http://identifiers.org/hco/6/GRCh38#40334806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49483157-C-A

40334806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: non coding transcript exon variant
orthologous variants: 49483157-C-T

http://identifiers.org/hco/6/GRCh38#40334850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49483115-C-A

http://identifiers.org/hco/6/GRCh38#40334863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49483097-C-A

40334898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: non coding transcript exon variant
orthologous variants: 49483063-G-T

40335073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: non coding transcript exon variant
orthologous variants: 49482893-T-C

40335116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: non coding transcript exon variant
orthologous variants: 49482850-T-C

40335135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49482829-G-T

40335160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49482808-A-G

http://identifiers.org/hco/6/GRCh38#40335220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49482735-C-A

40335220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49482735-C-T

40335316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49482648-C-T

40335338-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49482627-T-A

40335855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49482168-G-A

40335871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49482149-G-A

40335871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49482149-G-T

40335932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49482089-A-G

40336147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49481884-C-T

40336288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49481734-T-C

40336451-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49480682-C-G

40336527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49480611-G-A

40336875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49480369-A-G

40336901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49480347-G-A

40337073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49480194-A-G

http://identifiers.org/hco/6/GRCh38#40337094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49480163-C-A

40337094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49480163-C-T

40337097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49480160-G-A

40337121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: non coding transcript exon variant
orthologous variants: 49480137-C-T

40337339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49479938-A-G

40337341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49479936-T-C

40337386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49479892-C-T

40338219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49479382-G-A

40338238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49479363-A-G

40338356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49479266-G-A

40338404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49479234-T-C

40338483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49479132-T-C

40338556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49479070-A-G

40338585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49479048-G-A

40338608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49479025-G-A

40339334-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49478147-T-A

40339390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49478099-T-C

40339761-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49477889-A-T

40339777-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49477876-T-A

http://identifiers.org/hco/6/GRCh38#40340442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49477100-C-A

40340442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49477100-C-T

40340461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49477088-G-A

40340492-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49477058-T-A

40340492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49477058-T-C

40340530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49477020-G-A

40340530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49477020-G-T

http://identifiers.org/hco/6/GRCh38#40340559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49476991-C-A

40340589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49476965-T-C

40340754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49476811-G-A

40340814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49476752-T-C

40341122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49475681-C-T

40341234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49475591-G-A

40341234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49475591-G-T

40341571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49475312-C-T

40341719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49475097-C-T

40341980-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49465633-G-C

40342053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49465575-A-G

40342087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49465543-T-C

40342194-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49465412-C-G

40342318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49465325-A-G

http://identifiers.org/hco/6/GRCh38#40342320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49465323-C-A

40342320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49465323-C-T

40342363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49465280-C-T

40342377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49465268-C-T

40342433-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49465199-G-C

40342442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49465190-C-T

40342552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49465085-C-T

http://identifiers.org/hco/6/GRCh38#40342650-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49465026-A-C

40342765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49464902-A-G

40343164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49464586-G-A

40343164-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49464586-G-C

40343164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49464586-G-T

40343255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49464513-T-C

http://identifiers.org/hco/6/GRCh38#40343386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49464382-C-A

40343430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49464321-C-T

40343850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49463214-A-G

40344064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49463057-C-T

40344079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49463042-G-A

40344202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49462946-T-C

http://identifiers.org/hco/6/GRCh38#40344212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49462934-C-A

40344282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49462886-G-A

40344282-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49462886-G-C

40344282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49462886-G-T

40344329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49462858-G-T

http://identifiers.org/hco/6/GRCh38#40344335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49462853-C-A

http://identifiers.org/hco/6/GRCh38#40344337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49462851-C-A

40344337-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49462851-C-G

40344367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49462823-G-T

40344403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49462788-G-A

http://identifiers.org/hco/6/GRCh38#40344406-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49462785-A-C

40344438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49462757-T-C

40344513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49462698-A-G

40344531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49462689-G-A

40344569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49462652-T-C

40344610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49462612-A-G

40344613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49462609-A-G

40344762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 49462455-A-G

40344797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49462422-A-G

40344802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49462414-C-T

40344813-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49462403-T-A

40344850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49462369-G-A

http://identifiers.org/hco/6/GRCh38#40344876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49462340-C-A

40344876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49462340-C-T

40344883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49462334-A-G

40345025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49462180-T-C

40345064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49462142-C-T

40345146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49461956-C-T

40345237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49461815-T-C

40345237-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49461815-T-G

40345239-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49461812-G-C

40345239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49461812-G-T

40345273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 49461729-C-T

40345444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 49461554-C-T

40345492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49461503-T-C

http://identifiers.org/hco/6/GRCh38#40345890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49461104-C-A

40345915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49461080-T-C

40345920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49461074-G-A

40345920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49461074-G-T

40345997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49461003-T-C

40346206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49460867-G-T

40346827-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49460644-T-G

40348334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49459057-C-T

40348359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49459032-G-A

40348419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49458973-C-T

40348457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49458940-A-G

40348506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49458907-A-G

40348570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49458853-A-G

40348604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49458820-C-T

40349073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49458454-C-T

40349342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49458223-T-C

40349380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49458189-C-T

40349385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49458185-T-C

http://identifiers.org/hco/6/GRCh38#40349463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49458108-C-A

40349463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49458108-C-T

40349754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49457825-A-G

http://identifiers.org/hco/6/GRCh38#40349838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49457746-C-A

40349838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49457746-C-T

40350008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49457578-G-A

40350008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49457578-G-T

40355777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49454258-G-A

40355999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49454101-G-A

40356188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49453915-G-A

40356281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49453818-C-T

40356293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49453806-G-A

40356299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49453800-G-A

40356308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49453791-C-T

40356331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49453766-G-T

40356361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49453732-G-A

40356361-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49453732-G-C

40356419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49453679-C-T

40356441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49453657-G-A

40356452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49453646-A-G

40356804-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49452788-G-C

40357123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49452505-A-G

40357234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49452407-G-A

40357432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49452257-C-T

40357459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49452224-G-T

40377492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49421253-T-C

40377841-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49420909-G-C

40377841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49420909-G-T

40377872-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49420877-T-A

40378040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 49420746-T-C

40378293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 49420586-G-A

40378293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 49420586-G-T

40378382-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49420502-T-A

40378382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49420502-T-C

40378443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 49420442-G-A

40378443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 49420442-G-T

http://identifiers.org/hco/6/GRCh38#40378821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49420178-C-A

40378821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49420178-C-T

http://identifiers.org/hco/6/GRCh38#40378838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49420172-C-A

40378838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49420172-C-T

40378867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49420143-T-C

40378907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49420103-T-C

40379051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49420026-A-G

40379277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 49419880-T-C

40379311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: non coding transcript exon variant
orthologous variants: 49419840-A-G

40379326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: non coding transcript exon variant
orthologous variants: 49419827-G-A

40379360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: non coding transcript exon variant
orthologous variants: 49419789-G-T

http://identifiers.org/hco/6/GRCh38#40379401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49419715-C-A

40379401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: non coding transcript exon variant
orthologous variants: 49419715-C-T

40379419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: non coding transcript exon variant
orthologous variants: 49419697-G-A

40379419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: non coding transcript exon variant
orthologous variants: 49419697-G-T

40379425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: non coding transcript exon variant
orthologous variants: 49419691-G-A

40379425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: non coding transcript exon variant
orthologous variants: 49419691-G-T

40379436-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49419677-T-A

40379483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49419629-C-T

40379605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49419545-G-T

40379668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49419522-T-C

http://identifiers.org/hco/6/GRCh38#40379691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49419500-C-A

40379714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49419478-A-G

http://identifiers.org/hco/6/GRCh38#40380000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49419221-C-A

40380699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49417956-T-C

http://identifiers.org/hco/6/GRCh38#40380717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49417938-C-A

40380781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49417873-G-T

40380788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49417866-G-A

http://identifiers.org/hco/6/GRCh38#40380823-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49417831-A-C

40380966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49417695-T-C

40381533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49416232-C-T

40382071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49415530-C-T

40382399-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49415201-T-G

40382685-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49414933-T-G

40382912-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49414789-G-C

40382912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49414789-G-T

40382930-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49414781-T-G

40384190-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49413382-C-G

40384190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49413382-C-T

40384391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49412575-G-T

40384473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49412510-G-A

40384886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49412129-G-A

40384886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49412129-G-T

40384894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49412120-C-T

40385025-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49411984-T-G

40385200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49411644-T-C

40385283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49411583-A-G

40385329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49411537-A-G

40385660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49411033-C-T

40385798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49410931-C-T

40385857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49410880-T-C

40385857-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49410880-T-G

http://identifiers.org/hco/6/GRCh38#40386100-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49410268-A-C

40386165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49410198-G-T

40386317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49410055-T-C

40386501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: non coding transcript exon variant
orthologous variants: 49409876-C-T

40386503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: non coding transcript exon variant
orthologous variants: 49409875-G-A

40386514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: non coding transcript exon variant
orthologous variants: 49409864-T-C

40386587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: non coding transcript exon variant
orthologous variants: 49409790-A-G

40386843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49409118-G-A

40386843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49409118-G-T

40386902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49409062-A-G

40386912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49409052-C-T

40386971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49408993-C-T

40387033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49408937-G-A

40387523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43642
most severe consequence: non coding transcript exon variant
orthologous variants: 49408490-T-C