SNP Links for Gene (Select 22925) - SNP

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Select item 14915794641.

rs1491579464 [Homo sapiens]

Variant type:: DEL
Alleles:: TA>- [Show Flanks]
Chromosome:: 2:159948639 (GRCh38)
2:160805150 (GRCh37)
Canonical SPDI:: NC_000002.12:159948638:TA:
Gene:: PLA2R1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000002.12:g.159948639_159948640del, NC_000002.11:g.160805150_160805151del

Select item 14915569592.

rs1491556959 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->A,AA [Show Flanks]
Chromosome:: 2:159948639 (GRCh38)
2:160805151 (GRCh37)
Canonical SPDI:: NC_000002.12:159948639:AA:AAA,NC_000002.12:159948639:AA:AAAA
Gene:: PLA2R1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAA=0.00062/10 (ALFA)
A=0.00011/3 (TOMMO)
A=0.00234/10 (Estonian)
HGVS:: NC_000002.12:g.159948641dup, NC_000002.12:g.159948640_159948641dup, NC_000002.11:g.160805152dup, NC_000002.11:g.160805151_160805152dup

Select item 14915551223.

rs1491555122 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CA [Show Flanks]
Chromosome:: 2:159929873 (GRCh38)
2:160786385 (GRCh37)
Canonical SPDI:: NC_000002.12:159929873:A:ACA
Gene:: PLA2R1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant,3_prime_UTR_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: ACA=0./0 (ALFA)
HGVS:: NC_000002.12:g.159929874_159929875insCA, NC_000002.11:g.160786385_160786386insCA, XM_005246392.5:c.*2811_*2812insGT, XM_005246392.3:c.*2811_*2812insGT, XR_922892.4:n.7486_7487insGT, XR_922892.2:n.7374_7375insGT, XM_011510820.4:c.*2457_*2458insGT, XM_011510820.2:c.*2457_*2458insGT, XR_001738671.3:n.8123_8124insGT, XR_001738671.1:n.8011_8012insGT, XR_001738672.3:n.7605_7606insGT, XR_001738672.1:n.7493_7494insGT, XR_007071492.1:n.14883_14884insGT, XR_007071493.1:n.14164_14165insGT, XR_007071494.1:n.13898_13899insGT, XM_047443730.1:c.*2811_*2812insGT, XR_007071491.1:n.7251_7252insGT

Select item 14915531874.

rs1491553187 has merged into rs1205003993 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTT>-,TT,TTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 2:160048848 (GRCh38)
2:160905359 (GRCh37)
Canonical SPDI:: NC_000002.12:160048838:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000002.12:160048838:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000002.12:160048838:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000002.12:160048838:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000002.12:160048838:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000002.12:160048838:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000002.12:160048838:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000002.12:160048838:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000002.12:160048838:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:160048838:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:160048838:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:160048838:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: PLA2R1 (Varview), LOC105373717 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTT=0./0 (ALFA)
HGVS:: NC_000002.12:g.160048848_160048858del, NC_000002.12:g.160048850_160048858del, NC_000002.12:g.160048853_160048858del, NC_000002.12:g.160048855_160048858del, NC_000002.12:g.160048856_160048858del, NC_000002.12:g.160048857_160048858del, NC_000002.12:g.160048858del, NC_000002.12:g.160048858dup, NC_000002.12:g.160048857_160048858dup, NC_000002.12:g.160048856_160048858dup, NC_000002.12:g.160048855_160048858dup, NC_000002.12:g.160048854_160048858dup, NC_000002.11:g.160905359_160905369del, NC_000002.11:g.160905361_160905369del, NC_000002.11:g.160905364_160905369del, NC_000002.11:g.160905366_160905369del, NC_000002.11:g.160905367_160905369del, NC_000002.11:g.160905368_160905369del, NC_000002.11:g.160905369del, NC_000002.11:g.160905369dup, NC_000002.11:g.160905368_160905369dup, NC_000002.11:g.160905367_160905369dup, NC_000002.11:g.160905366_160905369dup, NC_000002.11:g.160905365_160905369dup

Select item 14915518825.

rs1491551882 [Homo sapiens]

Variant type:: DEL
Alleles:: TC>- [Show Flanks]
Chromosome:: 2:159983468 (GRCh38)
2:160839979 (GRCh37)
Canonical SPDI:: NC_000002.12:159983467:TC:
Gene:: PLA2R1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000002.12:g.159983468_159983469del, NC_000002.11:g.160839979_160839980del

Select item 14914684446.

rs1491468444 has merged into rs80154749 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAA>-,A,AA,AAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAAAAAAA [Show Flanks]
Chromosome:: 2:159988168 (GRCh38)
2:160844679 (GRCh37)
Canonical SPDI:: NC_000002.12:159988156:AAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000002.12:159988156:AAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000002.12:159988156:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000002.12:159988156:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000002.12:159988156:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000002.12:159988156:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000002.12:159988156:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000002.12:159988156:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA
Gene:: PLA2R1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAAAAA=0./0 (ALFA)
AAA=0.1617/810 (1000Genomes)
HGVS:: NC_000002.12:g.159988168_159988171del, NC_000002.12:g.159988169_159988171del, NC_000002.12:g.159988170_159988171del, NC_000002.12:g.159988171del, NC_000002.12:g.159988171dup, NC_000002.12:g.159988170_159988171dup, NC_000002.12:g.159988169_159988171dup, NC_000002.12:g.159988163_159988171dup, NC_000002.11:g.160844679_160844682del, NC_000002.11:g.160844680_160844682del, NC_000002.11:g.160844681_160844682del, NC_000002.11:g.160844682del, NC_000002.11:g.160844682dup, NC_000002.11:g.160844681_160844682dup, NC_000002.11:g.160844680_160844682dup, NC_000002.11:g.160844674_160844682dup

Select item 14914168767.

rs1491416876 [Homo sapiens]

Variant type:: DEL
Alleles:: AT>- [Show Flanks]
Chromosome:: 2:160048838 (GRCh38)
2:160905349 (GRCh37)
Canonical SPDI:: NC_000002.12:160048837:AT:
Gene:: PLA2R1 (Varview), LOC105373717 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.000015/2 (GnomAD)
HGVS:: NC_000002.12:g.160048838_160048839del, NC_000002.11:g.160905349_160905350del

Select item 14914035788.

rs1491403578 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 2:160025588 (GRCh38)
2:160882099 (GRCh37)
Canonical SPDI:: NC_000002.12:160025587:CA:
Gene:: PLA2R1 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: -=0.00017/2 (ALFA)
HGVS:: NC_000002.12:g.160025588_160025589del, NC_000002.11:g.160882099_160882100del

Select item 14913446989.

rs1491344698 has merged into rs1023098586 [Homo sapiens]

Variant type:: DELINS
Alleles:: CA>-,CACA,CACACACACACACACA [Show Flanks]
Chromosome:: 2:159971503 (GRCh38)
2:160828014 (GRCh37)
Canonical SPDI:: NC_000002.12:159971489:ACACACACACACACA:ACACACACACACA,NC_000002.12:159971489:ACACACACACACACA:ACACACACACACACACA,NC_000002.12:159971489:ACACACACACACACA:ACACACACACACACACACACACACACACA
Gene:: PLA2R1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ACACACACACACACACA=0./0 (ALFA)
ACACACACACACAC=0.00006/1 (TOMMO)
HGVS:: NC_000002.12:g.159971491CA[6], NC_000002.12:g.159971491CA[8], NC_000002.12:g.159971491CA[14], NC_000002.11:g.160828002CA[6], NC_000002.11:g.160828002CA[8], NC_000002.11:g.160828002CA[14]

Select item 149131158710.

rs1491311587 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->C [Show Flanks]
Chromosome:: 2:159943818 (GRCh38)
2:160800330 (GRCh37)
Canonical SPDI:: NC_000002.12:159943818:C:CC
Gene:: PLA2R1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: CC=0./0 (ALFA)
HGVS:: NC_000002.12:g.159943819dup, NC_000002.11:g.160800330dup

Select item 149130029911.

rs1491300299 has merged into rs56240008 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTTT>-,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 2:159935956 (GRCh38)
2:160792467 (GRCh37)
Canonical SPDI:: NC_000002.12:159935945:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000002.12:159935945:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000002.12:159935945:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000002.12:159935945:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000002.12:159935945:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000002.12:159935945:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000002.12:159935945:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000002.12:159935945:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000002.12:159935945:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000002.12:159935945:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000002.12:159935945:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:159935945:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:159935945:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:159935945:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:159935945:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:159935945:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:159935945:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:159935945:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:159935945:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:159935945:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:159935945:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:159935945:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:159935945:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:159935945:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:159935945:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:159935945:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:159935945:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:159935945:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:159935945:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:159935945:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:159935945:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:159935945:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:159935945:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:159935945:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:159935945:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:159935945:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:159935945:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:159935945:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:159935945:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:159935945:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:159935945:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:159935945:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:159935945:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:159935945:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:159935945:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:159935945:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:159935945:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:159935945:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:159935945:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:159935945:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:159935945:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:159935945:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:159935945:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:159935945:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:159935945:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:159935945:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:159935945:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:159935945:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:159935945:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:159935945:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:159935945:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:159935945:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: PLA2R1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant,3_prime_UTR_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTT=0./0 (ALFA)
HGVS:: NC_000002.12:g.159935956_159935969del, NC_000002.12:g.159935959_159935969del, NC_000002.12:g.159935960_159935969del, NC_000002.12:g.159935961_159935969del, NC_000002.12:g.159935962_159935969del, NC_000002.12:g.159935963_159935969del, NC_000002.12:g.159935964_159935969del, NC_000002.12:g.159935965_159935969del, NC_000002.12:g.159935966_159935969del, NC_000002.12:g.159935967_159935969del, NC_000002.12:g.159935968_159935969del, NC_000002.12:g.159935969del, NC_000002.12:g.159935969dup, NC_000002.12:g.159935968_159935969dup, NC_000002.12:g.159935967_159935969dup, NC_000002.12:g.159935966_159935969dup, NC_000002.12:g.159935965_159935969dup, NC_000002.12:g.159935964_159935969dup, NC_000002.12:g.159935963_159935969dup, NC_000002.12:g.159935962_159935969dup, NC_000002.12:g.159935961_159935969dup, NC_000002.12:g.159935960_159935969dup, NC_000002.12:g.159935959_159935969dup, NC_000002.12:g.159935958_159935969dup, NC_000002.12:g.159935957_159935969dup, NC_000002.12:g.159935956_159935969dup, NC_000002.12:g.159935955_159935969dup, NC_000002.12:g.159935954_159935969dup, NC_000002.12:g.159935953_159935969dup, NC_000002.12:g.159935952_159935969dup, NC_000002.12:g.159935951_159935969dup, NC_000002.12:g.159935950_159935969dup, NC_000002.12:g.159935949_159935969dup, NC_000002.12:g.159935948_159935969dup, NC_000002.12:g.159935947_159935969dup, NC_000002.12:g.159935946_159935969dup, NC_000002.12:g.159935969_159935970insTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.12:g.159935969_159935970insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.12:g.159935969_159935970insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.12:g.159935969_159935970insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.12:g.159935969_159935970insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.12:g.159935969_159935970insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.12:g.159935969_159935970insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.12:g.159935969_159935970insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.12:g.159935969_159935970insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.12:g.159935969_159935970insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.12:g.159935969_159935970insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.12:g.159935969_159935970insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.12:g.159935969_159935970insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.12:g.159935969_159935970insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.12:g.159935969_159935970insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.12:g.159935969_159935970insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.12:g.159935969_159935970insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.12:g.159935969_159935970insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.12:g.159935969_159935970insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.12:g.159935969_159935970insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.12:g.159935969_159935970insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.12:g.159935969_159935970insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.12:g.159935969_159935970insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.12:g.159935969_159935970insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.12:g.159935969_159935970insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.12:g.159935969_159935970insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.160792467_160792480del, NC_000002.11:g.160792470_160792480del, NC_000002.11:g.160792471_160792480del, NC_000002.11:g.160792472_160792480del, NC_000002.11:g.160792473_160792480del, NC_000002.11:g.160792474_160792480del, NC_000002.11:g.160792475_160792480del, NC_000002.11:g.160792476_160792480del, NC_000002.11:g.160792477_160792480del, NC_000002.11:g.160792478_160792480del, NC_000002.11:g.160792479_160792480del, NC_000002.11:g.160792480del, NC_000002.11:g.160792480dup, NC_000002.11:g.160792479_160792480dup, NC_000002.11:g.160792478_160792480dup, NC_000002.11:g.160792477_160792480dup, NC_000002.11:g.160792476_160792480dup, NC_000002.11:g.160792475_160792480dup, NC_000002.11:g.160792474_160792480dup, NC_000002.11:g.160792473_160792480dup, NC_000002.11:g.160792472_160792480dup, NC_000002.11:g.160792471_160792480dup, NC_000002.11:g.160792470_160792480dup, NC_000002.11:g.160792469_160792480dup, NC_000002.11:g.160792468_160792480dup, NC_000002.11:g.160792467_160792480dup, NC_000002.11:g.160792466_160792480dup, NC_000002.11:g.160792465_160792480dup, NC_000002.11:g.160792464_160792480dup, NC_000002.11:g.160792463_160792480dup, NC_000002.11:g.160792462_160792480dup, NC_000002.11:g.160792461_160792480dup, NC_000002.11:g.160792460_160792480dup, NC_000002.11:g.160792459_160792480dup, NC_000002.11:g.160792458_160792480dup, NC_000002.11:g.160792457_160792480dup, NC_000002.11:g.160792480_160792481insTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.160792480_160792481insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.160792480_160792481insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.160792480_160792481insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.160792480_160792481insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.160792480_160792481insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.160792480_160792481insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.160792480_160792481insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.160792480_160792481insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.160792480_160792481insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.160792480_160792481insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.160792480_160792481insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.160792480_160792481insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.160792480_160792481insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.160792480_160792481insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.160792480_160792481insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.160792480_160792481insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.160792480_160792481insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.160792480_160792481insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.160792480_160792481insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.160792480_160792481insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.160792480_160792481insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.160792480_160792481insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.160792480_160792481insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.160792480_160792481insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.160792480_160792481insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_007366.5:c.*5819_*5832del, NM_007366.5:c.*5822_*5832del, NM_007366.5:c.*5823_*5832del, NM_007366.5:c.*5824_*5832del, NM_007366.5:c.*5825_*5832del, NM_007366.5:c.*5826_*5832del, NM_007366.5:c.*5827_*5832del, NM_007366.5:c.*5828_*5832del, NM_007366.5:c.*5829_*5832del, NM_007366.5:c.*5830_*5832del, NM_007366.5:c.*5831_*5832del, NM_007366.5:c.*5832del, NM_007366.5:c.*5832dup, NM_007366.5:c.*5831_*5832dup, NM_007366.5:c.*5830_*5832dup, NM_007366.5:c.*5829_*5832dup, NM_007366.5:c.*5828_*5832dup, NM_007366.5:c.*5827_*5832dup, NM_007366.5:c.*5826_*5832dup, NM_007366.5:c.*5825_*5832dup, NM_007366.5:c.*5824_*5832dup, NM_007366.5:c.*5823_*5832dup, NM_007366.5:c.*5822_*5832dup, NM_007366.5:c.*5821_*5832dup, NM_007366.5:c.*5820_*5832dup, NM_007366.5:c.*5819_*5832dup, NM_007366.5:c.*5818_*5832dup, NM_007366.5:c.*5817_*5832dup, NM_007366.5:c.*5816_*5832dup, NM_007366.5:c.*5815_*5832dup, NM_007366.5:c.*5814_*5832dup, NM_007366.5:c.*5813_*5832dup, NM_007366.5:c.*5812_*5832dup, NM_007366.5:c.*5811_*5832dup, NM_007366.5:c.*5810_*5832dup, NM_007366.5:c.*5809_*5832dup, NM_007366.5:c.*5832_*5833insAAAAAAAAAAAAAAAAAAAAAAAAA, NM_007366.5:c.*5832_*5833insAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_007366.5:c.*5832_*5833insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_007366.5:c.*5832_*5833insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_007366.5:c.*5832_*5833insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_007366.5:c.*5832_*5833insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_007366.5:c.*5832_*5833insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_007366.5:c.*5832_*5833insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_007366.5:c.*5832_*5833insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_007366.5:c.*5832_*5833insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_007366.5:c.*5832_*5833insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_007366.5:c.*5832_*5833insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_007366.5:c.*5832_*5833insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_007366.5:c.*5832_*5833insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_007366.5:c.*5832_*5833insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_007366.5:c.*5832_*5833insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_007366.5:c.*5832_*5833insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_007366.5:c.*5832_*5833insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_007366.5:c.*5832_*5833insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_007366.5:c.*5832_*5833insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_007366.5:c.*5832_*5833insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_007366.5:c.*5832_*5833insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_007366.5:c.*5832_*5833insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_007366.5:c.*5832_*5833insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_007366.5:c.*5832_*5833insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_007366.5:c.*5832_*5833insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_001195641.2:c.*5819_*5832del, NM_001195641.2:c.*5822_*5832del, NM_001195641.2:c.*5823_*5832del, NM_001195641.2:c.*5824_*5832del, NM_001195641.2:c.*5825_*5832del, NM_001195641.2:c.*5826_*5832del, NM_001195641.2:c.*5827_*5832del, NM_001195641.2:c.*5828_*5832del, NM_001195641.2:c.*5829_*5832del, NM_001195641.2:c.*5830_*5832del, NM_001195641.2:c.*5831_*5832del, NM_001195641.2:c.*5832del, NM_001195641.2:c.*5832dup, NM_001195641.2:c.*5831_*5832dup, NM_001195641.2:c.*5830_*5832dup, NM_001195641.2:c.*5829_*5832dup, NM_001195641.2:c.*5828_*5832dup, NM_001195641.2:c.*5827_*5832dup, NM_001195641.2:c.*5826_*5832dup, NM_001195641.2:c.*5825_*5832dup, NM_001195641.2:c.*5824_*5832dup, NM_001195641.2:c.*5823_*5832dup, NM_001195641.2:c.*5822_*5832dup, NM_001195641.2:c.*5821_*5832dup, NM_001195641.2:c.*5820_*5832dup, NM_001195641.2:c.*5819_*5832dup, NM_001195641.2:c.*5818_*5832dup, NM_001195641.2:c.*5817_*5832dup, NM_001195641.2:c.*5816_*5832dup, NM_001195641.2:c.*5815_*5832dup, NM_001195641.2:c.*5814_*5832dup, NM_001195641.2:c.*5813_*5832dup, NM_001195641.2:c.*5812_*5832dup, NM_001195641.2:c.*5811_*5832dup, NM_001195641.2:c.*5810_*5832dup, NM_001195641.2:c.*5809_*5832dup, NM_001195641.2:c.*5832_*5833insAAAAAAAAAAAAAAAAAAAAAAAAA, NM_001195641.2:c.*5832_*5833insAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_001195641.2:c.*5832_*5833insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_001195641.2:c.*5832_*5833insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_001195641.2:c.*5832_*5833insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_001195641.2:c.*5832_*5833insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_001195641.2:c.*5832_*5833insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_001195641.2:c.*5832_*5833insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_001195641.2:c.*5832_*5833insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_001195641.2:c.*5832_*5833insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_001195641.2:c.*5832_*5833insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_001195641.2:c.*5832_*5833insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_001195641.2:c.*5832_*5833insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_001195641.2:c.*5832_*5833insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_001195641.2:c.*5832_*5833insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_001195641.2:c.*5832_*5833insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_001195641.2:c.*5832_*5833insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_001195641.2:c.*5832_*5833insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_001195641.2:c.*5832_*5833insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_001195641.2:c.*5832_*5833insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_001195641.2:c.*5832_*5833insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_001195641.2:c.*5832_*5833insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_001195641.2:c.*5832_*5833insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_001195641.2:c.*5832_*5833insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_001195641.2:c.*5832_*5833insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_001195641.2:c.*5832_*5833insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071492.1:n.9245_9258del, XR_007071492.1:n.9248_9258del, XR_007071492.1:n.9249_9258del, XR_007071492.1:n.9250_9258del, XR_007071492.1:n.9251_9258del, XR_007071492.1:n.9252_9258del, XR_007071492.1:n.9253_9258del, XR_007071492.1:n.9254_9258del, XR_007071492.1:n.9255_9258del, XR_007071492.1:n.9256_9258del, XR_007071492.1:n.9257_9258del, XR_007071492.1:n.9258del, XR_007071492.1:n.9258dup, XR_007071492.1:n.9257_9258dup, XR_007071492.1:n.9256_9258dup, XR_007071492.1:n.9255_9258dup, XR_007071492.1:n.9254_9258dup, XR_007071492.1:n.9253_9258dup, XR_007071492.1:n.9252_9258dup, XR_007071492.1:n.9251_9258dup, XR_007071492.1:n.9250_9258dup, XR_007071492.1:n.9249_9258dup, XR_007071492.1:n.9248_9258dup, XR_007071492.1:n.9247_9258dup, XR_007071492.1:n.9246_9258dup, XR_007071492.1:n.9245_9258dup, XR_007071492.1:n.9244_9258dup, XR_007071492.1:n.9243_9258dup, XR_007071492.1:n.9242_9258dup, XR_007071492.1:n.9241_9258dup, XR_007071492.1:n.9240_9258dup, XR_007071492.1:n.9239_9258dup, XR_007071492.1:n.9238_9258dup, XR_007071492.1:n.9237_9258dup, XR_007071492.1:n.9236_9258dup, XR_007071492.1:n.9235_9258dup, XR_007071492.1:n.9258_9259insAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071492.1:n.9258_9259insAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071492.1:n.9258_9259insAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071492.1:n.9258_9259insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071492.1:n.9258_9259insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071492.1:n.9258_9259insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071492.1:n.9258_9259insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071492.1:n.9258_9259insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071492.1:n.9258_9259insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071492.1:n.9258_9259insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071492.1:n.9258_9259insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071492.1:n.9258_9259insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071492.1:n.9258_9259insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071492.1:n.9258_9259insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071492.1:n.9258_9259insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071492.1:n.9258_9259insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071492.1:n.9258_9259insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071492.1:n.9258_9259insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071492.1:n.9258_9259insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071492.1:n.9258_9259insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071492.1:n.9258_9259insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071492.1:n.9258_9259insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071492.1:n.9258_9259insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071492.1:n.9258_9259insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071492.1:n.9258_9259insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071492.1:n.9258_9259insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071493.1:n.8526_8539del, XR_007071493.1:n.8529_8539del, XR_007071493.1:n.8530_8539del, XR_007071493.1:n.8531_8539del, XR_007071493.1:n.8532_8539del, XR_007071493.1:n.8533_8539del, XR_007071493.1:n.8534_8539del, XR_007071493.1:n.8535_8539del, XR_007071493.1:n.8536_8539del, XR_007071493.1:n.8537_8539del, XR_007071493.1:n.8538_8539del, XR_007071493.1:n.8539del, XR_007071493.1:n.8539dup, XR_007071493.1:n.8538_8539dup, XR_007071493.1:n.8537_8539dup, XR_007071493.1:n.8536_8539dup, XR_007071493.1:n.8535_8539dup, XR_007071493.1:n.8534_8539dup, XR_007071493.1:n.8533_8539dup, XR_007071493.1:n.8532_8539dup, XR_007071493.1:n.8531_8539dup, XR_007071493.1:n.8530_8539dup, XR_007071493.1:n.8529_8539dup, XR_007071493.1:n.8528_8539dup, XR_007071493.1:n.8527_8539dup, XR_007071493.1:n.8526_8539dup, XR_007071493.1:n.8525_8539dup, XR_007071493.1:n.8524_8539dup, XR_007071493.1:n.8523_8539dup, XR_007071493.1:n.8522_8539dup, XR_007071493.1:n.8521_8539dup, XR_007071493.1:n.8520_8539dup, XR_007071493.1:n.8519_8539dup, XR_007071493.1:n.8518_8539dup, XR_007071493.1:n.8517_8539dup, XR_007071493.1:n.8516_8539dup, XR_007071493.1:n.8539_8540insAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071493.1:n.8539_8540insAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071493.1:n.8539_8540insAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071493.1:n.8539_8540insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071493.1:n.8539_8540insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071493.1:n.8539_8540insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071493.1:n.8539_8540insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071493.1:n.8539_8540insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071493.1:n.8539_8540insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071493.1:n.8539_8540insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071493.1:n.8539_8540insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071493.1:n.8539_8540insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071493.1:n.8539_8540insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071493.1:n.8539_8540insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071493.1:n.8539_8540insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071493.1:n.8539_8540insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071493.1:n.8539_8540insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071493.1:n.8539_8540insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071493.1:n.8539_8540insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071493.1:n.8539_8540insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071493.1:n.8539_8540insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071493.1:n.8539_8540insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071493.1:n.8539_8540insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071493.1:n.8539_8540insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071493.1:n.8539_8540insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071493.1:n.8539_8540insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071494.1:n.8260_8273del, XR_007071494.1:n.8263_8273del, XR_007071494.1:n.8264_8273del, XR_007071494.1:n.8265_8273del, XR_007071494.1:n.8266_8273del, XR_007071494.1:n.8267_8273del, XR_007071494.1:n.8268_8273del, XR_007071494.1:n.8269_8273del, XR_007071494.1:n.8270_8273del, XR_007071494.1:n.8271_8273del, XR_007071494.1:n.8272_8273del, XR_007071494.1:n.8273del, XR_007071494.1:n.8273dup, XR_007071494.1:n.8272_8273dup, XR_007071494.1:n.8271_8273dup, XR_007071494.1:n.8270_8273dup, XR_007071494.1:n.8269_8273dup, XR_007071494.1:n.8268_8273dup, XR_007071494.1:n.8267_8273dup, XR_007071494.1:n.8266_8273dup, XR_007071494.1:n.8265_8273dup, XR_007071494.1:n.8264_8273dup, XR_007071494.1:n.8263_8273dup, XR_007071494.1:n.8262_8273dup, XR_007071494.1:n.8261_8273dup, XR_007071494.1:n.8260_8273dup, XR_007071494.1:n.8259_8273dup, XR_007071494.1:n.8258_8273dup, XR_007071494.1:n.8257_8273dup, XR_007071494.1:n.8256_8273dup, XR_007071494.1:n.8255_8273dup, XR_007071494.1:n.8254_8273dup, XR_007071494.1:n.8253_8273dup, XR_007071494.1:n.8252_8273dup, XR_007071494.1:n.8251_8273dup, XR_007071494.1:n.8250_8273dup, XR_007071494.1:n.8273_8274insAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071494.1:n.8273_8274insAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071494.1:n.8273_8274insAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071494.1:n.8273_8274insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071494.1:n.8273_8274insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071494.1:n.8273_8274insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071494.1:n.8273_8274insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071494.1:n.8273_8274insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071494.1:n.8273_8274insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071494.1:n.8273_8274insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071494.1:n.8273_8274insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071494.1:n.8273_8274insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071494.1:n.8273_8274insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071494.1:n.8273_8274insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071494.1:n.8273_8274insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071494.1:n.8273_8274insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071494.1:n.8273_8274insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071494.1:n.8273_8274insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071494.1:n.8273_8274insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071494.1:n.8273_8274insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071494.1:n.8273_8274insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071494.1:n.8273_8274insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071494.1:n.8273_8274insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071494.1:n.8273_8274insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071494.1:n.8273_8274insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XR_007071494.1:n.8273_8274insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Select item 149129641612.

rs1491296416 [Homo sapiens]

Variant type:: SNV:
Alleles:: TC>-
Chromosome:: no mapping
Canonical SPDI:

Select item 149123623113.

rs1491236231 [Homo sapiens]

Variant type:: INS
Alleles:: ->C [Show Flanks]
Chromosome:: 2:160013674 (GRCh38)
2:160870186 (GRCh37)
Canonical SPDI:: NC_000002.12:160013674::C
Gene:: PLA2R1 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency
MAF:: C=0.00025/7 (TOMMO)
HGVS:: NC_000002.12:g.160013674_160013675insC, NC_000002.11:g.160870185_160870186insC

Select item 149116407414.

rs1491164074 has merged into rs71000319 [Homo sapiens]

Variant type:: DELINS
Alleles:: AT>-,ATAT,ATATAT,ATATATAT,ATATATATAT,ATATATATATAT [Show Flanks]
Chromosome:: 2:159929886 (GRCh38)
2:160786397 (GRCh37)
Canonical SPDI:: NC_000002.12:159929872:TATATATATATATAT:TATATATATATAT,NC_000002.12:159929872:TATATATATATATAT:TATATATATATATATAT,NC_000002.12:159929872:TATATATATATATAT:TATATATATATATATATAT,NC_000002.12:159929872:TATATATATATATAT:TATATATATATATATATATAT,NC_000002.12:159929872:TATATATATATATAT:TATATATATATATATATATATAT,NC_000002.12:159929872:TATATATATATATAT:TATATATATATATATATATATATAT
Gene:: PLA2R1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant,non_coding_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TATATATATATATATAT=0./0 (ALFA)
TATA=0.13667/82 (NorthernSweden)
HGVS:: NC_000002.12:g.159929874AT[6], NC_000002.12:g.159929874AT[8], NC_000002.12:g.159929874AT[9], NC_000002.12:g.159929874AT[10], NC_000002.12:g.159929874AT[11], NC_000002.12:g.159929874AT[12], NC_000002.11:g.160786385AT[6], NC_000002.11:g.160786385AT[8], NC_000002.11:g.160786385AT[9], NC_000002.11:g.160786385AT[10], NC_000002.11:g.160786385AT[11], NC_000002.11:g.160786385AT[12], XM_005246392.5:c.*2799TA[6], XM_005246392.5:c.*2799TA[8], XM_005246392.5:c.*2799TA[9], XM_005246392.5:c.*2799TA[10], XM_005246392.5:c.*2799TA[11], XM_005246392.5:c.*2799TA[12], XM_005246392.3:c.*2799TA[6], XM_005246392.3:c.*2799TA[8], XM_005246392.3:c.*2799TA[9], XM_005246392.3:c.*2799TA[10], XM_005246392.3:c.*2799TA[11], XM_005246392.3:c.*2799TA[12], XR_922892.4:n.7474TA[6], XR_922892.4:n.7474TA[8], XR_922892.4:n.7474TA[9], XR_922892.4:n.7474TA[10], XR_922892.4:n.7474TA[11], XR_922892.4:n.7474TA[12], XR_922892.2:n.7362TA[6], XR_922892.2:n.7362TA[8], XR_922892.2:n.7362TA[9], XR_922892.2:n.7362TA[10], XR_922892.2:n.7362TA[11], XR_922892.2:n.7362TA[12], XM_011510820.4:c.*2445TA[6], XM_011510820.4:c.*2445TA[8], XM_011510820.4:c.*2445TA[9], XM_011510820.4:c.*2445TA[10], XM_011510820.4:c.*2445TA[11], XM_011510820.4:c.*2445TA[12], XM_011510820.2:c.*2445TA[6], XM_011510820.2:c.*2445TA[8], XM_011510820.2:c.*2445TA[9], XM_011510820.2:c.*2445TA[10], XM_011510820.2:c.*2445TA[11], XM_011510820.2:c.*2445TA[12], XR_001738671.3:n.8111TA[6], XR_001738671.3:n.8111TA[8], XR_001738671.3:n.8111TA[9], XR_001738671.3:n.8111TA[10], XR_001738671.3:n.8111TA[11], XR_001738671.3:n.8111TA[12], XR_001738671.1:n.7999TA[6], XR_001738671.1:n.7999TA[8], XR_001738671.1:n.7999TA[9], XR_001738671.1:n.7999TA[10], XR_001738671.1:n.7999TA[11], XR_001738671.1:n.7999TA[12], XR_001738672.3:n.7593TA[6], XR_001738672.3:n.7593TA[8], XR_001738672.3:n.7593TA[9], XR_001738672.3:n.7593TA[10], XR_001738672.3:n.7593TA[11], XR_001738672.3:n.7593TA[12], XR_001738672.1:n.7481TA[6], XR_001738672.1:n.7481TA[8], XR_001738672.1:n.7481TA[9], XR_001738672.1:n.7481TA[10], XR_001738672.1:n.7481TA[11], XR_001738672.1:n.7481TA[12], XR_007071492.1:n.14871TA[6], XR_007071492.1:n.14871TA[8], XR_007071492.1:n.14871TA[9], XR_007071492.1:n.14871TA[10], XR_007071492.1:n.14871TA[11], XR_007071492.1:n.14871TA[12], XR_007071493.1:n.14152TA[6], XR_007071493.1:n.14152TA[8], XR_007071493.1:n.14152TA[9], XR_007071493.1:n.14152TA[10], XR_007071493.1:n.14152TA[11], XR_007071493.1:n.14152TA[12], XR_007071494.1:n.13886TA[6], XR_007071494.1:n.13886TA[8], XR_007071494.1:n.13886TA[9], XR_007071494.1:n.13886TA[10], XR_007071494.1:n.13886TA[11], XR_007071494.1:n.13886TA[12], XM_047443730.1:c.*2799TA[6], XM_047443730.1:c.*2799TA[8], XM_047443730.1:c.*2799TA[9], XM_047443730.1:c.*2799TA[10], XM_047443730.1:c.*2799TA[11], XM_047443730.1:c.*2799TA[12], XR_007071491.1:n.7239TA[6], XR_007071491.1:n.7239TA[8], XR_007071491.1:n.7239TA[9], XR_007071491.1:n.7239TA[10], XR_007071491.1:n.7239TA[11], XR_007071491.1:n.7239TA[12]

Select item 149114071915.

rs1491140719 has merged into rs56857653 [Homo sapiens]

Variant type:: DELINS
Alleles:: CA>-,CACA,CACACA [Show Flanks]
Chromosome:: 2:159976359 (GRCh38)
2:160832870 (GRCh37)
Canonical SPDI:: NC_000002.12:159976347:ACACACACACACA:ACACACACACA,NC_000002.12:159976347:ACACACACACACA:ACACACACACACACA,NC_000002.12:159976347:ACACACACACACA:ACACACACACACACACA
Gene:: PLA2R1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ACACACACACACACACA=0./0 (ALFA)
AC=0.25703/1287 (1000Genomes)
AC=0.26852/58 (Vietnamese)
-=0.45491/454 (GoNL)
AC=0.49833/299 (NorthernSweden)
-=0.5/20 (GENOME_DK)
HGVS:: NC_000002.12:g.159976349CA[5], NC_000002.12:g.159976349CA[7], NC_000002.12:g.159976349CA[8], NC_000002.11:g.160832860CA[5], NC_000002.11:g.160832860CA[7], NC_000002.11:g.160832860CA[8]

Select item 149109817816.

rs1491098178 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CG [Show Flanks]
Chromosome:: 2:159929853 (GRCh38)
2:160786365 (GRCh37)
Canonical SPDI:: NC_000002.12:159929853:G:GCG
Gene:: PLA2R1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant,3_prime_UTR_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: GCG=0./0 (ALFA)
HGVS:: NC_000002.12:g.159929854_159929855insCG, NC_000002.11:g.160786365_160786366insCG, XM_005246392.5:c.*2831_*2832insGC, XM_005246392.3:c.*2831_*2832insGC, XR_922892.4:n.7506_7507insGC, XR_922892.2:n.7394_7395insGC, XM_011510820.4:c.*2477_*2478insGC, XM_011510820.2:c.*2477_*2478insGC, XR_001738671.3:n.8143_8144insGC, XR_001738671.1:n.8031_8032insGC, XR_001738672.3:n.7625_7626insGC, XR_001738672.1:n.7513_7514insGC, XR_007071492.1:n.14903_14904insGC, XR_007071493.1:n.14184_14185insGC, XR_007071494.1:n.13918_13919insGC, XM_047443730.1:c.*2831_*2832insGC, XR_007071491.1:n.7271_7272insGC

Select item 149109224117.

rs1491092241 [Homo sapiens]

Variant type:: INS
Alleles:: ->A,ATATAAATTAA [Show Flanks]
Chromosome:: 2:159935946 (GRCh38)
2:160792458 (GRCh37)
Canonical SPDI:: NC_000002.12:159935946::A,NC_000002.12:159935946::ATATAAATTAA
Gene:: PLA2R1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant,3_prime_UTR_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: ATATAAATTAA=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000002.12:g.159935946_159935947insA, NC_000002.12:g.159935946_159935947insATATAAATTAA, NC_000002.11:g.160792457_160792458insA, NC_000002.11:g.160792457_160792458insATATAAATTAA, NM_007366.5:c.*5831_*5832insT, NM_007366.5:c.*5831_*5832insTTAATTTATAT, NM_001195641.2:c.*5831_*5832insT, NM_001195641.2:c.*5831_*5832insTTAATTTATAT, XR_007071492.1:n.9257_9258insT, XR_007071492.1:n.9257_9258insTTAATTTATAT, XR_007071493.1:n.8538_8539insT, XR_007071493.1:n.8538_8539insTTAATTTATAT, XR_007071494.1:n.8272_8273insT, XR_007071494.1:n.8272_8273insTTAATTTATAT

Select item 149108394818.

rs1491083948 [Homo sapiens]

Variant type:: INS
Alleles:: ->C [Show Flanks]
Chromosome:: 2:160016472 (GRCh38)
2:160872984 (GRCh37)
Canonical SPDI:: NC_000002.12:160016472::C
Gene:: PLA2R1 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000002.12:g.160016472_160016473insC, NC_000002.11:g.160872983_160872984insC

Select item 149107784919.

rs1491077849 has merged into rs33933112 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAA>-,AA,AAAA,AAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 2:159939512 (GRCh38)
2:160796023 (GRCh37)
Canonical SPDI:: NC_000002.12:159939505:AAAAAAAAAAAAAAAAAA:AAAAAA,NC_000002.12:159939505:AAAAAAAAAAAAAAAAAA:AAAAAAAA,NC_000002.12:159939505:AAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000002.12:159939505:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000002.12:159939505:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000002.12:159939505:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000002.12:159939505:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000002.12:159939505:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000002.12:159939505:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000002.12:159939505:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000002.12:159939505:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000002.12:159939505:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000002.12:159939505:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000002.12:159939505:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000002.12:159939505:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: PLA2R1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant,3_prime_UTR_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAA=0./0 (ALFA)
-=0.1284/643 (1000Genomes)
HGVS:: NC_000002.12:g.159939512_159939523del, NC_000002.12:g.159939514_159939523del, NC_000002.12:g.159939516_159939523del, NC_000002.12:g.159939517_159939523del, NC_000002.12:g.159939520_159939523del, NC_000002.12:g.159939521_159939523del, NC_000002.12:g.159939522_159939523del, NC_000002.12:g.159939523del, NC_000002.12:g.159939523dup, NC_000002.12:g.159939522_159939523dup, NC_000002.12:g.159939521_159939523dup, NC_000002.12:g.159939520_159939523dup, NC_000002.12:g.159939516_159939523dup, NC_000002.12:g.159939513_159939523dup, NC_000002.12:g.159939523_159939524insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000002.11:g.160796023_160796034del, NC_000002.11:g.160796025_160796034del, NC_000002.11:g.160796027_160796034del, NC_000002.11:g.160796028_160796034del, NC_000002.11:g.160796031_160796034del, NC_000002.11:g.160796032_160796034del, NC_000002.11:g.160796033_160796034del, NC_000002.11:g.160796034del, NC_000002.11:g.160796034dup, NC_000002.11:g.160796033_160796034dup, NC_000002.11:g.160796032_160796034dup, NC_000002.11:g.160796031_160796034dup, NC_000002.11:g.160796027_160796034dup, NC_000002.11:g.160796024_160796034dup, NC_000002.11:g.160796034_160796035insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_007366.5:c.*2261_*2272del, NM_007366.5:c.*2263_*2272del, NM_007366.5:c.*2265_*2272del, NM_007366.5:c.*2266_*2272del, NM_007366.5:c.*2269_*2272del, NM_007366.5:c.*2270_*2272del, NM_007366.5:c.*2271_*2272del, NM_007366.5:c.*2272del, NM_007366.5:c.*2272dup, NM_007366.5:c.*2271_*2272dup, NM_007366.5:c.*2270_*2272dup, NM_007366.5:c.*2269_*2272dup, NM_007366.5:c.*2265_*2272dup, NM_007366.5:c.*2262_*2272dup, NM_007366.5:c.*2272_*2273insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001195641.2:c.*2261_*2272del, NM_001195641.2:c.*2263_*2272del, NM_001195641.2:c.*2265_*2272del, NM_001195641.2:c.*2266_*2272del, NM_001195641.2:c.*2269_*2272del, NM_001195641.2:c.*2270_*2272del, NM_001195641.2:c.*2271_*2272del, NM_001195641.2:c.*2272del, NM_001195641.2:c.*2272dup, NM_001195641.2:c.*2271_*2272dup, NM_001195641.2:c.*2270_*2272dup, NM_001195641.2:c.*2269_*2272dup, NM_001195641.2:c.*2265_*2272dup, NM_001195641.2:c.*2262_*2272dup, NM_001195641.2:c.*2272_*2273insTTTTTTTTTTTTTTTTTTTTTTTTTTT, XR_007071492.1:n.5687_5698del, XR_007071492.1:n.5689_5698del, XR_007071492.1:n.5691_5698del, XR_007071492.1:n.5692_5698del, XR_007071492.1:n.5695_5698del, XR_007071492.1:n.5696_5698del, XR_007071492.1:n.5697_5698del, XR_007071492.1:n.5698del, XR_007071492.1:n.5698dup, XR_007071492.1:n.5697_5698dup, XR_007071492.1:n.5696_5698dup, XR_007071492.1:n.5695_5698dup, XR_007071492.1:n.5691_5698dup, XR_007071492.1:n.5688_5698dup, XR_007071492.1:n.5698_5699insTTTTTTTTTTTTTTTTTTTTTTTTTTT, XR_007071493.1:n.4968_4979del, XR_007071493.1:n.4970_4979del, XR_007071493.1:n.4972_4979del, XR_007071493.1:n.4973_4979del, XR_007071493.1:n.4976_4979del, XR_007071493.1:n.4977_4979del, XR_007071493.1:n.4978_4979del, XR_007071493.1:n.4979del, XR_007071493.1:n.4979dup, XR_007071493.1:n.4978_4979dup, XR_007071493.1:n.4977_4979dup, XR_007071493.1:n.4976_4979dup, XR_007071493.1:n.4972_4979dup, XR_007071493.1:n.4969_4979dup, XR_007071493.1:n.4979_4980insTTTTTTTTTTTTTTTTTTTTTTTTTTT, XR_007071494.1:n.4702_4713del, XR_007071494.1:n.4704_4713del, XR_007071494.1:n.4706_4713del, XR_007071494.1:n.4707_4713del, XR_007071494.1:n.4710_4713del, XR_007071494.1:n.4711_4713del, XR_007071494.1:n.4712_4713del, XR_007071494.1:n.4713del, XR_007071494.1:n.4713dup, XR_007071494.1:n.4712_4713dup, XR_007071494.1:n.4711_4713dup, XR_007071494.1:n.4710_4713dup, XR_007071494.1:n.4706_4713dup, XR_007071494.1:n.4703_4713dup, XR_007071494.1:n.4713_4714insTTTTTTTTTTTTTTTTTTTTTTTTTTT

Select item 149106114220.

rs1491061142 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->G [Show Flanks]
Chromosome:: 2:160016480 (GRCh38)
2:160872992 (GRCh37)
Canonical SPDI:: NC_000002.12:160016480:G:GG
Gene:: PLA2R1 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GG=0.00008/1 (ALFA)
G=0.00001/1 (GnomAD)
HGVS:: NC_000002.12:g.160016481dup, NC_000002.11:g.160872992dup

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