45847242-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: 5 prime UTR variant
orthologous variants: 92264615-T-A

45847242-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: 5 prime UTR variant
orthologous variants: 92264615-T-G

45847394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron variant
orthologous variants: 92264461-T-C

45847394-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron variant
orthologous variants: 92264461-T-G

http://identifiers.org/hco/11/GRCh38#45847445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#92264410-C-A

45847445-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 92264410-C-G

45847446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, missense_variant
orthologous variants: 92264409-G-A

45847446-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, missense_variant
orthologous variants: 92264409-G-C

45847446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, missense_variant
orthologous variants: 92264409-G-T

45847461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, missense_variant
orthologous variants: 92264396-G-A

45847461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, missense_variant
orthologous variants: 92264396-G-T

45847479-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 92264378-G-C

45847479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 92264378-G-T

45847806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92264095-G-T

45847996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92263971-A-G

45848160-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92263844-A-T

45848436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92263443-C-T

45848711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92263174-C-T

45848755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92263130-G-A

45849258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92262589-A-G

45849266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92262581-A-G

45849286-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92262561-A-T

45849304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92262540-G-T

http://identifiers.org/hco/11/GRCh38#45849345-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#92262507-A-C

45849409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92262457-G-A

45849578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92262277-A-G

45850303-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92262208-C-G

45850303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92262208-C-T

45850411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92262103-T-C

45850501-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92262011-C-G

45850530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92261983-A-G

45850692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92261794-A-G

45850706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92261777-G-A

45850710-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92261773-A-T

45850809-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92261692-T-G

45850816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92261685-C-T

45851000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92261437-G-T

45851373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92261085-A-G

45851382-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92261076-A-T

45851469-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92261016-A-T

45852056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92260463-C-T

45852258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92260256-G-A

45852270-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92260245-C-G

45852278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92260238-C-T

45852368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92260146-A-G

45852391-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92260121-G-C

45852612-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92259910-C-G

45852986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92259444-T-C

45853092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92259312-C-T

45853278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92259143-T-C

45853729-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92258769-A-T

45854128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92258358-G-T

45854247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92258296-T-C

45854270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92258266-A-G

45854791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92258109-A-G

45855582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92257776-A-G

45855652-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92257720-T-A

45855956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92257379-T-C

45856049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 92257286-G-A

45856049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 92257286-G-T

45856141-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92257202-T-G

http://identifiers.org/hco/11/GRCh38#45856170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#92257173-C-A

45856170-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92257173-C-G

45856170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92257173-C-T

45856212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92257125-T-C

45856227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92257110-G-A

45856227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92257110-G-T

45856363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92256980-G-A

45856363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92256980-G-T

45856445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92256900-G-A

45856445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92256900-G-T

45857121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92256602-T-C

45857214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92256534-G-A

45857278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92256480-G-T

45857323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92256434-T-C

45857547-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92256130-C-G

45857867-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92255829-C-G

45857979-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92255744-C-G

45858232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92255510-A-G

45858232-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92255510-A-T

45858373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92255371-G-A

45858373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92255371-G-T

45858374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92255370-T-C

45858511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92255244-G-A

45858512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92255243-T-C

45858519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92255236-G-A

45858519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92255236-G-T

45858529-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92255226-T-A

http://identifiers.org/hco/11/GRCh38#45858622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#92255128-C-A

45858622-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92255128-C-G

45858640-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92255110-A-T

45858676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92255074-G-A

45858676-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92255074-G-C

45859008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92254779-G-T

45859179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92254613-C-T

45859182-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92254610-T-A

45859184-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92254608-C-G

45859203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92254586-C-T

45859815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92254334-G-A

45860029-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92254116-C-G

45860066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92254079-A-G

45860200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92253975-A-G

45860444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92253801-C-T

45860725-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92253531-A-T

45860746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92253511-G-T

45860770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92253487-T-C

45860771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92253486-G-T

45860787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92253467-G-A

45860812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92253441-A-G

45860996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92253257-G-A

45861026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92253227-G-A

45861115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92253109-T-C

http://identifiers.org/hco/11/GRCh38#45861170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#92253011-C-A

http://identifiers.org/hco/11/GRCh38#45861175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#92253006-C-A

45861175-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92253006-C-G

45861175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92253006-C-T

45861917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92252789-T-C

45861917-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92252789-T-G

45862173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92252479-A-G

45862212-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92252446-T-A

45862249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92252428-G-A

45862249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92252428-G-T

45862327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92252370-G-T

45862862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92251822-C-T

45862881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92251803-G-A

45862958-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92251714-G-C

45863140-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92251508-G-C

45863276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92251220-T-C

http://identifiers.org/hco/11/GRCh38#45863771-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#92250460-A-C

45863824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92250408-T-C

45864035-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92249982-G-C

45864035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92249982-G-T

45864224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92249803-T-C

45864247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92249796-A-G

45864301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92249739-A-G

45867287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92246932-G-A

45867287-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92246932-G-C

45867287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92246932-G-T

45867341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92246883-T-C

45867444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92246797-G-A

45867481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92246758-G-A

45867481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92246758-G-T

45867744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 92246505-T-C

45867837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92246424-G-A

45867837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92246424-G-T

45867881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92246390-G-A

45867881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92246390-G-T

45867947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92246325-A-G

45867963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92246309-A-G

http://identifiers.org/hco/11/GRCh38#45868010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#92246268-C-A

45868232-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92246088-G-C

45869276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92244504-T-C

45869335-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92244443-T-G

http://identifiers.org/hco/11/GRCh38#45869365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#92244416-C-A

45869367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92244414-A-G

45869367-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92244414-A-T

45869390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92244404-G-A

45869390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92244404-G-T

45869395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92244399-T-C

45869398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92244396-G-A

http://identifiers.org/hco/11/GRCh38#45869419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#92244380-C-A

45869419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92244380-C-T

45869569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 92244227-T-C

45869575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 92244221-G-A

45869584-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 92244212-A-T

45869611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 92244185-G-A

45869898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron variant
orthologous variants: 92243912-A-G

http://identifiers.org/hco/11/GRCh38#45869941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#92243869-C-A

45869941-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron variant
orthologous variants: 92243869-C-G

45870448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: missense variant
orthologous variants: 92243376-A-G

45870570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron variant
orthologous variants: 92243245-C-T

45870609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron variant
orthologous variants: 92243224-G-A

45870609-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron variant
orthologous variants: 92243224-G-C

45870703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 92243163-G-A

45870703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 92243163-G-T

45870847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 92243044-C-T

45870954-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92242927-C-G

45870954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92242927-C-T

45871485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92242532-G-T

45871613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92242449-A-G

45871725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92242394-C-T

45871861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92242272-G-A

45872079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92242123-C-T

45872094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 92242108-C-T

45872145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 92242057-G-A

45872145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 92242057-G-T

http://identifiers.org/hco/11/GRCh38#45872301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#92241937-C-A

45872301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92241937-C-T

http://identifiers.org/hco/11/GRCh38#45872307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#92241931-C-A

45872372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92241865-T-C

45872373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92241864-T-C

45872397-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92241824-G-C

45872630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92241650-T-C

45872886-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92241472-G-C

http://identifiers.org/hco/11/GRCh38#45872973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#92241414-C-A

45872990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92241404-T-C

45873001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92241393-G-A

45873298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92241066-G-A

45873298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92241066-G-T

45873336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92241040-C-T

45873341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92241035-A-G

45873575-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92240842-T-G

45873696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92240722-G-A

45873748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92240682-C-T

45873760-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92240673-A-T

http://identifiers.org/hco/11/GRCh38#45876504-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#92238852-A-C

45880892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92236185-T-C

45880942-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 92236135-C-G

45880942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 92236135-C-T

45880959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 92236121-C-T

45880999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: 3 prime UTR variant
orthologous variants: 92236081-A-G

http://identifiers.org/hco/11/GRCh38#45881044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#92236045-C-A

45881044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: 3 prime UTR variant
orthologous variants: 92236045-C-T

45881134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: 3 prime UTR variant
orthologous variants: 92235954-A-G

45881183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: 3 prime UTR variant
orthologous variants: 92235897-G-A

45881221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: 3 prime UTR variant
orthologous variants: 92235860-G-A

45881221-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: 3 prime UTR variant
orthologous variants: 92235860-G-C

45881233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: 3 prime UTR variant
orthologous variants: 92235848-G-A

45881242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 92235844-G-A

45881242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 92235844-G-T

http://identifiers.org/hco/11/GRCh38#45881296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#92235790-C-A

45881357-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: 3 prime UTR variant
orthologous variants: 92235729-A-T

45881403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: 3 prime UTR variant
orthologous variants: 92235679-G-A

45881403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: 3 prime UTR variant
orthologous variants: 92235679-G-T

45881420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: 3 prime UTR variant
orthologous variants: 92235661-G-T

http://identifiers.org/hco/11/GRCh38#45881635-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#92235557-A-C

45881686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: 3 prime UTR variant
orthologous variants: 92235504-A-G

http://identifiers.org/hco/11/GRCh38#45881710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#92235482-C-A

45881710-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: 3 prime UTR variant
orthologous variants: 92235482-C-G

45881751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: 3 prime UTR variant
orthologous variants: 92235443-T-C

45881751-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: 3 prime UTR variant
orthologous variants: 92235443-T-G

http://identifiers.org/hco/11/GRCh38#45882027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#92235192-C-A

45882027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: 3 prime UTR variant
orthologous variants: 92235192-C-T

http://identifiers.org/hco/11/GRCh38#45882034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#92235185-C-A

45882034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: 3 prime UTR variant
orthologous variants: 92235185-C-T

45882094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: 3 prime UTR variant
orthologous variants: 92235129-G-A

45882094-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: 3 prime UTR variant
orthologous variants: 92235129-G-C

45882094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: 3 prime UTR variant
orthologous variants: 92235129-G-T

45882118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: 3 prime UTR variant
orthologous variants: 92235105-T-C

45882204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: 3 prime UTR variant
orthologous variants: 92235035-G-A

45882204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: 3 prime UTR variant
orthologous variants: 92235035-G-T

45882240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: 3 prime UTR variant
orthologous variants: 92234999-T-C

45882263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: 3 prime UTR variant
orthologous variants: 92234931-A-G

45882263-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: 3 prime UTR variant
orthologous variants: 92234931-A-T

45882277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: 3 prime UTR variant
orthologous variants: 92234917-T-C

http://identifiers.org/hco/11/GRCh38#45882314-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#92234865-A-C

45882314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: 3 prime UTR variant
orthologous variants: 92234865-A-G

45882316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: 3 prime UTR variant
orthologous variants: 92234863-G-A

45882316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: 3 prime UTR variant
orthologous variants: 92234863-G-T

45882318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: 3 prime UTR variant
orthologous variants: 92234861-T-C

http://identifiers.org/hco/11/GRCh38#45882378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#92234801-C-A

http://identifiers.org/hco/11/GRCh38#45882487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#92234706-C-A

http://identifiers.org/hco/11/GRCh38#45882611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#92234586-C-A

45882611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: 3 prime UTR variant
orthologous variants: 92234586-C-T

45882659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: 3 prime UTR variant
orthologous variants: 92234536-A-G

45882704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: 3 prime UTR variant
orthologous variants: 92234493-G-A

45882704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: 3 prime UTR variant
orthologous variants: 92234493-G-T

45882748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: 3 prime UTR variant
orthologous variants: 92234449-T-C

http://identifiers.org/hco/11/GRCh38#45882761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#92234436-C-A

http://identifiers.org/hco/11/GRCh38#45882865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#92234340-C-A

45882920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2385
most severe consequence: 3 prime UTR variant
orthologous variants: 92234293-A-G