072 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.137+6291C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38608370 | |||||||
chr20:38608449 | C | T | 1 | a0001c0002t0005g0182 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.137+6370C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38608449 | |||||||
chr20:38608504 | T | C | 186 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(183): Show |
208 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.137+6425T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38608504 | |||||||
chr20:38608660 | G | A | 1 | a0001c0002t0005g0195 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.137+6581G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38608660 | |||||||
chr20:38608745 | T | C | 4 | a0001c0007t0001g0240 a0003c0005t0001g0194 a0004c0014t0005g0023 others(1): Show |
5 | HG02109.hp2 HG02622.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.137+6666T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38608745 | |||||||
chr20:38608851 | G | A | 9 | a0001c0002t0008g0073 a0001c0004t0002g0074 a0001c0004t0004g0044 others(6): Show |
10 | HG01243.hp2 HG01361.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.137+6772G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38608851 | |||||||
chr20:38608854 | G | T | 2 | a0001c0002t0008g0073 a0001c0004t0002g0074 |
2 | HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.137+6775G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38608854 | |||||||
chr20:38608858 | A | G | 3 | a0001c0001t0002g0071 a0001c0004t0007g0112 a0007c0009t0013g0041 |
3 | HG00741.hp2 HG02886.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.137+6779A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38608858 | |||||||
chr20:38609155 | G | A | 16 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(13): Show |
19 | HG01261.hp1 HG02055.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.137+7076G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38609155 | |||||||
chr20:38609304 | A | C | 2 | a0004c0011t0004g0308 a0004c0011t0004g0309 |
2 | HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.137+7225A>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38609304 | |||||||
chr20:38609372 | A | G | 7 | a0001c0004t0004g0044 a0003c0005t0002g0010 a0003c0005t0002g0046 others(4): Show |
8 | HG01243.hp2 HG01361.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.137+7293A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38609372 | |||||||
chr20:38609671 | C | T | 1 | a0001c0001t0001g0235 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.137+7592C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38609671 | |||||||
chr20:38609775 | G | A | 20 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0117 others(17): Show |
22 | HG00423.hp1 HG01099.hp1 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.137+7696G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38609775 | |||||||
chr20:38609903 | A | T | 1 | a0001c0001t0001g0186 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.137+7824A>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38609903 | |||||||
chr20:38609945 | C | T | 4 | a0004c0011t0007g0288 a0006c0013t0008g0027 a0006c0013t0008g0299 others(1): Show |
6 | HG01884.hp1 HG01891.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.137+7866C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38609945 | |||||||
chr20:38610060 | C | T | 87 | a0001c0001t0001g0098 a0001c0001t0002g0004 a0001c0001t0002g0008 others(84): Show |
97 | HG00438.hp2 HG00738.hp2 HG00741.hp2 others(94): Show |
intron_variant | MODIFIER | c.137+7981C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38610060 | |||||||
chr20:38610110 | C | T | 1 | a0001c0001t0003g0310 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.137+8031C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38610110 | |||||||
chr20:38610134 | C | T | 1 | a0004c0011t0004g0308 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.137+8055C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38610134 | |||||||
chr20:38610135 | G | A | 1 | a0001c0002t0010g0081 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.137+8056G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38610135 | |||||||
chr20:38610171 | C | T | 4 | a0001c0002t0004g0070 a0007c0009t0006g0067 a0007c0009t0006g0068 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.137+8092C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38610171 | |||||||
chr20:38610251 | C | T | 180 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(177): Show |
202 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.137+8172C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38610251 | |||||||
chr20:38610363 | C | T | 1 | a0001c0029t0003g0136 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.137+8284C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38610363 | |||||||
chr20:38610446 | A | G | 2 | a0001c0001t0001g0022 a0001c0001t0005g0185 |
3 | HG03491.hp2 HG03492.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.137+8367A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38610446 | |||||||
chr20:38610524 | G | T | 268 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(265): Show |
300 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(297): Show |
intron_variant | MODIFIER | c.137+8445G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38610524 | |||||||
chr20:38610543 | G | A | 1 | a0001c0001t0003g0199 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.137+8464G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38610543 | |||||||
chr20:38610568 | T | C | 268 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(265): Show |
300 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(297): Show |
intron_variant | MODIFIER | c.137+8489T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38610568 | |||||||
chr20:38610664 | A | C | 16 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(13): Show |
19 | HG01261.hp1 HG02055.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.137+8585A>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38610664 | |||||||
chr20:38610710 | G | A | 1 | a0004c0011t0004g0309 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.137+8631G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38610710 | |||||||
chr20:38610775 | G | A | 1 | a0006c0017t0008g0045 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.137+8696G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38610775 | |||||||
chr20:38610883 | C | CT | 177 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(174): Show |
199 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.137+8815dupT | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 38610883 | ||||||
chr20:38610894 | T | C | 1 | a0001c0001t0006g0029 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.137+8815T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38610894 | |||||||
chr20:38610895 | C | T | 2 | a0001c0001t0003g0262 a0001c0002t0005g0154 |
2 | HG01168.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.137+8816C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38610895 | |||||||
chr20:38610896 | T | C | 1 | a0001c0002t0005g0154 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.137+8817T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38610896 | |||||||
chr20:38610924 | C | T | 1 | a0001c0002t0005g0195 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.137+8845C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38610924 | |||||||
chr20:38610993 | G | A | 9 | a0001c0008t0004g0025 a0001c0008t0004g0305 a0001c0008t0006g0282 others(6): Show |
10 | HG02572.hp1 HG02723.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.137+8914G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38610993 | |||||||
chr20:38611106 | T | A | 4 | a0004c0011t0007g0288 a0006c0013t0008g0027 a0006c0013t0008g0299 others(1): Show |
6 | HG01884.hp1 HG01891.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.137+9027T>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38611106 | |||||||
chr20:38611166 | G | A | 4 | a0004c0011t0007g0288 a0006c0013t0008g0027 a0006c0013t0008g0299 others(1): Show |
6 | HG01884.hp1 HG01891.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.137+9087G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38611166 | |||||||
chr20:38611293 | C | T | 2 | a0001c0001t0001g0098 a0001c0001t0002g0040 |
2 | HG03710.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.137+9214C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38611293 | |||||||
chr20:38611401 | G | A | 1 | a0013c0015t0005g0245 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.137+9322G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38611401 | |||||||
chr20:38611413 | C | CT | 244 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(241): Show |
274 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.137+9355dupT | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 38611413 | ||||||
chr20:38611413 | C | CTT | 6 | a0001c0001t0001g0198 a0001c0001t0001g0234 a0001c0001t0003g0261 others(3): Show |
6 | HG03710.hp1 HG03831.hp1 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.137+9354_137+9355d others(4): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 38611413 | ||||||
chr20:38611504 | A | C | 1 | a0010c0012t0007g0097 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.137+9425A>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38611504 | |||||||
chr20:38611555 | C | T | 1 | a0011c0016t0004g0039 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.137+9476C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38611555 | |||||||
chr20:38611563 | A | G | 270 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(267): Show |
302 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(299): Show |
intron_variant | MODIFIER | c.137+9484A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38611563 | |||||||
chr20:38611665 | G | A | 181 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(178): Show |
203 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.137+9586G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38611665 | |||||||
chr20:38611667 | G | A | 9 | a0001c0008t0004g0025 a0001c0008t0004g0305 a0001c0008t0006g0282 others(6): Show |
10 | HG02572.hp1 HG02723.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.137+9588G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38611667 | |||||||
chr20:38611672 | C | T | 1 | a0006c0017t0008g0045 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.137+9593C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38611672 | |||||||
chr20:38611721 | G | A | 5 | a0001c0001t0003g0246 a0001c0001t0003g0247 a0001c0001t0003g0261 others(2): Show |
5 | HG02004.hp2 HG02273.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.137+9642G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38611721 | |||||||
chr20:38611764 | T | C | 1 | a0001c0001t0003g0203 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.137+9685T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38611764 | |||||||
chr20:38611796 | G | C | 2 | a0001c0001t0003g0263 a0001c0002t0005g0264 |
2 | HG02148.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.137+9717G>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38611796 | |||||||
chr20:38611825 | C | T | 9 | a0001c0002t0008g0073 a0001c0004t0002g0074 a0001c0004t0004g0044 others(6): Show |
10 | HG01243.hp2 HG01361.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.137+9746C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38611825 | |||||||
chr20:38611894 | A | AT | 16 | a0001c0001t0001g0146 a0001c0001t0002g0008 a0001c0001t0002g0037 others(13): Show |
17 | HG00438.hp2 HG01106.hp1 HG01978.hp1 others(14): Show |
intron_variant | MODIFIER | c.137+9825dupT | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 38611894 | ||||||
chr20:38612094 | G | T | 279 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(276): Show |
312 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(309): Show |
intron_variant | MODIFIER | c.137+10015G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38612094 | |||||||
chr20:38612123 | A | G | 270 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(267): Show |
302 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(299): Show |
intron_variant | MODIFIER | c.137+10044A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38612123 | |||||||
chr20:38612234 | T | A | 2 | a0001c0002t0007g0051 a0001c0002t0007g0080 |
2 | HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.137+10155T>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38612234 | |||||||
chr20:38612597 | G | A | 1 | a0004c0014t0005g0023 | 2 | HG02818.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.137+10518G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38612597 | |||||||
chr20:38612626 | C | T | 1 | a0001c0001t0003g0181 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.137+10547C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38612626 | |||||||
chr20:38612691 | A | G | 3 | a0002c0003t0004g0079 a0002c0024t0002g0050 a0004c0011t0004g0113 |
3 | HG02055.hp1 HG02559.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.137+10612A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38612691 | |||||||
chr20:38612928 | A | C | 1 | a0001c0001t0001g0180 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.138-10431A>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38612928 | |||||||
chr20:38613049 | T | C | 1 | a0003c0005t0001g0194 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.138-10310T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38613049 | |||||||
chr20:38613187 | G | A | 7 | a0001c0002t0005g0120 a0001c0002t0005g0156 a0001c0002t0005g0182 others(4): Show |
7 | HG01070.hp1 HG01071.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.138-10172G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38613187 | |||||||
chr20:38613191 | G | A | 2 | a0004c0011t0004g0308 a0004c0011t0004g0309 |
2 | HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.138-10168G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38613191 | |||||||
chr20:38613410 | T | C | 3 | a0007c0026t0002g0085 a0011c0016t0004g0039 a0011c0016t0004g0084 |
3 | HG02257.hp1 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.138-9949T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38613410 | |||||||
chr20:38613488 | G | T | 4 | a0001c0002t0004g0070 a0007c0009t0006g0067 a0007c0009t0006g0068 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.138-9871G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38613488 | |||||||
chr20:38613557 | C | T | 1 | a0001c0001t0003g0261 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.138-9802C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38613557 | |||||||
chr20:38613577 | C | A | 1 | a0001c0001t0002g0110 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.138-9782C>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38613577 | |||||||
chr20:38613844 | C | G | 9 | a0001c0001t0002g0287 a0001c0001t0002g0289 a0001c0001t0002g0294 others(6): Show |
9 | NA18941.hp1 NA18949.hp1 NA18962.hp2 others(6): Show |
intron_variant | MODIFIER | c.138-9515C>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38613844 | |||||||
chr20:38614056 | T | C | 287 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(284): Show |
321 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(318): Show |
intron_variant | MODIFIER | c.138-9303T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38614056 | |||||||
chr20:38614073 | C | T | 1 | a0001c0001t0006g0298 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.138-9286C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38614073 | |||||||
chr20:38614098 | C | T | 1 | a0001c0002t0003g0272 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.138-9261C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38614098 | |||||||
chr20:38614310 | C | T | 1 | a0001c0001t0006g0061 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.138-9049C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38614310 | |||||||
chr20:38614321 | A | G | 286 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(283): Show |
319 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(316): Show |
intron_variant | MODIFIER | c.138-9038A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38614321 | |||||||
chr20:38614424 | A | G | 44 | a0001c0001t0001g0098 a0001c0001t0002g0004 a0001c0001t0002g0011 others(41): Show |
49 | HG00738.hp2 HG00741.hp2 HG01167.hp2 others(46): Show |
intron_variant | MODIFIER | c.138-8935A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38614424 | |||||||
chr20:38614523 | A | G | 1 | a0001c0007t0002g0276 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.138-8836A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38614523 | |||||||
chr20:38614620 | G | T | 8 | a0001c0008t0004g0025 a0001c0008t0004g0305 a0001c0008t0006g0282 others(5): Show |
9 | HG02572.hp1 HG02723.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.138-8739G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38614620 | |||||||
chr20:38614628 | A | G | 2 | a0004c0011t0004g0308 a0004c0011t0004g0309 |
2 | HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.138-8731A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38614628 | |||||||
chr20:38614952 | G | T | 1 | a0001c0004t0002g0074 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.138-8407G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38614952 | |||||||
chr20:38615004 | T | G | 1 | a0004c0011t0004g0308 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.138-8355T>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38615004 | |||||||
chr20:38615073 | C | T | 15 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(12): Show |
18 | HG01261.hp1 HG02055.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.138-8286C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38615073 | |||||||
chr20:38615106 | C | G | 1 | a0001c0002t0007g0066 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.138-8253C>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38615106 | |||||||
chr20:38615109 | A | G | 1 | a0001c0001t0001g0138 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.138-8250A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38615109 | |||||||
chr20:38615129 | C | T | 1 | a0001c0001t0001g0260 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.138-8230C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38615129 | |||||||
chr20:38615286 | C | T | 1 | a0006c0017t0008g0045 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.138-8073C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38615286 | |||||||
chr20:38615287 | G | A | 1 | a0001c0007t0001g0187 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.138-8072G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38615287 | |||||||
chr20:38615298 | T | G | 1 | a0003c0005t0002g0075 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.138-8061T>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38615298 | |||||||
chr20:38615360 | C | A | 1 | a0003c0005t0001g0137 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.138-7999C>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38615360 | |||||||
chr20:38615480 | G | A | 2 | a0004c0011t0004g0308 a0004c0011t0004g0309 |
2 | HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.138-7879G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38615480 | |||||||
chr20:38615737 | A | T | 35 | a0001c0001t0001g0098 a0001c0001t0002g0004 a0001c0001t0002g0011 others(32): Show |
39 | HG00738.hp2 HG01167.hp2 HG01169.hp1 others(36): Show |
intron_variant | MODIFIER | c.138-7622A>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38615737 | |||||||
chr20:38615748 | C | T | 1 | a0001c0001t0003g0133 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.138-7611C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38615748 | |||||||
chr20:38615909 | T | C | 1 | a0016c0025t0004g0053 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.138-7450T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38615909 | |||||||
chr20:38615945 | A | G | 4 | a0001c0002t0004g0070 a0007c0009t0006g0067 a0007c0009t0006g0068 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.138-7414A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38615945 | |||||||
chr20:38616064 | G | A | 1 | a0003c0005t0002g0075 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.138-7295G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38616064 | |||||||
chr20:38616251 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.138-7108C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38616251 | |||||||
chr20:38616270 | G | A | 1 | a0001c0001t0001g0266 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.138-7089G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38616270 | |||||||
chr20:38616274 | G | A | 2 | a0004c0011t0004g0308 a0004c0011t0004g0309 |
2 | HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.138-7085G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38616274 | |||||||
chr20:38616301 | G | A | 1 | a0001c0002t0010g0081 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.138-7058G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38616301 | |||||||
chr20:38616327 | C | T | 1 | a0001c0001t0002g0065 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.138-7032C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38616327 | |||||||
chr20:38616788 | T | C | 1 | a0003c0005t0002g0075 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.138-6571T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38616788 | |||||||
chr20:38616914 | G | A | 13 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(10): Show |
16 | HG01261.hp1 HG02055.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.138-6445G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38616914 | |||||||
chr20:38616935 | C | CTTTA | 157 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(154): Show |
174 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.138-6400_138-6397d others(6): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 38616935 | ||||||
chr20:38616935 | C | CTTTATTT others(1): Show |
55 | a0001c0001t0001g0121 a0001c0001t0001g0158 a0001c0001t0001g0159 others(52): Show |
65 | HG00408.hp2 HG00423.hp2 HG00738.hp2 others(62): Show |
intron_variant | MODIFIER | c.138-6404_138-6397d others(10): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 38616935 | ||||||
chr20:38616935 | C | CTTTATTT others(5): Show |
45 | a0001c0001t0001g0022 a0001c0001t0001g0139 a0001c0001t0001g0238 others(42): Show |
49 | HG00140.hp2 HG00438.hp2 HG01256.hp2 others(46): Show |
intron_variant | MODIFIER | c.138-6408_138-6397d others(14): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 38616935 | ||||||
chr20:38616935 | C | CTTTATTT others(9): Show |
5 | a0001c0001t0002g0011 a0001c0002t0002g0062 a0001c0008t0004g0305 others(2): Show |
6 | HG01106.hp1 HG01175.hp2 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.138-6412_138-6397d others(18): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 38616935 | ||||||
chr20:38616998 | T | C | 1 | a0001c0007t0001g0240 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.138-6361T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38616998 | |||||||
chr20:38617235 | C | T | 38 | a0001c0001t0001g0022 a0001c0001t0001g0139 a0001c0001t0001g0238 others(35): Show |
42 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.138-6124C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38617235 | |||||||
chr20:38617273 | G | A | 1 | a0003c0005t0002g0075 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.138-6086G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38617273 | |||||||
chr20:38617315 | A | G | 121 | a0001c0001t0001g0022 a0001c0001t0001g0139 a0001c0001t0001g0207 others(118): Show |
137 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.138-6044A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38617315 | |||||||
chr20:38617395 | C | T | 101 | a0001c0001t0001g0022 a0001c0001t0001g0139 a0001c0001t0001g0207 others(98): Show |
116 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.138-5964C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38617395 | |||||||
chr20:38617577 | CCACCTA | C | 8 | a0001c0008t0004g0025 a0001c0008t0004g0305 a0001c0008t0006g0282 others(5): Show |
9 | HG02572.hp1 HG02723.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.138-5781_138-5776d others(8): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38617577 | |||||||
chr20:38617584 | G | A | 8 | a0001c0008t0004g0025 a0001c0008t0004g0305 a0001c0008t0006g0282 others(5): Show |
9 | HG02572.hp1 HG02723.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.138-5775G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38617584 | |||||||
chr20:38617655 | G | A | 4 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0186 others(1): Show |
4 | HG00558.hp2 NA18965.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.138-5704G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38617655 | |||||||
chr20:38617672 | C | T | 3 | a0001c0007t0002g0036 a0001c0007t0002g0092 a0001c0007t0002g0276 |
3 | HG02622.hp2 HG02717.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.138-5687C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38617672 | |||||||
chr20:38617675 | G | A | 1 | a0001c0004t0002g0074 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.138-5684G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38617675 | |||||||
chr20:38617687 | T | TC | 10 | a0001c0004t0002g0074 a0001c0004t0004g0044 a0003c0005t0001g0137 others(7): Show |
11 | HG01243.hp2 HG01361.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.138-5671dupC | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 38617687 | ||||||
chr20:38617708 | C | T | 10 | a0001c0004t0002g0074 a0001c0004t0004g0044 a0003c0005t0001g0137 others(7): Show |
11 | HG01243.hp2 HG01361.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.138-5651C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38617708 | |||||||
chr20:38617757 | A | T | 1 | a0001c0001t0006g0029 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.138-5602A>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38617757 | |||||||
chr20:38617763 | G | T | 1 | a0001c0001t0001g0259 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.138-5596G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38617763 | |||||||
chr20:38617908 | G | A | 2 | a0004c0011t0004g0308 a0004c0011t0004g0309 |
2 | HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.138-5451G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38617908 | |||||||
chr20:38617922 | G | A | 5 | a0001c0002t0004g0070 a0001c0002t0008g0073 a0007c0009t0006g0067 others(2): Show |
5 | HG02559.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.138-5437G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38617922 | |||||||
chr20:38617951 | T | A | 5 | a0001c0002t0004g0070 a0001c0002t0008g0073 a0007c0009t0006g0067 others(2): Show |
5 | HG02559.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.138-5408T>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38617951 | |||||||
chr20:38617990 | G | A | 3 | a0001c0007t0002g0036 a0001c0007t0002g0092 a0001c0007t0002g0276 |
3 | HG02622.hp2 HG02717.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.138-5369G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38617990 | |||||||
chr20:38618100 | C | CTT | 7 | a0001c0002t0004g0070 a0001c0002t0008g0073 a0002c0003t0005g0119 others(4): Show |
7 | HG02451.hp1 HG02559.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.138-5245_138-5244d others(4): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 38618100 | ||||||
chr20:38618100 | CT | C | 12 | a0001c0001t0001g0207 a0001c0001t0003g0249 a0001c0001t0006g0058 others(9): Show |
13 | HG01243.hp2 HG01361.hp2 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.138-5244delT | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 38618100 | ||||||
chr20:38618256 | C | T | 1 | a0006c0017t0008g0045 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.138-5103C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38618256 | |||||||
chr20:38618267 | T | G | 13 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(10): Show |
16 | HG01261.hp1 HG02055.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.138-5092T>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38618267 | |||||||
chr20:38618299 | G | A | 82 | a0001c0001t0001g0022 a0001c0001t0001g0139 a0001c0001t0001g0207 others(79): Show |
94 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.138-5060G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38618299 | |||||||
chr20:38618342 | T | C | 297 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(294): Show |
333 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(330): Show |
intron_variant | MODIFIER | c.138-5017T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38618342 | |||||||
chr20:38618355 | C | T | 2 | a0001c0002t0002g0052 a0001c0002t0002g0111 |
2 | NA18966.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.138-5004C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38618355 | |||||||
chr20:38618403 | A | G | 122 | a0001c0001t0001g0022 a0001c0001t0001g0139 a0001c0001t0001g0207 others(119): Show |
138 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.138-4956A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38618403 | |||||||
chr20:38618483 | G | T | 10 | a0001c0004t0002g0074 a0001c0004t0004g0044 a0003c0005t0001g0137 others(7): Show |
11 | HG01243.hp2 HG01361.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.138-4876G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38618483 | |||||||
chr20:38618489 | C | G | 10 | a0001c0004t0002g0074 a0001c0004t0004g0044 a0003c0005t0001g0137 others(7): Show |
11 | HG01243.hp2 HG01361.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.138-4870C>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38618489 | |||||||
chr20:38618586 | G | A | 5 | a0001c0002t0004g0070 a0001c0002t0008g0073 a0007c0009t0006g0067 others(2): Show |
5 | HG02559.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.138-4773G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38618586 | |||||||
chr20:38618848 | C | T | 11 | a0001c0001t0006g0029 a0001c0004t0002g0074 a0001c0004t0004g0044 others(8): Show |
12 | HG00639.hp1 HG01243.hp2 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.138-4511C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38618848 | |||||||
chr20:38619028 | A | T | 1 | a0001c0001t0005g0233 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.138-4331A>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38619028 | |||||||
chr20:38619061 | G | A | 16 | a0001c0002t0004g0070 a0001c0002t0008g0073 a0001c0004t0002g0074 others(13): Show |
17 | HG01243.hp2 HG01361.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.138-4298G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38619061 | |||||||
chr20:38619122 | A | G | 17 | a0001c0002t0004g0070 a0001c0002t0008g0073 a0001c0004t0002g0074 others(14): Show |
18 | HG01243.hp2 HG01361.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.138-4237A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38619122 | |||||||
chr20:38619177 | C | T | 1 | a0001c0020t0003g0202 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.138-4182C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38619177 | |||||||
chr20:38619288 | T | C | 1 | a0001c0001t0003g0133 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.138-4071T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38619288 | |||||||
chr20:38619333 | C | T | 1 | a0001c0001t0003g0176 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.138-4026C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38619333 | |||||||
chr20:38619375 | A | C | 22 | a0001c0001t0002g0106 a0001c0001t0002g0287 a0001c0001t0002g0289 others(19): Show |
24 | HG00642.hp2 HG01167.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.138-3984A>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38619375 | |||||||
chr20:38619457 | T | A | 1 | a0002c0003t0005g0132 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.138-3902T>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38619457 | |||||||
chr20:38619527 | T | C | 1 | a0001c0001t0001g0098 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.138-3832T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38619527 | |||||||
chr20:38619530 | G | A | 1 | a0006c0013t0008g0027 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.138-3829G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38619530 | |||||||
chr20:38619728 | C | T | 1 | a0016c0025t0004g0053 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.138-3631C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38619728 | |||||||
chr20:38619729 | G | A | 5 | a0001c0004t0002g0047 a0004c0011t0004g0308 a0004c0011t0004g0309 others(2): Show |
5 | HG02630.hp1 HG02647.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.138-3630G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38619729 | |||||||
chr20:38619809 | A | G | 3 | a0001c0004t0002g0047 a0012c0018t0004g0077 a0012c0018t0004g0087 |
3 | HG02647.hp2 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.138-3550A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38619809 | |||||||
chr20:38619860 | G | T | 7 | a0001c0002t0004g0070 a0007c0009t0006g0067 a0007c0009t0006g0068 others(4): Show |
7 | HG02257.hp1 HG02630.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.138-3499G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38619860 | |||||||
chr20:38619881 | C | T | 1 | a0001c0002t0010g0081 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.138-3478C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38619881 | |||||||
chr20:38619922 | A | T | 1 | a0008c0006t0002g0107 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.138-3437A>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38619922 | |||||||
chr20:38619952 | A | G | 7 | a0001c0002t0004g0072 a0001c0008t0004g0025 a0001c0008t0004g0305 others(4): Show |
8 | HG02258.hp1 HG02572.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.138-3407A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38619952 | |||||||
chr20:38619987 | G | A | 1 | a0001c0001t0001g0118 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.138-3372G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38619987 | |||||||
chr20:38620041 | G | A | 1 | a0006c0013t0008g0027 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.138-3318G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38620041 | |||||||
chr20:38620210 | C | T | 1 | a0001c0001t0003g0175 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.138-3149C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38620210 | |||||||
chr20:38620442 | C | T | 4 | a0001c0001t0002g0008 a0001c0001t0002g0063 a0001c0001t0002g0064 others(1): Show |
5 | HG02155.hp2 NA18963.hp1 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.138-2917C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38620442 | |||||||
chr20:38620738 | G | A | 2 | a0004c0011t0004g0308 a0004c0011t0004g0309 |
2 | HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.138-2621G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38620738 | |||||||
chr20:38621066 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.138-2293G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38621066 | |||||||
chr20:38621101 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.138-2258G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38621101 | |||||||
chr20:38621295 | T | A | 1 | a0001c0001t0002g0101 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.138-2064T>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38621295 | |||||||
chr20:38621298 | T | G | 1 | a0001c0001t0002g0101 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.138-2061T>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38621298 | |||||||
chr20:38621655 | G | A | 9 | a0003c0005t0001g0137 a0003c0005t0001g0194 a0003c0005t0002g0010 others(6): Show |
10 | HG01361.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.138-1704G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38621655 | |||||||
chr20:38621683 | A | G | 1 | a0001c0002t0001g0131 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.138-1676A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38621683 | |||||||
chr20:38621749 | T | A | 9 | a0003c0005t0001g0137 a0003c0005t0001g0194 a0003c0005t0002g0010 others(6): Show |
10 | HG01361.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.138-1610T>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38621749 | |||||||
chr20:38621783 | A | G | 2 | a0004c0014t0005g0023 a0020c0023t0011g0116 |
3 | HG02622.hp1 HG02818.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.138-1576A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38621783 | |||||||
chr20:38621827 | G | A | 181 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0022 others(178): Show |
205 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.138-1532G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38621827 | |||||||
chr20:38621881 | C | G | 1 | a0023c0032t0005g0227 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.138-1478C>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38621881 | |||||||
chr20:38621986 | C | T | 1 | a0019c0034t0007g0099 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.138-1373C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38621986 | |||||||
chr20:38622053 | C | CA | 9 | a0003c0005t0001g0137 a0003c0005t0001g0194 a0003c0005t0002g0010 others(6): Show |
10 | HG01361.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.138-1300dupA | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 38622053 | ||||||
chr20:38622110 | T | TA | 11 | a0001c0001t0003g0175 a0001c0002t0004g0072 a0001c0008t0004g0025 others(8): Show |
12 | HG01109.hp1 HG02258.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.138-1249_138-1248i others(3): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38622110 | |||||||
chr20:38622111 | T | A | 98 | a0001c0001t0001g0022 a0001c0001t0001g0126 a0001c0001t0001g0139 others(95): Show |
102 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.138-1248T>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38622111 | |||||||
chr20:38622113 | T | A | 13 | a0001c0002t0008g0073 a0004c0011t0004g0113 a0006c0017t0008g0045 others(10): Show |
13 | HG01261.hp1 HG01884.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.138-1246T>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38622113 | |||||||
chr20:38622119 | T | A | 3 | a0001c0001t0001g0238 a0001c0001t0003g0133 a0001c0001t0003g0188 |
3 | NA18950.hp2 NA18964.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.138-1240T>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38622119 | |||||||
chr20:38622119 | TA | T | 15 | a0001c0004t0002g0047 a0001c0004t0002g0074 a0001c0004t0004g0044 others(12): Show |
17 | HG01243.hp2 HG02486.hp1 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.138-1235delA | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 38622119 | ||||||
chr20:38622198 | A | G | 1 | a0001c0001t0006g0292 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.138-1161A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38622198 | |||||||
chr20:38622254 | A | G | 3 | a0001c0002t0005g0127 a0001c0002t0005g0154 a0001c0002t0005g0219 |
3 | HG00639.hp2 HG00741.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.138-1105A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38622254 | |||||||
chr20:38622321 | T | C | 1 | a0001c0001t0003g0135 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.138-1038T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38622321 | |||||||
chr20:38622325 | G | T | 4 | a0006c0013t0008g0027 a0006c0013t0008g0299 a0006c0017t0008g0045 others(1): Show |
5 | HG01261.hp1 HG01884.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.138-1034G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38622325 | |||||||
chr20:38622404 | C | T | 1 | a0001c0002t0004g0057 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.138-955C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38622404 | |||||||
chr20:38622421 | A | C | 1 | a0001c0002t0005g0182 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.138-938A>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38622421 | |||||||
chr20:38622516 | C | T | 2 | a0001c0021t0002g0278 a0001c0021t0002g0281 |
2 | HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.138-843C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38622516 | |||||||
chr20:38622519 | G | A | 18 | a0002c0003t0003g0167 a0002c0003t0004g0012 a0002c0003t0004g0026 others(15): Show |
20 | HG00642.hp2 HG01433.hp2 HG01516.hp2 others(17): Show |
intron_variant | MODIFIER | c.138-840G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38622519 | |||||||
chr20:38622611 | A | G | 1 | a0003c0005t0002g0075 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.138-748A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38622611 | |||||||
chr20:38622614 | G | C | 1 | a0004c0011t0004g0308 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.138-745G>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38622614 | |||||||
chr20:38622776 | A | G | 3 | a0001c0004t0002g0047 a0001c0004t0002g0074 a0001c0004t0016g0228 |
3 | HG02486.hp1 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.138-583A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38622776 | |||||||
chr20:38622886 | G | A | 1 | a0001c0001t0001g0255 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.138-473G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38622886 | |||||||
chr20:38622894 | T | G | 1 | a0001c0001t0006g0292 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.138-465T>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38622894 | |||||||
chr20:38622992 | A | G | 11 | a0001c0004t0002g0047 a0001c0004t0002g0074 a0001c0004t0004g0044 others(8): Show |
12 | HG01243.hp2 HG02486.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.138-367A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38622992 | |||||||
chr20:38623045 | G | A | 1 | a0016c0025t0004g0053 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.138-314G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38623045 | |||||||
chr20:38623181 | C | A | 1 | a0021c0039t0013g0280 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.138-178C>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38623181 | |||||||
chr20:38623183 | C | G | 11 | a0001c0004t0002g0047 a0001c0004t0002g0074 a0001c0004t0004g0044 others(8): Show |
12 | HG01243.hp2 HG02486.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.138-176C>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38623183 | |||||||
chr20:38623187 | G | A | 1 | a0001c0002t0005g0264 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.138-172G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38623187 | |||||||
chr20:38623282 | G | A | 67 | a0001c0001t0001g0022 a0001c0001t0001g0139 a0001c0001t0001g0271 others(64): Show |
71 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.138-77G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38623282 | |||||||
chr20:38623305 | C | G | 4 | a0001c0002t0008g0073 a0004c0011t0004g0113 a0004c0011t0007g0288 others(1): Show |
4 | HG02559.hp1 HG02559.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.138-54C>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38623305 | |||||||
chr20:38623567 | C | A | 83 | a0001c0001t0001g0022 a0001c0001t0001g0139 a0001c0001t0001g0271 others(80): Show |
89 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.337+9C>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38623567 | |||||||
chr20:38623590 | G | A | 4 | a0007c0009t0006g0067 a0007c0009t0006g0068 a0007c0009t0006g0069 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.337+32G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38623590 | |||||||
chr20:38623699 | C | A | 85 | a0001c0001t0001g0022 a0001c0001t0001g0139 a0001c0001t0001g0271 others(82): Show |
91 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.337+141C>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38623699 | |||||||
chr20:38623755 | G | A | 2 | a0001c0001t0005g0216 a0001c0001t0005g0250 |
2 | NA18969.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.337+197G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38623755 | |||||||
chr20:38623787 | C | A | 1 | a0003c0005t0001g0137 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.337+229C>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38623787 | |||||||
chr20:38624171 | A | G | 1 | a0001c0001t0001g0196 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.337+613A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38624171 | |||||||
chr20:38624283 | C | G | 9 | a0003c0005t0001g0137 a0003c0005t0001g0194 a0003c0005t0002g0010 others(6): Show |
10 | HG01361.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.337+725C>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38624283 | |||||||
chr20:38624294 | G | A | 11 | a0001c0004t0002g0047 a0001c0004t0002g0074 a0001c0004t0004g0044 others(8): Show |
12 | HG01243.hp2 HG02486.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.337+736G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38624294 | |||||||
chr20:38624548 | C | T | 67 | a0001c0001t0001g0022 a0001c0001t0001g0139 a0001c0001t0001g0271 others(64): Show |
71 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.337+990C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38624548 | |||||||
chr20:38624632 | C | T | 8 | a0003c0005t0001g0137 a0003c0005t0001g0194 a0003c0005t0002g0010 others(5): Show |
9 | HG01361.hp2 HG01891.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.337+1074C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38624632 | |||||||
chr20:38624644 | C | T | 1 | a0001c0021t0002g0278 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.337+1086C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38624644 | |||||||
chr20:38624648 | TG | T | 217 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0022 others(214): Show |
246 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(243): Show |
intron_variant | MODIFIER | c.337+1092delG | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr20 | 38624648 | ||||||
chr20:38624839 | T | A | 5 | a0001c0004t0007g0112 a0001c0004t0007g0283 a0004c0014t0005g0023 others(2): Show |
6 | HG01243.hp2 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.337+1281T>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38624839 | |||||||
chr20:38624845 | C | A | 1 | a0004c0011t0004g0308 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.337+1287C>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38624845 | |||||||
chr20:38624895 | A | G | 59 | a0001c0001t0001g0022 a0001c0001t0001g0139 a0001c0001t0001g0271 others(56): Show |
62 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.337+1337A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38624895 | |||||||
chr20:38624992 | C | T | 2 | a0001c0008t0004g0305 a0001c0038t0002g0306 |
2 | HG02572.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.337+1434C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38624992 | |||||||
chr20:38625307 | C | T | 57 | a0001c0001t0002g0083 a0001c0002t0001g0024 a0001c0002t0001g0124 others(54): Show |
59 | HG00558.hp1 HG00639.hp2 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.338-1688C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38625307 | |||||||
chr20:38625345 | G | T | 64 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0022 others(61): Show |
82 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.338-1650G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38625345 | |||||||
chr20:38625390 | G | GT | 33 | a0001c0001t0002g0071 a0001c0001t0002g0096 a0001c0002t0004g0089 others(30): Show |
36 | HG00642.hp2 HG00741.hp2 HG01433.hp2 others(33): Show |
intron_variant | MODIFIER | c.338-1594dupT | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr20 | 38625390 | ||||||
chr20:38625503 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.338-1492C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38625503 | |||||||
chr20:38625521 | C | T | 1 | a0001c0001t0003g0152 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.338-1474C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38625521 | |||||||
chr20:38625522 | G | A | 1 | a0001c0004t0007g0112 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.338-1473G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38625522 | |||||||
chr20:38625590 | C | T | 3 | a0007c0009t0006g0067 a0007c0009t0006g0068 a0007c0009t0006g0069 |
3 | HG02895.hp1 HG02897.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.338-1405C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38625590 | |||||||
chr20:38625670 | T | G | 1 | a0001c0001t0002g0063 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.338-1325T>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38625670 | |||||||
chr20:38625700 | T | A | 2 | a0008c0006t0002g0028 a0008c0006t0002g0086 |
3 | HG02886.hp2 HG02895.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.338-1295T>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38625700 | |||||||
chr20:38625736 | G | A | 310 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(307): Show |
347 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(344): Show |
intron_variant | MODIFIER | c.338-1259G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38625736 | |||||||
chr20:38625803 | G | C | 1 | a0005c0040t0004g0279 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.338-1192G>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38625803 | |||||||
chr20:38625831 | G | T | 8 | a0003c0005t0001g0137 a0003c0005t0001g0194 a0003c0005t0002g0010 others(5): Show |
9 | HG01361.hp2 HG01891.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.338-1164G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38625831 | |||||||
chr20:38625878 | C | G | 18 | a0001c0001t0002g0071 a0002c0003t0003g0167 a0002c0003t0004g0012 others(15): Show |
20 | HG00642.hp2 HG00741.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.338-1117C>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38625878 | |||||||
chr20:38625878 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.338-1117C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38625878 | |||||||
chr20:38626407 | C | T | 1 | a0001c0002t0010g0081 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.338-588C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38626407 | |||||||
chr20:38626465 | C | T | 1 | a0001c0001t0005g0233 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.338-530C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38626465 | |||||||
chr20:38626615 | C | T | 2 | a0012c0018t0004g0077 a0012c0018t0004g0087 |
2 | HG02647.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.338-380C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38626615 | |||||||
chr20:38626665 | G | A | 3 | a0001c0004t0007g0112 a0001c0004t0007g0283 a0014c0022t0007g0100 |
3 | HG01243.hp2 HG02647.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.338-330G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38626665 | |||||||
chr20:38626723 | C | T | 3 | a0007c0026t0002g0085 a0011c0016t0004g0039 a0011c0016t0004g0084 |
3 | HG02257.hp1 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.338-272C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38626723 | |||||||
chr20:38626727 | C | T | 2 | a0001c0001t0003g0142 a0001c0001t0003g0189 |
2 | NA18950.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.338-268C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38626727 | |||||||
chr20:38626810 | G | A | 73 | a0001c0002t0001g0024 a0001c0002t0001g0124 a0001c0002t0001g0125 others(70): Show |
78 | HG00558.hp1 HG00639.hp2 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.338-185G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38626810 | |||||||
chr20:38626820 | G | A | 1 | a0001c0004t0016g0228 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.338-175G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38626820 | |||||||
chr20:38626940 | G | A | 3 | a0007c0026t0002g0085 a0011c0016t0004g0039 a0011c0016t0004g0084 |
3 | HG02257.hp1 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.338-55G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38626940 | |||||||
chr20:38626942 | G | C | 2 | a0001c0001t0003g0170 a0001c0001t0006g0058 |
2 | NA19070.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.338-53G>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38626942 | |||||||
chr20:38627270 | C | T | 2 | a0001c0002t0008g0073 a0002c0024t0002g0050 |
2 | HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.558+55C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | chr20 | 38627270 | |||||||
chr20:38627352 | A | ATGTGTGT others(5): Show |
72 | a0001c0002t0001g0024 a0001c0002t0001g0124 a0001c0002t0001g0125 others(69): Show |
77 | HG00558.hp1 HG00639.hp2 HG00673.hp1 others(74): Show |
intron_variant | MODIFIER | c.558+139_558+150dup others(12): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr20 | 38627352 | ||||||
chr20:38627375 | GGTGTGTG others(9): Show |
G | 1 | a0002c0003t0004g0300 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.558+177_558+192del others(16): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr20 | 38627375 | ||||||
chr20:38627377 | T | G | 1 | a0001c0029t0003g0136 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.558+162T>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | chr20 | 38627377 | |||||||
chr20:38627422 | T | G | 2 | a0001c0001t0003g0229 a0001c0007t0002g0276 |
2 | HG02622.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.558+207T>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | chr20 | 38627422 | |||||||
chr20:38627495 | A | ATGTTGGT others(75): Show |
73 | a0001c0002t0001g0024 a0001c0002t0001g0124 a0001c0002t0001g0125 others(70): Show |
78 | HG00558.hp1 HG00639.hp2 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.558+289_558+290ins others(82): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr20 | 38627495 | ||||||
chr20:38627495 | A | ATGTTGGT others(72): Show |
1 | a0001c0002t0001g0215 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.558+289_558+290ins others(79): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr20 | 38627495 | ||||||
chr20:38627519 | G | A | 1 | a0001c0002t0005g0212 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.558+304G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | chr20 | 38627519 | |||||||
chr20:38627531 | ATG | A | 70 | a0001c0002t0001g0024 a0001c0002t0001g0124 a0001c0002t0001g0125 others(67): Show |
74 | HG00558.hp1 HG00639.hp2 HG00673.hp1 others(71): Show |
intron_variant | MODIFIER | c.558+328_558+329del others(2): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr20 | 38627531 | ||||||
chr20:38627531 | ATGTG | A | 9 | a0003c0005t0001g0137 a0003c0005t0001g0194 a0003c0005t0002g0010 others(6): Show |
10 | HG01361.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.558+326_558+329del others(4): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr20 | 38627531 | ||||||
chr20:38627553 | G | A | 2 | a0001c0021t0002g0278 a0001c0021t0002g0281 |
2 | HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.558+338G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | chr20 | 38627553 | |||||||
chr20:38627594 | GGTGTGCG others(7): Show |
G | 4 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0186 others(1): Show |
4 | HG00558.hp2 NA18965.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.558+385_558+398del others(14): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr20 | 38627594 | ||||||
chr20:38627600 | C | T | 234 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0022 others(231): Show |
262 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(259): Show |
intron_variant | MODIFIER | c.558+385C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | chr20 | 38627600 | |||||||
chr20:38627621 | G | GTGTA | 110 | a0001c0002t0001g0024 a0001c0002t0001g0124 a0001c0002t0001g0125 others(107): Show |
118 | HG00558.hp1 HG00639.hp2 HG00673.hp1 others(115): Show |
intron_variant | MODIFIER | c.558+409_558+410ins others(4): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr20 | 38627621 | ||||||
chr20:38627625 | G | A | 1 | a0021c0039t0013g0280 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.558+410G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | chr20 | 38627625 | |||||||
chr20:38627628 | TGTTGGGG others(10): Show |
T | 1 | a0021c0039t0013g0280 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.558+416_558+432del others(17): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr20 | 38627628 | ||||||
chr20:38627633 | G | GGGTGTGT others(11): Show |
4 | a0008c0006t0002g0028 a0008c0006t0002g0086 a0008c0006t0002g0105 others(1): Show |
5 | HG02886.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.558+426_558+427ins others(18): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr20 | 38627633 | ||||||
chr20:38627633 | G | GGGTGTGT others(13): Show |
70 | a0001c0002t0001g0024 a0001c0002t0001g0124 a0001c0002t0001g0125 others(67): Show |
74 | HG00558.hp1 HG00639.hp2 HG00673.hp1 others(71): Show |
intron_variant | MODIFIER | c.558+431_558+432ins others(20): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr20 | 38627633 | ||||||
chr20:38627655 | T | G | 1 | a0021c0039t0013g0280 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.558+440T>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | chr20 | 38627655 | |||||||
chr20:38627673 | GGTGTGTG others(4): Show |
G | 1 | a0001c0004t0016g0228 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.558+471_558+481del others(11): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr20 | 38627673 | ||||||
chr20:38627682 | GTT | G | 4 | a0008c0006t0002g0028 a0008c0006t0002g0086 a0008c0006t0002g0105 others(1): Show |
5 | HG02886.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.558+468_558+469del others(2): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | chr20 | 38627682 | |||||||
chr20:38627993 | A | G | 83 | a0001c0002t0001g0024 a0001c0002t0001g0124 a0001c0002t0001g0125 others(80): Show |
90 | HG00558.hp1 HG00639.hp2 HG00673.hp1 others(87): Show |
intron_variant | MODIFIER | c.558+778A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | chr20 | 38627993 | |||||||
chr20:38628074 | C | T | 2 | a0001c0021t0002g0278 a0001c0021t0002g0281 |
2 | HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.559-853C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | chr20 | 38628074 | |||||||
chr20:38628098 | A | G | 4 | a0008c0006t0002g0028 a0008c0006t0002g0086 a0008c0006t0002g0105 others(1): Show |
5 | HG02886.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.559-829A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | chr20 | 38628098 | |||||||
chr20:38628126 | T | C | 1 | a0001c0001t0001g0221 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.559-801T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | chr20 | 38628126 | |||||||
chr20:38628148 | G | A | 1 | a0001c0001t0003g0256 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.559-779G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | chr20 | 38628148 | |||||||
chr20:38628309 | C | CT | 83 | a0001c0001t0002g0289 a0001c0001t0006g0034 a0001c0001t0006g0082 others(80): Show |
88 | HG00558.hp1 HG00639.hp2 HG00673.hp1 others(85): Show |
intron_variant | MODIFIER | c.559-605dupT | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr20 | 38628309 | ||||||
chr20:38628309 | CT | C | 6 | a0001c0001t0001g0267 a0001c0001t0002g0096 a0008c0006t0002g0028 others(3): Show |
7 | HG02886.hp2 HG02895.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.559-605delT | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr20 | 38628309 | ||||||
chr20:38628310 | T | C | 1 | a0001c0001t0001g0222 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.559-617T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | chr20 | 38628310 | |||||||
chr20:38628324 | A | C | 4 | a0008c0006t0002g0028 a0008c0006t0002g0086 a0008c0006t0002g0105 others(1): Show |
5 | HG02886.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.559-603A>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | chr20 | 38628324 | |||||||
chr20:38628333 | C | T | 4 | a0008c0006t0002g0028 a0008c0006t0002g0086 a0008c0006t0002g0105 others(1): Show |
5 | HG02886.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.559-594C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | chr20 | 38628333 | |||||||
chr20:38628351 | CT | C | 4 | a0008c0006t0002g0028 a0008c0006t0002g0086 a0008c0006t0002g0105 others(1): Show |
5 | HG02886.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.559-575delT | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | chr20 | 38628351 | |||||||
chr20:38628373 | C | T | 1 | a0001c0002t0010g0081 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.559-554C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | chr20 | 38628373 | |||||||
chr20:38628375 | A | G | 4 | a0008c0006t0002g0028 a0008c0006t0002g0086 a0008c0006t0002g0105 others(1): Show |
5 | HG02886.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.559-552A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | chr20 | 38628375 | |||||||
chr20:38628498 | G | T | 9 | a0001c0002t0007g0009 a0001c0002t0007g0013 a0001c0002t0007g0043 others(6): Show |
11 | HG01069.hp2 HG01168.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.559-429G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | chr20 | 38628498 | |||||||
chr20:38628502 | C | G | 2 | a0012c0018t0004g0077 a0012c0018t0004g0087 |
2 | HG02647.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.559-425C>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | chr20 | 38628502 | |||||||
chr20:38628636 | T | A | 8 | a0003c0005t0001g0137 a0003c0005t0001g0194 a0003c0005t0002g0010 others(5): Show |
9 | HG01361.hp2 HG01891.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.559-291T>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | chr20 | 38628636 | |||||||
chr20:38628689 | C | T | 3 | a0001c0002t0001g0125 a0001c0002t0001g0165 a0001c0002t0001g0166 |
3 | NA18968.hp1 NA19002.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.559-238C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | chr20 | 38628689 | |||||||
chr20:38628714 | A | G | 4 | a0001c0021t0002g0278 a0001c0021t0002g0281 a0016c0025t0004g0053 others(1): Show |
4 | HG01884.hp2 HG02976.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.559-213A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | chr20 | 38628714 | |||||||
chr20:38628741 | A | G | 67 | a0001c0002t0001g0024 a0001c0002t0001g0124 a0001c0002t0001g0125 others(64): Show |
71 | HG00558.hp1 HG00639.hp2 HG00673.hp1 others(68): Show |
intron_variant | MODIFIER | c.559-186A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | chr20 | 38628741 | |||||||
chr20:38628833 | A | G | 1 | a0001c0004t0004g0044 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.559-94A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | chr20 | 38628833 | |||||||
chr20:38628893 | A | G | 1 | a0001c0001t0001g0129 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.559-34A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | chr20 | 38628893 | |||||||
chr20:38628921 | G | A | 4 | a0008c0006t0002g0028 a0008c0006t0002g0086 a0008c0006t0002g0105 others(1): Show |
5 | HG02886.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.559-6G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | chr20 | 38628921 | |||||||
chr20:38629071 | A | T | 3 | a0001c0004t0007g0112 a0001c0004t0007g0283 a0014c0022t0007g0100 |
3 | HG01243.hp2 HG02647.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.634+69A>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 4/14 | chr20 | 38629071 | |||||||
chr20:38629201 | T | A | 1 | a0001c0002t0001g0265 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.634+199T>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 4/14 | chr20 | 38629201 | |||||||
chr20:38629345 | C | A | 3 | a0001c0001t0003g0144 a0001c0001t0003g0191 a0001c0001t0003g0257 |
3 | HG00408.hp1 NA19074.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.635-157C>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 4/14 | chr20 | 38629345 | |||||||
chr20:38629378 | G | A | 1 | a0001c0002t0010g0081 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.635-124G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 4/14 | chr20 | 38629378 | |||||||
chr20:38629467 | C | T | 1 | a0001c0002t0010g0081 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.635-35C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 4/14 | chr20 | 38629467 | |||||||
chr20:38629492 | C | G | 2 | a0008c0006t0002g0105 a0008c0006t0002g0107 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.635-10C>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 4/14 | chr20 | 38629492 | |||||||
chr20:38629497 | C | T | 1 | a0001c0002t0001g0125 | 1 | NA19002.hp1 | splice_region_variant&intron_variant | LOW | c.635-5C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 4/14 | chr20 | 38629497 | |||||||
chr20:38629675 | G | A | 4 | a0001c0002t0005g0195 a0001c0002t0005g0201 a0001c0002t0005g0204 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.783+25G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38629675 | |||||||
chr20:38629686 | C | T | 1 | a0016c0025t0004g0053 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.783+36C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38629686 | |||||||
chr20:38629760 | A | C | 1 | a0021c0039t0013g0280 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.783+110A>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38629760 | |||||||
chr20:38629946 | A | G | 1 | a0001c0001t0003g0263 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.783+296A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38629946 | |||||||
chr20:38629982 | CAGAG | C | 4 | a0008c0006t0002g0028 a0008c0006t0002g0086 a0008c0006t0002g0105 others(1): Show |
5 | HG02886.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.783+338_783+341del others(4): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr20 | 38629982 | ||||||
chr20:38630060 | TTTTC | T | 5 | a0006c0013t0008g0027 a0006c0013t0008g0299 a0006c0017t0008g0045 others(2): Show |
6 | HG01261.hp1 HG01884.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.783+430_783+433del others(4): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr20 | 38630060 | ||||||
chr20:38630068 | C | CTTTCTTT others(3): Show |
2 | a0008c0006t0002g0028 a0008c0006t0002g0086 |
3 | HG02886.hp2 HG02895.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.783+420_783+429dup others(10): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr20 | 38630068 | ||||||
chr20:38630068 | CTTTCTTT others(7): Show |
C | 8 | a0001c0001t0006g0082 a0001c0001t0006g0090 a0001c0001t0006g0091 others(5): Show |
9 | HG00738.hp2 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.783+434_783+447del others(14): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr20 | 38630068 | ||||||
chr20:38630072 | CTTTCTTT others(3): Show |
C | 2 | a0004c0011t0004g0308 a0004c0011t0004g0309 |
2 | HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.783+434_783+443del others(10): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr20 | 38630072 | ||||||
chr20:38630080 | CTTTT | C | 4 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0122 others(1): Show |
8 | HG01433.hp1 HG01496.hp2 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.783+432_783+435del others(4): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr20 | 38630080 | ||||||
chr20:38630082 | T | TTC | 2 | a0008c0006t0002g0028 a0008c0006t0002g0086 |
3 | HG02886.hp2 HG02895.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.783+433_783+434ins others(2): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr20 | 38630082 | ||||||
chr20:38630082 | T | TTCTTTCT others(7): Show |
2 | a0008c0006t0002g0105 a0008c0006t0002g0107 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.783+433_783+434ins others(14): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr20 | 38630082 | ||||||
chr20:38630082 | T | TTTTC | 3 | a0001c0001t0001g0022 a0001c0001t0002g0083 a0001c0001t0005g0185 |
4 | HG02602.hp2 HG03491.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.783+448_783+451dup others(4): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr20 | 38630082 | ||||||
chr20:38630084 | T | G | 58 | a0001c0002t0001g0024 a0001c0002t0001g0124 a0001c0002t0001g0125 others(55): Show |
61 | HG00558.hp1 HG00639.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.783+434T>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38630084 | |||||||
chr20:38630085 | TCTTTCTT others(16): Show |
T | 58 | a0001c0002t0001g0024 a0001c0002t0001g0124 a0001c0002t0001g0125 others(55): Show |
61 | HG00558.hp1 HG00639.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.783+436_783+458del others(23): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38630085 | |||||||
chr20:38630103 | TTTTTC | T | 7 | a0004c0011t0004g0113 a0004c0011t0004g0308 a0004c0011t0004g0309 others(4): Show |
8 | HG02145.hp1 HG02559.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.783+462_783+466del others(5): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr20 | 38630103 | ||||||
chr20:38630105 | T | TTTCGTTT others(1): Show |
6 | a0001c0002t0004g0072 a0001c0004t0016g0228 a0001c0008t0004g0025 others(3): Show |
7 | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.783+458_783+459ins others(8): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr20 | 38630105 | ||||||
chr20:38630105 | T | TTTCTTTT others(1): Show |
4 | a0008c0006t0002g0028 a0008c0006t0002g0086 a0008c0006t0002g0105 others(1): Show |
5 | HG02886.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.783+458_783+465dup others(8): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr20 | 38630105 | ||||||
chr20:38630118 | TCTTTCTT others(2): Show |
T | 4 | a0007c0009t0006g0067 a0007c0009t0006g0068 a0007c0009t0006g0069 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.783+478_783+486del others(9): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr20 | 38630118 | ||||||
chr20:38630147 | T | TTCCC | 67 | a0001c0002t0001g0024 a0001c0002t0001g0124 a0001c0002t0001g0125 others(64): Show |
72 | HG00558.hp1 HG00639.hp2 HG00673.hp1 others(69): Show |
intron_variant | MODIFIER | c.783+511_783+514dup others(4): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr20 | 38630147 | ||||||
chr20:38630161 | CCCTT | C | 6 | a0001c0002t0004g0072 a0001c0004t0016g0228 a0001c0008t0004g0025 others(3): Show |
7 | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.783+525_783+528del others(4): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr20 | 38630161 | ||||||
chr20:38630238 | GA | G | 6 | a0001c0002t0004g0072 a0001c0004t0016g0228 a0001c0008t0004g0025 others(3): Show |
7 | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.783+589delA | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38630238 | |||||||
chr20:38630266 | C | T | 1 | a0007c0009t0013g0041 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.783+616C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38630266 | |||||||
chr20:38630299 | A | G | 1 | a0001c0001t0001g0138 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.783+649A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38630299 | |||||||
chr20:38630558 | G | T | 1 | a0001c0002t0010g0081 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.783+908G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38630558 | |||||||
chr20:38630793 | G | A | 4 | a0007c0009t0006g0067 a0007c0009t0006g0068 a0007c0009t0006g0069 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.783+1143G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38630793 | |||||||
chr20:38630802 | T | A | 5 | a0001c0002t0010g0081 a0006c0013t0008g0027 a0006c0013t0008g0299 others(2): Show |
6 | HG01261.hp1 HG01884.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.783+1152T>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38630802 | |||||||
chr20:38630874 | C | T | 4 | a0008c0006t0002g0028 a0008c0006t0002g0086 a0008c0006t0002g0105 others(1): Show |
5 | HG02886.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.783+1224C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38630874 | |||||||
chr20:38630915 | C | T | 3 | a0007c0026t0002g0085 a0011c0016t0004g0039 a0011c0016t0004g0084 |
3 | HG02257.hp1 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.783+1265C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38630915 | |||||||
chr20:38630921 | A | G | 2 | a0001c0002t0008g0073 a0002c0024t0002g0050 |
2 | HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.783+1271A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38630921 | |||||||
chr20:38630946 | G | C | 1 | a0001c0002t0010g0081 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.783+1296G>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38630946 | |||||||
chr20:38631148 | C | T | 1 | a0001c0002t0004g0089 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.783+1498C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38631148 | |||||||
chr20:38631210 | G | T | 6 | a0001c0002t0004g0072 a0001c0004t0016g0228 a0001c0008t0004g0025 others(3): Show |
7 | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.783+1560G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38631210 | |||||||
chr20:38631264 | T | C | 2 | a0001c0002t0002g0052 a0001c0002t0002g0111 |
2 | NA18966.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.783+1614T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38631264 | |||||||
chr20:38631304 | T | TA | 28 | a0001c0001t0002g0110 a0001c0001t0003g0189 a0001c0002t0005g0120 others(25): Show |
29 | HG01070.hp1 HG01109.hp1 HG01168.hp2 others(26): Show |
intron_variant | MODIFIER | c.783+1675dupA | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr20 | 38631304 | ||||||
chr20:38631304 | T | TAA | 38 | a0001c0002t0004g0032 a0001c0002t0004g0054 a0001c0002t0004g0056 others(35): Show |
40 | HG00639.hp2 HG00741.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.783+1674_783+1675d others(4): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr20 | 38631304 | ||||||
chr20:38631304 | TA | T | 18 | a0001c0001t0001g0117 a0001c0001t0001g0178 a0001c0001t0002g0037 others(15): Show |
20 | HG00323.hp1 HG00408.hp2 HG02523.hp2 others(17): Show |
intron_variant | MODIFIER | c.783+1675delA | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr20 | 38631304 | ||||||
chr20:38631407 | C | T | 1 | a0002c0003t0006g0042 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.783+1757C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38631407 | |||||||
chr20:38631519 | G | A | 47 | a0001c0002t0004g0032 a0001c0002t0004g0054 a0001c0002t0004g0056 others(44): Show |
50 | HG00639.hp2 HG00741.hp1 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.783+1869G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38631519 | |||||||
chr20:38631632 | G | A | 1 | a0001c0001t0002g0102 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.783+1982G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38631632 | |||||||
chr20:38631787 | T | C | 1 | a0001c0001t0006g0029 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.783+2137T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38631787 | |||||||
chr20:38631860 | T | C | 5 | a0004c0011t0004g0113 a0004c0011t0004g0308 a0004c0011t0004g0309 others(2): Show |
6 | HG02559.hp1 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.783+2210T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38631860 | |||||||
chr20:38631971 | T | G | 7 | a0001c0002t0008g0073 a0001c0021t0002g0278 a0001c0021t0002g0281 others(4): Show |
7 | HG01884.hp2 HG02559.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.783+2321T>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38631971 | |||||||
chr20:38631999 | T | A | 6 | a0001c0002t0004g0072 a0001c0004t0016g0228 a0001c0008t0004g0025 others(3): Show |
7 | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.783+2349T>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38631999 | |||||||
chr20:38632186 | A | C | 48 | a0001c0002t0004g0032 a0001c0002t0004g0054 a0001c0002t0004g0056 others(45): Show |
51 | HG00639.hp2 HG00741.hp1 HG01069.hp1 others(48): Show |
intron_variant | MODIFIER | c.784-2434A>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38632186 | |||||||
chr20:38632259 | C | A | 4 | a0008c0006t0002g0028 a0008c0006t0002g0086 a0008c0006t0002g0105 others(1): Show |
5 | HG02886.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.784-2361C>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38632259 | |||||||
chr20:38632267 | A | AT | 7 | a0001c0001t0001g0254 a0001c0001t0002g0008 a0001c0001t0002g0063 others(4): Show |
8 | HG00438.hp2 HG01884.hp2 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.784-2340dupT | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr20 | 38632267 | ||||||
chr20:38632267 | AT | A | 60 | a0001c0001t0006g0090 a0001c0002t0001g0124 a0001c0002t0004g0032 others(57): Show |
65 | HG00639.hp2 HG00741.hp1 HG01069.hp1 others(62): Show |
intron_variant | MODIFIER | c.784-2340delT | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr20 | 38632267 | ||||||
chr20:38632349 | G | A | 15 | a0001c0002t0008g0073 a0001c0021t0002g0278 a0001c0021t0002g0281 others(12): Show |
17 | HG01261.hp1 HG01884.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.784-2271G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38632349 | |||||||
chr20:38632349 | G | T | 1 | a0019c0034t0007g0099 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.784-2271G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38632349 | |||||||
chr20:38632357 | G | C | 4 | a0006c0013t0008g0027 a0006c0013t0008g0299 a0006c0017t0008g0045 others(1): Show |
5 | HG01261.hp1 HG01884.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.784-2263G>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38632357 | |||||||
chr20:38632383 | C | G | 1 | a0001c0004t0004g0044 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.784-2237C>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38632383 | |||||||
chr20:38632401 | ACAGGCGC others(7): Show |
A | 3 | a0001c0001t0001g0139 a0001c0001t0001g0180 a0001c0001t0001g0271 |
3 | HG00140.hp2 HG01361.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.784-2216_784-2203d others(16): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr20 | 38632401 | ||||||
chr20:38632410 | C | T | 42 | a0001c0002t0004g0032 a0001c0002t0004g0054 a0001c0002t0004g0056 others(39): Show |
44 | HG00639.hp2 HG00741.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.784-2210C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38632410 | |||||||
chr20:38632540 | C | T | 4 | a0008c0006t0002g0028 a0008c0006t0002g0086 a0008c0006t0002g0105 others(1): Show |
5 | HG02886.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.784-2080C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38632540 | |||||||
chr20:38632550 | C | T | 9 | a0001c0004t0004g0044 a0001c0004t0007g0112 a0001c0004t0007g0283 others(6): Show |
9 | HG01109.hp1 HG01243.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.784-2070C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38632550 | |||||||
chr20:38632686 | C | T | 1 | a0001c0001t0003g0176 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.784-1934C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38632686 | |||||||
chr20:38632754 | T | C | 42 | a0001c0002t0004g0032 a0001c0002t0004g0054 a0001c0002t0004g0056 others(39): Show |
44 | HG00639.hp2 HG00741.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.784-1866T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38632754 | |||||||
chr20:38632888 | C | T | 12 | a0001c0002t0007g0009 a0001c0002t0007g0013 a0001c0002t0007g0043 others(9): Show |
14 | HG01069.hp2 HG01168.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.784-1732C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38632888 | |||||||
chr20:38632893 | C | T | 3 | a0001c0002t0002g0033 a0001c0002t0002g0038 a0001c0002t0002g0062 |
3 | HG01106.hp1 HG01978.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.784-1727C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38632893 | |||||||
chr20:38632923 | G | A | 1 | a0001c0007t0001g0187 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.784-1697G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38632923 | |||||||
chr20:38632942 | G | A | 29 | a0001c0002t0004g0032 a0001c0002t0004g0054 a0001c0002t0004g0056 others(26): Show |
29 | HG00639.hp2 HG00741.hp1 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.784-1678G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38632942 | |||||||
chr20:38632982 | G | T | 8 | a0003c0005t0001g0137 a0003c0005t0001g0194 a0003c0005t0002g0010 others(5): Show |
9 | HG01361.hp2 HG01891.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.784-1638G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38632982 | |||||||
chr20:38633114 | C | T | 4 | a0006c0013t0008g0027 a0006c0013t0008g0299 a0006c0017t0008g0045 others(1): Show |
5 | HG01261.hp1 HG01884.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.784-1506C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38633114 | |||||||
chr20:38633117 | C | T | 4 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0186 others(1): Show |
4 | HG00558.hp2 NA18965.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.784-1503C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38633117 | |||||||
chr20:38633122 | C | CA | 18 | a0001c0001t0002g0110 a0001c0008t0004g0305 a0004c0011t0004g0113 others(15): Show |
21 | HG01261.hp1 HG01884.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.784-1484dupA | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr20 | 38633122 | ||||||
chr20:38633122 | CA | C | 48 | a0001c0001t0003g0173 a0001c0002t0004g0032 a0001c0002t0004g0054 others(45): Show |
50 | HG00639.hp2 HG00741.hp1 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.784-1484delA | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr20 | 38633122 | ||||||
chr20:38633136 | A | AT | 4 | a0001c0002t0004g0072 a0001c0008t0004g0025 a0001c0008t0006g0282 others(1): Show |
5 | HG02258.hp1 HG02723.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.784-1483dupT | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr20 | 38633136 | ||||||
chr20:38633138 | A | G | 4 | a0001c0002t0004g0072 a0001c0008t0004g0025 a0001c0008t0006g0282 others(1): Show |
5 | HG02258.hp1 HG02723.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.784-1482A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38633138 | |||||||
chr20:38633177 | C | G | 2 | a0001c0021t0002g0278 a0001c0021t0002g0281 |
2 | HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.784-1443C>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38633177 | |||||||
chr20:38633485 | C | T | 46 | a0001c0002t0004g0032 a0001c0002t0004g0054 a0001c0002t0004g0056 others(43): Show |
49 | HG00639.hp2 HG00741.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.784-1135C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38633485 | |||||||
chr20:38633539 | C | T | 4 | a0008c0006t0002g0028 a0008c0006t0002g0086 a0008c0006t0002g0105 others(1): Show |
5 | HG02886.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.784-1081C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38633539 | |||||||
chr20:38633570 | A | G | 1 | a0001c0002t0001g0184 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.784-1050A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38633570 | |||||||
chr20:38633593 | C | T | 33 | a0001c0002t0004g0032 a0001c0002t0004g0054 a0001c0002t0004g0056 others(30): Show |
34 | HG00639.hp2 HG00741.hp1 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.784-1027C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38633593 | |||||||
chr20:38633621 | G | A | 2 | a0001c0021t0002g0278 a0001c0021t0002g0281 |
2 | HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.784-999G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38633621 | |||||||
chr20:38633654 | C | T | 7 | a0001c0007t0001g0187 a0001c0007t0001g0240 a0001c0007t0002g0036 others(4): Show |
7 | HG02451.hp2 HG02622.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.784-966C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38633654 | |||||||
chr20:38634146 | G | T | 10 | a0001c0002t0004g0072 a0001c0008t0004g0025 a0001c0008t0004g0305 others(7): Show |
12 | HG02258.hp1 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.784-474G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38634146 | |||||||
chr20:38634314 | T | C | 1 | a0001c0001t0001g0242 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.784-306T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38634314 | |||||||
chr20:38634357 | A | G | 5 | a0001c0002t0004g0089 a0001c0002t0005g0195 a0001c0002t0005g0201 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.784-263A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38634357 | |||||||
chr20:38634497 | T | C | 1 | a0001c0002t0015g0270 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.784-123T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38634497 | |||||||
chr20:38634558 | C | T | 1 | a0016c0025t0004g0053 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.784-62C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38634558 | |||||||
chr20:38634831 | T | C | 1 | a0001c0002t0008g0073 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.949+46T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38634831 | |||||||
chr20:38634846 | G | A | 6 | a0001c0004t0004g0044 a0005c0010t0010g0224 a0005c0010t0010g0303 others(3): Show |
6 | HG01109.hp1 HG02896.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.949+61G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38634846 | |||||||
chr20:38634886 | C | CT | 149 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0022 others(146): Show |
170 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.949+115dupT | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr20 | 38634886 | ||||||
chr20:38634914 | G | A | 1 | a0011c0016t0004g0084 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.949+129G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38634914 | |||||||
chr20:38634947 | T | C | 3 | a0001c0002t0004g0072 a0001c0008t0004g0025 a0001c0008t0004g0305 |
4 | HG02258.hp1 HG02572.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.949+162T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38634947 | |||||||
chr20:38634974 | C | T | 1 | a0001c0001t0001g0207 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.949+189C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38634974 | |||||||
chr20:38634994 | G | T | 1 | a0001c0002t0001g0166 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.949+209G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38634994 | |||||||
chr20:38635007 | G | A | 1 | a0010c0012t0009g0236 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.949+222G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38635007 | |||||||
chr20:38635118 | G | A | 1 | a0001c0002t0009g0148 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.949+333G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38635118 | |||||||
chr20:38635161 | T | G | 1 | a0001c0001t0001g0243 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.949+376T>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38635161 | |||||||
chr20:38635213 | AT | A | 31 | a0001c0002t0004g0032 a0001c0002t0004g0054 a0001c0002t0004g0056 others(28): Show |
31 | HG00639.hp2 HG00741.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.949+437delT | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr20 | 38635213 | ||||||
chr20:38635366 | ATAT | A | 10 | a0001c0002t0004g0072 a0001c0008t0004g0025 a0001c0008t0004g0305 others(7): Show |
12 | HG02258.hp1 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.949+585_949+587del others(3): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr20 | 38635366 | ||||||
chr20:38635524 | G | C | 11 | a0001c0002t0004g0072 a0001c0002t0008g0073 a0001c0008t0004g0025 others(8): Show |
13 | HG02258.hp1 HG02559.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.949+739G>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38635524 | |||||||
chr20:38635540 | C | G | 57 | a0001c0002t0004g0032 a0001c0002t0004g0054 a0001c0002t0004g0056 others(54): Show |
62 | HG00639.hp2 HG00741.hp1 HG01069.hp1 others(59): Show |
intron_variant | MODIFIER | c.949+755C>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38635540 | |||||||
chr20:38635895 | C | A | 1 | a0001c0001t0002g0103 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.949+1110C>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38635895 | |||||||
chr20:38636140 | T | C | 4 | a0008c0006t0002g0028 a0008c0006t0002g0086 a0008c0006t0002g0105 others(1): Show |
5 | HG02886.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.949+1355T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38636140 | |||||||
chr20:38636237 | C | A | 14 | a0002c0003t0003g0167 a0002c0003t0004g0012 a0002c0003t0004g0026 others(11): Show |
16 | HG00642.hp2 HG01433.hp2 HG01516.hp2 others(13): Show |
intron_variant | MODIFIER | c.949+1452C>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38636237 | |||||||
chr20:38636264 | A | T | 2 | a0001c0001t0006g0001 a0001c0001t0006g0002 |
2 | HG02165.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.950-1444A>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38636264 | |||||||
chr20:38636264 | AT | A | 8 | a0001c0001t0001g0005 a0001c0001t0001g0139 a0001c0001t0001g0180 others(5): Show |
9 | HG00140.hp1 HG00140.hp2 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.950-1429delT | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr20 | 38636264 | ||||||
chr20:38636267 | T | A | 17 | a0001c0002t0004g0072 a0001c0008t0004g0025 a0001c0008t0004g0305 others(14): Show |
20 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.950-1441T>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38636267 | |||||||
chr20:38636267 | T | TA | 3 | a0001c0001t0001g0198 a0001c0002t0009g0134 a0001c0004t0004g0044 |
3 | HG02970.hp1 NA18995.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.950-1441_950-1440i others(3): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38636267 | |||||||
chr20:38636268 | T | A | 102 | a0001c0001t0001g0117 a0001c0001t0001g0149 a0001c0001t0001g0150 others(99): Show |
106 | HG00408.hp1 HG00423.hp2 HG00639.hp2 others(103): Show |
intron_variant | MODIFIER | c.950-1440T>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38636268 | |||||||
chr20:38636272 | T | A | 24 | a0001c0001t0006g0292 a0001c0001t0006g0301 a0001c0002t0004g0032 others(21): Show |
24 | HG00639.hp2 HG00741.hp1 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.950-1436T>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38636272 | |||||||
chr20:38636384 | G | A | 3 | a0002c0003t0004g0079 a0002c0003t0004g0291 a0009c0035t0011g0123 |
3 | HG02055.hp1 HG02602.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.950-1324G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38636384 | |||||||
chr20:38636482 | C | T | 10 | a0001c0002t0004g0072 a0001c0008t0004g0025 a0001c0008t0004g0305 others(7): Show |
12 | HG02258.hp1 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.950-1226C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38636482 | |||||||
chr20:38636504 | C | T | 5 | a0001c0007t0001g0187 a0001c0007t0001g0240 a0001c0007t0002g0036 others(2): Show |
5 | HG02451.hp2 HG02622.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.950-1204C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38636504 | |||||||
chr20:38636538 | C | T | 5 | a0001c0021t0002g0278 a0001c0021t0002g0281 a0012c0018t0004g0077 others(2): Show |
5 | HG01884.hp2 HG02647.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.950-1170C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38636538 | |||||||
chr20:38636777 | G | A | 1 | a0001c0002t0010g0081 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.950-931G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38636777 | |||||||
chr20:38636787 | G | T | 4 | a0006c0013t0008g0027 a0006c0013t0008g0299 a0006c0017t0008g0045 others(1): Show |
5 | HG01261.hp1 HG01884.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.950-921G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38636787 | |||||||
chr20:38636793 | A | G | 2 | a0004c0014t0005g0023 a0020c0023t0011g0116 |
3 | HG02622.hp1 HG02818.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.950-915A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38636793 | |||||||
chr20:38636804 | G | T | 57 | a0001c0002t0004g0032 a0001c0002t0004g0054 a0001c0002t0004g0056 others(54): Show |
62 | HG00639.hp2 HG00741.hp1 HG01069.hp1 others(59): Show |
intron_variant | MODIFIER | c.950-904G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38636804 | |||||||
chr20:38637144 | C | CT | 14 | a0001c0001t0003g0217 a0001c0002t0010g0081 a0001c0007t0001g0187 others(11): Show |
15 | HG01891.hp1 HG02109.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.950-550dupT | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr20 | 38637144 | ||||||
chr20:38637158 | T | C | 1 | a0001c0004t0002g0047 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.950-550T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38637158 | |||||||
chr20:38637200 | C | T | 8 | a0005c0040t0004g0279 a0006c0013t0008g0027 a0006c0013t0008g0299 others(5): Show |
9 | HG01261.hp1 HG01884.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.950-508C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38637200 | |||||||
chr20:38637241 | A | T | 2 | a0006c0017t0008g0045 a0006c0017t0008g0104 |
2 | HG01261.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.950-467A>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38637241 | |||||||
chr20:38637251 | T | C | 8 | a0001c0002t0010g0081 a0003c0005t0001g0137 a0003c0005t0001g0194 others(5): Show |
9 | HG01891.hp1 HG02109.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.950-457T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38637251 | |||||||
chr20:38637254 | T | A | 3 | a0007c0009t0006g0067 a0007c0009t0006g0068 a0007c0009t0006g0069 |
3 | HG02895.hp1 HG02897.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.950-454T>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38637254 | |||||||
chr20:38637289 | A | G | 1 | a0001c0002t0008g0073 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.950-419A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38637289 | |||||||
chr20:38637355 | G | C | 1 | a0001c0001t0001g0243 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.950-353G>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38637355 | |||||||
chr20:38637391 | C | T | 6 | a0001c0001t0001g0020 a0001c0021t0002g0278 a0001c0021t0002g0281 others(3): Show |
7 | HG01099.hp1 HG01884.hp2 HG02148.hp1 others(4): Show |
intron_variant | MODIFIER | c.950-317C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38637391 | |||||||
chr20:38637392 | G | A | 4 | a0008c0006t0002g0028 a0008c0006t0002g0086 a0008c0006t0002g0105 others(1): Show |
5 | HG02886.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.950-316G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38637392 | |||||||
chr20:38637468 | C | A | 5 | a0001c0021t0002g0278 a0001c0021t0002g0281 a0012c0018t0004g0077 others(2): Show |
5 | HG01884.hp2 HG02647.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.950-240C>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38637468 | |||||||
chr20:38637562 | C | A | 92 | a0001c0002t0004g0032 a0001c0002t0004g0054 a0001c0002t0004g0056 others(89): Show |
99 | HG00639.hp2 HG00741.hp1 HG01069.hp1 others(96): Show |
intron_variant | MODIFIER | c.950-146C>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38637562 | |||||||
chr20:38637918 | T | C | 164 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0022 others(161): Show |
188 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.1041+119T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 7/14 | chr20 | 38637918 | |||||||
chr20:38637937 | C | T | 8 | a0005c0040t0004g0279 a0006c0013t0008g0027 a0006c0013t0008g0299 others(5): Show |
9 | HG01261.hp1 HG01884.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.1041+138C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 7/14 | chr20 | 38637937 | |||||||
chr20:38638014 | T | C | 148 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0022 others(145): Show |
169 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.1041+215T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 7/14 | chr20 | 38638014 | |||||||
chr20:38638038 | C | G | 164 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0022 others(161): Show |
188 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.1041+239C>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 7/14 | chr20 | 38638038 | |||||||
chr20:38638045 | C | T | 2 | a0007c0009t0006g0068 a0007c0009t0006g0069 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1041+246C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 7/14 | chr20 | 38638045 | |||||||
chr20:38638050 | C | T | 4 | a0005c0010t0010g0224 a0005c0010t0010g0303 a0005c0010t0012g0128 others(1): Show |
4 | HG01109.hp1 HG02896.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1041+251C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 7/14 | chr20 | 38638050 | |||||||
chr20:38638081 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1041+282G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 7/14 | chr20 | 38638081 | |||||||
chr20:38638153 | C | CA | 148 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0022 others(145): Show |
169 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.1041+366dupA | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr20 | 38638153 | ||||||
chr20:38638166 | T | C | 1 | a0001c0001t0002g0106 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1041+367T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 7/14 | chr20 | 38638166 | |||||||
chr20:38638172 | G | A | 4 | a0008c0006t0002g0028 a0008c0006t0002g0086 a0008c0006t0002g0105 others(1): Show |
5 | HG02886.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1041+373G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 7/14 | chr20 | 38638172 | |||||||
chr20:38638183 | C | T | 1 | a0001c0001t0003g0220 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1041+384C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 7/14 | chr20 | 38638183 | |||||||
chr20:38638192 | G | A | 1 | a0001c0001t0003g0157 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1041+393G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 7/14 | chr20 | 38638192 | |||||||
chr20:38638228 | C | T | 1 | a0022c0031t0002g0286 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1041+429C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 7/14 | chr20 | 38638228 | |||||||
chr20:38638231 | T | C | 190 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0022 others(187): Show |
216 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.1041+432T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 7/14 | chr20 | 38638231 | |||||||
chr20:38638232 | G | A | 29 | a0001c0002t0004g0032 a0001c0002t0004g0054 a0001c0002t0004g0056 others(26): Show |
29 | HG00639.hp2 HG00741.hp1 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.1041+433G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 7/14 | chr20 | 38638232 | |||||||
chr20:38638272 | G | A | 1 | a0001c0001t0003g0252 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1041+473G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 7/14 | chr20 | 38638272 | |||||||
chr20:38638485 | A | G | 4 | a0008c0006t0002g0028 a0008c0006t0002g0086 a0008c0006t0002g0105 others(1): Show |
5 | HG02886.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1042-276A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 7/14 | chr20 | 38638485 | |||||||
chr20:38638606 | G | C | 7 | a0003c0005t0001g0137 a0003c0005t0001g0194 a0003c0005t0002g0010 others(4): Show |
8 | HG01891.hp1 HG02109.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1042-155G>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 7/14 | chr20 | 38638606 | |||||||
chr20:38638724 | G | A | 1 | a0001c0001t0001g0118 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1042-37G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 7/14 | chr20 | 38638724 | |||||||
chr20:38638726 | T | G | 1 | a0001c0001t0002g0014 | 2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1042-35T>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 7/14 | chr20 | 38638726 | |||||||
chr20:38638929 | G | A | 17 | a0001c0001t0001g0207 a0001c0001t0003g0001 a0001c0001t0003g0002 others(14): Show |
24 | HG00408.hp2 HG00544.hp2 HG01433.hp1 others(21): Show |
intron_variant | MODIFIER | c.1119+91G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 8/14 | chr20 | 38638929 | |||||||
chr20:38639003 | CAG | C | 3 | a0003c0005t0001g0137 a0003c0005t0001g0194 a0009c0019t0007g0307 |
3 | HG01891.hp1 HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1119+170_1119+171d others(4): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr20 | 38639003 | ||||||
chr20:38639086 | C | T | 4 | a0008c0006t0002g0028 a0008c0006t0002g0086 a0008c0006t0002g0105 others(1): Show |
5 | HG02886.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1120-141C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 8/14 | chr20 | 38639086 | |||||||
chr20:38639108 | G | A | 1 | a0001c0001t0003g0252 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1120-119G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 8/14 | chr20 | 38639108 | |||||||
chr20:38639215 | G | A | 1 | a0001c0001t0005g0233 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1120-12G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 8/14 | chr20 | 38639215 | |||||||
chr20:38639478 | C | T | 2 | a0001c0001t0005g0216 a0001c0001t0005g0250 |
2 | NA18969.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1279+92C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38639478 | |||||||
chr20:38639518 | T | G | 4 | a0005c0040t0004g0279 a0007c0026t0002g0085 a0011c0016t0004g0039 others(1): Show |
4 | HG02257.hp1 HG02630.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1279+132T>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38639518 | |||||||
chr20:38639537 | G | T | 11 | a0001c0002t0004g0072 a0001c0004t0004g0044 a0001c0008t0004g0025 others(8): Show |
13 | HG02258.hp1 HG02559.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.1279+151G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38639537 | |||||||
chr20:38639540 | C | T | 5 | a0001c0007t0001g0187 a0001c0007t0001g0240 a0001c0007t0002g0036 others(2): Show |
5 | HG02451.hp2 HG02622.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1279+154C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38639540 | |||||||
chr20:38639564 | A | T | 5 | a0001c0007t0001g0187 a0001c0007t0001g0240 a0001c0007t0002g0036 others(2): Show |
5 | HG02451.hp2 HG02622.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1279+178A>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38639564 | |||||||
chr20:38639576 | G | A | 3 | a0001c0001t0001g0098 a0001c0001t0001g0158 a0001c0001t0001g0221 |
3 | HG02735.hp2 HG03492.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1279+190G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38639576 | |||||||
chr20:38639577 | C | T | 1 | a0001c0008t0006g0282 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1279+191C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38639577 | |||||||
chr20:38639643 | A | G | 1 | a0001c0002t0015g0270 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1279+257A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38639643 | |||||||
chr20:38639852 | A | G | 2 | a0001c0021t0002g0278 a0001c0021t0002g0281 |
2 | HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1279+466A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38639852 | |||||||
chr20:38639945 | G | A | 4 | a0006c0013t0008g0027 a0006c0013t0008g0299 a0006c0017t0008g0045 others(1): Show |
5 | HG01261.hp1 HG01884.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.1279+559G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38639945 | |||||||
chr20:38639971 | C | T | 1 | a0016c0025t0004g0053 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1279+585C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38639971 | |||||||
chr20:38639980 | C | T | 51 | a0001c0002t0004g0072 a0001c0002t0008g0073 a0001c0002t0010g0081 others(48): Show |
57 | HG00642.hp2 HG01261.hp1 HG01433.hp2 others(54): Show |
intron_variant | MODIFIER | c.1279+594C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38639980 | |||||||
chr20:38640060 | C | T | 1 | a0001c0002t0005g0127 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1279+674C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38640060 | |||||||
chr20:38640076 | G | T | 46 | a0001c0002t0004g0072 a0001c0002t0008g0073 a0001c0002t0010g0081 others(43): Show |
51 | HG00642.hp2 HG01261.hp1 HG01433.hp2 others(48): Show |
intron_variant | MODIFIER | c.1279+690G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38640076 | |||||||
chr20:38640088 | G | C | 1 | a0001c0001t0001g0255 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1279+702G>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38640088 | |||||||
chr20:38640091 | C | G | 13 | a0001c0001t0001g0186 a0001c0002t0004g0089 a0001c0002t0005g0195 others(10): Show |
13 | HG00558.hp2 HG01069.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.1279+705C>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38640091 | |||||||
chr20:38640101 | TTCC | T | 15 | a0001c0002t0008g0073 a0001c0002t0010g0081 a0001c0007t0001g0187 others(12): Show |
16 | HG01261.hp1 HG01884.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1279+721_1279+723d others(5): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr20 | 38640101 | ||||||
chr20:38640104 | C | CTCTTCT | 31 | a0001c0002t0004g0072 a0001c0004t0004g0044 a0001c0004t0016g0228 others(28): Show |
35 | HG00642.hp2 HG01433.hp2 HG01516.hp2 others(32): Show |
intron_variant | MODIFIER | c.1279+720_1279+721i others(8): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr20 | 38640104 | ||||||
chr20:38640104 | C | T | 173 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0022 others(170): Show |
196 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.1279+718C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38640104 | |||||||
chr20:38640121 | C | CT | 34 | a0001c0002t0004g0072 a0001c0002t0008g0073 a0001c0004t0004g0044 others(31): Show |
38 | HG00642.hp2 HG01433.hp2 HG01516.hp2 others(35): Show |
intron_variant | MODIFIER | c.1279+737dupT | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr20 | 38640121 | ||||||
chr20:38640123 | TCC | T | 151 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0022 others(148): Show |
172 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.1279+738_1279+739d others(4): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38640123 | |||||||
chr20:38640125 | C | T | 34 | a0001c0002t0004g0072 a0001c0002t0008g0073 a0001c0004t0004g0044 others(31): Show |
38 | HG00642.hp2 HG01433.hp2 HG01516.hp2 others(35): Show |
intron_variant | MODIFIER | c.1279+739C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38640125 | |||||||
chr20:38640133 | T | C | 151 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0022 others(148): Show |
172 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.1279+747T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38640133 | |||||||
chr20:38640134 | C | T | 151 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0022 others(148): Show |
172 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.1279+748C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38640134 | |||||||
chr20:38640140 | CT | C | 151 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0022 others(148): Show |
172 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.1279+757delT | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr20 | 38640140 | ||||||
chr20:38640141 | T | C | 2 | a0001c0002t0008g0073 a0005c0040t0004g0279 |
2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1279+755T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38640141 | |||||||
chr20:38640145 | T | C | 153 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0022 others(150): Show |
174 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.1279+759T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38640145 | |||||||
chr20:38640145 | T | TTCTTCC | 64 | a0001c0002t0010g0081 a0001c0004t0004g0044 a0001c0004t0007g0112 others(61): Show |
70 | HG00642.hp2 HG01109.hp1 HG01243.hp2 others(67): Show |
intron_variant | MODIFIER | c.1279+765_1279+770d others(8): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr20 | 38640145 | ||||||
chr20:38640151 | C | CTCTTCTT | 37 | a0001c0004t0016g0228 a0001c0007t0001g0187 a0001c0007t0001g0240 others(34): Show |
41 | HG00642.hp2 HG01261.hp1 HG01433.hp2 others(38): Show |
intron_variant | MODIFIER | c.1279+780_1279+786d others(9): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr20 | 38640151 | ||||||
chr20:38640151 | C | T | 1 | a0005c0040t0004g0279 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1279+765C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38640151 | |||||||
chr20:38640156 | CT | C | 2 | a0001c0002t0004g0072 a0001c0008t0004g0025 |
3 | HG02258.hp1 HG03041.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1279+773delT | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr20 | 38640156 | ||||||
chr20:38640158 | T | C | 2 | a0001c0002t0004g0072 a0001c0008t0004g0025 |
3 | HG02258.hp1 HG03041.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1279+772T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38640158 | |||||||
chr20:38640167 | C | CTTCTTCT | 7 | a0003c0005t0001g0137 a0003c0005t0001g0194 a0003c0005t0002g0010 others(4): Show |
8 | HG01891.hp1 HG02109.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1279+791_1279+797d others(9): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr20 | 38640167 | ||||||
chr20:38640173 | C | T | 130 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0022 others(127): Show |
152 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.1279+787C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38640173 | |||||||
chr20:38640173 | CTTTCTTC others(1): Show |
C | 8 | a0001c0004t0007g0112 a0001c0004t0007g0283 a0005c0010t0010g0224 others(5): Show |
8 | HG01109.hp1 HG01243.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1279+806_1279+813d others(10): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr20 | 38640173 | ||||||
chr20:38640174 | T | C | 130 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0022 others(127): Show |
152 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.1279+788T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38640174 | |||||||
chr20:38640180 | CT | C | 130 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0022 others(127): Show |
152 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.1279+798delT | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr20 | 38640180 | ||||||
chr20:38640189 | TTTTCTTC | T | 30 | a0001c0001t0001g0098 a0001c0001t0001g0126 a0001c0001t0001g0140 others(27): Show |
31 | HG00558.hp2 HG00741.hp2 HG02015.hp1 others(28): Show |
intron_variant | MODIFIER | c.1279+824_1279+830d others(9): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr20 | 38640189 | ||||||
chr20:38640196 | C | CT | 130 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0022 others(127): Show |
152 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.1279+813dupT | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr20 | 38640196 | ||||||
chr20:38640218 | C | CT | 17 | a0001c0001t0001g0198 a0001c0001t0003g0199 a0001c0004t0007g0112 others(14): Show |
18 | HG00544.hp1 HG01891.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1279+847dupT | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr20 | 38640218 | ||||||
chr20:38640218 | CT | C | 8 | a0001c0001t0001g0140 a0001c0001t0001g0149 a0001c0001t0001g0197 others(5): Show |
8 | HG01169.hp2 HG01515.hp1 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.1279+847delT | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr20 | 38640218 | ||||||
chr20:38640220 | T | G | 4 | a0005c0010t0010g0224 a0005c0010t0010g0303 a0005c0010t0012g0128 others(1): Show |
4 | HG01109.hp1 HG02896.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1279+834T>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38640220 | |||||||
chr20:38640222 | T | C | 1 | a0007c0026t0002g0085 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1279+836T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38640222 | |||||||
chr20:38640238 | A | T | 1 | a0001c0001t0003g0248 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1279+852A>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38640238 | |||||||
chr20:38640251 | C | G | 1 | a0001c0029t0003g0136 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1279+865C>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38640251 | |||||||
chr20:38640376 | C | T | 2 | a0001c0002t0002g0052 a0001c0002t0002g0111 |
2 | NA18966.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.1279+990C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38640376 | |||||||
chr20:38640426 | C | T | 1 | a0001c0001t0006g0210 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1279+1040C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38640426 | |||||||
chr20:38640460 | G | A | 21 | a0001c0001t0001g0022 a0001c0001t0002g0037 a0001c0001t0002g0083 others(18): Show |
23 | HG00558.hp1 HG00673.hp1 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.1279+1074G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38640460 | |||||||
chr20:38640538 | A | G | 1 | a0019c0034t0007g0099 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1279+1152A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38640538 | |||||||
chr20:38640588 | T | C | 1 | a0001c0002t0008g0073 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1280-1138T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38640588 | |||||||
chr20:38640627 | C | T | 5 | a0001c0007t0001g0187 a0001c0007t0001g0240 a0001c0007t0002g0036 others(2): Show |
5 | HG02451.hp2 HG02622.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1280-1099C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38640627 | |||||||
chr20:38640670 | C | T | 1 | a0001c0002t0005g0163 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1280-1056C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38640670 | |||||||
chr20:38640809 | G | A | 1 | a0001c0001t0002g0083 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1280-917G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38640809 | |||||||
chr20:38640846 | G | A | 12 | a0001c0004t0007g0112 a0001c0004t0007g0283 a0005c0010t0010g0224 others(9): Show |
12 | HG01109.hp1 HG01243.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1280-880G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38640846 | |||||||
chr20:38640867 | C | A | 10 | a0001c0002t0004g0072 a0001c0004t0004g0044 a0001c0008t0004g0025 others(7): Show |
12 | HG02258.hp1 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1280-859C>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38640867 | |||||||
chr20:38640989 | A | G | 1 | a0001c0020t0003g0202 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1280-737A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38640989 | |||||||
chr20:38641024 | A | G | 6 | a0003c0005t0001g0137 a0003c0005t0001g0194 a0003c0005t0002g0010 others(3): Show |
7 | HG02109.hp2 HG02572.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1280-702A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38641024 | |||||||
chr20:38641079 | A | T | 1 | a0001c0001t0003g0248 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1280-647A>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38641079 | |||||||
chr20:38641079 | AGGAG | A | 16 | a0001c0001t0005g0185 a0001c0004t0016g0228 a0002c0003t0004g0012 others(13): Show |
18 | HG00642.hp2 HG01516.hp2 HG01517.hp1 others(15): Show |
intron_variant | MODIFIER | c.1280-629_1280-626d others(6): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr20 | 38641079 | ||||||
chr20:38641097 | G | C | 1 | a0001c0002t0002g0033 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1280-629G>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38641097 | |||||||
chr20:38641100 | G | A | 5 | a0001c0001t0003g0171 a0001c0001t0003g0230 a0001c0001t0003g0249 others(2): Show |
5 | HG00642.hp1 HG01243.hp1 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.1280-626G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38641100 | |||||||
chr20:38641136 | C | T | 4 | a0001c0004t0007g0112 a0001c0004t0007g0283 a0009c0019t0007g0307 others(1): Show |
4 | HG01243.hp2 HG01891.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1280-590C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38641136 | |||||||
chr20:38641159 | T | C | 3 | a0001c0002t0001g0125 a0001c0002t0001g0165 a0001c0002t0001g0166 |
3 | NA18968.hp1 NA19002.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1280-567T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38641159 | |||||||
chr20:38641235 | G | T | 2 | a0001c0021t0002g0278 a0001c0021t0002g0281 |
2 | HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1280-491G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38641235 | |||||||
chr20:38641290 | G | A | 6 | a0001c0007t0001g0187 a0001c0007t0001g0240 a0001c0007t0002g0036 others(3): Show |
6 | HG02451.hp2 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1280-436G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38641290 | |||||||
chr20:38641342 | A | C | 2 | a0001c0021t0002g0278 a0001c0021t0002g0281 |
2 | HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1280-384A>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38641342 | |||||||
chr20:38641367 | A | G | 160 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0022 others(157): Show |
178 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.1280-359A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38641367 | |||||||
chr20:38641386 | T | C | 14 | a0001c0004t0007g0112 a0001c0004t0007g0283 a0001c0021t0002g0278 others(11): Show |
14 | HG01109.hp1 HG01243.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1280-340T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38641386 | |||||||
chr20:38641403 | G | C | 1 | a0001c0004t0007g0283 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1280-323G>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38641403 | |||||||
chr20:38641464 | C | T | 1 | a0007c0026t0002g0085 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1280-262C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38641464 | |||||||
chr20:38641466 | G | T | 1 | a0001c0004t0007g0283 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1280-260G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38641466 | |||||||
chr20:38641469 | C | T | 1 | a0016c0025t0004g0053 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1280-257C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38641469 | |||||||
chr20:38641603 | G | A | 4 | a0008c0006t0002g0028 a0008c0006t0002g0086 a0008c0006t0002g0105 others(1): Show |
5 | HG02886.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1280-123G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38641603 | |||||||
chr20:38641869 | T | C | 4 | a0001c0004t0007g0112 a0001c0004t0007g0283 a0009c0019t0007g0307 others(1): Show |
4 | HG01243.hp2 HG01891.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1362+61T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 10/14 | chr20 | 38641869 | |||||||
chr20:38642032 | C | T | 1 | a0002c0003t0004g0030 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1362+224C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 10/14 | chr20 | 38642032 | |||||||
chr20:38642147 | A | G | 13 | a0001c0002t0010g0081 a0001c0007t0001g0187 a0001c0007t0001g0240 others(10): Show |
14 | HG02109.hp2 HG02451.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.1362+339A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 10/14 | chr20 | 38642147 | |||||||
chr20:38642245 | G | T | 1 | a0001c0001t0002g0037 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1362+437G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 10/14 | chr20 | 38642245 | |||||||
chr20:38642321 | A | T | 214 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(211): Show |
237 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(234): Show |
intron_variant | MODIFIER | c.1362+513A>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 10/14 | chr20 | 38642321 | |||||||
chr20:38642346 | C | T | 1 | a0001c0002t0004g0088 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1362+538C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 10/14 | chr20 | 38642346 | |||||||
chr20:38642495 | A | G | 156 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(153): Show |
173 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.1362+687A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 10/14 | chr20 | 38642495 | |||||||
chr20:38642509 | C | T | 4 | a0001c0001t0005g0185 a0002c0003t0004g0012 a0002c0003t0004g0030 others(1): Show |
5 | HG01516.hp2 HG01517.hp1 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.1362+701C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 10/14 | chr20 | 38642509 | |||||||
chr20:38642608 | T | TCCTC | 9 | a0001c0021t0002g0278 a0001c0021t0002g0281 a0005c0010t0010g0224 others(6): Show |
9 | HG01109.hp1 HG02257.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.1362+814_1362+817d others(6): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr20 | 38642608 | ||||||
chr20:38642653 | C | T | 1 | a0004c0011t0007g0288 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1362+845C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 10/14 | chr20 | 38642653 | |||||||
chr20:38642714 | ATCCATCC others(9): Show |
A | 156 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(153): Show |
173 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.1362+922_1362+937d others(18): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr20 | 38642714 | ||||||
chr20:38642765 | C | T | 5 | a0007c0026t0002g0085 a0008c0006t0002g0028 a0008c0006t0002g0086 others(2): Show |
6 | HG02630.hp2 HG02886.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1363-939C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 10/14 | chr20 | 38642765 | |||||||
chr20:38642911 | C | T | 48 | a0001c0001t0005g0185 a0001c0001t0005g0251 a0001c0002t0004g0072 others(45): Show |
54 | HG00642.hp2 HG01261.hp1 HG01516.hp2 others(51): Show |
intron_variant | MODIFIER | c.1363-793C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 10/14 | chr20 | 38642911 | |||||||
chr20:38642939 | G | C | 2 | a0012c0018t0004g0077 a0012c0018t0004g0087 |
2 | HG02647.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1363-765G>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 10/14 | chr20 | 38642939 | |||||||
chr20:38642970 | G | A | 3 | a0001c0001t0006g0082 a0001c0001t0006g0090 a0001c0001t0006g0091 |
3 | HG00738.hp2 HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1363-734G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 10/14 | chr20 | 38642970 | |||||||
chr20:38643008 | G | A | 12 | a0001c0007t0001g0187 a0001c0007t0001g0240 a0001c0007t0002g0036 others(9): Show |
13 | HG02109.hp2 HG02451.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.1363-696G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 10/14 | chr20 | 38643008 | |||||||
chr20:38643023 | C | T | 1 | a0001c0002t0010g0081 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1363-681C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 10/14 | chr20 | 38643023 | |||||||
chr20:38643031 | C | T | 13 | a0001c0002t0007g0009 a0001c0002t0007g0013 a0001c0002t0007g0043 others(10): Show |
15 | HG01069.hp2 HG01168.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.1363-673C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 10/14 | chr20 | 38643031 | |||||||
chr20:38643145 | C | CAA | 6 | a0006c0013t0008g0027 a0006c0013t0008g0299 a0006c0017t0008g0045 others(3): Show |
7 | HG01261.hp1 HG01884.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.1363-547_1363-546d others(4): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr20 | 38643145 | ||||||
chr20:38643145 | CA | C | 7 | a0001c0001t0001g0098 a0001c0001t0001g0221 a0001c0002t0004g0032 others(4): Show |
7 | HG00639.hp2 HG00741.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.1363-546delA | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr20 | 38643145 | ||||||
chr20:38643145 | CAA | C | 148 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(145): Show |
165 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.1363-547_1363-546d others(4): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr20 | 38643145 | ||||||
chr20:38643145 | CAAAA | C | 7 | a0005c0010t0010g0224 a0005c0010t0010g0303 a0005c0010t0012g0128 others(4): Show |
7 | HG01109.hp1 HG02257.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1363-549_1363-546d others(6): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr20 | 38643145 | ||||||
chr20:38643223 | T | C | 214 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(211): Show |
237 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(234): Show |
intron_variant | MODIFIER | c.1363-481T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 10/14 | chr20 | 38643223 | |||||||
chr20:38643551 | G | A | 6 | a0001c0001t0001g0145 a0001c0001t0001g0169 a0001c0001t0002g0004 others(3): Show |
8 | HG01074.hp1 HG01192.hp2 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.1363-153G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 10/14 | chr20 | 38643551 | |||||||
chr20:38643566 | C | T | 35 | a0001c0001t0005g0185 a0001c0001t0005g0251 a0001c0002t0004g0072 others(32): Show |
40 | HG00642.hp2 HG01261.hp1 HG01516.hp2 others(37): Show |
intron_variant | MODIFIER | c.1363-138C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 10/14 | chr20 | 38643566 | |||||||
chr20:38643572 | C | A | 1 | a0007c0009t0013g0041 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1363-132C>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 10/14 | chr20 | 38643572 | |||||||
chr20:38643657 | G | A | 7 | a0001c0004t0004g0044 a0004c0011t0004g0113 a0004c0011t0004g0308 others(4): Show |
8 | HG02559.hp1 HG02630.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1363-47G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 10/14 | chr20 | 38643657 | |||||||
chr20:38643946 | G | A | 156 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(153): Show |
173 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.1569+36G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/14 | chr20 | 38643946 | |||||||
chr20:38644027 | G | T | 1 | a0001c0002t0010g0081 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1569+117G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/14 | chr20 | 38644027 | |||||||
chr20:38644127 | G | C | 5 | a0001c0001t0002g0015 a0001c0001t0002g0048 a0001c0001t0002g0078 others(2): Show |
6 | HG02280.hp2 HG02818.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1569+217G>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/14 | chr20 | 38644127 | |||||||
chr20:38644150 | C | T | 4 | a0005c0010t0010g0224 a0005c0010t0010g0303 a0005c0010t0012g0128 others(1): Show |
4 | HG01109.hp1 HG02896.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1569+240C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/14 | chr20 | 38644150 | |||||||
chr20:38644326 | A | C | 1 | a0001c0001t0001g0232 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1569+416A>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/14 | chr20 | 38644326 | |||||||
chr20:38644333 | A | G | 1 | a0007c0009t0013g0041 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1569+423A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/14 | chr20 | 38644333 | |||||||
chr20:38644389 | T | C | 1 | a0007c0009t0013g0041 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1569+479T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/14 | chr20 | 38644389 | |||||||
chr20:38644533 | A | G | 1 | a0019c0034t0007g0099 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1569+623A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/14 | chr20 | 38644533 | |||||||
chr20:38644569 | A | G | 58 | a0001c0001t0005g0185 a0001c0001t0005g0251 a0001c0002t0004g0072 others(55): Show |
64 | HG00642.hp2 HG01109.hp1 HG01261.hp1 others(61): Show |
intron_variant | MODIFIER | c.1569+659A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/14 | chr20 | 38644569 | |||||||
chr20:38644613 | GTCACCCA others(5): Show |
G | 10 | a0001c0002t0004g0072 a0001c0004t0004g0044 a0001c0008t0004g0025 others(7): Show |
12 | HG02258.hp1 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1569+716_1569+727d others(14): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr20 | 38644613 | ||||||
chr20:38644636 | A | C | 1 | a0016c0025t0004g0053 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1569+726A>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/14 | chr20 | 38644636 | |||||||
chr20:38644709 | T | C | 214 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(211): Show |
237 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(234): Show |
intron_variant | MODIFIER | c.1569+799T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/14 | chr20 | 38644709 | |||||||
chr20:38644888 | T | C | 16 | a0001c0001t0005g0185 a0001c0001t0005g0251 a0001c0004t0016g0228 others(13): Show |
18 | HG00642.hp2 HG01516.hp2 HG01517.hp1 others(15): Show |
intron_variant | MODIFIER | c.1569+978T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/14 | chr20 | 38644888 | |||||||
chr20:38644925 | T | TC | 10 | a0001c0002t0004g0072 a0001c0004t0004g0044 a0001c0008t0004g0025 others(7): Show |
12 | HG02258.hp1 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1569+1018dupC | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr20 | 38644925 | ||||||
chr20:38644929 | T | C | 211 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(208): Show |
234 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.1569+1019T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/14 | chr20 | 38644929 | |||||||
chr20:38644931 | T | C | 1 | a0001c0001t0001g0206 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1569+1021T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/14 | chr20 | 38644931 | |||||||
chr20:38645149 | C | CT | 34 | a0001c0001t0004g0049 a0001c0001t0005g0216 a0001c0001t0005g0250 others(31): Show |
34 | HG00639.hp2 HG00741.hp1 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.1570-886dupT | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr20 | 38645149 | ||||||
chr20:38645149 | CT | C | 17 | a0001c0001t0003g0189 a0001c0002t0004g0072 a0001c0004t0004g0044 others(14): Show |
20 | HG02109.hp2 HG02258.hp1 HG02559.hp1 others(17): Show |
intron_variant | MODIFIER | c.1570-886delT | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr20 | 38645149 | ||||||
chr20:38645174 | G | A | 1 | a0007c0026t0002g0085 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1570-873G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/14 | chr20 | 38645174 | |||||||
chr20:38645233 | G | A | 1 | a0022c0031t0002g0286 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1570-814G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/14 | chr20 | 38645233 | |||||||
chr20:38645267 | T | C | 214 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(211): Show |
237 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(234): Show |
intron_variant | MODIFIER | c.1570-780T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/14 | chr20 | 38645267 | |||||||
chr20:38645607 | C | A | 7 | a0001c0007t0001g0187 a0001c0007t0001g0240 a0001c0007t0002g0036 others(4): Show |
7 | HG01884.hp2 HG02451.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1570-440C>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/14 | chr20 | 38645607 | |||||||
chr20:38645663 | C | A | 1 | a0001c0001t0003g0142 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1570-384C>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/14 | chr20 | 38645663 | |||||||
chr20:38645677 | C | G | 215 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(212): Show |
238 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(235): Show |
intron_variant | MODIFIER | c.1570-370C>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/14 | chr20 | 38645677 | |||||||
chr20:38645832 | C | A | 49 | a0001c0001t0005g0185 a0001c0001t0005g0233 a0001c0001t0005g0251 others(46): Show |
53 | HG00642.hp2 HG01109.hp1 HG01261.hp1 others(50): Show |
intron_variant | MODIFIER | c.1570-215C>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/14 | chr20 | 38645832 | |||||||
chr20:38645916 | C | CA | 156 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(153): Show |
173 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.1570-129dupA | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr20 | 38645916 | ||||||
chr20:38645965 | G | A | 10 | a0001c0002t0004g0072 a0001c0004t0004g0044 a0001c0008t0004g0025 others(7): Show |
12 | HG02258.hp1 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1570-82G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/14 | chr20 | 38645965 | |||||||
chr20:38646021 | G | A | 1 | a0001c0004t0016g0228 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1570-26G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/14 | chr20 | 38646021 | |||||||
chr20:38646218 | A | G | 156 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(153): Show |
173 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.1710+31A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 12/14 | chr20 | 38646218 | |||||||
chr20:38646231 | A | G | 1 | a0001c0001t0001g0237 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1710+44A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 12/14 | chr20 | 38646231 | |||||||
chr20:38646319 | G | C | 5 | a0006c0013t0008g0027 a0006c0013t0008g0299 a0006c0017t0008g0045 others(2): Show |
6 | HG01261.hp1 HG01884.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.1710+132G>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 12/14 | chr20 | 38646319 | |||||||
chr20:38646359 | C | A | 10 | a0001c0002t0004g0072 a0001c0004t0004g0044 a0001c0008t0004g0025 others(7): Show |
12 | HG02258.hp1 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1710+172C>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 12/14 | chr20 | 38646359 | |||||||
chr20:38646447 | C | T | 5 | a0006c0013t0008g0027 a0006c0013t0008g0299 a0006c0017t0008g0045 others(2): Show |
6 | HG01261.hp1 HG01884.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.1710+260C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 12/14 | chr20 | 38646447 | |||||||
chr20:38646511 | C | T | 19 | a0001c0002t0007g0009 a0001c0002t0007g0013 a0001c0002t0007g0043 others(16): Show |
22 | HG01069.hp2 HG01168.hp1 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.1710+324C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 12/14 | chr20 | 38646511 | |||||||
chr20:38646514 | G | A | 2 | a0001c0001t0001g0098 a0001c0001t0001g0158 |
2 | HG02735.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1710+327G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 12/14 | chr20 | 38646514 | |||||||
chr20:38646653 | A | G | 2 | a0001c0002t0004g0302 a0001c0002t0015g0270 |
2 | HG02071.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1711-304A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 12/14 | chr20 | 38646653 | |||||||
chr20:38647275 | A | G | 1 | a0001c0001t0006g0298 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1880+149A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 13/14 | chr20 | 38647275 | |||||||
chr20:38647290 | C | T | 9 | a0001c0002t0008g0073 a0006c0013t0008g0027 a0006c0013t0008g0299 others(6): Show |
10 | HG01261.hp1 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1880+164C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 13/14 | chr20 | 38647290 | |||||||
chr20:38647374 | CTGTTGGT others(1): Show |
C | 7 | a0001c0007t0001g0187 a0001c0007t0001g0240 a0001c0007t0002g0036 others(4): Show |
7 | HG01884.hp2 HG02451.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1880+253_1880+260d others(10): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr20 | 38647374 | ||||||
chr20:38647375 | TGTTG | T | 199 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(196): Show |
221 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(218): Show |
intron_variant | MODIFIER | c.1880+253_1880+256d others(6): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr20 | 38647375 | ||||||
chr20:38647379 | G | GGTTT | 4 | a0001c0001t0003g0229 a0001c0001t0003g0268 a0001c0002t0007g0009 others(1): Show |
5 | HG01069.hp2 HG01168.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.1880+278_1880+281d others(6): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr20 | 38647379 | ||||||
chr20:38647379 | G | T | 9 | a0001c0002t0010g0081 a0001c0004t0016g0228 a0003c0005t0001g0137 others(6): Show |
10 | HG02109.hp2 HG02486.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1880+253G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 13/14 | chr20 | 38647379 | |||||||
chr20:38647557 | A | AT | 33 | a0001c0001t0004g0049 a0001c0001t0005g0216 a0001c0001t0005g0250 others(30): Show |
33 | HG00639.hp2 HG00741.hp1 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.1880+438dupT | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr20 | 38647557 | ||||||
chr20:38647592 | T | C | 215 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(212): Show |
238 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(235): Show |
intron_variant | MODIFIER | c.1880+466T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 13/14 | chr20 | 38647592 | |||||||
chr20:38647714 | T | C | 3 | a0001c0002t0004g0072 a0001c0008t0004g0025 a0001c0008t0004g0305 |
4 | HG02258.hp1 HG02572.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1880+588T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 13/14 | chr20 | 38647714 | |||||||
chr20:38647744 | C | T | 17 | a0001c0002t0004g0072 a0001c0004t0004g0044 a0001c0007t0001g0187 others(14): Show |
19 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.1880+618C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 13/14 | chr20 | 38647744 | |||||||
chr20:38647797 | G | C | 17 | a0001c0001t0005g0185 a0001c0001t0005g0233 a0001c0001t0005g0251 others(14): Show |
19 | HG00642.hp2 HG01516.hp2 HG01517.hp1 others(16): Show |
intron_variant | MODIFIER | c.1880+671G>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 13/14 | chr20 | 38647797 | |||||||
chr20:38647802 | G | A | 26 | a0001c0001t0005g0185 a0001c0001t0005g0233 a0001c0001t0005g0251 others(23): Show |
29 | HG00642.hp2 HG01261.hp1 HG01516.hp2 others(26): Show |
intron_variant | MODIFIER | c.1880+676G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 13/14 | chr20 | 38647802 | |||||||
chr20:38647930 | G | T | 1 | a0010c0012t0007g0097 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1881-713G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 13/14 | chr20 | 38647930 | |||||||
chr20:38647992 | T | C | 1 | a0001c0001t0002g0065 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1881-651T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 13/14 | chr20 | 38647992 | |||||||
chr20:38648152 | G | C | 13 | a0001c0002t0007g0009 a0001c0002t0007g0013 a0001c0002t0007g0043 others(10): Show |
15 | HG01069.hp2 HG01168.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.1881-491G>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 13/14 | chr20 | 38648152 | |||||||
chr20:38648393 | C | T | 4 | a0001c0004t0004g0044 a0004c0011t0004g0113 a0004c0011t0004g0308 others(1): Show |
4 | HG02559.hp1 HG02630.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1881-250C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 13/14 | chr20 | 38648393 | |||||||
chr20:38648455 | C | T | 2 | a0007c0009t0013g0041 a0021c0039t0013g0280 |
2 | HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1881-188C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 13/14 | chr20 | 38648455 | |||||||
chr20:38648499 | G | T | 3 | a0005c0010t0010g0224 a0005c0010t0010g0303 a0005c0010t0012g0128 |
3 | HG01109.hp1 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1881-144G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 13/14 | chr20 | 38648499 | |||||||
chr20:38648505 | ATGC | A | 5 | a0006c0013t0008g0027 a0006c0013t0008g0299 a0006c0017t0008g0045 others(2): Show |
6 | HG01261.hp1 HG01884.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.1881-133_1881-131d others(5): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr20 | 38648505 | ||||||
chr20:38648510 | G | T | 210 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(207): Show |
232 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(229): Show |
intron_variant | MODIFIER | c.1881-133G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 13/14 | chr20 | 38648510 | |||||||
chr20:38648571 | C | T | 3 | a0001c0002t0005g0201 a0001c0002t0005g0204 a0001c0002t0005g0212 |
3 | HG01069.hp1 HG01071.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.1881-72C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 13/14 | chr20 | 38648571 | |||||||
chr20:38648613 | G | GT | 10 | a0001c0001t0002g0083 a0001c0002t0008g0073 a0006c0013t0008g0027 others(7): Show |
11 | HG01261.hp1 HG01884.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.1881-20dupT | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr20 | 38648613 | ||||||
chr20:38648622 | T | C | 1 | a0001c0001t0003g0122 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1881-21T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 13/14 | chr20 | 38648622 | |||||||
chr20:38648626 | C | T | 16 | a0001c0001t0005g0185 a0001c0001t0005g0233 a0001c0001t0005g0251 others(13): Show |
18 | HG00642.hp2 HG01516.hp2 HG01517.hp1 others(15): Show |
intron_variant | MODIFIER | c.1881-17C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 13/14 | chr20 | 38648626 | |||||||
chr20:38648628 | C | T | 198 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(195): Show |
219 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(216): Show |
intron_variant | MODIFIER | c.1881-15C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 13/14 | chr20 | 38648628 | |||||||
chr20:38648733 | G | C | 17 | a0001c0002t0004g0072 a0001c0004t0004g0044 a0001c0007t0001g0187 others(14): Show |
19 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.1936+35G>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 14/14 | chr20 | 38648733 | |||||||
chr20:38648758 | A | G | 2 | a0001c0001t0003g0170 a0001c0001t0006g0058 |
2 | NA19070.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1936+60A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 14/14 | chr20 | 38648758 | |||||||
chr20:38648920 | G | A | 17 | a0001c0002t0004g0072 a0001c0004t0004g0044 a0001c0007t0001g0187 others(14): Show |
19 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.1936+222G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 14/14 | chr20 | 38648920 | |||||||
chr20:38648975 | A | G | 232 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(229): Show |
257 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(254): Show |
intron_variant | MODIFIER | c.1936+277A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 14/14 | chr20 | 38648975 | |||||||
chr20:38649144 | C | A | 9 | a0001c0002t0004g0072 a0001c0004t0004g0044 a0001c0008t0004g0025 others(6): Show |
11 | HG02258.hp1 HG02559.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1936+446C>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 14/14 | chr20 | 38649144 | |||||||
chr20:38649269 | C | T | 2 | a0008c0006t0002g0105 a0008c0006t0002g0107 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1937-488C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 14/14 | chr20 | 38649269 | |||||||
chr20:38649364 | A | G | 6 | a0003c0005t0001g0137 a0003c0005t0001g0194 a0003c0005t0002g0010 others(3): Show |
7 | HG02109.hp2 HG02572.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1937-393A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 14/14 | chr20 | 38649364 | |||||||
chr20:38649422 | C | T | 5 | a0006c0013t0008g0027 a0006c0013t0008g0299 a0006c0017t0008g0045 others(2): Show |
6 | HG01261.hp1 HG01884.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.1937-335C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 14/14 | chr20 | 38649422 | |||||||
chr20:38649464 | A | T | 233 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(230): Show |
258 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(255): Show |
intron_variant | MODIFIER | c.1937-293A>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 14/14 | chr20 | 38649464 | |||||||
chr20:38649480 | G | A | 3 | a0001c0001t0001g0139 a0001c0001t0001g0180 a0001c0001t0001g0271 |
3 | HG00140.hp2 HG01361.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.1937-277G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 14/14 | chr20 | 38649480 | |||||||
chr20:38649542 | C | G | 1 | a0019c0034t0007g0099 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1937-215C>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 14/14 | chr20 | 38649542 | |||||||
chr20:38649553 | C | CG | 33 | a0001c0001t0004g0049 a0001c0001t0005g0216 a0001c0001t0005g0250 others(30): Show |
33 | HG00639.hp2 HG00741.hp1 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.1937-204_1937-203i others(3): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 14/14 | chr20 | 38649553 | |||||||
chr20:38649554 | A | G | 309 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(306): Show |
346 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(343): Show |
intron_variant | MODIFIER | c.1937-203A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 14/14 | chr20 | 38649554 |