Links from Gene
Items: 1 to 20 of 1000
1.
rs1491587307 has merged into rs1159173741 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- TTTTTTTTTTT>-,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
[Show Flanks]
- Chromosome:
- 4:52789666
(GRCh38)
4:53655833
(GRCh37)
- Canonical SPDI:
- NC_000004.12:52789656:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000004.12:52789656:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000004.12:52789656:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000004.12:52789656:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000004.12:52789656:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000004.12:52789656:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000004.12:52789656:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000004.12:52789656:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:52789656:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:52789656:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:52789656:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:52789656:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:52789656:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:52789656:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:52789656:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:52789656:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:52789656:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- Gene:
- LINC01618 (Varview)
- Functional Consequence:
- upstream_transcript_variant,2KB_upstream_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TTTTTTTTTTTTTTT=0./0
(
ALFA)
- HGVS:
NC_000004.12:g.52789666_52789676del, NC_000004.12:g.52789672_52789676del, NC_000004.12:g.52789673_52789676del, NC_000004.12:g.52789674_52789676del, NC_000004.12:g.52789675_52789676del, NC_000004.12:g.52789676del, NC_000004.12:g.52789676dup, NC_000004.12:g.52789675_52789676dup, NC_000004.12:g.52789674_52789676dup, NC_000004.12:g.52789673_52789676dup, NC_000004.12:g.52789672_52789676dup, NC_000004.12:g.52789671_52789676dup, NC_000004.12:g.52789670_52789676dup, NC_000004.12:g.52789669_52789676dup, NC_000004.12:g.52789668_52789676dup, NC_000004.12:g.52789665_52789676dup, NC_000004.12:g.52789676_52789677insTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.53655833_53655843del, NC_000004.11:g.53655839_53655843del, NC_000004.11:g.53655840_53655843del, NC_000004.11:g.53655841_53655843del, NC_000004.11:g.53655842_53655843del, NC_000004.11:g.53655843del, NC_000004.11:g.53655843dup, NC_000004.11:g.53655842_53655843dup, NC_000004.11:g.53655841_53655843dup, NC_000004.11:g.53655840_53655843dup, NC_000004.11:g.53655839_53655843dup, NC_000004.11:g.53655838_53655843dup, NC_000004.11:g.53655837_53655843dup, NC_000004.11:g.53655836_53655843dup, NC_000004.11:g.53655835_53655843dup, NC_000004.11:g.53655832_53655843dup, NC_000004.11:g.53655843_53655844insTTTTTTTTTTTTTTTTTTTTTTT
3.
rs1491500901 has merged into rs869285095 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- T>-,TT
[Show Flanks]
- Chromosome:
- 4:52794002
(GRCh38)
4:53660169
(GRCh37)
- Canonical SPDI:
- NC_000004.12:52794001:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000004.12:52794001:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT
- Gene:
- LINC01618 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TTTTTTTTTTTTTTTT=0./0
(
ALFA)
- HGVS:
4.
rs1491483072 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- ->CT
[Show Flanks]
- Chromosome:
- 4:52811271
(GRCh38)
4:53677439
(GRCh37)
- Canonical SPDI:
- NC_000004.12:52811271:T:TCT
- Gene:
- LINC01618 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa
- MAF:
TCT=0./0
(
ALFA)
TC=0.00002/1
(GnomAD)
- HGVS:
5.
rs1491412903 has merged into rs993411297 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- TTTTTTTTTTT>-,TT,TTT,TTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT
[Show Flanks]
- Chromosome:
- 4:52811282
(GRCh38)
4:53677449
(GRCh37)
- Canonical SPDI:
- NC_000004.12:52811270:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000004.12:52811270:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000004.12:52811270:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000004.12:52811270:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000004.12:52811270:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000004.12:52811270:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000004.12:52811270:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000004.12:52811270:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000004.12:52811270:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:52811270:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:52811270:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:52811270:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:52811270:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:52811270:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:52811270:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:52811270:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:52811270:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:52811270:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:52811270:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:52811270:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- Gene:
- LINC01618 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TTTTTTTTTTTTT=0./0
(
ALFA)
- HGVS:
NC_000004.12:g.52811282_52811292del, NC_000004.12:g.52811284_52811292del, NC_000004.12:g.52811285_52811292del, NC_000004.12:g.52811287_52811292del, NC_000004.12:g.52811289_52811292del, NC_000004.12:g.52811290_52811292del, NC_000004.12:g.52811291_52811292del, NC_000004.12:g.52811292del, NC_000004.12:g.52811292dup, NC_000004.12:g.52811291_52811292dup, NC_000004.12:g.52811290_52811292dup, NC_000004.12:g.52811289_52811292dup, NC_000004.12:g.52811288_52811292dup, NC_000004.12:g.52811287_52811292dup, NC_000004.12:g.52811286_52811292dup, NC_000004.12:g.52811285_52811292dup, NC_000004.12:g.52811284_52811292dup, NC_000004.12:g.52811283_52811292dup, NC_000004.12:g.52811282_52811292dup, NC_000004.12:g.52811280_52811292dup, NC_000004.11:g.53677449_53677459del, NC_000004.11:g.53677451_53677459del, NC_000004.11:g.53677452_53677459del, NC_000004.11:g.53677454_53677459del, NC_000004.11:g.53677456_53677459del, NC_000004.11:g.53677457_53677459del, NC_000004.11:g.53677458_53677459del, NC_000004.11:g.53677459del, NC_000004.11:g.53677459dup, NC_000004.11:g.53677458_53677459dup, NC_000004.11:g.53677457_53677459dup, NC_000004.11:g.53677456_53677459dup, NC_000004.11:g.53677455_53677459dup, NC_000004.11:g.53677454_53677459dup, NC_000004.11:g.53677453_53677459dup, NC_000004.11:g.53677452_53677459dup, NC_000004.11:g.53677451_53677459dup, NC_000004.11:g.53677450_53677459dup, NC_000004.11:g.53677449_53677459dup, NC_000004.11:g.53677447_53677459dup
6.
rs1491369565 [Homo sapiens]- Variant type:
- DEL
- Alleles:
- GG>-
[Show Flanks]
- Chromosome:
- 4:52794000
(GRCh38)
4:53660167
(GRCh37)
- Canonical SPDI:
- NC_000004.12:52793999:GG:
- Gene:
- LINC01618 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
-=0./0
(
ALFA)
-=0.0755/291
(ALSPAC)
-=0.0925/343
(TWINSUK)
- HGVS:
7.
rs1491154202 has merged into rs1273423998 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- AAAAA>-,A,AA,AAA,AAAA,AAAAAA,AAAAAAA,AAAAAAAA
[Show Flanks]
- Chromosome:
- 4:52811053
(GRCh38)
4:53677220
(GRCh37)
- Canonical SPDI:
- NC_000004.12:52811037:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000004.12:52811037:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000004.12:52811037:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000004.12:52811037:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000004.12:52811037:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000004.12:52811037:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000004.12:52811037:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:52811037:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA
- Gene:
- LINC01618 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
AAAAAAAAAAAAAAAAA=0./0
(
ALFA)
- HGVS:
NC_000004.12:g.52811053_52811057del, NC_000004.12:g.52811054_52811057del, NC_000004.12:g.52811055_52811057del, NC_000004.12:g.52811056_52811057del, NC_000004.12:g.52811057del, NC_000004.12:g.52811057dup, NC_000004.12:g.52811056_52811057dup, NC_000004.12:g.52811055_52811057dup, NC_000004.11:g.53677220_53677224del, NC_000004.11:g.53677221_53677224del, NC_000004.11:g.53677222_53677224del, NC_000004.11:g.53677223_53677224del, NC_000004.11:g.53677224del, NC_000004.11:g.53677224dup, NC_000004.11:g.53677223_53677224dup, NC_000004.11:g.53677222_53677224dup
8.
rs1491118538 has merged into rs200504067 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- ACACACACACACACACACAC>-,ACACACACAC,ACACACACACAC,ACACACACACACAC,ACACACACACACACAC,ACACACACACACACACAC,ACACACACACACACACACACAC,ACACACACACACACACACACACAC,ACACACACACACACACACACACACAC,ACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACACACAC
[Show Flanks]
- Chromosome:
- 4:52788881
(GRCh38)
4:53655048
(GRCh37)
- Canonical SPDI:
- NC_000004.12:52788875:CACACACACACACACACACACACAC:CACAC,NC_000004.12:52788875:CACACACACACACACACACACACAC:CACACACACACACAC,NC_000004.12:52788875:CACACACACACACACACACACACAC:CACACACACACACACAC,NC_000004.12:52788875:CACACACACACACACACACACACAC:CACACACACACACACACAC,NC_000004.12:52788875:CACACACACACACACACACACACAC:CACACACACACACACACACAC,NC_000004.12:52788875:CACACACACACACACACACACACAC:CACACACACACACACACACACAC,NC_000004.12:52788875:CACACACACACACACACACACACAC:CACACACACACACACACACACACACAC,NC_000004.12:52788875:CACACACACACACACACACACACAC:CACACACACACACACACACACACACACAC,NC_000004.12:52788875:CACACACACACACACACACACACAC:CACACACACACACACACACACACACACACAC,NC_000004.12:52788875:CACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACAC,NC_000004.12:52788875:CACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACAC,NC_000004.12:52788875:CACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACAC,NC_000004.12:52788875:CACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACAC
- Gene:
- LINC01618 (Varview)
- Functional Consequence:
- upstream_transcript_variant,2KB_upstream_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
CACACACACACACAC=0./0
(
ALFA)
-=0.000366/97
(TOPMED)
- HGVS:
NC_000004.12:g.52788877AC[2], NC_000004.12:g.52788877AC[7], NC_000004.12:g.52788877AC[8], NC_000004.12:g.52788877AC[9], NC_000004.12:g.52788877AC[10], NC_000004.12:g.52788877AC[11], NC_000004.12:g.52788877AC[13], NC_000004.12:g.52788877AC[14], NC_000004.12:g.52788877AC[15], NC_000004.12:g.52788877AC[16], NC_000004.12:g.52788877AC[17], NC_000004.12:g.52788877AC[18], NC_000004.12:g.52788877AC[19], NC_000004.11:g.53655044AC[2], NC_000004.11:g.53655044AC[7], NC_000004.11:g.53655044AC[8], NC_000004.11:g.53655044AC[9], NC_000004.11:g.53655044AC[10], NC_000004.11:g.53655044AC[11], NC_000004.11:g.53655044AC[13], NC_000004.11:g.53655044AC[14], NC_000004.11:g.53655044AC[15], NC_000004.11:g.53655044AC[16], NC_000004.11:g.53655044AC[17], NC_000004.11:g.53655044AC[18], NC_000004.11:g.53655044AC[19]
9.
rs1491087486 has merged into rs199641575 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- ACACACAC>-,AC,ACAC,ACACAC,ACACACACAC,ACACACACACAC,ACACACACACACAC,ACACACACACACACAC
[Show Flanks]
- Chromosome:
- 4:52797374
(GRCh38)
4:53663541
(GRCh37)
- Canonical SPDI:
- NC_000004.12:52797363:ACACACACACACACACAC:ACACACACAC,NC_000004.12:52797363:ACACACACACACACACAC:ACACACACACAC,NC_000004.12:52797363:ACACACACACACACACAC:ACACACACACACAC,NC_000004.12:52797363:ACACACACACACACACAC:ACACACACACACACAC,NC_000004.12:52797363:ACACACACACACACACAC:ACACACACACACACACACAC,NC_000004.12:52797363:ACACACACACACACACAC:ACACACACACACACACACACAC,NC_000004.12:52797363:ACACACACACACACACAC:ACACACACACACACACACACACAC,NC_000004.12:52797363:ACACACACACACACACAC:ACACACACACACACACACACACACAC
- Gene:
- LINC01618 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
ACACACACACAC=0./0
(
ALFA)
AC=0.00601/6
(GoNL)
AC=0.07308/366
(1000Genomes)
- HGVS:
NC_000004.12:g.52797364AC[5], NC_000004.12:g.52797364AC[6], NC_000004.12:g.52797364AC[7], NC_000004.12:g.52797364AC[8], NC_000004.12:g.52797364AC[10], NC_000004.12:g.52797364AC[11], NC_000004.12:g.52797364AC[12], NC_000004.12:g.52797364AC[13], NC_000004.11:g.53663531AC[5], NC_000004.11:g.53663531AC[6], NC_000004.11:g.53663531AC[7], NC_000004.11:g.53663531AC[8], NC_000004.11:g.53663531AC[10], NC_000004.11:g.53663531AC[11], NC_000004.11:g.53663531AC[12], NC_000004.11:g.53663531AC[13]
10.
rs1491016141 [Homo sapiens]- Variant type:
- INS
- Alleles:
- ->G
[Show Flanks]
- Chromosome:
- 4:52809252
(GRCh38)
4:53675420
(GRCh37)
- Canonical SPDI:
- NC_000004.12:52809252::G
- Gene:
- LINC01618 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency
- MAF:
G=0.000036/5
(GnomAD)
- HGVS:
12.
rs1490703098 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>A
[Show Flanks]
- Chromosome:
- 4:52788640
(GRCh38)
4:53654807
(GRCh37)
- Canonical SPDI:
- NC_000004.12:52788639:T:A
- Gene:
- LINC01618 (Varview)
- Functional Consequence:
- upstream_transcript_variant,2KB_upstream_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
A=0./0
(
ALFA)
A=0.000004/1
(TOPMED)
A=0.000007/1
(GnomAD)
- HGVS:
13.
rs1490659402 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- A>G
[Show Flanks]
- Chromosome:
- 4:52792782
(GRCh38)
4:53658949
(GRCh37)
- Canonical SPDI:
- NC_000004.12:52792781:A:G
- Gene:
- LINC01618 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
G=0./0
(
ALFA)
G=0.000004/1
(TOPMED)
G=0.000007/1
(GnomAD)
G=0.000248/4
(TOMMO)
G=0.000342/1
(KOREAN)
G=0.001092/2
(Korea1K)
- HGVS:
14.
rs1490643769 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>C
[Show Flanks]
- Chromosome:
- 4:52794919
(GRCh38)
4:53661086
(GRCh37)
- Canonical SPDI:
- NC_000004.12:52794918:T:C
- Gene:
- LINC01618 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
C=0.000071/1
(
ALFA)
C=0.000019/5
(TOPMED)
C=0.000021/3
(GnomAD)
- HGVS:
15.
rs1490413897 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- AA>-
[Show Flanks]
- Chromosome:
- 4:52795599
(GRCh38)
4:53661766
(GRCh37)
- Canonical SPDI:
- NC_000004.12:52795597:AAA:A
- Gene:
- LINC01618 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
A=0.000169/2
(
ALFA)
-=0.000534/64
(GnomAD)
-=0.001534/25
(TOMMO)
- HGVS:
16.
rs1490368422 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>A
[Show Flanks]
- Chromosome:
- 4:52795874
(GRCh38)
4:53662041
(GRCh37)
- Canonical SPDI:
- NC_000004.12:52795873:G:A
- Gene:
- LINC01618 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
A=0./0
(
ALFA)
A=0.000007/1
(GnomAD)
A=0.000008/2
(TOPMED)
- HGVS:
17.
rs1490329738 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- A>C,G
[Show Flanks]
- Chromosome:
- 4:52790511
(GRCh38)
4:53656678
(GRCh37)
- Canonical SPDI:
- NC_000004.12:52790510:A:C,NC_000004.12:52790510:A:G
- Gene:
- LINC01618 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa
- MAF:
G=0./0
(
ALFA)
C=0.000007/1
(GnomAD)
- HGVS:
18.
rs1490315462 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- A>G
[Show Flanks]
- Chromosome:
- 4:52793066
(GRCh38)
4:53659233
(GRCh37)
- Canonical SPDI:
- NC_000004.12:52793065:A:G
- Gene:
- LINC01618 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa
- MAF:
G=0./0
(
ALFA)
G=0.000007/1
(GnomAD)
- HGVS:
19.
rs1489947077 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>G
[Show Flanks]
- Chromosome:
- 4:52805070
(GRCh38)
4:53671237
(GRCh37)
- Canonical SPDI:
- NC_000004.12:52805069:T:G
- Gene:
- LINC01618 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa
- MAF:
G=0./0
(
ALFA)
G=0.000004/1
(TOPMED)
- HGVS:
20.
rs1489943496 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- A>C,G
[Show Flanks]
- Chromosome:
- 4:52810875
(GRCh38)
4:53677042
(GRCh37)
- Canonical SPDI:
- NC_000004.12:52810874:A:C,NC_000004.12:52810874:A:G
- Gene:
- LINC01618 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
G=0./0
(
ALFA)
G=0.000034/9
(TOPMED)
G=0.000043/6
(GnomAD)
- HGVS: