http://identifiers.org/hco/11/GRCh38#118894505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#44424687-C-A

118894520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 44424672-G-A

http://identifiers.org/hco/11/GRCh38#118894714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#44424469-C-A

118894714-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3 prime UTR variant
orthologous variants: 44424469-C-G

118894714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3 prime UTR variant
orthologous variants: 44424469-C-T

http://identifiers.org/hco/11/GRCh38#118894899-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#44424369-A-C

118894899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3 prime UTR variant
orthologous variants: 44424369-A-G

118894899-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3 prime UTR variant
orthologous variants: 44424369-A-T

http://identifiers.org/hco/11/GRCh38#118894904-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#44424364-A-C

http://identifiers.org/hco/11/GRCh38#118894948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#44424321-C-A

118894948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3 prime UTR variant
orthologous variants: 44424321-C-T

118894993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3 prime UTR variant
orthologous variants: 44424253-T-C

118894993-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3 prime UTR variant
orthologous variants: 44424253-T-G

118894999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3 prime UTR variant
orthologous variants: 44424247-T-C

118894999-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3 prime UTR variant
orthologous variants: 44424247-T-G

118895013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3 prime UTR variant
orthologous variants: 44424211-G-T

118895166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3 prime UTR variant
orthologous variants: 44424112-G-A

118895166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3 prime UTR variant
orthologous variants: 44424112-G-T

118895179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3 prime UTR variant
orthologous variants: 44424096-G-A

http://identifiers.org/hco/11/GRCh38#118895198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#44424079-C-A

118895355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3 prime UTR variant
orthologous variants: 44423927-G-A

http://identifiers.org/hco/11/GRCh38#118895465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#44423818-C-A

118895465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3 prime UTR variant
orthologous variants: 44423818-C-T

118895475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3 prime UTR variant
orthologous variants: 44423808-G-A

118895511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3 prime UTR variant
orthologous variants: 44423772-A-G

http://identifiers.org/hco/11/GRCh38#118895514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#44423769-C-A

118895514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3 prime UTR variant
orthologous variants: 44423769-C-T

118895523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3 prime UTR variant
orthologous variants: 44423760-G-A

118895523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3 prime UTR variant
orthologous variants: 44423760-G-T

http://identifiers.org/hco/11/GRCh38#118895538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#44423749-C-A

118895571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 44423715-G-A

118895572-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 44423714-T-A

118895572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 44423714-T-C

118895679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3 prime UTR variant
orthologous variants: 44423639-G-T

http://identifiers.org/hco/11/GRCh38#118895701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#44423611-C-A

118895701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 44423611-C-T

118895703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 44423609-A-G

118895732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3 prime UTR variant
orthologous variants: 44423586-G-T

118895762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 44423556-G-A

118895762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 44423556-G-T

118895763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 44423555-T-C

118895989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 44423342-G-T

118896122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3 prime UTR variant
orthologous variants: 44423214-A-G

118896435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44422889-C-T

118896438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44422886-G-A

118896438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44422886-G-T

118896462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44422867-G-T

118896466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44422863-G-A

118896544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44422800-A-G

118896544-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44422800-A-T

118896624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 44422715-A-G

118896691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44422652-G-A

118896691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44422652-G-T

118896832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44422509-A-G

118896832-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44422509-A-T

118897115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44422249-G-A

118897115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44422249-G-T

118897139-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44422225-A-T

118897180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44422197-T-C

118897250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44422129-G-A

118897250-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44422129-G-C

118897250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44422129-G-T

118897274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44422106-G-A

118897274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44422106-G-T

118897366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44422022-G-A

118897393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44421995-A-G

118897476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44421928-G-A

118897583-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44421809-T-G

118897680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44421783-G-A

118897753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44421702-T-C

118898152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44421344-T-C

118898169-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44421325-G-C

118898169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44421325-G-T

http://identifiers.org/hco/11/GRCh38#118898227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#44421268-C-A

118898227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44421268-C-T

http://identifiers.org/hco/11/GRCh38#118898230-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#44421265-A-C

http://identifiers.org/hco/11/GRCh38#118898306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#44421188-C-A

118898306-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44421188-C-G

118898306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44421188-C-T

118898355-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44421134-A-T

118898392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44421099-G-A

118898392-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44421099-G-C

118898392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44421099-G-T

118898803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44420690-G-A

118898812-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44420681-T-G

118899026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44420467-C-T

118899114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 44420379-G-A

118899114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 44420379-G-T

118899399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 44420100-G-A

118899399-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 44420100-G-C

118899399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 44420100-G-T

118899469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 44420030-G-T

118899514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 44419985-G-A

118899886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44419764-G-A

118899886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44419764-G-T

118900089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 44419557-T-C

118900150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44419496-G-A

118900177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44419469-G-A

118900180-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44419466-C-G

http://identifiers.org/hco/11/GRCh38#118900206-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#44419440-A-C

118900227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44419417-G-A

118900227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44419417-G-T

118900343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44419319-A-G

118900417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44419263-C-T

118900599-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44419185-T-A

118900599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44419185-T-C

118901092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 44418692-G-A

118901092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 44418692-G-T

http://identifiers.org/hco/11/GRCh38#118901107-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#44418677-A-C

118901506-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 44418278-C-G

118901506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 44418278-C-T

118901542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 44418242-G-A

118902299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 44417485-G-A

118902299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 44417485-G-T

118902373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 44417411-G-A

118902923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44416864-A-G

http://identifiers.org/hco/11/GRCh38#118903078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#44416707-C-A

118903078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 44416707-C-T

http://identifiers.org/hco/11/GRCh38#118903124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#44416663-C-A

118903124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44416663-C-T

118903125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44416662-C-T

118903475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44416324-A-G

118903476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44416323-G-A

118903492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44416307-G-A

118903492-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44416307-G-C

118904112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44415756-G-A

118907499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 44413200-G-T

118907656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44413036-C-T

118908098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44412613-C-T

118908284-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44412411-T-A

118908284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44412411-T-C

118908678-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44412017-T-G

118908698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44411997-G-A

118908698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44411997-G-T

118908749-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44411958-G-C

118908749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44411958-G-T

http://identifiers.org/hco/11/GRCh38#118908983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#44411748-C-A

118909255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44411477-A-G

118909733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44411018-G-A

http://identifiers.org/hco/11/GRCh38#118909807-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#44410945-A-C

118909983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 44410775-G-A

118909983-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 44410775-G-C

118909983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 44410775-G-T

118910072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44410686-G-A

http://identifiers.org/hco/11/GRCh38#118910197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#44410575-C-A

118910197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44410575-C-T

118910297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44410461-G-A

118910297-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44410461-G-C

118910297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44410461-G-T

118910309-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44410449-T-A

118910309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44410449-T-C

118910309-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44410449-T-G

http://identifiers.org/hco/11/GRCh38#118910528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#44410214-C-A

118910528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44410214-C-T

http://identifiers.org/hco/11/GRCh38#118910629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#44410109-C-A

118910629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44410109-C-T

118910695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44410030-G-A

118910695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44410030-G-T

118910769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 44409949-C-T

118910771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 44409947-G-A

118910771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 44409947-G-T

118910772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 44409946-G-A

118910846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44409880-G-A

118910846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44409880-G-T

118911088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44409615-T-C

118911270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44409442-G-A

118911270-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44409442-G-C

118911270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44409442-G-T

118911282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44409430-G-A

118911282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44409430-G-T

118911335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44409378-G-A

118911379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44409332-G-A

118911379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44409332-G-T

118911683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44409044-T-C

118911959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44408632-G-A

http://identifiers.org/hco/11/GRCh38#118912026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#44408591-C-A

118912026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44408591-C-T

118912060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44408558-G-A

118912352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44408290-G-A

118912420-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44408215-C-G

118912447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44408191-G-A

118912452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44408186-G-A

118912452-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44408186-G-C

118912452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44408186-G-T

118913205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44406981-T-C

http://identifiers.org/hco/11/GRCh38#118913490-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#44406701-A-C

118915444-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44405066-T-G

118915705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44404837-C-T

118916175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44404378-G-A

http://identifiers.org/hco/11/GRCh38#118916184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#44404369-C-A

http://identifiers.org/hco/11/GRCh38#118916427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#44404149-C-A

118916615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44403989-C-T

118916779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44403913-A-G

118916787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44403905-G-A

118916961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44403738-G-A

118917032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44403654-G-A

118917032-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44403654-G-C

118917802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44402105-C-T

118917895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44402012-C-T

118918016-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44401886-T-G

118918034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44401867-G-A

118918034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44401867-G-T

118918130-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44401759-A-T

118918281-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44401589-G-T

118918291-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44401579-C-G

118918293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44401577-G-A

118918308-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44401562-T-G

118918312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44401558-C-T

118918572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44401275-C-T

118918917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44400912-G-A

118919007-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44400810-T-A

118919007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44400810-T-C

118919032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44400758-T-C

118919032-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44400758-T-G

118919353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44400457-G-A

118919413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44400398-G-A

118919413-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44400398-G-C

118919782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44400034-A-G

118920056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44399763-T-C

118920271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44399551-T-C

118920338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44399475-A-G

118920419-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44399407-A-T

118920645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44399202-G-A

118920698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44399161-G-A

118920985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44398903-G-A

118921128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44398769-C-T

118921287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44398634-C-T

118921402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44398511-G-A

118921406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44398505-G-A

http://identifiers.org/hco/11/GRCh38#118921706-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#44398209-A-C

118921830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44398093-T-C

118922904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44396920-T-C

http://identifiers.org/hco/11/GRCh38#118923375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#44396472-C-A

118923443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44396418-G-A

118923907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44396127-C-T

118924384-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44395650-G-C

118924488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44395552-G-A

118924552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44395477-G-A

118924813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44395204-C-T

http://identifiers.org/hco/11/GRCh38#118925020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#44394999-C-A

118925020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44394999-C-T

http://identifiers.org/hco/11/GRCh38#118925270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#44394750-C-A

118925270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44394750-C-T

118925311-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44394709-T-A

118925315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44394705-G-A

118925315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44394705-G-T

http://identifiers.org/hco/11/GRCh38#118925405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#44394615-C-A

118925405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44394615-C-T

118925520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44394503-G-T

118925703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44394324-G-A

118925703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23688
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44394324-G-T