http://identifiers.org/hco/3/GRCh38#58633948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#14120828-C-A

58634011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 14120763-C-T

58634072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 14120709-G-A

58634072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 14120709-G-T

58634073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 14120708-G-T

58634083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 14120698-G-T

58634109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 14120667-G-A

58634109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 14120667-G-T

58634136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 14120640-G-A

58634136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 14120640-G-T

58634156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 14120620-A-G

http://identifiers.org/hco/3/GRCh38#58634193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#14120583-C-A

58634193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 14120583-C-T

58634212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 14120544-G-A

58634212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 14120544-G-T

58634231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 14120526-A-G

58634292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 14120481-G-A

58634401-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron_variant, undefined
orthologous variants: 14120375-G-C

58634401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron_variant, undefined
orthologous variants: 14120375-G-T

58634405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron_variant, undefined
orthologous variants: 14120371-G-T

58634413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron_variant, undefined
orthologous variants: 14120359-G-A

58634413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron_variant, undefined
orthologous variants: 14120359-G-T

58634475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron_variant, undefined
orthologous variants: 14120297-T-C

http://identifiers.org/hco/3/GRCh38#58634530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#14120244-C-A

58634530-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron_variant, undefined
orthologous variants: 14120244-C-G

58634530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron_variant, undefined
orthologous variants: 14120244-C-T

58634674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron_variant, undefined
orthologous variants: 14120109-A-G

58634692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron_variant, undefined
orthologous variants: 14120093-A-G

58636086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron_variant, undefined
orthologous variants: 14117913-T-C

58636126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron_variant, undefined
orthologous variants: 14117882-T-C

http://identifiers.org/hco/3/GRCh38#58636287-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#14117696-A-C

58636398-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 14117585-G-C

58636399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 14117584-T-C

http://identifiers.org/hco/3/GRCh38#58636431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#14117552-C-A

58636431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron_variant, undefined
orthologous variants: 14117552-C-T

58636484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron_variant, undefined
orthologous variants: 14117501-G-T

58636500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron_variant, undefined
orthologous variants: 14117488-G-T

58636857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron_variant, undefined
orthologous variants: 14116185-A-G

http://identifiers.org/hco/3/GRCh38#58637025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#14116035-C-A

58637025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron_variant, undefined
orthologous variants: 14116035-C-T

58637073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron_variant, undefined
orthologous variants: 14115989-G-A

58637073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron_variant, undefined
orthologous variants: 14115989-G-T

58637164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 14115899-G-A

58637253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 14115811-G-T

58637275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 14115789-G-T

58637318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 14115745-C-T

http://identifiers.org/hco/3/GRCh38#58637332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#14115731-C-A

58637332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 14115731-C-T

58640016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 14114376-T-C

58640019-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 14114373-A-T

58640116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 14114318-G-A

58640119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant, undefined
orthologous variants: 14114315-G-A

58640164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 14114270-A-G

58640164-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 14114270-A-T

58640170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 14114264-C-T

58640185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant, undefined
orthologous variants: 14114253-T-C

58640219-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 14114219-T-A

58640219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 14114219-T-C

58640274-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 14114164-A-T

http://identifiers.org/hco/3/GRCh38#58640275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#14114163-C-A

58640348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 14114084-G-T

58640456-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 14113983-C-G

58640491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 14113948-A-G

58640585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 14113865-C-T

58640593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 14113857-T-C

58640698-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 14113760-C-G

58640708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 14113750-G-A

58640708-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 14113750-G-C

58641002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 14113508-C-T

58641029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 14113481-T-C

58642943-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 14113137-C-G

58643589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 14112701-A-G

http://identifiers.org/hco/3/GRCh38#58643608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#14112682-C-A

58643608-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 14112682-C-G

58643608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 14112682-C-T

58643696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 14112627-A-G

58643708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, splice_acceptor_variant, synonymous_variant, undefined
orthologous variants: 14112615-A-G

58643720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, splice_region_variant, undefined
orthologous variants: 14112603-C-T

58643978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 14112350-T-C

58644112-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 14112235-C-G

58644703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14112096-G-A

58644727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14112075-T-C

58644862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14111957-T-C

58645332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14111596-C-T

58645405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14111521-G-T

58645496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14111446-C-T

http://identifiers.org/hco/3/GRCh38#58645644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14111298-C-A

58647790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14110637-C-T

http://identifiers.org/hco/3/GRCh38#58647862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14109419-C-A

58647897-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14109383-T-G

58648199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14109089-C-T

58648463-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14108856-C-G

58648493-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14108827-C-G

58648522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14108798-C-T

58648575-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14108747-A-T

58649051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14108537-G-A

58649181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14108399-A-G

58649192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14108388-C-T

58649212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14108368-A-G

58649212-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14108368-A-T

http://identifiers.org/hco/3/GRCh38#58649229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14108351-C-A

58649229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14108351-C-T

http://identifiers.org/hco/3/GRCh38#58649299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14108311-C-A

58649393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 14108222-G-A

58649393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 14108222-G-T

58649396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 14108219-G-A

58649421-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 14108202-A-T

58649426-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14108197-G-C

58649426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14108197-G-T

http://identifiers.org/hco/3/GRCh38#58649471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14108130-C-A

58649471-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14108130-C-G

58649471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14108130-C-T

58649513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14108088-G-A

58649513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14108088-G-T

58649528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14108073-G-T

http://identifiers.org/hco/3/GRCh38#58649677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14107961-C-A

58649677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14107961-C-T

58649758-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14107907-G-C

58649890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14107817-A-G

58649915-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14107792-A-T

58650068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14107693-C-T

58650077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14107684-A-G

58651269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14107092-G-T

58651300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14107060-G-A

58651618-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14106770-T-A

58651693-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14106725-C-G

58652515-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14105878-C-G

58652765-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14105727-C-G

58652809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14105709-C-T

58652897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14105624-T-C

58652909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14105612-C-T

http://identifiers.org/hco/3/GRCh38#58653054-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14105555-A-C

58653090-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14105519-G-C

58653331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14105255-A-G

58653335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14105251-T-C

http://identifiers.org/hco/3/GRCh38#58653774-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14104882-A-C

58653844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14104805-G-A

58653844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14104805-G-T

58653873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14104755-A-G

58653894-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14104734-T-A

58653894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14104734-T-C

58653894-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14104734-T-G

58654044-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14104604-C-G

http://identifiers.org/hco/3/GRCh38#58655414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14102915-C-A

58655414-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14102915-C-G

58655414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14102915-C-T

58655426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14102903-G-T

http://identifiers.org/hco/3/GRCh38#58655549-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14102739-A-C

58655584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 14102704-C-T

58655676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14102601-G-A

58655676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14102601-G-T

58656205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14101979-T-C

58656230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14101954-C-T

58656557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14101671-G-A

http://identifiers.org/hco/3/GRCh38#58656646-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14101593-A-C

58656752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14101504-C-T

58656843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14101427-G-A

58657032-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14101280-C-G

58657141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14101079-T-C

58657203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14101025-C-T

58657227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14100996-C-T

58657382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14100853-G-A

58657496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14100766-A-G

http://identifiers.org/hco/3/GRCh38#58657726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14100563-C-A

58657726-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: 14100563-C-G

58657786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron variant
orthologous variants: 14100497-G-A

58657786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron variant
orthologous variants: 14100497-G-T

58657819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron variant
orthologous variants: 14100464-A-G

58658231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron variant
orthologous variants: 14100060-G-A

58658231-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron variant
orthologous variants: 14100060-G-C

58658496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron variant
orthologous variants: 14099818-C-T

58659102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron variant
orthologous variants: 14099301-G-T

58659137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron variant
orthologous variants: 14099268-T-C

58659241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron variant
orthologous variants: 14099175-T-C

58659502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron_variant, undefined
orthologous variants: 14098790-A-G

58659574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron variant
orthologous variants: 14098720-G-T

58659635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron variant
orthologous variants: 14098659-G-A

58659635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron variant
orthologous variants: 14098659-G-T

58659968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron variant
orthologous variants: 14098160-A-G

58660096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron variant
orthologous variants: 14098025-T-C

58660096-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron variant
orthologous variants: 14098025-T-G

58661110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron variant
orthologous variants: 14096340-T-C

58661403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron variant
orthologous variants: 14096088-C-T

58661519-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron variant
orthologous variants: 14095972-C-G

58661559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron variant
orthologous variants: 14095916-C-T

http://identifiers.org/hco/3/GRCh38#58661561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14095914-C-A

58661635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron variant
orthologous variants: 14095848-C-T

http://identifiers.org/hco/3/GRCh38#58661755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14095721-C-A

58661755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron variant
orthologous variants: 14095721-C-T

58661815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron variant
orthologous variants: 14095659-G-A

58661832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron variant
orthologous variants: 14095642-C-T

58661888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron variant
orthologous variants: 14095595-T-C

58661905-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron variant
orthologous variants: 14095578-T-G

http://identifiers.org/hco/3/GRCh38#58661982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14095505-C-A

58662000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron variant
orthologous variants: 14095487-G-A

58662076-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron variant
orthologous variants: 14095425-C-G

58663243-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron variant
orthologous variants: 14094101-C-G

58663509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron variant
orthologous variants: 14093947-C-T

58663698-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron variant
orthologous variants: 14093787-G-C

58663783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron variant
orthologous variants: 14093726-A-G

58664345-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron variant
orthologous variants: 14093224-T-G

58664352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron variant
orthologous variants: 14093217-A-G

58664372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron variant
orthologous variants: 14093197-C-T

58664654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron_variant, undefined
orthologous variants: 14092843-G-A

http://identifiers.org/hco/3/GRCh38#58664748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#14092758-C-A

http://identifiers.org/hco/3/GRCh38#58664814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#14092671-C-A

http://identifiers.org/hco/3/GRCh38#58665129-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#14092397-A-C

58665130-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron_variant, undefined
orthologous variants: 14092396-C-G

58665130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron_variant, undefined
orthologous variants: 14092396-C-T

58665231-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron_variant, undefined
orthologous variants: 14092308-T-A

http://identifiers.org/hco/3/GRCh38#58665255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#14092282-C-A

58665322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron_variant, undefined
orthologous variants: 14092252-C-T

58665446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron_variant, undefined
orthologous variants: 14092172-T-C

58665549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron_variant, undefined
orthologous variants: 14092087-G-A

58665700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron_variant, undefined
orthologous variants: 14091987-C-T

58666434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron_variant, undefined
orthologous variants: 14091349-T-C

58666435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron_variant, undefined
orthologous variants: 14091348-G-T

58666437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron_variant, undefined
orthologous variants: 14091346-G-T

58666451-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron_variant, undefined
orthologous variants: 14091332-T-A

58666451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron_variant, undefined
orthologous variants: 14091332-T-C

http://identifiers.org/hco/3/GRCh38#58666484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#14091303-C-A

58666484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: intron_variant, undefined
orthologous variants: 14091303-C-T

58666539-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant, undefined
orthologous variants: 14091251-T-A

http://identifiers.org/hco/3/GRCh38#58666690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#14091099-C-A

58666690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18665
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 14091099-C-T