Links from Nucleotide
Items: 1 to 20 of 345
1.
rs1486413463 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- A>G
[Show Flanks]
- Chromosome:
- X:107895436
(GRCh38)
X:107138666
(GRCh37)
- Canonical SPDI:
- NC_000023.11:107895435:A:G
- Gene:
- MID2 (Varview), LOC101928335 (Varview)
- Functional Consequence:
- intron_variant,non_coding_transcript_variant
- Validated:
- by frequency,by alfa
- MAF:
G=0./0
(
ALFA)
G=0.00001/1
(GnomAD)
- HGVS:
3.
rs1481703198 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>C
[Show Flanks]
- Chromosome:
- X:107894809
(GRCh38)
X:107138039
(GRCh37)
- Canonical SPDI:
- NC_000023.11:107894808:T:C
- Gene:
- MID2 (Varview), LOC101928335 (Varview)
- Functional Consequence:
- intron_variant,non_coding_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
C=0./0
(
ALFA)
C=0.000008/2
(TOPMED)
C=0.000021/2
(GnomAD)
C=0.000416/2
(1000Genomes)
- HGVS:
4.
rs1479871903 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>C
[Show Flanks]
- Chromosome:
- X:107895245
(GRCh38)
X:107138475
(GRCh37)
- Canonical SPDI:
- NC_000023.11:107895244:T:C
- Gene:
- MID2 (Varview), LOC101928335 (Varview)
- Functional Consequence:
- intron_variant,non_coding_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
C=0.000142/2
(
ALFA)
C=0.000039/4
(GnomAD)
C=0.000053/14
(TOPMED)
- HGVS:
5.
rs1479741398 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>A
[Show Flanks]
- Chromosome:
- X:107895576
(GRCh38)
X:107138806
(GRCh37)
- Canonical SPDI:
- NC_000023.11:107895575:G:A
- Gene:
- MID2 (Varview), LOC101928335 (Varview)
- Functional Consequence:
- intron_variant,non_coding_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
A=0./0
(
ALFA)
A=0.000004/1
(TOPMED)
A=0.00001/1
(GnomAD)
A=0.000342/1
(KOREAN)
A=0.00108/14
(TOMMO)
- HGVS:
7.
rs1473463743 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>C
[Show Flanks]
- Chromosome:
- X:107895733
(GRCh38)
X:107138963
(GRCh37)
- Canonical SPDI:
- NC_000023.11:107895732:T:C
- Gene:
- MID2 (Varview), LOC101928335 (Varview)
- Functional Consequence:
- non_coding_transcript_variant,intron_variant
- Validated:
- by frequency,by alfa
- MAF:
C=0./0
(
ALFA)
C=0.000008/2
(TOPMED)
- HGVS:
10.
rs1467853252 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- A>T
[Show Flanks]
- Chromosome:
- X:107935836
(GRCh38)
X:107179066
(GRCh37)
- Canonical SPDI:
- NC_000023.11:107935835:A:T
- Gene:
- LOC101928335 (Varview)
- Functional Consequence:
- non_coding_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
T=0./0
(
ALFA)
T=0.000008/2
(TOPMED)
T=0.00001/1
(GnomAD)
- HGVS:
11.
rs1466390615 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>G,T
[Show Flanks]
- Chromosome:
- X:107896144
(GRCh38)
X:107139374
(GRCh37)
- Canonical SPDI:
- NC_000023.11:107896143:C:G,NC_000023.11:107896143:C:T
- Gene:
- MID2 (Varview), LOC101928335 (Varview)
- Functional Consequence:
- non_coding_transcript_variant,intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
T=0./0
(
ALFA)
T=0.000019/2
(GnomAD)
C=0.5/1
(SGDP_PRJ)
- HGVS:
12.
rs1465090088 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>T
[Show Flanks]
- Chromosome:
- X:107894604
(GRCh38)
X:107137834
(GRCh37)
- Canonical SPDI:
- NC_000023.11:107894603:C:T
- Gene:
- MID2 (Varview), LOC101928335 (Varview)
- Functional Consequence:
- non_coding_transcript_variant,intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
T=0.000184/3
(
ALFA)
T=0.000004/1
(TOPMED)
- HGVS:
13.
rs1464368505 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- A>G
[Show Flanks]
- Chromosome:
- X:107894927
(GRCh38)
X:107138157
(GRCh37)
- Canonical SPDI:
- NC_000023.11:107894926:A:G
- Gene:
- MID2 (Varview), LOC101928335 (Varview)
- Functional Consequence:
- non_coding_transcript_variant,intron_variant
- Validated:
- by frequency
- MAF:
G=0.00001/1
(GnomAD)
- HGVS:
14.
rs1463157528 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>A
[Show Flanks]
- Chromosome:
- X:107894712
(GRCh38)
X:107137942
(GRCh37)
- Canonical SPDI:
- NC_000023.11:107894711:G:A
- Gene:
- MID2 (Varview), LOC101928335 (Varview)
- Functional Consequence:
- non_coding_transcript_variant,intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
A=0./0
(
ALFA)
A=0.000004/1
(TOPMED)
A=0.00001/1
(GnomAD)
- HGVS:
15.
rs1460913749 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>G
[Show Flanks]
- Chromosome:
- X:107895426
(GRCh38)
X:107138656
(GRCh37)
- Canonical SPDI:
- NC_000023.11:107895425:T:G
- Gene:
- MID2 (Varview), LOC101928335 (Varview)
- Functional Consequence:
- non_coding_transcript_variant,intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
G=0./0
(
ALFA)
G=0.000029/3
(GnomAD)
G=0.000045/12
(TOPMED)
- HGVS:
16.
rs1459572653 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>T
[Show Flanks]
- Chromosome:
- X:107896174
(GRCh38)
X:107139404
(GRCh37)
- Canonical SPDI:
- NC_000023.11:107896173:C:T
- Gene:
- MID2 (Varview), LOC101928335 (Varview)
- Functional Consequence:
- non_coding_transcript_variant,intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
T=0./0
(
ALFA)
T=0.000008/2
(TOPMED)
T=0.00001/1
(GnomAD)
- HGVS:
17.
rs1458957928 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>G
[Show Flanks]
- Chromosome:
- X:107895932
(GRCh38)
X:107139162
(GRCh37)
- Canonical SPDI:
- NC_000023.11:107895931:C:G
- Gene:
- MID2 (Varview), LOC101928335 (Varview)
- Functional Consequence:
- non_coding_transcript_variant,intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
G=0./0
(
ALFA)
G=0.000004/1
(TOPMED)
G=0.00001/1
(GnomAD)
- HGVS:
18.
rs1454495647 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>C
[Show Flanks]
- Chromosome:
- X:107933108
(GRCh38)
X:107176338
(GRCh37)
- Canonical SPDI:
- NC_000023.11:107933107:T:C
- Gene:
- LOC101928335 (Varview)
- Functional Consequence:
- non_coding_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
C=0./0
(
ALFA)
C=0.000004/1
(TOPMED)
C=0.00001/1
(GnomAD)
- HGVS:
19.
rs1453527981 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>A
[Show Flanks]
- Chromosome:
- X:107894920
(GRCh38)
X:107138150
(GRCh37)
- Canonical SPDI:
- NC_000023.11:107894919:G:A
- Gene:
- MID2 (Varview), LOC101928335 (Varview)
- Functional Consequence:
- intron_variant,non_coding_transcript_variant
- Validated:
- by frequency,by alfa
- MAF:
A=0./0
(
ALFA)
A=0.000008/2
(TOPMED)
- HGVS:
20.
rs1452200235 has merged into rs1160011458 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- TGTGTGTGTGTGTGTGTG>-,TG,TGTG,TGTGTG,TGTGTGTG,TGTGTGTGTG,TGTGTGTGTGTG,TGTGTGTGTGTGTG,TGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG
[Show Flanks]
- Chromosome:
- X:107894848
(GRCh38)
X:107138078
(GRCh37)
- Canonical SPDI:
- NC_000023.11:107894828:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTG,NC_000023.11:107894828:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTG,NC_000023.11:107894828:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTG,NC_000023.11:107894828:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTG,NC_000023.11:107894828:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000023.11:107894828:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000023.11:107894828:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000023.11:107894828:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000023.11:107894828:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000023.11:107894828:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000023.11:107894828:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000023.11:107894828:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000023.11:107894828:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000023.11:107894828:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000023.11:107894828:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000023.11:107894828:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000023.11:107894828:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000023.11:107894828:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG
- Gene:
- MID2 (Varview), LOC101928335 (Varview)
- Functional Consequence:
- intron_variant,non_coding_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
GTGTGTGTGTGTGTGTGTGTG=0./0
(
ALFA)
- HGVS:
NC_000023.11:g.107894830TG[9], NC_000023.11:g.107894830TG[10], NC_000023.11:g.107894830TG[11], NC_000023.11:g.107894830TG[12], NC_000023.11:g.107894830TG[13], NC_000023.11:g.107894830TG[14], NC_000023.11:g.107894830TG[15], NC_000023.11:g.107894830TG[16], NC_000023.11:g.107894830TG[17], NC_000023.11:g.107894830TG[19], NC_000023.11:g.107894830TG[20], NC_000023.11:g.107894830TG[21], NC_000023.11:g.107894830TG[22], NC_000023.11:g.107894830TG[23], NC_000023.11:g.107894830TG[24], NC_000023.11:g.107894830TG[25], NC_000023.11:g.107894830TG[26], NC_000023.11:g.107894830TG[29], NC_000023.10:g.107138060TG[9], NC_000023.10:g.107138060TG[10], NC_000023.10:g.107138060TG[11], NC_000023.10:g.107138060TG[12], NC_000023.10:g.107138060TG[13], NC_000023.10:g.107138060TG[14], NC_000023.10:g.107138060TG[15], NC_000023.10:g.107138060TG[16], NC_000023.10:g.107138060TG[17], NC_000023.10:g.107138060TG[19], NC_000023.10:g.107138060TG[20], NC_000023.10:g.107138060TG[21], NC_000023.10:g.107138060TG[22], NC_000023.10:g.107138060TG[23], NC_000023.10:g.107138060TG[24], NC_000023.10:g.107138060TG[25], NC_000023.10:g.107138060TG[26], NC_000023.10:g.107138060TG[29], NG_011907.2:g.73977TG[9], NG_011907.2:g.73977TG[10], NG_011907.2:g.73977TG[11], NG_011907.2:g.73977TG[12], NG_011907.2:g.73977TG[13], NG_011907.2:g.73977TG[14], NG_011907.2:g.73977TG[15], NG_011907.2:g.73977TG[16], NG_011907.2:g.73977TG[17], NG_011907.2:g.73977TG[19], NG_011907.2:g.73977TG[20], NG_011907.2:g.73977TG[21], NG_011907.2:g.73977TG[22], NG_011907.2:g.73977TG[23], NG_011907.2:g.73977TG[24], NG_011907.2:g.73977TG[25], NG_011907.2:g.73977TG[26], NG_011907.2:g.73977TG[29], NR_110395.1:n.1823AC[9], NR_110395.1:n.1823AC[10], NR_110395.1:n.1823AC[11], NR_110395.1:n.1823AC[12], NR_110395.1:n.1823AC[13], NR_110395.1:n.1823AC[14], NR_110395.1:n.1823AC[15], NR_110395.1:n.1823AC[16], NR_110395.1:n.1823AC[17], NR_110395.1:n.1823AC[19], NR_110395.1:n.1823AC[20], NR_110395.1:n.1823AC[21], NR_110395.1:n.1823AC[22], NR_110395.1:n.1823AC[23], NR_110395.1:n.1823AC[24], NR_110395.1:n.1823AC[25], NR_110395.1:n.1823AC[26], NR_110395.1:n.1823AC[29]