26576770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53959672-C-T

26576784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53959684-A-G

26576784-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53959684-A-T

http://identifiers.org/hco/4/GRCh38#26576844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53959731-C-A

26576867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53959752-G-T

26576892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53959777-G-A

http://identifiers.org/hco/4/GRCh38#26576905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53959790-C-A

26576905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53959790-C-T

26576938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53959818-G-A

26576938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53959818-G-T

26576979-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53959858-A-T

26577021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53959875-G-A

26577119-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53959962-T-A

26577382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53960531-G-A

26577382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53960531-G-T

26577397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53960547-C-T

26577433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53960583-G-T

26577460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53960608-C-T

26577480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53960626-G-A

26577614-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53960745-G-C

26577614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53960745-G-T

26577727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53960854-G-A

26577821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53960958-G-T

26577882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53961025-C-T

26578009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53962341-T-C

26578255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53962579-T-C

26578493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53962806-T-C

26578506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53962819-G-T

26578686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53962970-G-A

http://identifiers.org/hco/4/GRCh38#26580643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53963309-C-A

26580903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53963546-C-T

26581029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53964012-A-G

26581073-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53964057-C-G

26581190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53964181-G-T

26581765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53964347-C-T

26581921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53964502-A-G

26582154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53964721-G-T

26582168-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53964735-G-C

26582255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53964811-T-C

26582349-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53964875-C-G

26582874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53965312-G-A

26583160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53965628-T-C

26584032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53966942-G-A

26584032-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53966942-G-C

26584032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53966942-G-T

26584153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53967063-G-A

26584153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53967063-G-T

http://identifiers.org/hco/4/GRCh38#26584176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53967084-C-A

26584176-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53967084-C-G

26584176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53967084-C-T

26584189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53967097-G-A

26584381-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53967286-C-G

26584381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53967286-C-T

http://identifiers.org/hco/4/GRCh38#26584393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53967298-C-A

26584393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53967298-C-T

26584481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53967324-T-C

26584583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53967427-G-A

26584678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53967520-C-T

26584686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53967528-G-A

26584833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53967663-T-C

26585097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53967881-A-G

26600001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53976112-G-T

26600157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53976276-T-C

26600554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53977058-G-T

26606561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53980559-T-C

26606562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53980560-A-G

26606577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53980587-T-C

26606587-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53980597-T-A

26606587-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53980597-T-G

26606588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53980598-A-G

http://identifiers.org/hco/4/GRCh38#26606629-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53980635-A-C

26607134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53981051-A-G

26607134-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53981051-A-T

26607138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53981055-A-G

26607248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53981152-C-T

26607290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53981196-C-T

26607400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53981303-C-T

26607410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53981313-A-G

26607989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53981725-G-T

26608381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53982073-T-C

http://identifiers.org/hco/4/GRCh38#26608416-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53982111-A-C

26608666-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53983039-C-G

26609369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53983367-C-T

26609389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53983388-T-C

26609417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53983415-T-C

26609442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53983438-G-A

26609583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53983569-T-C

26609684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53983664-G-A

26609715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53983694-T-C

26609721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53983700-C-T

http://identifiers.org/hco/4/GRCh38#26609742-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53983719-A-C

26609742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53983719-A-G

26609775-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53983753-A-T

26611635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53984815-T-C

26611825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53985188-A-G

26611845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53985219-C-T

26612259-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53985653-T-G

26612529-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53986099-G-C

26612720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53986285-A-G

26612773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53986332-T-C

26613186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 53986709-T-C

26613533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53986793-T-C

26613634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53986886-G-T

26613671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53986923-T-C

26613934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53987163-A-G

26614335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53987693-T-C

26614335-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53987693-T-G

http://identifiers.org/hco/4/GRCh38#26614391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53987774-C-A

26614391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53987774-C-T

26614470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53987861-A-G

http://identifiers.org/hco/4/GRCh38#26615842-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53989204-A-C

26615943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53989327-G-A

26620480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53990175-A-G

26620480-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53990175-A-T

http://identifiers.org/hco/4/GRCh38#26620488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53990183-C-A

26620490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53990185-G-T

26620495-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53990190-T-G

26620585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53990284-A-G

26620585-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53990284-A-T

26620634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53990333-T-C

26620661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53990360-A-G

26620670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53990369-A-G

http://identifiers.org/hco/4/GRCh38#26620726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53990425-C-A

26620755-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53990448-T-A

http://identifiers.org/hco/4/GRCh38#26620765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53990458-C-A

26620765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53990458-C-T

26620783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53990475-A-G

26620798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53990491-G-A

26620798-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53990491-G-C

26620798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53990491-G-T

26620919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53990607-A-G

26620987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53990667-G-A

26621108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53990815-G-A

26621151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53990829-G-T

26621210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53990876-T-C

26621237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53990903-T-C

26621510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53991140-C-T

26637065-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53992362-T-A

http://identifiers.org/hco/4/GRCh38#26637106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53992402-C-A

26637893-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53993162-C-G

26637893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53993162-C-T

26638448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53993656-G-A

26638477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53993686-A-G

26638585-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53993790-T-G

26638657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53993864-A-G

26638696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53993904-T-C

26638824-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53993991-T-A

26638824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53993991-T-C

26638850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53994026-T-C

26639393-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53994660-C-G

26639400-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53994667-A-T

http://identifiers.org/hco/4/GRCh38#26639628-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53994866-A-C

26639850-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53995038-T-A

26639942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53995076-A-G

http://identifiers.org/hco/4/GRCh38#26639993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53995121-C-A

26639993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53995121-C-T

26659461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53995346-G-T

26659499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53995386-T-C

26659499-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53995386-T-G

26659504-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53995391-T-G

26659583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53995455-A-G

26659824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53995701-G-A

26659824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53995701-G-T

26660033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53996742-G-T

26660225-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53996898-A-T

26660236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53996909-C-T

26660477-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53997080-T-A

26660511-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53997117-T-A

26660879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53997390-A-G

26660954-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53997466-A-T

26661340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53997790-C-T

26661507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53997953-A-G

26661644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53998130-A-G

26663941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53998754-G-A

26663973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53998772-G-A

26663976-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53998775-A-T

26664205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53998951-T-C

26664273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53999013-G-A

26664273-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53999013-G-C

26664372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53999100-T-C

http://identifiers.org/hco/4/GRCh38#26664528-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53999257-A-C

26665398-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53999394-G-C

26665699-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53999697-C-G

26665812-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54003130-G-C

26665906-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54003211-C-G

26666040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54003349-C-T

http://identifiers.org/hco/4/GRCh38#26666192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#54003475-C-A

26666192-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54003475-C-G

26666192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54003475-C-T

26666193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54003476-T-C

26666364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 54003574-T-C

http://identifiers.org/hco/4/GRCh38#26671078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#54004101-C-A

http://identifiers.org/hco/4/GRCh38#26671189-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#54004222-A-C

26671231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54004360-A-G

26671478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54004588-C-T

26671836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54005166-T-C

26672039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54005397-G-A

26672039-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54005397-G-C

26672039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54005397-G-T

http://identifiers.org/hco/4/GRCh38#26672165-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#54005520-A-C

26672165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 54005520-A-G

26672165-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 54005520-A-T

26672171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 54005526-A-G

26672171-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 54005526-A-T

26672197-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54005556-T-A

26672197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54005556-T-C

http://identifiers.org/hco/4/GRCh38#26672199-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#54005558-A-C

26672199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54005558-A-G

26672199-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54005558-A-T

26672219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54005574-T-C

26672225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54005580-G-A

26672225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54005580-G-T

http://identifiers.org/hco/4/GRCh38#26672231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#54005586-C-A

26672231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54005586-C-T

26672255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54005608-A-G

26672270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54005622-G-A

26672270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54005622-G-T

26672728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54006053-C-T

http://identifiers.org/hco/4/GRCh38#26672788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#54006112-C-A

26672788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54006112-C-T

26673191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54006484-T-C

26673560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54006942-G-A

26673677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54007077-G-T

26673742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54007146-G-A

26673742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54007146-G-T

http://identifiers.org/hco/4/GRCh38#26673760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#54007164-C-A

26673773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 54007177-T-C

http://identifiers.org/hco/4/GRCh38#26673903-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#54007307-A-C

26673903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54007307-A-G

26673920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54007321-A-G

26673921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54007322-G-A

26673929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54007330-G-A

26673929-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54007330-G-C

26673929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54007330-G-T

26674019-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54007397-A-T

26674408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54008010-G-A

26675197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54008731-A-G

26675231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54008757-A-G

26675372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54008907-C-T

26675391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54008928-A-G

26675399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54008936-A-G

26675424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54008961-C-T

http://identifiers.org/hco/4/GRCh38#26675438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#54008975-C-A

26680517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54009980-C-T

26680599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54010044-G-A

26680700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54010124-T-C

http://identifiers.org/hco/4/GRCh38#26683506-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#54014009-A-C

26683524-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54014026-T-A

26683527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54014029-A-G

26683527-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54014029-A-T

26683567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54014080-T-C

26683588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54014099-G-T

http://identifiers.org/hco/4/GRCh38#26683740-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#54014255-A-C

http://identifiers.org/hco/4/GRCh38#26683762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#54014277-C-A

26683793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54014307-T-C

26683799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54014313-T-C

26683820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54014334-A-G

26683825-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54014339-G-C

26683825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54014339-G-T

26686415-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54015184-T-G

26686938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54015661-T-C

26687015-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54015758-T-A

26687138-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54016062-T-G

26687431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54016634-C-T

26687460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54016658-C-T

26687671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54016832-A-G

26687794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54016946-G-A

26687936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54017082-G-T

26688243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54017382-A-G

26688253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54017392-T-C

26688253-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54017392-T-G

26688275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54017415-A-G

26688275-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54017415-A-T

26688312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54017452-G-A

26688312-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54017452-G-C

26688312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54017452-G-T

http://identifiers.org/hco/4/GRCh38#26702421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#54018788-C-A

26702421-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54018788-C-G

http://identifiers.org/hco/4/GRCh38#26702439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#54018806-C-A

26702539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54018892-G-A

26702836-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54019102-A-T

http://identifiers.org/hco/4/GRCh38#26702857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#54019122-C-A

26704414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54021319-C-T

26704450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54021343-T-C

26704504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54021388-C-T

26704505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54021389-G-A

26704522-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54021408-A-T

26704532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54021418-A-G

26704600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54021877-G-A

http://identifiers.org/hco/4/GRCh38#26704718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#54021991-C-A

26711663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54023303-T-C

26711860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54023449-A-G

26712157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54023756-T-C

26712237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54023837-C-T

26712251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54023860-G-T

26712300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54023922-G-A

26712335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54023957-T-C

26713419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54027083-A-G

26713465-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54027137-C-G

26717220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54028903-G-T

26717543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54029189-A-G

26717689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54029323-T-C

26717699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54029333-G-A

26717802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54029445-G-A

26717802-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54029445-G-C

26717802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54029445-G-T

26717829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54029472-G-A

26717829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54029472-G-T

26717833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54029476-G-A

26717833-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54029476-G-C

26717833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54029476-G-T

26717893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54029558-T-C

http://identifiers.org/hco/4/GRCh38#26718056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#54029722-C-A

26718056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54029722-C-T

26718064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54029730-T-C

26718064-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54029730-T-G

http://identifiers.org/hco/4/GRCh38#26718169-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#54029830-A-C

26718317-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54029966-T-A

26718422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54030085-C-T

26718585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54030240-A-G

26718629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54030284-C-T

26718678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54030322-A-G

26718685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54030329-G-A

26718690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54030334-G-T

26718731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54030375-A-G

26718955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54030845-A-G

26718991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54030873-C-T

26719623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54031836-G-A

26719636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54031849-A-G

26719696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54031889-A-G

http://identifiers.org/hco/4/GRCh38#26719959-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#54032109-A-C

26719959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54032109-A-G

26720066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54032214-G-A

26720068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54032216-T-C

26720138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54032284-C-T

http://identifiers.org/hco/4/GRCh38#26720150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#54032296-C-A

26720150-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54032296-C-G

26720168-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54032314-A-T

http://identifiers.org/hco/4/GRCh38#26720268-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#54032421-A-C

26720336-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54032485-C-G

26720414-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54032563-A-T

26720939-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54033041-T-G

26721021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54033099-G-A

26721021-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54033099-G-C

26721450-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54033364-C-G

26721502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54033401-C-T

26721582-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54033480-C-G

26721582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54033480-C-T

26721686-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54033576-C-G

26721686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54033576-C-T

26726622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54034147-C-T

26726863-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54034364-T-A

26727144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54034674-T-C

26727577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54035011-G-A

26727701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54035108-A-G

26727798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54035205-A-G

26728108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54035471-T-C

26728167-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54035523-A-T

26730164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54036115-G-A

26730376-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54036302-T-G

26730666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54036492-C-T

http://identifiers.org/hco/4/GRCh38#26730799-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#54036565-A-C

26731038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54036710-A-G

26731038-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54036710-A-T

26731199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54036884-C-T

26731771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54037466-G-A

26732286-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54037829-C-G

26732353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54037860-C-T

26732366-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54037873-C-G

26732689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54038182-A-G

26733883-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54039214-T-A

26734148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54039422-G-A

http://identifiers.org/hco/4/GRCh38#26734151-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#54039425-A-C

26734266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54039503-G-A

26734277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54039514-A-G

26734677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54039930-G-A

26734691-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54039944-G-C

26739738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54044579-G-T

26739787-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54044624-T-G

http://identifiers.org/hco/4/GRCh38#26739872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#54044704-C-A

http://identifiers.org/hco/4/GRCh38#26739988-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#54044820-A-C

26739988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54044820-A-G

26739988-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54044820-A-T

26739989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54044821-A-G

26740296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54045056-A-G

26740363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54045131-G-T

26740491-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54045226-A-T

26740916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54045578-A-G

26740934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54045596-A-G

26741002-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54045651-C-G

26741019-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54045668-T-A

26741689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54046025-T-C

26741691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54046027-C-T

26741927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54046262-A-G

26741927-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54046262-A-T

26742177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54046472-A-G

26742375-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54046549-T-A

26742375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54046549-T-C

26742375-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54046549-T-G

26742501-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 54046651-T-A

26742501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 54046651-T-C

http://identifiers.org/hco/4/GRCh38#26742504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#54046654-C-A

26742504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 54046654-C-T

26742540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 54046690-T-C

26742656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54046811-T-C

26742656-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54046811-T-G

http://identifiers.org/hco/4/GRCh38#26743030-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#54047244-A-C

26743042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54047256-A-G

26743247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54047426-A-G

26743478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54047665-T-C

26743521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54047707-T-C

26743544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54047729-T-C

26743627-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54047802-T-A

26748045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54054062-T-C

26748206-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54054144-C-G

26748381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54054304-A-G

26748381-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54054304-A-T

26748468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 54054390-T-C

http://identifiers.org/hco/4/GRCh38#26748597-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#54054504-A-C

http://identifiers.org/hco/4/GRCh38#26748623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#54054537-C-A

26748662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54054574-T-C

26749019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54054813-C-T

http://identifiers.org/hco/4/GRCh38#26749142-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#54054956-A-C

26749146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54054960-A-G

26749186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54055006-A-G

26749317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54055131-G-A

http://identifiers.org/hco/4/GRCh38#26750170-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#54056074-A-C

26750339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54056234-G-A

26750339-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54056234-G-C

26750404-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54056290-C-G

26750633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54056514-G-A

26750670-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54056549-T-A

26750747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54056605-A-G

26751129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54057001-T-C

26751250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54057117-G-A

26751295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54057135-T-C

26751513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54057348-A-G

26751651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54057480-C-T

26751870-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54057723-G-C

26751882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54057734-G-A

26752085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54057924-A-G

26752192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54057954-T-C

26752570-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54058091-T-G

26752580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54058101-T-C

http://identifiers.org/hco/4/GRCh38#26752582-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#54058103-A-C

26752605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54058126-C-T

26752716-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54058223-T-A

26753055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54058388-C-T

26753193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54058525-T-C

http://identifiers.org/hco/4/GRCh38#26753665-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#54058781-A-C

26753691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54058806-G-A

26753691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54058806-G-T

http://identifiers.org/hco/4/GRCh38#26753735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#54058842-C-A

26753735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54058842-C-T

http://identifiers.org/hco/4/GRCh38#26753736-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#54058843-A-C

26753736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54058843-A-G

26753753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54058859-G-A

26753755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54058861-A-G

26753755-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54058861-A-T

26753793-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54058892-G-C

26753793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54058892-G-T

http://identifiers.org/hco/4/GRCh38#26753798-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#54058897-A-C

26753910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54059009-A-G

http://identifiers.org/hco/4/GRCh38#26754146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#54059245-C-A

26754146-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54059245-C-G

26754186-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54059285-T-A

26754186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54059285-T-C

26754202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54059298-T-C

26754224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 54059315-G-A

26754224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 54059315-G-T

26754586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54060396-A-G

26754692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54060498-A-G

http://identifiers.org/hco/4/GRCh38#26754699-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#54060505-A-C

26754804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54060603-G-A

26754804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54060603-G-T

26755184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54060983-T-C

26755270-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54061051-A-T

http://identifiers.org/hco/4/GRCh38#26755273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#54061054-C-A

26755732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54061628-T-C

26756144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54062091-G-T

26756553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54062434-G-A

26756750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54062608-A-G

26756919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54062773-C-T

26756922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54062776-A-G

26757492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54063009-A-G

26857617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54152868-G-A

26857768-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 54152992-T-G

26857801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25624
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54153027-A-G