45388682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: 3 prime UTR variant
orthologous variants: 86292095-A-G

http://identifiers.org/hco/2/GRCh38#45388748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86292157-C-A

45388837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 86292245-G-A

45388837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 86292245-G-T

45388988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 86292390-G-A

45388988-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 86292390-G-C

45389061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 86292432-T-C

http://identifiers.org/hco/2/GRCh38#45389156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86292489-C-A

45389156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 86292489-C-T

45389179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 86292496-G-A

45389179-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 86292496-G-C

45389179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 86292496-G-T

45389214-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 86292527-T-A

http://identifiers.org/hco/2/GRCh38#45389215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86292528-C-A

45389215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 86292528-C-T

http://identifiers.org/hco/2/GRCh38#45389220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86292533-C-A

45389220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 86292533-C-T

45389222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 86292535-G-T

45389224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 86292537-T-C

45389243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 86292555-A-G

45389300-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 86292611-C-G

45389300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 86292611-C-T

45389348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 86292660-G-A

45389348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 86292660-G-T

45389357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 86292669-C-T

45389409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 86292721-T-C

45389409-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 86292721-T-G

45389416-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 86292728-T-A

http://identifiers.org/hco/2/GRCh38#45389585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86292897-C-A

45389628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86292948-A-G

45389817-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86293123-C-G

45389876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86293194-T-C

45390205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86293489-G-A

45390205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86293489-G-T

45390214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86293498-G-A

45390222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86293510-T-C

45390316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86293599-T-C

45390316-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86293599-T-G

45390332-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86293616-T-G

45390376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86293657-A-G

45390468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86293753-G-A

45390553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86293826-C-T

45390868-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86294143-C-G

45390868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86294143-C-T

45391021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86294276-C-T

http://identifiers.org/hco/2/GRCh38#45391034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86294288-C-A

45391034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86294288-C-T

45391042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86294296-G-T

45391076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86294322-C-T

45391532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86294752-G-A

45391802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86294924-T-C

45391853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86294974-T-C

45391858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86294979-G-A

45392672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86295497-T-C

45392793-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86295615-T-A

45392794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86295616-T-C

45392837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86295659-G-A

45392837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86295659-G-T

45392871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86295694-T-C

45392871-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86295694-T-G

45392875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86295698-T-C

45392888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86295711-G-A

http://identifiers.org/hco/2/GRCh38#45392902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86295725-C-A

45393104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 86295912-G-A

45393123-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 86295931-C-G

45393123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 86295931-C-T

http://identifiers.org/hco/2/GRCh38#45393152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86295956-C-A

45393152-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86295956-C-G

45393152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86295956-C-T

http://identifiers.org/hco/2/GRCh38#45393218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86296008-C-A

45393230-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86296020-G-C

45393230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86296020-G-T

45393240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86296029-T-C

45393717-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86296175-G-C

45393944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86296381-C-T

45393985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86296414-C-T

45394100-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86296583-T-A

45394108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86296591-A-G

45394240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86296698-T-C

45394284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86296733-T-C

45394690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86297117-C-T

45396046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86298164-T-C

45396047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86298165-A-G

45396356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86298429-G-T

45396394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86298468-A-G

45396815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86298885-T-C

45397451-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86299381-T-G

http://identifiers.org/hco/2/GRCh38#45397579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86299487-C-A

45397596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86299504-C-T

http://identifiers.org/hco/2/GRCh38#45397982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86299589-C-A

45397996-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86299603-T-A

45398015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86299622-T-C

45398405-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86299962-A-T

45398573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86300106-G-A

45398573-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86300106-G-C

45398696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86300221-C-T

45398903-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86300419-T-G

http://identifiers.org/hco/2/GRCh38#45399047-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86300550-A-C

45399252-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86300744-G-C

45399444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86300867-G-A

45399599-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86301011-T-G

45399694-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86301108-G-C

45399855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86301269-A-G

45399946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86301359-T-C

45399946-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86301359-T-G

45400201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86301617-G-A

45400201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86301617-G-T

45400450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86301834-G-T

http://identifiers.org/hco/2/GRCh38#45400572-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86301963-A-C

45400681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86302067-T-C

45400764-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86302138-T-A

45400764-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86302138-T-G

http://identifiers.org/hco/2/GRCh38#45400836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86302207-C-A

45400997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86302275-T-C

45401031-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86302303-C-G

45402166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86302802-C-T

45402308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86302920-T-C

45402312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86302924-C-T

45402379-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86302993-T-G

45402534-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86303136-G-T

45402657-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86303242-G-C

45402966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86303523-C-T

45403193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86303717-T-C

45403223-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86303736-G-C

45403273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86303778-T-C

45403306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86303803-T-C

45403716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86304167-A-G

http://identifiers.org/hco/2/GRCh38#45412988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86307635-C-A

45412988-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86307635-C-G

http://identifiers.org/hco/2/GRCh38#45413053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86307688-C-A

45413053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86307688-C-T

45413070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86307705-C-T

45413273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 86307881-C-T

45413315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86307927-C-T

45418298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86308790-G-A

45418298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86308790-G-T

45418299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86308791-G-A

45418299-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86308791-G-C

45418307-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86308799-G-C

45418323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86308815-G-A

45418323-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86308815-G-C

45418337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86308829-T-C

45418351-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86308842-A-T

http://identifiers.org/hco/2/GRCh38#45418579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86309096-C-A

45418581-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86309098-T-A

45418581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86309098-T-C

45418585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86309102-A-G

45418630-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86309147-T-A

45418630-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86309147-T-G

45419199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86310523-G-A

45419685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86311214-A-G

45419685-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86311214-A-T

45419934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86311424-G-A

45419934-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86311424-G-C

45419934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86311424-G-T

http://identifiers.org/hco/2/GRCh38#45419963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86311450-C-A

45419963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86311450-C-T

http://identifiers.org/hco/2/GRCh38#45420025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86311513-C-A

45420025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86311513-C-T

45424064-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86313068-T-A

45424263-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86313277-A-T

http://identifiers.org/hco/2/GRCh38#45424961-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86314363-A-C

45425191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86314636-G-A

45425357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86314806-T-C

45432529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86315271-T-C

45432529-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86315271-T-G

45432724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86315461-G-A

45432724-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86315461-G-C

45433028-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86315716-A-T

45433070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86315760-A-G

45433131-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86315811-C-G

45433171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86315836-T-C

45433171-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86315836-T-G

45433366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86315865-C-T

45433446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86315892-A-G

45433530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86315981-T-C

45433860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86316231-A-G

45433882-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86316253-G-C

45434026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86316399-A-G

http://identifiers.org/hco/2/GRCh38#45434394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86316715-C-A

45438033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86319553-T-C

45438049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86319564-A-G

45438049-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86319564-A-T

45438082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86319597-T-C

45438279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86319762-G-A

http://identifiers.org/hco/2/GRCh38#45438416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86319875-C-A

45438550-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86320012-C-G

http://identifiers.org/hco/2/GRCh38#45438689-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86320150-A-C

45438881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86320330-C-T

45439023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86320462-G-A

45439270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86320691-T-C

45439981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86321595-C-T

45440155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86321742-T-C

http://identifiers.org/hco/2/GRCh38#45440262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#86321844-C-A

45440488-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86322051-T-A

45440488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86322051-T-C

45441046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86322516-C-T

45441164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86322637-C-T

45441513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86322949-A-G

45441655-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86323089-T-G

45441656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86323090-T-C

45441748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86323182-G-A

45443637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86327783-C-T

http://identifiers.org/hco/2/GRCh38#45443754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86327898-C-A

45443754-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86327898-C-G

45444679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86331127-T-C

45444749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86331195-C-T

45445485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86332079-G-A

45445646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86332218-T-C

http://identifiers.org/hco/2/GRCh38#45445691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86332266-C-A

45445995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86332565-G-A

45446045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86332590-T-C

http://identifiers.org/hco/2/GRCh38#45446083-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86332628-A-C

45446115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86332659-G-T

45446768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86334614-T-C

45446808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86334656-T-C

45446901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86334743-T-C

45446901-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86334743-T-G

45450041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86336900-G-A

45450441-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86337243-C-G

45450467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86337269-T-C

45450492-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86337301-T-G

45450564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86337373-A-G

45450590-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86337404-T-A

http://identifiers.org/hco/2/GRCh38#45451243-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86338049-A-C

45451449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86338272-T-C

http://identifiers.org/hco/2/GRCh38#45451467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86338295-C-A

45451467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86338295-C-T

45451776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86338732-G-A

http://identifiers.org/hco/2/GRCh38#45452118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86339034-C-A

45452134-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86339048-T-A

45452162-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86339076-G-C

http://identifiers.org/hco/2/GRCh38#45452237-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86339157-A-C

http://identifiers.org/hco/2/GRCh38#45452465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86339366-C-A

45453416-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86340200-T-G

45453417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86340201-A-G

45453512-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86340293-C-G

45453553-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86340338-T-A

45453553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86340338-T-C

45453553-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86340338-T-G

45453760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86340547-A-G

45454273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86341020-G-A

45454273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86341020-G-T

45454279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86341026-T-C

45454329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86341074-T-C

45454353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86341098-C-T

45454884-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86341599-C-G

45455057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86341717-C-T

45455068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86341728-T-C

http://identifiers.org/hco/2/GRCh38#45455106-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86341772-A-C

45455136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86341803-G-T

45455167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86341834-T-C

45455227-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86341868-G-C

45455272-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86341909-T-G

45455363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86341952-G-A

45455369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86341958-T-C

45455419-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86341993-C-G

45455801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86342323-T-C

45455885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86342413-T-C

45456001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86342528-A-G

45456122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86342645-A-G

45456579-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86343346-G-C

45456713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86343494-G-A

45457692-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86344428-C-G

45457933-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86344645-T-A

45458156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86344886-A-G

45458231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86344935-A-G

45458443-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86345095-T-G

45458508-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86345160-T-A

45458508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86345160-T-C

45458804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86345475-C-T

45459122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86345790-C-T

http://identifiers.org/hco/2/GRCh38#45459155-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86345827-A-C

45459359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86346005-T-C

45459364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86346010-A-G

45459404-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86346045-G-C

45459820-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86346435-C-G

45459978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86346594-G-T

http://identifiers.org/hco/2/GRCh38#45460211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86346789-C-A

45460217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86346795-G-A

45460554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86347094-C-T

45460605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86347143-G-T

45460698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86347224-T-C

45460782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86347301-T-C

45460794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86347313-T-C

http://identifiers.org/hco/2/GRCh38#45460987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86347477-C-A

45460987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86347477-C-T

45461238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86347527-T-C

45461275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86347563-C-T

http://identifiers.org/hco/2/GRCh38#45461467-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86347778-A-C

45461467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86347778-A-G

45461535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86347848-C-T

45461645-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86347954-C-G

45461684-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86347969-G-C

45461740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86348016-T-C

45462083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86348332-T-C

45462251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86348504-C-T

45462412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86348657-T-C

http://identifiers.org/hco/2/GRCh38#45462667-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86348798-A-C

45462930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86348918-G-A

45462930-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86348918-G-C

45463078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86349063-A-G

45463148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86349132-T-C

45463180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86349169-T-C

45463276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86349262-T-C

45463305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86349290-T-C

45463379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86349357-C-T

45463404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86349381-T-C

45463471-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86349449-G-C

45463803-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86349868-C-G

45463873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86349922-A-G

45463969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86350009-A-G

http://identifiers.org/hco/2/GRCh38#45464852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86351386-C-A

45464852-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86351386-C-G

45464940-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86351480-T-A

45466953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86352656-T-C

45466999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86352707-T-C

45467742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86353340-T-C

45467742-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86353340-T-G

45467801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86353374-T-C

45467815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86353390-T-C

45467990-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86353534-C-G

http://identifiers.org/hco/2/GRCh38#45468030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86353552-C-A

45468077-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86353588-T-A

45468145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86353660-T-C

45469172-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86354073-T-A

45469202-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86354104-T-G

45469234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86354128-A-G

45469716-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86354557-T-A

45469716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86354557-T-C

45470098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86355241-A-G

45470103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86355246-T-C

45470169-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86355318-C-G

45470454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86355575-T-C

45471191-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86356287-C-G

45471283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86356368-G-A

45471350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86356431-T-C

45471454-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86356498-G-C

45471557-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86356546-T-G

45471596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86356585-G-A

45476272-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86357415-G-C

45476373-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86357507-A-T

45476781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86358326-T-C

45476849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86358389-T-C

45476894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86358418-G-T

http://identifiers.org/hco/2/GRCh38#45476915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86358439-C-A

45476915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86358439-C-T

45476926-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86358450-T-A

45476926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86358450-T-C

45477053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 86358574-T-C

45477104-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86358626-T-A

45477104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86358626-T-C

45477121-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86358643-C-G

45477504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86359209-C-T

45483557-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86360536-C-G

45483645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86360616-G-A

45483810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86361364-T-C

45484008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86361616-T-C

45484013-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86361625-T-A

45484013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86361625-T-C

45484087-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86361719-A-T

45484100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86361732-C-T

45484259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86361846-C-T

45484465-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86361999-C-G

45484465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86361999-C-T

45484839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86362352-G-A

45484866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86362379-C-T

45484988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86362509-T-C

45485563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86362815-A-G

45486063-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86363751-G-C

http://identifiers.org/hco/2/GRCh38#45486217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86363885-C-A

45486217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86363885-C-T

45487012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86364262-G-A

45487012-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86364262-G-C

45487084-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86364328-G-C

45487106-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86364350-A-T

45487107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86364351-A-G

http://identifiers.org/hco/2/GRCh38#45488090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86364959-C-A

45488090-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86364959-C-G

45488090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86364959-C-T

http://identifiers.org/hco/2/GRCh38#45488117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86364982-C-A

45488117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86364982-C-T

http://identifiers.org/hco/2/GRCh38#45488120-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86364985-A-C

45488154-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86365019-T-G

45488178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86365043-G-T

http://identifiers.org/hco/2/GRCh38#45488184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86365049-C-A

45488184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86365049-C-T

45488186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86365051-T-C

45488188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86365053-C-T

45488205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86365071-A-G

45488395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86365258-T-C

45488411-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86365272-T-A

45488417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86365278-G-A

45488417-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86365278-G-C

45488417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86365278-G-T

http://identifiers.org/hco/2/GRCh38#45488440-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86365306-A-C

45488442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86365308-T-C

45488442-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86365308-T-G

45488465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86365328-A-G

http://identifiers.org/hco/2/GRCh38#45488857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86365652-C-A

45488884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86365675-G-T

45488911-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86365704-G-C

http://identifiers.org/hco/2/GRCh38#45488971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86365746-C-A

45488971-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86365746-C-G

45489014-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86365787-C-G

45489023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86365791-T-C

45489025-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86365793-T-G

http://identifiers.org/hco/2/GRCh38#45489179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86365922-C-A

45489321-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86366061-T-A

45489768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86366559-T-C

45489771-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86366562-C-G

45489865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86366651-T-C

http://identifiers.org/hco/2/GRCh38#45489884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86366656-C-A

45490020-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86366782-T-A

45490020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86366782-T-C

45490127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86366887-T-C

45490285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86367250-G-A

45490321-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86367286-G-C

45490360-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86367322-T-G

45490519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86367459-T-C

http://identifiers.org/hco/2/GRCh38#45490615-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86367567-A-C

45490820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86367782-C-T

45490881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86367840-C-T

45491137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86368061-T-C

45491180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86368103-C-T

45491227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86368149-A-G

45491227-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86368149-A-T

45491617-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86368559-G-C

45491635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86368577-C-T

45492235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86368915-T-C

45492293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86368961-C-T

45492335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86369000-A-G

45492427-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86369080-T-G

http://identifiers.org/hco/2/GRCh38#45492782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86369130-C-A

45492782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86369130-C-T

45492844-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86369178-T-A

45492844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86369178-T-C

45493691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86369953-G-A

45493691-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86369953-G-C

45494348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86370554-G-T

45494556-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86370753-C-G

45494556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86370753-C-T

45494831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86371048-C-T

45494836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86371053-A-G

45494967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86371173-C-T

45495125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86371324-G-T

http://identifiers.org/hco/2/GRCh38#45495208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86371405-C-A

45495220-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86371417-G-C

45495220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86371417-G-T

http://identifiers.org/hco/2/GRCh38#45495235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86371432-C-A

45495258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86371455-G-A

45495304-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86371499-C-G

45496611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86373673-G-T

45496622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86373686-G-A

45496786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86373823-A-G

45496846-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86373892-G-C

http://identifiers.org/hco/2/GRCh38#45496857-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86373903-A-C

http://identifiers.org/hco/2/GRCh38#45496934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86373977-C-A

45496961-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86374014-C-G

45496975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86374026-T-C

45497088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86374125-G-A

45497298-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86374336-T-G

45497403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86374441-G-A

45497403-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86374441-G-C

45497410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86374448-A-G

http://identifiers.org/hco/2/GRCh38#45497417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86374455-C-A

45497537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86374577-A-G

http://identifiers.org/hco/2/GRCh38#45503188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86376814-C-A

45503188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86376814-C-T

45503227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86376855-G-A

45503325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86376922-G-A

45503334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86376931-A-G

45503507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86377084-T-C

45503542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86377154-T-C

45503629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86377238-G-A

45503629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86377238-G-T

45503630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86377239-G-A

45503663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86377264-T-C

http://identifiers.org/hco/2/GRCh38#45503671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86377272-C-A

45503685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86377286-G-A

45503744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86377317-G-A

45503744-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86377317-G-C

45503823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86377391-A-G

45503863-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86377430-A-T

45503988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86377553-T-C

http://identifiers.org/hco/2/GRCh38#45504018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86377575-C-A

45504088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86377646-A-G

45504205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86377727-C-T

45504224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86377744-T-C

45504558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86378045-T-C

45504719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86378228-G-A

45504753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86378258-G-A

45504768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86378272-C-T

45504891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86378388-G-T

45505020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86378516-T-C

45505020-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86378516-T-G

http://identifiers.org/hco/2/GRCh38#45505142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86378629-C-A

http://identifiers.org/hco/2/GRCh38#45505146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86378633-C-A

http://identifiers.org/hco/2/GRCh38#45505189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86378678-C-A

45505515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86378964-A-G

45505516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86378965-T-C

45505609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86379055-C-T

45505627-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86379073-G-C

45505635-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86379081-G-C

45505635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86379081-G-T

45505824-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86379398-T-G

45505892-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86379447-C-G

45506294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86379755-C-T

45506445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86379881-G-A

45506445-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86379881-G-C

45506674-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86380110-A-T

45506707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86380152-T-C

http://identifiers.org/hco/2/GRCh38#45506773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86380449-C-A

45506773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86380449-C-T

45506919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86380650-G-A

45507005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86380736-G-A

45507005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86380736-G-T

45507021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86380752-A-G

45507233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86380964-T-C

45507242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86380979-G-A

45507244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86380981-G-A

45507409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86381139-T-C

45507412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86381142-G-A

http://identifiers.org/hco/2/GRCh38#45507428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86381163-C-A

45507897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86381282-T-C

45507899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86381284-C-T

45507923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86381309-A-G

45508339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86381643-C-T

45508375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86381656-A-G

45509109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86382703-T-C

45510142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86382916-G-T

45510406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86383193-T-C

45510634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86383410-A-G

45510756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86383532-T-C

45511290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86384053-C-T

45511481-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86384219-A-T

45511605-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86384344-G-C

45511932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86384660-T-C

45512010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86384735-G-A

45512105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86384809-G-A

45512105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86384809-G-T

45512236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86384908-G-T

45512341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86385001-T-C

45512393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86385054-C-T

45512535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86385193-C-T

45512632-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86385284-C-G

45512731-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86385399-G-C

45512885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86385559-G-A

45512886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86385560-A-G

45513149-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86385747-C-G

45513395-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86385984-T-A

45513438-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86386017-T-A

45513899-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86386324-G-C

45513900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86386325-C-T

45513974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86386376-T-C

45514022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86386403-A-G

45514025-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86386406-T-A

45514078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86386446-T-C

http://identifiers.org/hco/2/GRCh38#45514378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86386956-C-A

45514421-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86387001-A-T

http://identifiers.org/hco/2/GRCh38#45514525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86387124-C-A

45514525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86387124-C-T

45514542-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86387141-A-T

45514839-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86387420-C-G

45515138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86387684-T-C

45515190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86387736-C-T

45515220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86387760-G-A

45515220-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86387760-G-C

45515276-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86387838-T-G

45515311-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86387872-G-C

45515430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86387986-C-T

45515535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86388101-A-G

45515648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86388211-C-T

45516259-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86388851-A-T

45516538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86389082-A-G

45516622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86389168-T-C

45516888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86389435-G-A

45517006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86389558-A-G

45517044-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86389594-A-T

45517429-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86389962-G-C

http://identifiers.org/hco/2/GRCh38#45517435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86389968-C-A

45517435-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86389968-C-G

45517598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86390131-C-T

45518103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86390306-G-A

45518537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86390901-T-C

45518567-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86390928-A-T

45518621-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86390978-C-G

45518695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86391051-T-C

45518695-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86391051-T-G

http://identifiers.org/hco/2/GRCh38#45518734-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86391089-A-C

45518734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86391089-A-G

45518921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86391257-G-A

45528846-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86393750-A-T

45528927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86393849-A-G

45529122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86394046-G-A

45529427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86394321-T-C

45529476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86394370-T-C

45529563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86394626-A-G

45529627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86394688-A-G

45529634-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86394695-G-C

45529651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86394712-C-T

http://identifiers.org/hco/2/GRCh38#45529661-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86394723-A-C

45529816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86394878-C-T

45530074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86395140-C-T

45530144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86395202-G-A

45530144-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86395202-G-C

45530256-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86395655-A-T

45530816-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86396123-C-G

45531044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86396219-C-T

45531181-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86396352-G-C

45531212-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86396382-T-A

45531273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86396439-T-C

45531328-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86396510-G-C

45531364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86396679-C-T

45531538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86396937-C-T

45531541-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86396940-C-G

45531734-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86397122-C-G

http://identifiers.org/hco/2/GRCh38#45531875-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86397231-A-C

45531875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86397231-A-G

45532022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86397374-A-G

45532028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86397382-A-G

45532041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86397396-C-T

45532106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86397457-C-T

45532107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86397458-T-C

45532119-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86397469-T-A

45532123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86397473-T-C

45532197-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86397546-C-G

http://identifiers.org/hco/2/GRCh38#45532396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86397746-C-A

45532396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86397746-C-T

45532397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86397747-G-A

45532397-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86397747-G-C

http://identifiers.org/hco/2/GRCh38#45532512-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86397862-A-C

45532743-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86398097-G-C

45532782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86398137-G-A

45532782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86398137-G-T

45532841-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86398185-G-C

45532886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86398230-G-A

45532991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86398332-T-C

45533080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86398428-G-A

45533232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86398564-A-G

45533361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86398673-A-G

45533394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86398709-T-C

45533490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86398799-T-C

45533701-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86399014-T-G

45534129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86399448-G-A

45534582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86399844-A-G

45534706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86400011-G-A

45534713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86400018-T-C

45534764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86400065-A-G

45535485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86400648-T-C

45535653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86400808-A-G

45535700-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86400859-T-G

45535743-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86400903-A-T

45535792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86400954-G-A

45536356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86401506-T-C

45536765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86401898-T-C

45536771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86401904-G-A

45536935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86402160-C-T

45537155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86402434-A-G

45537230-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86402499-T-G

45537382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86402638-C-T

45537403-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86402655-T-G

45543239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86404692-G-A

45543239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86404692-G-T

45543260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86404713-G-A

45543471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86404908-A-G

45543474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86404919-T-C

http://identifiers.org/hco/2/GRCh38#45546606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86405815-C-A

45546788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 86405996-A-G

45546886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86406096-T-C

45546948-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86406155-T-A

45547349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86406466-C-T

45547400-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86406515-A-T

45547434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86406546-T-C

45547469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86406581-A-G

45547482-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86406594-T-A

45547482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86406594-T-C

45547485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86406597-G-A

45548060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86407326-T-C

45548137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86407381-A-G

45548252-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86407570-A-T

45548325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86407641-G-T

45548472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86407768-T-C

45548477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86407773-A-G

45548661-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86407919-T-A

45548661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86407919-T-C

http://identifiers.org/hco/2/GRCh38#45548696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86407951-C-A

http://identifiers.org/hco/2/GRCh38#45548730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86407985-C-A

http://identifiers.org/hco/2/GRCh38#45548866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86408116-C-A

45548866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86408116-C-T

45548922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86408174-A-G

http://identifiers.org/hco/2/GRCh38#45548971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86408203-C-A

45548997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86408211-G-A

http://identifiers.org/hco/2/GRCh38#45549287-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86408460-A-C

45549437-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86408588-C-G

45549541-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86408690-T-A

45549669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86408758-G-A

45549770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86408834-G-A

45549803-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86408865-C-G

45549807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86408869-G-A

45549846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86408892-G-A

45549846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86408892-G-T

45549848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86408894-G-A

45549985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86408969-A-G

45550013-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86408991-T-A

http://identifiers.org/hco/2/GRCh38#45550465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86409390-C-A

45550611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86409553-A-G

http://identifiers.org/hco/2/GRCh38#45550739-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86409688-A-C

45550792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86409746-T-C

45550894-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86409831-C-G

45550928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86409898-T-C

http://identifiers.org/hco/2/GRCh38#45550989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86409952-C-A

45550989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86409952-C-T

http://identifiers.org/hco/2/GRCh38#45550994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86409957-C-A

45550999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86409994-G-A

45550999-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86409994-G-C

45550999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86409994-G-T

45551023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86410086-G-A

45551023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86410086-G-T

45551062-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86410211-G-C

45551387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86410552-T-C

45551459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86410600-T-C

45551503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86410643-A-G

45551542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86410676-A-G

http://identifiers.org/hco/2/GRCh38#45552257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86414998-C-A

45552257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86414998-C-T

45552322-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86415055-A-T

45552349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86415081-G-A

45552783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86415797-G-A

45552866-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86415868-C-G

http://identifiers.org/hco/2/GRCh38#45552870-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86415872-A-C

45552885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86415879-A-G

45552885-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86415879-A-T

45553128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86416105-C-T

45553296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86416258-T-C

45553560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86416601-T-C

45553560-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86416601-T-G

http://identifiers.org/hco/2/GRCh38#45553596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86416633-C-A

45553596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86416633-C-T

45553652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 86416684-A-G

45553819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86416838-G-A

45553819-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86416838-G-C

45553819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86416838-G-T

45555992-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86418321-C-G

45556113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86418415-T-C

45556176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86418478-C-T

45557210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86419279-G-A

45557211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86419280-T-C

45557230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86419299-G-A

45557238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86419307-C-T

45557512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86419587-C-T

45557539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86419614-G-A

45557901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86419950-A-G

45557909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86419958-T-C

45558063-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86420417-T-A

45558063-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86420417-T-G

45558344-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86420582-C-G

45558344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86420582-C-T

45558345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86420583-G-A

45558464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86420681-A-G

45558561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86420761-T-C

45558643-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86420838-T-A

45558665-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86420861-A-T

45562650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86422618-G-T

http://identifiers.org/hco/2/GRCh38#45562670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86422638-C-A

45562670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 86422638-C-T

45562733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 86422701-T-C

45562751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 86422719-C-T

45569673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86426262-C-T

45572699-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86426891-T-G

45572818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86427025-T-C

http://identifiers.org/hco/2/GRCh38#45572835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86427042-C-A

45573067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86427246-G-A

45573067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86427246-G-T

45573136-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86427299-A-T

45573160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86427311-T-C

45573160-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86427311-T-G

45573318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: synonymous variant
orthologous variants: 86427453-G-T

http://identifiers.org/hco/2/GRCh38#45573333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86427468-C-A

http://identifiers.org/hco/2/GRCh38#45573468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86427602-C-A

45573468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86427602-C-T

45574500-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86427954-G-C

45574500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86427954-G-T

45574590-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86428041-T-A

45575041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86428471-C-T

45575107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86428530-G-A

45575107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86428530-G-T

45575319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86428720-G-A

45575324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86428726-T-C

45575420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86428860-T-C

45575516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86428962-T-C

45575629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86429070-T-C

45575637-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86429078-G-C

45576511-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86429124-T-G

45576526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86429137-T-C

45576774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86429359-A-G

45576862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86429441-T-C

45576980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86429534-G-A

45576980-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86429534-G-C

45577079-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86429596-C-G

45577267-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86429772-A-T

45577452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86429928-A-G

45577496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86429972-C-T

45577550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86430026-T-C

45577666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86430130-A-G

http://identifiers.org/hco/2/GRCh38#45577670-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86430134-A-C

45577711-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86430176-T-A

45577711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86430176-T-C

45577721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86430186-G-A

45577810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86430286-T-C

http://identifiers.org/hco/2/GRCh38#45578062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86431782-C-A

45578509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, undefined
orthologous variants: 86432322-C-T

45578604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86432400-C-T

http://identifiers.org/hco/2/GRCh38#45578636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#86432432-C-A

45578636-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, undefined
orthologous variants: 86432432-C-G

45578664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86432460-T-C

45578741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86432531-A-G

45579386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86433102-G-T

http://identifiers.org/hco/2/GRCh38#45579884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86433548-C-A

45579884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: missense variant
orthologous variants: 86433548-C-T

45579921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: synonymous variant
orthologous variants: 86433585-T-C

http://identifiers.org/hco/2/GRCh38#45580141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86433804-C-A

45580187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86433833-T-C

45580332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86433988-T-C

45580337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86433993-C-T

45580352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86434008-T-C

45581472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86434919-G-A

45581472-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86434919-G-C

http://identifiers.org/hco/2/GRCh38#45581590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86435044-C-A

45581590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86435044-C-T

45581640-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86435096-C-G

45581640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86435096-C-T

45581696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: synonymous variant
orthologous variants: 86435147-G-A

45581696-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: missense variant
orthologous variants: 86435147-G-C

45582184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86435605-T-C

45582300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86435710-A-G

45582328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86435733-G-A

45582331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86435736-A-G

45582364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86435770-C-T

45582413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86435819-T-C

45582413-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86435819-T-G

45582441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86435845-G-A

45582472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86435868-C-T

45582545-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86435932-G-C

45582558-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86435945-G-C

45582696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86436083-T-C

45582857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86436217-T-C

45583122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86436487-G-A

45583122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86436487-G-T

45585019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86436886-G-A

45585048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86436914-G-T

45585083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86436959-G-A

45585200-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86437132-T-G

45585456-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86437360-A-T

45585478-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86437406-T-A

45585478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86437406-T-C

45585478-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86437406-T-G

45585512-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86437440-T-A

45585528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86437457-T-C

45585546-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86437475-C-G

45585600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 86437534-T-C

45585718-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: synonymous variant
orthologous variants: 86437652-G-C

45585741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: missense variant
orthologous variants: 86437675-C-T

45587827-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86437979-A-T

45588094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86438202-C-T

http://identifiers.org/hco/2/GRCh38#45593222-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86439930-A-C

http://identifiers.org/hco/2/GRCh38#45593295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86440005-C-A

45593505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86440174-T-C

45593541-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86440209-A-T

45593714-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86440384-C-G

45593714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86440384-C-T

45593756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86440426-T-C

45593772-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86440444-C-G

http://identifiers.org/hco/2/GRCh38#45593812-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86440471-A-C

45593867-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86440526-G-C

45593909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86440567-G-T

45593950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86440598-A-G

45594156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86440785-T-C

http://identifiers.org/hco/2/GRCh38#45594206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86440829-C-A

45594500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86441095-T-C

45596587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86441425-G-A

45596643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86441476-T-C

45596724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86441539-T-C

45598065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86442122-G-T

45598120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86442167-T-C

http://identifiers.org/hco/2/GRCh38#45598566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86442772-C-A

45598655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86442864-T-C

45598656-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86442865-G-C

45598808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86442991-C-T

45599116-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86443269-G-C

45599195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86443348-T-C

45599195-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86443348-T-G

45599205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86443355-T-C

45599234-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86443389-G-C

45599376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86443530-C-T

45599392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86443549-C-T

http://identifiers.org/hco/2/GRCh38#45599423-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86443569-A-C

45599495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: missense variant
orthologous variants: 86443638-G-A

45599632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: synonymous variant
orthologous variants: 86443772-T-C

45599635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: synonymous variant
orthologous variants: 86443775-T-C

45599779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: synonymous variant
orthologous variants: 86443907-A-G

45599809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: synonymous variant
orthologous variants: 86443937-A-G

http://identifiers.org/hco/2/GRCh38#45599931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86444053-C-A

45599931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86444053-C-T

45599966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86444088-G-T

45599982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86444102-A-G

45600004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86444124-T-C

45600071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86444227-G-A

45600087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86444249-A-G

http://identifiers.org/hco/2/GRCh38#45600191-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86444403-A-C

45600228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86444441-G-A

45600620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86445146-C-T

45600652-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86445178-G-C

45600708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86445201-C-T

45600847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86445342-T-C

http://identifiers.org/hco/2/GRCh38#45601006-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86445483-A-C

45601219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86445823-G-A

45601391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86445998-G-A

45601435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86446032-G-A

45601560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86446140-A-G

45601589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86446172-A-G

45601780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86446367-G-A

45601780-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86446367-G-C

45601780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86446367-G-T

45601826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron variant
orthologous variants: 86446414-A-G

http://identifiers.org/hco/2/GRCh38#45601964-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86446558-A-C

45601972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 86446566-C-T

http://identifiers.org/hco/2/GRCh38#45602038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86446632-C-A

45602171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86446760-A-G

45602171-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86446760-A-T

45602176-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86446763-G-C

45602240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86446828-T-C

45602263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86446845-G-A

45602796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86447315-T-C

45602814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86447329-T-C

45602878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86447385-G-A

45603056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86447556-G-T

45604178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86448337-A-G

45604287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86448453-T-C

45604757-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86449031-C-G

45605096-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86449388-T-G

45605218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86449645-G-A

45605218-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86449645-G-C

45605218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86449645-G-T

http://identifiers.org/hco/2/GRCh38#45605254-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86449681-A-C

http://identifiers.org/hco/2/GRCh38#45605302-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86449732-A-C

45605419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 86449845-G-A

45605419-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 86449845-G-C

45605447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 86449879-A-G

45605454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86449886-G-A

45605454-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86449886-G-C

45605510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86449942-T-C

45605510-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86449942-T-G

45605516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86449944-A-G

45605971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86450089-T-C

45606147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86450249-T-C

45606467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86450259-T-C

45606661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86450429-G-A

45606697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86450464-T-C

45606707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86450474-C-T

45606746-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86450511-T-G

45606894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86450594-C-T

http://identifiers.org/hco/2/GRCh38#45607230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86450970-C-A

45607371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86451108-C-T

45607469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86451196-A-G

45607593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86451291-A-G

45610379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86451869-A-G

45610481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86452004-G-A

45610481-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86452004-G-C

http://identifiers.org/hco/2/GRCh38#45610540-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#86452063-A-C

45610577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86452108-A-G

45610948-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86452314-T-A

45610948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86452314-T-C

45610948-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86452314-T-G

45610963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86452329-A-G

45611115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86452466-A-G

45611115-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86452466-A-T

45611141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86452489-G-A

45611141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86452489-G-T

http://identifiers.org/hco/2/GRCh38#45611184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#86452513-C-A

http://identifiers.org/hco/2/GRCh38#45611203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#86452533-C-A

45611203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86452533-C-T

45611312-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 86452635-G-C

45611312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 86452635-G-T

45611338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 86452652-C-T

45611409-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 86452720-G-C

http://identifiers.org/hco/2/GRCh38#45611423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#86452734-C-A

45611423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25521
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 86452734-C-T