42704753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121623640-G-T

42704778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121623659-A-G

42704778-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121623659-A-T

42704779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121623660-G-A

42704779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121623660-G-T

http://identifiers.org/hco/3/GRCh38#42704998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121623824-C-A

42705066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121623864-G-A

42705066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121623864-G-T

42705208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121623910-T-C

42705359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121624021-G-A

42706739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121625467-T-C

42706908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121625602-A-G

42706926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121625620-G-T

42707099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121625740-A-G

42707368-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121625974-T-A

42707412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121626018-T-C

42707602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121626089-G-A

42708089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121626448-C-T

http://identifiers.org/hco/3/GRCh38#42708175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121626505-C-A

42708416-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121626721-A-T

42708470-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121626761-T-G

42708547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121626814-G-A

42708547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121626814-G-T

42708609-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121626878-A-T

http://identifiers.org/hco/3/GRCh38#42708705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121626971-C-A

42708705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121626971-C-T

42708711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121626977-T-C

42708831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121627057-G-A

42708831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121627057-G-T

42708833-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121627059-T-A

42708833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121627059-T-C

http://identifiers.org/hco/3/GRCh38#42708834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121627060-C-A

42708834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121627060-C-T

42708844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121627064-G-T

42708855-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121627075-G-C

42708855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121627075-G-T

42708864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121627085-G-T

42709042-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121627208-G-C

http://identifiers.org/hco/3/GRCh38#42709162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121627329-C-A

42709566-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121627972-A-T

42709576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121627985-T-C

42709577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121627986-G-A

42709577-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121627986-G-C

42709577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121627986-G-T

42709609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121628021-C-T

42709611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121628023-C-T

42709746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121628154-G-A

http://identifiers.org/hco/3/GRCh38#42709866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121628263-C-A

42709866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121628263-C-T

42709886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121628269-G-A

42709886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121628269-G-T

42709891-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121628274-T-G

42709920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121628288-G-A

42709920-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121628288-G-C

42709920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121628288-G-T

http://identifiers.org/hco/3/GRCh38#42709947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121628309-C-A

42709947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121628309-C-T

42710029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121628384-G-A

42710029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121628384-G-T

42713009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121629473-A-G

42713084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121629518-A-G

42713085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121629519-G-A

42713085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121629519-G-T

http://identifiers.org/hco/3/GRCh38#42713265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121629666-C-A

42713289-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121629690-C-G

42713289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121629690-C-T

42713364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121629758-C-T

42713401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121629791-G-A

42713401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121629791-G-T

42713435-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121629829-T-A

42713435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121629829-T-C

http://identifiers.org/hco/3/GRCh38#42713447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121629841-C-A

42713447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121629841-C-T

42713744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121630110-G-A

42713957-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121630354-A-T

http://identifiers.org/hco/3/GRCh38#42714039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121630414-C-A

42714039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121630414-C-T

http://identifiers.org/hco/3/GRCh38#42714064-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121630429-A-C

42714064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121630429-A-G

http://identifiers.org/hco/3/GRCh38#42714124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121630470-C-A

42714132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121630476-T-C

42714171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121630515-G-T

42714409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121630665-T-C

42714414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121630670-T-C

http://identifiers.org/hco/3/GRCh38#42714478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121630719-C-A

42714538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121630788-G-T

http://identifiers.org/hco/3/GRCh38#42723839-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121633419-A-C

http://identifiers.org/hco/3/GRCh38#42723842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121633422-C-A

42724040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121633616-C-T

http://identifiers.org/hco/3/GRCh38#42728933-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121636069-A-C

42729392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121636412-A-G

http://identifiers.org/hco/3/GRCh38#42729583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121636543-C-A

42729750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121636641-G-T

42729885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121636774-G-A

42730023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121636902-G-A

42730023-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121636902-G-C

http://identifiers.org/hco/3/GRCh38#42730353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121637140-C-A

42730353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121637140-C-T

42730686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121637426-G-A

42730686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121637426-G-T

42730687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121637427-G-A

42730687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121637427-G-T

42730767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121637514-G-T

42732334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121637693-C-T

42732511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121637842-G-T

http://identifiers.org/hco/3/GRCh38#42732514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121637845-C-A

42732514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121637845-C-T

42732517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121637848-A-G

42732541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121637883-A-G

42732686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121637999-G-T

42732693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121638005-T-C

42732693-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121638005-T-G

42733049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121638285-G-A

42733049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121638285-G-T

42733068-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121638293-G-C

42733068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121638293-G-T

42733094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121638340-G-T

http://identifiers.org/hco/3/GRCh38#42733107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#121638353-C-A

42733213-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121638428-T-G

42733320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121638513-G-A

42733320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121638513-G-T

http://identifiers.org/hco/3/GRCh38#42733350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121638542-C-A

42733380-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121639062-G-C

42733380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121639062-G-T

42733666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121639344-G-A

42733670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121639348-G-T

42733874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121639518-G-A

42734948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121640272-C-T

42735570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121642236-A-G

42735570-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121642236-A-T

42735594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121642260-G-A

42735594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121642260-G-T

42735603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121642268-G-T

42735725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 121642370-G-A

42735725-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121642370-G-C

42735744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121642389-C-T

42735845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 121642490-G-A

42735851-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 121642496-T-A

42735937-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121642581-G-C

42735937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121642581-G-T

42735970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121642616-G-A

42735970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121642616-G-T

42736033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121642694-G-A

42736215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121642830-G-T

42736270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121642856-G-A

42736284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121642861-C-T

42739803-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121643405-G-C

http://identifiers.org/hco/3/GRCh38#42739878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121643471-C-A

http://identifiers.org/hco/3/GRCh38#42739904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121643497-C-A

http://identifiers.org/hco/3/GRCh38#42739951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121643540-C-A

42739951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121643540-C-T

http://identifiers.org/hco/3/GRCh38#42742762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121645608-C-A

42742762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121645608-C-T

42742816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121645620-A-G

42742861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121645638-C-T

42742868-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121645645-C-G

42742869-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121645646-C-G

42742869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121645646-C-T

42742941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121645704-C-T

42742973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121645736-G-A

42743037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121645800-T-C

http://identifiers.org/hco/3/GRCh38#42743154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121645915-C-A

42743154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121645915-C-T

42743384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121646229-A-G

42743384-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121646229-A-T

42743580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121646425-G-A

42743580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121646425-G-T

http://identifiers.org/hco/3/GRCh38#42745002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121647749-C-A

42745002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121647749-C-T

http://identifiers.org/hco/3/GRCh38#42745042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121647789-C-A

42745089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121647816-T-C

42745119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121647845-A-G

http://identifiers.org/hco/3/GRCh38#42745242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121647976-C-A

http://identifiers.org/hco/3/GRCh38#42745268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121648000-C-A

42745268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121648000-C-T

42745275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121648006-A-G

42745339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121648090-A-G

42745398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121648148-C-T

http://identifiers.org/hco/3/GRCh38#42745428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121648178-C-A

42745428-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121648178-C-G

42745428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121648178-C-T

42745533-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121648280-T-G

http://identifiers.org/hco/3/GRCh38#42745567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121648298-C-A

http://identifiers.org/hco/3/GRCh38#42745619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121648346-C-A

http://identifiers.org/hco/3/GRCh38#42745669-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121648391-A-C

42745677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121648399-G-A

42745677-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121648399-G-C

42745677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121648399-G-T

http://identifiers.org/hco/3/GRCh38#42745787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121648486-C-A

42745787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121648486-C-T

42745870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121648537-G-A

42745985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121648623-G-A

http://identifiers.org/hco/3/GRCh38#42746118-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121648777-A-C

42746133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121648792-G-A

42746133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121648792-G-T

42746223-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121648866-T-A

42746223-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121648866-T-G

42746399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121649001-A-G

42746455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121649048-T-C

42746587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121649164-T-C

42746710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121649267-G-T

42746811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121649340-T-C

http://identifiers.org/hco/3/GRCh38#42746872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121649407-C-A

42746872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121649407-C-T

42746962-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121649500-C-G

42746962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121649500-C-T

42746966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121649504-G-A

42746966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121649504-G-T

42747004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121649537-G-A

42747004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121649537-G-C

42747004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121649537-G-T

42747029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121649552-G-A

42747029-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121649552-G-C

42747029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121649552-G-T

42747162-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121649633-T-A

42747162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121649633-T-C

42747195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121649664-C-T

http://identifiers.org/hco/3/GRCh38#42747471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121649946-C-A

42747475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121649950-G-T

http://identifiers.org/hco/3/GRCh38#42747511-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121649968-A-C

42747511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121649968-A-G

http://identifiers.org/hco/3/GRCh38#42747512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121649969-C-A

42747710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121650145-G-A

42747908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121650328-G-A

http://identifiers.org/hco/3/GRCh38#42747951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121650364-C-A

42748366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121651028-G-A

42748414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121651085-C-T

42748501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121651167-C-T

42748816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121651423-A-G

http://identifiers.org/hco/3/GRCh38#42749099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121651464-C-A

42749474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121651725-A-G

42749475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121651726-G-A

http://identifiers.org/hco/3/GRCh38#42749694-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#121651859-A-C

42749870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121652012-G-A

42749910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121652036-G-A

42749910-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121652036-G-C

42749957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 121652079-G-A

42749993-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121652104-G-C

42749999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121652110-G-A

42749999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121652110-G-T

42750026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121652137-G-T

42750134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121652237-T-C

http://identifiers.org/hco/3/GRCh38#42750141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121652244-C-A

42750164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121652258-C-T

42750942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121652738-C-T

42750987-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121652774-A-T

42751001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121652788-C-T

42751114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121652856-C-T

42751123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121652865-G-T

42751190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121652929-G-A

42751215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121652951-C-T

42751368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121653109-C-T

42751512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121653647-T-C

42751753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121653885-G-A

42751819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121653946-G-A

42751819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121653946-G-T

http://identifiers.org/hco/3/GRCh38#42751960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121654058-C-A

42751960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121654058-C-T

http://identifiers.org/hco/3/GRCh38#42751998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121654096-C-A

42751998-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121654096-C-G

42751998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121654096-C-T

http://identifiers.org/hco/3/GRCh38#42752039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121654137-C-A

42752039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121654137-C-T

42752071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121654173-C-T

42752291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121654377-T-C

42752541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121656266-C-T

42752578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121656302-C-T

42752597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121656321-C-T

42752713-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121656437-T-A

42752713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121656437-T-C

http://identifiers.org/hco/3/GRCh38#42752809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121656545-C-A

42752824-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121656560-A-T

http://identifiers.org/hco/3/GRCh38#42752848-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121656578-A-C

42752848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121656578-A-G

http://identifiers.org/hco/3/GRCh38#42752849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121656579-C-A

42752849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121656579-C-T

http://identifiers.org/hco/3/GRCh38#42753106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121656761-C-A

42755794-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121659100-T-A

42755809-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121659115-C-G

42755809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121659115-C-T

http://identifiers.org/hco/3/GRCh38#42755878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#121659187-C-A

42755893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121659189-C-T

42756352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121659613-C-T

42757058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 121659935-G-T

42757271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121660135-G-T

http://identifiers.org/hco/3/GRCh38#42757278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121660142-C-A

http://identifiers.org/hco/3/GRCh38#42758199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121662867-C-A

42758199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121662867-C-T

42758396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121663051-G-A

42758396-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121663051-G-C

42758396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121663051-G-T

http://identifiers.org/hco/3/GRCh38#42758430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121663078-C-A

42758478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121663100-A-G

42758483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121663105-G-A

42758523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121663133-T-C

42758537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121663147-C-T

42758670-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121663223-T-G

42773033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121668302-G-T

http://identifiers.org/hco/3/GRCh38#42773034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121668303-C-A

42773041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121668310-C-T

42773098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121668373-G-A

42773098-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121668373-G-C

42773140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121668425-T-C