Links from Gene
Items: 1 to 20 of 47263
2.
rs1491547305 has merged into rs61043046 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- AAAAAA>-,AA,AAA,AAAA,AAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAGAAAAAAAAAAAAA,AAAAAAAGAAAAAAAAAAAAA
[Show Flanks]
- Chromosome:
- 9:27365170
(GRCh38)
9:27365168
(GRCh37)
- Canonical SPDI:
- NC_000009.12:27365162:AAAAAAAAAAAAA:AAAAAAA,NC_000009.12:27365162:AAAAAAAAAAAAA:AAAAAAAAA,NC_000009.12:27365162:AAAAAAAAAAAAA:AAAAAAAAAA,NC_000009.12:27365162:AAAAAAAAAAAAA:AAAAAAAAAAA,NC_000009.12:27365162:AAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000009.12:27365162:AAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000009.12:27365162:AAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000009.12:27365162:AAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000009.12:27365162:AAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000009.12:27365162:AAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000009.12:27365162:AAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000009.12:27365162:AAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000009.12:27365162:AAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000009.12:27365162:AAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000009.12:27365162:AAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000009.12:27365162:AAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000009.12:27365162:AAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000009.12:27365162:AAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000009.12:27365162:AAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000009.12:27365162:AAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000009.12:27365162:AAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000009.12:27365162:AAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000009.12:27365162:AAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000009.12:27365162:AAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000009.12:27365162:AAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000009.12:27365162:AAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000009.12:27365162:AAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000009.12:27365162:AAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000009.12:27365162:AAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000009.12:27365162:AAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000009.12:27365162:AAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000009.12:27365162:AAAAAAAAAAAAA:AAAAAAAAAAAAAAAGAAAAAAAAAAAAA,NC_000009.12:27365162:AAAAAAAAAAAAA:AAAAAAAAAAAAAAGAAAAAAAAAAAAA
- Gene:
- MOB3B (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
AAAAAAAAA=0./0
(
ALFA)
-=0.0509/255
(1000Genomes)
- HGVS:
NC_000009.12:g.27365170_27365175del, NC_000009.12:g.27365172_27365175del, NC_000009.12:g.27365173_27365175del, NC_000009.12:g.27365174_27365175del, NC_000009.12:g.27365175del, NC_000009.12:g.27365175dup, NC_000009.12:g.27365174_27365175dup, NC_000009.12:g.27365173_27365175dup, NC_000009.12:g.27365172_27365175dup, NC_000009.12:g.27365171_27365175dup, NC_000009.12:g.27365170_27365175dup, NC_000009.12:g.27365169_27365175dup, NC_000009.12:g.27365168_27365175dup, NC_000009.12:g.27365167_27365175dup, NC_000009.12:g.27365166_27365175dup, NC_000009.12:g.27365165_27365175dup, NC_000009.12:g.27365164_27365175dup, NC_000009.12:g.27365163_27365175dup, NC_000009.12:g.27365175_27365176insAAAAAAAAAAAAAA, NC_000009.12:g.27365175_27365176insAAAAAAAAAAAAAAA, NC_000009.12:g.27365175_27365176insAAAAAAAAAAAAAAAA, NC_000009.12:g.27365175_27365176insAAAAAAAAAAAAAAAAA, NC_000009.12:g.27365175_27365176insAAAAAAAAAAAAAAAAAA, NC_000009.12:g.27365175_27365176insAAAAAAAAAAAAAAAAAAA, NC_000009.12:g.27365175_27365176insAAAAAAAAAAAAAAAAAAAA, NC_000009.12:g.27365175_27365176insAAAAAAAAAAAAAAAAAAAAAA, NC_000009.12:g.27365175_27365176insAAAAAAAAAAAAAAAAAAAAAAA, NC_000009.12:g.27365175_27365176insAAAAAAAAAAAAAAAAAAAAAAAA, NC_000009.12:g.27365175_27365176insAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000009.12:g.27365175_27365176insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000009.12:g.27365175_27365176insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000009.12:g.27365163_27365175A[15]GAAAAAAAAAAAAA[1], NC_000009.12:g.27365163_27365175A[14]GAAAAAAAAAAAAA[1], NC_000009.11:g.27365168_27365173del, NC_000009.11:g.27365170_27365173del, NC_000009.11:g.27365171_27365173del, NC_000009.11:g.27365172_27365173del, NC_000009.11:g.27365173del, NC_000009.11:g.27365173dup, NC_000009.11:g.27365172_27365173dup, NC_000009.11:g.27365171_27365173dup, NC_000009.11:g.27365170_27365173dup, NC_000009.11:g.27365169_27365173dup, NC_000009.11:g.27365168_27365173dup, NC_000009.11:g.27365167_27365173dup, NC_000009.11:g.27365166_27365173dup, NC_000009.11:g.27365165_27365173dup, NC_000009.11:g.27365164_27365173dup, NC_000009.11:g.27365163_27365173dup, NC_000009.11:g.27365162_27365173dup, NC_000009.11:g.27365161_27365173dup, NC_000009.11:g.27365173_27365174insAAAAAAAAAAAAAA, NC_000009.11:g.27365173_27365174insAAAAAAAAAAAAAAA, NC_000009.11:g.27365173_27365174insAAAAAAAAAAAAAAAA, NC_000009.11:g.27365173_27365174insAAAAAAAAAAAAAAAAA, NC_000009.11:g.27365173_27365174insAAAAAAAAAAAAAAAAAA, NC_000009.11:g.27365173_27365174insAAAAAAAAAAAAAAAAAAA, NC_000009.11:g.27365173_27365174insAAAAAAAAAAAAAAAAAAAA, NC_000009.11:g.27365173_27365174insAAAAAAAAAAAAAAAAAAAAAA, NC_000009.11:g.27365173_27365174insAAAAAAAAAAAAAAAAAAAAAAA, NC_000009.11:g.27365173_27365174insAAAAAAAAAAAAAAAAAAAAAAAA, NC_000009.11:g.27365173_27365174insAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000009.11:g.27365173_27365174insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000009.11:g.27365173_27365174insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000009.11:g.27365161_27365173A[15]GAAAAAAAAAAAAA[1], NC_000009.11:g.27365161_27365173A[14]GAAAAAAAAAAAAA[1]
3.
rs1491544107 [Homo sapiens]- Variant type:
- DEL
- Alleles:
- AT>-
[Show Flanks]
- Chromosome:
- 9:27462219
(GRCh38)
9:27462217
(GRCh37)
- Canonical SPDI:
- NC_000009.12:27462218:AT:
- Gene:
- MOB3B (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
-=0./0
(
ALFA)
-=0.000008/2
(TOPMED)
-=0.000014/2
(GnomAD)
- HGVS:
4.
rs1491540996 has merged into rs756275032 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- TTTTTTTTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,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,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
[Show Flanks]
- Chromosome:
- 9:27404358
(GRCh38)
9:27404356
(GRCh37)
- Canonical SPDI:
- NC_000009.12:27404347:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000009.12:27404347:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000009.12:27404347:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000009.12:27404347:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000009.12:27404347:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000009.12:27404347:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000009.12:27404347:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000009.12:27404347:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000009.12:27404347:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000009.12:27404347:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000009.12:27404347:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000009.12:27404347:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000009.12:27404347:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000009.12:27404347:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000009.12:27404347:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000009.12:27404347:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000009.12:27404347:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000009.12:27404347:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000009.12:27404347:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000009.12:27404347:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000009.12:27404347:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000009.12:27404347:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000009.12:27404347:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000009.12:27404347:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000009.12:27404347:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000009.12:27404347:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000009.12:27404347:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000009.12:27404347:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000009.12:27404347:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000009.12:27404347:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000009.12:27404347:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000009.12:27404347:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000009.12:27404347:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000009.12:27404347:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000009.12:27404347:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000009.12:27404347:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000009.12:27404347:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000009.12:27404347:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000009.12:27404347:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000009.12:27404347:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000009.12:27404347:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000009.12:27404347:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000009.12:27404347:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000009.12:27404347:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000009.12:27404347:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000009.12:27404347:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- Gene:
- MOB3B (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TTTTTTTTTT=0./0
(
ALFA)
TTTTTT=0.075/3
(GENOME_DK)
- HGVS:
NC_000009.12:g.27404358_27404374del, NC_000009.12:g.27404359_27404374del, NC_000009.12:g.27404360_27404374del, NC_000009.12:g.27404361_27404374del, NC_000009.12:g.27404362_27404374del, NC_000009.12:g.27404363_27404374del, NC_000009.12:g.27404364_27404374del, NC_000009.12:g.27404365_27404374del, NC_000009.12:g.27404366_27404374del, NC_000009.12:g.27404367_27404374del, NC_000009.12:g.27404368_27404374del, NC_000009.12:g.27404369_27404374del, NC_000009.12:g.27404370_27404374del, NC_000009.12:g.27404371_27404374del, NC_000009.12:g.27404372_27404374del, NC_000009.12:g.27404373_27404374del, NC_000009.12:g.27404374del, NC_000009.12:g.27404374dup, NC_000009.12:g.27404373_27404374dup, NC_000009.12:g.27404372_27404374dup, NC_000009.12:g.27404371_27404374dup, NC_000009.12:g.27404370_27404374dup, NC_000009.12:g.27404369_27404374dup, NC_000009.12:g.27404368_27404374dup, NC_000009.12:g.27404367_27404374dup, NC_000009.12:g.27404366_27404374dup, NC_000009.12:g.27404365_27404374dup, NC_000009.12:g.27404364_27404374dup, NC_000009.12:g.27404363_27404374dup, NC_000009.12:g.27404362_27404374dup, NC_000009.12:g.27404361_27404374dup, NC_000009.12:g.27404360_27404374dup, NC_000009.12:g.27404359_27404374dup, NC_000009.12:g.27404358_27404374dup, NC_000009.12:g.27404357_27404374dup, NC_000009.12:g.27404356_27404374dup, NC_000009.12:g.27404355_27404374dup, NC_000009.12:g.27404354_27404374dup, NC_000009.12:g.27404353_27404374dup, NC_000009.12:g.27404352_27404374dup, NC_000009.12:g.27404351_27404374dup, NC_000009.12:g.27404350_27404374dup, NC_000009.12:g.27404349_27404374dup, NC_000009.12:g.27404348_27404374dup, NC_000009.12:g.27404374_27404375insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000009.12:g.27404374_27404375insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000009.11:g.27404356_27404372del, NC_000009.11:g.27404357_27404372del, NC_000009.11:g.27404358_27404372del, NC_000009.11:g.27404359_27404372del, NC_000009.11:g.27404360_27404372del, NC_000009.11:g.27404361_27404372del, NC_000009.11:g.27404362_27404372del, NC_000009.11:g.27404363_27404372del, NC_000009.11:g.27404364_27404372del, NC_000009.11:g.27404365_27404372del, NC_000009.11:g.27404366_27404372del, NC_000009.11:g.27404367_27404372del, NC_000009.11:g.27404368_27404372del, NC_000009.11:g.27404369_27404372del, NC_000009.11:g.27404370_27404372del, NC_000009.11:g.27404371_27404372del, NC_000009.11:g.27404372del, NC_000009.11:g.27404372dup, NC_000009.11:g.27404371_27404372dup, NC_000009.11:g.27404370_27404372dup, NC_000009.11:g.27404369_27404372dup, NC_000009.11:g.27404368_27404372dup, NC_000009.11:g.27404367_27404372dup, NC_000009.11:g.27404366_27404372dup, NC_000009.11:g.27404365_27404372dup, NC_000009.11:g.27404364_27404372dup, NC_000009.11:g.27404363_27404372dup, NC_000009.11:g.27404362_27404372dup, NC_000009.11:g.27404361_27404372dup, NC_000009.11:g.27404360_27404372dup, NC_000009.11:g.27404359_27404372dup, NC_000009.11:g.27404358_27404372dup, NC_000009.11:g.27404357_27404372dup, NC_000009.11:g.27404356_27404372dup, NC_000009.11:g.27404355_27404372dup, NC_000009.11:g.27404354_27404372dup, NC_000009.11:g.27404353_27404372dup, NC_000009.11:g.27404352_27404372dup, NC_000009.11:g.27404351_27404372dup, NC_000009.11:g.27404350_27404372dup, NC_000009.11:g.27404349_27404372dup, NC_000009.11:g.27404348_27404372dup, NC_000009.11:g.27404347_27404372dup, NC_000009.11:g.27404346_27404372dup, NC_000009.11:g.27404372_27404373insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000009.11:g.27404372_27404373insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
5.
rs1491518972 has merged into rs10602930 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- TTT>-,T,TT,TTTT
[Show Flanks]
- Chromosome:
- 9:27490989
(GRCh38)
9:27490987
(GRCh37)
- Canonical SPDI:
- NC_000009.12:27490979:TTTTTTTTTTTT:TTTTTTTTT,NC_000009.12:27490979:TTTTTTTTTTTT:TTTTTTTTTT,NC_000009.12:27490979:TTTTTTTTTTTT:TTTTTTTTTTT,NC_000009.12:27490979:TTTTTTTTTTTT:TTTTTTTTTTTTT
- Gene:
- MOB3B (Varview)
- Functional Consequence:
- genic_upstream_transcript_variant,intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TTTTTTTTTTTTT=0./0
(
ALFA)
TT=0.1281/446
(1000Genomes)
- HGVS:
6.
rs1491488991 has merged into rs756559270 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- AAAAAAAAAAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
[Show Flanks]
- Chromosome:
- 9:27517659
(GRCh38)
9:27517657
(GRCh37)
- Canonical SPDI:
- NC_000009.12:27517647:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000009.12:27517647:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000009.12:27517647:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000009.12:27517647:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000009.12:27517647:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000009.12:27517647:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000009.12:27517647:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000009.12:27517647:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000009.12:27517647:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000009.12:27517647:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000009.12:27517647:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000009.12:27517647:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000009.12:27517647:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000009.12:27517647:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000009.12:27517647:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000009.12:27517647:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000009.12:27517647:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000009.12:27517647:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000009.12:27517647:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000009.12:27517647:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000009.12:27517647:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000009.12:27517647:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000009.12:27517647:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
- Gene:
- MOB3B (Varview)
- Functional Consequence:
- genic_upstream_transcript_variant,intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
AAAAAAAAAAA=0./0
(
ALFA)
-=0.2/8
(GENOME_DK)
- HGVS:
NC_000009.12:g.27517659_27517672del, NC_000009.12:g.27517660_27517672del, NC_000009.12:g.27517661_27517672del, NC_000009.12:g.27517662_27517672del, NC_000009.12:g.27517663_27517672del, NC_000009.12:g.27517664_27517672del, NC_000009.12:g.27517665_27517672del, NC_000009.12:g.27517666_27517672del, NC_000009.12:g.27517667_27517672del, NC_000009.12:g.27517668_27517672del, NC_000009.12:g.27517669_27517672del, NC_000009.12:g.27517670_27517672del, NC_000009.12:g.27517671_27517672del, NC_000009.12:g.27517672del, NC_000009.12:g.27517672dup, NC_000009.12:g.27517671_27517672dup, NC_000009.12:g.27517670_27517672dup, NC_000009.12:g.27517669_27517672dup, NC_000009.12:g.27517668_27517672dup, NC_000009.12:g.27517667_27517672dup, NC_000009.12:g.27517664_27517672dup, NC_000009.12:g.27517662_27517672dup, NC_000009.12:g.27517672_27517673insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000009.11:g.27517657_27517670del, NC_000009.11:g.27517658_27517670del, NC_000009.11:g.27517659_27517670del, NC_000009.11:g.27517660_27517670del, NC_000009.11:g.27517661_27517670del, NC_000009.11:g.27517662_27517670del, NC_000009.11:g.27517663_27517670del, NC_000009.11:g.27517664_27517670del, NC_000009.11:g.27517665_27517670del, NC_000009.11:g.27517666_27517670del, NC_000009.11:g.27517667_27517670del, NC_000009.11:g.27517668_27517670del, NC_000009.11:g.27517669_27517670del, NC_000009.11:g.27517670del, NC_000009.11:g.27517670dup, NC_000009.11:g.27517669_27517670dup, NC_000009.11:g.27517668_27517670dup, NC_000009.11:g.27517667_27517670dup, NC_000009.11:g.27517666_27517670dup, NC_000009.11:g.27517665_27517670dup, NC_000009.11:g.27517662_27517670dup, NC_000009.11:g.27517660_27517670dup, NC_000009.11:g.27517670_27517671insAAAAAAAAAAAAAAAAAAAAAAAAAAAA
8.
rs1491472486 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- CA>-
[Show Flanks]
- Chromosome:
- 9:27339587
(GRCh38)
9:27339585
(GRCh37)
- Canonical SPDI:
- NC_000009.12:27339585:ACA:A
- Gene:
- MOB3B (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa
- MAF:
A=0./0
(
ALFA)
-=0.000007/1
(GnomAD)
- HGVS:
9.
rs1491439565 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- ->T
[Show Flanks]
- Chromosome:
- 9:27393397
(GRCh38)
9:27393396
(GRCh37)
- Canonical SPDI:
- NC_000009.12:27393397:T:TT
- Gene:
- MOB3B (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TT=0.000641/9
(
ALFA)
T=0.000318/44
(GnomAD)
T=0.000355/94
(TOPMED)
T=0.003333/2
(NorthernSweden)
- HGVS:
10.
rs1491417957 has merged into rs57574286 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- AAAAAA>-,AAA,AAAA,AAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
[Show Flanks]
- Chromosome:
- 9:27425384
(GRCh38)
9:27425382
(GRCh37)
- Canonical SPDI:
- NC_000009.12:27425373:AAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000009.12:27425373:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000009.12:27425373:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000009.12:27425373:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000009.12:27425373:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000009.12:27425373:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000009.12:27425373:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000009.12:27425373:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000009.12:27425373:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000009.12:27425373:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000009.12:27425373:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
- Gene:
- MOB3B (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
AAAAAAAAAAAAAA=0./0
(
ALFA)
-=0.0263/14
(NorthernSweden)
-=0.05/2
(GENOME_DK)
- HGVS:
NC_000009.12:g.27425384_27425389del, NC_000009.12:g.27425387_27425389del, NC_000009.12:g.27425388_27425389del, NC_000009.12:g.27425389del, NC_000009.12:g.27425389dup, NC_000009.12:g.27425388_27425389dup, NC_000009.12:g.27425387_27425389dup, NC_000009.12:g.27425386_27425389dup, NC_000009.12:g.27425385_27425389dup, NC_000009.12:g.27425384_27425389dup, NC_000009.12:g.27425389_27425390insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000009.11:g.27425382_27425387del, NC_000009.11:g.27425385_27425387del, NC_000009.11:g.27425386_27425387del, NC_000009.11:g.27425387del, NC_000009.11:g.27425387dup, NC_000009.11:g.27425386_27425387dup, NC_000009.11:g.27425385_27425387dup, NC_000009.11:g.27425384_27425387dup, NC_000009.11:g.27425383_27425387dup, NC_000009.11:g.27425382_27425387dup, NC_000009.11:g.27425387_27425388insAAAAAAAAAAAAAAAAAAAAAAAAAAA
11.
rs1491404210 [Homo sapiens]- Variant type:
- DEL
- Alleles:
- AG>-
[Show Flanks]
- Chromosome:
- 9:27372215
(GRCh38)
9:27372213
(GRCh37)
- Canonical SPDI:
- NC_000009.12:27372214:AG:
- Gene:
- MOB3B (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
-=0./0
(
ALFA)
-=0.000007/1
(GnomAD)
-=0.000071/1
(TOMMO)
- HGVS:
12.
rs1491400375 has merged into rs11339453 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- TTTT>-,T,TT,TTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTTTTTT
[Show Flanks]
- Chromosome:
- 9:27355574
(GRCh38)
9:27355572
(GRCh37)
- Canonical SPDI:
- NC_000009.12:27355562:TTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000009.12:27355562:TTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000009.12:27355562:TTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000009.12:27355562:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000009.12:27355562:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000009.12:27355562:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000009.12:27355562:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000009.12:27355562:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT
- Gene:
- MOB3B (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TTTTTTTTTTTTT=0./0
(
ALFA)
-=0.4327/2167
(1000Genomes)
- HGVS:
NC_000009.12:g.27355574_27355577del, NC_000009.12:g.27355575_27355577del, NC_000009.12:g.27355576_27355577del, NC_000009.12:g.27355577del, NC_000009.12:g.27355577dup, NC_000009.12:g.27355576_27355577dup, NC_000009.12:g.27355575_27355577dup, NC_000009.12:g.27355570_27355577dup, NC_000009.11:g.27355572_27355575del, NC_000009.11:g.27355573_27355575del, NC_000009.11:g.27355574_27355575del, NC_000009.11:g.27355575del, NC_000009.11:g.27355575dup, NC_000009.11:g.27355574_27355575dup, NC_000009.11:g.27355573_27355575dup, NC_000009.11:g.27355568_27355575dup
14.
rs1491342536 has merged into rs55684272 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- ATATATATATATATATATATATATATATATATATATATATAT>-,AT,ATAT,ATATAT,ATATATAT,ATATATATAT,ATATATATATAT,ATATATATATATAT,ATATATATATATATAT,ATATATATATATATATAT,ATATATATATATATATATAT,ATATATATATATATATATATAT,ATATATATATATATATATATATAT,ATATATATATATATATATATATATAT,ATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATATATATATATATATATATATATAT
[Show Flanks]
- Chromosome:
- 9:27420555
(GRCh38)
9:27420553
(GRCh37)
- Canonical SPDI:
- NC_000009.12:27420548:ATATATATATATATATATATATATATATATATATATATATATATATAT:ATATAT,NC_000009.12:27420548:ATATATATATATATATATATATATATATATATATATATATATATATAT:ATATATAT,NC_000009.12:27420548:ATATATATATATATATATATATATATATATATATATATATATATATAT:ATATATATAT,NC_000009.12:27420548:ATATATATATATATATATATATATATATATATATATATATATATATAT:ATATATATATAT,NC_000009.12:27420548:ATATATATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATAT,NC_000009.12:27420548:ATATATATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATAT,NC_000009.12:27420548:ATATATATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATAT,NC_000009.12:27420548:ATATATATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATAT,NC_000009.12:27420548:ATATATATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATAT,NC_000009.12:27420548:ATATATATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATAT,NC_000009.12:27420548:ATATATATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATAT,NC_000009.12:27420548:ATATATATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATAT,NC_000009.12:27420548:ATATATATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATAT,NC_000009.12:27420548:ATATATATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATAT,NC_000009.12:27420548:ATATATATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATAT,NC_000009.12:27420548:ATATATATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATAT,NC_000009.12:27420548:ATATATATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATAT,NC_000009.12:27420548:ATATATATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATAT,NC_000009.12:27420548:ATATATATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATAT,NC_000009.12:27420548:ATATATATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATAT,NC_000009.12:27420548:ATATATATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATATAT,NC_000009.12:27420548:ATATATATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATATATATAT,NC_000009.12:27420548:ATATATATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATATATATATAT,NC_000009.12:27420548:ATATATATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATATATATATATAT,NC_000009.12:27420548:ATATATATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATATATATATATATAT,NC_000009.12:27420548:ATATATATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATATATATATATATATAT,NC_000009.12:27420548:ATATATATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAT
- Gene:
- MOB3B (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
- HGVS:
NC_000009.12:g.27420549AT[3], NC_000009.12:g.27420549AT[4], NC_000009.12:g.27420549AT[5], NC_000009.12:g.27420549AT[6], NC_000009.12:g.27420549AT[7], NC_000009.12:g.27420549AT[8], NC_000009.12:g.27420549AT[9], NC_000009.12:g.27420549AT[10], NC_000009.12:g.27420549AT[11], NC_000009.12:g.27420549AT[12], NC_000009.12:g.27420549AT[13], NC_000009.12:g.27420549AT[14], NC_000009.12:g.27420549AT[15], NC_000009.12:g.27420549AT[16], NC_000009.12:g.27420549AT[17], NC_000009.12:g.27420549AT[18], NC_000009.12:g.27420549AT[19], NC_000009.12:g.27420549AT[20], NC_000009.12:g.27420549AT[21], NC_000009.12:g.27420549AT[22], NC_000009.12:g.27420549AT[23], NC_000009.12:g.27420549AT[25], NC_000009.12:g.27420549AT[26], NC_000009.12:g.27420549AT[27], NC_000009.12:g.27420549AT[28], NC_000009.12:g.27420549AT[29], NC_000009.12:g.27420549AT[30], NC_000009.11:g.27420547AT[3], NC_000009.11:g.27420547AT[4], NC_000009.11:g.27420547AT[5], NC_000009.11:g.27420547AT[6], NC_000009.11:g.27420547AT[7], NC_000009.11:g.27420547AT[8], NC_000009.11:g.27420547AT[9], NC_000009.11:g.27420547AT[10], NC_000009.11:g.27420547AT[11], NC_000009.11:g.27420547AT[12], NC_000009.11:g.27420547AT[13], NC_000009.11:g.27420547AT[14], NC_000009.11:g.27420547AT[15], NC_000009.11:g.27420547AT[16], NC_000009.11:g.27420547AT[17], NC_000009.11:g.27420547AT[18], NC_000009.11:g.27420547AT[19], NC_000009.11:g.27420547AT[20], NC_000009.11:g.27420547AT[21], NC_000009.11:g.27420547AT[22], NC_000009.11:g.27420547AT[23], NC_000009.11:g.27420547AT[25], NC_000009.11:g.27420547AT[26], NC_000009.11:g.27420547AT[27], NC_000009.11:g.27420547AT[28], NC_000009.11:g.27420547AT[29], NC_000009.11:g.27420547AT[30]
16.
rs1491318934 has merged into rs36090681 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- AAAAA>-,A,AA,AAA,AAAA,AAAAAA,AAAAAAA,AAAAAAAAAAAA
[Show Flanks]
- Chromosome:
- 9:27501778
(GRCh38)
9:27501776
(GRCh37)
- Canonical SPDI:
- NC_000009.12:27501766:AAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000009.12:27501766:AAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000009.12:27501766:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000009.12:27501766:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000009.12:27501766:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000009.12:27501766:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000009.12:27501766:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000009.12:27501766:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA
- Gene:
- MOB3B (Varview)
- Functional Consequence:
- genic_upstream_transcript_variant,intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
AAAAAAAAAAAAAA=0./0
(
ALFA)
AA=0.0877/439
(1000Genomes)
AA=0.1/4
(GENOME_DK)
- HGVS:
NC_000009.12:g.27501778_27501782del, NC_000009.12:g.27501779_27501782del, NC_000009.12:g.27501780_27501782del, NC_000009.12:g.27501781_27501782del, NC_000009.12:g.27501782del, NC_000009.12:g.27501782dup, NC_000009.12:g.27501781_27501782dup, NC_000009.12:g.27501776_27501782dup, NC_000009.11:g.27501776_27501780del, NC_000009.11:g.27501777_27501780del, NC_000009.11:g.27501778_27501780del, NC_000009.11:g.27501779_27501780del, NC_000009.11:g.27501780del, NC_000009.11:g.27501780dup, NC_000009.11:g.27501779_27501780dup, NC_000009.11:g.27501774_27501780dup
17.
rs1491286334 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- GA>-
[Show Flanks]
- Chromosome:
- 9:27370510
(GRCh38)
9:27370508
(GRCh37)
- Canonical SPDI:
- NC_000009.12:27370508:AGA:A
- Gene:
- MOB3B (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by cluster
- MAF:
-=0.0327/126
(ALSPAC)
-=0.0442/164
(TWINSUK)
- HGVS:
18.
rs1491245265 [Homo sapiens]- Variant type:
- DEL
- Alleles:
- CA>-
[Show Flanks]
- Chromosome:
- 9:27420548
(GRCh38)
9:27420546
(GRCh37)
- Canonical SPDI:
- NC_000009.12:27420547:CA:
- Gene:
- MOB3B (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
-=0./0
(
ALFA)
-=0.00004/1
(TOMMO)
-=0.00091/38
(GnomAD)
- HGVS:
20.
rs1491236758 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- ->CT
[Show Flanks]
- Chromosome:
- 9:27355563
(GRCh38)
9:27355562
(GRCh37)
- Canonical SPDI:
- NC_000009.12:27355563:T:TCT
- Gene:
- MOB3B (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TCT=0.00101/12
(
ALFA)
TC=0.00648/202
(GnomAD)
- HGVS: