134455759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: 3 prime UTR variant
orthologous variants: 127418420-T-C

134455795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 127418454-C-T

134455818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 127418477-G-A

134455893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 127418550-A-G

134455999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 127418646-T-C

134456138-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 127418782-C-G

134456138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 127418782-C-T

http://identifiers.org/hco/2/GRCh38#134456347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127418936-C-A

134456347-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 127418936-C-G

134456347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 127418936-C-T

134456389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 127418977-G-T

134456395-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 127418987-G-C

134456451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 127419043-T-C

134456451-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 127419043-T-G

134456467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 127419060-A-G

134456511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 127419107-T-C

134456511-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 127419107-T-G

134456527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 127419126-A-G

134456593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 127419191-G-A

134456593-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 127419191-G-C

134456593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 127419191-G-T

134456699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 127419300-G-A

http://identifiers.org/hco/2/GRCh38#134456700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127419301-C-A

134456700-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 127419301-C-G

134456700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 127419301-C-T

134456708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 127419321-G-A

134456827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127419441-G-A

134456827-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127419441-G-C

134456827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127419441-G-T

134456833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127419447-G-A

134456833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127419447-G-T

134457980-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127423396-A-T

134460726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127424651-C-T

134461218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127425314-G-A

134461226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127425322-G-A

134461226-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127425322-G-C

134461241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127425338-A-G

134461734-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127425905-A-T

134466012-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127427820-A-T

134466017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127427825-G-A

134466017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127427825-G-T

http://identifiers.org/hco/2/GRCh38#134466083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127427892-C-A

134466083-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127427892-C-G

134466087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127427896-G-A

134466087-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127427896-G-C

134466087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127427896-G-T

134466106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 127427913-T-C

134466175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 127427982-G-A

134466301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 127428107-G-T

134466403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127428202-A-G

134466535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127428309-G-A

http://identifiers.org/hco/2/GRCh38#134466721-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127428479-A-C

http://identifiers.org/hco/2/GRCh38#134466785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127428543-C-A

134466785-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127428543-C-G

134466815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127428573-T-C

134466907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127428668-T-C

134466918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127428695-A-G

134466928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127428705-G-A

134466928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127428705-G-T

http://identifiers.org/hco/2/GRCh38#134466950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127428727-C-A

134466950-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127428727-C-G

134466950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127428727-C-T

134467025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127428802-G-A

http://identifiers.org/hco/2/GRCh38#134467039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127428816-C-A

134467076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127428852-C-T

134467203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127428981-G-A

134467203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127428981-G-T

http://identifiers.org/hco/2/GRCh38#134479230-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127431171-A-C

134479414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127431351-A-G

http://identifiers.org/hco/2/GRCh38#134479425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127431362-C-A

134479425-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127431362-C-G

134479948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127432451-T-C

http://identifiers.org/hco/2/GRCh38#134480387-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127433552-A-C

134480479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127433651-G-A

134480497-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127433669-G-C

134480529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127433701-C-T

134480551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127433721-T-C

134480572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127433746-A-G

134481748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127435347-T-C

http://identifiers.org/hco/2/GRCh38#134481842-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127435410-A-C

134482474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127436269-C-T

134482651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127436446-C-T

134482913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127436679-G-A

http://identifiers.org/hco/2/GRCh38#134482916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127436682-C-A

134483081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127436836-C-T

134483107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127436861-C-T

134483167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127436939-G-A

134490718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127437615-A-G

134490765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127437645-C-T

134490903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127437785-G-A

134491045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127437935-G-A

134491045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127437935-G-T

134491230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127438357-C-T

134491456-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127438602-T-A

134491569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127438691-C-T

134492195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127439332-A-G

134492227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127439361-G-A

134492230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127439364-A-G

134492427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127439531-A-G

134494502-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127440274-C-G

134494541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127440311-A-G

134494609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127440374-A-G

134494853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127440798-G-T

http://identifiers.org/hco/2/GRCh38#134499625-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127442970-A-C

134501196-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127445528-T-G

134501328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127445669-C-T

134501356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127445697-T-C

134501364-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127445705-G-C

134501454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127445794-T-C

134501490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127445830-G-A

134501576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127445917-C-T

134501627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127445965-G-A

http://identifiers.org/hco/2/GRCh38#134501682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127446019-C-A

134501682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127446019-C-T

134502151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127446405-G-T

134502184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127446439-C-T

134502206-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127446453-A-T

134502274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127446521-C-T

134502280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127446527-C-T

http://identifiers.org/hco/2/GRCh38#134502376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127446604-C-A

134502376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127446604-C-T

134502377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127446605-G-A

134502457-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127446673-A-T

134502846-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127447026-G-C

134502846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127447026-G-T

134506671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127449594-G-A

134506796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127449735-G-A

134506864-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127449829-C-G

http://identifiers.org/hco/2/GRCh38#134506913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127449875-C-A

http://identifiers.org/hco/2/GRCh38#134515692-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127453193-A-C

134515692-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127453193-A-T

134515713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127453215-T-C

134515752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127453259-T-C

134515764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127453271-C-T

134515773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127453280-A-G

134517552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127457068-T-C

134517924-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127457439-A-T

134517949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127457464-G-A

134522500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127458633-G-T

134522865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127458967-G-A

134523109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127459207-C-T

134523159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127459257-A-G

134523160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127459258-A-G

http://identifiers.org/hco/2/GRCh38#134523198-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127459296-A-C

134523260-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127459357-C-G

134528576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127461834-C-T

134528638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127461886-G-T

134528739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127461975-G-A

134528836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127462059-T-C

134528869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127462090-G-T

134530194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127463264-T-C

134530619-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127463383-G-C

134530619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127463383-G-T

134530645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127463409-A-G

134530883-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127463642-A-T

134532177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127464719-C-T

134532222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127464757-C-T

134532325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127464872-C-T

134532533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127465089-G-A

http://identifiers.org/hco/2/GRCh38#134532739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127465303-C-A

134532739-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127465303-C-G

134532739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127465303-C-T

134532884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127465447-T-C

http://identifiers.org/hco/2/GRCh38#134532963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127465510-C-A

134532963-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127465510-C-G

134532963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127465510-C-T

134532985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127465532-G-T

134532999-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127465546-C-G

134533375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127466426-G-A

134533419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127466459-G-A

http://identifiers.org/hco/2/GRCh38#134533493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127466532-C-A

134533703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127466768-T-C

134533705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127466770-C-T

134533931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127466975-G-A

134534119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127467145-C-T

134535390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127468421-T-C

134535438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127468470-T-C

http://identifiers.org/hco/2/GRCh38#134543169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127468768-C-A

134543284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127468897-C-T

134543347-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127468951-A-T

134543423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127469027-G-A

http://identifiers.org/hco/2/GRCh38#134543661-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127469464-A-C

134543771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127469581-A-G

134543776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127469586-G-A

134543940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127469750-C-T

134544044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127469855-C-T

134544211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127470022-C-T

134544346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127470162-T-C

134544355-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127470171-C-G

http://identifiers.org/hco/2/GRCh38#134547438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127475710-C-A

134547438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127475710-C-T

134547734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127475982-G-A

134548221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127476883-A-G

134548236-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127476898-T-A

134549101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127477580-G-A

134549101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127477580-G-T

134549216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127477689-C-T

134549773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127478158-C-T

134549777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127478162-C-T

134549807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127478186-C-T

http://identifiers.org/hco/2/GRCh38#134549960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127478337-C-A

134549964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127478341-C-T

134550248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127478634-C-T

134550415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127478919-G-T

134550475-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127478977-A-T

134550734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127479223-T-C

134550741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127479230-T-C

134550873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127479356-C-T

134551222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127479715-T-C

134551256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127479748-G-A

134551296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127479811-G-A

134551737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127480197-C-T

134551843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127480295-A-G

134551874-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127480324-G-C

134551876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127480326-C-T

134551938-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127480384-A-T

http://identifiers.org/hco/2/GRCh38#134551948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127480394-C-A

134551948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127480394-C-T

134551964-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127480412-C-G

http://identifiers.org/hco/2/GRCh38#134552176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127480636-C-A

134552176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127480636-C-T

134552183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127480642-G-A

134552183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127480642-G-T

134552361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127480843-T-C

134554782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127481813-C-T

134554890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127481917-C-T

134554930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127481957-T-C

134555277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127482827-T-C

134558545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127483992-C-T

http://identifiers.org/hco/2/GRCh38#134558662-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127484103-A-C

134562700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127485880-A-G

http://identifiers.org/hco/2/GRCh38#134562794-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127485974-A-C

http://identifiers.org/hco/2/GRCh38#134567770-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127493486-A-C

http://identifiers.org/hco/2/GRCh38#134568089-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127494140-A-C

134568454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127494547-G-A

134568934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127495053-C-T

134569160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127495265-G-A

http://identifiers.org/hco/2/GRCh38#134571227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127495791-C-A

134571227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127495791-C-T

134571258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127495821-T-C

http://identifiers.org/hco/2/GRCh38#134571264-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127495827-A-C

134571264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127495827-A-G

134571273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127495835-C-T

134572096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127499697-C-T

134572279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127499831-C-T

134572303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127499857-C-T

134572415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127500173-C-T

134572916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127501484-T-C

http://identifiers.org/hco/2/GRCh38#134573566-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127502086-A-C

134573607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127502129-G-A

134573624-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127502145-T-G

134576629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127503561-C-T

134576686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, undefined
orthologous variants: 127503622-T-C

134578367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127504673-T-C

134578367-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127504673-T-G

134578430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127504736-G-A

134578499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127504807-C-T

134578648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127504968-G-A

134578849-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127505143-A-T

134578923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127505217-A-G

134579862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127505481-G-T

http://identifiers.org/hco/2/GRCh38#134579968-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127505585-A-C

134579996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127505623-T-C

134580126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127505922-G-A

134580171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127505965-G-A

134580634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127506432-G-A

134581042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127506783-A-G

134581045-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127506786-C-G

134581070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127506809-G-A

134581070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127506809-G-T

134581615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127507411-T-C

134581985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127508109-C-T

134582047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127508145-C-T

134582792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127508715-G-A

134582808-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127508733-G-C

http://identifiers.org/hco/2/GRCh38#134582934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127508861-C-A

134582964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127508892-T-C

134582989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127508938-G-A

134583168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127509483-C-T

134583203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127509519-A-G

134583238-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127509554-T-G

134584298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127510985-C-T

134585157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127512347-G-A

http://identifiers.org/hco/2/GRCh38#134585158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127512348-C-A

134585158-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127512348-C-G

134585164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127512354-C-T

134585386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127512434-C-T

134585444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127512487-A-G

134585760-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127512499-T-A

134586303-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127513727-T-G

134586619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127513935-G-A

134587049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127514317-C-T

134587177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127514421-G-A

134587446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127515465-G-A

134587751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127515746-A-G

134588170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127516587-T-C

134588172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127516590-G-A

134590097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127516985-C-T

134590138-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127517020-T-A

134590138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127517020-T-C

134591758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127517448-C-T

134591781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127517472-T-C

134591876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127517557-G-A

http://identifiers.org/hco/2/GRCh38#134591886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127517567-C-A

134591886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127517567-C-T

134593133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127518473-C-T

134593183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127521640-G-T

134593244-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127521702-T-G

134593308-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127521775-G-C

134593626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127522748-G-A

134593634-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127522779-G-C

134593663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127522828-G-A

134593830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127522994-G-T

134593894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127523036-C-T

134593915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127523057-T-C

http://identifiers.org/hco/2/GRCh38#134593946-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127523082-A-C

134594127-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127523727-C-G

134594267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127523841-G-A

134594616-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127524173-C-G

134594833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127524368-G-A

134599914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127526702-T-C

134599914-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127526702-T-G

http://identifiers.org/hco/2/GRCh38#134599943-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127526731-A-C

134600001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127526796-T-C

134600108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127526983-C-T

134601445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127528059-C-T

http://identifiers.org/hco/2/GRCh38#134601479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127528093-C-A

134601479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127528093-C-T

134629168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127528907-A-G

134629251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127528993-C-T

134629301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127529052-T-C

134629710-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127529776-G-C

134629848-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127529899-C-G

134629930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127529964-A-G

134630359-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127531271-A-T

134630404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127531318-T-C

134630463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127531372-T-C

134630464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127531373-G-A

134630559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127531496-G-A

http://identifiers.org/hco/2/GRCh38#134630610-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127531623-A-C

134630710-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127531703-C-G

134630716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127531709-G-A

134630923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127531919-C-T

134631243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127532229-A-G

134635241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127534807-T-C

134635274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127534840-G-T

134635291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127534857-G-T

134635439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127535857-A-G

134635543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127535963-G-A

134661330-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127547977-C-G

134661350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127547997-T-C

134661350-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127547997-T-G

134661450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127548092-C-T

http://identifiers.org/hco/2/GRCh38#134661504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127548146-C-A

134661504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127548146-C-T

134661532-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127548174-T-G

http://identifiers.org/hco/2/GRCh38#134661678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127548874-C-A

134661678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127548874-C-T

134661795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127549199-C-T

134662430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127550164-G-A

134662503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127550231-T-C

134662704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127550493-C-T

134662722-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127550716-T-G

134662764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127550828-C-T

134663010-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127551049-A-T

134663012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127551051-T-C

134663359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127552255-C-T

134663373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127552269-G-A

134663527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127552434-T-C

134663534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127552441-A-G

134663545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127552452-G-A

134668811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127553223-C-T

134668823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127553235-T-C

134668827-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127553239-T-G

134668831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127553243-G-A

134669277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127553690-C-T

134670386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, undefined
orthologous variants: 127555179-T-C

134672286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127557285-A-G

134672289-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127557288-T-A

http://identifiers.org/hco/2/GRCh38#134672308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127557303-C-A

134673905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127558660-A-G

134673947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127558891-C-T

134675103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127559204-A-G

134675137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127559238-A-G

http://identifiers.org/hco/2/GRCh38#134676134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127564318-C-A

http://identifiers.org/hco/2/GRCh38#134676386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127564584-C-A

134676462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127564705-A-G

134676535-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127564791-A-T

134676548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127564804-A-G

134676560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127564818-G-A

134676630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127564881-A-G

134676917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127565545-C-T

134677371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127565938-T-C

134677371-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127565938-T-G

134677708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127566277-A-G

134677891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127566841-T-C

134677978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127566919-G-A

134678577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127567486-G-A

http://identifiers.org/hco/2/GRCh38#134678618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127567551-C-A

134678648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127567605-T-C

134678693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127567668-C-T

134678696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127567707-G-A

134679025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127568057-A-G

134679079-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127568111-G-C

134680189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127568669-C-T

134680323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127568812-A-G

134680742-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127569075-T-A

134680822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127569132-T-C

134681325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127570563-G-A

http://identifiers.org/hco/2/GRCh38#134681390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127570619-C-A

134681390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127570619-C-T

134681392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127570621-C-T

134681406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127570635-G-A

134681474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127570690-C-T

134681489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127570707-C-T

134681569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127570830-A-G

134681585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127570846-G-A

134683679-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, undefined
orthologous variants: 127571069-C-G

134683851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, undefined
orthologous variants: 127571227-G-A

134684433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127572582-G-T

134684542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127572689-A-G

134684997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127573989-A-G

134685187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127574166-C-T

http://identifiers.org/hco/2/GRCh38#134685352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127574297-C-A

http://identifiers.org/hco/2/GRCh38#134685608-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127574521-A-C

134687872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127575319-G-A

134689469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127576256-G-A

134689493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127576291-C-T

134689686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127576473-T-C

134689781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127576568-G-A

134689825-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127576613-C-G

134691081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127577685-A-G

134692921-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127579578-T-A

134692926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127579583-G-T

134692987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127579645-G-T

134693230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127579821-T-C

134693344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127579928-T-C

http://identifiers.org/hco/2/GRCh38#134693491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127580008-C-A

http://identifiers.org/hco/2/GRCh38#134693638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127580065-C-A

134693638-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127580065-C-G

134693719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127580153-T-C

134693739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127580173-A-G

134693970-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127580425-A-T

http://identifiers.org/hco/2/GRCh38#134694138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127580587-C-A

134694271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127580682-G-T

134694312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127580728-A-G

134694398-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127581783-A-T

134694582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127582005-C-T

134694782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127582197-T-C

134705717-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127588785-G-C

134706040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127589070-G-A

134706044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127589074-G-A

134706183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127589216-C-T

134706220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127589243-G-T

134706465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127589519-C-T

134706598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127589653-G-T

134706687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, undefined
orthologous variants: 127590204-G-A

134706815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127590334-G-A

134706945-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127590458-G-C

134707224-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127590682-T-G

134707225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127590683-G-A

http://identifiers.org/hco/2/GRCh38#134708568-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127592696-A-C

134708661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127592788-A-G

http://identifiers.org/hco/2/GRCh38#134708867-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127592987-A-C

http://identifiers.org/hco/2/GRCh38#134708887-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127593077-A-C

134708910-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127593101-C-G

134709020-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127593642-T-G

134709173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127593795-C-T

134711696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127594823-T-C

134711737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127594863-G-A

134711944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127595067-A-G

134712118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127595242-G-A

134712240-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127595362-T-A

http://identifiers.org/hco/2/GRCh38#134712337-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127595444-A-C

134712337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127595444-A-G

134712464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127595648-A-G

134712486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127595671-G-A

134712894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127596076-C-T

http://identifiers.org/hco/2/GRCh38#134713014-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127596192-A-C

134713398-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127596587-A-T

134713444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127596631-G-A

134713444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127596631-G-T

134713488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127596692-C-T

134713727-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127596895-T-G

134713760-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127596928-G-C

134713760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127596928-G-T

134714164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127597632-A-G

134714184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127597652-T-C

134714358-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127598115-A-T

134714363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127598120-T-C

134714376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127598133-C-T

134714824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127600450-G-A

134714911-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127600533-C-G

134714911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127600533-C-T

134715082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127601194-G-T

http://identifiers.org/hco/2/GRCh38#134715125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127601237-C-A

134715622-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127602024-T-G

134715922-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127602292-C-G

134715969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127602321-G-A

134716160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127602616-G-A

134716160-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127602616-G-C

134716274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127602894-G-T

134716342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127602967-T-C

134716650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127603258-C-T

134716876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127603456-C-T

134717750-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron variant
orthologous variants: 127604360-C-G

134718113-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127604693-C-G

http://identifiers.org/hco/2/GRCh38#134718145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127604725-C-A

134718618-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127605082-C-G

134718618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127605082-C-T

134718672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127605125-G-A

134718672-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127605125-G-C

134718672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127605125-G-T

134718788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 127605222-G-A

134718788-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 127605222-G-C

134718788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 127605222-G-T

134718856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 127605284-G-A

134718856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 127605284-G-T

http://identifiers.org/hco/2/GRCh38#134718876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127605304-C-A

134718876-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 127605304-C-G

134718876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25380
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 127605304-C-T