126304159-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35087187-G-C

126304368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35086991-G-A

126304368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35086991-G-T

126304468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35086904-G-T

http://identifiers.org/hco/11/GRCh38#126304570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#35086814-C-A

126304743-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35086665-C-G

http://identifiers.org/hco/11/GRCh38#126304808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#35086597-C-A

126305875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35083802-G-T

126305880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35083797-T-C

126305911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35083766-A-G

126306125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35083189-C-T

126306243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35083121-T-C

126306262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35083103-A-G

126306355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35082990-A-G

126306369-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35082976-T-A

http://identifiers.org/hco/11/GRCh38#126306372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#35082973-C-A

http://identifiers.org/hco/11/GRCh38#126306422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#35083210-C-A

126306422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35083210-C-T

126306589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: missense variant
orthologous variants: 35082526-A-G

126306645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: stop gained
orthologous variants: 35082470-C-T

126306771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35082344-G-A

http://identifiers.org/hco/11/GRCh38#126306839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#35082283-C-A

126306839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35082283-C-T

126306884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35082223-G-A

126306884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35082223-G-T

126307773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35081759-A-G

126307816-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35081707-C-G

126307911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35081614-A-G

126308571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35080804-C-T

126309650-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35080405-C-G

126309835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35080215-C-T

126309930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35080187-T-C

126310230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35079880-C-T

126310426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35079683-C-T

126310428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35079681-G-A

126310466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35079645-A-G

126310487-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, undefined
orthologous variants: 35079624-G-C

126310871-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35077405-C-G

126311092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35077201-A-G

126311146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35077157-G-A

126311361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35076887-A-G

126311430-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35076833-T-A

126312695-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35076050-T-A

126312754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35075987-A-G

126312985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35075772-C-T

126313177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35075585-A-G

126313301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35075460-T-C

126313843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35075012-T-C

126313992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35074791-C-T

126314058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35074730-T-C

126315607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35073533-A-G

126315665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35073468-T-C

126317354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35072309-T-C

126317355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35072308-C-T

126317364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35072306-G-T

126317998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35068551-C-T

126318155-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35068433-C-G

126318339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35068282-T-C

126318586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35068087-T-C

126318586-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35068087-T-G

126318636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35068047-C-T

126318711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35067975-A-G

126318804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35067882-G-T

126319022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35067665-G-A

126319403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35067293-C-T

126324247-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35054012-T-G

126324326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35053942-A-G

126324359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35053909-A-G

126325095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35053390-G-A

126325113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35053372-G-A

126325664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35052936-A-G

126325794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35052808-G-T

126327182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35051972-G-A

126327363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35051817-A-G

126327810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35051319-G-T

126328046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35051127-G-A

126328367-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35050982-G-C

126328396-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35050958-G-C

126328537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35050851-C-T

126328660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35050748-G-A

126328859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35050526-C-T

126328889-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, splice_donor_variant
orthologous variants: 35050496-G-C

126329279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35050144-C-T

126329362-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35050075-T-A

126329567-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35049896-G-C

126329745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35049735-C-T

126329756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35049726-G-A

126330007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35049552-A-G

126331028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35048026-G-A

126331301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron variant
orthologous variants: 35047835-T-C

126331416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35047772-A-G

126331592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35047603-G-A

126331592-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35047603-G-C

126331594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35047601-C-T

126331607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35047588-T-C

126331613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35047582-G-A

126331758-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35047543-C-G

126331834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35047466-G-A

http://identifiers.org/hco/11/GRCh38#126332095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#35047238-C-A

126332095-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35047238-C-G

126332112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35047219-C-T

126332148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35047183-G-T

http://identifiers.org/hco/11/GRCh38#126332154-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#35047177-A-C

126332272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35047055-T-C

126332272-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35047055-T-G

126332829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35045664-A-G

126335047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35043482-A-G

126335172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35043368-G-T

126335642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35042984-A-G

126335657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35042969-G-A

http://identifiers.org/hco/11/GRCh38#126337274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#35041612-C-A

126337274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35041612-C-T

126337275-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35041611-T-A

126337275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35041611-T-C

http://identifiers.org/hco/11/GRCh38#126337301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#35041584-C-A

126337301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35041584-C-T

http://identifiers.org/hco/11/GRCh38#126337303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#35041582-C-A

126337303-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35041582-C-G

126337303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35041582-C-T

http://identifiers.org/hco/11/GRCh38#126337347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#35041559-C-A

126337347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 35041559-C-T

126337377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35041529-G-A

126337377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35041529-G-T

126337401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35041503-G-A

126337401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35041503-G-T

http://identifiers.org/hco/11/GRCh38#126337406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#35041498-C-A

http://identifiers.org/hco/11/GRCh38#126337446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#35041458-C-A

126337446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35041458-C-T

126337483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35041422-A-G

126337493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35041412-C-T

126337556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35041372-G-A

126337611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35041323-G-A

126337611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35041323-G-T

126337675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35041271-T-C

http://identifiers.org/hco/11/GRCh38#126337759-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#35041230-A-C

http://identifiers.org/hco/11/GRCh38#126337760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#35041229-C-A

126337760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35041229-C-T

http://identifiers.org/hco/11/GRCh38#126337794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#35041200-C-A

126337794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35041200-C-T

http://identifiers.org/hco/11/GRCh38#126337799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#35041195-C-A

126337799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35041195-C-T

http://identifiers.org/hco/11/GRCh38#126337817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#35041181-C-A

126337817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35041181-C-T

http://identifiers.org/hco/11/GRCh38#126337835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#35041163-C-A

126337835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35041163-C-T

126337967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35041089-G-A

126337967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35041089-G-T

126338008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35041064-G-A

126338014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35041058-G-T

126338078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35041009-G-T

126338111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35040987-A-G

126340951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35039684-G-A

126341036-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35039597-T-A

http://identifiers.org/hco/11/GRCh38#126341178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#35039469-C-A

126341215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35039435-T-C

126341325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35039374-T-C

126341402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35039300-G-T

http://identifiers.org/hco/11/GRCh38#126341723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#35039045-C-A

126341730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35039038-T-C

http://identifiers.org/hco/11/GRCh38#126341782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#35039000-C-A

126341782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35039000-C-T

126341802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35038977-G-T

126342023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35038793-G-T

http://identifiers.org/hco/11/GRCh38#126342040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#35038776-C-A

126342097-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35038719-T-A

http://identifiers.org/hco/11/GRCh38#126342288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#35038537-C-A

126342288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35038537-C-T

http://identifiers.org/hco/11/GRCh38#126342389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#35038454-C-A

126342660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35038284-T-C

126343161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35037853-G-A

126343161-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35037853-G-C

126343161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35037853-G-T

http://identifiers.org/hco/11/GRCh38#126343169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#35037845-C-A

126343169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35037845-C-T

126343176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35037840-C-T

126343463-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35037557-T-A

126343463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35037557-T-C

126343463-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35037557-T-G

126343476-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35037544-T-A

126343476-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35037544-T-G

126343477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35037543-G-A

126343477-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35037543-G-C

126343477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35037543-G-T

126343495-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35037523-T-A

126343495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35037523-T-C

http://identifiers.org/hco/11/GRCh38#126343553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#35037486-C-A

126343564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35037475-C-T

126343795-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35037275-T-G

126343908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35037160-G-A

126343908-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35037160-G-C

126343975-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35037103-C-G

126344167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35036925-C-T

126344277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35036872-A-G

126344588-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35036635-G-C

126344764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35036586-T-C

http://identifiers.org/hco/11/GRCh38#126344904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#35036492-C-A

126345165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35036305-T-C

126345198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35036279-A-G

126345217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35036260-G-T

126345218-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35036259-T-G

126345284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35036196-G-T

http://identifiers.org/hco/11/GRCh38#126345294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#35036186-C-A

http://identifiers.org/hco/11/GRCh38#126345306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#35036174-C-A

126345431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35036054-G-A

126345653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35035851-G-T

126345657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35035847-G-T

126345793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35035667-G-A

126345994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35035486-C-T

126346088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35035384-G-A

126346123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35035343-G-A

126346183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35035293-G-A

126346320-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35035153-C-G

126346581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35034913-A-G

126346715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35034778-G-T

126346809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35034671-T-C

126346891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35034573-A-G

126347196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35034492-T-C

126347645-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35034345-C-G

126347953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35034030-T-C

126348144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35033856-G-A

126348463-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35033543-C-G

126348524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35033481-C-T

126348560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35033449-A-G

126348645-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35033363-C-G

126349691-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29812
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35032509-G-C