regionname | pos | ref | alt | annotation | impact | samples | ahapids | achapids | acthapids | actghapids | ac | an | af | len | 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 | external |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGEF5_chr7_144350402_144385632 | 144381975 | CAAAA | C | downstream_gene_variant | MODIFIER | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(39): Show |
a0004a0006a0007others(4): Show | a0004c0003a0006c0005a0007c0007others(6): Show | a0004c0003t0001a0006c0005t0001a0007c0007t0003others(6): Show | a0004c0003t0001g0002a0004c0003t0001g0040a0004c0003t0001g0041others(22): Show | 42 | 288 | 0.1458 | -4 | c.*19 others(15): Show |
ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1344 | chr7 | TogoVar | ||||||
ARHGEF6_chrX_136660550_136785932 | 136662059 | TCTAA | T | downstream_gene_variant | MODIFIER | HG02683.hp1 HG03669.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0068a0001c0001t0001g0178 | 2 | 247 | 0.0081 | -4 | c.*59 others(15): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 3490 | chrX | TogoVar | ||||||
ARHGEF6_chrX_136660550_136785932 | 136667894 | GAAGA | G | 3_prime_UTR_variant | MODIFIER | HG03209.hp1 | a0001 | a0001c0001 | a0001c0001t0009 | a0001c0001t0009g0064 | 1 | 247 | 0.0041 | -4 | c.*13 others(13): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 22/22 | 131 | chrX | TogoVar | |||||
ARHGEF6_chrX_136660550_136785932 | 136681469 | ATTTG | A | intron_variant | MODIFIER | NA19076.hp1 | a0006 | a0006c0008 | a0006c0008t0001 | a0006c0008t0001g0124 | 1 | 247 | 0.0041 | -4 | c.155 others(21): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 14/21 | chrX | TogoVar | ||||||
ARHGEF6_chrX_136660550_136785932 | 136686535 | TTGCC | T | intron_variant | MODIFIER | NA18949.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0214 | 1 | 247 | 0.0041 | -4 | c.124 others(21): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | TogoVar | ||||||
ARHGEF6_chrX_136660550_136785932 | 136686619 | TATAC | T | intron_variant | MODIFIER | HG02738.hp1 HG03041.hp2 NA18940.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0062a0001c0001t0001g0085a0001c0001t0001g0228 | 3 | 247 | 0.0122 | -4 | c.124 others(21): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | TogoVar | ||||||
ARHGEF6_chrX_136660550_136785932 | 136686625 | CATAT | C | intron_variant | MODIFIER | NA18983.hp2 NA18985.hp1 |
a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0150a0001c0001t0005g0151 | 2 | 247 | 0.0081 | -4 | c.124 others(21): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | TogoVar | ||||||
ARHGEF6_chrX_136660550_136785932 | 136686639 | TATAC | T | intron_variant | MODIFIER | HG03540.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0003 | 1 | 247 | 0.0041 | -4 | c.124 others(21): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | TogoVar | ||||||
ARHGEF6_chrX_136660550_136785932 | 136686705 | TATAC | T | intron_variant | MODIFIER | HG02970.hp2 homoSapiens_chm13v2.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0033a0001c0001t0001g0242 | 2 | 247 | 0.0081 | -4 | c.124 others(21): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | TogoVar | ||||||
ARHGEF6_chrX_136660550_136785932 | 136686709 | CATAT | C | intron_variant | MODIFIER | HG00423.hp1 HG01168.hp2 HG01243.hp1 others(9): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0087others(9): Show | 12 | 247 | 0.0486 | -4 | c.124 others(21): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | TogoVar | ||||||
ARHGEF6_chrX_136660550_136785932 | 136691333 | TGAAG | T | intron_variant | MODIFIER | NA18949.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0214 | 1 | 247 | 0.0041 | -4 | c.104 others(21): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | TogoVar | ||||||
ARHGEF6_chrX_136660550_136785932 | 136691376 | GAAAA | G | intron_variant | MODIFIER | NA18949.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0214 | 1 | 247 | 0.0041 | -4 | c.104 others(21): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | TogoVar | ||||||
ARHGEF6_chrX_136660550_136785932 | 136693114 | ATGAC | A | intron_variant | MODIFIER | NA19058.hp1 | a0001 | a0001c0001 | a0001c0001t0011 | a0001c0001t0011g0174 | 1 | 247 | 0.0041 | -4 | c.104 others(23): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | TogoVar | ||||||
ARHGEF6_chrX_136660550_136785932 | 136710330 | CATAT | C | intron_variant | MODIFIER | HG02970.hp2 NA20805.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004 | a0001c0001t0001g0242a0001c0001t0004g0042 | 2 | 247 | 0.0081 | -4 | c.828 others(21): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 7/21 | chrX | TogoVar | ||||||
ARHGEF6_chrX_136660550_136785932 | 136727325 | TTTTC | T | intron_variant | MODIFIER | HG00639.hp2 HG01346.hp2 HG02559.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0016 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0001t0001g0031others(3): Show | 6 | 247 | 0.0243 | -4 | c.732 others(21): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | TogoVar | ||||||
ARHGEF6_chrX_136660550_136785932 | 136727411 | CTCTT | C | intron_variant | MODIFIER | NA19006.hp1 NA20129.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0101a0001c0001t0001g0162 | 2 | 247 | 0.0081 | -4 | c.732 others(21): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | TogoVar | ||||||
ARHGEF6_chrX_136660550_136785932 | 136727458 | CTTCT | C | intron_variant | MODIFIER | HG01981.hp2 HG01993.hp1 HG02004.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0073a0001c0001t0001g0085a0001c0001t0001g0153others(1): Show | 4 | 247 | 0.0162 | -4 | c.732 others(21): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | TogoVar | ||||||
ARHGEF6_chrX_136660550_136785932 | 136727503 | TCCTC | T | intron_variant | MODIFIER | NA18986.hp1 NA19012.hp1 NA19068.hp1 others(1): Show |
a0001a0006 | a0001c0001a0006c0008 | a0001c0001t0001a0006c0008t0001 | a0001c0001t0001g0009a0001c0001t0001g0209a0001c0001t0001g0210others(1): Show | 4 | 247 | 0.0162 | -4 | c.732 others(21): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | TogoVar | ||||||
ARHGEF6_chrX_136660550_136785932 | 136729000 | TTCTC | T | intron_variant | MODIFIER | HG01346.hp1 HG01928.hp1 HG02015.hp1 others(32): Show |
a0001a0006 | a0001c0001a0001c0002a0006c0008 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(5): Show | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(32): Show | 35 | 247 | 0.1417 | -4 | c.732 others(21): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | TogoVar | ||||||
ARHGEF6_chrX_136660550_136785932 | 136736618 | GGTGT | G | intron_variant | MODIFIER | HG01168.hp1 NA19030.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004 | a0001c0001t0001g0045a0001c0001t0004g0229 | 2 | 247 | 0.0081 | -4 | c.662 others(21): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | TogoVar | ||||||
ARHGEF6_chrX_136660550_136785932 | 136750971 | TTTTG | T | intron_variant | MODIFIER | HG02080.hp1 HG02886.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0012a0001c0001t0002g0207 | 2 | 247 | 0.0081 | -4 | c.250 others(21): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | TogoVar | ||||||
ARHGEF6_chrX_136660550_136785932 | 136758031 | CTTTT | C | intron_variant | MODIFIER | HG01952.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0239 | 1 | 247 | 0.0041 | -4 | c.250 others(23): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | TogoVar | ||||||
ARHGEF6_chrX_136660550_136785932 | 136776878 | GATAA | G | intron_variant | MODIFIER | HG01496.hp2 HG02071.hp1 HG02559.hp1 others(8): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0007a0001c0001t0014others(1): Show | a0001c0001t0001g0031a0001c0001t0001g0053a0001c0001t0001g0054others(8): Show | 11 | 247 | 0.0445 | -4 | c.249 others(21): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | TogoVar | ||||||
ARHGEF7_chr13_111110310_111310732 | 111111922 | CAGAG | C | upstream_gene_variant | MODIFIER | HG02280.hp2 HG02647.hp2 HG02895.hp2 others(5): Show |
a0001 | a0001c0001a0001c0012 | a0001c0001t0001a0001c0001t0008a0001c0001t0011others(3): Show | a0001c0001t0001g0074a0001c0001t0008g0073a0001c0001t0011g0070others(5): Show | 8 | 274 | 0.0292 | -4 | c.-36 others(15): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 3387 | chr13 | TogoVar | ||||||
ARHGEF7_chr13_111110310_111310732 | 111117727 | CTCCT | C | intron_variant | MODIFIER | HG02280.hp1 HG02280.hp2 HG02647.hp2 others(14): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0012others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(9): Show | a0001c0001t0001g0068a0001c0001t0001g0074a0001c0001t0002g0078others(14): Show | 17 | 274 | 0.0620 | -4 | c.165 others(21): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
ARHGEF7_chr13_111110310_111310732 | 111123492 | CACAT | C | intron_variant | MODIFIER | HG02280.hp2 HG02647.hp2 HG02895.hp2 others(6): Show |
a0001 | a0001c0001a0001c0012 | a0001c0001t0001a0001c0001t0008a0001c0001t0011others(4): Show | a0001c0001t0001g0074a0001c0001t0008g0073a0001c0001t0011g0070others(6): Show | 9 | 274 | 0.0329 | -4 | c.165 others(21): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
ARHGEF7_chr13_111110310_111310732 | 111133763 | TTATA | T | intron_variant | MODIFIER | HG01243.hp2 HG02572.hp2 HG03130.hp2 others(9): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0008others(4): Show | a0001c0001t0001g0019a0001c0001t0001g0027a0001c0001t0001g0056others(9): Show | 12 | 274 | 0.0438 | -4 | c.165 others(23): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
ARHGEF7_chr13_111110310_111310732 | 111134637 | GTTGT | G | intron_variant | MODIFIER | HG02257.hp2 HG03486.hp2 |
a0001a0007 | a0001c0001a0007c0010 | a0001c0001t0005a0007c0010t0001 | a0001c0001t0005g0062a0007c0010t0001g0095 | 2 | 274 | 0.0073 | -4 | c.165 others(23): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
ARHGEF7_chr13_111110310_111310732 | 111152180 | GAATT | G | intron_variant | MODIFIER | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(53): Show |
a0001a0003a0006others(1): Show | a0001c0001a0001c0002a0003c0011others(2): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(13): Show | a0001c0001t0001g0106a0001c0001t0001g0129a0001c0001t0001g0137others(53): Show | 56 | 274 | 0.2044 | -4 | c.166 others(21): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
ARHGEF7_chr13_111110310_111310732 | 111155914 | TAAAC | T | intron_variant | MODIFIER | HG00140.hp1 HG01099.hp1 HG01891.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0107a0001c0001t0003g0136a0001c0001t0003g0178others(4): Show | 7 | 274 | 0.0256 | -4 | c.252 others(21): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
ARHGEF7_chr13_111110310_111310732 | 111156080 | CAAAA | C | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(147): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0002a0001c0003others(12): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(40): Show | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0048others(147): Show | 150 | 274 | 0.5475 | -4 | c.252 others(21): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
ARHGEF7_chr13_111110310_111310732 | 111164061 | ATTAT | A | intron_variant | MODIFIER | HG00642.hp1 HG00741.hp1 HG01081.hp1 others(43): Show |
a0001a0004 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(13): Show | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0066others(43): Show | 46 | 274 | 0.1679 | -4 | c.252 others(23): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
ARHGEF7_chr13_111110310_111310732 | 111185961 | CGTGT | C | intron_variant | MODIFIER | HG00597.hp1 HG00642.hp2 HG02015.hp2 others(12): Show |
a0001a0007 | a0001c0001a0001c0004a0001c0012others(3): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(6): Show | a0001c0001t0002g0029a0001c0001t0002g0156a0001c0001t0003g0088others(12): Show | 15 | 274 | 0.0547 | -4 | c.253 others(23): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
ARHGEF7_chr13_111110310_111310732 | 111186384 | GAAAT | G | intron_variant | MODIFIER | HG00140.hp1 HG00597.hp1 HG00738.hp1 others(25): Show |
a0001 | a0001c0001a0001c0004a0001c0007others(1): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(7): Show | a0001c0001t0002g0029a0001c0001t0002g0156a0001c0001t0003g0087others(25): Show | 28 | 274 | 0.1022 | -4 | c.253 others(23): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
ARHGEF7_chr13_111110310_111310732 | 111192881 | AACAC | A | intron_variant | MODIFIER | HG03486.hp1 HG03579.hp1 |
a0002 | a0002c0009 | a0002c0009t0002 | a0002c0009t0002g0069a0002c0009t0002g0112 | 2 | 274 | 0.0073 | -4 | c.253 others(23): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
ARHGEF7_chr13_111110310_111310732 | 111214860 | AATAG | A | intron_variant | MODIFIER | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(73): Show |
a0001a0002a0006 | a0001c0001a0001c0002a0001c0006others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(20): Show | a0001c0001t0001g0129a0001c0001t0001g0137a0001c0001t0001g0144others(73): Show | 76 | 274 | 0.2774 | -4 | c.469 others(21): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
ARHGEF7_chr13_111110310_111310732 | 111220044 | GGCCT | G | intron_variant | MODIFIER | HG01243.hp2 HG02572.hp2 HG02818.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0018others(2): Show | 5 | 274 | 0.0183 | -4 | c.670 others(21): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
ARHGEF7_chr13_111110310_111310732 | 111220944 | TGTTA | T | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(102): Show |
a0001a0004a0005others(1): Show | a0001c0001a0001c0004a0001c0007others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(20): Show | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(102): Show | 105 | 274 | 0.3832 | -4 | c.670 others(21): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
ARHGEF7_chr13_111110310_111310732 | 111221297 | ATGTC | A | intron_variant | MODIFIER | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(5): Show |
a0001 | a0001c0001a0001c0016 | a0001c0001t0001a0001c0001t0007a0001c0001t0008others(1): Show | a0001c0001t0001g0084a0001c0001t0007g0094a0001c0001t0008g0003others(5): Show | 8 | 274 | 0.0292 | -4 | c.670 others(21): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
ARHGEF7_chr13_111110310_111310732 | 111221488 | TAGAC | T | intron_variant | MODIFIER | HG01891.hp2 HG02145.hp1 HG02572.hp1 others(5): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(1): Show | a0001c0001t0002g0029a0001c0001t0002g0156a0001c0001t0003g0107others(5): Show | 8 | 274 | 0.0292 | -4 | c.670 others(21): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
ARHGEF7_chr13_111110310_111310732 | 111221529 | ATATC | A | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(50): Show |
a0001 | a0001c0001a0001c0008a0001c0013 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(6): Show | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(50): Show | 53 | 274 | 0.1934 | -4 | c.670 others(21): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
ARHGEF7_chr13_111110310_111310732 | 111263402 | CTTAA | C | intron_variant | MODIFIER | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
a0001 | a0001c0001a0001c0016 | a0001c0001t0007a0001c0001t0008a0001c0016t0008 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | 274 | 0.0256 | -4 | c.951 others(21): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
ARHGEF7_chr13_111110310_111310732 | 111267924 | TAGTA | T | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00597.hp1 others(36): Show |
a0001a0004a0005 | a0001c0001a0001c0004a0001c0012others(2): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(8): Show | a0001c0001t0002g0029a0001c0001t0002g0156a0001c0001t0003g0087others(36): Show | 39 | 274 | 0.1423 | -4 | c.107 others(21): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
ARHGEF7_chr13_111110310_111310732 | 111281181 | CTTTT | C | intron_variant | MODIFIER | HG01109.hp1 HG02809.hp1 HG02818.hp2 others(7): Show |
a0001 | a0001c0001a0001c0016 | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(2): Show | a0001c0001t0001g0144a0001c0001t0002g0011a0001c0001t0007g0094others(7): Show | 10 | 274 | 0.0365 | -4 | c.172 others(21): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
ARHGEF9_chrX_63629967_63790214 | 63637846 | CTGTG | C | 3_prime_UTR_variant | MODIFIER | HG00738.hp1 HG01243.hp1 HG02055.hp1 others(15): Show |
a0001a0003 | a0001c0001a0003c0003 | a0001c0001t0003a0001c0001t0005a0001c0001t0020others(2): Show | a0001c0001t0003g0041a0001c0001t0003g0043a0001c0001t0003g0072others(15): Show | 18 | 168 | 0.1071 | -4 | c.*17 others(13): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 10/10 | 178 | chrX | TogoVar | |||||
ARHGEF9_chrX_63629967_63790214 | 63641380 | AAGAC | A | intron_variant | MODIFIER | HG02723.hp1 NA19240.hp2 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0019 | a0001c0001t0002g0037a0001c0001t0019g0034 | 2 | 168 | 0.0119 | -4 | c.139 others(23): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | TogoVar | ||||||
ARHGEF9_chrX_63629967_63790214 | 63653546 | GTTAC | G | intron_variant | MODIFIER | HG04115.hp1 | a0001 | a0001c0001 | a0001c0001t0010 | a0001c0001t0010g0080 | 1 | 168 | 0.0060 | -4 | c.132 others(23): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | TogoVar | ||||||
ARHGEF9_chrX_63629967_63790214 | 63661758 | TTCTC | T | intron_variant | MODIFIER | HG03486.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0024 | 1 | 168 | 0.0060 | -4 | c.107 others(23): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | TogoVar | ||||||
ARHGEF9_chrX_63629967_63790214 | 63666326 | CCTCT | C | intron_variant | MODIFIER | NA18940.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0053 | 1 | 168 | 0.0060 | -4 | c.946 others(19): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | TogoVar | ||||||
ARHGEF9_chrX_63629967_63790214 | 63666453 | TACAC | T | intron_variant | MODIFIER | HG00735.hp1 HG02647.hp1 HG02723.hp2 |
a0001 | a0001c0001 | a0001c0001t0008a0001c0001t0017 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0017g0003 | 3 | 168 | 0.0179 | -4 | c.946 others(19): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | TogoVar |