http://identifiers.org/hco/17/GRCh38#40475923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#98956582-C-A

40475923-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 98956582-C-G

http://identifiers.org/hco/17/GRCh38#40475966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#98956624-C-A

40475966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 98956624-C-T

http://identifiers.org/hco/17/GRCh38#40475987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#98956645-C-A

40476000-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 98956658-C-G

40476000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 98956658-C-T

40476002-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 98956660-G-C

40476002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 98956660-G-T

40476027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 98956685-G-T

http://identifiers.org/hco/17/GRCh38#40476073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#98956774-C-A

40476073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 98956774-C-T

40476228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 98956927-G-A

40476305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 98957005-T-C

http://identifiers.org/hco/17/GRCh38#40476494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#98957150-C-A

40477124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 98958569-C-T

40477252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 98958696-G-A

40477252-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 98958696-G-C

40477252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 98958696-G-T

40477351-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 98958799-G-C

40477351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 98958799-G-T

http://identifiers.org/hco/17/GRCh38#40477357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#98958804-C-A

40477357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 98958804-C-T

40477365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 98958812-T-C

40477365-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 98958812-T-G

40477366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 98958813-T-C

40477394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 98958839-A-G

http://identifiers.org/hco/17/GRCh38#40477433-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#98958875-A-C

40477433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 98958875-A-G

40477496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 98958938-T-C

40477654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 98959073-C-T

40477656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 98959075-T-C

http://identifiers.org/hco/17/GRCh38#40477855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#98959265-C-A

http://identifiers.org/hco/17/GRCh38#40477980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#98959775-C-A

40477980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 98959775-C-T

40478286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98961205-C-T

http://identifiers.org/hco/17/GRCh38#40478368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#98961292-C-A

http://identifiers.org/hco/17/GRCh38#40478436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#98961348-C-A

40478436-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98961348-C-G

40478493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98961397-G-T

http://identifiers.org/hco/17/GRCh38#40478733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#98961635-C-A

http://identifiers.org/hco/17/GRCh38#40478748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#98961650-C-A

40478748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98961650-C-T

40478858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98961744-T-C

40478884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98961770-A-G

40478927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98961798-G-A

40478935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98961806-G-A

40479075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98961925-G-A

40479075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98961925-G-T

40479100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98961928-G-A

40479127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98961956-T-C

40479579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98962063-A-G

40479607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98962073-G-T

http://identifiers.org/hco/17/GRCh38#40479634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#98962100-C-A

40479642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98962111-C-T

40479739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 98962208-G-A

40479739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 98962208-G-T

40479820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 98962289-G-A

http://identifiers.org/hco/17/GRCh38#40479934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#98962433-C-A

40479934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 98962433-C-T

http://identifiers.org/hco/17/GRCh38#40480113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#98962510-C-A

40480113-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 98962510-C-G

40480113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 98962510-C-T

http://identifiers.org/hco/17/GRCh38#40480114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#98962511-C-A

40480422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 98962756-G-A

40480422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 98962756-G-T

40480481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98962810-C-T

http://identifiers.org/hco/17/GRCh38#40480542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#98962879-C-A

40480542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 98962879-C-T

40480557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 98962894-G-A

40480557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 98962894-G-T

http://identifiers.org/hco/17/GRCh38#40480562-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#98962899-A-C

40480562-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 98962899-A-T

40480563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 98962900-G-A

40480563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 98962900-G-T

http://identifiers.org/hco/17/GRCh38#40480602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#98962941-C-A

40480602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 98962941-C-T

40480719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 98963054-G-A

40480822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98963155-G-A

40480822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98963155-G-T

40480834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 98963167-A-G

http://identifiers.org/hco/17/GRCh38#40480843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#98963176-C-A

http://identifiers.org/hco/17/GRCh38#40480881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#98963214-C-A

40480881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, undefined
orthologous variants: 98963214-C-T

40480914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, undefined
orthologous variants: 98963246-T-C

40480925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, undefined
orthologous variants: 98963257-G-A

40480925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, undefined
orthologous variants: 98963257-G-T

40480926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, undefined
orthologous variants: 98963258-G-A

40480926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, undefined
orthologous variants: 98963258-G-T

40480944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98963268-G-A

40480944-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98963268-G-C

40480944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98963268-G-T

http://identifiers.org/hco/17/GRCh38#40480969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#98963290-C-A

40480969-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98963290-C-G

40480995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98963318-G-A

40480995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98963318-G-T

40481041-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, undefined
orthologous variants: 98963365-C-G

40481183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98963479-C-T

40481184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98963480-A-G

40481202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98963496-A-G

40481246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98963521-G-T

40481380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98963585-G-A

40481530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98963699-A-G

http://identifiers.org/hco/17/GRCh38#40481531-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#98963700-A-C

40481731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98963871-G-A

40481979-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98964369-T-A

40481979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98964369-T-C

http://identifiers.org/hco/17/GRCh38#40481991-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#98964385-A-C

40481991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98964385-A-G

40481991-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98964385-A-T

http://identifiers.org/hco/17/GRCh38#40482004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#98964398-C-A

40482004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98964398-C-T

40482015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98964409-A-G

40482066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98964466-C-T

http://identifiers.org/hco/17/GRCh38#40482071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#98964471-C-A

40482115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 98964484-G-A

40482237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98964606-A-G

http://identifiers.org/hco/17/GRCh38#40482265-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#98964660-A-C

40482270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98964665-G-A

40482270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98964665-G-T

http://identifiers.org/hco/17/GRCh38#40482370-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#98964768-A-C

40483571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98965053-G-A

40483701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, undefined
orthologous variants: 98965148-G-A

40483701-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, undefined
orthologous variants: 98965148-G-C

40483746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98965211-A-G

40483887-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98965349-T-G

40484418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98965882-G-T

40484490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: stop gained
orthologous variants: 98965947-G-A

40484490-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: missense variant
orthologous variants: 98965947-G-C

40484490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: synonymous variant
orthologous variants: 98965947-G-T

40484506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: synonymous variant
orthologous variants: 98965963-G-A

40484506-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: synonymous variant
orthologous variants: 98965963-G-C

40484506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: synonymous variant
orthologous variants: 98965963-G-T

40484547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: stop gained
orthologous variants: 98966004-G-A

40484547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: synonymous variant
orthologous variants: 98966004-G-T

40484594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: missense variant
orthologous variants: 98966051-C-T

40484599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: synonymous variant
orthologous variants: 98966056-C-T

40484613-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 98966070-G-C

40484613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 98966070-G-T

40484642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98966096-G-A

40484642-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98966096-G-C

40484642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98966096-G-T

40484664-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98966116-C-G

40484673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98966125-T-C

40484743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98966172-T-C

40484868-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98966293-T-A

40484868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98966293-T-C

40484874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98966299-G-A

40484874-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98966299-G-C

40485030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98966468-G-A

40485031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98966469-A-G

40485035-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98966473-T-A

40485035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98966473-T-C

40485040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98966478-G-A

40485040-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98966478-G-C

40485040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98966478-G-T

40485064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98966502-T-C

40485065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98966503-G-A

40485065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98966503-G-T

http://identifiers.org/hco/17/GRCh38#40485071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#98966508-C-A

40485071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98966508-C-T

http://identifiers.org/hco/17/GRCh38#40485121-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#98966557-A-C

40485121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98966557-A-G

40485121-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98966557-A-T

40485125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98966562-A-G

40485125-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98966562-A-T

40485147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98966590-T-C

40485147-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98966590-T-G

40486194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, undefined
orthologous variants: 98967812-G-A

http://identifiers.org/hco/17/GRCh38#40486697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#98968307-C-A

40486697-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, undefined
orthologous variants: 98968307-C-G

40486977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98969167-C-T

http://identifiers.org/hco/17/GRCh38#40486994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#98969184-C-A

40486994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98969184-C-T

40487071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: missense_variant, undefined
orthologous variants: 98969267-G-A

40487155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: missense variant
orthologous variants: 98969351-C-T

40487241-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: missense variant
orthologous variants: 98969437-G-C

40487241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: stop gained
orthologous variants: 98969437-G-T

40487250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: synonymous variant
orthologous variants: 98969446-G-A

40487310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: synonymous variant
orthologous variants: 98969506-G-A

40487310-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: synonymous variant
orthologous variants: 98969506-G-C

40487421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: synonymous variant
orthologous variants: 98969617-C-T

http://identifiers.org/hco/17/GRCh38#40487540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#98969745-C-A

40487540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98969745-C-T

http://identifiers.org/hco/17/GRCh38#40487560-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#98969761-A-C

40487560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98969761-A-G

http://identifiers.org/hco/17/GRCh38#40487601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#98969802-C-A

40487601-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98969802-C-G

40487601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98969802-C-T

40487705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98969909-C-T

40488080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98970242-G-T

40488159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98970307-G-A

http://identifiers.org/hco/17/GRCh38#40488186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#98970357-C-A

40488186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98970357-C-T

40488224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98970469-G-A

40488250-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98970601-C-G

40488403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98970764-G-A

40488403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98970764-G-T

40488490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98970850-G-A

40488490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98970850-G-T

40488513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98970873-T-C

40488522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98970882-A-G

40488529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98970889-G-A

40488536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98970896-C-T

http://identifiers.org/hco/17/GRCh38#40488606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#98970966-C-A

40488606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: missense variant
orthologous variants: 98970966-C-T

http://identifiers.org/hco/17/GRCh38#40488686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#98971025-C-A

40488686-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: synonymous variant
orthologous variants: 98971025-C-G

40488686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: synonymous variant
orthologous variants: 98971025-C-T

http://identifiers.org/hco/17/GRCh38#40488691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#98971030-C-A

http://identifiers.org/hco/17/GRCh38#40488701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#98971040-C-A

40488825-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: missense variant
orthologous variants: 98971137-C-G

40488825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: missense variant
orthologous variants: 98971137-C-T

40488899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: synonymous variant
orthologous variants: 98971211-G-A

40488923-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: missense variant
orthologous variants: 98971235-A-T

40488933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: missense variant
orthologous variants: 98971245-C-T

40488937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: missense variant
orthologous variants: 98971249-A-G

40488975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 98971289-G-A

40488975-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 98971289-G-C

40488975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 98971289-G-T

40488984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98971298-A-G

40490478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98971684-T-C

40490526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, undefined
orthologous variants: 98971709-C-T

40490572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98971756-C-T

40490840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98971986-G-A

40490899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98972046-G-A

40491263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, undefined
orthologous variants: 98972606-A-G

40491311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98972631-C-T

40491483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98972803-A-G

40491804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98973114-G-A

40493736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98974311-C-T

40493786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98974356-C-T

40493984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98974562-T-C

40494028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98974600-C-T

40494044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98974612-T-C

http://identifiers.org/hco/17/GRCh38#40494084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#98974642-C-A

40494381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98974882-G-A

40494716-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98975187-T-A

40494716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98975187-T-C

40494716-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98975187-T-G

40494719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98975190-G-A

40495597-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98976077-C-G

40495783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98976284-G-A

40495853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98976354-G-T

40495860-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98976361-A-T

40495932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98976436-C-T

http://identifiers.org/hco/17/GRCh38#40495956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#98976464-C-A

40495956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98976464-C-T

http://identifiers.org/hco/17/GRCh38#40495974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#98976480-C-A

40495974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98976480-C-T

http://identifiers.org/hco/17/GRCh38#40496072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#98976578-C-A

http://identifiers.org/hco/17/GRCh38#40496108-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#98976614-A-C

40496207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: synonymous variant
orthologous variants: 98976713-C-T

40496237-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: synonymous variant
orthologous variants: 98976743-A-T

40496312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: synonymous variant
orthologous variants: 98976818-G-A

40496346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: missense variant
orthologous variants: 98976852-G-A

40496498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: 5 prime UTR variant
orthologous variants: 98976991-T-C

40496587-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98977074-T-A

40496587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98977074-T-C

40496587-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98977074-T-G

http://identifiers.org/hco/17/GRCh38#40496589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#98977076-C-A

40496589-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98977076-C-G

40496589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98977076-C-T

40497107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98977524-G-A

http://identifiers.org/hco/17/GRCh38#40497804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#98977862-C-A

40497853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, undefined
orthologous variants: 98977911-A-G

40497864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, undefined
orthologous variants: 98977922-A-G

40498073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98978134-G-T

40498091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98978152-G-T

40499630-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron_variant, undefined
orthologous variants: 98978780-C-G

40500329-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98979415-C-G

40500329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98979415-C-T

40500744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98979761-C-T

http://identifiers.org/hco/17/GRCh38#40500792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#98979802-C-A

40500792-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98979802-C-G

40500792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24352
most severe consequence: intron variant
orthologous variants: 98979802-C-T