14443592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: non coding transcript exon variant
orthologous variants: 113799923-T-C

http://identifiers.org/hco/11/GRCh38#14443623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#113799968-C-A

14443623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 113799968-C-T

14443630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 113799975-A-G

14443740-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 113800088-T-A

http://identifiers.org/hco/11/GRCh38#14443790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#113800126-C-A

http://identifiers.org/hco/11/GRCh38#14443847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#113800171-C-A

14443895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 113800223-A-G

14445973-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113801880-T-G

14446483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113802519-C-T

14446687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113802987-T-C

14446901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113803224-T-C

14448489-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113805021-T-A

14448741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113805590-G-A

14449112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113805947-T-C

14449122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113805957-T-C

14451868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113809183-T-C

14451940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 113809263-G-T

14452199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113809464-G-A

14452215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113809480-A-G

14452632-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113809550-C-G

14452632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113809550-C-T

14452747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113809654-A-G

14452815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113809724-C-T

14452821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113809727-C-T

14453109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113809987-G-A

http://identifiers.org/hco/11/GRCh38#14453158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#113810135-C-A

14453216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113810198-G-A

14453216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113810198-G-T

14453222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113810204-T-C

14453506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113812173-A-G

14453691-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113812678-A-T

http://identifiers.org/hco/11/GRCh38#14455112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#113812901-C-A

http://identifiers.org/hco/11/GRCh38#14455141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#113812930-C-A

14455141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113812930-C-T

http://identifiers.org/hco/11/GRCh38#14455194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#113812963-C-A

14455196-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113812965-G-C

14455196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113812965-G-T

14455235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 113813003-T-C

14455248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113813009-G-A

14455357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113813101-G-T

14455593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113813392-C-T

14455681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113813505-T-C

14455946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113813725-C-T

14456000-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113813779-A-T

14456213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113813978-G-A

14456213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113813978-G-T

http://identifiers.org/hco/11/GRCh38#14456267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#113814032-C-A

14456267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113814032-C-T

14456291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113814057-T-C

14456501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113814256-T-C

14456830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113814436-A-G

14457190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113814534-C-T

14457302-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113814599-T-A

http://identifiers.org/hco/11/GRCh38#14457354-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#113814636-A-C

14457586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113814862-G-T

14457634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113814914-G-A

14457634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113814914-G-T

14457894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113815183-A-G

http://identifiers.org/hco/11/GRCh38#14458484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#113815651-C-A

http://identifiers.org/hco/11/GRCh38#14458595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#113815761-C-A

14458619-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 113815785-T-G

http://identifiers.org/hco/11/GRCh38#14458676-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#113815842-A-C

14459373-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113816209-G-C

14459983-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113816626-T-A

14459990-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113816633-G-C

14459990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113816633-G-T

http://identifiers.org/hco/11/GRCh38#14460110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#113816754-C-A

14460110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113816754-C-T

14460145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113816791-A-G

http://identifiers.org/hco/11/GRCh38#14460169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#113816815-C-A

14460380-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113817008-C-G

14460380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113817008-C-T

14460397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113817022-G-A

14460397-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113817022-G-C

14460397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113817022-G-T

14460406-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113817031-G-C

14460406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113817031-G-T

14461124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113818708-C-T

14461419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113818971-A-G

14461458-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113818993-T-A

14461458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113818993-T-C

14461621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113819150-G-A

14461735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113819258-C-T

14464044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113820051-G-A

14464152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113820133-G-A

14464551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113820540-A-G

14464811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113820776-G-T

http://identifiers.org/hco/11/GRCh38#14465112-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#113821047-A-C

14465112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113821047-A-G

14465309-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113821235-G-T

14465958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113821754-G-A

http://identifiers.org/hco/11/GRCh38#14466138-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#113822105-A-C

14466157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113822124-G-T

14466180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113822334-A-G

14466180-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113822334-A-T

14466227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113822386-T-C

14466242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113822401-C-T

14466319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: synonymous variant
orthologous variants: 113822475-A-G

14467733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113824661-T-C

14467818-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113824750-C-G

14467885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113824807-A-G

14467915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113824835-T-C

http://identifiers.org/hco/11/GRCh38#14467977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#113824893-C-A

14467995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113824912-T-C

http://identifiers.org/hco/11/GRCh38#14468035-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#113825022-A-C

14468708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: synonymous variant
orthologous variants: 113825865-T-C

14469321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113826167-T-C

14469666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113826496-T-C

14469682-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113826509-T-A

14469704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113826531-T-C

14469704-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113826531-T-G

http://identifiers.org/hco/11/GRCh38#14469963-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#113827007-A-C

14470169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113827215-T-C

14474067-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113830767-T-A

http://identifiers.org/hco/11/GRCh38#14474076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#113830776-C-A

14474081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113830781-G-T

14474110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113830809-G-A

http://identifiers.org/hco/11/GRCh38#14474115-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#113830814-A-C

14474206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113831181-T-C

http://identifiers.org/hco/11/GRCh38#14474209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#113831184-C-A

http://identifiers.org/hco/11/GRCh38#14474428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#113831347-C-A

14474612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 113831527-A-G

http://identifiers.org/hco/11/GRCh38#14474640-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#113831555-A-C

14474664-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113831572-T-A

14475150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113831709-A-G

http://identifiers.org/hco/11/GRCh38#14475152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#113831711-C-A

14475152-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113831711-C-G

14475205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113831762-T-C

14475292-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113831864-T-A

14475292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113831864-T-C

http://identifiers.org/hco/11/GRCh38#14475327-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#113831897-A-C

14475355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113831925-T-C

14475408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113831998-T-C

14475575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113832250-T-C

14475700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113832370-G-A

14475700-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113832370-G-C

14475700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113832370-G-T

14475702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113832372-G-A

14475702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113832372-G-T

14475767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113832418-A-G

14475823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 113832470-G-A

14475823-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 113832470-G-C

14475823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 113832470-G-T

14475896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: missense variant
orthologous variants: 113832543-G-A

http://identifiers.org/hco/11/GRCh38#14475907-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#113832554-A-C

14475993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113832633-G-A

14475993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113832633-G-T

14476253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113832866-A-G

14476408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113832998-G-A

14476658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113833240-G-T

14476925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: synonymous variant
orthologous variants: 113834180-A-G

http://identifiers.org/hco/11/GRCh38#14477059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#113834316-C-A

14477064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113834321-A-G

14478237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113834531-C-T

14478246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113834540-C-T

http://identifiers.org/hco/11/GRCh38#14478751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#113835277-C-A

14478857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113835387-G-A

http://identifiers.org/hco/11/GRCh38#14479091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#113835575-C-A

14479091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113835575-C-T

14479364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113835856-G-A

14479540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113835994-C-T

http://identifiers.org/hco/11/GRCh38#14479664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#113836117-C-A

14479721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 113836174-G-A

14479721-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 113836174-G-C

14479721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 113836174-G-T

http://identifiers.org/hco/11/GRCh38#14479722-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#113836175-A-C

14479722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 113836175-A-G

http://identifiers.org/hco/11/GRCh38#14479733-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#113836186-A-C

14479733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113836186-A-G

14480720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113836492-T-C

14480729-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113836499-T-A

14480729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113836499-T-C

14480822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: synonymous variant
orthologous variants: 113836592-T-C

14480864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: synonymous variant
orthologous variants: 113836634-A-G

14480983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 113836755-C-T

14481167-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113836938-G-C

14481167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113836938-G-T

14481184-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113836955-T-G

14481237-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113837008-T-A

14481245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113837016-T-C

14481245-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113837016-T-G

14481437-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113837195-G-C

14481437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113837195-G-T

http://identifiers.org/hco/11/GRCh38#14482921-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#113837498-A-C

14482921-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113837498-A-T

14482947-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113837527-G-C

14482947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113837527-G-T

14483035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: synonymous variant
orthologous variants: 113837588-T-C

14483231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113837789-C-T

14483276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113837803-T-C

14483276-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113837803-T-G

14483298-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113837821-T-G

14483336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113837852-T-C

14483382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113837903-G-A

14483401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113837930-G-A

14483401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113837930-G-T

http://identifiers.org/hco/11/GRCh38#14484016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#113838686-C-A

14484016-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113838686-C-G

14484075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113838728-T-C

14484138-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113838794-C-G

14484212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113838842-T-C

14484250-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113838874-G-C

14484406-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113839024-G-C

14484412-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113839030-T-G

14484424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113839042-A-G

14485048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113839308-T-C

14485159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113839417-C-T

http://identifiers.org/hco/11/GRCh38#14485160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#113839418-C-A

14486418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: synonymous variant
orthologous variants: 113839911-A-G

14488519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: synonymous variant
orthologous variants: 113844686-C-T

http://identifiers.org/hco/11/GRCh38#14488645-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#113844807-A-C

14488645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113844807-A-G

14488645-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113844807-A-T

14488664-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113844829-T-A

14488664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113844829-T-C

http://identifiers.org/hco/11/GRCh38#14488682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#113844848-C-A

14488719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113844885-A-G

http://identifiers.org/hco/11/GRCh38#14490628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#113846026-C-A

14490628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: synonymous variant
orthologous variants: 113846026-C-T

14490685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 113846083-A-G

14490791-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113846189-G-C

14490791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113846189-G-T

14490798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113846196-T-C

14490805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113846203-T-C

14491704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113846237-A-G

14493374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113847717-G-A

14493449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113847786-T-C

14493472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113847810-G-A

14493499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113847839-T-C

http://identifiers.org/hco/11/GRCh38#14493598-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#113847952-A-C

14493598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113847952-A-G

14493629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113847976-T-C

14493629-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113847976-T-G

14493636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113848027-A-G

14493707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: synonymous variant
orthologous variants: 113848108-T-C

14493707-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: synonymous variant
orthologous variants: 113848108-T-G

14493868-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113848422-T-A

14493875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113848430-G-A

14493875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113848430-G-T

14493898-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113848453-A-T

14493984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113848543-C-T

http://identifiers.org/hco/11/GRCh38#14494163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#113849239-C-A

14494163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113849239-C-T

14494174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: 113849246-A-G

http://identifiers.org/hco/11/GRCh38#14494178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#113849250-C-A

14494464-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113849557-A-T

14494467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113849560-G-A

14494467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113849560-G-T

14494545-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113849620-T-A

14494545-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113849620-T-G

14494548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113849623-C-T

http://identifiers.org/hco/11/GRCh38#14494551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#113849626-C-A

14494551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113849626-C-T

http://identifiers.org/hco/11/GRCh38#14494574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#113849649-C-A

14494574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 113849649-C-T

http://identifiers.org/hco/11/GRCh38#14494651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#113849692-C-A

14494651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113849692-C-T

14494652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113849693-T-C

14494658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113849699-T-C

http://identifiers.org/hco/11/GRCh38#14494694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#113849735-C-A

http://identifiers.org/hco/11/GRCh38#14494714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#113849755-C-A

14494714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113849755-C-T

14498765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113853011-A-G

14498774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113853025-T-C

http://identifiers.org/hco/11/GRCh38#14499432-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#113853644-A-C

http://identifiers.org/hco/11/GRCh38#14499517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#113853691-C-A

14499517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113853691-C-T

14499555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 113853711-A-G

http://identifiers.org/hco/11/GRCh38#14499557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#113853713-C-A

14499557-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 113853713-C-G

14499673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113853779-A-G

14499676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113853782-A-G

14499713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 113853813-T-C

http://identifiers.org/hco/11/GRCh38#14499881-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#113853965-A-C

14499881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, undefined
orthologous variants: 113853965-A-G

14499897-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 113853981-G-C

14499897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 113853981-G-T

http://identifiers.org/hco/11/GRCh38#14499898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#113853982-C-A

14499898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 113853982-C-T

14499913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: 5 prime UTR variant
orthologous variants: 113853997-A-G

14499931-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 113854015-T-A

14499931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 113854015-T-C

14499935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 113854019-G-A

14499935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2231
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 113854019-G-T