Links from Gene
Items: 1 to 20 of 12302
1.
rs1491511073 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- T>-,TT
[Show Flanks]
- Chromosome:
- 14:35007035
(GRCh38)
14:35476241
(GRCh37)
- Canonical SPDI:
- NC_000014.9:35007034:TTTTTTT:TTTTTT,NC_000014.9:35007034:TTTTTTT:TTTTTTTT
- Gene:
- SRP54 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TTTTTTTT=0./0
(
ALFA)
-=0.000007/1
(GnomAD)
-=0.000015/4
(TOPMED)
- HGVS:
4.
rs1491479262 has merged into rs145307640 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- TTT>-,T,TT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
[Show Flanks]
- Chromosome:
- 14:35016842
(GRCh38)
14:35486048
(GRCh37)
- Canonical SPDI:
- NC_000014.9:35016840:TTTT:T,NC_000014.9:35016840:TTTT:TT,NC_000014.9:35016840:TTTT:TTT,NC_000014.9:35016840:TTTT:TTTTT,NC_000014.9:35016840:TTTT:TTTTTT,NC_000014.9:35016840:TTTT:TTTTTTT,NC_000014.9:35016840:TTTT:TTTTTTTT,NC_000014.9:35016840:TTTT:TTTTTTTTT,NC_000014.9:35016840:TTTT:TTTTTTTTTT,NC_000014.9:35016840:TTTT:TTTTTTTTTTT,NC_000014.9:35016840:TTTT:TTTTTTTTTTTT,NC_000014.9:35016840:TTTT:TTTTTTTTTTTTT,NC_000014.9:35016840:TTTT:TTTTTTTTTTTTTT,NC_000014.9:35016840:TTTT:TTTTTTTTTTTTTTT,NC_000014.9:35016840:TTTT:TTTTTTTTTTTTTTTT,NC_000014.9:35016840:TTTT:TTTTTTTTTTTTTTTTT,NC_000014.9:35016840:TTTT:TTTTTTTTTTTTTTTTTT,NC_000014.9:35016840:TTTT:TTTTTTTTTTTTTTTTTTT,NC_000014.9:35016840:TTTT:TTTTTTTTTTTTTTTTTTTT,NC_000014.9:35016840:TTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000014.9:35016840:TTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:35016840:TTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:35016840:TTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:35016840:TTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:35016840:TTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:35016840:TTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:35016840:TTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:35016840:TTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:35016840:TTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:35016840:TTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:35016840:TTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:35016840:TTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:35016840:TTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- Gene:
- SRP54 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
- HGVS:
NC_000014.9:g.35016842_35016844del, NC_000014.9:g.35016843_35016844del, NC_000014.9:g.35016844del, NC_000014.9:g.35016844dup, NC_000014.9:g.35016843_35016844dup, NC_000014.9:g.35016842_35016844dup, NC_000014.9:g.35016841_35016844dup, NC_000014.9:g.35016844_35016845insTTTTT, NC_000014.9:g.35016844_35016845insTTTTTT, NC_000014.9:g.35016844_35016845insTTTTTTT, NC_000014.9:g.35016844_35016845insTTTTTTTT, NC_000014.9:g.35016844_35016845insTTTTTTTTT, NC_000014.9:g.35016844_35016845insTTTTTTTTTT, NC_000014.9:g.35016844_35016845insTTTTTTTTTTT, NC_000014.9:g.35016844_35016845insTTTTTTTTTTTT, NC_000014.9:g.35016844_35016845insTTTTTTTTTTTTT, NC_000014.9:g.35016844_35016845insTTTTTTTTTTTTTT, NC_000014.9:g.35016844_35016845insTTTTTTTTTTTTTTT, NC_000014.9:g.35016844_35016845insTTTTTTTTTTTTTTTT, NC_000014.9:g.35016844_35016845insTTTTTTTTTTTTTTTTT, NC_000014.9:g.35016844_35016845insTTTTTTTTTTTTTTTTTT, NC_000014.9:g.35016844_35016845insTTTTTTTTTTTTTTTTTTT, NC_000014.9:g.35016844_35016845insTTTTTTTTTTTTTTTTTTTT, NC_000014.9:g.35016844_35016845insTTTTTTTTTTTTTTTTTTTTT, NC_000014.9:g.35016844_35016845insTTTTTTTTTTTTTTTTTTTTTT, NC_000014.9:g.35016844_35016845insTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.9:g.35016844_35016845insTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.9:g.35016844_35016845insTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.9:g.35016844_35016845insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.9:g.35016844_35016845insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.9:g.35016844_35016845insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.9:g.35016844_35016845insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.9:g.35016844_35016845insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.8:g.35486048_35486050del, NC_000014.8:g.35486049_35486050del, NC_000014.8:g.35486050del, NC_000014.8:g.35486050dup, NC_000014.8:g.35486049_35486050dup, NC_000014.8:g.35486048_35486050dup, NC_000014.8:g.35486047_35486050dup, NC_000014.8:g.35486050_35486051insTTTTT, NC_000014.8:g.35486050_35486051insTTTTTT, NC_000014.8:g.35486050_35486051insTTTTTTT, NC_000014.8:g.35486050_35486051insTTTTTTTT, NC_000014.8:g.35486050_35486051insTTTTTTTTT, NC_000014.8:g.35486050_35486051insTTTTTTTTTT, NC_000014.8:g.35486050_35486051insTTTTTTTTTTT, NC_000014.8:g.35486050_35486051insTTTTTTTTTTTT, NC_000014.8:g.35486050_35486051insTTTTTTTTTTTTT, NC_000014.8:g.35486050_35486051insTTTTTTTTTTTTTT, NC_000014.8:g.35486050_35486051insTTTTTTTTTTTTTTT, NC_000014.8:g.35486050_35486051insTTTTTTTTTTTTTTTT, NC_000014.8:g.35486050_35486051insTTTTTTTTTTTTTTTTT, NC_000014.8:g.35486050_35486051insTTTTTTTTTTTTTTTTTT, NC_000014.8:g.35486050_35486051insTTTTTTTTTTTTTTTTTTT, NC_000014.8:g.35486050_35486051insTTTTTTTTTTTTTTTTTTTT, NC_000014.8:g.35486050_35486051insTTTTTTTTTTTTTTTTTTTTT, NC_000014.8:g.35486050_35486051insTTTTTTTTTTTTTTTTTTTTTT, NC_000014.8:g.35486050_35486051insTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.8:g.35486050_35486051insTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.8:g.35486050_35486051insTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.8:g.35486050_35486051insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.8:g.35486050_35486051insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.8:g.35486050_35486051insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.8:g.35486050_35486051insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.8:g.35486050_35486051insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
5.
rs1491460783 has merged into rs373239357 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- CT>-
[Show Flanks]
- Chromosome:
- 14:35016845
(GRCh38)
14:35486051
(GRCh37)
- Canonical SPDI:
- NC_000014.9:35016843:TCT:T
- Gene:
- SRP54 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
T=0.16431/1949
(
ALFA)
-=0.00161/21
(GnomAD)
TC=0.01837/92
(1000Genomes)
TC=0.0807/311
(ALSPAC)
TC=0.14617/542
(TWINSUK)
- HGVS:
6.
rs1491438532 [Homo sapiens]- Variant type:
- INS
- Alleles:
- ->CAGAG
[Show Flanks]
- Chromosome:
- 14:35026169
(GRCh38)
14:35495376
(GRCh37)
- Canonical SPDI:
- NC_000014.9:35026169::CAGAG
- Gene:
- SRP54 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency
- MAF:
CAGAG=0.00021/6
(TOMMO)
- HGVS:
7.
rs1491414350 has merged into rs1160365086 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- AAAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA
[Show Flanks]
- Chromosome:
- 14:34988573
(GRCh38)
14:35457779
(GRCh37)
- Canonical SPDI:
- NC_000014.9:34988560:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000014.9:34988560:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000014.9:34988560:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000014.9:34988560:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000014.9:34988560:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000014.9:34988560:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000014.9:34988560:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000014.9:34988560:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000014.9:34988560:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000014.9:34988560:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:34988560:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:34988560:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:34988560:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:34988560:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:34988560:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:34988560:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:34988560:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:34988560:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:34988560:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:34988560:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:34988560:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
- Gene:
- SRP54 (Varview)
- Functional Consequence:
- intron_variant,genic_upstream_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
AAAAAAAAAAAAA=0./0
(
ALFA)
- HGVS:
NC_000014.9:g.34988573_34988579del, NC_000014.9:g.34988574_34988579del, NC_000014.9:g.34988575_34988579del, NC_000014.9:g.34988576_34988579del, NC_000014.9:g.34988577_34988579del, NC_000014.9:g.34988578_34988579del, NC_000014.9:g.34988579del, NC_000014.9:g.34988579dup, NC_000014.9:g.34988578_34988579dup, NC_000014.9:g.34988577_34988579dup, NC_000014.9:g.34988576_34988579dup, NC_000014.9:g.34988575_34988579dup, NC_000014.9:g.34988574_34988579dup, NC_000014.9:g.34988573_34988579dup, NC_000014.9:g.34988572_34988579dup, NC_000014.9:g.34988571_34988579dup, NC_000014.9:g.34988570_34988579dup, NC_000014.9:g.34988569_34988579dup, NC_000014.9:g.34988568_34988579dup, NC_000014.9:g.34988567_34988579dup, NC_000014.9:g.34988566_34988579dup, NC_000014.8:g.35457779_35457785del, NC_000014.8:g.35457780_35457785del, NC_000014.8:g.35457781_35457785del, NC_000014.8:g.35457782_35457785del, NC_000014.8:g.35457783_35457785del, NC_000014.8:g.35457784_35457785del, NC_000014.8:g.35457785del, NC_000014.8:g.35457785dup, NC_000014.8:g.35457784_35457785dup, NC_000014.8:g.35457783_35457785dup, NC_000014.8:g.35457782_35457785dup, NC_000014.8:g.35457781_35457785dup, NC_000014.8:g.35457780_35457785dup, NC_000014.8:g.35457779_35457785dup, NC_000014.8:g.35457778_35457785dup, NC_000014.8:g.35457777_35457785dup, NC_000014.8:g.35457776_35457785dup, NC_000014.8:g.35457775_35457785dup, NC_000014.8:g.35457774_35457785dup, NC_000014.8:g.35457773_35457785dup, NC_000014.8:g.35457772_35457785dup
9.
rs1491368266 has merged into rs1160365086 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- AAAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA
[Show Flanks]
- Chromosome:
- 14:34988573
(GRCh38)
14:35457779
(GRCh37)
- Canonical SPDI:
- NC_000014.9:34988560:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000014.9:34988560:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000014.9:34988560:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000014.9:34988560:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000014.9:34988560:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000014.9:34988560:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000014.9:34988560:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000014.9:34988560:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000014.9:34988560:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000014.9:34988560:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:34988560:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:34988560:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:34988560:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:34988560:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:34988560:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:34988560:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:34988560:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:34988560:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:34988560:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:34988560:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:34988560:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
- Gene:
- SRP54 (Varview)
- Functional Consequence:
- intron_variant,genic_upstream_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
AAAAAAAAAAAAA=0./0
(
ALFA)
- HGVS:
NC_000014.9:g.34988573_34988579del, NC_000014.9:g.34988574_34988579del, NC_000014.9:g.34988575_34988579del, NC_000014.9:g.34988576_34988579del, NC_000014.9:g.34988577_34988579del, NC_000014.9:g.34988578_34988579del, NC_000014.9:g.34988579del, NC_000014.9:g.34988579dup, NC_000014.9:g.34988578_34988579dup, NC_000014.9:g.34988577_34988579dup, NC_000014.9:g.34988576_34988579dup, NC_000014.9:g.34988575_34988579dup, NC_000014.9:g.34988574_34988579dup, NC_000014.9:g.34988573_34988579dup, NC_000014.9:g.34988572_34988579dup, NC_000014.9:g.34988571_34988579dup, NC_000014.9:g.34988570_34988579dup, NC_000014.9:g.34988569_34988579dup, NC_000014.9:g.34988568_34988579dup, NC_000014.9:g.34988567_34988579dup, NC_000014.9:g.34988566_34988579dup, NC_000014.8:g.35457779_35457785del, NC_000014.8:g.35457780_35457785del, NC_000014.8:g.35457781_35457785del, NC_000014.8:g.35457782_35457785del, NC_000014.8:g.35457783_35457785del, NC_000014.8:g.35457784_35457785del, NC_000014.8:g.35457785del, NC_000014.8:g.35457785dup, NC_000014.8:g.35457784_35457785dup, NC_000014.8:g.35457783_35457785dup, NC_000014.8:g.35457782_35457785dup, NC_000014.8:g.35457781_35457785dup, NC_000014.8:g.35457780_35457785dup, NC_000014.8:g.35457779_35457785dup, NC_000014.8:g.35457778_35457785dup, NC_000014.8:g.35457777_35457785dup, NC_000014.8:g.35457776_35457785dup, NC_000014.8:g.35457775_35457785dup, NC_000014.8:g.35457774_35457785dup, NC_000014.8:g.35457773_35457785dup, NC_000014.8:g.35457772_35457785dup
10.
rs1491324498 has merged into rs59058538 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- TTTTTTTTTTTTTTTTTT>-,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT
[Show Flanks]
- Chromosome:
- 14:34994942
(GRCh38)
14:35464148
(GRCh37)
- Canonical SPDI:
- NC_000014.9:34994932:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000014.9:34994932:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000014.9:34994932:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000014.9:34994932:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000014.9:34994932:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000014.9:34994932:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000014.9:34994932:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000014.9:34994932:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000014.9:34994932:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000014.9:34994932:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000014.9:34994932:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:34994932:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:34994932:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:34994932:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:34994932:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:34994932:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:34994932:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:34994932:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:34994932:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:34994932:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:34994932:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- Gene:
- SRP54 (Varview)
- Functional Consequence:
- intron_variant,genic_upstream_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TTTTTTTTT=0./0
(
ALFA)
-=0.0239/14
(NorthernSweden)
- HGVS:
NC_000014.9:g.34994942_34994959del, NC_000014.9:g.34994944_34994959del, NC_000014.9:g.34994945_34994959del, NC_000014.9:g.34994946_34994959del, NC_000014.9:g.34994947_34994959del, NC_000014.9:g.34994948_34994959del, NC_000014.9:g.34994949_34994959del, NC_000014.9:g.34994950_34994959del, NC_000014.9:g.34994951_34994959del, NC_000014.9:g.34994954_34994959del, NC_000014.9:g.34994955_34994959del, NC_000014.9:g.34994956_34994959del, NC_000014.9:g.34994957_34994959del, NC_000014.9:g.34994958_34994959del, NC_000014.9:g.34994959del, NC_000014.9:g.34994959dup, NC_000014.9:g.34994958_34994959dup, NC_000014.9:g.34994957_34994959dup, NC_000014.9:g.34994954_34994959dup, NC_000014.9:g.34994953_34994959dup, NC_000014.9:g.34994952_34994959dup, NC_000014.8:g.35464148_35464165del, NC_000014.8:g.35464150_35464165del, NC_000014.8:g.35464151_35464165del, NC_000014.8:g.35464152_35464165del, NC_000014.8:g.35464153_35464165del, NC_000014.8:g.35464154_35464165del, NC_000014.8:g.35464155_35464165del, NC_000014.8:g.35464156_35464165del, NC_000014.8:g.35464157_35464165del, NC_000014.8:g.35464160_35464165del, NC_000014.8:g.35464161_35464165del, NC_000014.8:g.35464162_35464165del, NC_000014.8:g.35464163_35464165del, NC_000014.8:g.35464164_35464165del, NC_000014.8:g.35464165del, NC_000014.8:g.35464165dup, NC_000014.8:g.35464164_35464165dup, NC_000014.8:g.35464163_35464165dup, NC_000014.8:g.35464160_35464165dup, NC_000014.8:g.35464159_35464165dup, NC_000014.8:g.35464158_35464165dup
12.
rs1491287346 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- ->TACATATATATATA
[Show Flanks]
- Chromosome:
- 14:34987276
(GRCh38)
14:35456483
(GRCh37)
- Canonical SPDI:
- NC_000014.9:34987276:ATATATATATA:ATATATATATATACATATATATATA
- Gene:
- SRP54 (Varview)
- Functional Consequence:
- genic_upstream_transcript_variant,intron_variant
- Validated:
- by frequency,by alfa
- MAF:
ATATATATATATACATATATATATA=0./0
(
ALFA)
ATATATATATATAC=0.00008/4
(GnomAD)
- HGVS:
13.
rs1491269843 has merged into rs67731588 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- TTTTT>-,TT,TTT,TTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT
[Show Flanks]
- Chromosome:
- 14:34999028
(GRCh38)
14:35468234
(GRCh37)
- Canonical SPDI:
- NC_000014.9:34999014:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000014.9:34999014:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000014.9:34999014:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000014.9:34999014:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000014.9:34999014:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000014.9:34999014:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000014.9:34999014:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000014.9:34999014:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:34999014:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:34999014:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:34999014:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:34999014:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- Gene:
- SRP54 (Varview)
- Functional Consequence:
- intron_variant,genic_upstream_transcript_variant,upstream_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TTTTTTTTTTTTTTT=0./0
(
ALFA)
T=0.01507/161
(TOMMO)
- HGVS:
NC_000014.9:g.34999028_34999032del, NC_000014.9:g.34999030_34999032del, NC_000014.9:g.34999031_34999032del, NC_000014.9:g.34999032del, NC_000014.9:g.34999032dup, NC_000014.9:g.34999031_34999032dup, NC_000014.9:g.34999030_34999032dup, NC_000014.9:g.34999028_34999032dup, NC_000014.9:g.34999027_34999032dup, NC_000014.9:g.34999026_34999032dup, NC_000014.9:g.34999024_34999032dup, NC_000014.9:g.34999022_34999032dup, NC_000014.8:g.35468234_35468238del, NC_000014.8:g.35468236_35468238del, NC_000014.8:g.35468237_35468238del, NC_000014.8:g.35468238del, NC_000014.8:g.35468238dup, NC_000014.8:g.35468237_35468238dup, NC_000014.8:g.35468236_35468238dup, NC_000014.8:g.35468234_35468238dup, NC_000014.8:g.35468233_35468238dup, NC_000014.8:g.35468232_35468238dup, NC_000014.8:g.35468230_35468238dup, NC_000014.8:g.35468228_35468238dup
14.
rs1491200870 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- ->GG
[Show Flanks]
- Chromosome:
- 14:34995132
(GRCh38)
14:35464339
(GRCh37)
- Canonical SPDI:
- NC_000014.9:34995132:GGG:GGGGG
- Gene:
- SRP54 (Varview)
- Functional Consequence:
- genic_upstream_transcript_variant,intron_variant
- Validated:
- by frequency,by alfa
- MAF:
GGGGG=0./0
(
ALFA)
GG=0.00004/2
(GnomAD)
- HGVS:
15.
rs1491161960 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- ->T
[Show Flanks]
- Chromosome:
- 14:35010157
(GRCh38)
14:35479364
(GRCh37)
- Canonical SPDI:
- NC_000014.9:35010157:TTTTTTT:TTTTTTTT
- Gene:
- SRP54 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TTTTTTTT=0.00092/15
(
ALFA)
T=0.000231/32
(GnomAD)
- HGVS:
17.
rs1491145281 has merged into rs369480971 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- TATA>-,TA,TATATA,TATATATA,TATATATATATA
[Show Flanks]
- Chromosome:
- 14:34987284
(GRCh38)
14:35456490
(GRCh37)
- Canonical SPDI:
- NC_000014.9:34987275:TATATATATATA:TATATATA,NC_000014.9:34987275:TATATATATATA:TATATATATA,NC_000014.9:34987275:TATATATATATA:TATATATATATATA,NC_000014.9:34987275:TATATATATATA:TATATATATATATATA,NC_000014.9:34987275:TATATATATATA:TATATATATATATATATATA
- Gene:
- SRP54 (Varview)
- Functional Consequence:
- intron_variant,genic_upstream_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TATATATATA=0./0
(
ALFA)
TA=0.26333/158
(NorthernSweden)
- HGVS:
18.
rs1491114090 [Homo sapiens]- Variant type:
- DEL
- Alleles:
- GT>-
[Show Flanks]
- Chromosome:
- 14:34999014
(GRCh38)
14:35468220
(GRCh37)
- Canonical SPDI:
- NC_000014.9:34999013:GT:
- Gene:
- SRP54 (Varview)
- Functional Consequence:
- upstream_transcript_variant,intron_variant,genic_upstream_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
-=0./0
(
ALFA)
-=0.00038/7
(TOMMO)
-=0.00364/136
(GnomAD)
- HGVS:
19.
rs1491111359 has merged into rs145956462 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- TT>-,T,TTT
[Show Flanks]
- Chromosome:
- 14:34986138
(GRCh38)
14:35455344
(GRCh37)
- Canonical SPDI:
- NC_000014.9:34986130:TTTTTTTTT:TTTTTTT,NC_000014.9:34986130:TTTTTTTTT:TTTTTTTT,NC_000014.9:34986130:TTTTTTTTT:TTTTTTTTTT
- Gene:
- SRP54 (Varview)
- Functional Consequence:
- genic_upstream_transcript_variant,intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TTTTTTTT=0.00568/79
(
ALFA)
-=0.00214/10
(1000Genomes)
-=0.02154/361
(TOMMO)
T=0.11743/508
(Estonian)
- HGVS:
20.
rs1491105063 has merged into rs71435838 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- TTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
[Show Flanks]
- Chromosome:
- 14:34991120
(GRCh38)
14:35460326
(GRCh37)
- Canonical SPDI:
- NC_000014.9:34991109:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000014.9:34991109:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000014.9:34991109:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000014.9:34991109:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000014.9:34991109:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000014.9:34991109:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000014.9:34991109:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000014.9:34991109:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000014.9:34991109:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000014.9:34991109:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000014.9:34991109:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000014.9:34991109:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:34991109:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:34991109:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:34991109:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:34991109:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:34991109:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:34991109:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:34991109:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:34991109:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:34991109:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:34991109:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:34991109:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:34991109:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:34991109:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:34991109:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:34991109:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:34991109:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:34991109:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:34991109:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:34991109:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:34991109:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:34991109:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:34991109:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:34991109:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:34991109:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:34991109:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- Gene:
- SRP54 (Varview)
- Functional Consequence:
- intron_variant,genic_upstream_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
- HGVS:
NC_000014.9:g.34991120_34991129del, NC_000014.9:g.34991121_34991129del, NC_000014.9:g.34991122_34991129del, NC_000014.9:g.34991123_34991129del, NC_000014.9:g.34991124_34991129del, NC_000014.9:g.34991125_34991129del, NC_000014.9:g.34991126_34991129del, NC_000014.9:g.34991127_34991129del, NC_000014.9:g.34991128_34991129del, NC_000014.9:g.34991129del, NC_000014.9:g.34991129dup, NC_000014.9:g.34991128_34991129dup, NC_000014.9:g.34991127_34991129dup, NC_000014.9:g.34991126_34991129dup, NC_000014.9:g.34991125_34991129dup, NC_000014.9:g.34991124_34991129dup, NC_000014.9:g.34991123_34991129dup, NC_000014.9:g.34991122_34991129dup, NC_000014.9:g.34991121_34991129dup, NC_000014.9:g.34991120_34991129dup, NC_000014.9:g.34991119_34991129dup, NC_000014.9:g.34991118_34991129dup, NC_000014.9:g.34991117_34991129dup, NC_000014.9:g.34991116_34991129dup, NC_000014.9:g.34991115_34991129dup, NC_000014.9:g.34991114_34991129dup, NC_000014.9:g.34991113_34991129dup, NC_000014.9:g.34991112_34991129dup, NC_000014.9:g.34991111_34991129dup, NC_000014.9:g.34991110_34991129dup, NC_000014.9:g.34991129_34991130insTTTTTTTTTTTTTTTTTTTTT, NC_000014.9:g.34991129_34991130insTTTTTTTTTTTTTTTTTTTTTT, NC_000014.9:g.34991129_34991130insTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.9:g.34991129_34991130insTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.9:g.34991129_34991130insTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.9:g.34991129_34991130insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.9:g.34991129_34991130insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.8:g.35460326_35460335del, NC_000014.8:g.35460327_35460335del, NC_000014.8:g.35460328_35460335del, NC_000014.8:g.35460329_35460335del, NC_000014.8:g.35460330_35460335del, NC_000014.8:g.35460331_35460335del, NC_000014.8:g.35460332_35460335del, NC_000014.8:g.35460333_35460335del, NC_000014.8:g.35460334_35460335del, NC_000014.8:g.35460335del, NC_000014.8:g.35460335dup, NC_000014.8:g.35460334_35460335dup, NC_000014.8:g.35460333_35460335dup, NC_000014.8:g.35460332_35460335dup, NC_000014.8:g.35460331_35460335dup, NC_000014.8:g.35460330_35460335dup, NC_000014.8:g.35460329_35460335dup, NC_000014.8:g.35460328_35460335dup, NC_000014.8:g.35460327_35460335dup, NC_000014.8:g.35460326_35460335dup, NC_000014.8:g.35460325_35460335dup, NC_000014.8:g.35460324_35460335dup, NC_000014.8:g.35460323_35460335dup, NC_000014.8:g.35460322_35460335dup, NC_000014.8:g.35460321_35460335dup, NC_000014.8:g.35460320_35460335dup, NC_000014.8:g.35460319_35460335dup, NC_000014.8:g.35460318_35460335dup, NC_000014.8:g.35460317_35460335dup, NC_000014.8:g.35460316_35460335dup, NC_000014.8:g.35460335_35460336insTTTTTTTTTTTTTTTTTTTTT, NC_000014.8:g.35460335_35460336insTTTTTTTTTTTTTTTTTTTTTT, NC_000014.8:g.35460335_35460336insTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.8:g.35460335_35460336insTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.8:g.35460335_35460336insTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.8:g.35460335_35460336insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.8:g.35460335_35460336insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT