88879794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant
orthologous variants: 34169239-G-T

88879796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant
orthologous variants: 34169241-G-A

88879796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant
orthologous variants: 34169241-G-T

88879836-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant
orthologous variants: 34169272-G-C

88879836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant
orthologous variants: 34169272-G-T

88879950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 34169360-G-A

88879950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 34169360-G-T

88879981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 34169394-G-T

88880002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 34169418-G-T

88880043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 34169455-A-G

88880043-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 34169455-A-T

88880050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 34169463-G-A

88880050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 34169463-G-T

http://identifiers.org/hco/10/GRCh38#88880076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34169489-C-A

http://identifiers.org/hco/10/GRCh38#88880144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34169549-C-A

88880222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 34169618-G-A

88880222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 34169618-G-T

88880267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 34169665-C-T

88880320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 34169704-G-A

88880320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 34169704-G-T

88880324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 34169708-G-A

88880324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 34169708-G-T

88880335-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 34169719-C-G

88880335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 34169719-C-T

http://identifiers.org/hco/10/GRCh38#88880470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34169828-C-A

88880470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34169828-C-T

88880531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34169888-C-T

88880758-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34170028-C-G

88880905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34170130-A-G

88881020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34170242-G-T

88881045-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34170284-G-C

http://identifiers.org/hco/10/GRCh38#88881217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34170455-C-A

88881271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34170506-C-T

88881427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34170663-G-A

http://identifiers.org/hco/10/GRCh38#88881858-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34170994-A-C

88881858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34170994-A-G

88881987-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34171349-A-T

88882010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 34171372-T-C

88882065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34171419-G-A

88882065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34171419-G-T

88882114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34171468-G-T

http://identifiers.org/hco/10/GRCh38#88882125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34171479-C-A

88882140-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34171491-A-T

http://identifiers.org/hco/10/GRCh38#88882206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34171537-C-A

http://identifiers.org/hco/10/GRCh38#88882299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34171586-C-A

88882390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34171676-G-A

88882501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34171766-G-A

88882501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34171766-G-T

88882683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34172558-G-T

88882808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34172683-C-T

88883233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34172794-A-G

88883444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34173170-T-C

88883982-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34173680-C-G

88884147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34173810-G-A

88884289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34173954-T-C

88884307-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34173972-A-T

88884390-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34174029-C-G

88884470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34174105-A-G

88884513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34174149-G-A

88884971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34174522-C-T

88884978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34174532-G-T

http://identifiers.org/hco/10/GRCh38#88885210-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34174941-A-C

88885210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34174941-A-G

88885556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34176194-G-A

88885602-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34176249-C-G

88885675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34176318-T-C

88885942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34176575-T-C

88886431-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34176812-G-C

88886491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34176871-A-G

88886533-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34176916-T-A

88886813-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34177197-T-A

88886835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34177215-G-A

88886841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34177221-C-T

88887041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34177457-A-G

88887041-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34177457-A-T

88887453-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34177821-G-C

88887470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34177831-G-A

88887858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34177920-G-T

88887936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34177995-C-T

88888322-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34178397-C-G

88888322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34178397-C-T

88888324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34178399-G-A

88888373-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34178448-T-G

88888393-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34178468-G-C

88888423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34178490-G-A

88888769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34178701-G-A

88888957-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34178867-T-A

88889588-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34180469-A-T

88889613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34180506-G-A

88889979-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34180936-G-C

88890006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34180963-A-G

88890121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34181072-G-A

88890187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34181142-G-A

88890423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34182082-C-T

88890509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34182158-G-A

88890563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34182204-G-A

88890566-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34182207-T-A

88890566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34182207-T-C

88890909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34182442-C-T

88890964-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34182496-T-A

88891056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34182592-C-T

88891846-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34184193-G-C

88892014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34184340-T-C

88892388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34184683-C-T

88892710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34185020-G-T

88892725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34185035-G-A

88892816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34185150-G-A

88892879-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34185213-A-T

88893016-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34185333-A-T

88893093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34185410-C-T

88893257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34185572-G-A

88893276-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34185604-T-A

88893298-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34185630-T-A

88893298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34185630-T-C

88893358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34185690-G-A

88893427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34185736-C-T

88893442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34185755-G-A

88893442-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34185755-G-C

http://identifiers.org/hco/10/GRCh38#88893826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34185830-C-A

88893826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34185830-C-T

http://identifiers.org/hco/10/GRCh38#88893875-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34185878-A-C

88896397-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, undefined
orthologous variants: 34188322-A-T

88896741-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34188656-C-G

88896741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34188656-C-T

88896749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34188664-G-T

88896981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34189495-T-C

88897231-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, undefined
orthologous variants: 34189654-G-C

88897431-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34189843-T-A

88897470-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, undefined
orthologous variants: 34189880-G-T

88897521-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, undefined
orthologous variants: 34189907-A-T

88897526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, undefined
orthologous variants: 34189912-G-A

http://identifiers.org/hco/10/GRCh38#88897567-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#34189955-A-C

88897652-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, undefined
orthologous variants: 34190032-C-G

88897652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, undefined
orthologous variants: 34190032-C-T

88897848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34190207-G-A

88898398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34194054-A-G

88898520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34194124-A-G

88898811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34194414-A-G

88898834-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34194437-G-T

88898876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34194463-G-T

88898964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, undefined
orthologous variants: 34194547-C-T

88900841-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34196749-G-C

88901110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 34197036-G-A

88901147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 34197067-G-T

88901244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 34197169-T-C

http://identifiers.org/hco/10/GRCh38#88901337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34197276-C-A

88901337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 34197276-C-T

http://identifiers.org/hco/10/GRCh38#88901442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#34197385-C-A

88901442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 34197385-C-T

88901446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 34197389-C-T

http://identifiers.org/hco/10/GRCh38#88901485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34197428-C-A

88901485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 34197428-C-T

88901487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 34197430-G-A

88901487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 34197430-G-T

88901541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 34197483-A-G

88901541-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 34197483-A-T

88901558-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 34197499-G-C

88901558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 34197499-G-T

http://identifiers.org/hco/10/GRCh38#88901585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#34197515-C-A

88901585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 34197515-C-T

88901598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 34197528-G-T

88901631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 34197562-G-A

88901631-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 34197562-G-C

http://identifiers.org/hco/10/GRCh38#88901637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34197568-C-A

88901637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 34197568-C-T

88901661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5 prime UTR variant
orthologous variants: 34197592-G-A

88901728-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: missense_variant, undefined
orthologous variants: 34197656-T-A

88901786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34197714-A-G

http://identifiers.org/hco/10/GRCh38#88901816-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#34197740-A-C

88901825-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, undefined
orthologous variants: 34197749-T-A

88901848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, undefined
orthologous variants: 34197773-T-C

88901881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, undefined
orthologous variants: 34197806-T-C

http://identifiers.org/hco/10/GRCh38#88901891-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#34197816-A-C

88902052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, undefined
orthologous variants: 34197960-T-C

88902202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34198114-C-T

88902208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34198123-A-G

88902212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34198127-C-T

88902287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34198823-C-T

88903935-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34202460-C-G

88904329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34202780-C-T

88904669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34203106-A-G

88905369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34203863-T-C

88907126-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34205250-T-A

88907177-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34205300-A-T

88907182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34205307-C-T

88907275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34205397-A-G

88907277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34205399-G-A

88907277-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34205399-G-C

88907285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34205407-A-G

88907308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34205428-C-T

http://identifiers.org/hco/10/GRCh38#88907761-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34206202-A-C

88907766-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34206207-T-G

88907833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34206278-A-G

88907922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34206357-A-G

88908105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34206537-G-A

88908105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34206537-G-T

88908115-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34206547-G-C

88908171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34206620-G-A

88908171-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34206620-G-C

http://identifiers.org/hco/10/GRCh38#88908207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34206648-C-A

88908327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34206767-G-A

88908327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34206767-G-T

88908601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34207406-A-G

88908601-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34207406-A-T

http://identifiers.org/hco/10/GRCh38#88908610-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34207415-A-C

88908610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34207415-A-G

88908611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34207416-T-C

88908613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34207418-T-C

88908614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34207419-T-C

88908673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34207465-A-G

88908686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34207478-G-A

88908786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34207577-G-T

http://identifiers.org/hco/10/GRCh38#88908827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34207616-C-A

88908827-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34207616-C-G

88908827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34207616-C-T

http://identifiers.org/hco/10/GRCh38#88908843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34207632-C-A

88908843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34207632-C-T

http://identifiers.org/hco/10/GRCh38#88908884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34207653-C-A

88908884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34207653-C-T

88908889-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34207658-G-C

88908889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34207658-G-T

88910192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34208227-G-A

88910319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34208348-A-G

88910337-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34208366-T-A

88910416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34208444-T-C

88910794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34208743-A-G

http://identifiers.org/hco/10/GRCh38#88910852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34208766-C-A

88910852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34208766-C-T

88910890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34208805-T-C

88911065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34208986-T-C

88911133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34209046-G-A

88912073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34210347-G-A

88912212-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34210467-A-T

88912221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34210475-T-C

88912254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34210510-G-A

88912254-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34210510-G-C

88912254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34210510-G-T

88912286-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34210541-T-G

88912333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34210608-C-T

http://identifiers.org/hco/10/GRCh38#88912376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34210652-C-A

88912484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34210752-G-A

88912484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34210752-G-T

88912493-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34210761-T-A

88912552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34210821-G-A

88912552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34210821-G-T

88912567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34210835-T-C

88912569-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34210837-G-C

88912569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34210837-G-T

88912573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34210841-T-C

88912578-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34210846-T-G

88912769-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34211011-T-G

88912781-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34211023-T-G

88912909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34211140-T-C

88912985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34211210-G-A

88912985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34211210-G-T

88913093-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 34211353-C-G

88913093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 34211353-C-T

88913241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 34211501-A-G

88913241-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 34211501-A-T

88913262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 34211522-G-A

88913280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 34211540-A-G

88913336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 34211596-A-G

88913346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 34211606-G-A

88913653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34211783-A-G

88913826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34211919-G-A

88913959-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34212042-T-A

88914139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34212213-C-T

88914198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34212270-G-A

88914221-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34212289-C-G

88914272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34212341-T-C

88914392-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34212481-T-A

88914392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34212481-T-C

88914409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34212498-A-G

88914415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34212504-A-G

88914417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34212506-A-G

88914492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34212572-A-G

88914550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 34212626-A-G

88914562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 34212638-A-G

88914637-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 34212713-T-A

88914637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 34212713-T-C

88914662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34212738-T-C

88914689-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34212747-T-A

88914689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34212747-T-C

88914693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34212751-T-C

88915975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34213068-C-T

88916110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34213187-T-C

88916234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34213292-C-T

88916517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34213571-G-A

http://identifiers.org/hco/10/GRCh38#88916529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34213580-C-A

http://identifiers.org/hco/10/GRCh38#88916530-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34213581-A-C

88916530-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34213581-A-T

88916657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34213651-T-C

88916760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 34213756-A-G

88916832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34213828-T-C

88916834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34213830-G-A

88916834-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34213830-G-T

88916835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34213831-G-A

88916835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34213831-G-T

88916866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34213860-A-G

88916866-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34213860-A-T

88916886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34213877-G-A

88916886-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34213877-G-C

88916886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34213877-G-T

88916891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34213882-G-T

http://identifiers.org/hco/10/GRCh38#88916895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34213886-C-A

88917069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34213995-A-G

88919368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34214911-T-C

88919402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34215073-C-T

88919425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34215095-C-T

88919610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34215279-A-G

88919627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34215296-T-C

88919674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34215341-C-T

88920943-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34215658-T-A

88920945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34215660-T-C

http://identifiers.org/hco/10/GRCh38#88921021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34215723-C-A

88921035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34215735-G-A

88921124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34215819-G-T

88921477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34216313-G-T

http://identifiers.org/hco/10/GRCh38#88921481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34216317-C-A

88921481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34216317-C-T

88921485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34216321-G-A

88921485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34216321-G-T

http://identifiers.org/hco/10/GRCh38#88921508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34216336-C-A

88921508-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34216336-C-G

88921508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34216336-C-T

88921808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34216479-C-T

88921864-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34216513-T-G

88921932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34216585-G-A

88922045-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34216673-C-G

88922047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34216675-C-T

88922167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34216774-C-T

http://identifiers.org/hco/10/GRCh38#88922205-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34216790-A-C

88922205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34216790-A-G

88922209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34216794-T-C

88922258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34216847-T-C

88922323-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34216891-G-C

88922323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34216891-G-T

http://identifiers.org/hco/10/GRCh38#88922433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34216999-C-A

88922433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 34216999-C-T

88923075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34217329-T-C

88923083-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34217337-T-A

88923083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34217337-T-C

http://identifiers.org/hco/10/GRCh38#88923084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34217338-C-A

88923084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34217338-C-T

88923091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34217345-T-C

http://identifiers.org/hco/10/GRCh38#88923092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34217346-C-A

88923092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34217346-C-T

88923095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34217349-C-T

http://identifiers.org/hco/10/GRCh38#88923096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34217350-C-A

88923096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34217350-C-T

88923114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34217368-G-A

88923114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34217368-G-T

http://identifiers.org/hco/10/GRCh38#88923119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34217373-C-A

88923119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34217373-C-T

http://identifiers.org/hco/10/GRCh38#88923133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34217386-C-A

88923133-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34217386-C-G

88923143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34217396-G-A

88923151-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34217400-A-T

http://identifiers.org/hco/10/GRCh38#88923295-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34217527-A-C

88923295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34217527-A-G

88923295-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34217527-A-T

88923390-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34217632-T-G

http://identifiers.org/hco/10/GRCh38#88923409-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34217651-A-C

88923418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34217660-A-G

88923418-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34217660-A-T

88923537-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34217764-T-A

88933954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34218139-G-A

88933954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34218139-G-T

88934131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34218300-A-G

88934159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34218330-C-T

88934179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34218348-G-T

88934202-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34218372-A-T

88934414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34218527-G-A

88934820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34218668-G-A

88934870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34218723-T-C

88934941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34218792-T-C

88934955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34218804-A-G

88934956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 34218805-T-C

88934956-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 34218805-T-G

88935058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34218906-A-G

88935058-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34218906-A-T

http://identifiers.org/hco/10/GRCh38#88935108-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34218959-A-C

88935108-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34218959-A-T

http://identifiers.org/hco/10/GRCh38#88935196-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#34219047-A-C

88935196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 34219047-A-G

http://identifiers.org/hco/10/GRCh38#88935262-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34219106-A-C

http://identifiers.org/hco/10/GRCh38#88935389-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#34219229-A-C

88935389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34219229-A-G

http://identifiers.org/hco/10/GRCh38#88935394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#34219234-C-A

http://identifiers.org/hco/10/GRCh38#88935418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#34219251-C-A

88935418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34219251-C-T

88935446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34219261-G-A

88935446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34219261-G-T

http://identifiers.org/hco/10/GRCh38#88935466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#34219271-C-A

88935466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34219271-C-T

http://identifiers.org/hco/10/GRCh38#88935482-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#34219287-A-C

88935499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34219302-A-G

http://identifiers.org/hco/10/GRCh38#88935503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#34219306-C-A

88935503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34219306-C-T

88935517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34219320-T-C

http://identifiers.org/hco/10/GRCh38#88935572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34219334-C-A

88935599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34219393-G-A

88935599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34219393-G-T

88935649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34219443-A-G

http://identifiers.org/hco/10/GRCh38#88935719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#34219506-C-A

88935719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34219506-C-T

88935748-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34219531-G-C

88935750-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34219533-C-G

88935853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34219636-T-C

88936275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34220150-C-T

88936312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34220175-A-G

88936882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34220294-C-T

88937058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34220451-T-C

88937281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34220637-T-C

88937338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34220692-G-A

88937338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34220692-G-T

88938169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 34220825-G-A

88938253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34220909-G-A

88938405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34221104-G-T

88938407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34221106-T-C

88938407-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34221106-T-G

http://identifiers.org/hco/10/GRCh38#88938414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34221113-C-A

88938414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34221113-C-T

88938430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34221133-T-C

88938475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 34221179-A-G

http://identifiers.org/hco/10/GRCh38#88938481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34221185-C-A

88938492-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34221196-T-A

88938492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34221196-T-C

http://identifiers.org/hco/10/GRCh38#88938499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34221203-C-A

88938499-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34221203-C-G

88938499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34221203-C-T

http://identifiers.org/hco/10/GRCh38#88938543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34221243-C-A

88938543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34221243-C-T

88938554-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34221254-A-T

88938709-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34221547-A-T

88938747-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34221591-T-G

88938753-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34221598-T-G

88938822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34221669-G-A

88938924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34221765-T-C

88938939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34221780-T-C

88939022-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34221835-G-T

http://identifiers.org/hco/10/GRCh38#88939271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34222082-C-A

88939271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34222082-C-T

88939273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34222084-C-T

88939305-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34222115-A-T

http://identifiers.org/hco/10/GRCh38#88939341-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34222150-C-A

88939347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34222156-A-G

88939347-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34222156-A-T

88939349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34222158-G-T

88939389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 34222192-G-A

88939389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 34222192-G-T

88939446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34222263-T-C

88939529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 34222334-G-A

88939529-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 34222334-G-C

88939619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 34222424-G-A

88939753-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34222555-A-T

88940117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34222595-C-T

88940171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34222654-G-T

http://identifiers.org/hco/10/GRCh38#88941040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34222968-C-A

88941113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34223036-A-G

http://identifiers.org/hco/10/GRCh38#88941116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34223039-C-A

88941116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34223039-C-T

88941220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34223469-A-G

88941263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 34223512-G-T

88941455-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34223709-T-A

88941457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34223711-G-A

88941457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34223711-G-T

88941475-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34223724-G-C

88941482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34223731-T-C

88941558-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34223804-A-T

88941602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34223835-G-A

88941645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34223888-G-A

88941667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34223931-G-T

88941698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34223962-G-T

88941718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34223982-A-G

88941766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34224033-G-A

88941766-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34224033-G-C

88941767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34224034-T-C

88941770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34224037-C-T

http://identifiers.org/hco/10/GRCh38#88941774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34224041-C-A

88941774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34224041-C-T

88941843-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 34224110-T-G

88941925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34224190-G-A

88941925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34224190-G-T

http://identifiers.org/hco/10/GRCh38#88941927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34224192-C-A

88941927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34224192-C-T

88941983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34224235-G-A

88942083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34224328-G-A

88942085-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34224330-A-T

88942101-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34224350-T-G

88942223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34224466-G-T

88942289-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34224515-T-A

88942289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34224515-T-C

88942504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34224687-G-A

88942525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34224707-G-A

88942570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34224752-C-T

http://identifiers.org/hco/10/GRCh38#88942641-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34224812-A-C

88942651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34224822-C-T

88942652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34224823-G-A

88942674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34224836-G-A

http://identifiers.org/hco/10/GRCh38#88942714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34224875-C-A

88942714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34224875-C-T

88942760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34224915-T-C

88942764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34224919-C-T

88942765-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34224920-A-T

http://identifiers.org/hco/10/GRCh38#88942823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34224938-C-A

88942972-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34225065-G-C

88942972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34225065-G-T

88943056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34225146-C-T

88943410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34225517-G-A

88943432-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34225530-C-G

88943536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34225601-A-G

88943536-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34225601-A-T

88943582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34225625-C-T

88943602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34225648-A-G

88943617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34225663-A-G

88943645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34225686-T-C

http://identifiers.org/hco/10/GRCh38#88943647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34225688-C-A

88943662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34225703-C-T

88943729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34225760-G-A

88943729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34225760-G-T

88943884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 34225911-A-G

88943947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34225970-C-T

88944005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34226031-A-G

http://identifiers.org/hco/10/GRCh38#88944083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34226086-C-A

88944083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34226086-C-T

88944091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34226094-A-G

88944171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34226181-C-T

http://identifiers.org/hco/10/GRCh38#88944186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34226197-C-A

88944193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34226204-T-C

88944668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34226636-T-C

88944846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34226816-G-A

88944846-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34226816-G-C

88944850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34226825-A-G

88944855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34226830-C-T

88944933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34226896-T-C

88945103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34228083-C-T

88945169-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34228127-C-G

88945175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34228133-A-G

88945190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34228148-G-A

88945417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34228390-C-T

88945553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34228572-A-G

88947111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34229009-G-T

88947223-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34229085-T-A

88947300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 34229172-C-T

88947312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 34229184-G-A

http://identifiers.org/hco/10/GRCh38#88947423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34229296-C-A

88947434-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34229307-A-T

88948431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34229391-T-C

88948459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34229427-G-T

88948499-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34229467-T-G

88948777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34229799-A-G

88948779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34229801-G-A

88948880-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 34229903-C-G

88948880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 34229903-C-T

88948886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 34229909-G-A

88948990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34230009-T-C

88948990-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34230009-T-G

http://identifiers.org/hco/10/GRCh38#88948995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34230014-C-A

88949019-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34230038-T-G

http://identifiers.org/hco/10/GRCh38#88949191-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34230202-A-C

88949197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34230208-C-T

88949198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34230209-G-A

88949296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34230304-C-T

88949604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34230646-G-A

88949814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34230782-C-T

88949879-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34230849-T-A

88949879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34230849-T-C

88951072-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34231144-C-G

88951083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34231156-C-T

88951595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34231619-A-G

88951652-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34231676-C-G

88951680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34231711-G-A

88951680-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34231711-G-T

88951896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34231938-C-T

88951968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34231993-A-G

88952008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34232029-G-T

88952093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34232077-C-T

88952351-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34232304-G-C

88952382-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34232329-T-A

88952693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34232652-G-T

88952786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34232749-A-G

88952786-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34232749-A-T

88952854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34232817-A-G

http://identifiers.org/hco/10/GRCh38#88952926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34232889-C-A

88953453-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34233397-G-C

88953548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34233504-G-A

88953548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron variant
orthologous variants: 34233504-G-T

88954092-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34233691-T-A

88954193-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34233777-T-G

88954209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34233793-G-A

88954605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34234200-G-A

88954763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34234334-T-C

http://identifiers.org/hco/10/GRCh38#88955014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34234558-C-A

88959235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34235271-G-A

88959304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34235339-C-T

88959379-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34235412-C-G

88959659-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34235668-T-A

88960181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34236139-G-A

88960225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34236181-A-G

88960255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34236191-T-C

88960285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34236225-A-G

88960536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34236489-G-A

88960559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34236515-G-A

88960675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34236646-C-T

88960711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34236679-A-G

88964184-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34239365-A-T

88964326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34239506-G-A

88964326-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34239506-G-C

88964453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34239610-A-G

88965198-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34240061-T-G

88965359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34240197-A-G

http://identifiers.org/hco/10/GRCh38#88965561-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34240396-A-C

http://identifiers.org/hco/10/GRCh38#88965664-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: -A-C

88965795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34240618-A-G

88966186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34240934-A-G

88967005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34241172-G-A

http://identifiers.org/hco/10/GRCh38#88967033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34241200-C-A

http://identifiers.org/hco/10/GRCh38#88967204-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34241367-A-C

88967287-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34241456-T-A

88967329-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34241498-G-C

88967448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34241605-G-A

88967576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34241726-C-T

88967786-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34241934-C-G

88967786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34241934-C-T

88969087-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34243533-T-G

88969101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34243547-A-G

88969224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34243661-A-G

88969240-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34243677-T-A

http://identifiers.org/hco/10/GRCh38#88969308-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34243706-A-C

88969458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34243812-A-G

88969703-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34244672-T-A

88969913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34244876-T-C

88970366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34245298-A-G

88970422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34245354-T-C

88970452-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34245385-G-C

88971063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34245644-C-T

88971238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34245810-C-T

88971262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34245834-G-A

88971463-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34246245-T-G

88972249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34246699-A-G

88972362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34246809-T-C

88972455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34246886-C-T

88972522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34246945-T-C

88972755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34247175-T-C

88972842-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34247244-C-G

88972884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34247286-T-C

88972983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34247387-A-G

88973152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34247534-C-T

88973171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34247553-G-A

88973171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34247553-G-T

88973274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 34247646-G-A

88973332-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34247700-T-A

88973332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34247700-T-C

http://identifiers.org/hco/10/GRCh38#88973400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34247781-C-A

88973400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34247781-C-T

http://identifiers.org/hco/10/GRCh38#88973411-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34247792-A-C

88973411-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34247792-A-T

88973437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34247818-G-T

88973492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34247884-G-T

88973505-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34247902-T-A

88973505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34247902-T-C

88973512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34247910-A-G

http://identifiers.org/hco/10/GRCh38#88973523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34247922-C-A

88973539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34247943-G-T

88973540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34247944-G-A

88973540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34247944-G-T

http://identifiers.org/hco/10/GRCh38#88973782-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34248315-A-C

http://identifiers.org/hco/10/GRCh38#88973793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34248339-C-A

88973793-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34248339-C-G

88973793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34248339-C-T

88973976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34248490-A-G

88974011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34248520-A-G

88974072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34248577-G-A

http://identifiers.org/hco/10/GRCh38#88974077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34248582-C-A

88974077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34248582-C-T

http://identifiers.org/hco/10/GRCh38#88974215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#34248766-C-A

88974215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34248766-C-T

88974270-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34248845-T-A

88974270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34248845-T-C

88974450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34249026-G-A