130172432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 5 prime UTR variant
orthologous variants: 31135905-G-A

130172444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 5 prime UTR variant
orthologous variants: 31135917-G-A

130172489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 31135964-G-A

130172489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 31135964-G-T

130172609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 5 prime UTR variant
orthologous variants: 31136137-G-A

130172609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 5 prime UTR variant
orthologous variants: 31136137-G-T

http://identifiers.org/hco/9/GRCh38#130172740-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31136267-A-C

130172740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31136267-A-G

130172740-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31136267-A-T

http://identifiers.org/hco/9/GRCh38#130172902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31136338-C-A

130172941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31136387-G-A

130173307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31136757-G-A

130173759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, undefined
orthologous variants: 31137030-G-T

130173821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, undefined
orthologous variants: 31137074-C-T

130173837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31137091-C-T

130174056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31137283-G-A

130175016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31137885-A-G

130175102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31137955-G-A

http://identifiers.org/hco/9/GRCh38#130175938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31139318-C-A

130177260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31140586-T-C

130177352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31140661-A-G

130177404-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31140706-G-C

130177592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31140829-G-A

130177592-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31140829-G-C

130177681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31140893-C-T

130177799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31141003-G-A

130178396-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31141338-C-G

130178417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31141346-C-T

130178733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31141595-A-G

130178816-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31141662-A-T

130181318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31143896-G-A

130181414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31143948-G-A

130181504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31144025-T-C

130181667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31144168-G-A

130181725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31144206-C-T

130181729-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31144210-T-A

130181756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31144236-C-T

130181762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31144242-C-T

130181865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31144343-C-T

130182002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31144446-C-T

130182166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31144646-C-T

130182309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31144786-C-T

130182367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31144819-C-T

130182648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31145072-C-T

130182681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31145220-G-A

130182742-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31145341-C-G

130182742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31145341-C-T

130182948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31145665-C-T

130183348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31146035-G-A

130183470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31146134-G-A

130183590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31146261-C-T

130185273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31146948-G-A

130185303-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31146984-T-A

130185303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31146984-T-C

130186159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31147743-A-G

130186252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31147830-G-A

130186280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31147858-C-T

130186299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31147878-A-G

130187111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31148847-C-T

130187170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31148908-G-A

130187260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31148974-T-C

130187503-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31149211-T-A

130187582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31149274-C-T

130187770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31149434-A-G

130187803-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31149467-G-C

130187969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31149609-G-A

130188021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31149648-G-A

130188021-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31149648-G-C

130188513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31150055-G-A

130188560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31150093-T-C

130190473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31151105-C-T

130190535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31151145-C-T

http://identifiers.org/hco/9/GRCh38#130190544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31151154-C-A

130190561-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31151164-T-A

http://identifiers.org/hco/9/GRCh38#130191584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31153753-C-A

130192092-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31154184-G-C

130192253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31154313-G-A

130192268-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31154329-A-T

130193752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31155530-A-G

http://identifiers.org/hco/9/GRCh38#130193775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31155550-C-A

130193775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31155550-C-T

130193803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31155569-G-A

130193803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31155569-G-T

130193873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31155626-G-A

130193873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31155626-G-T

130193902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31155651-G-A

130193902-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31155651-G-C

http://identifiers.org/hco/9/GRCh38#130193927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31155676-C-A

130193927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31155676-C-T

130194081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31155830-G-A

130194276-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31156031-T-A

130194533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31156245-G-A

130194727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31156399-A-G

130194881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31156513-G-A

130195186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31156744-C-T

130195240-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31156804-G-C

130195241-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31156805-G-C

130195551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31157109-G-T

130195558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31157115-G-A

130195572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31157129-C-T

130195584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31157141-C-T

130195585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31157142-G-T

130196110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31157838-C-T

130196235-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31157942-G-C

130199488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31159228-G-A

130199543-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31159282-C-G

130200344-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31160027-T-G

130200348-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31160031-T-A

130200348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31160031-T-C

http://identifiers.org/hco/9/GRCh38#130200380-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31160062-A-C

130200380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31160062-A-G

130200380-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31160062-A-T

130200390-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31160069-T-A

130200427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31160100-G-A

130200427-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31160100-G-C

130200427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31160100-G-T

http://identifiers.org/hco/9/GRCh38#130200430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31160103-C-A

130200430-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31160103-C-G

130200430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31160103-C-T

http://identifiers.org/hco/9/GRCh38#130200435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31160108-C-A

130200435-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31160108-C-G

130200435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31160108-C-T

130200507-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31160186-A-T

http://identifiers.org/hco/9/GRCh38#130200660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31160372-C-A

130200660-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31160372-C-G

130200660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31160372-C-T

130200689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31160400-G-T

130200693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31160404-T-C

130200811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31160488-G-T

130200835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31160510-G-A

130200859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31160539-G-A

http://identifiers.org/hco/9/GRCh38#130200869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31160546-C-A

130200869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31160546-C-T

130200873-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31160550-A-T

130200883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31160560-C-T

130200939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31160607-T-C

130200968-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31160634-G-C

130201612-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31162326-G-C

130201727-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31162415-C-G

130201727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31162415-C-T

130201753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31162434-C-T

130211049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31166468-T-C

130211050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31166469-G-T

130211501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31166878-C-T

130211561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31166926-G-A

130211561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31166926-G-T

130211694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31167035-C-T

130211843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31167147-A-G

130211844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31167148-A-G

130212163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31167393-C-T

http://identifiers.org/hco/9/GRCh38#130212430-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31167535-A-C

130212433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31167538-A-G

http://identifiers.org/hco/9/GRCh38#130212477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31167580-C-A

130212477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31167580-C-T

130212955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31167899-G-A

130213887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31168191-G-A

130213990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31168272-C-T

130214045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31168312-C-T

130214722-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31168544-G-C

130214738-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31168562-G-C

130214785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31168616-A-G

130214793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31168624-G-T

130217006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31170030-A-G

130217133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31170125-C-T

130217174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31170156-G-A

http://identifiers.org/hco/9/GRCh38#130217214-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31170176-A-C

130217214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31170176-A-G

130217215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31170177-C-T

130217696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31170543-G-T

130217786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31170647-T-C

130217844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31170690-C-T

130218024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31170856-C-T

130218030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31170862-C-T

130218091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31170910-T-C

http://identifiers.org/hco/9/GRCh38#130218107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31170926-C-A

http://identifiers.org/hco/9/GRCh38#130218119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31170935-C-A

130218119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31170935-C-T

130218183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31170987-A-G

http://identifiers.org/hco/9/GRCh38#130219540-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31172164-A-C

http://identifiers.org/hco/9/GRCh38#130219598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31172230-C-A

130219598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31172230-C-T

130219631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31172258-G-A

130219631-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31172258-G-C

130219631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31172258-G-T

130219691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31172288-A-G

130219704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31172301-A-G

130219713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31172310-C-T

130219890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31172460-G-A

130219890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31172460-G-T

http://identifiers.org/hco/9/GRCh38#130219900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31172470-C-A

130219900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31172470-C-T

http://identifiers.org/hco/9/GRCh38#130219907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31172477-C-A

130219907-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31172477-C-G

130219907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31172477-C-T

http://identifiers.org/hco/9/GRCh38#130219916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31172486-C-A

http://identifiers.org/hco/9/GRCh38#130219931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31172500-C-A

130219955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31172539-G-A

130220069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31172642-C-T

130220198-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31172793-C-G

130220467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31173016-G-A

130220630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31173207-G-T

130220954-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31173484-C-G

130220985-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31173512-A-T

130220989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31173516-C-T

130221146-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31173758-C-G

130222444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31173970-T-C

130222444-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31173970-T-G

130222445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31173971-G-A

130222593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31174104-A-G

130222599-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31174110-C-G

130222789-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31174324-G-C

130222806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31174344-A-G

130222807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31174345-G-A

130222807-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31174345-G-C

130222807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31174345-G-T

130222867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31174409-G-A

130222867-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31174409-G-C

130222920-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31174462-T-G

130223008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31174539-G-T

130223016-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31174552-A-T

http://identifiers.org/hco/9/GRCh38#130223032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31174568-C-A

130223032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31174568-C-T

http://identifiers.org/hco/9/GRCh38#130223057-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31174617-A-C

130223162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31174754-G-A

130223162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31174754-G-T

130223237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31174805-G-T

http://identifiers.org/hco/9/GRCh38#130223241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31174809-C-A

130223244-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31174812-G-C

130223244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31174812-G-T

http://identifiers.org/hco/9/GRCh38#130223273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31174836-C-A

130223273-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31174836-C-G

130223273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31174836-C-T

130223401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31174931-C-T

130223490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31175022-G-A

http://identifiers.org/hco/9/GRCh38#130226271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31177205-C-A

130226271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31177205-C-T

http://identifiers.org/hco/9/GRCh38#130226277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31177211-C-A

130226277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31177211-C-T

130226302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31177220-G-A

130226302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31177220-G-T

http://identifiers.org/hco/9/GRCh38#130226314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31177232-C-A

130226314-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31177232-C-G

130226314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31177232-C-T

130226439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: synonymous variant
orthologous variants: 31177349-A-G

130226475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: synonymous variant
orthologous variants: 31177385-C-T

http://identifiers.org/hco/9/GRCh38#130232937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31182243-C-A

130232937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: intron variant
orthologous variants: 31182243-C-T

130233066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3 prime UTR variant
orthologous variants: 31182369-G-A

130233066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3 prime UTR variant
orthologous variants: 31182369-G-T

130233127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3 prime UTR variant
orthologous variants: 31182427-T-C

http://identifiers.org/hco/9/GRCh38#130233130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31182430-C-A

130233134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3 prime UTR variant
orthologous variants: 31182434-T-C

http://identifiers.org/hco/9/GRCh38#130233201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31182502-C-A

130233201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3 prime UTR variant
orthologous variants: 31182502-C-T

http://identifiers.org/hco/9/GRCh38#130233269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31182571-C-A

130233291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3 prime UTR variant
orthologous variants: 31182593-G-T

130233392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3 prime UTR variant
orthologous variants: 31182685-C-T

130233923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3 prime UTR variant
orthologous variants: 31183114-T-C

130234138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3 prime UTR variant
orthologous variants: 31183336-C-T

130234147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3 prime UTR variant
orthologous variants: 31183354-G-T

130234148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3 prime UTR variant
orthologous variants: 31183355-G-A

http://identifiers.org/hco/9/GRCh38#130234182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31183380-C-A

130234197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3 prime UTR variant
orthologous variants: 31183389-T-C

130234570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3 prime UTR variant
orthologous variants: 31183622-A-G

http://identifiers.org/hco/9/GRCh38#130234617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31183668-C-A

130234617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3 prime UTR variant
orthologous variants: 31183668-C-T

130234788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3 prime UTR variant
orthologous variants: 31183847-C-T

130234829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3 prime UTR variant
orthologous variants: 31183882-G-A

130234829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3 prime UTR variant
orthologous variants: 31183882-G-T

http://identifiers.org/hco/9/GRCh38#130234957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31184006-C-A

130234958-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3 prime UTR variant
orthologous variants: 31184007-T-A

130234993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3 prime UTR variant
orthologous variants: 31184083-G-A

http://identifiers.org/hco/9/GRCh38#130235009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31184106-C-A

130235009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3 prime UTR variant
orthologous variants: 31184106-C-T

130235035-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3 prime UTR variant
orthologous variants: 31184135-T-A

130235035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3 prime UTR variant
orthologous variants: 31184135-T-C

http://identifiers.org/hco/9/GRCh38#130235283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31184270-C-A

130235283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3 prime UTR variant
orthologous variants: 31184270-C-T

130235286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3 prime UTR variant
orthologous variants: 31184273-G-A

130235286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3 prime UTR variant
orthologous variants: 31184273-G-T

130235380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3 prime UTR variant
orthologous variants: 31184331-G-T

130235424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3 prime UTR variant
orthologous variants: 31184364-T-C

130235453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3 prime UTR variant
orthologous variants: 31184403-T-C

http://identifiers.org/hco/9/GRCh38#130235517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31184464-C-A

130235517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3 prime UTR variant
orthologous variants: 31184464-C-T

130235574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3 prime UTR variant
orthologous variants: 31184521-T-C

http://identifiers.org/hco/9/GRCh38#130235792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31184699-C-A

130235792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3 prime UTR variant
orthologous variants: 31184699-C-T

130235797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3 prime UTR variant
orthologous variants: 31184704-G-A

130235797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3 prime UTR variant
orthologous variants: 31184704-G-T

http://identifiers.org/hco/9/GRCh38#130235863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31184788-C-A

130235863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3 prime UTR variant
orthologous variants: 31184788-C-T

130235965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3 prime UTR variant
orthologous variants: 31184861-T-C

130235988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3 prime UTR variant
orthologous variants: 31184884-A-G

http://identifiers.org/hco/9/GRCh38#130236000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31184896-C-A

130236000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3 prime UTR variant
orthologous variants: 31184896-C-T

130236285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 31185150-G-T

130236409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3 prime UTR variant
orthologous variants: 31185261-G-A

130236409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3 prime UTR variant
orthologous variants: 31185261-G-T

130236429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3 prime UTR variant
orthologous variants: 31185279-T-C

130236432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 31185282-G-T

http://identifiers.org/hco/9/GRCh38#130236447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#31185303-C-A

130236986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3 prime UTR variant
orthologous variants: 31185718-T-C

130236986-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3 prime UTR variant
orthologous variants: 31185718-T-G

http://identifiers.org/hco/9/GRCh38#130237102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31185806-C-A

130237102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3 prime UTR variant
orthologous variants: 31185806-C-T

http://identifiers.org/hco/9/GRCh38#130237109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31185813-C-A

130237109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3 prime UTR variant
orthologous variants: 31185813-C-T

http://identifiers.org/hco/9/GRCh38#130237258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31185959-C-A

130237258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3 prime UTR variant
orthologous variants: 31185959-C-T

130237302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3953
most severe consequence: 3 prime UTR variant
orthologous variants: 31186001-G-A