Item | Value |
---|---|
geneid | 55285 |
ensemblid | ENSG00000089682.17 |
hgncid | 25617 |
symbol | RBM41 |
name | RNA binding motif protein 41 |
refseq_nuc | NM_001324242.2 |
refseq_prot | NP_001311171.1 |
ensembl_nuc | ENST00000685964.1 |
ensembl_prot | ENSP00000509650.1 |
mane_status | MANE Select |
chr | chrX |
start | 107061885 |
end | 107118822 |
strand | - |
ver | v1.2 |
region | chrX:107061885-107118822 |
region5000 | chrX:107056885-107123822 |
regionname0 | RBM41_chrX_107061885_107118822 |
regionname5000 | RBM41_chrX_107056885_107123822 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1311 | 286 | 72 | 49 | 138 | 7 | 20 | RBM41_chrX_107056885_107123822 | RBM41 | ATGAA others(1306): Show |
chrX | 107056885 | 107123822 | ||
a0001c0002 | 0/0 | 1311 | 2 | 2 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | ATGAA others(1306): Show |
chrX | 107056885 | 107123822 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 7004 | 105 | 4 | 24 | 62 | 4 | 11 | RBM41_chrX_107056885_107123822 | RBM41 | GAGGT others(6999): Show |
chrX | 107056885 | 107123822 |
a0001c0001t0002 | 0/0 | 7004 | 56 | 4 | 13 | 35 | 2 | 2 | RBM41_chrX_107056885_107123822 | RBM41 | GAGGT others(6999): Show |
chrX | 107056885 | 107123822 |
a0001c0001t0003 | 0/0 | 7004 | 17 | 1 | 2 | 14 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | GAGGT others(6999): Show |
chrX | 107056885 | 107123822 |
a0001c0001t0004 | 0/0 | 7006 | 10 | 10 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | GAGGT others(7001): Show |
chrX | 107056885 | 107123822 |
a0001c0001t0005 | 0/0 | 7003 | 8 | 8 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | GAGGT others(6998): Show |
chrX | 107056885 | 107123822 |
a0001c0001t0006 | 0/0 | 7004 | 8 | 7 | 0 | 0 | 0 | 1 | RBM41_chrX_107056885_107123822 | RBM41 | GAGGT others(6999): Show |
chrX | 107056885 | 107123822 |
a0001c0001t0007 | 0/0 | 7004 | 8 | 0 | 0 | 8 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | GAGGT others(6999): Show |
chrX | 107056885 | 107123822 |
a0001c0001t0008 | 0/0 | 7004 | 7 | 6 | 1 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | GAGGT others(6999): Show |
chrX | 107056885 | 107123822 |
a0001c0001t0009 | 0/0 | 7004 | 7 | 0 | 3 | 0 | 1 | 3 | RBM41_chrX_107056885_107123822 | RBM41 | GAGGT others(6999): Show |
chrX | 107056885 | 107123822 |
a0001c0001t0010 | 0/0 | 7004 | 5 | 0 | 0 | 5 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | GAGGT others(6999): Show |
chrX | 107056885 | 107123822 |
a0001c0001t0011 | 0/0 | 7004 | 4 | 0 | 0 | 4 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | GAGGT others(6999): Show |
chrX | 107056885 | 107123822 |
a0001c0001t0012 | 0/0 | 7003 | 3 | 3 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | GAGGT others(6998): Show |
chrX | 107056885 | 107123822 |
a0001c0001t0013 | 0/0 | 7003 | 3 | 3 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | GAGGT others(6998): Show |
chrX | 107056885 | 107123822 |
a0001c0001t0014 | 0/0 | 7003 | 3 | 3 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | GAGGT others(6998): Show |
chrX | 107056885 | 107123822 |
a0001c0001t0015 | 0/0 | 7003 | 2 | 2 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | GAGGT others(6998): Show |
chrX | 107056885 | 107123822 |
a0001c0001t0016 | 0/0 | 7003 | 2 | 0 | 0 | 1 | 0 | 1 | RBM41_chrX_107056885_107123822 | RBM41 | GAGGT others(6998): Show |
chrX | 107056885 | 107123822 |
a0001c0001t0017 | 0/0 | 7005 | 2 | 2 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | GAGGT others(7000): Show |
chrX | 107056885 | 107123822 |
a0001c0001t0018 | 0/0 | 7004 | 2 | 2 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | GAGGT others(6999): Show |
chrX | 107056885 | 107123822 |
a0001c0001t0019 | 0/0 | 7005 | 2 | 0 | 0 | 2 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | GAGGT others(7000): Show |
chrX | 107056885 | 107123822 |
a0001c0001t0020 | 0/0 | 7000 | 2 | 0 | 0 | 2 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | GAGGT others(6995): Show |
chrX | 107056885 | 107123822 |
a0001c0001t0021 | 0/0 | 7006 | 2 | 2 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | GAGGT others(7001): Show |
chrX | 107056885 | 107123822 |
a0001c0001t0023 | 0/0 | 7003 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | GAGGT others(6998): Show |
chrX | 107056885 | 107123822 |
a0001c0001t0024 | 0/0 | 7004 | 1 | 0 | 1 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | GAGGT others(6999): Show |
chrX | 107056885 | 107123822 |
a0001c0001t0025 | 0/0 | 7003 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | GAGGT others(6998): Show |
chrX | 107056885 | 107123822 |
a0001c0001t0026 | 0/0 | 7003 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | GAGGT others(6998): Show |
chrX | 107056885 | 107123822 |
a0001c0001t0027 | 0/0 | 7003 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | GAGGT others(6998): Show |
chrX | 107056885 | 107123822 |
a0001c0001t0028 | 0/0 | 7004 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | GAGGT others(6999): Show |
chrX | 107056885 | 107123822 |
a0001c0001t0029 | 0/0 | 7004 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | GAGGT others(6999): Show |
chrX | 107056885 | 107123822 |
a0001c0001t0030 | 0/0 | 7003 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | GAGGT others(6998): Show |
chrX | 107056885 | 107123822 |
a0001c0001t0031 | 0/0 | 7004 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | GAGGT others(6999): Show |
chrX | 107056885 | 107123822 |
a0001c0001t0032 | 0/0 | 7004 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | GAGGT others(6999): Show |
chrX | 107056885 | 107123822 |
a0001c0001t0033 | 0/0 | 7003 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | GAGGT others(6998): Show |
chrX | 107056885 | 107123822 |
a0001c0001t0034 | 0/0 | 7004 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | GAGGT others(6999): Show |
chrX | 107056885 | 107123822 |
a0001c0001t0035 | 0/0 | 7007 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | GAGGT others(7002): Show |
chrX | 107056885 | 107123822 |
a0001c0001t0036 | 0/0 | 7005 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | GAGGT others(7000): Show |
chrX | 107056885 | 107123822 |
a0001c0001t0037 | 0/0 | 7004 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | GAGGT others(6999): Show |
chrX | 107056885 | 107123822 |
a0001c0001t0038 | 0/0 | 7005 | 1 | 0 | 1 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | GAGGT others(7000): Show |
chrX | 107056885 | 107123822 |
a0001c0001t0039 | 0/0 | 7004 | 1 | 0 | 0 | 0 | 0 | 1 | RBM41_chrX_107056885_107123822 | RBM41 | GAGGT others(6999): Show |
chrX | 107056885 | 107123822 |
a0001c0001t0040 | 0/0 | 7000 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | GAGGT others(6995): Show |
chrX | 107056885 | 107123822 |
a0001c0001t0041 | 0/0 | 7004 | 1 | 0 | 0 | 0 | 0 | 1 | RBM41_chrX_107056885_107123822 | RBM41 | GAGGT others(6999): Show |
chrX | 107056885 | 107123822 |
a0001c0001t0042 | 0/0 | 7004 | 1 | 0 | 1 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | GAGGT others(6999): Show |
chrX | 107056885 | 107123822 |
a0001c0001t0043 | 0/0 | 7004 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | GAGGT others(6999): Show |
chrX | 107056885 | 107123822 |
a0001c0001t0045 | 0/0 | 7004 | 1 | 0 | 1 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | GAGGT others(6999): Show |
chrX | 107056885 | 107123822 |
a0001c0001t0046 | 0/0 | 7004 | 1 | 0 | 1 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | GAGGT others(6999): Show |
chrX | 107056885 | 107123822 |
a0001c0001t0047 | 0/0 | 7001 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | GAGGT others(6996): Show |
chrX | 107056885 | 107123822 |
a0001c0001t0048 | 0/0 | 7004 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | GAGGT others(6999): Show |
chrX | 107056885 | 107123822 |
a0001c0001t0049 | 0/0 | 7007 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | GAGGT others(7002): Show |
chrX | 107056885 | 107123822 |
a0001c0001t0050 | 0/0 | 7006 | 1 | 0 | 1 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | GAGGT others(7001): Show |
chrX | 107056885 | 107123822 |
a0001c0001t0051 | 0/0 | 7005 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | GAGGT others(7000): Show |
chrX | 107056885 | 107123822 |
a0001c0002t0022 | 0/0 | 7005 | 2 | 2 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | GAGGT others(7000): Show |
chrX | 107056885 | 107123822 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0004 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0023 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0002g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0003g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0003g0006 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0003g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0003g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0004g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0004g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0004g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0004g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0004g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0004g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0004g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0004g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0004g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0005g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0005g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0005g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0005g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0005g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0005g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0005g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0006g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0006g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0006g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0006g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0006g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0006g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0006g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0007g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0007g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0007g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0007g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0008g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0008g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0008g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0008g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0008g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0009g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0009g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0009g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0009g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0009g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0009g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0010g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0010g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0010g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0011g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0011g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0012g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0012g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0012g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0013g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0013g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0013g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0014g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0014g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0014g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0015g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0015g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0016g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0016g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0017g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0017g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0018g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0018g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0019g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0019g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0020g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0021g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0021g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0023g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0024g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0025g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0026g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0027g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0028g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0029g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0030g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0031g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0032g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0033g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0034g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0035g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0036g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0037g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0038g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0039g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0040g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0041g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0042g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0043g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0045g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0046g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0047g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0048g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0049g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0050g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0001t0051g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
a0001c0002t0022g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0002 | g0130 | EUR | GBR | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0023 | EUR | FIN | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG00408 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG00438 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | CHS | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | CHS | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | CHS | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG00673 | hp1 | a0001 | c0001 | t0010 | g0021 | EAS | CHS | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG00741 | hp1 | a0001 | c0001 | t0009 | g0184 | AMR | PUR | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG00741 | hp2 | a0001 | c0001 | t0046 | g0134 | AMR | PUR | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG01071 | hp1 | a0001 | c0001 | t0009 | g0186 | AMR | PUR | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0089 | AMR | PUR | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0097 | AMR | PUR | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0117 | AMR | PUR | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG01109 | hp1 | a0001 | c0001 | t0050 | g0236 | AMR | PUR | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG01175 | hp1 | a0001 | c0001 | t0045 | g0158 | AMR | PUR | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0128 | AMR | PUR | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG01243 | hp1 | a0001 | c0001 | t0008 | g0060 | AMR | PUR | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG01255 | hp1 | a0001 | c0001 | t0009 | g0187 | AMR | CLM | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0096 | AMR | CLM | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | CLM | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | CLM | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG01433 | hp1 | a0001 | c0001 | t0024 | g0142 | AMR | CLM | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | IBS | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | IBS | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG01517 | hp2 | a0001 | c0001 | t0009 | g0185 | EUR | IBS | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG01884 | hp2 | a0001 | c0001 | t0005 | g0062 | AFR | ACB | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0109 | AMR | PEL | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG01934 | hp1 | a0001 | c0001 | t0042 | g0119 | AMR | PEL | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0091 | AMR | PEL | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0072 | AMR | PEL | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PEL | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG01978 | hp2 | a0001 | c0001 | t0038 | g0090 | AMR | PEL | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0103 | AMR | PEL | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0105 | AMR | PEL | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0047 | AMR | PEL | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG02027 | hp1 | a0001 | c0001 | t0029 | g0210 | EAS | KHV | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG02055 | hp1 | a0001 | c0001 | t0006 | g0107 | AFR | ACB | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | KHV | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG02074 | hp1 | a0001 | c0001 | t0010 | g0025 | EAS | KHV | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | KHV | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG02132 | hp1 | a0001 | c0001 | t0010 | g0025 | EAS | KHV | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG02135 | hp1 | a0001 | c0001 | t0007 | g0001 | EAS | KHV | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG02145 | hp1 | a0001 | c0001 | t0005 | g0064 | AFR | ACB | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PEL | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG02148 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | PEL | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG02155 | hp1 | a0001 | c0001 | t0010 | g0021 | EAS | CDX | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | CDX | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | CDX | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG02165 | hp2 | a0001 | c0001 | t0007 | g0001 | EAS | CDX | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG02257 | hp1 | a0001 | c0001 | t0018 | g0220 | AFR | ACB | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG02257 | hp2 | a0001 | c0001 | t0004 | g0238 | AFR | ACB | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG02258 | hp1 | a0001 | c0001 | t0031 | g0059 | AFR | ACB | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG02280 | hp1 | a0001 | c0001 | t0006 | g0058 | AFR | ACB | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG02280 | hp2 | a0001 | c0001 | t0017 | g0199 | AFR | ACB | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0070 | AMR | PEL | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG02451 | hp1 | a0001 | c0001 | t0004 | g0235 | AFR | ACB | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG02451 | hp2 | a0001 | c0001 | t0017 | g0200 | AFR | ACB | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG02572 | hp1 | a0001 | c0001 | t0005 | g0063 | AFR | GWD | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG02602 | hp1 | a0001 | c0001 | t0041 | g0082 | SAS | PJL | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG02622 | hp1 | a0001 | c0001 | t0008 | g0005 | AFR | GWD | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG02622 | hp2 | a0001 | c0001 | t0051 | g0241 | AFR | GWD | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG02630 | hp1 | a0001 | c0002 | t0022 | g0037 | AFR | GWD | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG02630 | hp2 | a0001 | c0001 | t0006 | g0114 | AFR | GWD | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG02647 | hp1 | a0001 | c0001 | t0013 | g0214 | AFR | GWD | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG02717 | hp1 | a0001 | c0001 | t0049 | g0230 | AFR | GWD | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG02809 | hp1 | a0001 | c0001 | t0014 | g0212 | AFR | GWD | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG02809 | hp2 | a0001 | c0001 | t0032 | g0126 | AFR | GWD | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG02818 | hp1 | a0001 | c0001 | t0013 | g0215 | AFR | GWD | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG02818 | hp2 | a0001 | c0002 | t0022 | g0037 | AFR | GWD | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG02886 | hp1 | a0001 | c0001 | t0026 | g0203 | AFR | GWD | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG02886 | hp2 | a0001 | c0001 | t0043 | g0221 | AFR | GWD | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG02895 | hp1 | a0001 | c0001 | t0005 | g0061 | AFR | GWD | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG02897 | hp1 | a0001 | c0001 | t0005 | g0125 | AFR | GWD | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG02897 | hp2 | a0001 | c0001 | t0014 | g0211 | AFR | GWD | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG02922 | hp1 | a0001 | c0001 | t0004 | g0231 | AFR | ESN | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG02922 | hp2 | a0001 | c0001 | t0023 | g0039 | AFR | ESN | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG02965 | hp1 | a0001 | c0001 | t0006 | g0065 | AFR | ESN | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG02970 | hp1 | a0001 | c0001 | t0005 | g0008 | AFR | ESN | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG02970 | hp2 | a0001 | c0001 | t0015 | g0204 | AFR | ESN | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG02976 | hp1 | a0001 | c0001 | t0004 | g0240 | AFR | ESN | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG02976 | hp2 | a0001 | c0001 | t0015 | g0202 | AFR | ESN | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0080 | SAS | PJL | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG03041 | hp1 | a0001 | c0001 | t0021 | g0233 | AFR | GWD | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG03098 | hp1 | a0001 | c0001 | t0028 | g0213 | AFR | MSL | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG03130 | hp1 | a0001 | c0001 | t0012 | g0206 | AFR | ESN | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG03139 | hp1 | a0001 | c0001 | t0005 | g0008 | AFR | ESN | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG03195 | hp1 | a0001 | c0001 | t0012 | g0208 | AFR | ESN | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG03195 | hp2 | a0001 | c0001 | t0004 | g0038 | AFR | ESN | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG03209 | hp1 | a0001 | c0001 | t0006 | g0013 | AFR | MSL | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG03225 | hp1 | a0001 | c0001 | t0013 | g0218 | AFR | MSL | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG03453 | hp1 | a0001 | c0001 | t0014 | g0216 | AFR | MSL | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG03453 | hp2 | a0001 | c0001 | t0006 | g0013 | AFR | MSL | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0110 | AFR | MSL | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG03486 | hp2 | a0001 | c0001 | t0008 | g0005 | AFR | MSL | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG03490 | hp1 | a0001 | c0001 | t0016 | g0104 | SAS | PJL | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG03492 | hp1 | a0001 | c0001 | t0009 | g0183 | SAS | PJL | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG03516 | hp1 | a0001 | c0001 | t0021 | g0234 | AFR | ESN | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG03516 | hp2 | a0001 | c0001 | t0008 | g0056 | AFR | ESN | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0111 | AFR | GWD | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG03540 | hp2 | a0001 | c0001 | t0008 | g0005 | AFR | GWD | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG03579 | hp1 | a0001 | c0001 | t0004 | g0229 | AFR | MSL | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG03669 | hp1 | a0001 | c0001 | t0006 | g0112 | SAS | PJL | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0100 | SAS | PJL | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | STU | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG03831 | hp1 | a0001 | c0001 | t0009 | g0036 | SAS | BEB | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG03831 | hp2 | a0001 | c0001 | t0039 | g0081 | SAS | BEB | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | BEB | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | STU | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | STU | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG04204 | hp1 | a0001 | c0001 | t0009 | g0036 | SAS | STU | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | STU | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18522 | hp1 | a0001 | c0001 | t0008 | g0055 | AFR | YRI | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | CHB | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | CHB | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0068 | AFR | YRI | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18906 | hp2 | a0001 | c0001 | t0004 | g0237 | AFR | YRI | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18940 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18942 | hp1 | a0001 | c0001 | t0003 | g0121 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18949 | hp1 | a0001 | c0001 | t0019 | g0154 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18953 | hp1 | a0001 | c0001 | t0019 | g0137 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18960 | hp1 | a0001 | c0001 | t0020 | g0015 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18962 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18970 | hp1 | a0001 | c0001 | t0003 | g0116 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18973 | hp1 | a0001 | c0001 | t0003 | g0120 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18977 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18978 | hp2 | a0001 | c0001 | t0003 | g0115 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18980 | hp2 | a0001 | c0001 | t0007 | g0011 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18981 | hp2 | a0001 | c0001 | t0007 | g0066 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18983 | hp1 | a0001 | c0001 | t0007 | g0001 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18985 | hp1 | a0001 | c0001 | t0035 | g0227 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18987 | hp1 | a0001 | c0001 | t0034 | g0101 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18987 | hp2 | a0001 | c0001 | t0020 | g0015 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18988 | hp1 | a0001 | c0001 | t0011 | g0029 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18990 | hp1 | a0001 | c0001 | t0011 | g0029 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18993 | hp1 | a0001 | c0001 | t0016 | g0084 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18994 | hp1 | a0001 | c0001 | t0003 | g0124 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18995 | hp1 | a0001 | c0001 | t0007 | g0086 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA19001 | hp1 | a0001 | c0001 | t0011 | g0030 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA19001 | hp2 | a0001 | c0001 | t0036 | g0118 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA19004 | hp1 | a0001 | c0001 | t0010 | g0161 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA19011 | hp1 | a0001 | c0001 | t0003 | g0123 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA19011 | hp2 | a0001 | c0001 | t0011 | g0030 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA19012 | hp1 | a0001 | c0001 | t0007 | g0001 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA19030 | hp1 | a0001 | c0001 | t0030 | g0217 | AFR | LWK | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA19030 | hp2 | a0001 | c0001 | t0037 | g0098 | AFR | LWK | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA19043 | hp1 | a0001 | c0001 | t0047 | g0209 | AFR | LWK | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA19055 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA19066 | hp1 | a0001 | c0001 | t0007 | g0011 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA19072 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA19078 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA19080 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA19084 | hp1 | a0001 | c0001 | t0040 | g0075 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA19085 | hp1 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA19091 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA19240 | hp1 | a0001 | c0001 | t0004 | g0239 | AFR | YRI | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA19240 | hp2 | a0001 | c0001 | t0005 | g0040 | AFR | YRI | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0044 | AFR | ASW | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ASW | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0168 | EUR | TSI | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0083 | EUR | TSI | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | GIH | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG02109 | hp1 | a0001 | c0001 | t0004 | g0232 | AFR | ACB | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG02109 | hp2 | a0001 | c0001 | t0027 | g0205 | AFR | ACB | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG02486 | hp1 | a0001 | c0001 | t0018 | g0222 | AFR | ACB | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG02559 | hp2 | a0001 | c0001 | t0008 | g0106 | AFR | ACB | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG03471 | hp1 | a0001 | c0001 | t0025 | g0207 | AFR | MSL | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG06807 | hp1 | a0001 | c0001 | t0012 | g0201 | AFR | USA | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
HG06807 | hp2 | a0001 | c0001 | t0033 | g0228 | AFR | USA | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA20300 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | USA | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA20300 | hp2 | a0001 | c0001 | t0004 | g0038 | AFR | USA | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA21309 | hp1 | a0001 | c0001 | t0006 | g0127 | AFR | LWK | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
NA21309 | hp2 | a0001 | c0001 | t0048 | g0054 | AFR | LWK | RBM41_chrX_107056885_107123822 | RBM41 | chrX | 107056885 | 107123822 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:107088619 | G | A | 1 | a0001c0002 | 2 | HG02630.hp1 HG02818.hp2 |
synonymous_variant | LOW | c.816C>T | p.Gly272Gly | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/8 | 865/7005 | 816/1314 | 272/437 | chrX | 107088619 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:107061910 | A | G | 1 | a0001c0001t0025 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5617T>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 8/8 | 5617 | chrX | 107061910 | ||||||
chrX:107062094 | A | T | 3 | a0001c0001t0017 a0001c0001t0018 a0001c0001t0043 |
5 | HG02257.hp1 HG02280.hp2 HG02451.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5433T>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 8/8 | 5433 | chrX | 107062094 | ||||||
chrX:107062159 | A | G | 1 | a0001c0001t0032 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5368T>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 8/8 | 5368 | chrX | 107062159 | ||||||
chrX:107062419 | A | G | 2 | a0001c0001t0015 a0001c0001t0026 |
3 | HG02886.hp1 HG02970.hp2 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5108T>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 8/8 | 5108 | chrX | 107062419 | ||||||
chrX:107062427 | G | GC | 1 | a0001c0001t0035 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5099dupG | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 8/8 | 5099 | chrX | 107062427 | ||||||
chrX:107062640 | T | TA | 6 | a0001c0001t0004 a0001c0001t0021 a0001c0001t0049 others(3): Show |
17 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*4886dupT | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 8/8 | 4886 | chrX | 107062640 | ||||||
chrX:107062677 | A | C | 1 | a0001c0001t0039 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4850T>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 8/8 | 4850 | chrX | 107062677 | ||||||
chrX:107062684 | C | T | 1 | a0001c0001t0050 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4843G>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 8/8 | 4843 | chrX | 107062684 | ||||||
chrX:107062746 | T | A | 1 | a0001c0001t0045 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4781A>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 8/8 | 4781 | chrX | 107062746 | ||||||
chrX:107062752 | ACTTT | A | 1 | a0001c0001t0040 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4771_*4774delAAAG | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 8/8 | 4771 | chrX | 107062752 | ||||||
chrX:107062792 | C | G | 1 | a0001c0001t0042 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4735G>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 8/8 | 4735 | chrX | 107062792 | ||||||
chrX:107063264 | T | C | 1 | a0001c0001t0043 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4263A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 8/8 | 4263 | chrX | 107063264 | ||||||
chrX:107063344 | C | T | 2 | a0001c0001t0007 a0001c0001t0035 |
9 | HG02135.hp1 HG02165.hp2 NA18980.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4183G>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 8/8 | 4183 | chrX | 107063344 | ||||||
chrX:107063672 | C | T | 1 | a0001c0001t0011 | 4 | NA18988.hp1 NA18990.hp1 NA19001.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3855G>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 8/8 | 3855 | chrX | 107063672 | ||||||
chrX:107063742 | G | C | 1 | a0001c0001t0041 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3785C>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 8/8 | 3785 | chrX | 107063742 | ||||||
chrX:107063749 | A | C | 1 | a0001c0001t0021 | 2 | HG03041.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3778T>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 8/8 | 3778 | chrX | 107063749 | ||||||
chrX:107063923 | A | G | 1 | a0001c0001t0031 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3604T>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 8/8 | 3604 | chrX | 107063923 | ||||||
chrX:107063948 | TTTTC | T | 1 | a0001c0001t0020 | 2 | NA18960.hp1 NA18987.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3575_*3578delGAAA | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 8/8 | 3575 | chrX | 107063948 | ||||||
chrX:107063952 | C | CT | 4 | a0001c0001t0017 a0001c0001t0019 a0001c0001t0035 others(1): Show |
6 | HG01978.hp2 HG02280.hp2 HG02451.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3574dupA | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 8/8 | 3574 | chrX | 107063952 | ||||||
chrX:107063952 | CT | C | 13 | a0001c0001t0012 a0001c0001t0013 a0001c0001t0014 others(10): Show |
21 | HG02109.hp2 HG02622.hp2 HG02647.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*3574delA | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 8/8 | 3574 | chrX | 107063952 | ||||||
chrX:107064017 | T | C | 5 | a0001c0001t0013 a0001c0001t0014 a0001c0001t0028 others(2): Show |
9 | HG02027.hp1 HG02647.hp1 HG02809.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3510A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 8/8 | 3510 | chrX | 107064017 | ||||||
chrX:107064034 | C | T | 1 | a0001c0001t0037 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3493G>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 8/8 | 3493 | chrX | 107064034 | ||||||
chrX:107064146 | T | C | 3 | a0001c0001t0003 a0001c0001t0036 a0001c0001t0042 |
19 | HG00408.hp1 HG00438.hp2 HG01099.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*3381A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 8/8 | 3381 | chrX | 107064146 | ||||||
chrX:107064332 | G | A | 5 | a0001c0001t0004 a0001c0001t0021 a0001c0001t0049 others(2): Show |
15 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3195C>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 8/8 | 3195 | chrX | 107064332 | ||||||
chrX:107064404 | A | AT | 1 | a0001c0001t0049 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3122dupA | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 8/8 | 3122 | chrX | 107064404 | ||||||
chrX:107064404 | AT | A | 41 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(38): Show |
263 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(260): Show |
3_prime_UTR_variant | MODIFIER | c.*3122delA | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 8/8 | 3122 | chrX | 107064404 | ||||||
chrX:107064404 | ATT | A | 1 | a0001c0001t0005 | 8 | HG01884.hp2 HG02145.hp1 HG02572.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3121_*3122delAA | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 8/8 | 3121 | chrX | 107064404 | ||||||
chrX:107064469 | G | C | 1 | a0001c0001t0047 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3058C>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 8/8 | 3058 | chrX | 107064469 | ||||||
chrX:107064604 | T | C | 1 | a0001c0001t0026 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2923A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 8/8 | 2923 | chrX | 107064604 | ||||||
chrX:107064641 | G | C | 1 | a0001c0001t0030 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2886C>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 8/8 | 2886 | chrX | 107064641 | ||||||
chrX:107064741 | T | C | 3 | a0001c0001t0017 a0001c0001t0018 a0001c0001t0043 |
5 | HG02257.hp1 HG02280.hp2 HG02451.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2786A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 8/8 | 2786 | chrX | 107064741 | ||||||
chrX:107064773 | A | G | 1 | a0001c0001t0013 | 3 | HG02647.hp1 HG02818.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2754T>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 8/8 | 2754 | chrX | 107064773 | ||||||
chrX:107065063 | G | A | 14 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(11): Show |
101 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*2464C>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 8/8 | 2464 | chrX | 107065063 | ||||||
chrX:107065157 | A | G | 1 | a0001c0001t0011 | 4 | NA18988.hp1 NA18990.hp1 NA19001.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2370T>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 8/8 | 2370 | chrX | 107065157 | ||||||
chrX:107065174 | A | G | 1 | a0001c0001t0023 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2353T>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 8/8 | 2353 | chrX | 107065174 | ||||||
chrX:107065186 | G | T | 42 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(39): Show |
168 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*2341C>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 8/8 | 2341 | chrX | 107065186 | ||||||
chrX:107065397 | G | A | 1 | a0001c0001t0046 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2130C>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 8/8 | 2130 | chrX | 107065397 | ||||||
chrX:107065403 | G | T | 6 | a0001c0001t0013 a0001c0001t0014 a0001c0001t0028 others(3): Show |
10 | HG02027.hp1 HG02647.hp1 HG02809.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2124C>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 8/8 | 2124 | chrX | 107065403 | ||||||
chrX:107065473 | T | C | 1 | a0001c0001t0027 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2054A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 8/8 | 2054 | chrX | 107065473 | ||||||
chrX:107065772 | A | G | 1 | a0001c0001t0034 | 1 | NA18987.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1755T>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 8/8 | 1755 | chrX | 107065772 | ||||||
chrX:107066314 | T | G | 1 | a0001c0001t0047 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1213A>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 8/8 | 1213 | chrX | 107066314 | ||||||
chrX:107066353 | T | C | 13 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0007 others(10): Show |
93 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*1174A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 8/8 | 1174 | chrX | 107066353 | ||||||
chrX:107066666 | C | T | 5 | a0001c0001t0013 a0001c0001t0014 a0001c0001t0028 others(2): Show |
9 | HG02027.hp1 HG02647.hp1 HG02809.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*861G>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 8/8 | 861 | chrX | 107066666 | ||||||
chrX:107066671 | C | G | 32 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(29): Show |
139 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(136): Show |
3_prime_UTR_variant | MODIFIER | c.*856G>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 8/8 | 856 | chrX | 107066671 | ||||||
chrX:107066912 | A | C | 6 | a0001c0001t0013 a0001c0001t0014 a0001c0001t0028 others(3): Show |
10 | HG02027.hp1 HG02647.hp1 HG02809.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*615T>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 8/8 | 615 | chrX | 107066912 | ||||||
chrX:107066942 | AAAT | A | 1 | a0001c0001t0047 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*582_*584delATT | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 8/8 | 582 | chrX | 107066942 | ||||||
chrX:107067069 | G | T | 5 | a0001c0001t0012 a0001c0001t0015 a0001c0001t0025 others(2): Show |
8 | HG02109.hp2 HG02886.hp1 HG02970.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*458C>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 8/8 | 458 | chrX | 107067069 | ||||||
chrX:107067240 | G | T | 1 | a0001c0001t0024 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*287C>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 8/8 | 287 | chrX | 107067240 | ||||||
chrX:107067282 | T | C | 1 | a0001c0001t0048 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*245A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 8/8 | 245 | chrX | 107067282 | ||||||
chrX:107067513 | A | T | 1 | a0001c0001t0010 | 5 | HG00673.hp1 HG02074.hp1 HG02132.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*14T>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 8/8 | 14 | chrX | 107067513 | ||||||
chrX:107118788 | C | T | 1 | a0001c0001t0023 | 1 | HG02922.hp2 | 5_prime_UTR_variant | MODIFIER | c.-15G>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 1/8 | 15 | chrX | 107118788 | ||||||
chrX:107118803 | G | A | 6 | a0001c0001t0004 a0001c0001t0021 a0001c0001t0049 others(3): Show |
17 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(14): Show |
5_prime_UTR_variant | MODIFIER | c.-30C>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 1/8 | 30 | chrX | 107118803 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:107067745 | C | T | 2 | a0001c0001t0002g0070 a0001c0001t0002g0072 |
2 | HG01975.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.1148-52G>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 7/7 | chrX | 107067745 | |||||||
chrX:107067965 | G | A | 2 | a0001c0001t0017g0199 a0001c0001t0017g0200 |
2 | HG02280.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1148-272C>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 7/7 | chrX | 107067965 | |||||||
chrX:107068340 | A | T | 142 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0012 others(139): Show |
161 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(158): Show |
intron_variant | MODIFIER | c.1148-647T>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 7/7 | chrX | 107068340 | |||||||
chrX:107068454 | G | C | 1 | a0001c0001t0038g0090 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1148-761C>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 7/7 | chrX | 107068454 | |||||||
chrX:107068607 | G | C | 7 | a0001c0001t0002g0073 a0001c0001t0002g0074 a0001c0001t0002g0092 others(4): Show |
7 | NA18948.hp1 NA18987.hp1 NA18998.hp1 others(4): Show |
intron_variant | MODIFIER | c.1147+648C>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 7/7 | chrX | 107068607 | |||||||
chrX:107068694 | C | T | 14 | a0001c0001t0004g0038 a0001c0001t0004g0229 a0001c0001t0004g0231 others(11): Show |
15 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.1147+561G>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 7/7 | chrX | 107068694 | |||||||
chrX:107068757 | T | C | 142 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0012 others(139): Show |
161 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(158): Show |
intron_variant | MODIFIER | c.1147+498A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 7/7 | chrX | 107068757 | |||||||
chrX:107069082 | T | A | 1 | a0001c0001t0033g0228 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1147+173A>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 7/7 | chrX | 107069082 | |||||||
chrX:107069122 | A | G | 1 | a0001c0001t0033g0228 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1147+133T>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 7/7 | chrX | 107069122 | |||||||
chrX:107069130 | C | T | 1 | a0001c0001t0029g0210 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1147+125G>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 7/7 | chrX | 107069130 | |||||||
chrX:107069444 | G | T | 1 | a0001c0002t0022g0037 | 2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1000-42C>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107069444 | |||||||
chrX:107069642 | G | A | 142 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0012 others(139): Show |
161 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(158): Show |
intron_variant | MODIFIER | c.1000-240C>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107069642 | |||||||
chrX:107069671 | T | A | 1 | a0001c0001t0008g0106 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1000-269A>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107069671 | |||||||
chrX:107069785 | T | C | 1 | a0001c0001t0014g0212 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1000-383A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107069785 | |||||||
chrX:107069866 | T | TA | 2 | a0001c0001t0001g0131 a0001c0001t0001g0219 |
2 | HG03654.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.1000-465dupT | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107069866 | |||||||
chrX:107069866 | TA | T | 102 | a0001c0001t0001g0016 a0001c0001t0001g0135 a0001c0001t0001g0136 others(99): Show |
120 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.1000-465delT | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107069866 | |||||||
chrX:107069866 | TAA | T | 24 | a0001c0001t0001g0139 a0001c0001t0002g0012 a0001c0001t0002g0047 others(21): Show |
25 | HG00642.hp1 HG01074.hp1 HG01261.hp1 others(22): Show |
intron_variant | MODIFIER | c.1000-466_1000-465d others(4): Show |
RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107069866 | |||||||
chrX:107069866 | TAAA | T | 3 | a0001c0001t0004g0232 a0001c0001t0051g0241 a0001c0002t0022g0037 |
4 | HG02109.hp1 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1000-467_1000-465d others(5): Show |
RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107069866 | |||||||
chrX:107069866 | TAAAA | T | 12 | a0001c0001t0004g0038 a0001c0001t0004g0229 a0001c0001t0004g0231 others(9): Show |
13 | HG01109.hp1 HG02257.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1000-468_1000-465d others(6): Show |
RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107069866 | |||||||
chrX:107069878 | A | C | 1 | a0001c0001t0001g0170 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1000-476T>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107069878 | |||||||
chrX:107069905 | G | C | 102 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0012 others(99): Show |
119 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.1000-503C>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107069905 | |||||||
chrX:107070278 | G | A | 112 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0012 others(109): Show |
129 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.1000-876C>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107070278 | |||||||
chrX:107070749 | C | T | 4 | a0001c0001t0002g0068 a0001c0001t0002g0110 a0001c0001t0002g0111 others(1): Show |
4 | HG03486.hp1 HG03540.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1000-1347G>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107070749 | |||||||
chrX:107071045 | AC | A | 14 | a0001c0001t0004g0038 a0001c0001t0004g0229 a0001c0001t0004g0231 others(11): Show |
15 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.1000-1644delG | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107071045 | |||||||
chrX:107071054 | C | CA | 2 | a0001c0001t0001g0159 a0001c0001t0001g0165 |
2 | HG00738.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1000-1653dupT | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107071054 | |||||||
chrX:107071054 | CA | C | 109 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0012 others(106): Show |
126 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.1000-1653delT | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107071054 | |||||||
chrX:107071054 | CAA | C | 2 | a0001c0001t0002g0049 a0001c0001t0023g0039 |
2 | HG02922.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.1000-1654_1000-165 others(6): Show |
RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107071054 | |||||||
chrX:107071207 | C | CA | 12 | a0001c0001t0001g0033 a0001c0001t0001g0160 a0001c0001t0001g0167 others(9): Show |
13 | HG01081.hp2 HG01106.hp1 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.1000-1806dupT | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107071207 | |||||||
chrX:107071207 | C | CAA | 1 | a0001c0001t0028g0213 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1000-1807_1000-180 others(6): Show |
RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107071207 | |||||||
chrX:107071207 | CA | C | 96 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0001t0002g0042 others(93): Show |
108 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.1000-1806delT | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107071207 | |||||||
chrX:107071218 | A | C | 1 | a0001c0001t0016g0104 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1000-1816T>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107071218 | |||||||
chrX:107071354 | C | G | 15 | a0001c0001t0004g0038 a0001c0001t0004g0229 a0001c0001t0004g0231 others(12): Show |
17 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.1000-1952G>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107071354 | |||||||
chrX:107071459 | A | G | 1 | a0001c0001t0001g0198 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1000-2057T>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107071459 | |||||||
chrX:107071970 | T | C | 1 | a0001c0001t0007g0011 | 2 | NA18980.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1000-2568A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107071970 | |||||||
chrX:107072036 | A | G | 1 | a0001c0001t0008g0056 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1000-2634T>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107072036 | |||||||
chrX:107072238 | TA | T | 122 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0012 others(119): Show |
139 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.1000-2837delT | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107072238 | |||||||
chrX:107072634 | GA | G | 7 | a0001c0001t0005g0008 a0001c0001t0005g0040 a0001c0001t0005g0061 others(4): Show |
8 | HG01884.hp2 HG02145.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1000-3233delT | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107072634 | |||||||
chrX:107072718 | A | G | 1 | a0001c0001t0002g0052 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1000-3316T>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107072718 | |||||||
chrX:107072908 | A | G | 1 | a0001c0001t0006g0065 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1000-3506T>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107072908 | |||||||
chrX:107072934 | C | G | 8 | a0001c0001t0012g0201 a0001c0001t0012g0206 a0001c0001t0012g0208 others(5): Show |
8 | HG02109.hp2 HG02886.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.1000-3532G>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107072934 | |||||||
chrX:107073015 | C | CA | 1 | a0001c0001t0001g0153 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1000-3614_1000-361 others(5): Show |
RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107073015 | |||||||
chrX:107073334 | A | C | 6 | a0001c0001t0001g0024 a0001c0001t0001g0141 a0001c0001t0001g0143 others(3): Show |
7 | NA18947.hp1 NA18949.hp1 NA18952.hp1 others(4): Show |
intron_variant | MODIFIER | c.1000-3932T>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107073334 | |||||||
chrX:107073362 | A | C | 1 | a0001c0001t0006g0114 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1000-3960T>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107073362 | |||||||
chrX:107073413 | A | C | 14 | a0001c0001t0004g0038 a0001c0001t0004g0229 a0001c0001t0004g0231 others(11): Show |
15 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.1000-4011T>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107073413 | |||||||
chrX:107073737 | C | G | 1 | a0001c0001t0023g0039 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1000-4335G>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107073737 | |||||||
chrX:107073816 | G | A | 1 | a0001c0001t0002g0068 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1000-4414C>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107073816 | |||||||
chrX:107073819 | A | C | 1 | a0001c0001t0008g0060 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1000-4417T>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107073819 | |||||||
chrX:107074084 | ATATAT | A | 10 | a0001c0001t0001g0150 a0001c0001t0013g0214 a0001c0001t0013g0215 others(7): Show |
10 | HG00438.hp1 HG02027.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1000-4687_1000-468 others(9): Show |
RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107074084 | |||||||
chrX:107074242 | T | C | 142 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0012 others(139): Show |
161 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(158): Show |
intron_variant | MODIFIER | c.1000-4840A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107074242 | |||||||
chrX:107074373 | C | T | 1 | a0001c0001t0002g0083 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1000-4971G>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107074373 | |||||||
chrX:107075036 | A | G | 5 | a0001c0001t0017g0199 a0001c0001t0017g0200 a0001c0001t0018g0220 others(2): Show |
5 | HG02257.hp1 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1000-5634T>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107075036 | |||||||
chrX:107075227 | C | T | 112 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0012 others(109): Show |
129 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.1000-5825G>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107075227 | |||||||
chrX:107075600 | G | C | 11 | a0001c0001t0002g0042 a0001c0001t0002g0043 a0001c0001t0002g0046 others(8): Show |
11 | HG00558.hp2 HG00597.hp1 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.1000-6198C>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107075600 | |||||||
chrX:107075705 | C | T | 1 | a0001c0001t0002g0085 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1000-6303G>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107075705 | |||||||
chrX:107075740 | G | A | 1 | a0001c0001t0002g0096 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1000-6338C>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107075740 | |||||||
chrX:107075989 | C | T | 141 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0012 others(138): Show |
160 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(157): Show |
intron_variant | MODIFIER | c.1000-6587G>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107075989 | |||||||
chrX:107076195 | T | C | 1 | a0001c0001t0008g0060 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1000-6793A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107076195 | |||||||
chrX:107076295 | C | T | 1 | a0001c0001t0006g0127 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1000-6893G>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107076295 | |||||||
chrX:107076312 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1000-6910C>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107076312 | |||||||
chrX:107076316 | C | CAAAT | 64 | a0001c0001t0001g0023 a0001c0001t0001g0033 a0001c0001t0001g0138 others(61): Show |
78 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.1000-6918_1000-691 others(8): Show |
RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107076316 | |||||||
chrX:107076316 | C | CAAATAAA others(1): Show |
10 | a0001c0001t0002g0043 a0001c0001t0002g0049 a0001c0001t0002g0053 others(7): Show |
11 | HG00558.hp2 HG01934.hp1 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.1000-6922_1000-691 others(12): Show |
RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107076316 | |||||||
chrX:107076316 | CAAAT | C | 32 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0022 others(29): Show |
39 | HG00609.hp1 HG00738.hp1 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.1000-6918_1000-691 others(8): Show |
RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107076316 | |||||||
chrX:107076316 | CAAATAAA others(1): Show |
C | 11 | a0001c0001t0001g0150 a0001c0001t0001g0168 a0001c0001t0001g0223 others(8): Show |
11 | HG00438.hp1 HG01071.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1000-6922_1000-691 others(12): Show |
RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107076316 | |||||||
chrX:107076316 | CAAATAAA others(5): Show |
C | 6 | a0001c0001t0001g0146 a0001c0001t0001g0151 a0001c0001t0002g0044 others(3): Show |
8 | HG02630.hp1 HG02630.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1000-6926_1000-691 others(16): Show |
RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107076316 | |||||||
chrX:107076316 | CAAATAAA others(9): Show |
C | 9 | a0001c0001t0013g0214 a0001c0001t0013g0215 a0001c0001t0013g0218 others(6): Show |
9 | HG02027.hp1 HG02647.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1000-6930_1000-691 others(20): Show |
RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107076316 | |||||||
chrX:107076403 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1000-7001C>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107076403 | |||||||
chrX:107076443 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1000-7041G>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107076443 | |||||||
chrX:107076444 | G | A | 1 | a0001c0001t0004g0240 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1000-7042C>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107076444 | |||||||
chrX:107076463 | A | C | 10 | a0001c0001t0013g0214 a0001c0001t0013g0215 a0001c0001t0013g0218 others(7): Show |
10 | HG02027.hp1 HG02647.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.1000-7061T>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107076463 | |||||||
chrX:107076730 | A | T | 2 | a0001c0001t0017g0199 a0001c0001t0017g0200 |
2 | HG02280.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1000-7328T>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107076730 | |||||||
chrX:107076840 | C | T | 1 | a0001c0001t0012g0201 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1000-7438G>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107076840 | |||||||
chrX:107076880 | TATAA | T | 9 | a0001c0001t0013g0214 a0001c0001t0013g0215 a0001c0001t0013g0218 others(6): Show |
9 | HG02027.hp1 HG02647.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1000-7482_1000-747 others(8): Show |
RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107076880 | |||||||
chrX:107076957 | T | G | 6 | a0001c0001t0004g0038 a0001c0001t0004g0229 a0001c0001t0004g0237 others(3): Show |
7 | HG01109.hp1 HG02976.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.1000-7555A>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107076957 | |||||||
chrX:107077260 | T | C | 10 | a0001c0001t0012g0201 a0001c0001t0012g0206 a0001c0001t0012g0208 others(7): Show |
10 | HG02109.hp2 HG02886.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.1000-7858A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107077260 | |||||||
chrX:107077269 | T | C | 2 | a0001c0001t0001g0028 a0001c0001t0001g0163 |
3 | HG02056.hp1 HG02165.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1000-7867A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107077269 | |||||||
chrX:107077453 | A | T | 14 | a0001c0001t0004g0038 a0001c0001t0004g0229 a0001c0001t0004g0231 others(11): Show |
15 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.1000-8051T>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107077453 | |||||||
chrX:107077573 | A | AAC | 18 | a0001c0001t0001g0033 a0001c0001t0001g0153 a0001c0001t0001g0169 others(15): Show |
20 | HG01081.hp2 HG01106.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.1000-8173_1000-817 others(6): Show |
RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107077573 | |||||||
chrX:107077573 | A | AACAC | 4 | a0001c0001t0002g0078 a0001c0001t0004g0232 a0001c0001t0012g0208 others(1): Show |
4 | HG02080.hp1 HG02109.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1000-8175_1000-817 others(8): Show |
RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107077573 | |||||||
chrX:107077573 | A | AACACAC | 15 | a0001c0001t0002g0012 a0001c0001t0002g0045 a0001c0001t0002g0047 others(12): Show |
16 | HG00140.hp1 HG00642.hp1 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.1000-8177_1000-817 others(10): Show |
RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107077573 | |||||||
chrX:107077573 | A | AACACACA others(1): Show |
46 | a0001c0001t0002g0010 a0001c0001t0002g0042 a0001c0001t0002g0046 others(43): Show |
57 | HG00408.hp1 HG00438.hp2 HG01099.hp1 others(54): Show |
intron_variant | MODIFIER | c.1000-8179_1000-817 others(12): Show |
RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107077573 | |||||||
chrX:107077573 | A | AACACACA others(3): Show |
19 | a0001c0001t0002g0009 a0001c0001t0002g0068 a0001c0001t0002g0076 others(16): Show |
22 | HG00597.hp1 HG01243.hp1 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.1000-8181_1000-817 others(14): Show |
RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107077573 | |||||||
chrX:107077573 | A | AACACACA others(5): Show |
12 | a0001c0001t0002g0080 a0001c0001t0002g0096 a0001c0001t0002g0099 others(9): Show |
12 | HG01257.hp2 HG02818.hp1 HG02897.hp2 others(9): Show |
intron_variant | MODIFIER | c.1000-8183_1000-817 others(16): Show |
RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107077573 | |||||||
chrX:107077573 | A | AACACACA others(7): Show |
12 | a0001c0001t0002g0043 a0001c0001t0002g0044 a0001c0001t0002g0097 others(9): Show |
14 | HG00558.hp2 HG01081.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.1000-8185_1000-817 others(18): Show |
RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107077573 | |||||||
chrX:107077573 | A | AACACACA others(9): Show |
4 | a0001c0001t0005g0040 a0001c0001t0005g0062 a0001c0001t0005g0063 others(1): Show |
4 | HG01884.hp2 HG02055.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1000-8187_1000-817 others(20): Show |
RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107077573 | |||||||
chrX:107077573 | A | AACACACA others(11): Show |
2 | a0001c0001t0013g0214 a0001c0001t0013g0218 |
2 | HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1000-8189_1000-817 others(22): Show |
RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107077573 | |||||||
chrX:107077573 | AAC | A | 6 | a0001c0001t0001g0035 a0001c0001t0001g0132 a0001c0001t0009g0185 others(3): Show |
7 | HG01361.hp1 HG01517.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1000-8173_1000-817 others(6): Show |
RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107077573 | |||||||
chrX:107077573 | AACAC | A | 3 | a0001c0001t0001g0018 a0001c0001t0001g0193 a0001c0001t0001g0197 |
4 | HG00735.hp2 HG01515.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.1000-8175_1000-817 others(8): Show |
RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107077573 | |||||||
chrX:107077720 | G | A | 18 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0031 others(15): Show |
22 | HG00408.hp2 HG00621.hp1 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.1000-8318C>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107077720 | |||||||
chrX:107077733 | A | G | 1 | a0001c0001t0002g0080 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1000-8331T>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107077733 | |||||||
chrX:107077947 | ATGT | A | 1 | a0001c0001t0032g0126 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1000-8548_1000-854 others(7): Show |
RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107077947 | |||||||
chrX:107077991 | C | T | 1 | a0001c0001t0047g0209 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1000-8589G>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107077991 | |||||||
chrX:107078369 | A | C | 1 | a0001c0001t0002g0043 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1000-8967T>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107078369 | |||||||
chrX:107078658 | G | A | 1 | a0001c0001t0003g0121 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1000-9256C>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107078658 | |||||||
chrX:107078752 | G | A | 15 | a0001c0001t0004g0038 a0001c0001t0004g0229 a0001c0001t0004g0231 others(12): Show |
16 | HG01109.hp1 HG02027.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1000-9350C>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107078752 | |||||||
chrX:107078883 | C | CA | 10 | a0001c0001t0013g0214 a0001c0001t0013g0215 a0001c0001t0013g0218 others(7): Show |
10 | HG02027.hp1 HG02647.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.1000-9482dupT | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107078883 | |||||||
chrX:107078918 | C | A | 5 | a0001c0001t0017g0199 a0001c0001t0017g0200 a0001c0001t0018g0220 others(2): Show |
5 | HG02257.hp1 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1000-9516G>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107078918 | |||||||
chrX:107079186 | T | TA | 1 | a0001c0001t0002g0053 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.999+9249dupT | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107079186 | |||||||
chrX:107079290 | T | C | 1 | a0001c0001t0008g0056 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.999+9146A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107079290 | |||||||
chrX:107079395 | T | G | 102 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0012 others(99): Show |
119 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.999+9041A>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107079395 | |||||||
chrX:107079435 | T | C | 122 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0012 others(119): Show |
139 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.999+9001A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107079435 | |||||||
chrX:107079658 | A | G | 1 | a0001c0001t0008g0060 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.999+8778T>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107079658 | |||||||
chrX:107079714 | C | G | 1 | a0001c0001t0002g0113 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.999+8722G>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107079714 | |||||||
chrX:107079750 | G | A | 3 | a0001c0001t0001g0164 a0001c0001t0001g0171 a0001c0001t0012g0201 |
3 | HG06807.hp1 NA19006.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.999+8686C>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107079750 | |||||||
chrX:107079762 | C | T | 1 | a0001c0001t0029g0210 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.999+8674G>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107079762 | |||||||
chrX:107079763 | CCT | C | 10 | a0001c0001t0013g0214 a0001c0001t0013g0215 a0001c0001t0013g0218 others(7): Show |
10 | HG02027.hp1 HG02647.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.999+8671_999+8672d others(4): Show |
RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107079763 | |||||||
chrX:107080123 | A | G | 1 | a0001c0001t0002g0079 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.999+8313T>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107080123 | |||||||
chrX:107080278 | T | TA | 16 | a0001c0001t0001g0131 a0001c0001t0013g0214 a0001c0001t0013g0215 others(13): Show |
17 | HG02257.hp1 HG02280.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.999+8157dupT | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107080278 | |||||||
chrX:107080278 | TA | T | 4 | a0001c0001t0001g0143 a0001c0001t0006g0013 a0001c0001t0006g0114 others(1): Show |
5 | HG02630.hp2 HG03209.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.999+8157delT | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107080278 | |||||||
chrX:107080300 | C | T | 8 | a0001c0001t0013g0214 a0001c0001t0013g0215 a0001c0001t0013g0218 others(5): Show |
8 | HG02647.hp1 HG02809.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.999+8136G>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107080300 | |||||||
chrX:107080301 | G | A | 2 | a0001c0001t0002g0042 a0001c0001t0002g0043 |
2 | HG00558.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.999+8135C>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107080301 | |||||||
chrX:107080449 | G | A | 1 | a0001c0001t0027g0205 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.999+7987C>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107080449 | |||||||
chrX:107080477 | T | C | 1 | a0001c0001t0002g0047 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.999+7959A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107080477 | |||||||
chrX:107080587 | G | GAAACA | 57 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0135 others(54): Show |
67 | HG00735.hp1 HG01071.hp1 HG01243.hp1 others(64): Show |
intron_variant | MODIFIER | c.999+7844_999+7848d others(7): Show |
RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107080587 | |||||||
chrX:107080587 | G | GAAACAAA others(3): Show |
56 | a0001c0001t0002g0009 a0001c0001t0002g0012 a0001c0001t0002g0042 others(53): Show |
63 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.999+7839_999+7848d others(12): Show |
RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107080587 | |||||||
chrX:107080587 | G | GAAACAAA others(8): Show |
14 | a0001c0001t0002g0110 a0001c0001t0002g0111 a0001c0001t0003g0002 others(11): Show |
20 | HG00408.hp1 HG00438.hp2 HG01934.hp1 others(17): Show |
intron_variant | MODIFIER | c.999+7834_999+7848d others(17): Show |
RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107080587 | |||||||
chrX:107080587 | G | GAAACAAA others(13): Show |
7 | a0001c0001t0002g0073 a0001c0001t0002g0074 a0001c0001t0002g0092 others(4): Show |
7 | NA18948.hp1 NA18987.hp1 NA18998.hp1 others(4): Show |
intron_variant | MODIFIER | c.999+7829_999+7848d others(22): Show |
RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107080587 | |||||||
chrX:107080587 | GAAACA | G | 14 | a0001c0001t0004g0038 a0001c0001t0004g0229 a0001c0001t0004g0231 others(11): Show |
15 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.999+7844_999+7848d others(7): Show |
RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107080587 | |||||||
chrX:107080661 | A | T | 122 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0012 others(119): Show |
139 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.999+7775T>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107080661 | |||||||
chrX:107080721 | G | A | 6 | a0001c0001t0006g0107 a0001c0001t0017g0199 a0001c0001t0017g0200 others(3): Show |
6 | HG02055.hp1 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.999+7715C>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107080721 | |||||||
chrX:107080915 | T | C | 1 | a0001c0001t0047g0209 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.999+7521A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107080915 | |||||||
chrX:107081142 | C | A | 223 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(220): Show |
266 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.999+7294G>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107081142 | |||||||
chrX:107081220 | A | AT | 7 | a0001c0001t0001g0146 a0001c0001t0009g0036 a0001c0001t0009g0183 others(4): Show |
8 | HG00741.hp1 HG01071.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.999+7215dupA | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107081220 | |||||||
chrX:107081312 | A | C | 5 | a0001c0001t0017g0199 a0001c0001t0017g0200 a0001c0001t0018g0220 others(2): Show |
5 | HG02257.hp1 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.999+7124T>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107081312 | |||||||
chrX:107081452 | T | C | 15 | a0001c0001t0004g0038 a0001c0001t0004g0229 a0001c0001t0004g0231 others(12): Show |
17 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.999+6984A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107081452 | |||||||
chrX:107081566 | T | C | 1 | a0001c0001t0033g0228 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.999+6870A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107081566 | |||||||
chrX:107081589 | A | G | 1 | a0001c0001t0002g0067 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.999+6847T>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107081589 | |||||||
chrX:107081834 | T | C | 1 | a0001c0001t0005g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.999+6602A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107081834 | |||||||
chrX:107081901 | TTA | T | 2 | a0001c0001t0012g0206 a0001c0001t0012g0208 |
2 | HG03130.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.999+6533_999+6534d others(4): Show |
RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107081901 | |||||||
chrX:107081907 | T | A | 2 | a0001c0001t0004g0231 a0001c0001t0004g0238 |
2 | HG02257.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.999+6529A>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107081907 | |||||||
chrX:107081926 | T | C | 1 | a0001c0001t0025g0207 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.999+6510A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107081926 | |||||||
chrX:107081943 | A | G | 1 | a0001c0001t0040g0075 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.999+6493T>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107081943 | |||||||
chrX:107081987 | C | A | 102 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0012 others(99): Show |
119 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.999+6449G>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107081987 | |||||||
chrX:107082019 | G | GT | 1 | a0001c0001t0023g0039 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.999+6416dupA | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107082019 | |||||||
chrX:107082139 | G | T | 1 | a0001c0001t0002g0110 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.999+6297C>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107082139 | |||||||
chrX:107082159 | T | C | 5 | a0001c0001t0017g0199 a0001c0001t0017g0200 a0001c0001t0018g0220 others(2): Show |
5 | HG02257.hp1 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.999+6277A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107082159 | |||||||
chrX:107082286 | T | C | 2 | a0001c0001t0023g0039 a0001c0001t0033g0228 |
2 | HG02922.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.999+6150A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107082286 | |||||||
chrX:107082405 | G | T | 1 | a0001c0001t0010g0021 | 2 | HG00673.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.999+6031C>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107082405 | |||||||
chrX:107082414 | A | ATC | 1 | a0001c0001t0002g0074 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.999+6021_999+6022i others(4): Show |
RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107082414 | |||||||
chrX:107082415 | C | T | 1 | a0001c0001t0002g0074 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.999+6021G>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107082415 | |||||||
chrX:107082734 | C | T | 1 | a0001c0001t0002g0099 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.999+5702G>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107082734 | |||||||
chrX:107082816 | A | G | 1 | a0001c0001t0037g0098 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.999+5620T>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107082816 | |||||||
chrX:107082956 | A | C | 1 | a0001c0002t0022g0037 | 2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.999+5480T>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107082956 | |||||||
chrX:107083107 | G | GA | 1 | a0001c0001t0024g0142 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.999+5328dupT | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107083107 | |||||||
chrX:107083172 | A | AT | 4 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0031 others(1): Show |
7 | HG00408.hp2 HG00621.hp1 NA18943.hp1 others(4): Show |
intron_variant | MODIFIER | c.999+5263dupA | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107083172 | |||||||
chrX:107083172 | A | ATT | 1 | a0001c0001t0001g0188 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.999+5262_999+5263d others(4): Show |
RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107083172 | |||||||
chrX:107083172 | AT | A | 128 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0012 others(125): Show |
146 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.999+5263delA | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107083172 | |||||||
chrX:107083412 | T | C | 1 | a0001c0001t0001g0169 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.999+5024A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107083412 | |||||||
chrX:107083651 | T | A | 1 | a0001c0001t0027g0205 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.999+4785A>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107083651 | |||||||
chrX:107083835 | C | G | 1 | a0001c0001t0009g0183 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.999+4601G>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107083835 | |||||||
chrX:107083890 | C | T | 142 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0012 others(139): Show |
161 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(158): Show |
intron_variant | MODIFIER | c.999+4546G>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107083890 | |||||||
chrX:107083917 | G | GT | 4 | a0001c0001t0001g0175 a0001c0001t0001g0223 a0001c0001t0014g0216 others(1): Show |
4 | HG02738.hp1 HG03098.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.999+4518dupA | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107083917 | |||||||
chrX:107083918 | T | TC | 4 | a0001c0001t0012g0201 a0001c0001t0012g0206 a0001c0001t0012g0208 others(1): Show |
4 | HG03130.hp1 HG03195.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.999+4517_999+4518i others(3): Show |
RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107083918 | |||||||
chrX:107083919 | T | C | 108 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0012 others(105): Show |
125 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.999+4517A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107083919 | |||||||
chrX:107084017 | G | T | 5 | a0001c0001t0017g0199 a0001c0001t0017g0200 a0001c0001t0018g0220 others(2): Show |
5 | HG02257.hp1 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.999+4419C>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107084017 | |||||||
chrX:107084134 | C | CA | 34 | a0001c0001t0001g0145 a0001c0001t0001g0165 a0001c0001t0001g0175 others(31): Show |
38 | HG01109.hp1 HG01346.hp1 HG01975.hp2 others(35): Show |
intron_variant | MODIFIER | c.999+4301dupT | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107084134 | |||||||
chrX:107084134 | C | CAA | 105 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0012 others(102): Show |
122 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.999+4300_999+4301d others(4): Show |
RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107084134 | |||||||
chrX:107084134 | C | CAAA | 11 | a0001c0001t0002g0095 a0001c0001t0002g0103 a0001c0001t0002g0108 others(8): Show |
11 | HG01981.hp2 HG02572.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.999+4299_999+4301d others(5): Show |
RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107084134 | |||||||
chrX:107084134 | CA | C | 3 | a0001c0001t0001g0018 a0001c0001t0001g0156 a0001c0001t0001g0193 |
4 | HG00735.hp2 HG01069.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.999+4301delT | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107084134 | |||||||
chrX:107084490 | T | C | 10 | a0001c0001t0013g0214 a0001c0001t0013g0215 a0001c0001t0013g0218 others(7): Show |
10 | HG02027.hp1 HG02647.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.999+3946A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107084490 | |||||||
chrX:107084553 | G | A | 1 | a0001c0002t0022g0037 | 2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.999+3883C>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107084553 | |||||||
chrX:107084843 | T | G | 1 | a0001c0001t0001g0193 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.999+3593A>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107084843 | |||||||
chrX:107084844 | G | C | 5 | a0001c0001t0017g0199 a0001c0001t0017g0200 a0001c0001t0018g0220 others(2): Show |
5 | HG02257.hp1 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.999+3592C>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107084844 | |||||||
chrX:107084972 | T | C | 1 | a0001c0001t0016g0104 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.999+3464A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107084972 | |||||||
chrX:107085025 | T | C | 2 | a0001c0001t0014g0212 a0001c0001t0030g0217 |
2 | HG02809.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.999+3411A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107085025 | |||||||
chrX:107085032 | T | A | 3 | a0001c0001t0005g0008 a0001c0001t0005g0040 a0001c0001t0005g0064 |
4 | HG02145.hp1 HG02970.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.999+3404A>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107085032 | |||||||
chrX:107085095 | G | A | 1 | a0001c0001t0004g0231 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.999+3341C>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107085095 | |||||||
chrX:107085145 | T | C | 5 | a0001c0001t0017g0199 a0001c0001t0017g0200 a0001c0001t0018g0220 others(2): Show |
5 | HG02257.hp1 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.999+3291A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107085145 | |||||||
chrX:107085155 | CA | C | 1 | a0001c0001t0002g0099 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.999+3280delT | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107085155 | |||||||
chrX:107085224 | A | G | 1 | a0001c0001t0033g0228 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.999+3212T>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107085224 | |||||||
chrX:107085250 | T | C | 5 | a0001c0001t0017g0199 a0001c0001t0017g0200 a0001c0001t0018g0220 others(2): Show |
5 | HG02257.hp1 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.999+3186A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107085250 | |||||||
chrX:107085252 | TTCTTTTT others(1): Show |
T | 5 | a0001c0001t0017g0199 a0001c0001t0017g0200 a0001c0001t0018g0220 others(2): Show |
5 | HG02257.hp1 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.999+3176_999+3183d others(10): Show |
RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107085252 | |||||||
chrX:107085260 | C | CT | 4 | a0001c0001t0001g0155 a0001c0001t0001g0181 a0001c0001t0019g0154 others(1): Show |
5 | HG01993.hp1 HG02630.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.999+3175dupA | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107085260 | |||||||
chrX:107085260 | CT | C | 1 | a0001c0001t0001g0167 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.999+3175delA | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107085260 | |||||||
chrX:107085264 | T | TTC | 2 | a0001c0001t0002g0068 a0001c0001t0027g0205 |
2 | HG02109.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.999+3171_999+3172i others(4): Show |
RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107085264 | |||||||
chrX:107085265 | T | C | 1 | a0001c0001t0002g0053 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.999+3171A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107085265 | |||||||
chrX:107085265 | T | TC | 119 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0012 others(116): Show |
136 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.999+3170_999+3171i others(3): Show |
RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107085265 | |||||||
chrX:107085394 | G | A | 122 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0012 others(119): Show |
139 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.999+3042C>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107085394 | |||||||
chrX:107085456 | C | T | 2 | a0001c0001t0048g0054 a0001c0002t0022g0037 |
3 | HG02630.hp1 HG02818.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.999+2980G>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107085456 | |||||||
chrX:107085572 | C | CA | 1 | a0001c0001t0002g0053 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.999+2863_999+2864i others(3): Show |
RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107085572 | |||||||
chrX:107085726 | T | G | 1 | a0001c0001t0006g0112 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.999+2710A>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107085726 | |||||||
chrX:107085731 | T | C | 2 | a0001c0001t0001g0170 a0001c0001t0001g0182 |
2 | HG02155.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.999+2705A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107085731 | |||||||
chrX:107085737 | T | C | 2 | a0001c0001t0002g0096 a0001c0001t0002g0097 |
2 | HG01081.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.999+2699A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107085737 | |||||||
chrX:107085850 | T | A | 15 | a0001c0001t0004g0038 a0001c0001t0004g0229 a0001c0001t0004g0231 others(12): Show |
17 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.999+2586A>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107085850 | |||||||
chrX:107085943 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.999+2493C>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107085943 | |||||||
chrX:107086384 | C | T | 1 | a0001c0001t0002g0073 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.999+2052G>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107086384 | |||||||
chrX:107087210 | G | C | 1 | a0001c0001t0001g0034 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.999+1226C>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107087210 | |||||||
chrX:107087385 | ATTTT | A | 14 | a0001c0001t0004g0038 a0001c0001t0004g0229 a0001c0001t0004g0231 others(11): Show |
15 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.999+1047_999+1050d others(6): Show |
RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107087385 | |||||||
chrX:107087453 | A | G | 1 | a0001c0001t0047g0209 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.999+983T>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107087453 | |||||||
chrX:107087477 | T | C | 142 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0012 others(139): Show |
161 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(158): Show |
intron_variant | MODIFIER | c.999+959A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107087477 | |||||||
chrX:107087584 | TACA | T | 1 | a0001c0001t0002g0045 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.999+849_999+851del others(3): Show |
RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107087584 | |||||||
chrX:107087634 | C | T | 5 | a0001c0001t0017g0199 a0001c0001t0017g0200 a0001c0001t0018g0220 others(2): Show |
5 | HG02257.hp1 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.999+802G>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107087634 | |||||||
chrX:107087743 | A | G | 80 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0012 others(77): Show |
93 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.999+693T>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107087743 | |||||||
chrX:107087869 | T | C | 1 | a0001c0001t0001g0031 | 2 | HG00408.hp2 HG00621.hp1 |
intron_variant | MODIFIER | c.999+567A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107087869 | |||||||
chrX:107087923 | C | T | 2 | a0001c0001t0001g0131 a0001c0001t0001g0195 |
2 | HG03654.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.999+513G>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107087923 | |||||||
chrX:107088152 | C | T | 122 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0012 others(119): Show |
139 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.999+284G>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107088152 | |||||||
chrX:107088161 | G | A | 10 | a0001c0001t0012g0201 a0001c0001t0012g0206 a0001c0001t0012g0208 others(7): Show |
10 | HG02109.hp2 HG02886.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.999+275C>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107088161 | |||||||
chrX:107088250 | C | G | 14 | a0001c0001t0004g0038 a0001c0001t0004g0229 a0001c0001t0004g0231 others(11): Show |
15 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.999+186G>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107088250 | |||||||
chrX:107088397 | G | A | 5 | a0001c0001t0017g0199 a0001c0001t0017g0200 a0001c0001t0018g0220 others(2): Show |
5 | HG02257.hp1 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.999+39C>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 6/7 | chrX | 107088397 | |||||||
chrX:107089063 | A | G | 2 | a0001c0001t0001g0033 a0001c0001t0001g0153 |
3 | HG01081.hp2 HG01106.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.596-224T>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107089063 | |||||||
chrX:107089182 | T | C | 14 | a0001c0001t0004g0038 a0001c0001t0004g0229 a0001c0001t0004g0231 others(11): Show |
15 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.596-343A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107089182 | |||||||
chrX:107089255 | A | G | 3 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0130 |
3 | HG00140.hp1 HG01175.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.596-416T>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107089255 | |||||||
chrX:107089290 | C | T | 1 | a0001c0001t0009g0183 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.596-451G>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107089290 | |||||||
chrX:107089387 | C | A | 1 | a0001c0001t0016g0104 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.596-548G>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107089387 | |||||||
chrX:107089522 | G | A | 1 | a0001c0001t0002g0097 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.596-683C>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107089522 | |||||||
chrX:107089790 | G | T | 87 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0012 others(84): Show |
101 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.596-951C>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107089790 | |||||||
chrX:107089795 | C | T | 142 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0012 others(139): Show |
161 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(158): Show |
intron_variant | MODIFIER | c.596-956G>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107089795 | |||||||
chrX:107090021 | T | A | 1 | a0001c0001t0037g0098 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.596-1182A>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107090021 | |||||||
chrX:107090058 | A | T | 4 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0133 others(1): Show |
6 | NA18943.hp1 NA18978.hp1 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.596-1219T>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107090058 | |||||||
chrX:107090090 | T | C | 3 | a0001c0001t0002g0044 a0001c0001t0006g0013 a0001c0001t0006g0114 |
4 | HG02630.hp2 HG03209.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.596-1251A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107090090 | |||||||
chrX:107090248 | C | G | 14 | a0001c0001t0004g0038 a0001c0001t0004g0229 a0001c0001t0004g0231 others(11): Show |
15 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.596-1409G>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107090248 | |||||||
chrX:107090342 | G | C | 142 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0012 others(139): Show |
161 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(158): Show |
intron_variant | MODIFIER | c.596-1503C>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107090342 | |||||||
chrX:107090634 | G | T | 1 | a0001c0001t0033g0228 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.596-1795C>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107090634 | |||||||
chrX:107090774 | GTTTTA | G | 1 | a0001c0001t0006g0127 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.596-1940_596-1936d others(7): Show |
RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107090774 | |||||||
chrX:107090793 | A | T | 14 | a0001c0001t0004g0038 a0001c0001t0004g0229 a0001c0001t0004g0231 others(11): Show |
15 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.596-1954T>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107090793 | |||||||
chrX:107090995 | T | C | 1 | a0001c0001t0032g0126 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.596-2156A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107090995 | |||||||
chrX:107091022 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.596-2183T>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107091022 | |||||||
chrX:107091135 | T | C | 3 | a0001c0001t0001g0032 a0001c0001t0001g0150 a0001c0001t0001g0166 |
4 | HG00438.hp1 HG02015.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.596-2296A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107091135 | |||||||
chrX:107091215 | T | C | 1 | a0001c0001t0002g0099 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.596-2376A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107091215 | |||||||
chrX:107091855 | T | C | 1 | a0001c0001t0002g0100 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.596-3016A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107091855 | |||||||
chrX:107091927 | G | A | 1 | a0001c0001t0001g0167 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.596-3088C>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107091927 | |||||||
chrX:107092267 | C | CA | 15 | a0001c0001t0003g0124 a0001c0001t0004g0238 a0001c0001t0013g0214 others(12): Show |
15 | HG02027.hp1 HG02257.hp2 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.596-3429dupT | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107092267 | |||||||
chrX:107092267 | CA | C | 1 | a0001c0001t0002g0048 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.596-3429delT | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107092267 | |||||||
chrX:107092592 | AT | A | 1 | a0001c0001t0001g0168 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.596-3754delA | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107092592 | |||||||
chrX:107092957 | T | C | 15 | a0001c0001t0004g0038 a0001c0001t0004g0229 a0001c0001t0004g0231 others(12): Show |
17 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.596-4118A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107092957 | |||||||
chrX:107093000 | C | T | 2 | a0001c0001t0017g0199 a0001c0001t0017g0200 |
2 | HG02280.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.596-4161G>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107093000 | |||||||
chrX:107093121 | G | C | 1 | a0001c0001t0006g0107 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.596-4282C>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107093121 | |||||||
chrX:107093533 | C | A | 3 | a0001c0001t0015g0202 a0001c0001t0015g0204 a0001c0001t0026g0203 |
3 | HG02886.hp1 HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.596-4694G>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107093533 | |||||||
chrX:107093641 | A | G | 1 | a0001c0001t0002g0109 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.596-4802T>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107093641 | |||||||
chrX:107094483 | T | C | 10 | a0001c0001t0013g0214 a0001c0001t0013g0215 a0001c0001t0013g0218 others(7): Show |
10 | HG02027.hp1 HG02647.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.596-5644A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107094483 | |||||||
chrX:107094553 | G | A | 1 | a0001c0001t0012g0208 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.596-5714C>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107094553 | |||||||
chrX:107095149 | C | CA | 115 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0169 others(112): Show |
134 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.596-6311dupT | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107095149 | |||||||
chrX:107095149 | C | CAA | 18 | a0001c0001t0002g0053 a0001c0001t0004g0038 a0001c0001t0004g0229 others(15): Show |
20 | HG01109.hp1 HG02109.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.596-6312_596-6311d others(4): Show |
RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107095149 | |||||||
chrX:107095149 | C | CAAA | 1 | a0001c0001t0025g0207 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.596-6313_596-6311d others(5): Show |
RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107095149 | |||||||
chrX:107095149 | C | CAAAA | 8 | a0001c0001t0013g0214 a0001c0001t0013g0215 a0001c0001t0013g0218 others(5): Show |
8 | HG02027.hp1 HG02647.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.596-6314_596-6311d others(6): Show |
RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107095149 | |||||||
chrX:107095149 | C | CAAAAA | 2 | a0001c0001t0014g0216 a0001c0001t0030g0217 |
2 | HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.596-6315_596-6311d others(7): Show |
RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107095149 | |||||||
chrX:107095323 | T | C | 122 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0012 others(119): Show |
139 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.596-6484A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107095323 | |||||||
chrX:107095456 | C | G | 2 | a0001c0001t0017g0199 a0001c0001t0017g0200 |
2 | HG02280.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.596-6617G>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107095456 | |||||||
chrX:107095498 | A | G | 3 | a0001c0001t0015g0202 a0001c0001t0015g0204 a0001c0001t0026g0203 |
3 | HG02886.hp1 HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.596-6659T>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107095498 | |||||||
chrX:107095594 | T | TA | 1 | a0001c0001t0001g0171 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.596-6756dupT | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107095594 | |||||||
chrX:107095720 | T | C | 3 | a0001c0001t0003g0014 a0001c0001t0003g0123 a0001c0001t0003g0124 |
4 | NA18962.hp1 NA18977.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.596-6881A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107095720 | |||||||
chrX:107095949 | G | T | 10 | a0001c0001t0013g0214 a0001c0001t0013g0215 a0001c0001t0013g0218 others(7): Show |
10 | HG02027.hp1 HG02647.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.596-7110C>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107095949 | |||||||
chrX:107096010 | C | T | 1 | a0001c0001t0001g0151 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.596-7171G>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107096010 | |||||||
chrX:107096096 | C | T | 1 | a0001c0001t0006g0112 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.596-7257G>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107096096 | |||||||
chrX:107096358 | T | C | 9 | a0001c0001t0013g0214 a0001c0001t0013g0215 a0001c0001t0013g0218 others(6): Show |
9 | HG02027.hp1 HG02647.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.596-7519A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107096358 | |||||||
chrX:107096653 | A | G | 5 | a0001c0001t0017g0199 a0001c0001t0017g0200 a0001c0001t0018g0220 others(2): Show |
5 | HG02257.hp1 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.596-7814T>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107096653 | |||||||
chrX:107097288 | A | C | 2 | a0001c0001t0004g0231 a0001c0001t0004g0238 |
2 | HG02257.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.596-8449T>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107097288 | |||||||
chrX:107097383 | T | C | 2 | a0001c0001t0017g0199 a0001c0001t0017g0200 |
2 | HG02280.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.596-8544A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107097383 | |||||||
chrX:107097425 | G | A | 1 | a0001c0001t0014g0211 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.596-8586C>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107097425 | |||||||
chrX:107097448 | TC | T | 1 | a0001c0001t0003g0115 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.596-8610delG | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107097448 | |||||||
chrX:107097578 | T | TC | 1 | a0001c0001t0003g0115 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.596-8740dupG | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107097578 | |||||||
chrX:107097581 | G | A | 3 | a0001c0001t0015g0202 a0001c0001t0015g0204 a0001c0001t0026g0203 |
3 | HG02886.hp1 HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.596-8742C>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107097581 | |||||||
chrX:107097701 | TA | T | 1 | a0001c0001t0003g0115 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.596-8863delT | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107097701 | |||||||
chrX:107097895 | G | A | 1 | a0001c0001t0002g0046 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.596-9056C>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107097895 | |||||||
chrX:107097945 | T | C | 1 | a0001c0001t0006g0065 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.596-9106A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107097945 | |||||||
chrX:107098197 | T | C | 5 | a0001c0001t0017g0199 a0001c0001t0017g0200 a0001c0001t0018g0220 others(2): Show |
5 | HG02257.hp1 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.596-9358A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107098197 | |||||||
chrX:107098466 | C | CA | 1 | a0001c0001t0002g0052 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.596-9628dupT | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107098466 | |||||||
chrX:107098471 | A | T | 1 | a0001c0001t0002g0071 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.596-9632T>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107098471 | |||||||
chrX:107098483 | A | C | 1 | a0001c0001t0004g0239 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.596-9644T>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107098483 | |||||||
chrX:107098485 | A | G | 1 | a0001c0001t0001g0150 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.596-9646T>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107098485 | |||||||
chrX:107098585 | G | A | 10 | a0001c0001t0013g0214 a0001c0001t0013g0215 a0001c0001t0013g0218 others(7): Show |
10 | HG02027.hp1 HG02647.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.596-9746C>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107098585 | |||||||
chrX:107098601 | G | GA | 1 | a0001c0001t0001g0219 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.596-9763dupT | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107098601 | |||||||
chrX:107098608 | G | A | 3 | a0001c0001t0014g0211 a0001c0001t0014g0212 a0001c0001t0030g0217 |
3 | HG02809.hp1 HG02897.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.596-9769C>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107098608 | |||||||
chrX:107098678 | G | A | 15 | a0001c0001t0004g0038 a0001c0001t0004g0229 a0001c0001t0004g0231 others(12): Show |
17 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.596-9839C>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107098678 | |||||||
chrX:107098729 | G | A | 1 | a0001c0001t0002g0102 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.596-9890C>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107098729 | |||||||
chrX:107098882 | T | C | 1 | a0001c0001t0047g0209 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.596-10043A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107098882 | |||||||
chrX:107098998 | G | GA | 1 | a0001c0001t0027g0205 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.596-10160dupT | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107098998 | |||||||
chrX:107099291 | C | T | 1 | a0001c0001t0002g0046 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.596-10452G>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107099291 | |||||||
chrX:107099378 | A | T | 4 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(1): Show |
4 | NA18955.hp1 NA18971.hp1 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.596-10539T>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107099378 | |||||||
chrX:107099481 | G | A | 1 | a0001c0001t0033g0228 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.596-10642C>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107099481 | |||||||
chrX:107099690 | T | TAC | 98 | a0001c0001t0001g0019 a0001c0001t0001g0035 a0001c0001t0001g0041 others(95): Show |
116 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.596-10853_596-1085 others(6): Show |
RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107099690 | |||||||
chrX:107099690 | T | TACAC | 8 | a0001c0001t0002g0103 a0001c0001t0003g0124 a0001c0001t0006g0065 others(5): Show |
8 | HG01981.hp2 HG02055.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.596-10855_596-1085 others(8): Show |
RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107099690 | |||||||
chrX:107099690 | T | TACACAC | 4 | a0001c0001t0001g0176 a0001c0001t0017g0199 a0001c0001t0017g0200 others(1): Show |
4 | HG00597.hp2 HG02280.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.596-10857_596-1085 others(10): Show |
RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107099690 | |||||||
chrX:107099690 | TAC | T | 10 | a0001c0001t0001g0149 a0001c0001t0002g0009 a0001c0001t0002g0067 others(7): Show |
11 | HG02129.hp1 HG02257.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.596-10853_596-1085 others(6): Show |
RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107099690 | |||||||
chrX:107099690 | TACAC | T | 15 | a0001c0001t0001g0195 a0001c0001t0004g0038 a0001c0001t0004g0229 others(12): Show |
17 | HG01109.hp1 HG02109.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.596-10855_596-1085 others(8): Show |
RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107099690 | |||||||
chrX:107099696 | C | A | 1 | a0001c0001t0023g0039 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.596-10857G>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107099696 | |||||||
chrX:107099700 | C | A | 1 | a0001c0001t0023g0039 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.596-10861G>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107099700 | |||||||
chrX:107100312 | G | A | 5 | a0001c0001t0017g0199 a0001c0001t0017g0200 a0001c0001t0018g0220 others(2): Show |
5 | HG02257.hp1 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.596-11473C>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107100312 | |||||||
chrX:107100379 | C | G | 102 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0012 others(99): Show |
119 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.596-11540G>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107100379 | |||||||
chrX:107100448 | T | C | 10 | a0001c0001t0012g0201 a0001c0001t0012g0206 a0001c0001t0012g0208 others(7): Show |
10 | HG02109.hp2 HG02886.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.596-11609A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107100448 | |||||||
chrX:107100490 | CA | C | 143 | a0001c0001t0001g0148 a0001c0001t0002g0009 a0001c0001t0002g0010 others(140): Show |
162 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(159): Show |
intron_variant | MODIFIER | c.596-11652delT | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107100490 | |||||||
chrX:107100828 | C | T | 122 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0012 others(119): Show |
139 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.596-11989G>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107100828 | |||||||
chrX:107100835 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.596-11996G>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107100835 | |||||||
chrX:107100866 | A | G | 1 | a0001c0001t0001g0189 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.596-12027T>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107100866 | |||||||
chrX:107100916 | A | G | 5 | a0001c0001t0017g0199 a0001c0001t0017g0200 a0001c0001t0018g0220 others(2): Show |
5 | HG02257.hp1 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.596-12077T>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107100916 | |||||||
chrX:107101209 | G | A | 122 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0012 others(119): Show |
139 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.595+12188C>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107101209 | |||||||
chrX:107101241 | TA | T | 1 | a0001c0001t0003g0115 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.595+12155delT | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107101241 | |||||||
chrX:107101493 | G | A | 1 | a0001c0001t0013g0218 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.595+11904C>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107101493 | |||||||
chrX:107101523 | TCAA | T | 10 | a0001c0001t0013g0214 a0001c0001t0013g0215 a0001c0001t0013g0218 others(7): Show |
10 | HG02027.hp1 HG02647.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.595+11871_595+1187 others(7): Show |
RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107101523 | |||||||
chrX:107101657 | T | C | 9 | a0001c0001t0013g0214 a0001c0001t0013g0215 a0001c0001t0013g0218 others(6): Show |
9 | HG02027.hp1 HG02647.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.595+11740A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107101657 | |||||||
chrX:107101690 | G | GT | 1 | a0001c0001t0007g0066 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.595+11706dupA | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107101690 | |||||||
chrX:107101734 | A | AG | 1 | a0001c0001t0003g0115 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.595+11662dupC | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107101734 | |||||||
chrX:107101784 | A | AT | 1 | a0001c0001t0001g0219 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.595+11612dupA | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107101784 | |||||||
chrX:107102158 | C | CT | 1 | a0001c0001t0003g0115 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.595+11238dupA | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107102158 | |||||||
chrX:107102282 | G | A | 79 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0012 others(76): Show |
92 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.595+11115C>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107102282 | |||||||
chrX:107102298 | T | G | 15 | a0001c0001t0004g0038 a0001c0001t0004g0229 a0001c0001t0004g0231 others(12): Show |
17 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.595+11099A>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107102298 | |||||||
chrX:107102774 | GC | G | 1 | a0001c0001t0003g0115 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.595+10622delG | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107102774 | |||||||
chrX:107102857 | T | C | 1 | a0001c0001t0002g0105 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.595+10540A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107102857 | |||||||
chrX:107103154 | A | G | 1 | a0001c0001t0015g0202 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.595+10243T>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107103154 | |||||||
chrX:107103440 | CT | C | 240 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(237): Show |
289 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(286): Show |
intron_variant | MODIFIER | c.595+9956delA | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107103440 | |||||||
chrX:107103551 | G | C | 122 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0012 others(119): Show |
139 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.595+9846C>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107103551 | |||||||
chrX:107103584 | TATA | T | 1 | a0001c0001t0027g0205 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.595+9810_595+9812d others(5): Show |
RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107103584 | |||||||
chrX:107103639 | C | CAG | 2 | a0001c0001t0002g0046 a0001c0001t0002g0057 |
2 | NA19056.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.595+9757_595+9758i others(4): Show |
RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107103639 | |||||||
chrX:107103762 | G | T | 9 | a0001c0001t0012g0201 a0001c0001t0012g0206 a0001c0001t0012g0208 others(6): Show |
9 | HG02109.hp2 HG02886.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.595+9635C>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107103762 | |||||||
chrX:107103836 | G | A | 2 | a0001c0001t0004g0239 a0001c0001t0004g0240 |
2 | HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.595+9561C>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107103836 | |||||||
chrX:107104069 | T | TC | 1 | a0001c0001t0001g0177 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.595+9327dupG | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107104069 | |||||||
chrX:107104076 | T | TC | 1 | a0001c0001t0001g0219 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.595+9320dupG | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107104076 | |||||||
chrX:107104087 | A | AC | 3 | a0001c0001t0001g0181 a0001c0001t0001g0219 a0001c0001t0035g0227 |
3 | NA18985.hp1 NA19067.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.595+9309dupG | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107104087 | |||||||
chrX:107104089 | C | T | 4 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(1): Show |
4 | HG00558.hp1 HG01978.hp1 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.595+9308G>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107104089 | |||||||
chrX:107104197 | G | A | 1 | a0001c0001t0008g0106 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.595+9200C>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107104197 | |||||||
chrX:107104238 | T | C | 1 | a0001c0001t0002g0053 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.595+9159A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107104238 | |||||||
chrX:107104253 | C | T | 1 | a0001c0001t0023g0039 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.595+9144G>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107104253 | |||||||
chrX:107104331 | AT | A | 5 | a0001c0001t0017g0199 a0001c0001t0017g0200 a0001c0001t0018g0220 others(2): Show |
5 | HG02257.hp1 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.595+9065delA | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107104331 | |||||||
chrX:107104334 | G | A | 5 | a0001c0001t0017g0199 a0001c0001t0017g0200 a0001c0001t0018g0220 others(2): Show |
5 | HG02257.hp1 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.595+9063C>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107104334 | |||||||
chrX:107104414 | T | C | 1 | a0001c0001t0001g0146 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.595+8983A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107104414 | |||||||
chrX:107104441 | T | C | 1 | a0001c0001t0001g0178 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.595+8956A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107104441 | |||||||
chrX:107104507 | T | C | 1 | a0001c0001t0002g0108 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.595+8890A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107104507 | |||||||
chrX:107104684 | A | T | 112 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0012 others(109): Show |
129 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.595+8713T>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107104684 | |||||||
chrX:107104703 | G | A | 9 | a0001c0001t0013g0214 a0001c0001t0013g0215 a0001c0001t0013g0218 others(6): Show |
9 | HG02027.hp1 HG02647.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.595+8694C>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107104703 | |||||||
chrX:107104823 | T | C | 1 | a0001c0001t0006g0107 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.595+8574A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107104823 | |||||||
chrX:107104970 | C | A | 1 | a0001c0001t0009g0187 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.595+8427G>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107104970 | |||||||
chrX:107105045 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.595+8352C>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107105045 | |||||||
chrX:107105045 | G | C | 1 | a0001c0001t0001g0179 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.595+8352C>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107105045 | |||||||
chrX:107105083 | T | C | 1 | a0001c0001t0004g0240 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.595+8314A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107105083 | |||||||
chrX:107105159 | T | C | 6 | a0001c0001t0009g0036 a0001c0001t0009g0183 a0001c0001t0009g0184 others(3): Show |
7 | HG00741.hp1 HG01071.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.595+8238A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107105159 | |||||||
chrX:107105169 | G | C | 6 | a0001c0001t0009g0036 a0001c0001t0009g0183 a0001c0001t0009g0184 others(3): Show |
7 | HG00741.hp1 HG01071.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.595+8228C>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107105169 | |||||||
chrX:107105490 | A | C | 1 | a0001c0001t0006g0112 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.595+7907T>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107105490 | |||||||
chrX:107105548 | T | C | 1 | a0001c0001t0033g0228 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.595+7849A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107105548 | |||||||
chrX:107105550 | C | T | 1 | a0001c0001t0033g0228 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.595+7847G>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107105550 | |||||||
chrX:107105599 | A | G | 1 | a0001c0001t0002g0044 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.595+7798T>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107105599 | |||||||
chrX:107105635 | A | AACCAAAA others(15): Show |
1 | a0001c0001t0049g0230 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.595+7740_595+7761d others(24): Show |
RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107105635 | |||||||
chrX:107105688 | C | G | 4 | a0001c0001t0008g0005 a0001c0001t0008g0055 a0001c0001t0008g0056 others(1): Show |
6 | HG02622.hp1 HG03486.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.595+7709G>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107105688 | |||||||
chrX:107105713 | G | A | 1 | a0001c0001t0047g0209 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.595+7684C>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107105713 | |||||||
chrX:107105830 | A | T | 141 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0012 others(138): Show |
160 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(157): Show |
intron_variant | MODIFIER | c.595+7567T>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107105830 | |||||||
chrX:107105831 | C | G | 141 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0012 others(138): Show |
160 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(157): Show |
intron_variant | MODIFIER | c.595+7566G>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107105831 | |||||||
chrX:107105949 | T | C | 1 | a0001c0001t0033g0228 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.595+7448A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107105949 | |||||||
chrX:107105955 | C | T | 6 | a0001c0001t0002g0048 a0001c0001t0002g0049 a0001c0001t0002g0050 others(3): Show |
6 | NA18949.hp2 NA18959.hp1 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.595+7442G>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107105955 | |||||||
chrX:107106051 | C | T | 14 | a0001c0001t0004g0038 a0001c0001t0004g0229 a0001c0001t0004g0231 others(11): Show |
15 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.595+7346G>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107106051 | |||||||
chrX:107106151 | A | T | 1 | a0001c0001t0001g0146 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.595+7246T>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107106151 | |||||||
chrX:107106152 | C | G | 1 | a0001c0001t0001g0146 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.595+7245G>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107106152 | |||||||
chrX:107106189 | G | C | 16 | a0001c0001t0002g0108 a0001c0001t0004g0038 a0001c0001t0004g0229 others(13): Show |
18 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.595+7208C>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107106189 | |||||||
chrX:107106204 | C | T | 1 | a0001c0002t0022g0037 | 2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.595+7193G>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107106204 | |||||||
chrX:107106314 | A | G | 15 | a0001c0001t0004g0038 a0001c0001t0004g0229 a0001c0001t0004g0231 others(12): Show |
17 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.595+7083T>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107106314 | |||||||
chrX:107106376 | CTGGA | C | 1 | a0001c0001t0001g0145 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.595+7017_595+7020d others(6): Show |
RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107106376 | |||||||
chrX:107106413 | T | C | 5 | a0001c0001t0017g0199 a0001c0001t0017g0200 a0001c0001t0018g0220 others(2): Show |
5 | HG02257.hp1 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.595+6984A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107106413 | |||||||
chrX:107106427 | T | G | 1 | a0001c0001t0023g0039 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.595+6970A>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107106427 | |||||||
chrX:107106451 | T | G | 1 | a0001c0001t0002g0109 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.595+6946A>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107106451 | |||||||
chrX:107106562 | A | T | 2 | a0001c0001t0001g0144 a0001c0001t0001g0194 |
2 | HG01346.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.595+6835T>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107106562 | |||||||
chrX:107106563 | T | C | 2 | a0001c0001t0002g0110 a0001c0001t0002g0111 |
2 | HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.595+6834A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107106563 | |||||||
chrX:107106754 | C | A | 1 | a0001c0001t0006g0112 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.595+6643G>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107106754 | |||||||
chrX:107106858 | G | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0180 a0001c0001t0001g0219 |
5 | NA18965.hp1 NA18973.hp2 NA19063.hp1 others(2): Show |
intron_variant | MODIFIER | c.595+6539C>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107106858 | |||||||
chrX:107106874 | T | TG | 3 | a0001c0001t0001g0181 a0001c0001t0001g0219 a0001c0001t0003g0124 |
3 | NA18994.hp1 NA19067.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.595+6522dupC | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107106874 | |||||||
chrX:107106881 | A | AG | 1 | a0001c0001t0035g0227 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.595+6515dupC | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107106881 | |||||||
chrX:107106883 | T | G | 122 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0012 others(119): Show |
139 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.595+6514A>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107106883 | |||||||
chrX:107106925 | C | T | 1 | a0001c0001t0002g0047 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.595+6472G>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107106925 | |||||||
chrX:107107015 | A | T | 1 | a0001c0001t0001g0135 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.595+6382T>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107107015 | |||||||
chrX:107107136 | A | G | 8 | a0001c0001t0013g0214 a0001c0001t0013g0215 a0001c0001t0013g0218 others(5): Show |
8 | HG02647.hp1 HG02809.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.595+6261T>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107107136 | |||||||
chrX:107107245 | T | C | 1 | a0001c0001t0051g0241 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.595+6152A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107107245 | |||||||
chrX:107107277 | T | A | 1 | a0001c0001t0047g0209 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.595+6120A>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107107277 | |||||||
chrX:107107450 | C | G | 1 | a0001c0001t0014g0211 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.595+5947G>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107107450 | |||||||
chrX:107107518 | C | T | 1 | a0001c0001t0001g0143 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.595+5879G>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107107518 | |||||||
chrX:107107617 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.595+5780C>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107107617 | |||||||
chrX:107107840 | G | A | 1 | a0001c0001t0002g0113 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.595+5557C>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107107840 | |||||||
chrX:107107919 | A | G | 102 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0012 others(99): Show |
119 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.595+5478T>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107107919 | |||||||
chrX:107107953 | A | G | 7 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0035 others(4): Show |
10 | HG00735.hp2 HG00741.hp2 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.595+5444T>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107107953 | |||||||
chrX:107108287 | C | T | 1 | a0001c0001t0004g0229 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.595+5110G>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107108287 | |||||||
chrX:107108326 | C | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0193 |
3 | HG00735.hp2 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.595+5071G>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107108326 | |||||||
chrX:107108448 | G | A | 10 | a0001c0001t0013g0214 a0001c0001t0013g0215 a0001c0001t0013g0218 others(7): Show |
10 | HG02027.hp1 HG02647.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.595+4949C>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107108448 | |||||||
chrX:107108619 | T | C | 1 | a0001c0001t0001g0035 | 2 | HG01361.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.595+4778A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107108619 | |||||||
chrX:107108887 | AC | A | 6 | a0001c0001t0009g0036 a0001c0001t0009g0183 a0001c0001t0009g0184 others(3): Show |
7 | HG00741.hp1 HG01071.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.595+4509delG | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107108887 | |||||||
chrX:107108959 | A | C | 1 | a0001c0001t0027g0205 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.595+4438T>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107108959 | |||||||
chrX:107109294 | C | A | 2 | a0001c0001t0006g0013 a0001c0001t0006g0114 |
3 | HG02630.hp2 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.595+4103G>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107109294 | |||||||
chrX:107109490 | T | C | 5 | a0001c0001t0017g0199 a0001c0001t0017g0200 a0001c0001t0018g0220 others(2): Show |
5 | HG02257.hp1 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.595+3907A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107109490 | |||||||
chrX:107109599 | A | AT | 1 | a0001c0001t0001g0017 | 2 | NA18943.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.595+3797dupA | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107109599 | |||||||
chrX:107110133 | C | T | 5 | a0001c0001t0017g0199 a0001c0001t0017g0200 a0001c0001t0018g0220 others(2): Show |
5 | HG02257.hp1 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.595+3264G>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107110133 | |||||||
chrX:107110143 | C | CA | 1 | a0001c0001t0001g0188 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.595+3253dupT | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107110143 | |||||||
chrX:107110143 | CA | C | 1 | a0001c0001t0001g0141 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.595+3253delT | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107110143 | |||||||
chrX:107110244 | T | C | 14 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0014 others(11): Show |
20 | HG00408.hp1 HG00438.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.595+3153A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107110244 | |||||||
chrX:107110313 | A | G | 10 | a0001c0001t0013g0214 a0001c0001t0013g0215 a0001c0001t0013g0218 others(7): Show |
10 | HG02027.hp1 HG02647.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.595+3084T>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107110313 | |||||||
chrX:107110567 | A | AT | 8 | a0001c0001t0001g0016 a0001c0001t0001g0135 a0001c0001t0001g0136 others(5): Show |
10 | HG00735.hp1 HG01256.hp1 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.595+2829dupA | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107110567 | |||||||
chrX:107110567 | A | G | 1 | a0001c0001t0006g0127 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.595+2830T>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107110567 | |||||||
chrX:107110678 | C | T | 1 | a0001c0001t0046g0134 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.595+2719G>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107110678 | |||||||
chrX:107110710 | A | G | 112 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0012 others(109): Show |
129 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.595+2687T>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107110710 | |||||||
chrX:107110766 | G | T | 1 | a0001c0001t0001g0133 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.595+2631C>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107110766 | |||||||
chrX:107111000 | T | C | 1 | a0001c0001t0005g0125 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.595+2397A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107111000 | |||||||
chrX:107111060 | C | T | 1 | a0001c0001t0029g0210 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.595+2337G>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107111060 | |||||||
chrX:107111082 | C | A | 4 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(1): Show |
4 | HG00558.hp1 HG01978.hp1 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.595+2315G>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107111082 | |||||||
chrX:107111133 | C | T | 1 | a0001c0001t0047g0209 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.595+2264G>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107111133 | |||||||
chrX:107111354 | C | T | 10 | a0001c0001t0013g0214 a0001c0001t0013g0215 a0001c0001t0013g0218 others(7): Show |
10 | HG02027.hp1 HG02647.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.595+2043G>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107111354 | |||||||
chrX:107112217 | C | T | 15 | a0001c0001t0004g0038 a0001c0001t0004g0229 a0001c0001t0004g0231 others(12): Show |
17 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.595+1180G>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107112217 | |||||||
chrX:107112307 | A | G | 122 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0012 others(119): Show |
139 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.595+1090T>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107112307 | |||||||
chrX:107112343 | C | G | 5 | a0001c0001t0017g0199 a0001c0001t0017g0200 a0001c0001t0018g0220 others(2): Show |
5 | HG02257.hp1 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.595+1054G>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107112343 | |||||||
chrX:107112416 | T | C | 122 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0012 others(119): Show |
139 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.595+981A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107112416 | |||||||
chrX:107112913 | T | C | 15 | a0001c0001t0004g0038 a0001c0001t0004g0229 a0001c0001t0004g0231 others(12): Show |
17 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.595+484A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107112913 | |||||||
chrX:107113049 | G | A | 1 | a0001c0001t0032g0126 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.595+348C>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107113049 | |||||||
chrX:107113244 | C | G | 1 | a0001c0001t0001g0132 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.595+153G>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 5/7 | chrX | 107113244 | |||||||
chrX:107113509 | A | T | 1 | a0001c0001t0002g0046 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.524-41T>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 4/7 | chrX | 107113509 | |||||||
chrX:107113619 | C | T | 1 | a0001c0001t0002g0045 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.524-151G>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 4/7 | chrX | 107113619 | |||||||
chrX:107113659 | T | C | 1 | a0001c0001t0006g0127 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.524-191A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 4/7 | chrX | 107113659 | |||||||
chrX:107113698 | T | TG | 4 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(1): Show |
4 | NA18955.hp1 NA18971.hp1 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.524-231dupC | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 4/7 | chrX | 107113698 | |||||||
chrX:107114318 | C | A | 1 | a0001c0001t0001g0193 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.524-850G>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 4/7 | chrX | 107114318 | |||||||
chrX:107114476 | A | G | 1 | a0001c0001t0002g0044 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.523+876T>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 4/7 | chrX | 107114476 | |||||||
chrX:107114558 | T | C | 14 | a0001c0001t0004g0038 a0001c0001t0004g0229 a0001c0001t0004g0231 others(11): Show |
15 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.523+794A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 4/7 | chrX | 107114558 | |||||||
chrX:107114593 | CTCT | C | 3 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0130 |
3 | HG00140.hp1 HG01175.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.523+756_523+758del others(3): Show |
RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 4/7 | chrX | 107114593 | |||||||
chrX:107114665 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.523+687G>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 4/7 | chrX | 107114665 | |||||||
chrX:107114872 | C | G | 3 | a0001c0001t0015g0202 a0001c0001t0015g0204 a0001c0001t0026g0203 |
3 | HG02886.hp1 HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.523+480G>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 4/7 | chrX | 107114872 | |||||||
chrX:107114959 | T | C | 15 | a0001c0001t0004g0038 a0001c0001t0004g0229 a0001c0001t0004g0231 others(12): Show |
17 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.523+393A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 4/7 | chrX | 107114959 | |||||||
chrX:107115110 | T | G | 1 | a0001c0001t0033g0228 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.523+242A>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 4/7 | chrX | 107115110 | |||||||
chrX:107115266 | C | CT | 1 | a0001c0001t0035g0227 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.523+85dupA | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 4/7 | chrX | 107115266 | |||||||
chrX:107115837 | C | CA | 2 | a0001c0001t0001g0194 a0001c0001t0001g0195 |
2 | HG01346.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.318+24dupT | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 3/7 | chrX | 107115837 | |||||||
chrX:107116133 | AG | A | 1 | a0001c0001t0035g0227 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.126-80delC | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 2/7 | chrX | 107116133 | |||||||
chrX:107116490 | TC | T | 1 | a0001c0001t0035g0227 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.125+159delG | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 2/7 | chrX | 107116490 | |||||||
chrX:107116785 | T | C | 15 | a0001c0001t0004g0038 a0001c0001t0004g0229 a0001c0001t0004g0231 others(12): Show |
17 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.9-19A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 1/7 | chrX | 107116785 | |||||||
chrX:107116798 | C | T | 10 | a0001c0001t0012g0201 a0001c0001t0012g0206 a0001c0001t0012g0208 others(7): Show |
10 | HG02109.hp2 HG02886.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.9-32G>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 1/7 | chrX | 107116798 | |||||||
chrX:107116827 | T | C | 3 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0198 |
3 | HG01346.hp1 HG02004.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.9-61A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 1/7 | chrX | 107116827 | |||||||
chrX:107116856 | C | A | 102 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0012 others(99): Show |
119 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.9-90G>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 1/7 | chrX | 107116856 | |||||||
chrX:107117026 | GAGA | G | 2 | a0001c0001t0002g0042 a0001c0001t0002g0043 |
2 | HG00558.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.9-263_9-261delTCT | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 1/7 | chrX | 107117026 | |||||||
chrX:107117211 | C | A | 142 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0012 others(139): Show |
161 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(158): Show |
intron_variant | MODIFIER | c.9-445G>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 1/7 | chrX | 107117211 | |||||||
chrX:107117216 | AAGG | A | 1 | a0001c0001t0002g0130 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.9-453_9-451delCCT | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 1/7 | chrX | 107117216 | |||||||
chrX:107117282 | A | C | 1 | a0001c0001t0012g0201 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.9-516T>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 1/7 | chrX | 107117282 | |||||||
chrX:107117575 | T | C | 122 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0012 others(119): Show |
139 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.9-809A>G | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 1/7 | chrX | 107117575 | |||||||
chrX:107117652 | G | T | 102 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0012 others(99): Show |
119 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.9-886C>A | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 1/7 | chrX | 107117652 | |||||||
chrX:107117718 | A | G | 1 | a0001c0001t0001g0041 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.9-952T>C | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 1/7 | chrX | 107117718 | |||||||
chrX:107117783 | TG | T | 1 | a0001c0001t0005g0040 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.8+982delC | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 1/7 | chrX | 107117783 | |||||||
chrX:107118208 | T | TC | 1 | a0001c0001t0001g0219 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.8+557dupG | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 1/7 | chrX | 107118208 | |||||||
chrX:107118230 | C | A | 3 | a0001c0001t0018g0220 a0001c0001t0018g0222 a0001c0001t0043g0221 |
3 | HG02257.hp1 HG02486.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.8+536G>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 1/7 | chrX | 107118230 | |||||||
chrX:107118367 | G | A | 4 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(1): Show |
4 | HG00558.hp1 HG01978.hp1 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.8+399C>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 1/7 | chrX | 107118367 | |||||||
chrX:107118518 | T | A | 1 | a0001c0001t0023g0039 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.8+248A>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 1/7 | chrX | 107118518 | |||||||
chrX:107118639 | T | TC | 1 | a0001c0001t0035g0227 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.8+126dupG | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 1/7 | chrX | 107118639 | |||||||
chrX:107118684 | C | A | 2 | a0001c0001t0023g0039 a0001c0001t0033g0228 |
2 | HG02922.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.8+82G>T | RBM41 | ENSG00000089682.17 | transcript | ENST00000685964.1 | protein_coding | 1/7 | chrX | 107118684 |