80454278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 5 prime UTR variant
orthologous variants: 40688823-G-A

http://identifiers.org/hco/10/GRCh38#80454413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40688691-C-A

80454413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40688691-C-T

http://identifiers.org/hco/10/GRCh38#80454452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40688655-C-A

http://identifiers.org/hco/10/GRCh38#80454489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40688618-C-A

http://identifiers.org/hco/10/GRCh38#80454506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40688601-C-A

80454506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40688601-C-T

80454521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40688591-G-A

80454581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40688532-C-T

80454700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40688453-C-T

80455025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40688241-C-T

80455121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40688154-C-T

80455464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40687866-C-T

80455532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40687789-T-C

80455535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40687786-C-T

80455969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40687446-C-T

80455972-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40687443-C-G

80456006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40687409-C-T

80456024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40687392-C-T

80456179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40687295-A-G

80456307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40687183-G-A

80456343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40687151-C-T

80456402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40687084-A-G

80456515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40686961-C-T

80456570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40686906-G-A

80456570-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40686906-G-C

80458071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40685619-G-T

80458151-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40685552-G-C

80458151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40685552-G-T

80458701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40684940-C-T

80458788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40684848-G-A

http://identifiers.org/hco/10/GRCh38#80459122-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40684553-A-C

80459158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40684515-A-G

80459209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40684464-G-A

80459209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40684464-G-T

http://identifiers.org/hco/10/GRCh38#80459242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40684419-C-A

80459322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40684345-T-C

80459349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40684318-T-C

http://identifiers.org/hco/10/GRCh38#80459404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40684275-C-A

80459404-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40684275-C-G

80459404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40684275-C-T

80459499-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40684205-T-A

80459499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40684205-T-C

http://identifiers.org/hco/10/GRCh38#80459544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40684153-C-A

80459586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 40684123-T-C

http://identifiers.org/hco/10/GRCh38#80459587-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40684122-A-C

80459607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40684102-A-G

80459672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40684047-T-C

80459902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40682605-C-T

80460082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40682423-A-G

80460283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40682244-A-G

80460501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40682059-C-T

80460683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40681876-C-T

80460732-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40681847-C-G

80460895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40681672-C-T

80461603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40681128-T-C

80462251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40680750-T-C

80462302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40680697-T-C

80462307-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40680692-G-C

80462464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40680593-C-T

80462563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40680497-G-A

http://identifiers.org/hco/10/GRCh38#80462948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40680120-C-A

80462948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40680120-C-T

80462966-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40680098-T-A

80463184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40679772-T-C

80463889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40679096-G-A

80464059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40678928-A-G

80464714-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40678532-T-A

80464714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40678532-T-C

80464943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40678318-G-A

80464950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40678311-A-G

80464997-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40678271-C-G

80464997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40678271-C-T

http://identifiers.org/hco/10/GRCh38#80465119-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40678133-A-C

80465350-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40677916-T-A

80465490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40677773-G-T

80465866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40677360-A-G

80467395-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40676510-T-G

80467438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40676464-G-T

80467472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40676428-G-A

80467482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40676413-C-T

80467509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40676382-G-A

80467698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40676203-G-A

80468220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40675683-T-C

80468430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40675404-A-G

80468537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40675313-T-C

http://identifiers.org/hco/10/GRCh38#80468818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40675162-C-A

80468818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40675162-C-T

80468988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40675038-G-A

80469021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40675006-G-A

80469068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

80469780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40673575-C-T

80470597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40673078-T-C

80470618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40673048-A-G

80470632-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40673034-T-G

80470715-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40673000-T-A

80471188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40672674-C-T

80471202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40672668-G-A

80471202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40672668-G-T

80471335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40672560-T-C

80471385-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40672502-A-T

80471431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40672460-T-C

80471619-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40672323-T-G

80472850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40671594-A-G

80472975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40671506-G-A

80472977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40671504-C-T

80473000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40671479-T-C

80473059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40671432-G-T

80473498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40671030-G-A

http://identifiers.org/hco/10/GRCh38#80473675-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40670873-A-C

80473827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40670838-G-T

80473880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40670787-C-T

80473894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40670773-A-G

80473927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40670704-C-T

80473940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40670691-C-T

80474137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40670489-C-T

80474304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40670307-C-T

80474347-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40670267-A-T

80474356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40670258-A-G

80474480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40670140-G-A

http://identifiers.org/hco/10/GRCh38#80474865-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40669762-A-C

80474977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40669658-G-A

80474985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40669650-A-G

80477548-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40664219-C-G

80477593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40664176-G-T

80477661-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40664102-T-A

80477676-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40664085-C-G

80477732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40664051-A-G

80477854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40663926-G-T

80477874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40663912-G-A

80477994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40663789-G-A

80482737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40661286-T-C

80482821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40661216-C-T

80483059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40661005-G-A

80483059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40661005-G-T

http://identifiers.org/hco/10/GRCh38#80483587-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40660506-A-C

80483587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40660506-A-G

80484558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40660398-T-C

80485201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40659884-G-A

80485201-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40659884-G-C

80485467-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40659659-G-C

80485604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40659542-G-A

80485604-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40659542-G-C

80485678-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40659510-C-G

80485678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40659510-C-T

80485682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40659506-G-A

80485712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40659434-C-T

80485880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40659288-G-T

80486084-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40659126-G-C

80486185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40659015-G-A

80486224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40658974-C-T

80486372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40658835-T-C

80486454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40658758-C-T

80487547-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40658006-T-A

80487636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40657920-G-T

80487727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40657827-A-G

80487727-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40657827-A-T

80487763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40657789-G-A

80487836-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40657718-G-C

80487968-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40657596-C-G

80487968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40657596-C-T

80488166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40657336-G-A

80488224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40657273-C-T

80488296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40657241-T-C

80488381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40657201-T-C

80488400-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40657197-C-G

80488405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40657192-A-G

80488577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40657037-C-T

80488757-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40656823-G-C

80488757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40656823-G-T

80488803-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40656778-C-G

80488803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40656778-C-T

80488929-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40656515-A-T

80488943-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40656501-T-A

80488985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40656459-T-C

80489018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40656444-T-C

http://identifiers.org/hco/10/GRCh38#80489067-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40656395-A-C

80489070-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40656392-T-A

80489354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40656099-T-C

http://identifiers.org/hco/10/GRCh38#80489382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40656071-C-A

80489382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40656071-C-T

http://identifiers.org/hco/10/GRCh38#80489383-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40656070-A-C

80489383-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40656070-A-T

http://identifiers.org/hco/10/GRCh38#80489414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40656041-C-A

80489414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40656041-C-T

80489423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40656032-G-T

80489435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40656020-G-A

80489435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40656020-G-T

80489447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40656008-C-T

80489618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40655859-C-T

80489898-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40655597-T-A

80490196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40654697-T-C

80490205-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40654688-G-C

80490285-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40654624-A-T

80490431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40654508-A-G

80490433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40654506-T-C

80490646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40654380-A-G

80490775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40654257-A-G

80490889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40654148-A-G

80491590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40653450-C-T

80491613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40653426-G-A

http://identifiers.org/hco/10/GRCh38#80491684-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40653367-A-C

80492009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40653066-C-T

80492015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40653060-A-G

80492104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40652959-G-T

80492864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40652540-A-G

80493031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40652436-T-C

80493166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40652279-A-G

80493389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40652062-C-T

80493654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40651814-A-G

80493951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40650659-T-C

80494074-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40650541-T-G

80494195-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40650410-C-G

80494283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40650329-C-T

80494308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40650304-A-G

80494316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40650296-A-G

80494340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40650274-A-G

80494486-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40650132-G-C

80494538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40650024-T-C

80494550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40649996-C-T

80494651-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40649882-T-G

80494783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40649754-A-G

http://identifiers.org/hco/10/GRCh38#80494873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40649683-C-A

80494880-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40649676-G-C

http://identifiers.org/hco/10/GRCh38#80494985-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40649570-A-C

80495483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40649117-G-A

80495534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40649088-G-A

80497276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40647032-T-C

80497356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40646952-A-G

80497467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40646860-A-G

80497678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40646686-C-T

http://identifiers.org/hco/10/GRCh38#80498168-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40645847-A-C

80498174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40645841-A-G

80498207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40645811-G-T

80498367-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40645674-G-C

80498367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40645674-G-T

80498790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40645019-C-T

80498791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40645018-C-T

80498948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40644819-G-T

80498979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40644788-G-A

80499063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40644719-G-T

80499194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40644602-C-T

80499199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40644597-C-T

80499279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40644546-T-C

80500096-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40643454-C-G

80500096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40643454-C-T

80500176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40643386-G-T

80500228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40643336-T-C

80503959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40641389-C-T

80504131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40641257-C-T

80504132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40641256-G-A

80504132-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40641256-G-C

80504190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40641202-C-T

80504211-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40641189-T-A

80504215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40641185-C-T

80504500-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40640901-T-G

80504576-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40640821-A-T

80504691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40640692-A-G

80504831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40640554-G-A

80504831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40640554-G-T

80505026-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40640365-T-G

80505041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40640341-A-G

80505095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40640289-G-A

80505176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40640234-G-A

80505176-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40640234-G-C

80505176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40640234-G-T

80505531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40640000-C-T

80506902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40639233-T-C

80507061-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40639071-G-C

80507061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40639071-G-T

http://identifiers.org/hco/10/GRCh38#80507182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40638950-C-A

80507182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40638950-C-T

80507452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40638686-G-A

80507452-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40638686-G-C

80507453-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40638685-G-C

80507453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40638685-G-T

http://identifiers.org/hco/10/GRCh38#80507455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40638683-C-A

80507477-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40638658-G-C

80507477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40638658-G-T

80507594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40638553-G-A

80507604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40638543-A-G

80508643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40637950-C-T

80509091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40637613-G-A

80509120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40637588-G-A

http://identifiers.org/hco/10/GRCh38#80509150-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40637557-A-C

80509150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40637557-A-G

80509150-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40637557-A-T

80509152-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40637555-G-C

80509152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40637555-G-T

80509272-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40637531-A-T

80509439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 40637367-C-T

80509536-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40637271-C-G

http://identifiers.org/hco/10/GRCh38#80509577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40637235-C-A

http://identifiers.org/hco/10/GRCh38#80509618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40637193-C-A

80509618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40637193-C-T

80509630-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40637181-G-C

80509630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40637181-G-T

80509696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 40637108-G-A

80509696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 40637108-G-T

http://identifiers.org/hco/10/GRCh38#80509774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#40637059-C-A

http://identifiers.org/hco/10/GRCh38#80509785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40637045-C-A

80509785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40637045-C-T

80509786-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40637044-C-G

80509786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40637044-C-T

80509793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40637037-A-G

http://identifiers.org/hco/10/GRCh38#80509834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#40636977-C-A

80509834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 40636977-C-T

80509910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 40636926-G-A

80509910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 40636926-G-T

80509919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40636917-C-T

80509952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, undefined
orthologous variants: 40636884-A-G

http://identifiers.org/hco/10/GRCh38#80509986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#40636853-C-A

80510031-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, undefined
orthologous variants: 40636809-T-G

http://identifiers.org/hco/10/GRCh38#80510039-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#40636801-A-C

80510039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, undefined
orthologous variants: 40636801-A-G

80510039-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, undefined
orthologous variants: 40636801-A-T

http://identifiers.org/hco/10/GRCh38#80510051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#40636791-C-A

80510051-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, undefined
orthologous variants: 40636791-C-G

80510115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron variant
orthologous variants: 40636737-C-T

80510212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron variant
orthologous variants: 40636663-A-G

80510416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron variant
orthologous variants: 40636477-C-T

80512210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: missense variant
orthologous variants: 40635376-G-A

80512308-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron variant
orthologous variants: 40635301-T-G

80512315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron variant
orthologous variants: 40635294-G-T

http://identifiers.org/hco/10/GRCh38#80512317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40635292-C-A

http://identifiers.org/hco/10/GRCh38#80512372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40635232-C-A

80512394-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron variant
orthologous variants: 40635208-C-G

80512435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron variant
orthologous variants: 40635171-T-C

80513794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron variant
orthologous variants: 40633363-C-T

80514025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: missense variant
orthologous variants: 40633106-G-A

80514025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: missense variant
orthologous variants: 40633106-G-T

80514167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron variant
orthologous variants: 40632954-G-T

80514189-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron variant
orthologous variants: 40632933-A-T

80515385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron variant
orthologous variants: 40632417-G-T

80515612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40632218-A-G

80515633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40632200-G-A

80515637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40632196-T-C

80515768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40632077-G-T

80515811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40632030-T-C

80515829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40632009-C-T

80515830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40632008-T-C

80515854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40631981-T-C

http://identifiers.org/hco/10/GRCh38#80515895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40631938-C-A

80515895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40631938-C-T

80515937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40631911-A-G

80515938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40631910-G-A

80515938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40631910-G-T

80515991-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40631882-T-G

80516043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40631833-A-G

80516043-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40631833-A-T

80516051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40631824-T-C

80516051-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40631824-T-G

http://identifiers.org/hco/10/GRCh38#80516117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40631746-C-A

80516117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40631746-C-T

80516150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40631712-G-A

http://identifiers.org/hco/10/GRCh38#80516472-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40631438-A-C

80516492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40631418-T-C

80516960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40630907-G-T

80517086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40630799-G-A

80517207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40630671-G-A

80517249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40630629-A-G

80517319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40630584-C-T

80517408-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40630501-C-G

http://identifiers.org/hco/10/GRCh38#80517761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40630195-C-A

80517761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40630195-C-T

http://identifiers.org/hco/10/GRCh38#80517785-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40630174-A-C

80517785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40630174-A-G

80517785-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40630174-A-T

80517786-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40630173-G-C

80517786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40630173-G-T

80517807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40630157-G-T

80518022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 40629969-A-G

http://identifiers.org/hco/10/GRCh38#80518286-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40629717-C-A

http://identifiers.org/hco/10/GRCh38#80518300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40629703-C-A

http://identifiers.org/hco/10/GRCh38#80518323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40629682-C-A

80518363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 40629647-T-C

http://identifiers.org/hco/10/GRCh38#80518508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40629523-C-A

http://identifiers.org/hco/10/GRCh38#80518550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40629484-C-A

80518550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 40629484-C-T

80518663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 40629379-T-C

http://identifiers.org/hco/10/GRCh38#80518879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40629199-C-A

http://identifiers.org/hco/10/GRCh38#80518945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40629144-C-A

80518945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 40629144-C-T

80519044-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 40629071-G-C

80519044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 40629071-G-T

80519175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 40628945-G-A

80519177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 40628943-T-C

80519216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 40628910-G-T

http://identifiers.org/hco/10/GRCh38#80519276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40628867-C-A

80519276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 40628867-C-T

80519306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 40628826-G-T

80519399-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 40628729-T-A

80519552-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 40628553-A-T

80519815-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3 prime UTR variant
orthologous variants: 40628293-T-A

80519821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3 prime UTR variant
orthologous variants: 40628287-T-C

80520159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3 prime UTR variant
orthologous variants: 40628035-G-T

http://identifiers.org/hco/10/GRCh38#80520196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40627993-C-A

80520196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3 prime UTR variant
orthologous variants: 40627993-C-T

80520209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3 prime UTR variant
orthologous variants: 40627972-G-A

80520209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3 prime UTR variant
orthologous variants: 40627972-G-T

80520612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3 prime UTR variant
orthologous variants: 40627685-T-C

80520688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3 prime UTR variant
orthologous variants: 40627656-A-G

80520935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3 prime UTR variant
orthologous variants: 40627443-G-T

80521008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3 prime UTR variant
orthologous variants: 40627374-T-C

80521034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3 prime UTR variant
orthologous variants: 40627348-T-C

80521916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3 prime UTR variant
orthologous variants: 40626375-A-G

http://identifiers.org/hco/10/GRCh38#80521933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40626358-C-A

80521951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3 prime UTR variant
orthologous variants: 40626339-C-T

80522835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3 prime UTR variant
orthologous variants: 40625544-G-A

80522835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3 prime UTR variant
orthologous variants: 40625544-G-T

80523017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3 prime UTR variant
orthologous variants: 40625366-T-C

80523019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3 prime UTR variant
orthologous variants: 40625364-C-T

80523039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3 prime UTR variant
orthologous variants: 40625343-C-T

80523057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3 prime UTR variant
orthologous variants: 40625321-G-A

http://identifiers.org/hco/10/GRCh38#80523060-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40625318-A-C

80523060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3 prime UTR variant
orthologous variants: 40625318-A-G

80523105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3 prime UTR variant
orthologous variants: 40625269-T-C

80524047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3 prime UTR variant
orthologous variants: 40624403-G-A

80524047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3 prime UTR variant
orthologous variants: 40624403-G-T

http://identifiers.org/hco/10/GRCh38#80524069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40624383-C-A

80524069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3 prime UTR variant
orthologous variants: 40624383-C-T

80524119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3 prime UTR variant
orthologous variants: 40624330-G-T

80524158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3 prime UTR variant
orthologous variants: 40624284-T-C

80524229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3 prime UTR variant
orthologous variants: 40624219-C-T

80524316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3 prime UTR variant
orthologous variants: 40624123-G-A

80524337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3 prime UTR variant
orthologous variants: 40624102-T-C

80524382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3 prime UTR variant
orthologous variants: 40624073-T-C

80524427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3 prime UTR variant
orthologous variants: 40624042-G-A

80524427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3 prime UTR variant
orthologous variants: 40624042-G-T

http://identifiers.org/hco/10/GRCh38#80524478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40623994-C-A

http://identifiers.org/hco/10/GRCh38#80524540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40623944-C-A

80524540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3 prime UTR variant
orthologous variants: 40623944-C-T

80524613-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3 prime UTR variant
orthologous variants: 40623815-T-G

http://identifiers.org/hco/10/GRCh38#80524619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40623809-C-A

80524626-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3 prime UTR variant
orthologous variants: 40623802-T-A

80524693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3 prime UTR variant
orthologous variants: 40623738-A-G

80524705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3 prime UTR variant
orthologous variants: 40623726-G-A

80524705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3 prime UTR variant
orthologous variants: 40623726-G-T

http://identifiers.org/hco/10/GRCh38#80524720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40623708-C-A

80524721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3 prime UTR variant
orthologous variants: 40623707-A-G

80524848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3 prime UTR variant
orthologous variants: 40623577-G-T

80524851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3 prime UTR variant
orthologous variants: 40623574-G-T

80524952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3 prime UTR variant
orthologous variants: 40623423-A-G

80532835-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40617481-A-T

http://identifiers.org/hco/10/GRCh38#80532876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40617450-C-A

80532876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40617450-C-T

http://identifiers.org/hco/10/GRCh38#80532878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40617448-C-A

80532985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40617364-G-A

80532985-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40617364-G-C

80532985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23303
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40617364-G-T