55256109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113106514-G-A

55256109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113106514-G-T

55256208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113106000-A-G

55256209-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113105999-G-C

55256209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113105999-G-T

55256356-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113105851-A-T

55256363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113105844-T-C

55256416-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113105791-A-T

http://identifiers.org/hco/5/GRCh38#55256553-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113105655-A-C

55256553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113105655-A-G

55256553-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113105655-A-T

http://identifiers.org/hco/5/GRCh38#55256565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113105641-C-A

55256832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113105278-A-G

55257044-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113105020-C-G

55257044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113105020-C-T

http://identifiers.org/hco/5/GRCh38#55257063-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113105001-A-C

55257197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113104878-A-G

55257212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113104863-A-G

55257690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113104539-T-C

55257787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113104422-T-C

55257808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113104382-A-G

55257809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113104381-T-C

55257846-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113104337-G-C

55258113-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113104088-G-C

55258364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113103840-C-T

55258491-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113103734-T-G

55258513-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113103713-T-A

55258563-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113103668-G-C

55259782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113103246-A-G

55259812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113103205-G-T

55260027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113102990-T-C

55260027-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113102990-T-G

55260068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113102948-A-G

55260494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113102671-G-A

55260716-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113102404-G-C

55260882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113102268-T-C

55260947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113102216-G-A

55261277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113101961-T-C

http://identifiers.org/hco/5/GRCh38#55261317-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113101921-A-C

55261317-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113101921-A-T

55261513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113101733-A-G

55261548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113101699-G-A

55261548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113101699-G-T

55261549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113101698-G-A

55261549-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113101698-G-C

55261569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113101675-A-G

55261578-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113101666-T-A

55262355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113101535-T-C

55262504-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113101383-A-T

55262607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113101294-G-A

55262637-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113101265-T-A

55262637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113101265-T-C

55262642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 113101260-T-C

55262724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113101178-C-T

55262880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113101031-G-A

55262937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 113100974-A-G

55262946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113100968-T-C

http://identifiers.org/hco/5/GRCh38#55263016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113100903-C-A

55263016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113100903-C-T

http://identifiers.org/hco/5/GRCh38#55263037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113100882-C-A

55263037-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113100882-C-G

55263074-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113100847-T-A

55263074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113100847-T-C

55263075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113100846-A-G

55263075-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113100846-A-T

55263652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113100724-T-C

55267119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113099907-G-A

55267119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113099907-G-T

55267128-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113099898-T-A

55267128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113099898-T-C

55267128-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113099898-T-G

55267303-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113099730-G-C

55267303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113099730-G-T

55267345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113099687-G-A

http://identifiers.org/hco/5/GRCh38#55267370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113099662-C-A

55267377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113099655-A-G

55267536-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113099551-T-A

http://identifiers.org/hco/5/GRCh38#55267609-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113099479-A-C

55267609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113099479-A-G

55267620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113099471-A-G

55267658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113099430-A-G

55267818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113099270-G-A

55267818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113099270-G-T

55267832-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113099256-A-T

55267833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113099255-A-G

55267864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113099237-G-T

55267896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113099207-A-G

55267896-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113099207-A-T

http://identifiers.org/hco/5/GRCh38#55267910-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113099197-A-C

55267910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113099197-A-G

55267931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113099177-T-C

55267931-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113099177-T-G

55268138-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113099045-T-G

http://identifiers.org/hco/5/GRCh38#55268217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113098967-C-A

55268711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113098379-A-G

55269268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113097957-A-G

55269268-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113097957-A-T

http://identifiers.org/hco/5/GRCh38#55269276-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113097949-A-C

55269276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113097949-A-G

55269276-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113097949-A-T

55269303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113097922-A-G

55269303-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113097922-A-T

55269341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113097886-T-C

55269378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113097847-T-C

55269519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113097711-T-C

55269665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113097573-G-A

55269665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113097573-G-T

55269667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113097571-A-G

55269784-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113097475-T-A

55269784-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113097475-T-G

55269822-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113097455-A-T

55270064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113097276-G-T

55270187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113097160-T-C

55270376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113096966-G-A

55270376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113096966-G-T

55270428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113096914-A-G

55270517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113096837-T-C

55270559-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113096796-T-G

55270563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113096792-A-G

55270566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113096789-G-A

55270749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113096608-A-G

55270977-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113096245-G-C

55270986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113096237-C-T

55271149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113096091-T-C

55271182-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113096062-G-C

55271851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113095726-T-C

55271942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113095639-T-C

55272099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113095521-G-T

55272113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 113095507-A-G

55272138-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113095482-G-C

55272191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113095429-A-G

55272227-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113095394-C-G

http://identifiers.org/hco/5/GRCh38#55273153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113093091-C-A

55273153-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113093091-C-G

55273153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113093091-C-T

55273172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113093072-A-G

55273172-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113093072-A-T

55273235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113093047-G-A

55273235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113093047-G-T

55273314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 113092977-A-G

http://identifiers.org/hco/5/GRCh38#55273392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113092899-C-A

55273392-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113092899-C-G

http://identifiers.org/hco/5/GRCh38#55273413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113092878-C-A

http://identifiers.org/hco/5/GRCh38#55273442-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113092849-A-C

55273442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113092849-A-G

55273491-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113092802-A-T

55273527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113092768-A-G

http://identifiers.org/hco/5/GRCh38#55273536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113092759-C-A

55273571-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113092694-T-G

http://identifiers.org/hco/5/GRCh38#55273646-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113092571-A-C

55273709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113092508-G-A

http://identifiers.org/hco/5/GRCh38#55274496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113092146-C-A

http://identifiers.org/hco/5/GRCh38#55274497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113092145-C-A

55274497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113092145-C-T

55274523-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113092119-A-T

55274530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113092114-T-C

http://identifiers.org/hco/5/GRCh38#55274560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113092097-C-A

55274560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113092097-C-T

55274716-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113091947-A-T

55274752-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113091913-C-G

55274752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113091913-C-T

http://identifiers.org/hco/5/GRCh38#55274927-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113091763-A-C

55274927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 113091763-A-G

55275071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113091523-G-A

55275077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113091517-A-G

55275130-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113091445-T-A

55275130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113091445-T-C

55275168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113091411-A-G

55275347-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113091103-G-C

55275348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113091102-T-C

55275410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113091036-G-A

55275410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113091036-G-T

http://identifiers.org/hco/5/GRCh38#55275827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113090725-C-A

55276076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113090508-A-G

http://identifiers.org/hco/5/GRCh38#55276148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113090439-C-A

55276148-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113090439-C-G

55276148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113090439-C-T

55276149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113090438-C-T

55276206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113090400-T-C

55276233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113090377-T-C

55276239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113090373-A-G

55276247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113090365-C-T

55276257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113090355-T-C

55276257-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113090355-T-G

55276324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113090288-T-C

55276363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113090249-A-G

55276418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113090197-A-G

55276420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113090195-G-A

55276420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113090195-G-T

55276429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113090191-A-G

http://identifiers.org/hco/5/GRCh38#55276451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113090171-C-A

55276451-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113090171-C-G

55276451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113090171-C-T

55276456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113090166-A-G

55276535-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113090095-T-G

55276550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113090080-G-A

55276550-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113090080-G-C

55276550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113090080-G-T

55276565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113090065-T-C

55276571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113090059-T-C

http://identifiers.org/hco/5/GRCh38#55276989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113089665-C-A

55277087-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113089574-C-G

55277158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113089459-T-C

55277296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113089325-G-A

55277296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113089325-G-T

55277343-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113089289-T-A

55277343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113089289-T-C

http://identifiers.org/hco/5/GRCh38#55277358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113089273-C-A

55277358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113089273-C-T

http://identifiers.org/hco/5/GRCh38#55277359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113089272-C-A

55277391-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113089244-T-A

55277396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113089239-T-C

http://identifiers.org/hco/5/GRCh38#55277398-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113089237-A-C

55277398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113089237-A-G

55277399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113089236-G-A

55277399-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113089236-G-C

55277406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113089229-T-C

55277501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113089136-T-C

55278147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113088812-G-T

55278157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113088802-G-A

55278323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113088661-A-G

55278353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113088632-T-C

55278356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113088629-C-T

55278384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113088596-T-C

55278466-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113088522-G-C

55278476-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113088510-T-A

55278476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113088510-T-C

55278496-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113088495-C-G

55278601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113088406-A-G

55278641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113088366-T-C

55278795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113088064-T-C

55278930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113087926-G-T

55278952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113087901-T-C

55278996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113087852-G-A

55279043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113087815-T-C

55279209-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113087649-T-G

55279337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113087567-G-A

55279396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113087523-G-A

55281199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113085061-A-G

http://identifiers.org/hco/5/GRCh38#55281327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113084934-C-A

55281327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113084934-C-T

55281355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113084904-C-T

55281376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113084883-T-C

http://identifiers.org/hco/5/GRCh38#55281427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113084832-C-A

http://identifiers.org/hco/5/GRCh38#55281572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113084701-C-A

55281590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113084684-A-G

55281718-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113084449-C-G

55281751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113084416-A-G

55281752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113084415-T-C

http://identifiers.org/hco/5/GRCh38#55282903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113084038-C-A

55282914-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113084027-G-C

55282914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113084027-G-T

55283141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113083966-A-G

55283152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 113083955-G-A

55283152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 113083955-G-T

http://identifiers.org/hco/5/GRCh38#55283174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113083937-C-A

55283174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113083937-C-T

55283182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113083929-T-C

55283182-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113083929-T-G

55283210-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113083899-C-G

55283408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113083701-C-T

55283431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 113083678-G-A

55283431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113083678-G-T

55283432-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113083677-T-G

55283654-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113083455-T-A

55283767-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 113083339-C-G

55283868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113083238-T-C

55283870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113083236-G-A

55283870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113083236-G-T

55284145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113083062-T-C

55284188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113083036-C-T

55284234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113083024-T-C

http://identifiers.org/hco/5/GRCh38#55284311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113082932-C-A

55284539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113082713-C-T

55284599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113082264-G-A

55285387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113081631-A-G

55285387-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113081631-A-T

http://identifiers.org/hco/5/GRCh38#55285491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113081521-C-A

55285491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113081521-C-T

55285632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113081241-T-C

55285663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113081210-G-A

55285913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113080963-T-C

55286836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113080145-G-A

55286836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113080145-G-T

55286848-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113080134-T-A

http://identifiers.org/hco/5/GRCh38#55287536-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113079601-A-C

55288687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113079549-A-G

55288691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113079545-C-T

55288701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113079535-T-C

55288900-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113079362-C-G

55288956-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113079308-C-G

55289281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113078352-T-C

55289313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 113078320-A-G

http://identifiers.org/hco/5/GRCh38#55289342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113078291-C-A

55289400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 113078233-T-C

55289404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113078229-G-A

55289404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113078229-G-T

55289415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 113078218-T-C

http://identifiers.org/hco/5/GRCh38#55289570-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113078131-A-C

55289570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113078131-A-G

55289603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113078097-T-C

55289662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113078037-T-C

55289743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113077968-G-T

55290078-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113077127-T-A

55290078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113077127-T-C

55290085-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113077120-A-T

55290099-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113077105-C-G

http://identifiers.org/hco/5/GRCh38#55290100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113077104-C-A

55290100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113077104-C-T

55290109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113077095-A-G

55290120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113077084-A-G

http://identifiers.org/hco/5/GRCh38#55290126-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113077078-A-C

55290276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 113076973-T-C

55290375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113076877-A-G

55290467-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113076798-T-A

http://identifiers.org/hco/5/GRCh38#55290469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113076796-C-A

55292764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113074753-C-T

55293648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113072493-A-G

55293730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113072410-G-A

55293890-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113072256-T-A

http://identifiers.org/hco/5/GRCh38#55293908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113072241-C-A

55293990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113072156-A-G

55294018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 113072128-G-A

55294018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 113072128-G-T

55294027-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113072119-T-A

55294078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113072068-T-C

55294087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113072059-G-A

55294087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113072059-G-T

55294111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113072035-A-G

55294127-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113072019-T-A

55294127-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113072019-T-G

55294158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113071988-A-G

55294164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113071982-T-C

55294183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113071964-A-G

http://identifiers.org/hco/5/GRCh38#55294188-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113071957-A-C

http://identifiers.org/hco/5/GRCh38#55294230-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113071915-A-C

55294623-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113071637-C-G

55294623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113071637-C-T

55294658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113071603-A-G

55294660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113071593-C-T

55294696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113071532-A-G

55294734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113071493-G-T

55294756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113071470-T-C

55294757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113071469-T-C

55294760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113071466-A-G

http://identifiers.org/hco/5/GRCh38#55294805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113071412-C-A

55294805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113071412-C-T

http://identifiers.org/hco/5/GRCh38#55294843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113071372-C-A

55294876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113071339-G-A

55294887-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113071328-A-T

55294989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113070907-G-A

55294989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113070907-G-T

55295032-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113070850-A-T

http://identifiers.org/hco/5/GRCh38#55295123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113070754-C-A

55295379-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 113069761-C-G

55295414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113069726-T-C

55295592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113069556-T-C

55296121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113069180-G-A

55296121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113069180-G-T

55296122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113069179-A-G

55296395-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113068996-T-G

55296396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113068995-T-C

55296396-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113068995-T-G

http://identifiers.org/hco/5/GRCh38#55296398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113068993-C-A

55296401-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113068990-T-A

55296401-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113068990-T-G

http://identifiers.org/hco/5/GRCh38#55296416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113068970-C-A

55296416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113068970-C-T

http://identifiers.org/hco/5/GRCh38#55296462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113068928-C-A

55296721-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113068104-G-C

55296844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113067999-T-C

55296989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113067851-T-C

55297047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113067797-T-C

55297147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113067722-T-C

55297158-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113067711-T-A

55297189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113067680-C-T

http://identifiers.org/hco/5/GRCh38#55297209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113067657-C-A

55297209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113067657-C-T

55297340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113067432-T-C

http://identifiers.org/hco/5/GRCh38#55297357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113067415-C-A

55297481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113067297-T-C

http://identifiers.org/hco/5/GRCh38#55297483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113067295-C-A

http://identifiers.org/hco/5/GRCh38#55297484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113067294-C-A

55297491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113067287-G-A

55297491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113067287-G-T

55297584-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113067206-T-A

55297772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113067023-A-G

55297806-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113066994-G-C

http://identifiers.org/hco/5/GRCh38#55297923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113066880-C-A

55297923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113066880-C-T

55298356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113066561-A-G

http://identifiers.org/hco/5/GRCh38#55298555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113066269-C-A

55298555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113066269-C-T

55298561-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113066263-T-A

55298561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113066263-T-C

55298571-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113066253-T-A

55298571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113066253-T-C

55298571-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113066253-T-G

55298595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113066228-A-G

55305969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113065991-T-C

55306076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113065888-C-T

55306292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113065494-T-C

55306397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113065418-A-G

55306404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113065411-C-T

55306526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113065292-G-A

55306959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113064916-T-C

http://identifiers.org/hco/5/GRCh38#55306966-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113064909-A-C

55307273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113064610-G-A

55307273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113064610-G-T

http://identifiers.org/hco/5/GRCh38#55307302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113064582-C-A

55307302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113064582-C-T

55307315-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113064571-C-G

55307328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113064560-C-T

55307408-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 113064484-T-A

55307408-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 113064484-T-G

55307647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 113064249-A-G

http://identifiers.org/hco/5/GRCh38#55307667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#113064229-C-A

55307667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15815
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 113064229-C-T