http://identifiers.org/hco/5/GRCh38#36192708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#9110428-C-A

36193041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 9110096-C-T

36193563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 9109908-G-T

36193803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 9109691-C-T

36193895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 9109583-G-T

36193997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 9109481-A-G

36194052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 9109427-A-G

36194122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 9109376-G-A

36194563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 9108985-T-C

36194698-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 9108852-A-T

36194751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 9108799-T-C

36194938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 9108640-T-C

http://identifiers.org/hco/5/GRCh38#36194947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#9108631-C-A

http://identifiers.org/hco/5/GRCh38#36194951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#9108627-C-A

36194951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 9108627-C-T

36195011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 9108579-T-C

http://identifiers.org/hco/5/GRCh38#36195013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#9108577-C-A

36195013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 9108577-C-T

http://identifiers.org/hco/5/GRCh38#36195046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#9108536-C-A

36195046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 9108536-C-T

http://identifiers.org/hco/5/GRCh38#36195070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#9108514-C-A

36195070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 9108514-C-T

36195106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 9108479-T-C

36195148-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 9108439-T-A

36195229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 9108358-G-T

36195268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 9108319-G-A

36195300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9108287-T-C

36195300-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9108287-T-G

http://identifiers.org/hco/5/GRCh38#36195359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#9108234-C-A

36195359-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9108234-C-G

36195359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9108234-C-T

36195474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9108116-T-C

http://identifiers.org/hco/5/GRCh38#36197688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#9106795-C-A

36197688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9106795-C-T

http://identifiers.org/hco/5/GRCh38#36200186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#9103506-C-A

36200186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9103506-C-T

36200211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9103481-A-G

36200290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9103402-A-G

36201165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 9103065-G-A

36207096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9100374-C-T

http://identifiers.org/hco/5/GRCh38#36207130-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#9100326-A-C

36207130-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9100326-A-T

36207147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9100311-A-G

36207282-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9100176-T-A

36207282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9100176-T-C

36207446-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-A

36207446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

36207483-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9099999-A-T

36207542-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9099942-T-G

36207560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9099933-T-C

36207588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9099909-G-A

36207646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9099861-G-A

36208258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9099303-T-C

36208279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9099290-T-C

36208532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9099059-G-A

36208532-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9099059-G-C

36208532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9099059-G-T

http://identifiers.org/hco/5/GRCh38#36208702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#9098884-C-A

36208702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9098884-C-T

36208714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9098872-A-G

36208866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9098722-C-T

36208943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9098646-A-G

36209656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9098114-T-C

36209787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9097937-T-C

36209875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9097772-T-C

36209911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9097732-T-C

http://identifiers.org/hco/5/GRCh38#36209987-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#9097641-A-C

36211717-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9096274-A-T

36211828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9096195-A-G

36212364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9095331-T-C

36212441-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9095259-C-G

36212576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9095150-T-C

36212650-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9095041-C-G

36212986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9094739-T-C

36217843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 9092842-G-A

36217843-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 9092842-G-C

http://identifiers.org/hco/5/GRCh38#36217936-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#9092747-A-C

http://identifiers.org/hco/5/GRCh38#36217997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#9092393-C-A

http://identifiers.org/hco/5/GRCh38#36218030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#9092360-C-A

36218037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9092353-T-C

36218072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9092317-T-C

36218091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9092300-C-T

http://identifiers.org/hco/5/GRCh38#36218118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#9092277-C-A

http://identifiers.org/hco/5/GRCh38#36218978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#9091618-C-A

36218978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9091618-C-T

36219542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9091390-A-G

36219550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9091382-T-C

36219641-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: missense variant
orthologous variants: 9091291-T-A

36219695-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9091248-A-T

36219704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9091239-G-A

36219704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9091239-G-T

36219765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9091184-A-G

36220175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9090834-C-T

36220722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9089981-T-C

36220978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9089749-T-C

http://identifiers.org/hco/5/GRCh38#36220980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#9089747-C-A

36221102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9089642-T-C

36221202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9089575-T-C

36222126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9088976-G-T

http://identifiers.org/hco/5/GRCh38#36222244-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#9088858-A-C

36222244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9088858-A-G

36222244-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9088858-A-T

36222333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9088796-A-G

36222513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9088628-T-C

36222803-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9088338-T-A

36223006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9088085-G-T

36223571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9087376-T-C

36224235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9086798-G-A

36224235-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9086798-G-C

36224251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9086782-G-A

36224631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9086699-G-A

36224646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9086684-G-A

36224830-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9086510-T-A

http://identifiers.org/hco/5/GRCh38#36225338-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#9086086-A-C

36225429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9085994-G-T

36225496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9085936-A-G

http://identifiers.org/hco/5/GRCh38#36225502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#9085930-C-A

36225502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9085930-C-T

36225524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9085902-G-A

36225524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9085902-G-T

36225526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9085900-A-G

36225700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9085737-A-G

36225722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9085711-C-T

36225737-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9085696-T-A

36225737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9085696-T-C

36226077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9084808-A-G

36226260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9084524-C-T

36226439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9084364-T-C

36226534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 9084269-T-C

36226534-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 9084269-T-G

36226543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 9084260-C-T

36226569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 9084234-A-G

36226583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9084227-G-A

36226583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9084227-G-T

36226640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9084170-G-T

36226670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9084117-T-C

36226751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9084057-T-C

36226810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9084006-A-G

36227134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9083732-T-C

36227209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9083684-G-A

36227364-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9083538-G-C

36227364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9083538-G-T

36227409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9083502-T-C

http://identifiers.org/hco/5/GRCh38#36227483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#9083430-C-A

36227483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 9083430-C-T

36227605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9083310-A-G

36227652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9083271-A-G

36227688-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9083229-T-A

36227688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9083229-T-C

36228026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9083039-G-A

36228171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9082893-T-C

36228219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9082849-T-C

36228219-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9082849-T-G

36228301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9082770-C-T

36229350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9082211-T-C

36229539-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9081988-C-G

36229539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9081988-C-T

36229582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9081952-G-A

36229666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9081876-A-G

36230034-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9081631-A-T

36230506-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9081285-G-C

36230535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9081257-T-C

36230708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9081017-G-A

36230757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9080969-T-C

36230876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9080848-A-G

36231160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9080578-G-A

36232050-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9079928-T-A

36232304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9079700-A-G

36232476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9079561-C-T

http://identifiers.org/hco/5/GRCh38#36232679-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#9079366-A-C

36232809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9079254-C-T

36232934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9079167-T-C

36232953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9079148-A-G

36233491-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9078668-C-G

http://identifiers.org/hco/5/GRCh38#36233504-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#9078655-A-C

36233694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9078575-A-G

36233750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9078522-A-G

36233819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9078463-C-T

36234099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9078236-G-T

http://identifiers.org/hco/5/GRCh38#36234407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#9077977-C-A

36234407-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9077977-C-G

36234407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9077977-C-T

36234437-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9077947-T-A

36234437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9077947-T-C

36234522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9077869-C-T

36234599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9077794-G-A

36234599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9077794-G-T

36234731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9077308-T-C

36234777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9077264-T-C

36234916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9077128-A-G

36235033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9077047-G-A

36235033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9077047-G-T

http://identifiers.org/hco/5/GRCh38#36235087-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#9077004-A-C

36235734-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9076330-C-G

36235734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9076330-C-T

36236043-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9076013-G-C

36236130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9075907-T-C

36236152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9075884-A-G

36236582-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9075422-G-C

36236712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9075300-C-T

36238137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9074825-T-C

36238143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9074819-A-G

36238564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9074470-T-C

36238757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9074282-A-G

36238757-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9074282-A-T

http://identifiers.org/hco/5/GRCh38#36238792-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#9074245-A-C

36239359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9073703-T-C

36239446-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9073646-T-G

36239511-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9073592-C-G

36239511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9073592-C-T

36240353-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9072770-C-G

36240691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9072465-T-C

http://identifiers.org/hco/5/GRCh38#36241027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#9072160-C-A

36241027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9072160-C-T

36241072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9072117-G-A

http://identifiers.org/hco/5/GRCh38#36241319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#9071958-C-A

36241319-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, undefined
orthologous variants: 9071958-C-G

36241319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, undefined
orthologous variants: 9071958-C-T

http://identifiers.org/hco/5/GRCh38#36241411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#9071892-C-A

36241411-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9071892-C-G

36241411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9071892-C-T

36241438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9071886-G-A

36241438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9071886-G-T

36241444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9071880-G-A

36241444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron variant
orthologous variants: 9071880-G-T

36241722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 9071653-G-A

36241722-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 9071653-G-C

36241722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 9071653-G-T

36241740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, missense_variant
orthologous variants: 9071638-G-A

36241740-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, missense_variant
orthologous variants: 9071638-G-C

36241740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, missense_variant
orthologous variants: 9071638-G-T

36241773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 9071605-A-G

36241773-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 9071605-A-T

36241954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 9071473-G-A

36242027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 9071414-A-G

http://identifiers.org/hco/5/GRCh38#36242052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#9071401-C-A

36242052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9071401-C-T

36242071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9071382-T-C

36242079-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9071374-T-G

36242258-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9071199-A-T