Item | Value |
---|---|
geneid | 399979 |
ensemblid | ENSG00000120451.11 |
hgncid | 21532 |
symbol | SNX19 |
name | sorting nexin 19 |
refseq_nuc | NM_014758.3 |
refseq_prot | NP_055573.3 |
ensembl_nuc | ENST00000265909.9 |
ensembl_prot | ENSP00000265909.4 |
mane_status | MANE Select |
chr | chr11 |
start | 130866250 |
end | 130916479 |
strand | - |
ver | v1.2 |
region | chr11:130866250-130916479 |
region5000 | chr11:130861250-130921479 |
regionname0 | SNX19_chr11_130866250_130916479 |
regionname5000 | SNX19_chr11_130861250_130921479 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 992 | 178 | 30 | 35 | 72 | 8 | 33 | 53 | SNX19_chr11_130861250_130921479 | SNX19 | MKTET others(987): Show |
chr11 | 130861250 | 130921479 |
a0002 | 1/0 | 992 | 81 | 1 | 21 | 50 | 3 | 5 | 36 | SNX19_chr11_130861250_130921479 | SNX19 | MKTET others(987): Show |
chr11 | 130861250 | 130921479 |
a0003 | 0/0 | 992 | 53 | 6 | 5 | 40 | 1 | 1 | 34 | SNX19_chr11_130861250_130921479 | SNX19 | MKTET others(987): Show |
chr11 | 130861250 | 130921479 |
a0004 | 0/0 | 992 | 35 | 22 | 3 | 8 | 1 | 1 | 8 | SNX19_chr11_130861250_130921479 | SNX19 | MKTET others(987): Show |
chr11 | 130861250 | 130921479 |
a0005 | 0/0 | 992 | 17 | 17 | 0 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | MKTET others(987): Show |
chr11 | 130861250 | 130921479 |
a0006 | 0/0 | 992 | 16 | 14 | 1 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | MKTET others(987): Show |
chr11 | 130861250 | 130921479 |
a0007 | 0/0 | 992 | 14 | 0 | 0 | 14 | 0 | 0 | 12 | SNX19_chr11_130861250_130921479 | SNX19 | MKTET others(987): Show |
chr11 | 130861250 | 130921479 |
a0008 | 0/0 | 992 | 4 | 0 | 0 | 4 | 0 | 0 | 3 | SNX19_chr11_130861250_130921479 | SNX19 | MKTET others(987): Show |
chr11 | 130861250 | 130921479 |
a0009 | 0/0 | 992 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | MKTET others(987): Show |
chr11 | 130861250 | 130921479 |
a0010 | 0/0 | 992 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | MKTET others(987): Show |
chr11 | 130861250 | 130921479 |
a0011 | 0/0 | 992 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | MKTET others(987): Show |
chr11 | 130861250 | 130921479 |
a0012 | 0/0 | 992 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | MKTET others(987): Show |
chr11 | 130861250 | 130921479 |
a0013 | 0/0 | 992 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | MKTET others(987): Show |
chr11 | 130861250 | 130921479 |
a0014 | 0/0 | 992 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | MKTET others(987): Show |
chr11 | 130861250 | 130921479 |
a0015 | 0/0 | 992 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | MKTET others(987): Show |
chr11 | 130861250 | 130921479 |
a0016 | 0/0 | 992 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | MKTET others(987): Show |
chr11 | 130861250 | 130921479 |
a0017 | 0/0 | 992 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | MKTET others(987): Show |
chr11 | 130861250 | 130921479 |
a0018 | 0/0 | 992 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | MKTET others(987): Show |
chr11 | 130861250 | 130921479 |
a0019 | 0/0 | 992 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | MKTET others(987): Show |
chr11 | 130861250 | 130921479 |
a0020 | 0/0 | 992 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | MKTET others(987): Show |
chr11 | 130861250 | 130921479 |
a0021 | 0/0 | 992 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | MKTET others(987): Show |
chr11 | 130861250 | 130921479 |
a0022 | 0/0 | 992 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | MKTET others(987): Show |
chr11 | 130861250 | 130921479 |
a0023 | 0/1 | 992 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | MKTET others(987): Show |
chr11 | 130861250 | 130921479 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2976 | 165 | 24 | 31 | 72 | 7 | 31 | SNX19_chr11_130861250_130921479 | SNX19 | ATGAA others(2971): Show |
chr11 | 130861250 | 130921479 | ||
a0001c0010 | 0/0 | 2976 | 6 | 5 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | ATGAA others(2971): Show |
chr11 | 130861250 | 130921479 | ||
a0001c0011 | 0/0 | 2976 | 5 | 0 | 2 | 0 | 1 | 2 | SNX19_chr11_130861250_130921479 | SNX19 | ATGAA others(2971): Show |
chr11 | 130861250 | 130921479 | ||
a0001c0014 | 0/0 | 2976 | 2 | 1 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | ATGAA others(2971): Show |
chr11 | 130861250 | 130921479 | ||
a0002c0002 | 1/0 | 2976 | 81 | 1 | 21 | 50 | 3 | 5 | SNX19_chr11_130861250_130921479 | SNX19 | ATGAA others(2971): Show |
chr11 | 130861250 | 130921479 | ||
a0003c0003 | 0/0 | 2976 | 53 | 6 | 5 | 40 | 1 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | ATGAA others(2971): Show |
chr11 | 130861250 | 130921479 | ||
a0004c0005 | 0/0 | 2976 | 16 | 5 | 1 | 8 | 1 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | ATGAA others(2971): Show |
chr11 | 130861250 | 130921479 | ||
a0004c0008 | 0/0 | 2976 | 11 | 11 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | ATGAA others(2971): Show |
chr11 | 130861250 | 130921479 | ||
a0004c0009 | 0/0 | 2976 | 7 | 5 | 2 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | ATGAA others(2971): Show |
chr11 | 130861250 | 130921479 | ||
a0004c0025 | 0/0 | 2976 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | ATGAA others(2971): Show |
chr11 | 130861250 | 130921479 | ||
a0005c0004 | 0/0 | 2976 | 16 | 16 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | ATGAA others(2971): Show |
chr11 | 130861250 | 130921479 | ||
a0005c0017 | 0/0 | 2976 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | ATGAA others(2971): Show |
chr11 | 130861250 | 130921479 | ||
a0006c0006 | 0/0 | 2976 | 15 | 13 | 1 | 0 | 1 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | ATGAA others(2971): Show |
chr11 | 130861250 | 130921479 | ||
a0006c0019 | 0/0 | 2976 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | ATGAA others(2971): Show |
chr11 | 130861250 | 130921479 | ||
a0007c0007 | 0/0 | 2976 | 14 | 0 | 0 | 14 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | ATGAA others(2971): Show |
chr11 | 130861250 | 130921479 | ||
a0008c0012 | 0/0 | 2976 | 4 | 0 | 0 | 4 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | ATGAA others(2971): Show |
chr11 | 130861250 | 130921479 | ||
a0009c0013 | 0/0 | 2976 | 2 | 0 | 0 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | ATGAA others(2971): Show |
chr11 | 130861250 | 130921479 | ||
a0010c0024 | 0/0 | 2976 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | ATGAA others(2971): Show |
chr11 | 130861250 | 130921479 | ||
a0011c0020 | 0/0 | 2976 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | ATGAA others(2971): Show |
chr11 | 130861250 | 130921479 | ||
a0012c0018 | 0/0 | 2976 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | ATGAA others(2971): Show |
chr11 | 130861250 | 130921479 | ||
a0013c0028 | 0/0 | 2976 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | ATGAA others(2971): Show |
chr11 | 130861250 | 130921479 | ||
a0014c0026 | 0/0 | 2976 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | ATGAA others(2971): Show |
chr11 | 130861250 | 130921479 | ||
a0015c0031 | 0/0 | 2976 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | ATGAA others(2971): Show |
chr11 | 130861250 | 130921479 | ||
a0016c0023 | 0/0 | 2976 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | ATGAA others(2971): Show |
chr11 | 130861250 | 130921479 | ||
a0017c0029 | 0/0 | 2976 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | ATGAA others(2971): Show |
chr11 | 130861250 | 130921479 | ||
a0018c0027 | 0/0 | 2976 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | ATGAA others(2971): Show |
chr11 | 130861250 | 130921479 | ||
a0019c0022 | 0/0 | 2976 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | ATGAA others(2971): Show |
chr11 | 130861250 | 130921479 | ||
a0020c0015 | 0/0 | 2976 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | ATGAA others(2971): Show |
chr11 | 130861250 | 130921479 | ||
a0021c0030 | 0/0 | 2976 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | ATGAA others(2971): Show |
chr11 | 130861250 | 130921479 | ||
a0022c0016 | 0/0 | 2976 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | ATGAA others(2971): Show |
chr11 | 130861250 | 130921479 | ||
a0023c0021 | 0/1 | 2976 | 1 | 0 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | ATGAA others(2971): Show |
chr11 | 130861250 | 130921479 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 15691 | 73 | 2 | 18 | 37 | 5 | 11 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0001c0001t0004 | 0/0 | 15687 | 2 | 0 | 0 | 1 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15682): Show |
chr11 | 130861250 | 130921479 |
a0001c0001t0006 | 0/0 | 15692 | 13 | 0 | 1 | 2 | 1 | 9 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15687): Show |
chr11 | 130861250 | 130921479 |
a0001c0001t0007 | 0/0 | 15687 | 13 | 4 | 3 | 3 | 0 | 3 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15682): Show |
chr11 | 130861250 | 130921479 |
a0001c0001t0011 | 0/0 | 15690 | 4 | 3 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15685): Show |
chr11 | 130861250 | 130921479 |
a0001c0001t0014 | 0/0 | 15691 | 4 | 0 | 0 | 4 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0001c0001t0015 | 0/0 | 15692 | 4 | 0 | 0 | 4 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15687): Show |
chr11 | 130861250 | 130921479 |
a0001c0001t0017 | 0/0 | 15691 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0001c0001t0018 | 0/0 | 15691 | 4 | 3 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0001c0001t0028 | 0/0 | 15691 | 3 | 0 | 0 | 3 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0001c0001t0037 | 0/0 | 15687 | 2 | 0 | 1 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15682): Show |
chr11 | 130861250 | 130921479 |
a0001c0001t0038 | 0/0 | 15687 | 2 | 2 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15682): Show |
chr11 | 130861250 | 130921479 |
a0001c0001t0042 | 0/0 | 15692 | 2 | 0 | 1 | 0 | 1 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15687): Show |
chr11 | 130861250 | 130921479 |
a0001c0001t0043 | 0/0 | 15692 | 2 | 0 | 0 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15687): Show |
chr11 | 130861250 | 130921479 |
a0001c0001t0044 | 0/0 | 15691 | 2 | 0 | 2 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0001c0001t0045 | 0/0 | 15691 | 2 | 0 | 0 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0001c0001t0046 | 0/0 | 15691 | 2 | 0 | 0 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0001c0001t0047 | 0/0 | 15691 | 2 | 0 | 0 | 0 | 0 | 2 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0001c0001t0056 | 0/0 | 15691 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0001c0001t0075 | 0/0 | 15691 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0001c0001t0076 | 0/0 | 15687 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15682): Show |
chr11 | 130861250 | 130921479 |
a0001c0001t0077 | 0/0 | 15689 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15684): Show |
chr11 | 130861250 | 130921479 |
a0001c0001t0078 | 0/0 | 15691 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0001c0001t0080 | 0/0 | 15692 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15687): Show |
chr11 | 130861250 | 130921479 |
a0001c0001t0086 | 0/0 | 15692 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15687): Show |
chr11 | 130861250 | 130921479 |
a0001c0001t0087 | 0/0 | 15691 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0001c0001t0088 | 0/0 | 15692 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15687): Show |
chr11 | 130861250 | 130921479 |
a0001c0001t0089 | 0/0 | 15692 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15687): Show |
chr11 | 130861250 | 130921479 |
a0001c0001t0090 | 0/0 | 15693 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15688): Show |
chr11 | 130861250 | 130921479 |
a0001c0001t0091 | 0/0 | 15692 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15687): Show |
chr11 | 130861250 | 130921479 |
a0001c0001t0092 | 0/0 | 15693 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15688): Show |
chr11 | 130861250 | 130921479 |
a0001c0001t0093 | 0/0 | 15691 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0001c0001t0095 | 0/0 | 15691 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0001c0001t0096 | 0/0 | 15691 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0001c0001t0097 | 0/0 | 15691 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0001c0001t0098 | 0/0 | 15691 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0001c0001t0099 | 0/0 | 15691 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0001c0001t0100 | 0/0 | 15691 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0001c0001t0101 | 0/0 | 15692 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15687): Show |
chr11 | 130861250 | 130921479 |
a0001c0001t0104 | 0/0 | 15691 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0001c0001t0105 | 0/0 | 15691 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0001c0001t0106 | 0/0 | 15691 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0001c0001t0108 | 0/0 | 15692 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15687): Show |
chr11 | 130861250 | 130921479 |
a0001c0001t0111 | 0/0 | 15691 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0001c0001t0114 | 0/0 | 15690 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15685): Show |
chr11 | 130861250 | 130921479 |
a0001c0001t0115 | 0/0 | 15692 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15687): Show |
chr11 | 130861250 | 130921479 |
a0001c0010t0010 | 0/0 | 15691 | 5 | 4 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0001c0010t0053 | 0/0 | 15691 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0001c0011t0016 | 0/0 | 15691 | 3 | 0 | 2 | 0 | 1 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0001c0011t0102 | 0/0 | 15692 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15687): Show |
chr11 | 130861250 | 130921479 |
a0001c0011t0107 | 0/0 | 15691 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0001c0014t0041 | 0/0 | 15691 | 2 | 1 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0002c0002t0002 | 1/0 | 15691 | 49 | 0 | 15 | 29 | 2 | 2 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0002c0002t0005 | 0/0 | 15691 | 15 | 0 | 0 | 15 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0002c0002t0012 | 0/0 | 15691 | 4 | 0 | 2 | 0 | 1 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0002c0002t0024 | 0/0 | 15691 | 3 | 0 | 2 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0002c0002t0025 | 0/0 | 15690 | 3 | 0 | 1 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15685): Show |
chr11 | 130861250 | 130921479 |
a0002c0002t0061 | 0/0 | 15690 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15685): Show |
chr11 | 130861250 | 130921479 |
a0002c0002t0062 | 0/0 | 15691 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0002c0002t0063 | 0/0 | 15691 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0002c0002t0064 | 0/0 | 15691 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0002c0002t0065 | 0/0 | 15691 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0002c0002t0067 | 0/0 | 15690 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15685): Show |
chr11 | 130861250 | 130921479 |
a0002c0002t0079 | 0/0 | 15691 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0003c0003t0003 | 0/0 | 15687 | 27 | 5 | 4 | 16 | 1 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15682): Show |
chr11 | 130861250 | 130921479 |
a0003c0003t0004 | 0/0 | 15687 | 20 | 0 | 1 | 19 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15682): Show |
chr11 | 130861250 | 130921479 |
a0003c0003t0036 | 0/0 | 15691 | 2 | 0 | 0 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0003c0003t0070 | 0/0 | 15692 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15687): Show |
chr11 | 130861250 | 130921479 |
a0003c0003t0071 | 0/0 | 15687 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15682): Show |
chr11 | 130861250 | 130921479 |
a0003c0003t0073 | 0/0 | 15688 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15683): Show |
chr11 | 130861250 | 130921479 |
a0003c0003t0113 | 0/0 | 15688 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15683): Show |
chr11 | 130861250 | 130921479 |
a0004c0005t0020 | 0/0 | 15690 | 3 | 3 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15685): Show |
chr11 | 130861250 | 130921479 |
a0004c0005t0022 | 0/0 | 15691 | 3 | 0 | 1 | 1 | 1 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0004c0005t0023 | 0/0 | 15691 | 3 | 0 | 0 | 3 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0004c0005t0030 | 0/0 | 15692 | 2 | 2 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15687): Show |
chr11 | 130861250 | 130921479 |
a0004c0005t0031 | 0/0 | 15691 | 2 | 0 | 0 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0004c0005t0055 | 0/0 | 15692 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15687): Show |
chr11 | 130861250 | 130921479 |
a0004c0005t0057 | 0/0 | 15692 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15687): Show |
chr11 | 130861250 | 130921479 |
a0004c0005t0058 | 0/0 | 15691 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0004c0008t0019 | 0/0 | 15692 | 4 | 4 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15687): Show |
chr11 | 130861250 | 130921479 |
a0004c0008t0029 | 0/0 | 15692 | 3 | 3 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15687): Show |
chr11 | 130861250 | 130921479 |
a0004c0008t0048 | 0/0 | 15691 | 2 | 2 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0004c0008t0116 | 0/0 | 15692 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15687): Show |
chr11 | 130861250 | 130921479 |
a0004c0008t0117 | 0/0 | 15692 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15687): Show |
chr11 | 130861250 | 130921479 |
a0004c0009t0009 | 0/0 | 15687 | 7 | 5 | 2 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15682): Show |
chr11 | 130861250 | 130921479 |
a0004c0025t0051 | 0/0 | 15691 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0005c0004t0021 | 0/0 | 15691 | 3 | 3 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0005c0004t0027 | 0/0 | 15691 | 3 | 3 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0005c0004t0039 | 0/0 | 15691 | 2 | 2 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0005c0004t0040 | 0/0 | 15692 | 2 | 2 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15687): Show |
chr11 | 130861250 | 130921479 |
a0005c0004t0049 | 0/0 | 15691 | 2 | 2 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0005c0004t0074 | 0/0 | 15692 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15687): Show |
chr11 | 130861250 | 130921479 |
a0005c0004t0081 | 0/0 | 15691 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0005c0004t0082 | 0/0 | 15691 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0005c0004t0084 | 0/0 | 15692 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15687): Show |
chr11 | 130861250 | 130921479 |
a0005c0017t0083 | 0/0 | 15691 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0006c0006t0008 | 0/0 | 15691 | 9 | 7 | 1 | 0 | 1 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0006c0006t0032 | 0/0 | 15687 | 2 | 2 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15682): Show |
chr11 | 130861250 | 130921479 |
a0006c0006t0052 | 0/0 | 15691 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0006c0006t0060 | 0/0 | 15687 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15682): Show |
chr11 | 130861250 | 130921479 |
a0006c0006t0068 | 0/0 | 15690 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15685): Show |
chr11 | 130861250 | 130921479 |
a0006c0006t0069 | 0/0 | 15689 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15684): Show |
chr11 | 130861250 | 130921479 |
a0006c0019t0008 | 0/0 | 15691 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0007c0007t0013 | 0/0 | 15687 | 4 | 0 | 0 | 4 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15682): Show |
chr11 | 130861250 | 130921479 |
a0007c0007t0026 | 0/0 | 15689 | 3 | 0 | 0 | 3 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15684): Show |
chr11 | 130861250 | 130921479 |
a0007c0007t0033 | 0/0 | 15689 | 2 | 0 | 0 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15684): Show |
chr11 | 130861250 | 130921479 |
a0007c0007t0034 | 0/0 | 15688 | 2 | 0 | 0 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15683): Show |
chr11 | 130861250 | 130921479 |
a0007c0007t0054 | 0/0 | 15689 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15684): Show |
chr11 | 130861250 | 130921479 |
a0007c0007t0059 | 0/0 | 15687 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15682): Show |
chr11 | 130861250 | 130921479 |
a0007c0007t0066 | 0/0 | 15689 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15684): Show |
chr11 | 130861250 | 130921479 |
a0008c0012t0017 | 0/0 | 15691 | 3 | 0 | 0 | 3 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0008c0012t0103 | 0/0 | 15692 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15687): Show |
chr11 | 130861250 | 130921479 |
a0009c0013t0110 | 0/0 | 15691 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0009c0013t0112 | 0/0 | 15691 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0010c0024t0035 | 0/0 | 15691 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0011c0020t0011 | 0/0 | 15690 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15685): Show |
chr11 | 130861250 | 130921479 |
a0012c0018t0085 | 0/0 | 16023 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(16018): Show |
chr11 | 130861250 | 130921479 |
a0013c0028t0094 | 0/0 | 15691 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0014c0026t0072 | 0/0 | 15687 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15682): Show |
chr11 | 130861250 | 130921479 |
a0015c0031t0118 | 0/0 | 15690 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15685): Show |
chr11 | 130861250 | 130921479 |
a0016c0023t0001 | 0/0 | 15691 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0017c0029t0001 | 0/0 | 15691 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0018c0027t0035 | 0/0 | 15691 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0019c0022t0006 | 0/0 | 15692 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15687): Show |
chr11 | 130861250 | 130921479 |
a0020c0015t0002 | 0/0 | 15691 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0021c0030t0050 | 0/0 | 15691 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
a0022c0016t0109 | 0/0 | 15687 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15682): Show |
chr11 | 130861250 | 130921479 |
a0023c0021t0016 | 0/1 | 15691 | 1 | 0 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | AGCTG others(15686): Show |
chr11 | 130861250 | 130921479 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 19 | 0 | 2 | 17 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0001g0002 | 0/0 | 13 | 0 | 5 | 5 | 0 | 3 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0001g0003 | 0/0 | 9 | 0 | 5 | 2 | 1 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0001g0006 | 0/0 | 7 | 0 | 0 | 4 | 1 | 2 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0001g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0004g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0004g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0006g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0006g0039 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0006g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0006g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0006g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0006g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0006g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0006g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0006g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0006g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0006g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0007g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0007g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0007g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0007g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0007g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0007g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0007g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0007g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0007g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0007g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0007g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0007g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0007g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0011g0036 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0011g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0011g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0014g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0014g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0014g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0014g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0015g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0015g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0017g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0018g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0018g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0018g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0028g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0028g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0028g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0037g0032 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0038g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0038g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0042g0040 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0043g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0043g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0044g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0044g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0045g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0045g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0046g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0047g0041 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0056g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0075g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0076g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0077g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0078g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0080g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0086g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0087g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0088g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0089g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0090g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0091g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0092g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0093g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0095g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0096g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0097g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0098g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0099g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0100g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0101g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0104g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0105g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0106g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0108g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0111g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0114g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0001t0115g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0010t0010g0010 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0010t0010g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0010t0053g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0011t0016g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0011t0016g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0011t0016g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0011t0102g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0011t0107g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0014t0041g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0001c0014t0041g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0002c0002t0002g0008 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0002c0002t0002g0009 | 0/0 | 6 | 0 | 3 | 3 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0002c0002t0002g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0002c0002t0002g0014 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0002c0002t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0002c0002t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0002c0002t0002g0023 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0002c0002t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0002c0002t0002g0071 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0002c0002t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0002c0002t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0002c0002t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0002c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0002c0002t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0002c0002t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0002c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0002c0002t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0002c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0002c0002t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0002c0002t0005g0004 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0002c0002t0005g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0002c0002t0005g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0002c0002t0005g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0002c0002t0005g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0002c0002t0005g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0002c0002t0005g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0002c0002t0012g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0002c0002t0012g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0002c0002t0012g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0002c0002t0024g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0002c0002t0024g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0002c0002t0024g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0002c0002t0025g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0002c0002t0025g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0002c0002t0025g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0002c0002t0061g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0002c0002t0062g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0002c0002t0063g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0002c0002t0064g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0002c0002t0065g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0002c0002t0067g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0002c0002t0079g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0003c0003t0003g0005 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0003c0003t0003g0029 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0003c0003t0003g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0003c0003t0003g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0003c0003t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0003c0003t0003g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0003c0003t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0003c0003t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0003c0003t0003g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0003c0003t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0003c0003t0003g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0003c0003t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0003c0003t0003g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0003c0003t0003g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0003c0003t0003g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0003c0003t0003g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0003c0003t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0003c0003t0004g0007 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0003c0003t0004g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0003c0003t0004g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0003c0003t0004g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0003c0003t0004g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0003c0003t0004g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0003c0003t0004g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0003c0003t0004g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0003c0003t0004g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0003c0003t0004g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0003c0003t0004g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0003c0003t0036g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0003c0003t0036g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0003c0003t0070g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0003c0003t0071g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0003c0003t0073g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0003c0003t0113g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0004c0005t0020g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0004c0005t0020g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0004c0005t0022g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0004c0005t0022g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0004c0005t0022g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0004c0005t0023g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0004c0005t0030g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0004c0005t0031g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0004c0005t0031g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0004c0005t0055g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0004c0005t0057g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0004c0005t0058g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0004c0008t0019g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0004c0008t0019g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0004c0008t0019g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0004c0008t0019g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0004c0008t0029g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0004c0008t0029g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0004c0008t0029g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0004c0008t0048g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0004c0008t0116g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0004c0008t0117g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0004c0009t0009g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0004c0009t0009g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0004c0009t0009g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0004c0009t0009g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0004c0009t0009g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0004c0009t0009g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0004c0025t0051g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0005c0004t0021g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0005c0004t0021g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0005c0004t0021g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0005c0004t0027g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0005c0004t0027g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0005c0004t0039g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0005c0004t0039g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0005c0004t0040g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0005c0004t0040g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0005c0004t0049g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0005c0004t0049g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0005c0004t0074g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0005c0004t0081g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0005c0004t0082g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0005c0004t0084g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0005c0017t0083g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0006c0006t0008g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0006c0006t0008g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0006c0006t0008g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0006c0006t0008g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0006c0006t0008g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0006c0006t0008g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0006c0006t0008g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0006c0006t0008g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0006c0006t0032g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0006c0006t0032g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0006c0006t0052g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0006c0006t0060g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0006c0006t0068g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0006c0006t0069g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0006c0019t0008g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0007c0007t0013g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0007c0007t0013g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0007c0007t0013g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0007c0007t0026g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0007c0007t0026g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0007c0007t0033g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0007c0007t0034g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0007c0007t0054g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0007c0007t0059g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0007c0007t0066g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0008c0012t0017g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0008c0012t0017g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0008c0012t0103g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0009c0013t0110g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0009c0013t0112g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0010c0024t0035g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0011c0020t0011g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0012c0018t0085g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0013c0028t0094g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0014c0026t0072g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0015c0031t0118g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0016c0023t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0017c0029t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0018c0027t0035g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0019c0022t0006g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0020c0015t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0021c0030t0050g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0022c0016t0109g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
a0023c0021t0016g0237 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0012 | g0074 | EUR | GBR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0214 | EUR | GBR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0204 | EUR | FIN | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG00280 | hp2 | a0001 | c0011 | t0016 | g0226 | EUR | FIN | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0205 | EUR | FIN | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG00323 | hp2 | a0001 | c0001 | t0042 | g0040 | EUR | FIN | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG00408 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | CHS | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG00423 | hp1 | a0001 | c0001 | t0078 | g0158 | EAS | CHS | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG00423 | hp2 | a0003 | c0003 | t0003 | g0144 | EAS | CHS | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG00438 | hp1 | a0002 | c0002 | t0005 | g0092 | EAS | CHS | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG00544 | hp1 | a0001 | c0001 | t0108 | g0187 | EAS | CHS | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | CHS | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG00558 | hp2 | a0003 | c0003 | t0004 | g0272 | EAS | CHS | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG00597 | hp1 | a0002 | c0002 | t0002 | g0011 | EAS | CHS | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG00609 | hp1 | a0010 | c0024 | t0035 | g0124 | EAS | CHS | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG00609 | hp2 | a0009 | c0013 | t0112 | g0185 | EAS | CHS | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG00642 | hp1 | a0002 | c0002 | t0002 | g0008 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG00642 | hp2 | a0001 | c0001 | t0007 | g0150 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG00673 | hp1 | a0001 | c0001 | t0089 | g0256 | EAS | CHS | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG00673 | hp2 | a0001 | c0001 | t0106 | g0206 | EAS | CHS | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG00733 | hp1 | a0003 | c0003 | t0003 | g0139 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG00733 | hp2 | a0002 | c0002 | t0002 | g0008 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG00735 | hp1 | a0002 | c0002 | t0024 | g0089 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG00738 | hp1 | a0002 | c0002 | t0024 | g0101 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG00738 | hp2 | a0006 | c0006 | t0008 | g0061 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG00741 | hp1 | a0001 | c0001 | t0097 | g0192 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG00741 | hp2 | a0004 | c0009 | t0009 | g0044 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG01069 | hp1 | a0002 | c0002 | t0002 | g0087 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG01070 | hp2 | a0004 | c0009 | t0009 | g0044 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG01071 | hp2 | a0002 | c0002 | t0002 | g0088 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG01074 | hp1 | a0001 | c0011 | t0016 | g0231 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG01074 | hp2 | a0001 | c0001 | t0007 | g0154 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG01081 | hp1 | a0001 | c0011 | t0016 | g0230 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG01099 | hp1 | a0001 | c0014 | t0041 | g0233 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG01099 | hp2 | a0001 | c0001 | t0100 | g0195 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG01106 | hp2 | a0002 | c0002 | t0012 | g0019 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG01109 | hp1 | a0001 | c0001 | t0011 | g0036 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG01167 | hp1 | a0003 | c0003 | t0003 | g0143 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG01167 | hp2 | a0002 | c0002 | t0002 | g0114 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG01168 | hp1 | a0011 | c0020 | t0011 | g0240 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG01168 | hp2 | a0002 | c0002 | t0002 | g0009 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG01175 | hp1 | a0002 | c0002 | t0063 | g0103 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG01175 | hp2 | a0002 | c0002 | t0012 | g0019 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG01243 | hp1 | a0001 | c0010 | t0010 | g0010 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG01243 | hp2 | a0001 | c0001 | t0098 | g0193 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG01255 | hp1 | a0001 | c0001 | t0037 | g0032 | AMR | CLM | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG01256 | hp1 | a0002 | c0002 | t0002 | g0009 | AMR | CLM | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | CLM | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG01258 | hp1 | a0002 | c0002 | t0002 | g0009 | AMR | CLM | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG01258 | hp2 | a0004 | c0005 | t0022 | g0106 | AMR | CLM | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG01261 | hp1 | a0003 | c0003 | t0003 | g0135 | AMR | CLM | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG01261 | hp2 | a0002 | c0002 | t0025 | g0104 | AMR | CLM | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG01361 | hp2 | a0002 | c0002 | t0002 | g0080 | AMR | CLM | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG01433 | hp2 | a0002 | c0002 | t0002 | g0105 | AMR | CLM | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG01496 | hp2 | a0001 | c0001 | t0018 | g0277 | AMR | CLM | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG01516 | hp1 | a0002 | c0002 | t0002 | g0023 | EUR | IBS | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG01517 | hp1 | a0002 | c0002 | t0002 | g0023 | EUR | IBS | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG01517 | hp2 | a0003 | c0003 | t0003 | g0133 | EUR | IBS | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG01884 | hp1 | a0001 | c0001 | t0091 | g0250 | AFR | ACB | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG01884 | hp2 | a0004 | c0008 | t0019 | g0291 | AFR | ACB | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG01891 | hp1 | a0004 | c0005 | t0030 | g0017 | AFR | ACB | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG01891 | hp2 | a0005 | c0004 | t0027 | g0033 | AFR | ACB | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG01934 | hp1 | a0001 | c0001 | t0044 | g0242 | AMR | PEL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG01934 | hp2 | a0001 | c0001 | t0007 | g0162 | AMR | PEL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG01943 | hp2 | a0002 | c0002 | t0002 | g0110 | AMR | PEL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG01952 | hp1 | a0001 | c0001 | t0042 | g0040 | AMR | PEL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG01975 | hp1 | a0002 | c0002 | t0002 | g0014 | AMR | PEL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG01978 | hp1 | a0001 | c0001 | t0006 | g0039 | AMR | PEL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG01978 | hp2 | a0003 | c0003 | t0003 | g0141 | AMR | PEL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG01993 | hp1 | a0001 | c0001 | t0044 | g0200 | AMR | PEL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG01993 | hp2 | a0002 | c0002 | t0002 | g0107 | AMR | PEL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02004 | hp1 | a0002 | c0002 | t0002 | g0014 | AMR | PEL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02015 | hp1 | a0002 | c0002 | t0064 | g0082 | EAS | KHV | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02027 | hp1 | a0002 | c0002 | t0005 | g0091 | EAS | KHV | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02040 | hp2 | a0007 | c0007 | t0059 | g0118 | EAS | KHV | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02055 | hp1 | a0012 | c0018 | t0085 | g0173 | AFR | ACB | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02055 | hp2 | a0001 | c0001 | t0056 | g0056 | AFR | ACB | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02056 | hp1 | a0013 | c0028 | t0094 | g0275 | EAS | KHV | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02056 | hp2 | a0002 | c0002 | t0002 | g0083 | EAS | KHV | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02071 | hp1 | a0001 | c0001 | t0007 | g0163 | EAS | KHV | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02071 | hp2 | a0003 | c0003 | t0004 | g0007 | EAS | KHV | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02074 | hp1 | a0003 | c0003 | t0036 | g0142 | EAS | KHV | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02074 | hp2 | a0002 | c0002 | t0002 | g0081 | EAS | KHV | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02080 | hp1 | a0001 | c0001 | t0006 | g0260 | EAS | KHV | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02080 | hp2 | a0001 | c0001 | t0101 | g0203 | EAS | KHV | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02083 | hp1 | a0002 | c0002 | t0005 | g0020 | EAS | KHV | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02083 | hp2 | a0002 | c0002 | t0002 | g0112 | EAS | KHV | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02129 | hp2 | a0003 | c0003 | t0004 | g0273 | EAS | KHV | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02135 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | KHV | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02155 | hp1 | a0003 | c0003 | t0003 | g0005 | EAS | CDX | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02155 | hp2 | a0002 | c0002 | t0005 | g0069 | EAS | CDX | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02165 | hp1 | a0014 | c0026 | t0072 | g0125 | EAS | CDX | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CDX | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02257 | hp1 | a0004 | c0008 | t0029 | g0280 | AFR | ACB | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02257 | hp2 | a0003 | c0003 | t0071 | g0132 | AFR | ACB | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02258 | hp1 | a0001 | c0010 | t0010 | g0010 | AFR | ACB | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02258 | hp2 | a0004 | c0025 | t0051 | g0046 | AFR | ACB | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02280 | hp1 | a0004 | c0008 | t0117 | g0289 | AFR | ACB | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02280 | hp2 | a0006 | c0006 | t0069 | g0066 | AFR | ACB | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02293 | hp1 | a0002 | c0002 | t0002 | g0014 | AMR | PEL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02451 | hp1 | a0004 | c0009 | t0009 | g0283 | AFR | ACB | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02451 | hp2 | a0001 | c0001 | t0007 | g0148 | AFR | ACB | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02523 | hp1 | a0002 | c0002 | t0005 | g0095 | EAS | KHV | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02523 | hp2 | a0001 | c0001 | t0017 | g0219 | EAS | KHV | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02572 | hp1 | a0004 | c0005 | t0020 | g0016 | AFR | GWD | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02572 | hp2 | a0005 | c0004 | t0021 | g0050 | AFR | GWD | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02602 | hp2 | a0001 | c0001 | t0037 | g0032 | SAS | PJL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02615 | hp1 | a0006 | c0006 | t0060 | g0053 | AFR | GWD | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02615 | hp2 | a0001 | c0001 | t0075 | g0146 | AFR | GWD | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02622 | hp1 | a0005 | c0004 | t0027 | g0172 | AFR | GWD | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02622 | hp2 | a0004 | c0005 | t0020 | g0016 | AFR | GWD | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02630 | hp1 | a0001 | c0001 | t0018 | g0278 | AFR | GWD | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02630 | hp2 | a0005 | c0004 | t0039 | g0176 | AFR | GWD | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02647 | hp1 | a0006 | c0006 | t0032 | g0055 | AFR | GWD | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02647 | hp2 | a0001 | c0001 | t0007 | g0166 | AFR | GWD | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02683 | hp1 | a0002 | c0002 | t0012 | g0073 | SAS | PJL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02698 | hp1 | a0001 | c0001 | t0006 | g0039 | SAS | PJL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02698 | hp2 | a0003 | c0003 | t0003 | g0140 | SAS | PJL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02717 | hp1 | a0001 | c0001 | t0007 | g0149 | AFR | GWD | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02717 | hp2 | a0004 | c0009 | t0009 | g0287 | AFR | GWD | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02723 | hp1 | a0003 | c0003 | t0003 | g0126 | AFR | GWD | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02723 | hp2 | a0015 | c0031 | t0118 | g0294 | AFR | GWD | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02735 | hp1 | a0001 | c0001 | t0099 | g0194 | SAS | PJL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02735 | hp2 | a0002 | c0002 | t0024 | g0100 | SAS | PJL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02738 | hp1 | a0001 | c0001 | t0006 | g0244 | SAS | PJL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02809 | hp1 | a0006 | c0006 | t0068 | g0062 | AFR | GWD | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02809 | hp2 | a0005 | c0004 | t0021 | g0051 | AFR | GWD | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02818 | hp1 | a0001 | c0001 | t0076 | g0147 | AFR | GWD | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02818 | hp2 | a0005 | c0004 | t0082 | g0175 | AFR | GWD | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02886 | hp1 | a0006 | c0006 | t0008 | g0018 | AFR | GWD | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02886 | hp2 | a0004 | c0008 | t0029 | g0282 | AFR | GWD | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02895 | hp1 | a0001 | c0001 | t0086 | g0183 | AFR | GWD | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02895 | hp2 | a0004 | c0008 | t0048 | g0042 | AFR | GWD | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02896 | hp1 | a0006 | c0006 | t0008 | g0064 | AFR | GWD | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02896 | hp2 | a0001 | c0001 | t0011 | g0190 | AFR | GWD | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02897 | hp1 | a0006 | c0006 | t0008 | g0063 | AFR | GWD | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02897 | hp2 | a0004 | c0008 | t0048 | g0042 | AFR | GWD | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02922 | hp1 | a0005 | c0004 | t0040 | g0177 | AFR | ESN | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02922 | hp2 | a0001 | c0010 | t0010 | g0057 | AFR | ESN | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02965 | hp1 | a0006 | c0006 | t0008 | g0068 | AFR | ESN | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02965 | hp2 | a0005 | c0017 | t0083 | g0171 | AFR | ESN | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02970 | hp1 | a0004 | c0008 | t0019 | g0290 | AFR | ESN | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02970 | hp2 | a0001 | c0001 | t0115 | g0279 | AFR | ESN | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02976 | hp1 | a0006 | c0006 | t0008 | g0060 | AFR | ESN | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02976 | hp2 | a0005 | c0004 | t0084 | g0180 | AFR | ESN | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG03017 | hp2 | a0001 | c0001 | t0093 | g0188 | SAS | PJL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG03041 | hp1 | a0005 | c0004 | t0040 | g0179 | AFR | GWD | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG03041 | hp2 | a0001 | c0001 | t0018 | g0043 | AFR | GWD | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG03098 | hp1 | a0006 | c0006 | t0032 | g0054 | AFR | MSL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG03098 | hp2 | a0001 | c0014 | t0041 | g0234 | AFR | MSL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG03130 | hp1 | a0003 | c0003 | t0003 | g0029 | AFR | ESN | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG03130 | hp2 | a0004 | c0009 | t0009 | g0286 | AFR | ESN | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG03139 | hp1 | a0003 | c0003 | t0003 | g0134 | AFR | ESN | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG03139 | hp2 | a0005 | c0004 | t0049 | g0295 | AFR | ESN | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG03195 | hp1 | a0001 | c0001 | t0018 | g0043 | AFR | ESN | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG03195 | hp2 | a0006 | c0006 | t0052 | g0048 | AFR | ESN | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG03209 | hp1 | a0005 | c0004 | t0021 | g0052 | AFR | MSL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG03209 | hp2 | a0004 | c0005 | t0020 | g0045 | AFR | MSL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG03225 | hp1 | a0005 | c0004 | t0081 | g0174 | AFR | MSL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG03225 | hp2 | a0003 | c0003 | t0003 | g0127 | AFR | MSL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG03453 | hp1 | a0004 | c0008 | t0019 | g0293 | AFR | MSL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG03453 | hp2 | a0001 | c0010 | t0010 | g0010 | AFR | MSL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG03486 | hp1 | a0005 | c0004 | t0049 | g0296 | AFR | MSL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG03486 | hp2 | a0005 | c0004 | t0039 | g0178 | AFR | MSL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG03491 | hp1 | a0001 | c0001 | t0047 | g0041 | SAS | PJL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG03491 | hp2 | a0002 | c0002 | t0065 | g0093 | SAS | PJL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG03492 | hp1 | a0001 | c0011 | t0102 | g0227 | SAS | PJL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG03492 | hp2 | a0001 | c0001 | t0047 | g0041 | SAS | PJL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG03516 | hp1 | a0006 | c0019 | t0008 | g0059 | AFR | ESN | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG03516 | hp2 | a0005 | c0004 | t0074 | g0145 | AFR | ESN | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG03540 | hp1 | a0001 | c0001 | t0038 | g0152 | AFR | GWD | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG03540 | hp2 | a0001 | c0001 | t0114 | g0189 | AFR | GWD | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG03579 | hp1 | a0001 | c0001 | t0011 | g0036 | AFR | MSL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG03579 | hp2 | a0001 | c0010 | t0053 | g0058 | AFR | MSL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG03654 | hp1 | a0016 | c0023 | t0001 | g0264 | SAS | PJL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG03654 | hp2 | a0001 | c0001 | t0006 | g0038 | SAS | PJL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG03669 | hp1 | a0001 | c0001 | t0007 | g0160 | SAS | PJL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG03669 | hp2 | a0001 | c0001 | t0104 | g0191 | SAS | PJL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG03688 | hp1 | a0002 | c0002 | t0002 | g0102 | SAS | STU | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | STU | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG03704 | hp1 | a0001 | c0001 | t0006 | g0246 | SAS | PJL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG03704 | hp2 | a0017 | c0029 | t0001 | g0276 | SAS | PJL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG03710 | hp2 | a0004 | c0005 | t0055 | g0070 | SAS | PJL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG03831 | hp1 | a0001 | c0001 | t0006 | g0038 | SAS | BEB | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG03831 | hp2 | a0001 | c0001 | t0006 | g0261 | SAS | BEB | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG03834 | hp1 | a0001 | c0011 | t0107 | g0228 | SAS | BEB | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG03942 | hp2 | a0001 | c0001 | t0006 | g0247 | SAS | BEB | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG04115 | hp1 | a0002 | c0002 | t0002 | g0078 | SAS | STU | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG04115 | hp2 | a0001 | c0001 | t0006 | g0262 | SAS | STU | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG04199 | hp1 | a0001 | c0001 | t0007 | g0165 | SAS | STU | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | STU | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | STU | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG04204 | hp2 | a0001 | c0001 | t0088 | g0257 | SAS | STU | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | STU | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG04228 | hp2 | a0001 | c0001 | t0004 | g0182 | SAS | STU | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18522 | hp1 | a0004 | c0008 | t0116 | g0288 | AFR | YRI | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18522 | hp2 | a0004 | c0009 | t0009 | g0284 | AFR | YRI | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18612 | hp1 | a0002 | c0002 | t0005 | g0004 | EAS | CHB | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18612 | hp2 | a0008 | c0012 | t0017 | g0037 | EAS | CHB | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18747 | hp1 | a0002 | c0002 | t0005 | g0004 | EAS | CHB | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18747 | hp2 | a0007 | c0007 | t0013 | g0122 | EAS | CHB | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18906 | hp1 | a0004 | c0009 | t0009 | g0285 | AFR | YRI | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18906 | hp2 | a0001 | c0001 | t0011 | g0216 | AFR | YRI | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18942 | hp1 | a0002 | c0002 | t0002 | g0075 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18942 | hp2 | a0003 | c0003 | t0003 | g0031 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18944 | hp1 | a0002 | c0002 | t0005 | g0004 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18945 | hp1 | a0007 | c0007 | t0013 | g0119 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18945 | hp2 | a0002 | c0002 | t0005 | g0004 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18948 | hp1 | a0001 | c0001 | t0028 | g0186 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18948 | hp2 | a0001 | c0001 | t0007 | g0159 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18949 | hp1 | a0001 | c0001 | t0045 | g0202 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18949 | hp2 | a0003 | c0003 | t0003 | g0005 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18950 | hp2 | a0003 | c0003 | t0003 | g0030 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18952 | hp1 | a0002 | c0002 | t0005 | g0004 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18952 | hp2 | a0003 | c0003 | t0003 | g0030 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18956 | hp2 | a0002 | c0002 | t0002 | g0109 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18957 | hp1 | a0003 | c0003 | t0004 | g0007 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18959 | hp1 | a0007 | c0007 | t0034 | g0028 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18959 | hp2 | a0002 | c0002 | t0002 | g0021 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18960 | hp1 | a0001 | c0001 | t0006 | g0245 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18960 | hp2 | a0007 | c0007 | t0013 | g0026 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18961 | hp1 | a0002 | c0002 | t0002 | g0079 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18961 | hp2 | a0003 | c0003 | t0003 | g0005 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18962 | hp1 | a0003 | c0003 | t0003 | g0129 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18963 | hp1 | a0002 | c0002 | t0002 | g0117 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18963 | hp2 | a0002 | c0002 | t0005 | g0004 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18964 | hp1 | a0003 | c0003 | t0003 | g0005 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18964 | hp2 | a0007 | c0007 | t0033 | g0025 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18965 | hp1 | a0002 | c0002 | t0002 | g0024 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18965 | hp2 | a0003 | c0003 | t0003 | g0005 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18966 | hp1 | a0001 | c0001 | t0043 | g0255 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18966 | hp2 | a0004 | c0005 | t0031 | g0085 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18967 | hp1 | a0008 | c0012 | t0017 | g0037 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18967 | hp2 | a0002 | c0002 | t0002 | g0011 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18969 | hp1 | a0001 | c0001 | t0015 | g0015 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18970 | hp1 | a0001 | c0001 | t0007 | g0161 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18970 | hp2 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18972 | hp1 | a0001 | c0001 | t0014 | g0157 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18972 | hp2 | a0002 | c0002 | t0002 | g0077 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18973 | hp1 | a0007 | c0007 | t0054 | g0123 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18973 | hp2 | a0002 | c0002 | t0002 | g0022 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18974 | hp1 | a0002 | c0002 | t0002 | g0076 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18974 | hp2 | a0004 | c0005 | t0058 | g0096 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18975 | hp1 | a0018 | c0027 | t0035 | g0130 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18975 | hp2 | a0001 | c0001 | t0111 | g0253 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18977 | hp2 | a0007 | c0007 | t0034 | g0028 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18978 | hp1 | a0001 | c0001 | t0015 | g0252 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18978 | hp2 | a0004 | c0005 | t0022 | g0108 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18979 | hp1 | a0003 | c0003 | t0004 | g0269 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18979 | hp2 | a0002 | c0002 | t0002 | g0090 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18980 | hp1 | a0002 | c0002 | t0002 | g0024 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18981 | hp1 | a0007 | c0007 | t0013 | g0026 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18981 | hp2 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18983 | hp1 | a0003 | c0003 | t0003 | g0005 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18983 | hp2 | a0001 | c0001 | t0028 | g0197 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18984 | hp1 | a0002 | c0002 | t0005 | g0115 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18984 | hp2 | a0019 | c0022 | t0006 | g0263 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18985 | hp1 | a0002 | c0002 | t0002 | g0084 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18985 | hp2 | a0003 | c0003 | t0004 | g0266 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18986 | hp1 | a0001 | c0001 | t0046 | g0035 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18986 | hp2 | a0003 | c0003 | t0003 | g0029 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18988 | hp1 | a0003 | c0003 | t0004 | g0012 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18988 | hp2 | a0007 | c0007 | t0026 | g0120 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18989 | hp1 | a0002 | c0002 | t0005 | g0004 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18990 | hp2 | a0003 | c0003 | t0073 | g0136 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18992 | hp1 | a0001 | c0001 | t0095 | g0225 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18992 | hp2 | a0003 | c0003 | t0004 | g0012 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18993 | hp1 | a0004 | c0005 | t0023 | g0013 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18994 | hp1 | a0002 | c0002 | t0005 | g0020 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18994 | hp2 | a0003 | c0003 | t0004 | g0265 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18998 | hp1 | a0002 | c0002 | t0002 | g0022 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18998 | hp2 | a0003 | c0003 | t0004 | g0007 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA18999 | hp2 | a0007 | c0007 | t0026 | g0027 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19000 | hp1 | a0001 | c0001 | t0043 | g0259 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19000 | hp2 | a0001 | c0001 | t0046 | g0035 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19001 | hp1 | a0001 | c0001 | t0096 | g0201 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19001 | hp2 | a0002 | c0002 | t0002 | g0021 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19002 | hp1 | a0003 | c0003 | t0070 | g0137 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19002 | hp2 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19004 | hp1 | a0001 | c0001 | t0004 | g0222 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19004 | hp2 | a0007 | c0007 | t0026 | g0027 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19006 | hp1 | a0003 | c0003 | t0113 | g0270 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19006 | hp2 | a0002 | c0002 | t0067 | g0098 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19007 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19007 | hp2 | a0001 | c0001 | t0092 | g0258 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19009 | hp1 | a0001 | c0001 | t0015 | g0015 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19009 | hp2 | a0009 | c0013 | t0110 | g0248 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19010 | hp1 | a0007 | c0007 | t0033 | g0025 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19010 | hp2 | a0003 | c0003 | t0003 | g0005 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19011 | hp2 | a0003 | c0003 | t0004 | g0007 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19012 | hp2 | a0003 | c0003 | t0004 | g0007 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19030 | hp1 | a0004 | c0008 | t0019 | g0292 | AFR | LWK | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19030 | hp2 | a0001 | c0001 | t0007 | g0167 | AFR | LWK | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19043 | hp1 | a0001 | c0001 | t0077 | g0153 | AFR | LWK | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19043 | hp2 | a0001 | c0001 | t0087 | g0181 | AFR | LWK | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19054 | hp1 | a0003 | c0003 | t0036 | g0131 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19055 | hp1 | a0002 | c0002 | t0002 | g0072 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19056 | hp1 | a0001 | c0001 | t0015 | g0015 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19060 | hp1 | a0007 | c0007 | t0066 | g0121 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19060 | hp2 | a0008 | c0012 | t0017 | g0210 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19062 | hp1 | a0001 | c0001 | t0028 | g0223 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19062 | hp2 | a0001 | c0001 | t0105 | g0196 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19063 | hp1 | a0004 | c0005 | t0057 | g0099 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19063 | hp2 | a0008 | c0012 | t0103 | g0198 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19064 | hp2 | a0002 | c0002 | t0062 | g0116 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19067 | hp1 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19067 | hp2 | a0003 | c0003 | t0004 | g0007 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19068 | hp2 | a0002 | c0002 | t0002 | g0011 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19070 | hp1 | a0003 | c0003 | t0004 | g0268 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19072 | hp1 | a0004 | c0005 | t0023 | g0013 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19074 | hp1 | a0001 | c0001 | t0014 | g0156 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19074 | hp2 | a0003 | c0003 | t0004 | g0012 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19077 | hp1 | a0004 | c0005 | t0023 | g0013 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19077 | hp2 | a0003 | c0003 | t0003 | g0005 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19079 | hp1 | a0001 | c0001 | t0045 | g0232 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19079 | hp2 | a0003 | c0003 | t0003 | g0128 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19080 | hp1 | a0001 | c0001 | t0014 | g0155 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19080 | hp2 | a0002 | c0002 | t0025 | g0113 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19081 | hp2 | a0002 | c0002 | t0002 | g0011 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19083 | hp2 | a0003 | c0003 | t0004 | g0012 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19084 | hp1 | a0003 | c0003 | t0004 | g0267 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19084 | hp2 | a0001 | c0001 | t0014 | g0164 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19085 | hp1 | a0002 | c0002 | t0005 | g0004 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19086 | hp1 | a0002 | c0002 | t0061 | g0097 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19087 | hp1 | a0001 | c0001 | t0090 | g0249 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19087 | hp2 | a0020 | c0015 | t0002 | g0049 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19088 | hp1 | a0003 | c0003 | t0004 | g0271 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19088 | hp2 | a0004 | c0005 | t0031 | g0086 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19090 | hp1 | a0002 | c0002 | t0025 | g0094 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19090 | hp2 | a0003 | c0003 | t0004 | g0007 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19091 | hp2 | a0003 | c0003 | t0003 | g0031 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19240 | hp1 | a0004 | c0005 | t0030 | g0017 | AFR | YRI | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA19240 | hp2 | a0005 | c0004 | t0027 | g0033 | AFR | YRI | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | ASW | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA20129 | hp2 | a0006 | c0006 | t0008 | g0067 | AFR | ASW | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA20752 | hp1 | a0001 | c0001 | t0006 | g0251 | EUR | TSI | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA20752 | hp2 | a0006 | c0006 | t0008 | g0065 | EUR | TSI | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA20805 | hp1 | a0004 | c0005 | t0022 | g0111 | EUR | TSI | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA20905 | hp1 | a0001 | c0001 | t0007 | g0168 | SAS | GIH | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA20905 | hp2 | a0001 | c0001 | t0006 | g0208 | SAS | GIH | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG01123 | hp2 | a0003 | c0003 | t0004 | g0274 | AMR | CLM | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02109 | hp1 | a0001 | c0010 | t0010 | g0010 | AFR | ACB | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02109 | hp2 | a0003 | c0003 | t0003 | g0138 | AFR | ACB | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02559 | hp1 | a0002 | c0002 | t0079 | g0169 | AFR | ACB | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG02559 | hp2 | a0004 | c0008 | t0029 | g0281 | AFR | ACB | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG03471 | hp1 | a0006 | c0006 | t0008 | g0018 | AFR | MSL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
HG03471 | hp2 | a0001 | c0001 | t0038 | g0151 | AFR | MSL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA20300 | hp1 | a0001 | c0001 | t0080 | g0241 | AFR | USA | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA20300 | hp2 | a0021 | c0030 | t0050 | g0047 | AFR | USA | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | LWK | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
NA21309 | hp2 | a0022 | c0016 | t0109 | g0170 | AFR | LWK | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
homoSapiens | chm13v2 | a0023 | c0021 | t0016 | g0237 | REF | REF | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
homoSapiens | grch38p0 | a0002 | c0002 | t0002 | g0071 | REF | REF | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:130879634 | G | C | 1 | a0011 | 1 | HG01168.hp1 | missense_variant | MODERATE | c.2836C>G | p.Leu946Val | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 10/11 | 3376/15691 | 2836/2979 | 946/992 | chr11 | 130879634 | |||
chr11:130880747 | A | C | 17 | a0001 a0003 a0004 others(14): Show |
327 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(324): Show |
missense_variant | MODERATE | c.2633T>G | p.Leu878Arg | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 9/11 | 3173/15691 | 2633/2979 | 878/992 | chr11 | 130880747 | |||
chr11:130880766 | G | A | 2 | a0008 a0012 |
5 | HG02055.hp1 NA18612.hp2 NA18967.hp1 others(2): Show |
missense_variant | MODERATE | c.2614C>T | p.Arg872Cys | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 9/11 | 3154/15691 | 2614/2979 | 872/992 | chr11 | 130880766 | |||
chr11:130906629 | T | C | 14 | a0001 a0003 a0005 others(11): Show |
263 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(260): Show |
missense_variant | MODERATE | c.2258A>G | p.Asn753Ser | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 6/11 | 2798/15691 | 2258/2979 | 753/992 | chr11 | 130906629 | |||
chr11:130914273 | G | A | 1 | a0019 | 1 | NA18984.hp2 | missense_variant | MODERATE | c.1667C>T | p.Thr556Ile | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 2207/15691 | 1667/2979 | 556/992 | chr11 | 130914273 | |||
chr11:130914501 | G | A | 3 | a0003 a0014 a0018 |
55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
missense_variant | MODERATE | c.1439C>T | p.Pro480Leu | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 1979/15691 | 1439/2979 | 480/992 | chr11 | 130914501 | |||
chr11:130914559 | C | T | 1 | a0014 | 1 | HG02165.hp1 | missense_variant | MODERATE | c.1381G>A | p.Val461Ile | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 1921/15691 | 1381/2979 | 461/992 | chr11 | 130914559 | |||
chr11:130914679 | C | T | 2 | a0005 a0012 |
18 | HG01891.hp2 HG02055.hp1 HG02572.hp2 others(15): Show |
missense_variant | MODERATE | c.1261G>A | p.Gly421Arg | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 1801/15691 | 1261/2979 | 421/992 | chr11 | 130914679 | |||
chr11:130914694 | C | A | 1 | a0007 | 14 | HG02040.hp2 NA18747.hp2 NA18945.hp1 others(11): Show |
missense_variant | MODERATE | c.1246G>T | p.Gly416Cys | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 1786/15691 | 1246/2979 | 416/992 | chr11 | 130914694 | |||
chr11:130914721 | T | C | 3 | a0003 a0014 a0018 |
55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
missense_variant | MODERATE | c.1219A>G | p.Ser407Gly | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 1759/15691 | 1219/2979 | 407/992 | chr11 | 130914721 | |||
chr11:130914752 | G | C | 3 | a0003 a0014 a0018 |
55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
missense_variant | MODERATE | c.1188C>G | p.Asp396Glu | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 1728/15691 | 1188/2979 | 396/992 | chr11 | 130914752 | |||
chr11:130914799 | C | T | 3 | a0003 a0014 a0018 |
55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
missense_variant | MODERATE | c.1141G>A | p.Gly381Ser | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 1681/15691 | 1141/2979 | 381/992 | chr11 | 130914799 | |||
chr11:130914859 | C | G | 16 | a0001 a0003 a0005 others(13): Show |
293 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(290): Show |
missense_variant | MODERATE | c.1081G>C | p.Val361Leu | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 1621/15691 | 1081/2979 | 361/992 | chr11 | 130914859 | |||
chr11:130914933 | A | G | 1 | a0022 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.1007T>C | p.Val336Ala | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 1547/15691 | 1007/2979 | 336/992 | chr11 | 130914933 | |||
chr11:130914991 | T | C | 1 | a0016 | 1 | HG03654.hp1 | missense_variant | MODERATE | c.949A>G | p.Ser317Gly | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 1489/15691 | 949/2979 | 317/992 | chr11 | 130914991 | |||
chr11:130915185 | C | T | 1 | a0015 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.755G>A | p.Ser252Asn | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 1295/15691 | 755/2979 | 252/992 | chr11 | 130915185 | |||
chr11:130915359 | C | T | 1 | a0020 | 1 | NA19087.hp2 | missense_variant | MODERATE | c.581G>A | p.Arg194Gln | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 1121/15691 | 581/2979 | 194/992 | chr11 | 130915359 | |||
chr11:130915537 | T | G | 1 | a0013 | 1 | HG02056.hp1 | missense_variant | MODERATE | c.403A>C | p.Met135Leu | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 943/15691 | 403/2979 | 135/992 | chr11 | 130915537 | |||
chr11:130915665 | G | C | 1 | a0017 | 1 | HG03704.hp2 | missense_variant | MODERATE | c.275C>G | p.Pro92Arg | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 815/15691 | 275/2979 | 92/992 | chr11 | 130915665 | |||
chr11:130915689 | G | A | 1 | a0021 | 1 | NA20300.hp2 | missense_variant | MODERATE | c.251C>T | p.Pro84Leu | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 791/15691 | 251/2979 | 84/992 | chr11 | 130915689 | |||
chr11:130915862 | G | C | 1 | a0015 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.78C>G | p.Ser26Arg | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 618/15691 | 78/2979 | 26/992 | chr11 | 130915862 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:130906122 | A | C | 1 | a0001c0014 | 2 | HG01099.hp1 HG03098.hp2 |
synonymous_variant | LOW | c.2274T>G | p.Thr758Thr | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/11 | 2814/15691 | 2274/2979 | 758/992 | chr11 | 130906122 | |||
chr11:130906661 | T | C | 1 | a0001c0011 | 5 | HG00280.hp2 HG01074.hp1 HG01081.hp1 others(2): Show |
synonymous_variant | LOW | c.2226A>G | p.Gln742Gln | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 6/11 | 2766/15691 | 2226/2979 | 742/992 | chr11 | 130906661 | |||
chr11:130906718 | A | G | 18 | a0001c0001 a0001c0010 a0001c0011 others(15): Show |
263 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(260): Show |
synonymous_variant | LOW | c.2169T>C | p.Ser723Ser | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 6/11 | 2709/15691 | 2169/2979 | 723/992 | chr11 | 130906718 | |||
chr11:130907991 | G | A | 4 | a0003c0003 a0010c0024 a0014c0026 others(1): Show |
56 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(53): Show |
synonymous_variant | LOW | c.2127C>T | p.Thr709Thr | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 5/11 | 2667/15691 | 2127/2979 | 709/992 | chr11 | 130907991 | |||
chr11:130908003 | A | G | 1 | a0006c0019 | 1 | HG03516.hp1 | synonymous_variant | LOW | c.2115T>C | p.Ser705Ser | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 5/11 | 2655/15691 | 2115/2979 | 705/992 | chr11 | 130908003 | |||
chr11:130910120 | C | T | 13 | a0001c0001 a0001c0011 a0003c0003 others(10): Show |
237 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(234): Show |
synonymous_variant | LOW | c.1932G>A | p.Pro644Pro | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 4/11 | 2472/15691 | 1932/2979 | 644/992 | chr11 | 130910120 | |||
chr11:130911736 | G | C | 1 | a0005c0017 | 1 | HG02965.hp2 | synonymous_variant | LOW | c.1710C>G | p.Gly570Gly | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 2/11 | 2250/15691 | 1710/2979 | 570/992 | chr11 | 130911736 | |||
chr11:130914443 | T | A | 1 | a0004c0025 | 1 | HG02258.hp2 | synonymous_variant | LOW | c.1497A>T | p.Pro499Pro | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 2037/15691 | 1497/2979 | 499/992 | chr11 | 130914443 | |||
chr11:130914538 | A | G | 1 | a0005c0017 | 1 | HG02965.hp2 | synonymous_variant | LOW | c.1402T>C | p.Leu468Leu | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 1942/15691 | 1402/2979 | 468/992 | chr11 | 130914538 | |||
chr11:130914593 | A | G | 3 | a0003c0003 a0014c0026 a0018c0027 |
55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
synonymous_variant | LOW | c.1347T>C | p.Ile449Ile | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 1887/15691 | 1347/2979 | 449/992 | chr11 | 130914593 | |||
chr11:130914788 | G | A | 2 | a0004c0008 a0015c0031 |
12 | HG01884.hp2 HG02257.hp1 HG02280.hp1 others(9): Show |
synonymous_variant | LOW | c.1152C>T | p.Thr384Thr | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 1692/15691 | 1152/2979 | 384/992 | chr11 | 130914788 | |||
chr11:130914812 | C | T | 3 | a0003c0003 a0014c0026 a0018c0027 |
55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
synonymous_variant | LOW | c.1128G>A | p.Pro376Pro | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 1668/15691 | 1128/2979 | 376/992 | chr11 | 130914812 | |||
chr11:130915076 | C | G | 24 | a0001c0001 a0001c0010 a0001c0011 others(21): Show |
312 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(309): Show |
synonymous_variant | LOW | c.864G>C | p.Pro288Pro | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 1404/15691 | 864/2979 | 288/992 | chr11 | 130915076 | |||
chr11:130915310 | G | A | 3 | a0003c0003 a0014c0026 a0018c0027 |
55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
synonymous_variant | LOW | c.630C>T | p.Thr210Thr | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 1170/15691 | 630/2979 | 210/992 | chr11 | 130915310 | |||
chr11:130915409 | T | C | 3 | a0003c0003 a0014c0026 a0018c0027 |
55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
synonymous_variant | LOW | c.531A>G | p.Ala177Ala | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 1071/15691 | 531/2979 | 177/992 | chr11 | 130915409 | |||
chr11:130915580 | G | A | 1 | a0007c0007 | 14 | HG02040.hp2 NA18747.hp2 NA18945.hp1 others(11): Show |
synonymous_variant | LOW | c.360C>T | p.Ser120Ser | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 900/15691 | 360/2979 | 120/992 | chr11 | 130915580 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:130866254 | T | C | 1 | a0001c0001t0056 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*12168A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 12168 | chr11 | 130866254 | ||||||
chr11:130866272 | A | G | 8 | a0001c0001t0092 a0007c0007t0013 a0007c0007t0026 others(5): Show |
15 | HG02040.hp2 NA18747.hp2 NA18945.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*12150T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 12150 | chr11 | 130866272 | ||||||
chr11:130866339 | C | T | 1 | a0012c0018t0085 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*12083G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 12083 | chr11 | 130866339 | ||||||
chr11:130866376 | T | G | 3 | a0001c0011t0016 a0001c0011t0102 a0001c0011t0107 |
5 | HG00280.hp2 HG01074.hp1 HG01081.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*12046A>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 12046 | chr11 | 130866376 | ||||||
chr11:130866388 | T | C | 1 | a0001c0001t0099 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*12034A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 12034 | chr11 | 130866388 | ||||||
chr11:130866655 | C | T | 1 | a0002c0002t0065 | 1 | HG03491.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11767G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 11767 | chr11 | 130866655 | ||||||
chr11:130866668 | G | A | 1 | a0006c0006t0032 | 2 | HG02647.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*11754C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 11754 | chr11 | 130866668 | ||||||
chr11:130866739 | T | C | 1 | a0009c0013t0112 | 1 | HG00609.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11683A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 11683 | chr11 | 130866739 | ||||||
chr11:130866790 | C | T | 4 | a0001c0001t0007 a0001c0001t0037 a0001c0001t0076 others(1): Show |
17 | HG00642.hp2 HG01074.hp2 HG01255.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*11632G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 11632 | chr11 | 130866790 | ||||||
chr11:130866936 | C | T | 2 | a0001c0001t0007 a0001c0001t0037 |
15 | HG00642.hp2 HG01074.hp2 HG01255.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*11486G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 11486 | chr11 | 130866936 | ||||||
chr11:130866960 | A | AAAGCTCT others(325): Show |
1 | a0012c0018t0085 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11461_*11462insGG others(330): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 11461 | chr11 | 130866960 | ||||||
chr11:130867107 | G | A | 1 | a0004c0009t0009 | 7 | HG00741.hp2 HG01070.hp2 HG02451.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*11315C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 11315 | chr11 | 130867107 | ||||||
chr11:130867249 | A | G | 2 | a0001c0001t0105 a0001c0001t0106 |
2 | HG00673.hp2 NA19062.hp2 |
3_prime_UTR_variant | MODIFIER | c.*11173T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 11173 | chr11 | 130867249 | ||||||
chr11:130867299 | G | A | 1 | a0001c0001t0100 | 1 | HG01099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11123C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 11123 | chr11 | 130867299 | ||||||
chr11:130867349 | T | C | 2 | a0004c0008t0116 a0004c0008t0117 |
2 | HG02280.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*11073A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 11073 | chr11 | 130867349 | ||||||
chr11:130867359 | C | T | 4 | a0001c0001t0007 a0001c0001t0037 a0001c0001t0076 others(1): Show |
17 | HG00642.hp2 HG01074.hp2 HG01255.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*11063G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 11063 | chr11 | 130867359 | ||||||
chr11:130867377 | T | G | 8 | a0001c0001t0092 a0007c0007t0013 a0007c0007t0026 others(5): Show |
15 | HG02040.hp2 NA18747.hp2 NA18945.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*11045A>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 11045 | chr11 | 130867377 | ||||||
chr11:130867386 | A | G | 109 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(106): Show |
326 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(323): Show |
3_prime_UTR_variant | MODIFIER | c.*11036T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 11036 | chr11 | 130867386 | ||||||
chr11:130867551 | A | G | 1 | a0009c0013t0112 | 1 | HG00609.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10871T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 10871 | chr11 | 130867551 | ||||||
chr11:130867611 | C | T | 1 | a0001c0001t0046 | 2 | NA18986.hp1 NA19000.hp2 |
3_prime_UTR_variant | MODIFIER | c.*10811G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 10811 | chr11 | 130867611 | ||||||
chr11:130867901 | G | C | 1 | a0005c0004t0082 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10521C>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 10521 | chr11 | 130867901 | ||||||
chr11:130867983 | C | A | 7 | a0001c0001t0017 a0001c0001t0095 a0004c0005t0023 others(4): Show |
11 | HG02523.hp2 NA18612.hp2 NA18967.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*10439G>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 10439 | chr11 | 130867983 | ||||||
chr11:130868016 | C | G | 2 | a0007c0007t0033 a0007c0007t0066 |
3 | NA18964.hp2 NA19010.hp1 NA19060.hp1 |
3_prime_UTR_variant | MODIFIER | c.*10406G>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 10406 | chr11 | 130868016 | ||||||
chr11:130868016 | C | T | 1 | a0004c0009t0009 | 7 | HG00741.hp2 HG01070.hp2 HG02451.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*10406G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 10406 | chr11 | 130868016 | ||||||
chr11:130868058 | C | G | 1 | a0001c0001t0099 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10364G>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 10364 | chr11 | 130868058 | ||||||
chr11:130868357 | A | G | 1 | a0004c0009t0009 | 7 | HG00741.hp2 HG01070.hp2 HG02451.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*10065T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 10065 | chr11 | 130868357 | ||||||
chr11:130868375 | C | T | 1 | a0001c0001t0098 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10047G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 10047 | chr11 | 130868375 | ||||||
chr11:130868673 | A | C | 59 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0014 others(56): Show |
178 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(175): Show |
3_prime_UTR_variant | MODIFIER | c.*9749T>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 9749 | chr11 | 130868673 | ||||||
chr11:130868695 | C | A | 22 | a0001c0001t0006 a0001c0001t0015 a0001c0001t0042 others(19): Show |
50 | HG00323.hp2 HG01243.hp1 HG01884.hp1 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*9727G>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 9727 | chr11 | 130868695 | ||||||
chr11:130868708 | T | C | 1 | a0004c0005t0030 | 2 | HG01891.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*9714A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 9714 | chr11 | 130868708 | ||||||
chr11:130868761 | C | T | 1 | a0001c0001t0097 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9661G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 9661 | chr11 | 130868761 | ||||||
chr11:130868829 | T | C | 9 | a0001c0001t0011 a0001c0001t0114 a0004c0008t0048 others(6): Show |
21 | HG00738.hp2 HG01109.hp1 HG01168.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*9593A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 9593 | chr11 | 130868829 | ||||||
chr11:130868873 | G | A | 3 | a0001c0010t0010 a0005c0004t0027 a0005c0004t0081 |
9 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*9549C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 9549 | chr11 | 130868873 | ||||||
chr11:130868953 | C | T | 21 | a0001c0001t0006 a0001c0001t0015 a0001c0001t0042 others(18): Show |
49 | HG00323.hp2 HG00673.hp1 HG01243.hp1 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*9469G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 9469 | chr11 | 130868953 | ||||||
chr11:130869051 | T | A | 63 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0014 others(60): Show |
182 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(179): Show |
3_prime_UTR_variant | MODIFIER | c.*9371A>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 9371 | chr11 | 130869051 | ||||||
chr11:130869159 | A | G | 2 | a0001c0001t0007 a0001c0001t0037 |
15 | HG00642.hp2 HG01074.hp2 HG01255.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*9263T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 9263 | chr11 | 130869159 | ||||||
chr11:130869204 | T | G | 1 | a0004c0008t0117 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9218A>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 9218 | chr11 | 130869204 | ||||||
chr11:130869223 | C | T | 1 | a0001c0001t0045 | 2 | NA18949.hp1 NA19079.hp1 |
3_prime_UTR_variant | MODIFIER | c.*9199G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 9199 | chr11 | 130869223 | ||||||
chr11:130869238 | C | T | 36 | a0001c0001t0001 a0001c0001t0014 a0001c0001t0017 others(33): Show |
127 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*9184G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 9184 | chr11 | 130869238 | ||||||
chr11:130869389 | G | A | 62 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0014 others(59): Show |
181 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(178): Show |
3_prime_UTR_variant | MODIFIER | c.*9033C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 9033 | chr11 | 130869389 | ||||||
chr11:130869452 | C | T | 3 | a0001c0010t0010 a0005c0004t0027 a0005c0004t0081 |
9 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*8970G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 8970 | chr11 | 130869452 | ||||||
chr11:130869478 | G | C | 23 | a0001c0001t0006 a0001c0001t0015 a0001c0001t0042 others(20): Show |
51 | HG00323.hp2 HG00673.hp1 HG01243.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*8944C>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 8944 | chr11 | 130869478 | ||||||
chr11:130869492 | T | C | 5 | a0001c0001t0007 a0001c0001t0037 a0001c0001t0076 others(2): Show |
24 | HG00642.hp2 HG00741.hp2 HG01070.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*8930A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 8930 | chr11 | 130869492 | ||||||
chr11:130869536 | C | G | 3 | a0006c0006t0032 a0006c0006t0060 a0022c0016t0109 |
4 | HG02615.hp1 HG02647.hp1 HG03098.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*8886G>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 8886 | chr11 | 130869536 | ||||||
chr11:130869568 | C | T | 1 | a0014c0026t0072 | 1 | HG02165.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8854G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 8854 | chr11 | 130869568 | ||||||
chr11:130869585 | T | G | 10 | a0001c0001t0004 a0001c0001t0038 a0001c0001t0111 others(7): Show |
58 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*8837A>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 8837 | chr11 | 130869585 | ||||||
chr11:130869638 | A | C | 2 | a0001c0001t0015 a0003c0003t0070 |
5 | NA18969.hp1 NA18978.hp1 NA19002.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*8784T>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 8784 | chr11 | 130869638 | ||||||
chr11:130869705 | C | T | 1 | a0005c0004t0081 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8717G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 8717 | chr11 | 130869705 | ||||||
chr11:130869765 | A | G | 5 | a0001c0001t0007 a0001c0001t0037 a0001c0001t0076 others(2): Show |
24 | HG00642.hp2 HG00741.hp2 HG01070.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*8657T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 8657 | chr11 | 130869765 | ||||||
chr11:130869769 | T | C | 8 | a0001c0001t0092 a0007c0007t0013 a0007c0007t0026 others(5): Show |
15 | HG02040.hp2 NA18747.hp2 NA18945.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*8653A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 8653 | chr11 | 130869769 | ||||||
chr11:130869909 | G | GA | 26 | a0001c0001t0007 a0001c0001t0011 a0001c0001t0018 others(23): Show |
67 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*8512dupT | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 8512 | chr11 | 130869909 | ||||||
chr11:130869909 | G | GAA | 3 | a0001c0001t0115 a0004c0008t0019 a0004c0008t0029 |
8 | HG01884.hp2 HG02257.hp1 HG02559.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*8511_*8512dupTT | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 8512 | chr11 | 130869909 | ||||||
chr11:130869942 | T | TGAA | 16 | a0001c0001t0011 a0001c0001t0018 a0001c0001t0114 others(13): Show |
36 | HG00738.hp2 HG01109.hp1 HG01168.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*8477_*8479dupTTC | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 8479 | chr11 | 130869942 | ||||||
chr11:130869953 | A | G | 109 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(106): Show |
326 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(323): Show |
3_prime_UTR_variant | MODIFIER | c.*8469T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 8469 | chr11 | 130869953 | ||||||
chr11:130869958 | T | C | 105 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(102): Show |
319 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(316): Show |
3_prime_UTR_variant | MODIFIER | c.*8464A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 8464 | chr11 | 130869958 | ||||||
chr11:130869992 | G | T | 64 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0014 others(61): Show |
183 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*8430C>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 8430 | chr11 | 130869992 | ||||||
chr11:130870040 | A | G | 1 | a0002c0002t0063 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8382T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 8382 | chr11 | 130870040 | ||||||
chr11:130870268 | T | C | 1 | a0006c0006t0060 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8154A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 8154 | chr11 | 130870268 | ||||||
chr11:130870440 | T | C | 63 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0014 others(60): Show |
182 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(179): Show |
3_prime_UTR_variant | MODIFIER | c.*7982A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 7982 | chr11 | 130870440 | ||||||
chr11:130870445 | G | T | 1 | a0009c0013t0112 | 1 | HG00609.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7977C>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 7977 | chr11 | 130870445 | ||||||
chr11:130870460 | C | T | 1 | a0001c0001t0091 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7962G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 7962 | chr11 | 130870460 | ||||||
chr11:130870462 | T | C | 64 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0014 others(61): Show |
183 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*7960A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 7960 | chr11 | 130870462 | ||||||
chr11:130870529 | G | A | 13 | a0001c0001t0006 a0001c0001t0015 a0001c0001t0042 others(10): Show |
30 | HG00323.hp2 HG00673.hp1 HG01884.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*7893C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 7893 | chr11 | 130870529 | ||||||
chr11:130870805 | A | C | 7 | a0004c0008t0048 a0004c0008t0116 a0004c0008t0117 others(4): Show |
16 | HG00738.hp2 HG02280.hp1 HG02809.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*7617T>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 7617 | chr11 | 130870805 | ||||||
chr11:130870825 | T | TG | 14 | a0001c0001t0077 a0003c0003t0073 a0003c0003t0113 others(11): Show |
27 | HG00738.hp2 HG01891.hp1 HG02280.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*7596dupC | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 7596 | chr11 | 130870825 | ||||||
chr11:130870825 | TG | T | 66 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(63): Show |
210 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(207): Show |
3_prime_UTR_variant | MODIFIER | c.*7596delC | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 7596 | chr11 | 130870825 | ||||||
chr11:130870849 | T | A | 1 | a0001c0001t0087 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7573A>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 7573 | chr11 | 130870849 | ||||||
chr11:130870896 | T | C | 1 | a0004c0025t0051 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7526A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 7526 | chr11 | 130870896 | ||||||
chr11:130871072 | G | A | 67 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(64): Show |
199 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(196): Show |
3_prime_UTR_variant | MODIFIER | c.*7350C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 7350 | chr11 | 130871072 | ||||||
chr11:130871132 | C | G | 105 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(102): Show |
319 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(316): Show |
3_prime_UTR_variant | MODIFIER | c.*7290G>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 7290 | chr11 | 130871132 | ||||||
chr11:130871180 | G | A | 1 | a0002c0002t0012 | 4 | HG00099.hp1 HG01106.hp2 HG01175.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*7242C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 7242 | chr11 | 130871180 | ||||||
chr11:130871205 | A | G | 1 | a0002c0002t0064 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7217T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 7217 | chr11 | 130871205 | ||||||
chr11:130871295 | C | T | 4 | a0001c0001t0007 a0001c0001t0037 a0001c0001t0076 others(1): Show |
17 | HG00642.hp2 HG01074.hp2 HG01255.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*7127G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 7127 | chr11 | 130871295 | ||||||
chr11:130871387 | C | T | 9 | a0001c0001t0004 a0001c0001t0038 a0003c0003t0003 others(6): Show |
56 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*7035G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 7035 | chr11 | 130871387 | ||||||
chr11:130871508 | T | G | 1 | a0012c0018t0085 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6914A>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 6914 | chr11 | 130871508 | ||||||
chr11:130871520 | G | A | 42 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 others(39): Show |
137 | HG00423.hp2 HG00558.hp2 HG00642.hp2 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*6902C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 6902 | chr11 | 130871520 | ||||||
chr11:130871578 | C | T | 3 | a0001c0001t0043 a0001c0001t0089 a0001c0001t0090 |
4 | HG00673.hp1 NA18966.hp1 NA19000.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6844G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 6844 | chr11 | 130871578 | ||||||
chr11:130871711 | A | G | 63 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0014 others(60): Show |
182 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(179): Show |
3_prime_UTR_variant | MODIFIER | c.*6711T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 6711 | chr11 | 130871711 | ||||||
chr11:130871866 | A | G | 63 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0014 others(60): Show |
182 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(179): Show |
3_prime_UTR_variant | MODIFIER | c.*6556T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 6556 | chr11 | 130871866 | ||||||
chr11:130872010 | G | A | 1 | a0015c0031t0118 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6412C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 6412 | chr11 | 130872010 | ||||||
chr11:130872045 | A | G | 62 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0014 others(59): Show |
179 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(176): Show |
3_prime_UTR_variant | MODIFIER | c.*6377T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 6377 | chr11 | 130872045 | ||||||
chr11:130872260 | G | T | 63 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0014 others(60): Show |
182 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(179): Show |
3_prime_UTR_variant | MODIFIER | c.*6162C>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 6162 | chr11 | 130872260 | ||||||
chr11:130872280 | G | C | 1 | a0001c0001t0104 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6142C>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 6142 | chr11 | 130872280 | ||||||
chr11:130872310 | C | T | 1 | a0001c0001t0095 | 1 | NA18992.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6112G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 6112 | chr11 | 130872310 | ||||||
chr11:130872319 | C | T | 1 | a0004c0025t0051 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6103G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 6103 | chr11 | 130872319 | ||||||
chr11:130872349 | G | A | 1 | a0001c0001t0105 | 1 | NA19062.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6073C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 6073 | chr11 | 130872349 | ||||||
chr11:130872508 | A | G | 1 | a0007c0007t0033 | 2 | NA18964.hp2 NA19010.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5914T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 5914 | chr11 | 130872508 | ||||||
chr11:130872735 | G | A | 64 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0014 others(61): Show |
183 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*5687C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 5687 | chr11 | 130872735 | ||||||
chr11:130872847 | T | C | 1 | a0001c0001t0106 | 1 | HG00673.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5575A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 5575 | chr11 | 130872847 | ||||||
chr11:130872893 | T | C | 65 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0014 others(62): Show |
184 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(181): Show |
3_prime_UTR_variant | MODIFIER | c.*5529A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 5529 | chr11 | 130872893 | ||||||
chr11:130872906 | C | T | 1 | a0005c0004t0084 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5516G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 5516 | chr11 | 130872906 | ||||||
chr11:130872917 | G | A | 24 | a0001c0001t0006 a0001c0001t0015 a0001c0001t0042 others(21): Show |
52 | HG00323.hp2 HG00673.hp1 HG01243.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*5505C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 5505 | chr11 | 130872917 | ||||||
chr11:130872932 | C | T | 1 | a0001c0001t0042 | 2 | HG00323.hp2 HG01952.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5490G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 5490 | chr11 | 130872932 | ||||||
chr11:130873346 | T | G | 1 | a0001c0001t0087 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5076A>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 5076 | chr11 | 130873346 | ||||||
chr11:130873493 | T | C | 65 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0014 others(62): Show |
184 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(181): Show |
3_prime_UTR_variant | MODIFIER | c.*4929A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 4929 | chr11 | 130873493 | ||||||
chr11:130873539 | G | A | 3 | a0005c0004t0040 a0005c0004t0074 a0005c0004t0084 |
4 | HG02922.hp1 HG02976.hp2 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4883C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 4883 | chr11 | 130873539 | ||||||
chr11:130873578 | C | T | 1 | a0001c0001t0037 | 2 | HG01255.hp1 HG02602.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4844G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 4844 | chr11 | 130873578 | ||||||
chr11:130873939 | T | C | 3 | a0002c0002t0005 a0002c0002t0062 a0009c0013t0112 |
17 | HG00438.hp1 HG00609.hp2 HG02027.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*4483A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 4483 | chr11 | 130873939 | ||||||
chr11:130874026 | G | T | 3 | a0001c0001t0114 a0006c0006t0032 a0006c0006t0060 |
4 | HG02615.hp1 HG02647.hp1 HG03098.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4396C>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 4396 | chr11 | 130874026 | ||||||
chr11:130874029 | T | TTA | 12 | a0001c0001t0006 a0001c0001t0015 a0001c0001t0042 others(9): Show |
29 | HG00323.hp2 HG00673.hp1 HG01884.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*4392_*4393insTA | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 4392 | chr11 | 130874029 | ||||||
chr11:130874030 | T | TA | 53 | a0001c0001t0001 a0001c0001t0014 a0001c0001t0017 others(50): Show |
155 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(152): Show |
3_prime_UTR_variant | MODIFIER | c.*4391_*4392insT | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 4391 | chr11 | 130874030 | ||||||
chr11:130874089 | C | T | 1 | a0001c0001t0088 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4333G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 4333 | chr11 | 130874089 | ||||||
chr11:130874184 | C | T | 1 | a0002c0002t0063 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4238G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 4238 | chr11 | 130874184 | ||||||
chr11:130874317 | C | T | 2 | a0001c0001t0044 a0004c0005t0022 |
5 | HG01258.hp2 HG01934.hp1 HG01993.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4105G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 4105 | chr11 | 130874317 | ||||||
chr11:130874348 | G | A | 1 | a0006c0006t0069 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4074C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 4074 | chr11 | 130874348 | ||||||
chr11:130874353 | A | G | 1 | a0002c0002t0062 | 1 | NA19064.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4069T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 4069 | chr11 | 130874353 | ||||||
chr11:130874373 | A | C | 65 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0014 others(62): Show |
184 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(181): Show |
3_prime_UTR_variant | MODIFIER | c.*4049T>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 4049 | chr11 | 130874373 | ||||||
chr11:130874430 | G | A | 1 | a0007c0007t0059 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3992C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 3992 | chr11 | 130874430 | ||||||
chr11:130874441 | C | T | 1 | a0002c0002t0061 | 1 | NA19086.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3981G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 3981 | chr11 | 130874441 | ||||||
chr11:130874507 | G | A | 1 | a0004c0005t0058 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3915C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 3915 | chr11 | 130874507 | ||||||
chr11:130874578 | G | A | 64 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0014 others(61): Show |
183 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*3844C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 3844 | chr11 | 130874578 | ||||||
chr11:130874595 | T | G | 65 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0014 others(62): Show |
184 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(181): Show |
3_prime_UTR_variant | MODIFIER | c.*3827A>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 3827 | chr11 | 130874595 | ||||||
chr11:130874614 | A | G | 65 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0014 others(62): Show |
184 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(181): Show |
3_prime_UTR_variant | MODIFIER | c.*3808T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 3808 | chr11 | 130874614 | ||||||
chr11:130874628 | C | T | 1 | a0013c0028t0094 | 1 | HG02056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3794G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 3794 | chr11 | 130874628 | ||||||
chr11:130874746 | A | G | 3 | a0004c0005t0020 a0004c0005t0030 a0021c0030t0050 |
6 | HG01891.hp1 HG02572.hp1 HG02622.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3676T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 3676 | chr11 | 130874746 | ||||||
chr11:130874775 | A | G | 65 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0014 others(62): Show |
184 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(181): Show |
3_prime_UTR_variant | MODIFIER | c.*3647T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 3647 | chr11 | 130874775 | ||||||
chr11:130874872 | T | G | 65 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0014 others(62): Show |
184 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(181): Show |
3_prime_UTR_variant | MODIFIER | c.*3550A>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 3550 | chr11 | 130874872 | ||||||
chr11:130875082 | G | A | 64 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0014 others(61): Show |
183 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*3340C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 3340 | chr11 | 130875082 | ||||||
chr11:130875150 | T | C | 65 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0014 others(62): Show |
184 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(181): Show |
3_prime_UTR_variant | MODIFIER | c.*3272A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 3272 | chr11 | 130875150 | ||||||
chr11:130875175 | C | T | 1 | a0001c0001t0093 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3247G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 3247 | chr11 | 130875175 | ||||||
chr11:130875464 | G | A | 1 | a0001c0001t0078 | 1 | HG00423.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2958C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 2958 | chr11 | 130875464 | ||||||
chr11:130875696 | A | G | 64 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0014 others(61): Show |
183 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*2726T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 2726 | chr11 | 130875696 | ||||||
chr11:130875783 | T | G | 1 | a0001c0011t0107 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2639A>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 2639 | chr11 | 130875783 | ||||||
chr11:130875824 | C | T | 36 | a0001c0001t0001 a0001c0001t0014 a0001c0001t0017 others(33): Show |
126 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(123): Show |
3_prime_UTR_variant | MODIFIER | c.*2598G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 2598 | chr11 | 130875824 | ||||||
chr11:130875845 | A | C | 3 | a0001c0001t0080 a0001c0001t0086 a0001c0001t0087 |
3 | HG02895.hp1 NA19043.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2577T>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 2577 | chr11 | 130875845 | ||||||
chr11:130876235 | T | TCCAG | 64 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0014 others(61): Show |
183 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*2186_*2187insCTGG | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 2186 | chr11 | 130876235 | ||||||
chr11:130876251 | T | C | 36 | a0001c0001t0001 a0001c0001t0014 a0001c0001t0017 others(33): Show |
126 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(123): Show |
3_prime_UTR_variant | MODIFIER | c.*2171A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 2171 | chr11 | 130876251 | ||||||
chr11:130876262 | A | G | 1 | a0004c0008t0048 | 2 | HG02895.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2160T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 2160 | chr11 | 130876262 | ||||||
chr11:130876373 | A | G | 2 | a0001c0014t0041 a0012c0018t0085 |
3 | HG01099.hp1 HG02055.hp1 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2049T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 2049 | chr11 | 130876373 | ||||||
chr11:130876601 | AAGGT | A | 103 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(100): Show |
316 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(313): Show |
3_prime_UTR_variant | MODIFIER | c.*1817_*1820delACCT | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 1817 | chr11 | 130876601 | ||||||
chr11:130876631 | A | C | 2 | a0004c0008t0116 a0004c0008t0117 |
2 | HG02280.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1791T>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 1791 | chr11 | 130876631 | ||||||
chr11:130876759 | A | G | 1 | a0003c0003t0071 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1663T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 1663 | chr11 | 130876759 | ||||||
chr11:130876842 | C | T | 1 | a0001c0010t0053 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1580G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 1580 | chr11 | 130876842 | ||||||
chr11:130876865 | C | T | 1 | a0002c0002t0024 | 3 | HG00735.hp1 HG00738.hp1 HG02735.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1557G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 1557 | chr11 | 130876865 | ||||||
chr11:130877005 | T | C | 1 | a0001c0001t0028 | 3 | NA18948.hp1 NA18983.hp2 NA19062.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1417A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 1417 | chr11 | 130877005 | ||||||
chr11:130877100 | C | T | 12 | a0001c0010t0010 a0001c0010t0053 a0005c0004t0021 others(9): Show |
23 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1322G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 1322 | chr11 | 130877100 | ||||||
chr11:130877107 | T | C | 1 | a0001c0001t0047 | 2 | HG03491.hp1 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1315A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 1315 | chr11 | 130877107 | ||||||
chr11:130877147 | G | A | 1 | a0004c0008t0048 | 2 | HG02895.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1275C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 1275 | chr11 | 130877147 | ||||||
chr11:130877265 | C | T | 3 | a0006c0006t0032 a0006c0006t0060 a0022c0016t0109 |
4 | HG02615.hp1 HG02647.hp1 HG03098.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1157G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 1157 | chr11 | 130877265 | ||||||
chr11:130877336 | C | G | 65 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0014 others(62): Show |
184 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(181): Show |
3_prime_UTR_variant | MODIFIER | c.*1086G>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 1086 | chr11 | 130877336 | ||||||
chr11:130877364 | A | G | 1 | a0007c0007t0059 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1058T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 1058 | chr11 | 130877364 | ||||||
chr11:130877423 | A | G | 1 | a0001c0010t0053 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*999T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 999 | chr11 | 130877423 | ||||||
chr11:130877491 | C | G | 65 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0014 others(62): Show |
184 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(181): Show |
3_prime_UTR_variant | MODIFIER | c.*931G>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 931 | chr11 | 130877491 | ||||||
chr11:130877633 | T | C | 1 | a0002c0002t0067 | 1 | NA19006.hp2 | 3_prime_UTR_variant | MODIFIER | c.*789A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 789 | chr11 | 130877633 | ||||||
chr11:130877918 | G | A | 1 | a0004c0009t0009 | 7 | HG00741.hp2 HG01070.hp2 HG02451.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*504C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 504 | chr11 | 130877918 | ||||||
chr11:130878130 | AG | A | 9 | a0001c0001t0011 a0001c0001t0114 a0004c0008t0048 others(6): Show |
21 | HG00738.hp2 HG01109.hp1 HG01168.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*291delC | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 291 | chr11 | 130878130 | ||||||
chr11:130878180 | C | G | 1 | a0001c0001t0080 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*242G>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 242 | chr11 | 130878180 | ||||||
chr11:130878236 | A | G | 68 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0014 others(65): Show |
190 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(187): Show |
3_prime_UTR_variant | MODIFIER | c.*186T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 186 | chr11 | 130878236 | ||||||
chr11:130878332 | C | G | 5 | a0001c0001t0007 a0001c0001t0037 a0001c0001t0076 others(2): Show |
24 | HG00642.hp2 HG00741.hp2 HG01070.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*90G>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 90 | chr11 | 130878332 | ||||||
chr11:130915957 | G | T | 9 | a0001c0001t0007 a0001c0001t0014 a0001c0001t0037 others(6): Show |
26 | HG00423.hp1 HG00642.hp2 HG01074.hp2 others(23): Show |
5_prime_UTR_variant | MODIFIER | c.-18C>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 18 | chr11 | 130915957 | ||||||
chr11:130916164 | C | A | 2 | a0001c0001t0018 a0001c0001t0115 |
5 | HG01496.hp2 HG02630.hp1 HG02970.hp2 others(2): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-225G>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | chr11 | 130916164 | |||||||
chr11:130916211 | C | G | 1 | a0004c0008t0029 | 3 | HG02257.hp1 HG02559.hp2 HG02886.hp2 |
5_prime_UTR_variant | MODIFIER | c.-272G>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 272 | chr11 | 130916211 | ||||||
chr11:130916333 | C | T | 4 | a0004c0005t0020 a0004c0005t0030 a0004c0025t0051 others(1): Show |
7 | HG01891.hp1 HG02258.hp2 HG02572.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-394G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 394 | chr11 | 130916333 | ||||||
chr11:130916391 | C | T | 1 | a0001c0001t0075 | 1 | HG02615.hp2 | 5_prime_UTR_variant | MODIFIER | c.-452G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 452 | chr11 | 130916391 | ||||||
chr11:130916403 | G | A | 6 | a0004c0008t0019 a0004c0008t0029 a0004c0008t0116 others(3): Show |
17 | HG00741.hp2 HG01070.hp2 HG01884.hp2 others(14): Show |
5_prime_UTR_variant | MODIFIER | c.-464C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 464 | chr11 | 130916403 | ||||||
chr11:130916413 | T | C | 8 | a0003c0003t0003 a0003c0003t0036 a0003c0003t0070 others(5): Show |
35 | HG00423.hp2 HG00609.hp1 HG00733.hp1 others(32): Show |
5_prime_UTR_variant | MODIFIER | c.-474A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 474 | chr11 | 130916413 | ||||||
chr11:130916430 | C | T | 1 | a0005c0004t0074 | 1 | HG03516.hp2 | 5_prime_UTR_variant | MODIFIER | c.-491G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 491 | chr11 | 130916430 | ||||||
chr11:130916441 | G | C | 1 | a0005c0004t0049 | 2 | HG03139.hp2 HG03486.hp1 |
5_prime_UTR_variant | MODIFIER | c.-502C>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 502 | chr11 | 130916441 | ||||||
chr11:130916450 | C | A | 79 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(76): Show |
239 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(236): Show |
5_prime_UTR_variant | MODIFIER | c.-511G>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 511 | chr11 | 130916450 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:130878565 | T | C | 1 | a0001c0001t0001g0207 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2847-11A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 10/10 | chr11 | 130878565 | |||||||
chr11:130878630 | C | A | 3 | a0001c0001t0006g0208 a0001c0001t0006g0261 a0001c0001t0006g0262 |
3 | HG03831.hp2 HG04115.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2847-76G>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 10/10 | chr11 | 130878630 | |||||||
chr11:130878816 | A | G | 1 | a0001c0001t0001g0205 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2847-262T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 10/10 | chr11 | 130878816 | |||||||
chr11:130878931 | T | C | 1 | a0004c0009t0009g0283 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2847-377A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 10/10 | chr11 | 130878931 | |||||||
chr11:130879164 | G | A | 79 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(76): Show |
129 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.2846+460C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 10/10 | chr11 | 130879164 | |||||||
chr11:130879222 | A | G | 2 | a0005c0004t0049g0295 a0005c0004t0049g0296 |
2 | HG03139.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2846+402T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 10/10 | chr11 | 130879222 | |||||||
chr11:130879249 | C | T | 3 | a0001c0014t0041g0233 a0001c0014t0041g0234 a0012c0018t0085g0173 |
3 | HG01099.hp1 HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2846+375G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 10/10 | chr11 | 130879249 | |||||||
chr11:130879312 | C | T | 1 | a0001c0001t0007g0160 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2846+312G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 10/10 | chr11 | 130879312 | |||||||
chr11:130879361 | C | A | 42 | a0001c0001t0006g0038 a0001c0001t0006g0039 a0001c0001t0006g0208 others(39): Show |
51 | HG00323.hp2 HG00673.hp1 HG01243.hp1 others(48): Show |
intron_variant | MODIFIER | c.2846+263G>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 10/10 | chr11 | 130879361 | |||||||
chr11:130879452 | T | C | 5 | a0004c0005t0020g0016 a0004c0005t0020g0045 a0004c0005t0030g0017 others(2): Show |
7 | HG01891.hp1 HG02258.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.2846+172A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 10/10 | chr11 | 130879452 | |||||||
chr11:130879456 | TAG | T | 191 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(188): Show |
260 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.2846+166_2846+167d others(4): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 10/10 | chr11 | 130879456 | |||||||
chr11:130879579 | G | T | 1 | a0001c0001t0104g0191 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2846+45C>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 10/10 | chr11 | 130879579 | |||||||
chr11:130879820 | A | G | 236 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(233): Show |
326 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(323): Show |
intron_variant | MODIFIER | c.2759-109T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 9/10 | chr11 | 130879820 | |||||||
chr11:130879951 | A | G | 2 | a0005c0004t0021g0050 a0005c0004t0039g0178 |
2 | HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2759-240T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 9/10 | chr11 | 130879951 | |||||||
chr11:130880006 | A | G | 3 | a0002c0002t0002g0081 a0002c0002t0002g0083 a0002c0002t0064g0082 |
3 | HG02015.hp1 HG02056.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.2759-295T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 9/10 | chr11 | 130880006 | |||||||
chr11:130880253 | G | A | 1 | a0001c0001t0014g0164 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2758+369C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 9/10 | chr11 | 130880253 | |||||||
chr11:130880354 | AC | A | 4 | a0001c0011t0016g0226 a0001c0011t0016g0231 a0001c0011t0102g0227 others(1): Show |
4 | HG00280.hp2 HG01074.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.2758+267delG | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 9/10 | chr11 | 130880354 | |||||||
chr11:130880505 | T | G | 1 | a0004c0009t0009g0283 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2758+117A>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 9/10 | chr11 | 130880505 | |||||||
chr11:130880558 | A | G | 4 | a0006c0006t0032g0054 a0006c0006t0032g0055 a0006c0006t0060g0053 others(1): Show |
4 | HG02615.hp1 HG02647.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2758+64T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 9/10 | chr11 | 130880558 | |||||||
chr11:130880597 | T | C | 5 | a0004c0005t0020g0016 a0004c0005t0020g0045 a0004c0005t0030g0017 others(2): Show |
7 | HG01891.hp1 HG02258.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.2758+25A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 9/10 | chr11 | 130880597 | |||||||
chr11:130881007 | G | C | 1 | a0001c0001t0093g0188 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2574-201C>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130881007 | |||||||
chr11:130881199 | G | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
189 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.2574-393C>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130881199 | |||||||
chr11:130881335 | C | G | 1 | a0001c0001t0045g0232 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2574-529G>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130881335 | |||||||
chr11:130881335 | C | T | 2 | a0001c0001t0001g0209 a0001c0001t0001g0220 |
2 | HG00735.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2574-529G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130881335 | |||||||
chr11:130881366 | A | C | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(126): Show |
188 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.2574-560T>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130881366 | |||||||
chr11:130881372 | C | T | 1 | a0012c0018t0085g0173 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2574-566G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130881372 | |||||||
chr11:130881413 | C | G | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(126): Show |
188 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.2574-607G>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130881413 | |||||||
chr11:130881525 | T | C | 4 | a0006c0006t0032g0054 a0006c0006t0032g0055 a0006c0006t0060g0053 others(1): Show |
4 | HG02615.hp1 HG02647.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2574-719A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130881525 | |||||||
chr11:130881535 | G | C | 1 | a0002c0002t0005g0095 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2574-729C>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130881535 | |||||||
chr11:130881582 | T | C | 32 | a0001c0001t0011g0036 a0001c0001t0011g0190 a0001c0001t0011g0216 others(29): Show |
36 | HG00738.hp2 HG01109.hp1 HG01168.hp1 others(33): Show |
intron_variant | MODIFIER | c.2574-776A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130881582 | |||||||
chr11:130881874 | T | G | 1 | a0003c0003t0003g0144 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2574-1068A>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130881874 | |||||||
chr11:130882145 | A | C | 126 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(123): Show |
185 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.2574-1339T>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130882145 | |||||||
chr11:130882594 | C | T | 6 | a0004c0009t0009g0044 a0004c0009t0009g0283 a0004c0009t0009g0284 others(3): Show |
7 | HG00741.hp2 HG01070.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.2574-1788G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130882594 | |||||||
chr11:130882657 | A | T | 1 | a0003c0003t0071g0132 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2574-1851T>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130882657 | |||||||
chr11:130882672 | A | G | 237 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(234): Show |
327 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(324): Show |
intron_variant | MODIFIER | c.2574-1866T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130882672 | |||||||
chr11:130882793 | C | T | 1 | a0001c0010t0053g0058 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2574-1987G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130882793 | |||||||
chr11:130882802 | T | C | 4 | a0006c0006t0032g0054 a0006c0006t0032g0055 a0006c0006t0060g0053 others(1): Show |
4 | HG02615.hp1 HG02647.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2574-1996A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130882802 | |||||||
chr11:130882834 | G | T | 2 | a0005c0004t0049g0295 a0005c0004t0049g0296 |
2 | HG03139.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2574-2028C>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130882834 | |||||||
chr11:130883174 | A | G | 39 | a0001c0001t0004g0182 a0001c0001t0004g0222 a0001c0001t0038g0151 others(36): Show |
58 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.2574-2368T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130883174 | |||||||
chr11:130883220 | T | C | 32 | a0001c0001t0011g0036 a0001c0001t0011g0190 a0001c0001t0011g0216 others(29): Show |
36 | HG00738.hp2 HG01109.hp1 HG01168.hp1 others(33): Show |
intron_variant | MODIFIER | c.2574-2414A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130883220 | |||||||
chr11:130883438 | A | G | 1 | a0001c0001t0043g0255 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2574-2632T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130883438 | |||||||
chr11:130883446 | C | T | 2 | a0001c0010t0053g0058 a0005c0017t0083g0171 |
2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2574-2640G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130883446 | |||||||
chr11:130883479 | C | A | 3 | a0001c0001t0080g0241 a0001c0001t0086g0183 a0001c0001t0087g0181 |
3 | HG02895.hp1 NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2574-2673G>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130883479 | |||||||
chr11:130883608 | G | A | 4 | a0006c0006t0032g0054 a0006c0006t0032g0055 a0006c0006t0060g0053 others(1): Show |
4 | HG02615.hp1 HG02647.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2574-2802C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130883608 | |||||||
chr11:130883672 | C | T | 1 | a0002c0002t0002g0112 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2574-2866G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130883672 | |||||||
chr11:130883799 | G | A | 19 | a0001c0010t0010g0010 a0001c0010t0010g0057 a0001c0010t0053g0058 others(16): Show |
23 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.2574-2993C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130883799 | |||||||
chr11:130883823 | A | G | 39 | a0001c0001t0004g0182 a0001c0001t0004g0222 a0001c0001t0038g0151 others(36): Show |
58 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.2574-3017T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130883823 | |||||||
chr11:130883950 | T | C | 1 | a0015c0031t0118g0294 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2574-3144A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130883950 | |||||||
chr11:130884017 | T | A | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(96): Show |
151 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.2574-3211A>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130884017 | |||||||
chr11:130884191 | T | C | 1 | a0005c0004t0082g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2574-3385A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130884191 | |||||||
chr11:130884243 | G | C | 6 | a0004c0009t0009g0044 a0004c0009t0009g0283 a0004c0009t0009g0284 others(3): Show |
7 | HG00741.hp2 HG01070.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.2574-3437C>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130884243 | |||||||
chr11:130884351 | A | G | 10 | a0001c0001t0092g0258 a0007c0007t0013g0026 a0007c0007t0013g0119 others(7): Show |
14 | HG02040.hp2 NA18747.hp2 NA18945.hp1 others(11): Show |
intron_variant | MODIFIER | c.2574-3545T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130884351 | |||||||
chr11:130884352 | T | C | 19 | a0001c0010t0010g0010 a0001c0010t0010g0057 a0001c0010t0053g0058 others(16): Show |
23 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.2574-3546A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130884352 | |||||||
chr11:130884400 | G | GAT | 4 | a0006c0006t0032g0054 a0006c0006t0032g0055 a0006c0006t0060g0053 others(1): Show |
4 | HG02615.hp1 HG02647.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2574-3595_2574-359 others(6): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130884400 | |||||||
chr11:130884541 | C | A | 2 | a0001c0001t0056g0056 a0001c0001t0075g0146 |
2 | HG02055.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.2574-3735G>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130884541 | |||||||
chr11:130884589 | C | T | 1 | a0001c0001t0006g0251 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2574-3783G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130884589 | |||||||
chr11:130884590 | G | A | 1 | a0002c0002t0002g0076 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2574-3784C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130884590 | |||||||
chr11:130884607 | C | G | 1 | a0001c0001t0080g0241 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2574-3801G>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130884607 | |||||||
chr11:130884626 | G | C | 64 | a0001c0001t0007g0148 a0001c0001t0007g0149 a0001c0001t0007g0150 others(61): Show |
74 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.2574-3820C>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130884626 | |||||||
chr11:130884627 | G | A | 18 | a0001c0001t0011g0036 a0001c0001t0011g0190 a0001c0001t0011g0216 others(15): Show |
21 | HG00738.hp2 HG01109.hp1 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.2574-3821C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130884627 | |||||||
chr11:130884696 | G | A | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(126): Show |
188 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.2574-3890C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130884696 | |||||||
chr11:130884713 | A | G | 39 | a0001c0001t0004g0182 a0001c0001t0004g0222 a0001c0001t0038g0151 others(36): Show |
58 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.2574-3907T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130884713 | |||||||
chr11:130884718 | A | C | 1 | a0021c0030t0050g0047 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2574-3912T>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130884718 | |||||||
chr11:130884763 | C | T | 1 | a0003c0003t0003g0140 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2574-3957G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130884763 | |||||||
chr11:130884828 | C | A | 1 | a0001c0001t0078g0158 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2574-4022G>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130884828 | |||||||
chr11:130884828 | C | T | 36 | a0001c0001t0004g0182 a0001c0001t0004g0222 a0001c0001t0038g0151 others(33): Show |
55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.2574-4022G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130884828 | |||||||
chr11:130884871 | C | CA | 35 | a0001c0001t0004g0182 a0001c0001t0004g0222 a0001c0001t0111g0253 others(32): Show |
46 | HG00423.hp2 HG00438.hp1 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.2574-4066dupT | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130884871 | |||||||
chr11:130884871 | CA | C | 42 | a0001c0001t0007g0149 a0001c0001t0007g0150 a0001c0001t0007g0159 others(39): Show |
51 | HG00099.hp1 HG00642.hp2 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.2574-4066delT | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130884871 | |||||||
chr11:130884878 | A | G | 1 | a0001c0001t0087g0181 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2574-4072T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130884878 | |||||||
chr11:130884890 | A | AG | 27 | a0001c0001t0006g0038 a0001c0001t0006g0039 a0001c0001t0006g0208 others(24): Show |
32 | HG00323.hp2 HG00673.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.2574-4085_2574-408 others(5): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130884890 | |||||||
chr11:130884890 | A | G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(100): Show |
157 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.2574-4084T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130884890 | |||||||
chr11:130884921 | A | G | 1 | a0001c0001t0076g0147 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2574-4115T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130884921 | |||||||
chr11:130884955 | G | T | 5 | a0001c0010t0010g0010 a0001c0010t0010g0057 a0005c0004t0027g0033 others(2): Show |
9 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.2574-4149C>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130884955 | |||||||
chr11:130884984 | G | C | 2 | a0001c0001t0001g0214 a0016c0023t0001g0264 |
2 | HG00099.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.2574-4178C>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130884984 | |||||||
chr11:130885149 | G | C | 28 | a0001c0001t0011g0036 a0001c0001t0011g0190 a0001c0001t0011g0216 others(25): Show |
31 | HG00738.hp2 HG01109.hp1 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.2574-4343C>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130885149 | |||||||
chr11:130885345 | G | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
189 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.2574-4539C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130885345 | |||||||
chr11:130885353 | G | C | 1 | a0022c0016t0109g0170 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2574-4547C>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130885353 | |||||||
chr11:130885488 | A | C | 3 | a0007c0007t0033g0025 a0007c0007t0059g0118 a0007c0007t0066g0121 |
4 | HG02040.hp2 NA18964.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.2574-4682T>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130885488 | |||||||
chr11:130885530 | A | C | 1 | a0012c0018t0085g0173 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2574-4724T>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130885530 | |||||||
chr11:130885543 | G | A | 1 | a0001c0001t0087g0181 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2574-4737C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130885543 | |||||||
chr11:130885680 | A | G | 127 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(124): Show |
184 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.2574-4874T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130885680 | |||||||
chr11:130885769 | C | CCTTAT | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(120): Show |
180 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.2574-4964_2574-496 others(9): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130885769 | |||||||
chr11:130885805 | A | C | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(120): Show |
180 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.2574-4999T>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130885805 | |||||||
chr11:130885844 | G | A | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(120): Show |
180 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.2574-5038C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130885844 | |||||||
chr11:130885889 | G | T | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(120): Show |
180 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.2574-5083C>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130885889 | |||||||
chr11:130885918 | T | C | 103 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(100): Show |
156 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.2574-5112A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130885918 | |||||||
chr11:130885933 | C | T | 4 | a0005c0004t0040g0177 a0005c0004t0040g0179 a0005c0004t0074g0145 others(1): Show |
4 | HG02922.hp1 HG02976.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2574-5127G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130885933 | |||||||
chr11:130885934 | G | A | 22 | a0001c0001t0007g0148 a0001c0001t0007g0149 a0001c0001t0007g0150 others(19): Show |
24 | HG00642.hp2 HG00741.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.2574-5128C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130885934 | |||||||
chr11:130886034 | A | T | 1 | a0003c0003t0003g0133 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.2574-5228T>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130886034 | |||||||
chr11:130886057 | T | C | 1 | a0001c0001t0014g0156 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.2574-5251A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130886057 | |||||||
chr11:130886095 | C | T | 1 | a0012c0018t0085g0173 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2574-5289G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130886095 | |||||||
chr11:130886103 | C | T | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(120): Show |
180 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.2574-5297G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130886103 | |||||||
chr11:130886127 | A | G | 32 | a0001c0001t0011g0036 a0001c0001t0011g0190 a0001c0001t0011g0216 others(29): Show |
36 | HG00738.hp2 HG01109.hp1 HG01168.hp1 others(33): Show |
intron_variant | MODIFIER | c.2574-5321T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130886127 | |||||||
chr11:130886181 | C | T | 2 | a0001c0001t0006g0039 a0001c0001t0091g0250 |
3 | HG01884.hp1 HG01978.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.2574-5375G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130886181 | |||||||
chr11:130886281 | T | C | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(120): Show |
180 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.2574-5475A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130886281 | |||||||
chr11:130886295 | T | C | 2 | a0001c0014t0041g0233 a0001c0014t0041g0234 |
2 | HG01099.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2574-5489A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130886295 | |||||||
chr11:130886356 | C | T | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(120): Show |
180 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.2574-5550G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130886356 | |||||||
chr11:130886358 | C | T | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(120): Show |
180 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.2574-5552G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130886358 | |||||||
chr11:130886394 | G | C | 1 | a0003c0003t0003g0128 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2574-5588C>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130886394 | |||||||
chr11:130886548 | G | T | 1 | a0001c0001t0001g0229 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.2574-5742C>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130886548 | |||||||
chr11:130886559 | T | C | 1 | a0001c0001t0042g0040 | 2 | HG00323.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.2574-5753A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130886559 | |||||||
chr11:130886624 | A | C | 1 | a0001c0001t0001g0229 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.2574-5818T>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130886624 | |||||||
chr11:130886737 | T | C | 122 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(119): Show |
179 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.2574-5931A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130886737 | |||||||
chr11:130886769 | C | G | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(118): Show |
178 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.2574-5963G>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130886769 | |||||||
chr11:130886940 | C | A | 28 | a0001c0001t0011g0036 a0001c0001t0011g0190 a0001c0001t0011g0216 others(25): Show |
31 | HG00738.hp2 HG01109.hp1 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.2574-6134G>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130886940 | |||||||
chr11:130887148 | A | G | 51 | a0001c0001t0006g0038 a0001c0001t0006g0039 a0001c0001t0006g0208 others(48): Show |
60 | HG00323.hp2 HG00673.hp1 HG01099.hp1 others(57): Show |
intron_variant | MODIFIER | c.2574-6342T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130887148 | |||||||
chr11:130887166 | T | G | 1 | a0005c0004t0084g0180 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2574-6360A>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130887166 | |||||||
chr11:130887266 | G | A | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(118): Show |
178 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.2574-6460C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130887266 | |||||||
chr11:130887277 | C | CA | 4 | a0005c0004t0040g0177 a0005c0004t0040g0179 a0005c0004t0074g0145 others(1): Show |
4 | HG02922.hp1 HG02976.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2574-6472dupT | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130887277 | |||||||
chr11:130887502 | A | C | 21 | a0001c0010t0010g0010 a0001c0010t0010g0057 a0001c0010t0053g0058 others(18): Show |
25 | HG01099.hp1 HG01243.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.2574-6696T>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130887502 | |||||||
chr11:130887562 | C | T | 1 | a0002c0002t0002g0022 | 2 | NA18973.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.2574-6756G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130887562 | |||||||
chr11:130887683 | T | G | 1 | a0001c0001t0001g0229 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.2574-6877A>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130887683 | |||||||
chr11:130887791 | G | A | 1 | a0005c0004t0021g0051 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2574-6985C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130887791 | |||||||
chr11:130887844 | C | T | 1 | a0001c0001t0093g0188 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2574-7038G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130887844 | |||||||
chr11:130887925 | T | G | 1 | a0002c0002t0002g0110 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2574-7119A>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130887925 | |||||||
chr11:130887960 | T | C | 3 | a0008c0012t0017g0037 a0008c0012t0017g0210 a0008c0012t0103g0198 |
4 | NA18612.hp2 NA18967.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.2574-7154A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130887960 | |||||||
chr11:130888030 | C | T | 1 | a0004c0025t0051g0046 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2574-7224G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130888030 | |||||||
chr11:130888099 | C | CA | 9 | a0002c0002t0002g0077 a0002c0002t0002g0081 a0002c0002t0002g0105 others(6): Show |
9 | HG01168.hp1 HG01433.hp2 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.2574-7294dupT | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130888099 | |||||||
chr11:130888099 | CAA | C | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(116): Show |
176 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.2574-7295_2574-729 others(6): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130888099 | |||||||
chr11:130888136 | T | C | 1 | a0002c0002t0005g0020 | 2 | HG02083.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.2574-7330A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130888136 | |||||||
chr11:130888185 | G | A | 1 | a0003c0003t0003g0139 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2574-7379C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130888185 | |||||||
chr11:130888218 | G | A | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(118): Show |
178 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.2574-7412C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130888218 | |||||||
chr11:130888257 | G | T | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(113): Show |
169 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.2574-7451C>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130888257 | |||||||
chr11:130888258 | A | T | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(113): Show |
169 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.2574-7452T>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130888258 | |||||||
chr11:130888271 | C | T | 1 | a0003c0003t0003g0135 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2574-7465G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130888271 | |||||||
chr11:130888415 | C | T | 4 | a0006c0006t0032g0054 a0006c0006t0032g0055 a0006c0006t0060g0053 others(1): Show |
4 | HG02615.hp1 HG02647.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2574-7609G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130888415 | |||||||
chr11:130888510 | A | G | 1 | a0002c0002t0005g0091 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2574-7704T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130888510 | |||||||
chr11:130888554 | C | T | 7 | a0003c0003t0004g0007 a0003c0003t0004g0265 a0003c0003t0004g0266 others(4): Show |
13 | HG00558.hp2 HG02071.hp2 HG02129.hp2 others(10): Show |
intron_variant | MODIFIER | c.2574-7748G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130888554 | |||||||
chr11:130888579 | G | A | 1 | a0004c0005t0057g0099 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2574-7773C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130888579 | |||||||
chr11:130888584 | C | T | 1 | a0001c0001t0001g0229 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.2574-7778G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130888584 | |||||||
chr11:130888661 | G | A | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(114): Show |
170 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.2574-7855C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130888661 | |||||||
chr11:130888867 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2574-8061G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130888867 | |||||||
chr11:130889029 | G | A | 124 | a0001c0001t0001g0199 a0001c0001t0004g0222 a0001c0001t0006g0038 others(121): Show |
162 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(159): Show |
intron_variant | MODIFIER | c.2574-8223C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130889029 | |||||||
chr11:130889034 | T | A | 2 | a0003c0003t0003g0126 a0003c0003t0003g0127 |
2 | HG02723.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2574-8228A>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130889034 | |||||||
chr11:130889047 | C | T | 1 | a0001c0001t0093g0188 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2574-8241G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130889047 | |||||||
chr11:130889094 | C | T | 7 | a0001c0010t0053g0058 a0001c0014t0041g0233 a0001c0014t0041g0234 others(4): Show |
7 | HG01099.hp1 HG02055.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.2574-8288G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130889094 | |||||||
chr11:130889228 | C | T | 7 | a0001c0001t0056g0056 a0004c0008t0019g0290 a0004c0008t0019g0291 others(4): Show |
7 | HG01168.hp1 HG01884.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.2574-8422G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130889228 | |||||||
chr11:130889238 | G | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0209 others(52): Show |
87 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.2574-8432C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130889238 | |||||||
chr11:130889269 | C | T | 3 | a0001c0001t0007g0161 a0001c0001t0046g0035 a0007c0007t0034g0028 |
5 | NA18959.hp1 NA18970.hp1 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.2574-8463G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130889269 | |||||||
chr11:130889292 | T | C | 1 | a0001c0001t0001g0209 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2574-8486A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130889292 | |||||||
chr11:130889305 | CTT | C | 3 | a0006c0006t0008g0061 a0006c0006t0008g0063 a0006c0006t0008g0064 |
3 | HG00738.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2574-8501_2574-850 others(6): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130889305 | |||||||
chr11:130889310 | T | C | 43 | a0001c0001t0007g0149 a0001c0001t0007g0150 a0001c0001t0011g0190 others(40): Show |
50 | HG00642.hp2 HG00738.hp2 HG01243.hp1 others(47): Show |
intron_variant | MODIFIER | c.2574-8504A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130889310 | |||||||
chr11:130889328 | G | T | 187 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0034 others(184): Show |
275 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(272): Show |
intron_variant | MODIFIER | c.2574-8522C>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130889328 | |||||||
chr11:130889369 | A | G | 3 | a0002c0002t0002g0014 a0002c0002t0002g0107 a0002c0002t0002g0110 |
5 | HG01943.hp2 HG01975.hp1 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.2574-8563T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130889369 | |||||||
chr11:130889409 | C | A | 6 | a0007c0007t0013g0026 a0007c0007t0013g0122 a0007c0007t0026g0027 others(3): Show |
10 | NA18747.hp2 NA18959.hp1 NA18960.hp2 others(7): Show |
intron_variant | MODIFIER | c.2574-8603G>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130889409 | |||||||
chr11:130889490 | C | T | 1 | a0002c0002t0002g0107 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2574-8684G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130889490 | |||||||
chr11:130889515 | G | A | 37 | a0001c0001t0038g0152 a0001c0010t0053g0058 a0001c0011t0016g0230 others(34): Show |
59 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(56): Show |
intron_variant | MODIFIER | c.2574-8709C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130889515 | |||||||
chr11:130889526 | A | T | 1 | a0001c0001t0087g0181 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2574-8720T>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130889526 | |||||||
chr11:130889530 | C | A | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(117): Show |
189 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.2574-8724G>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130889530 | |||||||
chr11:130889531 | T | A | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(117): Show |
189 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.2574-8725A>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130889531 | |||||||
chr11:130889532 | T | TGCC | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(117): Show |
189 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.2574-8727_2574-872 others(7): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130889532 | |||||||
chr11:130889600 | T | C | 1 | a0002c0002t0062g0116 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.2574-8794A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130889600 | |||||||
chr11:130889611 | C | T | 3 | a0001c0001t0076g0147 a0001c0001t0077g0153 a0005c0004t0049g0295 |
3 | HG02818.hp1 HG03139.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2574-8805G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130889611 | |||||||
chr11:130889805 | C | T | 1 | a0005c0004t0082g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2574-8999G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130889805 | |||||||
chr11:130889819 | T | C | 1 | a0009c0013t0112g0185 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2574-9013A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130889819 | |||||||
chr11:130889904 | T | C | 1 | a0002c0002t0002g0110 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2574-9098A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130889904 | |||||||
chr11:130890043 | G | C | 2 | a0001c0010t0010g0010 a0001c0010t0010g0057 |
5 | HG01243.hp1 HG02109.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.2574-9237C>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130890043 | |||||||
chr11:130890092 | A | G | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(150): Show |
227 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.2574-9286T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130890092 | |||||||
chr11:130890099 | T | C | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
233 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.2574-9293A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130890099 | |||||||
chr11:130890100 | G | A | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
232 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.2574-9294C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130890100 | |||||||
chr11:130890185 | T | C | 2 | a0001c0001t0080g0241 a0001c0001t0086g0183 |
2 | HG02895.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2574-9379A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130890185 | |||||||
chr11:130890205 | C | T | 157 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(154): Show |
234 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.2574-9399G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130890205 | |||||||
chr11:130890297 | A | C | 16 | a0006c0006t0008g0018 a0006c0006t0008g0060 a0006c0006t0008g0061 others(13): Show |
17 | HG00738.hp2 HG01168.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.2574-9491T>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130890297 | |||||||
chr11:130890308 | C | T | 157 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(154): Show |
234 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.2574-9502G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130890308 | |||||||
chr11:130890390 | T | C | 1 | a0001c0001t0017g0219 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2574-9584A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130890390 | |||||||
chr11:130890471 | T | C | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(155): Show |
235 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.2574-9665A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130890471 | |||||||
chr11:130890577 | T | C | 10 | a0007c0007t0013g0026 a0007c0007t0013g0119 a0007c0007t0013g0122 others(7): Show |
14 | HG02040.hp2 NA18747.hp2 NA18945.hp1 others(11): Show |
intron_variant | MODIFIER | c.2574-9771A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130890577 | |||||||
chr11:130890599 | A | T | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(155): Show |
235 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.2574-9793T>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130890599 | |||||||
chr11:130890667 | T | C | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(155): Show |
235 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.2574-9861A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130890667 | |||||||
chr11:130890698 | G | T | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
233 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.2574-9892C>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130890698 | |||||||
chr11:130890699 | C | T | 2 | a0003c0003t0004g0267 a0003c0003t0004g0268 |
2 | NA19070.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.2574-9893G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130890699 | |||||||
chr11:130890890 | C | CT | 21 | a0001c0001t0001g0211 a0002c0002t0002g0090 a0002c0002t0005g0020 others(18): Show |
23 | HG00438.hp1 HG00738.hp2 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.2574-10085dupA | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130890890 | |||||||
chr11:130890890 | C | CTT | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(149): Show |
229 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.2574-10086_2574-10 others(8): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130890890 | |||||||
chr11:130890979 | G | A | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(155): Show |
235 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.2574-10173C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130890979 | |||||||
chr11:130891048 | A | G | 5 | a0004c0005t0020g0016 a0004c0005t0020g0045 a0004c0005t0030g0017 others(2): Show |
7 | HG01891.hp1 HG02258.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.2574-10242T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130891048 | |||||||
chr11:130891077 | T | C | 36 | a0001c0001t0007g0148 a0001c0001t0007g0149 a0001c0001t0007g0150 others(33): Show |
39 | HG00423.hp1 HG00642.hp2 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.2574-10271A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130891077 | |||||||
chr11:130891104 | G | T | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(155): Show |
235 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.2574-10298C>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130891104 | |||||||
chr11:130891249 | G | T | 4 | a0004c0008t0019g0290 a0004c0008t0019g0291 a0004c0008t0019g0292 others(1): Show |
4 | HG01884.hp2 HG02970.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2574-10443C>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130891249 | |||||||
chr11:130891283 | C | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
232 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.2574-10477G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130891283 | |||||||
chr11:130891337 | T | C | 2 | a0005c0004t0049g0295 a0005c0004t0049g0296 |
2 | HG03139.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2574-10531A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130891337 | |||||||
chr11:130891359 | C | T | 21 | a0001c0001t0007g0148 a0001c0001t0007g0149 a0001c0001t0007g0150 others(18): Show |
22 | HG00423.hp1 HG00642.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.2574-10553G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130891359 | |||||||
chr11:130891367 | T | TG | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(155): Show |
235 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.2574-10562dupC | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130891367 | |||||||
chr11:130891685 | G | A | 1 | a0001c0001t0007g0168 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2574-10879C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130891685 | |||||||
chr11:130891718 | A | G | 2 | a0005c0004t0049g0295 a0005c0004t0049g0296 |
2 | HG03139.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2574-10912T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130891718 | |||||||
chr11:130891720 | A | T | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(155): Show |
235 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.2574-10914T>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130891720 | |||||||
chr11:130891790 | C | A | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
232 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.2574-10984G>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130891790 | |||||||
chr11:130891831 | T | A | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(155): Show |
235 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.2574-11025A>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130891831 | |||||||
chr11:130891846 | C | CTT | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(121): Show |
195 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.2574-11042_2574-11 others(8): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130891846 | |||||||
chr11:130891846 | C | CTTT | 33 | a0001c0001t0001g0214 a0001c0001t0001g0243 a0001c0001t0001g0254 others(30): Show |
39 | HG00099.hp2 HG00323.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.2574-11043_2574-11 others(9): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130891846 | |||||||
chr11:130891864 | A | G | 1 | a0002c0002t0079g0169 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2574-11058T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130891864 | |||||||
chr11:130891888 | T | G | 1 | a0004c0008t0048g0042 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2574-11082A>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130891888 | |||||||
chr11:130891995 | G | C | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(155): Show |
235 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.2574-11189C>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130891995 | |||||||
chr11:130892140 | G | A | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(155): Show |
235 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.2573+11115C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130892140 | |||||||
chr11:130892162 | G | A | 157 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(154): Show |
234 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.2573+11093C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130892162 | |||||||
chr11:130892229 | C | T | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(155): Show |
235 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.2573+11026G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130892229 | |||||||
chr11:130892230 | C | T | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(155): Show |
235 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.2573+11025G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130892230 | |||||||
chr11:130892245 | C | T | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(155): Show |
235 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.2573+11010G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130892245 | |||||||
chr11:130892285 | C | T | 1 | a0015c0031t0118g0294 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2573+10970G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130892285 | |||||||
chr11:130892580 | T | C | 1 | a0001c0001t0001g0213 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2573+10675A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130892580 | |||||||
chr11:130892603 | T | C | 28 | a0001c0001t0001g0214 a0001c0001t0001g0243 a0001c0001t0001g0254 others(25): Show |
34 | HG00099.hp2 HG00323.hp2 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.2573+10652A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130892603 | |||||||
chr11:130892610 | C | G | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(155): Show |
235 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.2573+10645G>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130892610 | |||||||
chr11:130892634 | A | G | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(155): Show |
235 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.2573+10621T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130892634 | |||||||
chr11:130892655 | C | T | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(155): Show |
235 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.2573+10600G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130892655 | |||||||
chr11:130892667 | T | C | 1 | a0001c0001t0014g0157 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.2573+10588A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130892667 | |||||||
chr11:130892674 | G | A | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(155): Show |
235 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.2573+10581C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130892674 | |||||||
chr11:130892751 | C | T | 16 | a0006c0006t0008g0018 a0006c0006t0008g0060 a0006c0006t0008g0061 others(13): Show |
17 | HG00738.hp2 HG01168.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.2573+10504G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130892751 | |||||||
chr11:130892860 | T | A | 1 | a0002c0002t0002g0022 | 2 | NA18973.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.2573+10395A>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130892860 | |||||||
chr11:130893025 | G | C | 9 | a0005c0004t0021g0050 a0005c0004t0021g0051 a0005c0004t0021g0052 others(6): Show |
9 | HG02572.hp2 HG02630.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.2573+10230C>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130893025 | |||||||
chr11:130893066 | T | C | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(155): Show |
235 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.2573+10189A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130893066 | |||||||
chr11:130893075 | G | A | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(155): Show |
235 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.2573+10180C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130893075 | |||||||
chr11:130893121 | C | G | 1 | a0004c0025t0051g0046 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2573+10134G>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130893121 | |||||||
chr11:130893218 | C | T | 4 | a0005c0004t0027g0033 a0005c0004t0027g0172 a0005c0004t0081g0174 others(1): Show |
5 | HG01891.hp2 HG02055.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2573+10037G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130893218 | |||||||
chr11:130893257 | G | C | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(155): Show |
235 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.2573+9998C>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130893257 | |||||||
chr11:130893445 | A | C | 25 | a0001c0001t0007g0148 a0001c0001t0007g0149 a0001c0001t0007g0150 others(22): Show |
27 | HG00423.hp1 HG00642.hp2 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.2573+9810T>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130893445 | |||||||
chr11:130893559 | A | C | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(156): Show |
236 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.2573+9696T>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130893559 | |||||||
chr11:130893595 | G | A | 4 | a0005c0004t0027g0033 a0005c0004t0027g0172 a0005c0004t0081g0174 others(1): Show |
5 | HG01891.hp2 HG02055.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2573+9660C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130893595 | |||||||
chr11:130893618 | G | A | 52 | a0001c0001t0007g0148 a0001c0001t0007g0149 a0001c0001t0007g0150 others(49): Show |
60 | HG00423.hp1 HG00642.hp2 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.2573+9637C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130893618 | |||||||
chr11:130893689 | G | A | 2 | a0005c0004t0049g0295 a0005c0004t0049g0296 |
2 | HG03139.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2573+9566C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130893689 | |||||||
chr11:130893692 | TAATA | T | 3 | a0006c0006t0032g0054 a0006c0006t0032g0055 a0006c0006t0060g0053 |
3 | HG02615.hp1 HG02647.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2573+9559_2573+956 others(8): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130893692 | |||||||
chr11:130893817 | C | T | 1 | a0007c0007t0059g0118 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2573+9438G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130893817 | |||||||
chr11:130893877 | C | T | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(155): Show |
235 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.2573+9378G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130893877 | |||||||
chr11:130894051 | G | A | 17 | a0004c0008t0019g0290 a0004c0008t0019g0291 a0004c0008t0019g0292 others(14): Show |
19 | HG00741.hp2 HG01070.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.2573+9204C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130894051 | |||||||
chr11:130894100 | C | G | 58 | a0001c0001t0038g0151 a0001c0001t0038g0152 a0001c0010t0010g0010 others(55): Show |
81 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(78): Show |
intron_variant | MODIFIER | c.2573+9155G>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130894100 | |||||||
chr11:130894114 | CA | C | 41 | a0001c0001t0038g0151 a0001c0001t0038g0152 a0001c0010t0010g0010 others(38): Show |
63 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.2573+9140delT | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130894114 | |||||||
chr11:130894122 | A | G | 10 | a0007c0007t0013g0026 a0007c0007t0013g0119 a0007c0007t0013g0122 others(7): Show |
14 | HG02040.hp2 NA18747.hp2 NA18945.hp1 others(11): Show |
intron_variant | MODIFIER | c.2573+9133T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130894122 | |||||||
chr11:130894197 | G | T | 127 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(124): Show |
198 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.2573+9058C>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130894197 | |||||||
chr11:130894503 | A | C | 10 | a0007c0007t0013g0026 a0007c0007t0013g0119 a0007c0007t0013g0122 others(7): Show |
14 | HG02040.hp2 NA18747.hp2 NA18945.hp1 others(11): Show |
intron_variant | MODIFIER | c.2573+8752T>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130894503 | |||||||
chr11:130894514 | T | C | 40 | a0001c0001t0038g0151 a0001c0001t0038g0152 a0001c0014t0041g0233 others(37): Show |
59 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(56): Show |
intron_variant | MODIFIER | c.2573+8741A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130894514 | |||||||
chr11:130894523 | C | G | 31 | a0001c0001t0001g0214 a0001c0001t0001g0243 a0001c0001t0001g0254 others(28): Show |
37 | HG00099.hp2 HG00323.hp2 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.2573+8732G>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130894523 | |||||||
chr11:130894554 | G | T | 59 | a0001c0001t0001g0214 a0001c0001t0001g0243 a0001c0001t0001g0254 others(56): Show |
68 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.2573+8701C>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130894554 | |||||||
chr11:130894581 | ATTGT | A | 17 | a0005c0004t0021g0050 a0005c0004t0021g0051 a0005c0004t0021g0052 others(14): Show |
18 | HG01891.hp2 HG02055.hp1 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.2573+8670_2573+867 others(8): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130894581 | |||||||
chr11:130894631 | C | T | 173 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(170): Show |
252 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.2573+8624G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130894631 | |||||||
chr11:130894635 | G | A | 2 | a0005c0004t0049g0295 a0005c0004t0049g0296 |
2 | HG03139.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2573+8620C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130894635 | |||||||
chr11:130894645 | A | T | 66 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(63): Show |
114 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.2573+8610T>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130894645 | |||||||
chr11:130894670 | C | T | 17 | a0005c0004t0021g0050 a0005c0004t0021g0051 a0005c0004t0021g0052 others(14): Show |
18 | HG01891.hp2 HG02055.hp1 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.2573+8585G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130894670 | |||||||
chr11:130894852 | C | T | 47 | a0001c0001t0007g0150 a0001c0014t0041g0233 a0001c0014t0041g0234 others(44): Show |
54 | HG00642.hp2 HG00741.hp2 HG01070.hp2 others(51): Show |
intron_variant | MODIFIER | c.2573+8403G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130894852 | |||||||
chr11:130894944 | C | T | 1 | a0001c0001t0006g0262 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2573+8311G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130894944 | |||||||
chr11:130894953 | A | G | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(175): Show |
254 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.2573+8302T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130894953 | |||||||
chr11:130894962 | G | A | 1 | a0001c0001t0075g0146 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2573+8293C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130894962 | |||||||
chr11:130894989 | G | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
260 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.2573+8266C>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130894989 | |||||||
chr11:130894990 | C | T | 1 | a0001c0010t0053g0058 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2573+8265G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130894990 | |||||||
chr11:130895008 | T | A | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
260 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.2573+8247A>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130895008 | |||||||
chr11:130895136 | G | A | 37 | a0001c0001t0038g0151 a0001c0001t0038g0152 a0003c0003t0003g0005 others(34): Show |
56 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.2573+8119C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130895136 | |||||||
chr11:130895145 | G | A | 2 | a0001c0014t0041g0233 a0001c0014t0041g0234 |
2 | HG01099.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2573+8110C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130895145 | |||||||
chr11:130895183 | T | C | 1 | a0002c0002t0002g0023 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.2573+8072A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130895183 | |||||||
chr11:130895365 | T | G | 3 | a0001c0010t0010g0010 a0001c0010t0010g0057 a0001c0010t0053g0058 |
6 | HG01243.hp1 HG02109.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2573+7890A>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130895365 | |||||||
chr11:130895482 | T | C | 2 | a0006c0006t0008g0063 a0006c0006t0008g0064 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2573+7773A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130895482 | |||||||
chr11:130895492 | G | A | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(175): Show |
254 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.2573+7763C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130895492 | |||||||
chr11:130895503 | C | T | 1 | a0002c0002t0024g0089 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2573+7752G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130895503 | |||||||
chr11:130895555 | A | T | 2 | a0003c0003t0003g0126 a0003c0003t0003g0127 |
2 | HG02723.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2573+7700T>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130895555 | |||||||
chr11:130895567 | G | T | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
260 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.2573+7688C>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130895567 | |||||||
chr11:130895589 | T | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
260 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.2573+7666A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130895589 | |||||||
chr11:130895590 | G | A | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(175): Show |
254 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.2573+7665C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130895590 | |||||||
chr11:130895627 | T | C | 4 | a0005c0004t0027g0033 a0005c0004t0027g0172 a0005c0004t0081g0174 others(1): Show |
5 | HG01891.hp2 HG02055.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2573+7628A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130895627 | |||||||
chr11:130895734 | T | C | 1 | a0001c0001t0087g0181 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2573+7521A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130895734 | |||||||
chr11:130895738 | A | G | 1 | a0015c0031t0118g0294 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2573+7517T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130895738 | |||||||
chr11:130895742 | T | A | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
260 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.2573+7513A>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130895742 | |||||||
chr11:130895780 | A | T | 16 | a0006c0006t0008g0018 a0006c0006t0008g0060 a0006c0006t0008g0061 others(13): Show |
17 | HG00738.hp2 HG01168.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.2573+7475T>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130895780 | |||||||
chr11:130895790 | T | C | 1 | a0002c0002t0005g0069 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2573+7465A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130895790 | |||||||
chr11:130895811 | A | G | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(175): Show |
257 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.2573+7444T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130895811 | |||||||
chr11:130895828 | C | G | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
260 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.2573+7427G>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130895828 | |||||||
chr11:130895833 | A | T | 3 | a0002c0002t0012g0019 a0002c0002t0012g0073 a0002c0002t0012g0074 |
4 | HG00099.hp1 HG01106.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.2573+7422T>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130895833 | |||||||
chr11:130895834 | T | C | 3 | a0002c0002t0012g0019 a0002c0002t0012g0073 a0002c0002t0012g0074 |
4 | HG00099.hp1 HG01106.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.2573+7421A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130895834 | |||||||
chr11:130895917 | T | C | 1 | a0002c0002t0025g0104 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2573+7338A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130895917 | |||||||
chr11:130895929 | T | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
260 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.2573+7326A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130895929 | |||||||
chr11:130896023 | C | T | 2 | a0002c0002t0002g0087 a0002c0002t0002g0088 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2573+7232G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130896023 | |||||||
chr11:130896074 | A | T | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
260 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.2573+7181T>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130896074 | |||||||
chr11:130896110 | G | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
260 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.2573+7145C>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130896110 | |||||||
chr11:130896149 | G | T | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
260 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.2573+7106C>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130896149 | |||||||
chr11:130896171 | C | T | 1 | a0001c0001t0087g0181 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2573+7084G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130896171 | |||||||
chr11:130896205 | G | C | 115 | a0001c0001t0001g0243 a0001c0001t0001g0254 a0001c0001t0006g0038 others(112): Show |
146 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.2573+7050C>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130896205 | |||||||
chr11:130896205 | G | T | 66 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(63): Show |
114 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.2573+7050C>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130896205 | |||||||
chr11:130896237 | A | G | 4 | a0002c0002t0002g0072 a0002c0002t0002g0084 a0004c0005t0031g0085 others(1): Show |
4 | NA18966.hp2 NA18985.hp1 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.2573+7018T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130896237 | |||||||
chr11:130896240 | T | G | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
260 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.2573+7015A>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130896240 | |||||||
chr11:130896310 | G | A | 4 | a0005c0004t0027g0033 a0005c0004t0027g0172 a0005c0004t0081g0174 others(1): Show |
5 | HG01891.hp2 HG02055.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2573+6945C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130896310 | |||||||
chr11:130896330 | T | C | 38 | a0001c0001t0038g0151 a0001c0001t0038g0152 a0003c0003t0003g0005 others(35): Show |
57 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.2573+6925A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130896330 | |||||||
chr11:130896347 | T | C | 17 | a0005c0004t0021g0050 a0005c0004t0021g0051 a0005c0004t0021g0052 others(14): Show |
18 | HG01891.hp2 HG02055.hp1 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.2573+6908A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130896347 | |||||||
chr11:130896637 | T | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
260 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.2573+6618A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130896637 | |||||||
chr11:130896643 | C | T | 26 | a0001c0001t0001g0243 a0001c0001t0001g0254 a0001c0001t0006g0038 others(23): Show |
32 | HG00323.hp2 HG00673.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.2573+6612G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130896643 | |||||||
chr11:130896650 | T | A | 1 | a0022c0016t0109g0170 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2573+6605A>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130896650 | |||||||
chr11:130896674 | T | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
260 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.2573+6581A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130896674 | |||||||
chr11:130896713 | C | T | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
260 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.2573+6542G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130896713 | |||||||
chr11:130896821 | A | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
260 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.2573+6434T>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130896821 | |||||||
chr11:130896866 | T | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
260 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.2573+6389A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130896866 | |||||||
chr11:130896937 | A | ACT | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
260 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.2573+6317_2573+631 others(6): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130896937 | |||||||
chr11:130896945 | C | T | 10 | a0007c0007t0013g0026 a0007c0007t0013g0119 a0007c0007t0013g0122 others(7): Show |
14 | HG02040.hp2 NA18747.hp2 NA18945.hp1 others(11): Show |
intron_variant | MODIFIER | c.2573+6310G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130896945 | |||||||
chr11:130896946 | G | A | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
260 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.2573+6309C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130896946 | |||||||
chr11:130896968 | A | C | 1 | a0001c0001t0001g0239 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2573+6287T>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130896968 | |||||||
chr11:130896991 | T | C | 1 | a0001c0001t0014g0164 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2573+6264A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130896991 | |||||||
chr11:130897038 | G | A | 3 | a0001c0010t0010g0010 a0001c0010t0010g0057 a0001c0010t0053g0058 |
6 | HG01243.hp1 HG02109.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2573+6217C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130897038 | |||||||
chr11:130897050 | A | C | 180 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(177): Show |
259 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.2573+6205T>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130897050 | |||||||
chr11:130897050 | A | T | 1 | a0003c0003t0003g0140 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2573+6205T>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130897050 | |||||||
chr11:130897083 | C | G | 4 | a0005c0004t0027g0033 a0005c0004t0027g0172 a0005c0004t0081g0174 others(1): Show |
5 | HG01891.hp2 HG02055.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2573+6172G>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130897083 | |||||||
chr11:130897163 | T | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
260 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.2573+6092A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130897163 | |||||||
chr11:130897187 | T | C | 180 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(177): Show |
259 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.2573+6068A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130897187 | |||||||
chr11:130897192 | G | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
260 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.2573+6063C>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130897192 | |||||||
chr11:130897244 | C | T | 3 | a0001c0001t0080g0241 a0001c0001t0086g0183 a0001c0001t0087g0181 |
3 | HG02895.hp1 NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2573+6011G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130897244 | |||||||
chr11:130897303 | T | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
260 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.2573+5952A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130897303 | |||||||
chr11:130897352 | A | G | 4 | a0005c0004t0027g0033 a0005c0004t0027g0172 a0005c0004t0081g0174 others(1): Show |
5 | HG01891.hp2 HG02055.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2573+5903T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130897352 | |||||||
chr11:130897363 | G | A | 17 | a0005c0004t0021g0050 a0005c0004t0021g0051 a0005c0004t0021g0052 others(14): Show |
18 | HG01891.hp2 HG02055.hp1 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.2573+5892C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130897363 | |||||||
chr11:130897373 | T | TAC | 3 | a0001c0001t0080g0241 a0001c0001t0086g0183 a0001c0001t0087g0181 |
3 | HG02895.hp1 NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2573+5880_2573+588 others(6): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130897373 | |||||||
chr11:130897411 | T | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
260 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.2573+5844A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130897411 | |||||||
chr11:130897506 | C | T | 10 | a0007c0007t0013g0026 a0007c0007t0013g0119 a0007c0007t0013g0122 others(7): Show |
14 | HG02040.hp2 NA18747.hp2 NA18945.hp1 others(11): Show |
intron_variant | MODIFIER | c.2573+5749G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130897506 | |||||||
chr11:130897560 | C | T | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
260 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.2573+5695G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130897560 | |||||||
chr11:130897591 | G | T | 38 | a0001c0001t0038g0151 a0001c0001t0038g0152 a0003c0003t0003g0005 others(35): Show |
57 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.2573+5664C>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130897591 | |||||||
chr11:130897593 | C | T | 2 | a0001c0001t0090g0249 a0009c0013t0110g0248 |
2 | NA19009.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.2573+5662G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130897593 | |||||||
chr11:130897840 | T | G | 6 | a0004c0009t0009g0044 a0004c0009t0009g0283 a0004c0009t0009g0284 others(3): Show |
7 | HG00741.hp2 HG01070.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.2573+5415A>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130897840 | |||||||
chr11:130897857 | G | C | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(175): Show |
257 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.2573+5398C>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130897857 | |||||||
chr11:130898152 | G | GT | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(175): Show |
257 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.2573+5102dupA | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130898152 | |||||||
chr11:130898369 | C | T | 180 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(177): Show |
259 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.2573+4886G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130898369 | |||||||
chr11:130898442 | C | T | 1 | a0001c0001t0111g0253 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2573+4813G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130898442 | |||||||
chr11:130898468 | C | T | 1 | a0001c0001t0006g0038 | 2 | HG03654.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.2573+4787G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130898468 | |||||||
chr11:130898530 | T | G | 4 | a0001c0001t0018g0043 a0001c0001t0018g0277 a0001c0001t0018g0278 others(1): Show |
5 | HG01496.hp2 HG02630.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2573+4725A>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130898530 | |||||||
chr11:130898673 | A | C | 4 | a0005c0004t0040g0177 a0005c0004t0040g0179 a0005c0004t0074g0145 others(1): Show |
4 | HG02922.hp1 HG02976.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2573+4582T>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130898673 | |||||||
chr11:130898673 | A | G | 13 | a0005c0004t0021g0050 a0005c0004t0021g0051 a0005c0004t0021g0052 others(10): Show |
14 | HG01891.hp2 HG02055.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.2573+4582T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130898673 | |||||||
chr11:130899138 | T | C | 56 | a0001c0010t0010g0010 a0001c0010t0010g0057 a0001c0010t0053g0058 others(53): Show |
79 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(76): Show |
intron_variant | MODIFIER | c.2573+4117A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130899138 | |||||||
chr11:130899294 | T | C | 1 | a0001c0001t0028g0223 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2573+3961A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130899294 | |||||||
chr11:130899343 | T | C | 3 | a0002c0002t0002g0081 a0002c0002t0002g0083 a0002c0002t0064g0082 |
3 | HG02015.hp1 HG02056.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.2573+3912A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130899343 | |||||||
chr11:130899479 | A | G | 2 | a0005c0004t0027g0172 a0005c0004t0081g0174 |
2 | HG02622.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2573+3776T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130899479 | |||||||
chr11:130899506 | C | T | 1 | a0019c0022t0006g0263 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.2573+3749G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130899506 | |||||||
chr11:130899710 | C | T | 10 | a0007c0007t0013g0026 a0007c0007t0013g0119 a0007c0007t0013g0122 others(7): Show |
14 | HG02040.hp2 NA18747.hp2 NA18945.hp1 others(11): Show |
intron_variant | MODIFIER | c.2573+3545G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130899710 | |||||||
chr11:130899791 | A | C | 17 | a0004c0008t0029g0282 a0006c0006t0008g0018 a0006c0006t0008g0060 others(14): Show |
18 | HG00738.hp2 HG01168.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.2573+3464T>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130899791 | |||||||
chr11:130899843 | T | C | 1 | a0003c0003t0004g0272 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2573+3412A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130899843 | |||||||
chr11:130900056 | G | C | 1 | a0022c0016t0109g0170 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2573+3199C>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130900056 | |||||||
chr11:130900088 | C | T | 10 | a0007c0007t0013g0026 a0007c0007t0013g0119 a0007c0007t0013g0122 others(7): Show |
14 | HG02040.hp2 NA18747.hp2 NA18945.hp1 others(11): Show |
intron_variant | MODIFIER | c.2573+3167G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130900088 | |||||||
chr11:130900124 | T | C | 1 | a0003c0003t0003g0129 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2573+3131A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130900124 | |||||||
chr11:130900185 | T | G | 1 | a0001c0001t0001g0215 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2573+3070A>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130900185 | |||||||
chr11:130900247 | G | A | 1 | a0001c0001t0011g0216 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2573+3008C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130900247 | |||||||
chr11:130900284 | C | T | 1 | a0002c0002t0002g0112 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2573+2971G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130900284 | |||||||
chr11:130900364 | A | G | 1 | a0006c0006t0008g0060 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2573+2891T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130900364 | |||||||
chr11:130900441 | G | A | 1 | a0003c0003t0004g0272 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2573+2814C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130900441 | |||||||
chr11:130900461 | C | T | 4 | a0002c0002t0002g0081 a0002c0002t0002g0083 a0002c0002t0064g0082 others(1): Show |
4 | HG00609.hp1 HG02015.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.2573+2794G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130900461 | |||||||
chr11:130900663 | A | G | 2 | a0001c0014t0041g0233 a0001c0014t0041g0234 |
2 | HG01099.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2573+2592T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130900663 | |||||||
chr11:130900690 | T | C | 4 | a0002c0002t0002g0105 a0004c0005t0022g0106 a0004c0005t0022g0111 others(1): Show |
4 | HG01258.hp2 HG01433.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.2573+2565A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130900690 | |||||||
chr11:130900828 | A | G | 2 | a0001c0014t0041g0233 a0001c0014t0041g0234 |
2 | HG01099.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2573+2427T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130900828 | |||||||
chr11:130900872 | G | A | 1 | a0001c0001t0014g0155 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.2573+2383C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130900872 | |||||||
chr11:130900873 | A | G | 1 | a0001c0001t0014g0155 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.2573+2382T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130900873 | |||||||
chr11:130900916 | C | A | 16 | a0006c0006t0008g0018 a0006c0006t0008g0060 a0006c0006t0008g0061 others(13): Show |
17 | HG00738.hp2 HG01168.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.2573+2339G>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130900916 | |||||||
chr11:130901481 | A | G | 1 | a0002c0002t0002g0080 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2573+1774T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130901481 | |||||||
chr11:130901488 | G | A | 3 | a0004c0005t0020g0016 a0004c0005t0020g0045 a0004c0025t0051g0046 |
4 | HG02258.hp2 HG02572.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.2573+1767C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130901488 | |||||||
chr11:130901519 | T | G | 2 | a0003c0003t0003g0140 a0003c0003t0003g0141 |
2 | HG01978.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.2573+1736A>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130901519 | |||||||
chr11:130901600 | C | T | 26 | a0001c0001t0007g0148 a0001c0001t0007g0149 a0001c0001t0007g0150 others(23): Show |
28 | HG00423.hp1 HG00642.hp2 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.2573+1655G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130901600 | |||||||
chr11:130901767 | G | T | 210 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(207): Show |
295 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.2573+1488C>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130901767 | |||||||
chr11:130901770 | G | T | 1 | a0001c0001t0093g0188 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2573+1485C>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130901770 | |||||||
chr11:130901818 | A | AG | 17 | a0005c0004t0021g0050 a0005c0004t0021g0051 a0005c0004t0021g0052 others(14): Show |
18 | HG01891.hp2 HG02055.hp1 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.2573+1436dupC | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130901818 | |||||||
chr11:130901856 | T | C | 4 | a0005c0004t0021g0050 a0005c0004t0021g0051 a0005c0004t0021g0052 others(1): Show |
4 | HG02572.hp2 HG02630.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2573+1399A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130901856 | |||||||
chr11:130901873 | T | C | 69 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(66): Show |
117 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.2573+1382A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130901873 | |||||||
chr11:130901921 | T | C | 3 | a0001c0001t0080g0241 a0001c0001t0086g0183 a0001c0001t0087g0181 |
3 | HG02895.hp1 NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2573+1334A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130901921 | |||||||
chr11:130901942 | A | C | 4 | a0005c0004t0040g0177 a0005c0004t0040g0179 a0005c0004t0074g0145 others(1): Show |
4 | HG02922.hp1 HG02976.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2573+1313T>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130901942 | |||||||
chr11:130902054 | G | A | 1 | a0004c0009t0009g0287 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2573+1201C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130902054 | |||||||
chr11:130902166 | G | A | 1 | a0005c0004t0081g0174 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2573+1089C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130902166 | |||||||
chr11:130902298 | A | C | 4 | a0004c0008t0019g0290 a0004c0008t0019g0291 a0004c0008t0019g0292 others(1): Show |
4 | HG01884.hp2 HG02970.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2573+957T>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130902298 | |||||||
chr11:130902391 | C | T | 1 | a0001c0001t0001g0220 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2573+864G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130902391 | |||||||
chr11:130902488 | T | C | 1 | a0001c0001t0007g0150 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2573+767A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130902488 | |||||||
chr11:130902521 | G | A | 5 | a0004c0009t0009g0044 a0004c0009t0009g0284 a0004c0009t0009g0285 others(2): Show |
6 | HG00741.hp2 HG01070.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2573+734C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130902521 | |||||||
chr11:130902658 | C | G | 11 | a0004c0008t0019g0290 a0004c0008t0019g0291 a0004c0008t0019g0292 others(8): Show |
12 | HG01884.hp2 HG02257.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.2573+597G>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130902658 | |||||||
chr11:130902896 | A | G | 6 | a0002c0002t0002g0011 a0002c0002t0002g0076 a0002c0002t0002g0077 others(3): Show |
9 | HG00597.hp1 HG04115.hp1 NA18961.hp1 others(6): Show |
intron_variant | MODIFIER | c.2573+359T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130902896 | |||||||
chr11:130903012 | A | G | 1 | a0022c0016t0109g0170 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2573+243T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130903012 | |||||||
chr11:130903091 | T | G | 2 | a0001c0001t0001g0217 a0001c0001t0001g0218 |
2 | HG03710.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.2573+164A>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130903091 | |||||||
chr11:130903154 | T | C | 2 | a0005c0004t0049g0295 a0005c0004t0049g0296 |
2 | HG03139.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2573+101A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130903154 | |||||||
chr11:130903164 | C | T | 27 | a0005c0004t0021g0050 a0005c0004t0021g0051 a0005c0004t0021g0052 others(24): Show |
32 | HG01891.hp2 HG02040.hp2 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.2573+91G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130903164 | |||||||
chr11:130903172 | G | T | 2 | a0005c0004t0049g0295 a0005c0004t0049g0296 |
2 | HG03139.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2573+83C>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130903172 | |||||||
chr11:130903181 | G | A | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(142): Show |
205 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.2573+74C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130903181 | |||||||
chr11:130903205 | C | T | 2 | a0001c0001t0038g0151 a0001c0001t0038g0152 |
2 | HG03471.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2573+50G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130903205 | |||||||
chr11:130903501 | T | C | 4 | a0005c0004t0021g0050 a0005c0004t0021g0051 a0005c0004t0021g0052 others(1): Show |
4 | HG02572.hp2 HG02630.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2444-117A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130903501 | |||||||
chr11:130903593 | T | C | 2 | a0001c0014t0041g0233 a0001c0014t0041g0234 |
2 | HG01099.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2444-209A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130903593 | |||||||
chr11:130903643 | A | G | 1 | a0001c0001t0017g0219 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2444-259T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130903643 | |||||||
chr11:130903696 | CAT | C | 4 | a0002c0002t0002g0024 a0002c0002t0002g0075 a0004c0025t0051g0046 others(1): Show |
5 | HG02258.hp2 HG02280.hp2 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.2444-314_2444-313d others(4): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130903696 | |||||||
chr11:130903710 | T | C | 2 | a0004c0005t0020g0016 a0004c0005t0020g0045 |
3 | HG02572.hp1 HG02622.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2444-326A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130903710 | |||||||
chr11:130903712 | C | T | 1 | a0001c0001t0006g0247 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2444-328G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130903712 | |||||||
chr11:130903714 | C | T | 2 | a0004c0005t0020g0016 a0004c0005t0020g0045 |
3 | HG02572.hp1 HG02622.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2444-330G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130903714 | |||||||
chr11:130903716 | T | C | 5 | a0001c0001t0006g0247 a0001c0014t0041g0233 a0001c0014t0041g0234 others(2): Show |
6 | HG01099.hp1 HG02572.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.2444-332A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130903716 | |||||||
chr11:130903716 | T | TAC | 22 | a0001c0001t0043g0259 a0001c0001t0092g0258 a0002c0002t0002g0014 others(19): Show |
26 | HG01167.hp1 HG01261.hp1 HG01517.hp2 others(23): Show |
intron_variant | MODIFIER | c.2444-334_2444-333d others(4): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130903716 | |||||||
chr11:130903716 | T | TACAC | 41 | a0001c0010t0010g0010 a0001c0010t0010g0057 a0002c0002t0002g0112 others(38): Show |
66 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.2444-336_2444-333d others(6): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130903716 | |||||||
chr11:130903716 | T | TACACAC | 8 | a0003c0003t0004g0266 a0003c0003t0004g0273 a0003c0003t0036g0142 others(5): Show |
8 | HG02074.hp1 HG02129.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2444-338_2444-333d others(8): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130903716 | |||||||
chr11:130903716 | T | TACACACA others(1): Show |
3 | a0003c0003t0004g0274 a0003c0003t0036g0131 a0004c0009t0009g0283 |
3 | HG01123.hp2 HG02451.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.2444-340_2444-333d others(10): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130903716 | |||||||
chr11:130903716 | T | TACACACA others(3): Show |
1 | a0004c0009t0009g0286 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2444-342_2444-333d others(12): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130903716 | |||||||
chr11:130903716 | T | TACACACA others(7): Show |
1 | a0004c0009t0009g0044 | 2 | HG00741.hp2 HG01070.hp2 |
intron_variant | MODIFIER | c.2444-346_2444-333d others(16): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130903716 | |||||||
chr11:130903716 | T | TACACACA others(9): Show |
1 | a0004c0009t0009g0287 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2444-348_2444-333d others(18): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130903716 | |||||||
chr11:130903716 | TAC | T | 102 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(99): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.2444-334_2444-333d others(4): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130903716 | |||||||
chr11:130903716 | TACAC | T | 8 | a0001c0001t0001g0224 a0001c0001t0037g0032 a0001c0001t0044g0242 others(5): Show |
9 | HG01074.hp1 HG01081.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.2444-336_2444-333d others(6): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130903716 | |||||||
chr11:130903716 | TACACAC | T | 8 | a0001c0001t0007g0148 a0001c0001t0007g0149 a0001c0001t0007g0150 others(5): Show |
9 | HG00544.hp1 HG00642.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2444-338_2444-333d others(8): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130903716 | |||||||
chr11:130903716 | TACACACA others(3): Show |
T | 1 | a0001c0001t0028g0186 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2444-342_2444-333d others(12): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130903716 | |||||||
chr11:130903718 | C | T | 3 | a0001c0001t0006g0247 a0001c0014t0041g0233 a0001c0014t0041g0234 |
3 | HG01099.hp1 HG03098.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.2444-334G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130903718 | |||||||
chr11:130903747 | A | G | 1 | a0001c0001t0056g0056 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2444-363T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130903747 | |||||||
chr11:130903764 | CTACT | C | 3 | a0001c0010t0010g0010 a0001c0010t0010g0057 a0001c0010t0053g0058 |
6 | HG01243.hp1 HG02109.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2444-384_2444-381d others(6): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130903764 | |||||||
chr11:130903925 | AAGTGGGG others(4): Show |
A | 10 | a0005c0004t0021g0050 a0005c0004t0021g0051 a0005c0004t0021g0052 others(7): Show |
10 | HG02572.hp2 HG02630.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.2444-552_2444-542d others(13): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130903925 | |||||||
chr11:130904079 | G | A | 1 | a0001c0001t0076g0147 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2444-695C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130904079 | |||||||
chr11:130904182 | G | A | 3 | a0001c0010t0010g0010 a0001c0010t0010g0057 a0001c0010t0053g0058 |
6 | HG01243.hp1 HG02109.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2444-798C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130904182 | |||||||
chr11:130904381 | C | T | 1 | a0004c0009t0009g0283 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2444-997G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130904381 | |||||||
chr11:130904439 | A | T | 1 | a0003c0003t0004g0265 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2444-1055T>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130904439 | |||||||
chr11:130904536 | G | A | 17 | a0005c0004t0021g0050 a0005c0004t0021g0051 a0005c0004t0021g0052 others(14): Show |
18 | HG01891.hp2 HG02055.hp1 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.2444-1152C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130904536 | |||||||
chr11:130904595 | C | T | 1 | a0009c0013t0112g0185 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2444-1211G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130904595 | |||||||
chr11:130904642 | T | C | 1 | a0001c0014t0041g0234 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2444-1258A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130904642 | |||||||
chr11:130904642 | TAAG | T | 37 | a0003c0003t0003g0005 a0003c0003t0003g0029 a0003c0003t0003g0030 others(34): Show |
56 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.2444-1261_2444-125 others(7): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130904642 | |||||||
chr11:130904689 | G | C | 17 | a0005c0004t0021g0050 a0005c0004t0021g0051 a0005c0004t0021g0052 others(14): Show |
18 | HG01891.hp2 HG02055.hp1 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.2443+1264C>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130904689 | |||||||
chr11:130904694 | A | AT | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(137): Show |
200 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.2443+1258dupA | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130904694 | |||||||
chr11:130904694 | A | ATT | 40 | a0001c0001t0006g0246 a0001c0001t0014g0155 a0001c0001t0014g0156 others(37): Show |
59 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.2443+1257_2443+125 others(6): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130904694 | |||||||
chr11:130904704 | G | T | 184 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(181): Show |
263 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.2443+1249C>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130904704 | |||||||
chr11:130904798 | G | A | 14 | a0005c0004t0021g0050 a0005c0004t0021g0051 a0005c0004t0021g0052 others(11): Show |
15 | HG01891.hp2 HG02055.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.2443+1155C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130904798 | |||||||
chr11:130904809 | A | T | 1 | a0001c0001t0001g0184 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2443+1144T>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130904809 | |||||||
chr11:130905028 | G | C | 1 | a0022c0016t0109g0170 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2443+925C>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130905028 | |||||||
chr11:130905045 | C | T | 1 | a0005c0017t0083g0171 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2443+908G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130905045 | |||||||
chr11:130905105 | G | A | 1 | a0001c0001t0001g0238 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.2443+848C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130905105 | |||||||
chr11:130905207 | C | CCTGGAAG others(11): Show |
1 | a0001c0001t0006g0246 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2443+728_2443+745d others(20): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130905207 | |||||||
chr11:130905360 | CA | C | 184 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(181): Show |
263 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.2443+592delT | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130905360 | |||||||
chr11:130905453 | CAT | C | 10 | a0007c0007t0013g0026 a0007c0007t0013g0119 a0007c0007t0013g0122 others(7): Show |
14 | HG02040.hp2 NA18747.hp2 NA18945.hp1 others(11): Show |
intron_variant | MODIFIER | c.2443+498_2443+499d others(4): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130905453 | |||||||
chr11:130905561 | C | G | 184 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(181): Show |
263 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.2443+392G>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130905561 | |||||||
chr11:130905584 | A | G | 184 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(181): Show |
263 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.2443+369T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130905584 | |||||||
chr11:130905601 | C | T | 26 | a0001c0001t0001g0243 a0001c0001t0001g0254 a0001c0001t0006g0038 others(23): Show |
32 | HG00323.hp2 HG00673.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.2443+352G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130905601 | |||||||
chr11:130905671 | A | T | 1 | a0001c0001t0001g0034 | 2 | HG01109.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2443+282T>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130905671 | |||||||
chr11:130905690 | T | A | 1 | a0004c0025t0051g0046 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2443+263A>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130905690 | |||||||
chr11:130905793 | C | T | 184 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(181): Show |
263 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.2443+160G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130905793 | |||||||
chr11:130905808 | C | T | 2 | a0001c0001t0080g0241 a0001c0001t0086g0183 |
2 | HG02895.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2443+145G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130905808 | |||||||
chr11:130905887 | C | A | 1 | a0004c0025t0051g0046 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2443+66G>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130905887 | |||||||
chr11:130905887 | C | T | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(224): Show |
313 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(310): Show |
intron_variant | MODIFIER | c.2443+66G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130905887 | |||||||
chr11:130906458 | C | A | 17 | a0004c0008t0019g0290 a0004c0008t0019g0291 a0004c0008t0019g0292 others(14): Show |
19 | HG00741.hp2 HG01070.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.2262+167G>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 6/10 | chr11 | 130906458 | |||||||
chr11:130906507 | G | A | 184 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(181): Show |
263 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.2262+118C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 6/10 | chr11 | 130906507 | |||||||
chr11:130906525 | C | T | 1 | a0001c0001t0076g0147 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2262+100G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 6/10 | chr11 | 130906525 | |||||||
chr11:130906542 | C | T | 184 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(181): Show |
263 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.2262+83G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 6/10 | chr11 | 130906542 | |||||||
chr11:130906548 | A | G | 1 | a0001c0010t0053g0058 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2262+77T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 6/10 | chr11 | 130906548 | |||||||
chr11:130906559 | A | G | 184 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(181): Show |
263 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.2262+66T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 6/10 | chr11 | 130906559 | |||||||
chr11:130906751 | T | A | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(224): Show |
313 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(310): Show |
intron_variant | MODIFIER | c.2166-30A>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 5/10 | chr11 | 130906751 | |||||||
chr11:130906795 | C | T | 184 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(181): Show |
263 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.2166-74G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 5/10 | chr11 | 130906795 | |||||||
chr11:130906806 | A | C | 4 | a0001c0001t0018g0043 a0001c0001t0018g0277 a0001c0001t0018g0278 others(1): Show |
5 | HG01496.hp2 HG02630.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2166-85T>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 5/10 | chr11 | 130906806 | |||||||
chr11:130906806 | A | T | 180 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(177): Show |
258 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.2166-85T>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 5/10 | chr11 | 130906806 | |||||||
chr11:130906957 | A | C | 4 | a0005c0004t0040g0177 a0005c0004t0040g0179 a0005c0004t0074g0145 others(1): Show |
4 | HG02922.hp1 HG02976.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2166-236T>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 5/10 | chr11 | 130906957 | |||||||
chr11:130906970 | T | C | 184 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(181): Show |
263 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.2166-249A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 5/10 | chr11 | 130906970 | |||||||
chr11:130907023 | A | T | 1 | a0001c0001t0004g0182 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2166-302T>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 5/10 | chr11 | 130907023 | |||||||
chr11:130907144 | T | A | 184 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(181): Show |
263 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.2166-423A>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 5/10 | chr11 | 130907144 | |||||||
chr11:130907283 | G | A | 11 | a0004c0008t0019g0290 a0004c0008t0019g0291 a0004c0008t0019g0292 others(8): Show |
12 | HG01884.hp2 HG02257.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.2166-562C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 5/10 | chr11 | 130907283 | |||||||
chr11:130907313 | T | C | 1 | a0002c0002t0025g0113 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.2166-592A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 5/10 | chr11 | 130907313 | |||||||
chr11:130907329 | G | GACAC | 35 | a0003c0003t0003g0005 a0003c0003t0003g0029 a0003c0003t0003g0030 others(32): Show |
54 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.2166-612_2166-609d others(6): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 5/10 | chr11 | 130907329 | |||||||
chr11:130907341 | T | C | 37 | a0003c0003t0003g0005 a0003c0003t0003g0029 a0003c0003t0003g0030 others(34): Show |
56 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.2165+612A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 5/10 | chr11 | 130907341 | |||||||
chr11:130907349 | T | C | 37 | a0003c0003t0003g0005 a0003c0003t0003g0029 a0003c0003t0003g0030 others(34): Show |
56 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.2165+604A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 5/10 | chr11 | 130907349 | |||||||
chr11:130907536 | T | C | 1 | a0001c0001t0001g0229 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.2165+417A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 5/10 | chr11 | 130907536 | |||||||
chr11:130907665 | G | A | 3 | a0004c0008t0048g0042 a0004c0008t0116g0288 a0004c0008t0117g0289 |
4 | HG02280.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2165+288C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 5/10 | chr11 | 130907665 | |||||||
chr11:130907694 | T | C | 37 | a0003c0003t0003g0005 a0003c0003t0003g0029 a0003c0003t0003g0030 others(34): Show |
56 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.2165+259A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 5/10 | chr11 | 130907694 | |||||||
chr11:130907778 | G | A | 27 | a0004c0008t0019g0290 a0004c0008t0019g0291 a0004c0008t0019g0292 others(24): Show |
33 | HG00741.hp2 HG01070.hp2 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.2165+175C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 5/10 | chr11 | 130907778 | |||||||
chr11:130907918 | G | A | 37 | a0003c0003t0003g0005 a0003c0003t0003g0029 a0003c0003t0003g0030 others(34): Show |
56 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.2165+35C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 5/10 | chr11 | 130907918 | |||||||
chr11:130908432 | C | T | 10 | a0007c0007t0013g0026 a0007c0007t0013g0119 a0007c0007t0013g0122 others(7): Show |
14 | HG02040.hp2 NA18747.hp2 NA18945.hp1 others(11): Show |
intron_variant | MODIFIER | c.2035-349G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 4/10 | chr11 | 130908432 | |||||||
chr11:130908502 | A | G | 1 | a0001c0001t0006g0245 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2035-419T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 4/10 | chr11 | 130908502 | |||||||
chr11:130908589 | A | T | 1 | a0002c0002t0002g0072 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2035-506T>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 4/10 | chr11 | 130908589 | |||||||
chr11:130908615 | A | G | 37 | a0003c0003t0003g0005 a0003c0003t0003g0029 a0003c0003t0003g0030 others(34): Show |
56 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.2035-532T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 4/10 | chr11 | 130908615 | |||||||
chr11:130908632 | T | A | 2 | a0001c0001t0056g0056 a0001c0001t0075g0146 |
2 | HG02055.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.2035-549A>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 4/10 | chr11 | 130908632 | |||||||
chr11:130908709 | AC | A | 37 | a0003c0003t0003g0005 a0003c0003t0003g0029 a0003c0003t0003g0030 others(34): Show |
56 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.2035-627delG | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 4/10 | chr11 | 130908709 | |||||||
chr11:130908983 | C | A | 2 | a0001c0011t0016g0230 a0001c0011t0016g0231 |
2 | HG01074.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.2035-900G>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 4/10 | chr11 | 130908983 | |||||||
chr11:130909001 | G | A | 1 | a0001c0001t0045g0232 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2035-918C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 4/10 | chr11 | 130909001 | |||||||
chr11:130909010 | C | T | 37 | a0003c0003t0003g0005 a0003c0003t0003g0029 a0003c0003t0003g0030 others(34): Show |
56 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.2035-927G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 4/10 | chr11 | 130909010 | |||||||
chr11:130909095 | T | C | 37 | a0003c0003t0003g0005 a0003c0003t0003g0029 a0003c0003t0003g0030 others(34): Show |
56 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.2034+923A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 4/10 | chr11 | 130909095 | |||||||
chr11:130909157 | G | A | 37 | a0003c0003t0003g0005 a0003c0003t0003g0029 a0003c0003t0003g0030 others(34): Show |
56 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.2034+861C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 4/10 | chr11 | 130909157 | |||||||
chr11:130909173 | G | C | 37 | a0003c0003t0003g0005 a0003c0003t0003g0029 a0003c0003t0003g0030 others(34): Show |
56 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.2034+845C>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 4/10 | chr11 | 130909173 | |||||||
chr11:130909244 | ACCCAGTT others(3): Show |
A | 4 | a0005c0004t0040g0177 a0005c0004t0040g0179 a0005c0004t0074g0145 others(1): Show |
4 | HG02922.hp1 HG02976.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2034+764_2034+773d others(12): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 4/10 | chr11 | 130909244 | |||||||
chr11:130909262 | T | C | 1 | a0001c0010t0053g0058 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2034+756A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 4/10 | chr11 | 130909262 | |||||||
chr11:130909378 | T | C | 37 | a0003c0003t0003g0005 a0003c0003t0003g0029 a0003c0003t0003g0030 others(34): Show |
56 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.2034+640A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 4/10 | chr11 | 130909378 | |||||||
chr11:130909515 | C | A | 26 | a0001c0001t0001g0243 a0001c0001t0001g0254 a0001c0001t0006g0038 others(23): Show |
32 | HG00323.hp2 HG00673.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.2034+503G>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 4/10 | chr11 | 130909515 | |||||||
chr11:130909584 | C | T | 37 | a0003c0003t0003g0005 a0003c0003t0003g0029 a0003c0003t0003g0030 others(34): Show |
56 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.2034+434G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 4/10 | chr11 | 130909584 | |||||||
chr11:130909620 | G | A | 1 | a0002c0002t0002g0114 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2034+398C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 4/10 | chr11 | 130909620 | |||||||
chr11:130909726 | C | T | 37 | a0003c0003t0003g0005 a0003c0003t0003g0029 a0003c0003t0003g0030 others(34): Show |
56 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.2034+292G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 4/10 | chr11 | 130909726 | |||||||
chr11:130909751 | A | G | 37 | a0003c0003t0003g0005 a0003c0003t0003g0029 a0003c0003t0003g0030 others(34): Show |
56 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.2034+267T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 4/10 | chr11 | 130909751 | |||||||
chr11:130909773 | T | C | 125 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(122): Show |
181 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.2034+245A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 4/10 | chr11 | 130909773 | |||||||
chr11:130909779 | C | T | 37 | a0003c0003t0003g0005 a0003c0003t0003g0029 a0003c0003t0003g0030 others(34): Show |
56 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.2034+239G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 4/10 | chr11 | 130909779 | |||||||
chr11:130909869 | G | A | 1 | a0005c0004t0021g0052 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2034+149C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 4/10 | chr11 | 130909869 | |||||||
chr11:130909892 | T | G | 16 | a0006c0006t0008g0018 a0006c0006t0008g0060 a0006c0006t0008g0061 others(13): Show |
17 | HG00738.hp2 HG01168.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.2034+126A>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 4/10 | chr11 | 130909892 | |||||||
chr11:130909908 | C | T | 37 | a0003c0003t0003g0005 a0003c0003t0003g0029 a0003c0003t0003g0030 others(34): Show |
56 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.2034+110G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 4/10 | chr11 | 130909908 | |||||||
chr11:130910009 | T | A | 12 | a0001c0001t0007g0159 a0001c0001t0007g0160 a0001c0001t0007g0161 others(9): Show |
12 | HG00423.hp1 HG01934.hp2 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.2034+9A>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 4/10 | chr11 | 130910009 | |||||||
chr11:130910373 | TC | T | 14 | a0001c0001t0001g0235 a0001c0001t0006g0244 a0001c0001t0087g0181 others(11): Show |
17 | HG02040.hp2 HG02738.hp1 HG03195.hp2 others(14): Show |
splice_region_variant&intron_variant | LOW | c.1814-4delG | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 2/10 | chr11 | 130910373 | |||||||
chr11:130910374 | C | CA | 7 | a0001c0001t0015g0252 a0001c0001t0017g0219 a0001c0001t0075g0146 others(4): Show |
7 | HG01099.hp1 HG02523.hp2 HG02615.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.1814-5_1814-4insT | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 2/10 | chr11 | 130910374 | |||||||
chr11:130910374 | CCA | C | 3 | a0001c0010t0010g0010 a0001c0010t0010g0057 a0001c0010t0053g0058 |
6 | HG01243.hp1 HG02109.hp1 HG02258.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.1814-6_1814-5delTG | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 2/10 | chr11 | 130910374 | |||||||
chr11:130910374 | CCAAAA | C | 37 | a0003c0003t0003g0005 a0003c0003t0003g0029 a0003c0003t0003g0030 others(34): Show |
55 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(52): Show |
splice_region_variant&intron_variant | LOW | c.1814-9_1814-5delTT others(3): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 2/10 | chr11 | 130910374 | |||||||
chr11:130910375 | C | A | 240 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(237): Show |
333 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(330): Show |
splice_region_variant&intron_variant | LOW | c.1814-5G>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 2/10 | chr11 | 130910375 | |||||||
chr11:130910517 | G | A | 2 | a0001c0001t0056g0056 a0001c0001t0075g0146 |
2 | HG02055.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1814-147C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 2/10 | chr11 | 130910517 | |||||||
chr11:130910580 | A | T | 36 | a0003c0003t0003g0005 a0003c0003t0003g0029 a0003c0003t0003g0030 others(33): Show |
55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1814-210T>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 2/10 | chr11 | 130910580 | |||||||
chr11:130910588 | T | G | 36 | a0003c0003t0003g0005 a0003c0003t0003g0029 a0003c0003t0003g0030 others(33): Show |
55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1814-218A>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 2/10 | chr11 | 130910588 | |||||||
chr11:130910692 | C | T | 36 | a0003c0003t0003g0005 a0003c0003t0003g0029 a0003c0003t0003g0030 others(33): Show |
55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1814-322G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 2/10 | chr11 | 130910692 | |||||||
chr11:130910700 | C | T | 37 | a0003c0003t0003g0005 a0003c0003t0003g0029 a0003c0003t0003g0030 others(34): Show |
57 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.1814-330G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 2/10 | chr11 | 130910700 | |||||||
chr11:130910721 | T | C | 36 | a0003c0003t0003g0005 a0003c0003t0003g0029 a0003c0003t0003g0030 others(33): Show |
55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1814-351A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 2/10 | chr11 | 130910721 | |||||||
chr11:130910754 | A | G | 36 | a0003c0003t0003g0005 a0003c0003t0003g0029 a0003c0003t0003g0030 others(33): Show |
55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1814-384T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 2/10 | chr11 | 130910754 | |||||||
chr11:130910876 | C | T | 36 | a0003c0003t0003g0005 a0003c0003t0003g0029 a0003c0003t0003g0030 others(33): Show |
55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1814-506G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 2/10 | chr11 | 130910876 | |||||||
chr11:130910933 | A | G | 36 | a0003c0003t0003g0005 a0003c0003t0003g0029 a0003c0003t0003g0030 others(33): Show |
55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1814-563T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 2/10 | chr11 | 130910933 | |||||||
chr11:130910970 | A | G | 36 | a0003c0003t0003g0005 a0003c0003t0003g0029 a0003c0003t0003g0030 others(33): Show |
55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1814-600T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 2/10 | chr11 | 130910970 | |||||||
chr11:130911012 | T | C | 1 | a0002c0002t0005g0115 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1813+621A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 2/10 | chr11 | 130911012 | |||||||
chr11:130911075 | A | G | 36 | a0003c0003t0003g0005 a0003c0003t0003g0029 a0003c0003t0003g0030 others(33): Show |
55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1813+558T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 2/10 | chr11 | 130911075 | |||||||
chr11:130911079 | T | C | 36 | a0003c0003t0003g0005 a0003c0003t0003g0029 a0003c0003t0003g0030 others(33): Show |
55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1813+554A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 2/10 | chr11 | 130911079 | |||||||
chr11:130911126 | C | T | 26 | a0001c0001t0001g0243 a0001c0001t0001g0254 a0001c0001t0006g0038 others(23): Show |
32 | HG00323.hp2 HG00673.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.1813+507G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 2/10 | chr11 | 130911126 | |||||||
chr11:130911194 | C | CA | 12 | a0004c0008t0019g0292 a0005c0004t0039g0178 a0007c0007t0013g0026 others(9): Show |
16 | HG02040.hp2 HG03486.hp2 NA18747.hp2 others(13): Show |
intron_variant | MODIFIER | c.1813+438dupT | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 2/10 | chr11 | 130911194 | |||||||
chr11:130911194 | C | CAAA | 31 | a0003c0003t0003g0005 a0003c0003t0003g0029 a0003c0003t0003g0030 others(28): Show |
50 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.1813+436_1813+438d others(5): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 2/10 | chr11 | 130911194 | |||||||
chr11:130911210 | AG | A | 3 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0004c0009t0009g0283 |
3 | HG02451.hp1 NA18977.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.1813+422delC | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 2/10 | chr11 | 130911210 | |||||||
chr11:130911211 | G | A | 291 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(288): Show |
409 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(406): Show |
intron_variant | MODIFIER | c.1813+422C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 2/10 | chr11 | 130911211 | |||||||
chr11:130911331 | G | A | 1 | a0004c0008t0019g0292 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1813+302C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 2/10 | chr11 | 130911331 | |||||||
chr11:130911371 | A | G | 1 | a0006c0006t0060g0053 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1813+262T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 2/10 | chr11 | 130911371 | |||||||
chr11:130911462 | T | C | 1 | a0002c0002t0062g0116 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1813+171A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 2/10 | chr11 | 130911462 | |||||||
chr11:130911533 | C | T | 1 | a0001c0001t0001g0243 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1813+100G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 2/10 | chr11 | 130911533 | |||||||
chr11:130911580 | C | G | 36 | a0003c0003t0003g0005 a0003c0003t0003g0029 a0003c0003t0003g0030 others(33): Show |
55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1813+53G>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 2/10 | chr11 | 130911580 | |||||||
chr11:130911587 | C | T | 2 | a0003c0003t0003g0126 a0003c0003t0003g0127 |
2 | HG02723.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1813+46G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 2/10 | chr11 | 130911587 | |||||||
chr11:130911611 | A | T | 1 | a0002c0002t0005g0069 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1813+22T>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 2/10 | chr11 | 130911611 | |||||||
chr11:130911780 | C | T | 36 | a0003c0003t0003g0005 a0003c0003t0003g0029 a0003c0003t0003g0030 others(33): Show |
55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1675-9G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130911780 | |||||||
chr11:130911788 | T | C | 1 | a0001c0001t0001g0238 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1675-17A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130911788 | |||||||
chr11:130911790 | G | C | 36 | a0003c0003t0003g0005 a0003c0003t0003g0029 a0003c0003t0003g0030 others(33): Show |
55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1675-19C>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130911790 | |||||||
chr11:130911799 | A | C | 2 | a0004c0008t0116g0288 a0004c0008t0117g0289 |
2 | HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1675-28T>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130911799 | |||||||
chr11:130911807 | G | A | 1 | a0004c0008t0019g0293 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1675-36C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130911807 | |||||||
chr11:130911872 | C | A | 36 | a0003c0003t0003g0005 a0003c0003t0003g0029 a0003c0003t0003g0030 others(33): Show |
55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1675-101G>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130911872 | |||||||
chr11:130911908 | T | G | 1 | a0001c0001t0007g0166 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1675-137A>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130911908 | |||||||
chr11:130912151 | T | C | 2 | a0001c0001t0006g0261 a0001c0001t0006g0262 |
2 | HG03831.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1675-380A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130912151 | |||||||
chr11:130912163 | G | A | 36 | a0003c0003t0003g0005 a0003c0003t0003g0029 a0003c0003t0003g0030 others(33): Show |
55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1675-392C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130912163 | |||||||
chr11:130912169 | A | G | 36 | a0003c0003t0003g0005 a0003c0003t0003g0029 a0003c0003t0003g0030 others(33): Show |
55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1675-398T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130912169 | |||||||
chr11:130912192 | G | C | 36 | a0003c0003t0003g0005 a0003c0003t0003g0029 a0003c0003t0003g0030 others(33): Show |
55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1675-421C>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130912192 | |||||||
chr11:130912206 | A | T | 36 | a0003c0003t0003g0005 a0003c0003t0003g0029 a0003c0003t0003g0030 others(33): Show |
55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1675-435T>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130912206 | |||||||
chr11:130912237 | A | G | 4 | a0004c0005t0020g0016 a0004c0005t0020g0045 a0004c0005t0030g0017 others(1): Show |
6 | HG01891.hp1 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1675-466T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130912237 | |||||||
chr11:130912264 | C | G | 36 | a0003c0003t0003g0005 a0003c0003t0003g0029 a0003c0003t0003g0030 others(33): Show |
55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1675-493G>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130912264 | |||||||
chr11:130912330 | T | G | 1 | a0001c0001t0001g0239 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1675-559A>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130912330 | |||||||
chr11:130912369 | G | A | 17 | a0004c0008t0019g0290 a0004c0008t0019g0291 a0004c0008t0019g0292 others(14): Show |
19 | HG00741.hp2 HG01070.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.1675-598C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130912369 | |||||||
chr11:130912422 | C | T | 17 | a0005c0004t0021g0050 a0005c0004t0021g0051 a0005c0004t0021g0052 others(14): Show |
18 | HG01891.hp2 HG02055.hp1 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.1675-651G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130912422 | |||||||
chr11:130912449 | G | A | 36 | a0003c0003t0003g0005 a0003c0003t0003g0029 a0003c0003t0003g0030 others(33): Show |
55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1675-678C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130912449 | |||||||
chr11:130912454 | T | C | 3 | a0001c0010t0010g0010 a0001c0010t0010g0057 a0001c0010t0053g0058 |
6 | HG01243.hp1 HG02109.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1675-683A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130912454 | |||||||
chr11:130912460 | G | A | 6 | a0004c0009t0009g0044 a0004c0009t0009g0283 a0004c0009t0009g0284 others(3): Show |
7 | HG00741.hp2 HG01070.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1675-689C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130912460 | |||||||
chr11:130912532 | T | C | 1 | a0001c0001t0007g0167 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1675-761A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130912532 | |||||||
chr11:130912553 | C | T | 4 | a0001c0001t0018g0043 a0001c0001t0018g0277 a0001c0001t0018g0278 others(1): Show |
5 | HG01496.hp2 HG02630.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1675-782G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130912553 | |||||||
chr11:130912674 | A | G | 36 | a0003c0003t0003g0005 a0003c0003t0003g0029 a0003c0003t0003g0030 others(33): Show |
55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1675-903T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130912674 | |||||||
chr11:130912716 | G | A | 1 | a0001c0001t0007g0168 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1675-945C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130912716 | |||||||
chr11:130912754 | G | A | 13 | a0006c0006t0008g0018 a0006c0006t0008g0060 a0006c0006t0008g0061 others(10): Show |
14 | HG00738.hp2 HG01168.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.1675-983C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130912754 | |||||||
chr11:130912794 | G | C | 1 | a0002c0002t0002g0117 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1675-1023C>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130912794 | |||||||
chr11:130912862 | T | C | 1 | a0004c0008t0048g0042 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1675-1091A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130912862 | |||||||
chr11:130912877 | G | A | 5 | a0004c0009t0009g0044 a0004c0009t0009g0284 a0004c0009t0009g0285 others(2): Show |
6 | HG00741.hp2 HG01070.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1675-1106C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130912877 | |||||||
chr11:130913063 | A | G | 27 | a0004c0008t0019g0290 a0004c0008t0019g0291 a0004c0008t0019g0292 others(24): Show |
33 | HG00741.hp2 HG01070.hp2 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.1674+1203T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130913063 | |||||||
chr11:130913364 | T | C | 1 | a0001c0001t0080g0241 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1674+902A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130913364 | |||||||
chr11:130913446 | C | T | 2 | a0004c0005t0020g0016 a0004c0005t0020g0045 |
3 | HG02572.hp1 HG02622.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1674+820G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130913446 | |||||||
chr11:130913595 | TGG | T | 36 | a0003c0003t0003g0005 a0003c0003t0003g0029 a0003c0003t0003g0030 others(33): Show |
55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1674+669_1674+670d others(4): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130913595 | |||||||
chr11:130913648 | C | A | 36 | a0003c0003t0003g0005 a0003c0003t0003g0029 a0003c0003t0003g0030 others(33): Show |
55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1674+618G>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130913648 | |||||||
chr11:130913802 | A | G | 36 | a0003c0003t0003g0005 a0003c0003t0003g0029 a0003c0003t0003g0030 others(33): Show |
55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1674+464T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130913802 | |||||||
chr11:130913833 | G | A | 36 | a0003c0003t0003g0005 a0003c0003t0003g0029 a0003c0003t0003g0030 others(33): Show |
55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1674+433C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130913833 | |||||||
chr11:130913870 | T | C | 36 | a0003c0003t0003g0005 a0003c0003t0003g0029 a0003c0003t0003g0030 others(33): Show |
55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1674+396A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130913870 | |||||||
chr11:130913884 | A | G | 26 | a0001c0001t0001g0243 a0001c0001t0001g0254 a0001c0001t0006g0038 others(23): Show |
32 | HG00323.hp2 HG00673.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.1674+382T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130913884 | |||||||
chr11:130913891 | T | C | 1 | a0001c0001t0044g0242 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1674+375A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130913891 | |||||||
chr11:130913894 | G | GAAATAT | 36 | a0003c0003t0003g0005 a0003c0003t0003g0029 a0003c0003t0003g0030 others(33): Show |
55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1674+371_1674+372i others(8): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130913894 | |||||||
chr11:130913922 | AC | A | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(223): Show |
312 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(309): Show |
intron_variant | MODIFIER | c.1674+343delG | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130913922 | |||||||
chr11:130913980 | C | T | 36 | a0003c0003t0003g0005 a0003c0003t0003g0029 a0003c0003t0003g0030 others(33): Show |
55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1674+286G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130913980 | |||||||
chr11:130914009 | G | A | 2 | a0005c0004t0040g0179 a0005c0004t0084g0180 |
2 | HG02976.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1674+257C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130914009 | |||||||
chr11:130914112 | TA | T | 26 | a0001c0001t0001g0243 a0001c0001t0001g0254 a0001c0001t0006g0038 others(23): Show |
32 | HG00323.hp2 HG00673.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.1674+153delT | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130914112 | |||||||
chr11:130914116 | T | A | 26 | a0001c0001t0001g0243 a0001c0001t0001g0254 a0001c0001t0006g0038 others(23): Show |
32 | HG00323.hp2 HG00673.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.1674+150A>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130914116 | |||||||
chr11:130914127 | G | C | 1 | a0003c0003t0003g0144 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1674+139C>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130914127 | |||||||
chr11:130914172 | T | C | 17 | a0004c0008t0019g0290 a0004c0008t0019g0291 a0004c0008t0019g0292 others(14): Show |
19 | HG00741.hp2 HG01070.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.1674+94A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130914172 |