SNP Links for Nucleotide (Select 300797028) - SNP - NCBI

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Links from Nucleotide

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Select item 14909081631.

rs1490908163 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: X:10447104 (GRCh38)
X:10415144 (GRCh37)
Canonical SPDI:: NC_000023.11:10447103:T:C
Gene:: MID1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: C=0.000071/1 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000023.11:g.10447104T>C, NC_000023.10:g.10415144T>C, NG_008197.2:g.391587A>G, NM_033290.4:c.*2264A>G, NM_033290.3:c.*2264A>G, NM_000381.4:c.*2264A>G, NM_000381.3:c.*2264A>G, NM_001347733.2:c.*2264A>G, NM_001347733.1:c.*2264A>G, NM_001098624.2:c.*2264A>G, NM_033289.2:c.*2264A>G, NM_033289.1:c.*2264A>G, NM_001193277.1:c.*2264A>G

Select item 14908514952.

rs1490851495 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:10445575 (GRCh38)
X:10413615 (GRCh37)
Canonical SPDI:: NC_000023.11:10445574:A:G
Gene:: MID1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.10445575A>G, NC_000023.10:g.10413615A>G, NG_008197.2:g.393116T>C, NM_033290.4:c.*3793T>C, NM_033290.3:c.*3793T>C, NM_000381.4:c.*3793T>C, NM_000381.3:c.*3793T>C, NM_001347733.2:c.*3793T>C, NM_001347733.1:c.*3793T>C, NM_001098624.2:c.*3793T>C, NM_033289.2:c.*3793T>C, NM_033289.1:c.*3793T>C, NM_001193277.1:c.*3793T>C

Select item 14902435453.

rs1490243545 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:10445414 (GRCh38)
X:10413454 (GRCh37)
Canonical SPDI:: NC_000023.11:10445413:A:G
Gene:: MID1 (Varview)
Functional Consequence:: downstream_transcript_variant,genic_downstream_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000023.11:g.10445414A>G, NC_000023.10:g.10413454A>G, NG_008197.2:g.393277T>C, NM_033290.4:c.*3954T>C, NM_033290.3:c.*3954T>C, NM_001347733.2:c.*3954T>C, NM_001347733.1:c.*3954T>C, NM_001098624.2:c.*3954T>C, NM_033289.2:c.*3954T>C, NM_033289.1:c.*3954T>C, NM_001193277.1:c.*3954T>C, NM_000381.3:c.*3954T>C

Select item 14896809564.

rs1489680956 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: X:10447831 (GRCh38)
X:10415871 (GRCh37)
Canonical SPDI:: NC_000023.11:10447830:G:C
Gene:: MID1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.10447831G>C, NC_000023.10:g.10415871G>C, NG_008197.2:g.390860C>G, NM_033290.4:c.*1537C>G, NM_033290.3:c.*1537C>G, NM_000381.4:c.*1537C>G, NM_000381.3:c.*1537C>G, NM_001347733.2:c.*1537C>G, NM_001347733.1:c.*1537C>G, NM_001098624.2:c.*1537C>G, NM_033289.2:c.*1537C>G, NM_033289.1:c.*1537C>G, NM_001193277.1:c.*1537C>G

Select item 14892997535.

rs1489299753 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:10449687 (GRCh38)
X:10417727 (GRCh37)
Canonical SPDI:: NC_000023.11:10449686:G:A
Gene:: MID1 (Varview)
Functional Consequence:: coding_sequence_variant,genic_downstream_transcript_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
A=0.000045/1 (TOMMO)
HGVS:: NC_000023.11:g.10449687G>A, NC_000023.10:g.10417727G>A, NG_008197.2:g.389004C>T, NM_033290.4:c.1685C>T, NM_033290.3:c.1685C>T, NM_000381.4:c.1685C>T, NM_000381.3:c.1685C>T, NM_001347733.2:c.1685C>T, NM_001347733.1:c.1685C>T, NM_001098624.2:c.1685C>T, NM_033289.2:c.1571C>T, NM_033289.1:c.1571C>T, NM_001193277.1:c.1685C>T, NP_150632.1:p.Ala562Val, NP_000372.1:p.Ala562Val, NP_001334662.1:p.Ala562Val, NP_001092094.1:p.Ala562Val, NP_150631.1:p.Ala524Val, NP_001180206.1:p.Ala562Val

Select item 14876624916.

rs1487662491 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:10459708 (GRCh38)
X:10427748 (GRCh37)
Canonical SPDI:: NC_000023.11:10459707:A:G
Gene:: MID1 (Varview)
Functional Consequence:: coding_sequence_variant,genic_downstream_transcript_variant,missense_variant
Validated:: by frequency
MAF:: G=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.10459708A>G, NC_000023.10:g.10427748A>G, NG_008197.2:g.378983T>C, NM_033290.4:c.1385T>C, NM_033290.3:c.1385T>C, NM_000381.4:c.1385T>C, NM_000381.3:c.1385T>C, NM_001347733.2:c.1385T>C, NM_001347733.1:c.1385T>C, NM_001098624.2:c.1385T>C, NM_033289.2:c.1271T>C, NM_033289.1:c.1271T>C, NM_001193277.1:c.1385T>C, NM_033291.1:c.1385T>C, NP_150632.1:p.Met462Thr, NP_000372.1:p.Met462Thr, NP_001334662.1:p.Met462Thr, NP_001092094.1:p.Met462Thr, NP_150631.1:p.Met424Thr, NP_001180206.1:p.Met462Thr

Select item 14861457907.

rs1486145790 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:10469817 (GRCh38)
X:10437857 (GRCh37)
Canonical SPDI:: NC_000023.11:10469816:C:T
Gene:: MID1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.10469817C>T, NC_000023.10:g.10437857C>T, NG_008197.2:g.368874G>A, NM_033290.4:c.1165G>A, NM_033290.3:c.1165G>A, NM_000381.4:c.1165G>A, NM_000381.3:c.1165G>A, NM_001347733.2:c.1165G>A, NM_001347733.1:c.1165G>A, NM_001098624.2:c.1165G>A, NM_033289.2:c.1051G>A, NM_033289.1:c.1051G>A, NM_001193277.1:c.1165G>A, NM_001193278.1:c.1318G>A, NM_001193279.1:c.1165G>A, NM_001193280.1:c.1051G>A, NM_033291.1:c.1165G>A, NP_150632.1:p.Glu389Lys, NP_000372.1:p.Glu389Lys, NP_001334662.1:p.Glu389Lys, NP_001092094.1:p.Glu389Lys, NP_150631.1:p.Glu351Lys, NP_001180206.1:p.Glu389Lys, NP_001180207.1:p.Glu440Lys, NP_001180208.1:p.Glu389Lys, NP_001180209.1:p.Glu351Lys

Select item 14847563118.

rs1484756311 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:10447131 (GRCh38)
X:10415171 (GRCh37)
Canonical SPDI:: NC_000023.11:10447130:A:G
Gene:: MID1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
G=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.10447131A>G, NC_000023.10:g.10415171A>G, NG_008197.2:g.391560T>C, NM_033290.4:c.*2237T>C, NM_033290.3:c.*2237T>C, NM_000381.4:c.*2237T>C, NM_000381.3:c.*2237T>C, NM_001347733.2:c.*2237T>C, NM_001347733.1:c.*2237T>C, NM_001098624.2:c.*2237T>C, NM_033289.2:c.*2237T>C, NM_033289.1:c.*2237T>C, NM_001193277.1:c.*2237T>C

Select item 14837949679.

rs1483794967 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:10523156 (GRCh38)
X:10491196 (GRCh37)
Canonical SPDI:: NC_000023.11:10523155:A:G
Gene:: MID1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
G=0.000045/1 (TOMMO)
HGVS:: NC_000023.11:g.10523156A>G, NC_000023.10:g.10491196A>G, NG_008197.2:g.315535T>C, NM_033290.4:c.692T>C, NM_033290.3:c.692T>C, NM_000381.4:c.692T>C, NM_000381.3:c.692T>C, NM_001347733.2:c.692T>C, NM_001347733.1:c.692T>C, NM_001098624.2:c.692T>C, NM_033289.2:c.578T>C, NM_033289.1:c.578T>C, NM_001193277.1:c.692T>C, NM_001193278.1:c.692T>C, NM_001193279.1:c.692T>C, NM_001193280.1:c.578T>C, NM_033291.1:c.692T>C, NM_001193281.1:c.578T>C, NP_150632.1:p.Ile231Thr, NP_000372.1:p.Ile231Thr, NP_001334662.1:p.Ile231Thr, NP_001092094.1:p.Ile231Thr, NP_150631.1:p.Ile193Thr, NP_001180206.1:p.Ile231Thr, NP_001180207.1:p.Ile231Thr, NP_001180208.1:p.Ile231Thr, NP_001180209.1:p.Ile193Thr

Select item 148373535210.

rs1483735352 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:10447811 (GRCh38)
X:10415851 (GRCh37)
Canonical SPDI:: NC_000023.11:10447810:C:T
Gene:: MID1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000023.11:g.10447811C>T, NC_000023.10:g.10415851C>T, NG_008197.2:g.390880G>A, NM_033290.4:c.*1557G>A, NM_033290.3:c.*1557G>A, NM_000381.4:c.*1557G>A, NM_000381.3:c.*1557G>A, NM_001347733.2:c.*1557G>A, NM_001347733.1:c.*1557G>A, NM_001098624.2:c.*1557G>A, NM_033289.2:c.*1557G>A, NM_033289.1:c.*1557G>A, NM_001193277.1:c.*1557G>A

Select item 148364572711.

rs1483645727 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:10482514 (GRCh38)
X:10450554 (GRCh37)
Canonical SPDI:: NC_000023.11:10482513:G:A
Gene:: MID1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000015/4 (TOPMED)
HGVS:: NC_000023.11:g.10482514G>A, NC_000023.10:g.10450554G>A, NG_008197.2:g.356177C>T, NM_033290.4:c.979C>T, NM_033290.3:c.979C>T, NM_000381.4:c.979C>T, NM_000381.3:c.979C>T, NM_001347733.2:c.979C>T, NM_001347733.1:c.979C>T, NM_001098624.2:c.979C>T, NM_033289.2:c.865C>T, NM_033289.1:c.865C>T, NM_001193277.1:c.979C>T, NM_001193278.1:c.1132C>T, NM_001193279.1:c.979C>T, NM_001193280.1:c.865C>T, NM_033291.1:c.979C>T, NP_150632.1:p.Arg327Cys, NP_000372.1:p.Arg327Cys, NP_001334662.1:p.Arg327Cys, NP_001092094.1:p.Arg327Cys, NP_150631.1:p.Arg289Cys, NP_001180206.1:p.Arg327Cys, NP_001180207.1:p.Arg378Cys, NP_001180208.1:p.Arg327Cys, NP_001180209.1:p.Arg289Cys

Select item 148340589112.

rs1483405891 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: X:10446983 (GRCh38)
X:10415023 (GRCh37)
Canonical SPDI:: NC_000023.11:10446982:C:G,NC_000023.11:10446982:C:T
Gene:: MID1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.00001/1 (GnomAD)
T=0.000208/1 (1000Genomes)
HGVS:: NC_000023.11:g.10446983C>G, NC_000023.11:g.10446983C>T, NC_000023.10:g.10415023C>G, NC_000023.10:g.10415023C>T, NG_008197.2:g.391708G>C, NG_008197.2:g.391708G>A, NM_033290.4:c.*2385G>C, NM_033290.4:c.*2385G>A, NM_033290.3:c.*2385G>C, NM_033290.3:c.*2385G>A, NM_000381.4:c.*2385G>C, NM_000381.4:c.*2385G>A, NM_000381.3:c.*2385G>C, NM_000381.3:c.*2385G>A, NM_001347733.2:c.*2385G>C, NM_001347733.2:c.*2385G>A, NM_001347733.1:c.*2385G>C, NM_001347733.1:c.*2385G>A, NM_001098624.2:c.*2385G>C, NM_001098624.2:c.*2385G>A, NM_033289.2:c.*2385G>C, NM_033289.2:c.*2385G>A, NM_033289.1:c.*2385G>C, NM_033289.1:c.*2385G>A, NM_001193277.1:c.*2385G>C, NM_001193277.1:c.*2385G>A

Select item 148326084113.

rs1483260841 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:10567359 (GRCh38)
X:10535399 (GRCh37)
Canonical SPDI:: NC_000023.11:10567358:G:A
Gene:: MID1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
HGVS:: NC_000023.11:g.10567359G>A, NC_000023.10:g.10535399G>A, NG_008197.2:g.271332C>T, NM_033290.4:c.189C>T, NM_033290.3:c.189C>T, NM_000381.4:c.189C>T, NM_000381.3:c.189C>T, NM_001347733.2:c.189C>T, NM_001347733.1:c.189C>T, NM_001098624.2:c.189C>T, NM_033289.2:c.189C>T, NM_033289.1:c.189C>T, NM_001193277.1:c.189C>T, NM_001193278.1:c.189C>T, NM_001193279.1:c.189C>T, NM_001193280.1:c.189C>T, NM_033291.1:c.189C>T, NM_001193281.1:c.189C>T

Select item 148309956114.

rs1483099561 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G,T [Show Flanks]
Chromosome:: X:10446803 (GRCh38)
X:10414843 (GRCh37)
Canonical SPDI:: NC_000023.11:10446802:C:A,NC_000023.11:10446802:C:G,NC_000023.11:10446802:C:T
Gene:: MID1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
T=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.10446803C>A, NC_000023.11:g.10446803C>G, NC_000023.11:g.10446803C>T, NC_000023.10:g.10414843C>A, NC_000023.10:g.10414843C>G, NC_000023.10:g.10414843C>T, NG_008197.2:g.391888G>T, NG_008197.2:g.391888G>C, NG_008197.2:g.391888G>A, NM_033290.4:c.*2565G>T, NM_033290.4:c.*2565G>C, NM_033290.4:c.*2565G>A, NM_033290.3:c.*2565G>T, NM_033290.3:c.*2565G>C, NM_033290.3:c.*2565G>A, NM_000381.4:c.*2565G>T, NM_000381.4:c.*2565G>C, NM_000381.4:c.*2565G>A, NM_000381.3:c.*2565G>T, NM_000381.3:c.*2565G>C, NM_000381.3:c.*2565G>A, NM_001347733.2:c.*2565G>T, NM_001347733.2:c.*2565G>C, NM_001347733.2:c.*2565G>A, NM_001347733.1:c.*2565G>T, NM_001347733.1:c.*2565G>C, NM_001347733.1:c.*2565G>A, NM_001098624.2:c.*2565G>T, NM_001098624.2:c.*2565G>C, NM_001098624.2:c.*2565G>A, NM_033289.2:c.*2565G>T, NM_033289.2:c.*2565G>C, NM_033289.2:c.*2565G>A, NM_033289.1:c.*2565G>T, NM_033289.1:c.*2565G>C, NM_033289.1:c.*2565G>A, NM_001193277.1:c.*2565G>T, NM_001193277.1:c.*2565G>C, NM_001193277.1:c.*2565G>A

Select item 148252414015.

rs1482524140 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:10448457 (GRCh38)
X:10416497 (GRCh37)
Canonical SPDI:: NC_000023.11:10448456:G:A
Gene:: MID1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000029/3 (GnomAD)
A=0.00003/8 (TOPMED)
HGVS:: NC_000023.11:g.10448457G>A, NC_000023.10:g.10416497G>A, NG_008197.2:g.390234C>T, NM_033290.4:c.*911C>T, NM_033290.3:c.*911C>T, NM_000381.4:c.*911C>T, NM_000381.3:c.*911C>T, NM_001347733.2:c.*911C>T, NM_001347733.1:c.*911C>T, NM_001098624.2:c.*911C>T, NM_033289.2:c.*911C>T, NM_033289.1:c.*911C>T, NM_001193277.1:c.*911C>T, NM_033291.1:c.*1155C>T

Select item 148248608616.

rs1482486086 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:10446344 (GRCh38)
X:10414384 (GRCh37)
Canonical SPDI:: NC_000023.11:10446343:C:T
Gene:: MID1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.10446344C>T, NC_000023.10:g.10414384C>T, NG_008197.2:g.392347G>A, NM_033290.4:c.*3024G>A, NM_033290.3:c.*3024G>A, NM_000381.4:c.*3024G>A, NM_000381.3:c.*3024G>A, NM_001347733.2:c.*3024G>A, NM_001347733.1:c.*3024G>A, NM_001098624.2:c.*3024G>A, NM_033289.2:c.*3024G>A, NM_033289.1:c.*3024G>A, NM_001193277.1:c.*3024G>A

Select item 148215389717.

rs1482153897 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:10448448 (GRCh38)
X:10416488 (GRCh37)
Canonical SPDI:: NC_000023.11:10448447:G:A
Gene:: MID1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.00027/3 (TOMMO)
HGVS:: NC_000023.11:g.10448448G>A, NC_000023.10:g.10416488G>A, NG_008197.2:g.390243C>T, NM_033290.4:c.*920C>T, NM_033290.3:c.*920C>T, NM_000381.4:c.*920C>T, NM_000381.3:c.*920C>T, NM_001347733.2:c.*920C>T, NM_001347733.1:c.*920C>T, NM_001098624.2:c.*920C>T, NM_033289.2:c.*920C>T, NM_033289.1:c.*920C>T, NM_001193277.1:c.*920C>T, NM_033291.1:c.*1164C>T

Select item 148161633518.

rs1481616335 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: X:10455025 (GRCh38)
X:10423065 (GRCh37)
Canonical SPDI:: NC_000023.11:10455024:G:C
Gene:: MID1 (Varview)
Functional Consequence:: coding_sequence_variant,genic_downstream_transcript_variant,synonymous_variant
Validated:: by frequency
MAF:: C=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.10455025G>C, NC_000023.10:g.10423065G>C, NG_008197.2:g.383666C>G, NM_033290.4:c.1500C>G, NM_033290.3:c.1500C>G, NM_000381.4:c.1500C>G, NM_000381.3:c.1500C>G, NM_001347733.2:c.1500C>G, NM_001347733.1:c.1500C>G, NM_001098624.2:c.1500C>G, NM_033289.2:c.1386C>G, NM_033289.1:c.1386C>G, NM_001193277.1:c.1500C>G, NM_033291.1:c.1500C>G

Select item 148144151919.

rs1481441519 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:10447279 (GRCh38)
X:10415319 (GRCh37)
Canonical SPDI:: NC_000023.11:10447278:A:G
Gene:: MID1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.10447279A>G, NC_000023.10:g.10415319A>G, NG_008197.2:g.391412T>C, NM_033290.4:c.*2089T>C, NM_033290.3:c.*2089T>C, NM_000381.4:c.*2089T>C, NM_000381.3:c.*2089T>C, NM_001347733.2:c.*2089T>C, NM_001347733.1:c.*2089T>C, NM_001098624.2:c.*2089T>C, NM_033289.2:c.*2089T>C, NM_033289.1:c.*2089T>C, NM_001193277.1:c.*2089T>C

Select item 148093897920.

rs1480938979 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:10677478 (GRCh38)
X:10645518 (GRCh37)
Canonical SPDI:: NC_000023.11:10677477:C:T
Gene:: MID1 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant,5_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: T=0.000671/3 (ALFA)
T=0.000029/3 (GnomAD)
HGVS:: NC_000023.11:g.10677478C>T, NC_000023.10:g.10645518C>T, NG_008197.2:g.161213G>A, NM_001098624.2:c.-70G>A

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