http://identifiers.org/hco/11/GRCh38#122655834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#41068894-C-A

122655834-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41068894-C-G

122655834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41068894-C-T

122655841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41068887-G-A

122655841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41068887-G-T

http://identifiers.org/hco/11/GRCh38#122655957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#41068798-C-A

122655957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41068798-C-T

http://identifiers.org/hco/11/GRCh38#122655980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#41068786-C-A

122655980-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41068786-C-G

122655980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41068786-C-T

122656573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41068350-G-T

122656829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41068079-G-A

122657068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41067831-G-A

http://identifiers.org/hco/11/GRCh38#122657118-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#41067798-A-C

122657263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41067673-C-T

122658802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41066832-C-T

122658849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41066781-T-C

122659080-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41066575-G-C

http://identifiers.org/hco/11/GRCh38#122659504-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#41065169-A-C

122659647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41064990-G-A

122659994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41064716-A-G

122660032-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41064681-T-G

122660057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41064656-G-A

122660309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41064456-G-A

122660476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41064286-T-C

122660490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41064272-C-T

122660552-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41064223-A-T

122660646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41064141-G-A

122660699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41064092-T-C

122660817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41063604-T-C

122661139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41063198-G-A

122661225-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41063120-G-C

122661352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41063000-G-A

122661356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41062996-C-T

122661710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41062657-G-A

122662808-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41061925-T-A

122663323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41061738-G-A

122663482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41061590-C-T

122663547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41061543-G-A

http://identifiers.org/hco/11/GRCh38#122663890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#41061172-C-A

http://identifiers.org/hco/11/GRCh38#122664849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#41060107-C-A

122664849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41060107-C-T

http://identifiers.org/hco/11/GRCh38#122664866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#41060085-C-A

http://identifiers.org/hco/11/GRCh38#122664889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#41060059-C-A

122665735-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41059222-A-T

122665908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41059057-T-C

122666037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41058927-A-G

122666096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41058870-G-A

122666096-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41058870-G-C

122666256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41058724-G-A

122668378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41056994-G-A

http://identifiers.org/hco/11/GRCh38#122668741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#41055571-C-A

http://identifiers.org/hco/11/GRCh38#122668785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#41055508-C-A

122669465-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41054736-T-A

122669523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41054692-C-T

122669525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41054690-T-C

122669526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41054689-G-A

122669555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41054659-G-T

122669557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41054657-C-T

122669909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41052840-A-G

122669937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41052813-T-C

122669959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41052791-A-G

122669990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41052760-A-G

122670048-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41052702-C-G

122670058-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41052692-G-C

122670058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41052692-G-T

122670107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41052646-A-G

122670137-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41052625-C-G

122670235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41052564-A-G

122670266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41052534-C-T

122670380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41052426-C-T

122670457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41052350-C-T

122670521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41052278-G-A

122670568-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41052231-G-C

122671535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41051044-G-A

122671566-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41051014-G-C

122671640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41050950-G-T

122671793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41050883-T-C

122671862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41050813-G-T

122672806-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41050240-A-T

122672973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41050098-C-T

122673041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41050042-G-A

122675268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41048321-T-C

122675268-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41048321-T-G

122675552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41048050-G-T

122675931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41047731-C-T

122676778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41047364-C-T

122678235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41045463-C-T

122678310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41045371-C-T

122678312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41045369-C-T

122678394-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41045280-T-G

122678442-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41045232-T-A

122678442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41045232-T-C

122678442-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41045232-T-G

122678557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41045121-C-T

http://identifiers.org/hco/11/GRCh38#122678645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#41045027-C-A

122678645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41045027-C-T

122678682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41044990-G-A

http://identifiers.org/hco/11/GRCh38#122678808-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#41044874-A-C

122678959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41044740-A-G

122679052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41044648-G-A

122680887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41042870-T-C

122680928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41042829-G-A

122680928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41042829-G-T

122681138-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41042479-C-G

122681155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41042464-G-A

122681482-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41042015-C-G

122681563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41041962-C-T

122682016-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41041444-T-G

122682214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41041202-T-C

122682267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41041137-A-G

http://identifiers.org/hco/11/GRCh38#122682279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#41041125-C-A

122682390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41041012-A-G

122685565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41038951-G-T

http://identifiers.org/hco/11/GRCh38#122685616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#41038887-C-A

122685693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41038811-T-C

122686256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41038252-G-T

122686408-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41038121-A-T

122686434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41038095-C-T

122686567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41037969-G-A

122686830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41037764-T-C

122687729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41035897-G-A

122687785-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41035847-C-G

http://identifiers.org/hco/11/GRCh38#122687880-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#41035753-A-C

122687880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41035753-A-G

122690364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41034795-A-G

122690386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41034773-C-T

122690472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41034690-T-C

122690671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41034476-C-T

122691112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41034009-A-G

122691547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41033505-C-T

122691562-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41033490-T-G

122691727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41033321-A-G

122691829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41033221-C-T

122691894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41033153-G-A

122692041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41033020-G-T

122692071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41032991-A-G

122692120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41032949-T-C

122694908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41031233-T-C

122695089-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-G

122695138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

122695138-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-T

122695253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

122695805-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41029991-C-G

http://identifiers.org/hco/11/GRCh38#122696758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#41029636-C-A

122697837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41028886-G-T

122697909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41028954-C-T

122698141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41029177-G-A

122698146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41029182-G-A

122698213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41029217-C-T

http://identifiers.org/hco/11/GRCh38#122698248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#41029253-C-A

122698272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41029277-C-T

122698538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41028522-G-A

122698643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41028429-A-G

122700027-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41027355-A-T

122701025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41026186-T-C

122701025-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41026186-T-G

122701092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41026135-G-A

122701390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41025862-A-G

http://identifiers.org/hco/11/GRCh38#122701841-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#41025473-A-C

122702135-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41025381-T-G

122702460-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41025161-T-G

122702461-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41025160-G-C

122703787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41024703-A-G

122704387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41023817-G-A

122704484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41023738-C-T

122704595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41023595-T-C

122704748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41023407-G-T

122704807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41023348-T-C

122704851-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41023335-T-G

http://identifiers.org/hco/11/GRCh38#122705118-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#41023081-A-C

122705751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41022882-T-C

122705777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41022843-A-G

122705911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41022710-A-G

122705937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41022683-T-C

122705961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41022658-G-A

122705989-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41022628-C-G

122706021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41022591-A-G

122706044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41022568-A-G

122706048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41022564-T-C

122706091-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41022475-C-G

122706091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41022475-C-T

http://identifiers.org/hco/11/GRCh38#122706146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#41022368-C-A

122706146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41022368-C-T

122706288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41022327-G-A

122706479-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41021852-C-G

122706479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41021852-C-T

122706502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41021829-A-G

122706571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41021764-G-A

122706706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41021696-C-T

122706717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41021685-G-A

122706717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41021685-G-T

122706738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41021662-G-A

122706829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41021556-C-T

122707142-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41021270-A-T

122707163-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41021252-C-G

122707163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41021252-C-T

122707292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41021115-C-T

122707301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41021106-A-G

122707430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41020980-G-A

122707430-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41020980-G-C

http://identifiers.org/hco/11/GRCh38#122708165-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#41020550-A-C

http://identifiers.org/hco/11/GRCh38#122708194-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#41020529-A-C

122712087-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41019964-A-T

122712530-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41019539-G-C

122712553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41019518-T-C

122712643-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41019420-C-G

122712756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41019334-C-T

122712864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41019237-C-T

122714533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41019074-G-A

http://identifiers.org/hco/11/GRCh38#122714748-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#41018852-A-C

122714880-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41018728-G-C

http://identifiers.org/hco/11/GRCh38#122715288-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#41018638-A-C

122715388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41018528-A-G

122715539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41018367-T-C

122715712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41018201-A-G

122715712-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41018201-A-T

http://identifiers.org/hco/11/GRCh38#122715801-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#41018121-A-C

122715919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41018025-T-C

122715945-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41018001-T-G

122715994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41017964-C-T

122716779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41017612-G-A

122716908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41017499-T-C

122716929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41017480-A-G

122717045-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41017376-T-G

http://identifiers.org/hco/11/GRCh38#122717080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#41017348-C-A

122717091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41017337-T-C

122717109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41017321-G-T

122717255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41017187-C-T

122717282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41017160-C-T

122717612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41016780-A-G

122717673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41016719-T-C

122718414-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41016151-T-G

122719166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41015520-C-T

122719538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41015230-C-T

122719818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41014955-G-A

122720414-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41012783-T-A

122720646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41013191-G-T

122720776-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41013320-T-A

122720902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41013454-C-T

122720974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41013538-G-A

122720974-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41013538-G-C

122720974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41013538-G-T

122721399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41013863-G-A

122721496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41013969-A-G

122721553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41014026-C-T

122722198-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41011736-C-G

122722271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41011668-T-C

122722382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41011560-G-A

122723439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41010946-C-T

122723561-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41010811-G-C

122723619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41010752-G-A

122723844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41010471-G-T

122723852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41010463-A-G

122724114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41010240-A-G

122726848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41009896-G-A

122727373-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41009386-G-C

http://identifiers.org/hco/11/GRCh38#122727668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#41009069-C-A

122727668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41009069-C-T

122728256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41008634-C-T

122728262-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41008628-G-C

122728371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41008527-T-C

122728378-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41008525-T-A

122728378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41008525-T-C

122728507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41008393-C-T

122728897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41008060-C-T

122729100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41007779-T-C

122729236-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41007671-T-G

122730398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41006657-C-T

122731972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41006156-A-G

http://identifiers.org/hco/11/GRCh38#122731990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#41006130-C-A

122732097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41006045-C-T

122732169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41005974-G-A

122732183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41005960-A-G

122732349-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41005852-T-A

122732402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41005797-G-A

122732509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41005517-G-T

122732561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41005466-G-A

122732561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41005466-G-T

122732716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41005321-C-T

122732939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41005061-G-T

122732964-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41005046-A-T

http://identifiers.org/hco/11/GRCh38#122732967-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#41005043-A-C

122732967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41005043-A-G

122732974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41005032-C-T

122732990-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41005016-T-A

122732990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41005016-T-C

122733020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41004989-T-C

122733185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41004372-G-A

122733274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41004288-G-A

122733274-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41004288-G-C

http://identifiers.org/hco/11/GRCh38#122733836-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#41003756-A-C

122734288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41003639-T-C

122734469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41003472-G-A

122734487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41003454-A-G

122734577-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41003379-A-T

122734612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41003344-G-A

122735037-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41002887-C-G

122735037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41002887-C-T

122735604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41002042-A-G

122735648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41001999-C-T

122735674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41001956-A-G

122735748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41001886-G-T

122735817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41001820-T-C

122735820-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41001817-G-C

122735930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41001706-T-C

122735977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41001659-A-G

122735986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41001651-T-C

122736087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41001565-C-T

http://identifiers.org/hco/11/GRCh38#122736137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#41001515-C-A

122736266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41001407-T-C

122736308-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41001365-T-G

http://identifiers.org/hco/11/GRCh38#122739985-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40997484-A-C

122740075-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40997397-T-G

122740140-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40997329-T-A

122740216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40997241-T-C

122740273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40997189-A-G

122741408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40996471-C-T

http://identifiers.org/hco/11/GRCh38#122741536-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40996376-A-C

122741554-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40996358-G-C

122741561-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40996351-C-G

122741561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40996351-C-T

122741613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40996310-C-T

122741681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40996233-A-G

http://identifiers.org/hco/11/GRCh38#122741895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40996049-C-A

122742151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40995844-G-A

122742173-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40995822-C-G

122742399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40995608-A-G

122742632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40995406-C-T

http://identifiers.org/hco/11/GRCh38#122742657-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40995382-A-C

122742735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40995308-T-C

122743135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40994628-T-C

122743945-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40994447-G-C

http://identifiers.org/hco/11/GRCh38#122744140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40994269-C-A

122744140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40994269-C-T

122744373-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40994060-C-G

122744485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40993979-T-C

122744764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40993805-C-T

122745108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40993614-G-A

122745421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40993328-G-A

122745421-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40993328-G-C

122745427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40993322-G-A

122745554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40993188-G-A

122745621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40992982-T-C

122745805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40992802-A-G

122745811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40992796-G-T

122745896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40992720-A-G

122745979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40992656-G-A

122746307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40992506-G-T

122746436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40992398-T-C

122746506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40992380-A-G

122746763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40991919-C-T

122746764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40991918-G-A

122746764-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40991918-G-C

http://identifiers.org/hco/11/GRCh38#122746832-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40991851-A-C

http://identifiers.org/hco/11/GRCh38#122746903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40991768-C-A

122746903-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40991768-C-G

http://identifiers.org/hco/11/GRCh38#122746963-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40991703-A-C

122747002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40991667-G-A

122747363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40991342-A-G

122747554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40991005-C-T

122747735-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40990789-T-G

122747829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40990697-T-C

122748087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40990447-A-G

122748383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40990346-A-G

http://identifiers.org/hco/11/GRCh38#122748501-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40990313-A-C

122748708-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40990120-G-C

122748708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40990120-G-T

122748851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40989999-T-C

122749049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40989875-A-G

122749663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40989289-T-C

122751286-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40987879-C-G

122751364-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40987787-G-C

122751418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40987744-G-A

122751453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40987709-G-T

http://identifiers.org/hco/11/GRCh38#122751501-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40987666-A-C

122751835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40987335-C-T

122752089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40987115-A-G

http://identifiers.org/hco/11/GRCh38#122752126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40987084-C-A

122752126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40987084-C-T

122752268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40986669-C-T

122754496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40985190-G-T

122754585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40985106-G-T

122754676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40985035-A-G

122754871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40984840-A-G

122754980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40984735-G-A

122755068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40984645-C-T

http://identifiers.org/hco/11/GRCh38#122755095-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40984609-A-C

122755109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40984602-A-G

122755345-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40984391-T-A

122755355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40984381-G-A

122755871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40983862-A-G

122755877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40983856-A-G

122755945-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40983790-T-A

122755945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40983790-T-C

122756042-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40983693-A-T

122756069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40983666-A-G

http://identifiers.org/hco/11/GRCh38#122756119-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40983616-A-C

122756124-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40983611-C-G

122756152-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40983583-A-T

122756261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40983477-G-A

122756319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40983426-T-C

122756585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40982213-G-A

122756743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40982073-T-C

122756907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40981917-G-A

122757015-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40981847-G-C

122757681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40980529-C-T

122758057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40980470-G-T

http://identifiers.org/hco/11/GRCh38#122758116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40980410-C-A

122758190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40980344-C-T

122758581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40979958-T-C

122758693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40979868-G-A

122759094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40979445-G-A

122759320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40979240-G-A

122760751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40978631-G-T

122760784-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40978597-T-A

122760942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40978420-T-C

http://identifiers.org/hco/11/GRCh38#122761061-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40978328-A-C

122761061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40978328-A-G

122761144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40978246-T-C

122761144-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40978246-T-G

122761593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40975701-G-A

122762606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40974028-C-T

122762630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40974009-C-T

122762635-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40974004-T-A

122762635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40974004-T-C

122762994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40973654-A-G

122763018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40973633-G-A

122763018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40973633-G-T

122763403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40973252-C-T

122763470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40973222-A-G

122763539-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40973153-T-A

122763652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40973028-G-A

122763795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40972915-A-G

122763795-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40972915-A-T

122763980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40972764-A-G

122764547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40972284-C-T

122764682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40972165-T-C

122764705-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40972142-G-C

122764953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40971895-T-C

122764980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40971868-C-T

http://identifiers.org/hco/11/GRCh38#122764986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40971862-C-A

122765998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40969605-G-A

122765998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40969605-G-T

122766015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40969588-G-T

122766018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40969585-G-A

122766032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40969571-C-T

122766082-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40969541-T-A

122766111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40969513-C-T

122766207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40969438-T-C

122769517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40968495-T-C

122772674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40966192-C-T

http://identifiers.org/hco/11/GRCh38#122773708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40964949-C-A

122773770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40964876-A-G

122774156-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40964552-G-C

122774191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 40964520-C-T

122774193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 40964518-G-A

122774193-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40964518-G-C

122774228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40964491-G-T

122774290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40964430-T-C

http://identifiers.org/hco/11/GRCh38#122774294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40964426-C-A

122774294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40964426-C-T

122774400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40964370-A-G

122774400-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40964370-A-T

122774589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40964187-G-T

122774638-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40964136-T-G

122775052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40963742-A-G

122775226-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40963357-G-C

122775503-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40963141-G-C

122775549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40963088-G-A

http://identifiers.org/hco/11/GRCh38#122775551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40963086-C-A

122775551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40963086-C-T

122775560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40963077-T-C

122775833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40963048-G-T

122775835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40963046-G-A

122775835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40963046-G-T

122775850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40963033-T-C

http://identifiers.org/hco/11/GRCh38#122775851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40963032-C-A

122775851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40963032-C-T

122775855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40963028-T-C

122775888-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40962995-G-C

http://identifiers.org/hco/11/GRCh38#122775975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40962907-C-A

122775975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40962907-C-T

http://identifiers.org/hco/11/GRCh38#122775979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40962897-C-A

122775979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40962897-C-T

http://identifiers.org/hco/11/GRCh38#122776010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40962866-C-A

122776010-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40962866-C-G

122776018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40962858-A-G

122776018-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40962858-A-T

122776072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40962816-G-A

122776072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40962816-G-T

http://identifiers.org/hco/11/GRCh38#122776097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40962791-C-A

http://identifiers.org/hco/11/GRCh38#122776104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40962784-C-A

122776104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40962784-C-T

122776106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40962782-G-A

122776106-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40962782-G-C

122776106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40962782-G-T

122776120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40962764-A-G

122776281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40962602-G-A

122776299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40962584-A-G

122776358-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40962526-T-A

122776358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40962526-T-C

http://identifiers.org/hco/11/GRCh38#122776400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40962498-C-A

122776400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40962498-C-T

122776401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40962497-A-G

122776401-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40962497-A-T

http://identifiers.org/hco/11/GRCh38#122776406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40962492-C-A

122776406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40962492-C-T

122776552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40962352-G-A

122776585-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40962319-G-C

122776598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40962306-C-T

122776850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40962071-A-G

122776886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40962036-T-C

122776888-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40962034-T-A

122776888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40962034-T-C

122777154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40961790-G-A

http://identifiers.org/hco/11/GRCh38#122777190-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40961754-A-C

122777225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40961719-C-T

122777249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40961706-C-T

122777254-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40961701-A-T

http://identifiers.org/hco/11/GRCh38#122777285-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40961670-A-C

122777285-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40961670-A-T

122777321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40961632-A-G

122777325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40961628-T-C

122777325-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40961628-T-G

122777341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40961612-A-G

122777341-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40961612-A-T

122777361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40961592-G-A

122777361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40961592-G-T

http://identifiers.org/hco/11/GRCh38#122777486-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40961459-A-C

122777912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40960883-T-C

122778064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40960676-A-G

122778126-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40960626-C-G

http://identifiers.org/hco/11/GRCh38#122778141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40960611-C-A

http://identifiers.org/hco/11/GRCh38#122779101-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40958802-A-C

122779268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40958659-G-A

122779268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40958659-G-T

122779273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40958654-G-A

122779273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40958654-G-T

122779314-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40958558-G-C

122779389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40958482-G-A

122779389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40958482-G-T

122779448-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40958428-T-G

122779450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40958422-C-T

122779456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40958416-C-T

122779462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40958410-G-T

122779770-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40958101-G-C

122779770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40958101-G-T

122779825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40957689-G-A

122779825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40957689-G-T

122779882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40957648-G-A

122779985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40957549-T-C

122780095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40957443-A-G

122780165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40957398-T-C

122781473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40956233-A-G

http://identifiers.org/hco/11/GRCh38#122781495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#40956211-C-A

122781495-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40956211-C-G

122782036-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40955729-T-A

122782481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40955461-A-G

http://identifiers.org/hco/11/GRCh38#122782484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40955458-C-A

122782484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40955458-C-T

http://identifiers.org/hco/11/GRCh38#122782506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40955436-C-A

122782506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40955436-C-T

http://identifiers.org/hco/11/GRCh38#122782510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40955432-C-A

122782510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40955432-C-T

http://identifiers.org/hco/11/GRCh38#122782531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40955413-C-A

122782620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40955334-G-A

122782620-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40955334-G-C

122782620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40955334-G-T

122782635-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40955319-T-A

122782635-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40955319-T-G

122782644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40955311-A-G

122782644-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40955311-A-T

http://identifiers.org/hco/11/GRCh38#122782650-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40955305-A-C

122782650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40955305-A-G

122782684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40955273-G-A

122782684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40955273-G-T

122782685-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40955272-C-G

122782698-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40955259-C-G

122782726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40955231-A-G

122782726-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40955231-A-T

122782774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40955185-G-A

122782774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40955185-G-T

122782879-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40955071-T-A

122782879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40955071-T-C

122782879-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40955071-T-G

http://identifiers.org/hco/11/GRCh38#122782895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40955055-C-A

122782895-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40955055-C-G

122782895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40955055-C-T

122782906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40955045-T-C

http://identifiers.org/hco/11/GRCh38#122782972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40955001-C-A

122782972-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40955001-C-G

http://identifiers.org/hco/11/GRCh38#122782976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40954997-C-A

122782978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40954995-A-G

http://identifiers.org/hco/11/GRCh38#122783058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40954933-C-A

122783088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40954903-G-A

122784571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40953373-A-G

122784814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40953127-A-G

122784872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40953078-G-A

122784925-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40953029-T-G

122784979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40952974-G-A

122786805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40951394-G-A

122786988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40951040-C-T

http://identifiers.org/hco/11/GRCh38#122787001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40951003-C-A

122787002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40951002-C-T

122787040-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40950951-T-A

122787188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40950832-A-G

122787281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40950739-A-G

122787349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40950681-T-C

122787356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40950674-G-A

122787483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40950566-C-T

122787484-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40950565-T-G

122787617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40950277-G-A

122788025-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40949863-A-T

122788114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40949767-G-A

122788794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40949224-G-A

122788837-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40949178-G-C

122788899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40949119-C-T

http://identifiers.org/hco/11/GRCh38#122788974-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40949057-A-C

122788974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40949057-A-G

122788974-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40949057-A-T

122788976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40949055-G-T

122789005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40949026-T-C

122789005-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40949026-T-G

122789007-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40949024-T-G

122789013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40949019-A-G

122789057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40948983-A-G

122789115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40948924-T-C

122789309-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 40948730-G-T

122789499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40948708-C-T

122789520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40948687-C-T

122789594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40948620-C-T

122789602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40948613-C-T

122789916-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40948371-C-G

122790182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40948104-A-G

122790326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40948006-C-T

122790339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40947993-C-T

122790395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40947939-A-G

122790416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40947923-A-G

122790421-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40947918-G-C

122791224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40946615-A-G

122791248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40946592-G-A

122791375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40946493-C-T

122791418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40946453-T-C

122791488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40946392-T-C

122791653-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40946245-C-G

122791696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40946198-A-G

122791749-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40946152-C-G

122791889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40946015-C-T

122792853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40945404-G-A

http://identifiers.org/hco/11/GRCh38#122792931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40945342-C-A

122793499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40943774-T-C

http://identifiers.org/hco/11/GRCh38#122793660-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40943634-A-C

122793660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40943634-A-G

122793662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40943632-T-C

122793784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40943510-G-A

122793965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40943337-C-T

122794164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40943122-T-C

http://identifiers.org/hco/11/GRCh38#122794579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40943026-C-A

122794579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40943026-C-T

http://identifiers.org/hco/11/GRCh38#122794583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40943022-C-A

122794583-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40943022-C-G

122794583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40943022-C-T

122794605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40943002-G-T

122794736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40942873-T-C

122794737-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40942872-C-G

http://identifiers.org/hco/11/GRCh38#122794742-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40942867-A-C

122794742-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40942867-A-T

122794751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40942858-G-A

122794760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 40942849-T-C

122794844-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40942765-A-T

122794964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40942479-A-G

http://identifiers.org/hco/11/GRCh38#122794965-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40942478-A-C

122795148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40942319-T-C

122795148-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40942319-T-G

122795176-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40942262-G-C

122795413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40942007-A-G

122795813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40941393-G-T

http://identifiers.org/hco/11/GRCh38#122795825-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40941377-A-C

122795984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40941259-T-C

122795987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40941256-T-C

http://identifiers.org/hco/11/GRCh38#122795993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40941250-C-A

122796012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40941231-G-T

http://identifiers.org/hco/11/GRCh38#122796046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40941154-C-A

122796046-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40941154-C-G

122796334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40939962-A-G

122796335-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40939961-C-G

122796335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40939961-C-T

122796596-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40939707-T-A

122796597-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40939706-C-G

http://identifiers.org/hco/11/GRCh38#122796766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40939567-C-A

122796773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40939560-T-C

122796773-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40939560-T-G

http://identifiers.org/hco/11/GRCh38#122796787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40939546-C-A

122796787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40939546-C-T

http://identifiers.org/hco/11/GRCh38#122796931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40939413-C-A

122796931-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40939413-C-G

122796979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40939365-T-C

http://identifiers.org/hco/11/GRCh38#122797096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40939256-C-A

122797096-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40939256-C-G

122797096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40939256-C-T

122797101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40939251-G-A

122797113-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40939240-A-T

http://identifiers.org/hco/11/GRCh38#122797114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40939239-C-A

122797114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40939239-C-T

http://identifiers.org/hco/11/GRCh38#122797152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40939209-C-A

http://identifiers.org/hco/11/GRCh38#122797160-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40939199-A-C

122797160-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40939199-A-T

http://identifiers.org/hco/11/GRCh38#122797202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40939151-C-A

122797202-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40939151-C-G

122797210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40939134-G-T

122797243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40939095-T-C

122797252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40939086-A-G

http://identifiers.org/hco/11/GRCh38#122797256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40939082-C-A

122797256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40939082-C-T

122797267-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40939074-A-T

http://identifiers.org/hco/11/GRCh38#122797335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40939017-C-A

122797335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40939017-C-T

122797353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40939003-G-A

122797377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40938978-G-T

122797386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40938969-T-C

122797389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40938966-A-G

122797395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40938959-T-C

122797398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40938956-A-G

122797526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40938842-A-G

122797675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40938675-T-C

122798769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40937775-C-T

122798890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40937684-G-T

122798893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40937681-G-A

122798893-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40937681-G-C

122798935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 40937643-T-C

122799025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 40937553-A-G

http://identifiers.org/hco/11/GRCh38#122799075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40937502-C-A

122799075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40937502-C-T

122799116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40937474-T-C

122799765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40936813-C-T

122799942-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40936664-C-G

122799960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40936646-A-G

122800306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40936268-G-A

122800341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40936241-C-T

122801096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40935927-A-G

122801182-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 40934865-C-G

122801271-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 40934776-C-G

122801366-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40934691-G-C

122801405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40934660-A-G

122801466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40934600-T-C

122801548-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40934516-A-T

122801626-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40934435-C-G

122801668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40934402-G-A

122801907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40933906-G-A

122802716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40933079-T-C

122803027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40932809-A-G

122803273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40932446-T-C

122803773-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40931739-G-C

http://identifiers.org/hco/11/GRCh38#122804273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40931281-C-A

122804282-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40931272-T-G

122804332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40931221-G-A

122804367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40931186-T-C

122804393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40931164-A-G

122804401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40931156-G-A

122805782-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40930062-C-G

122805907-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40929942-C-G

122805907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40929942-C-T

122806086-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40929753-G-C

122806240-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40929587-C-G

http://identifiers.org/hco/11/GRCh38#122806348-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40929487-A-C

122806348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40929487-A-G

122806402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 40929425-T-C

122806504-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 40929323-T-G

122806581-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40929236-G-C

122806581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40929236-G-T

122806833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40928982-A-G

http://identifiers.org/hco/11/GRCh38#122806844-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40928973-A-C

122806903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40928909-C-T

http://identifiers.org/hco/11/GRCh38#122806964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40928854-C-A

122806993-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40928818-G-C

122807109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40928723-C-T

122807178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40928662-C-T

122807280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40928563-A-G

122807407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40928444-G-A

http://identifiers.org/hco/11/GRCh38#122807532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40928316-C-A

122807532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40928316-C-T

http://identifiers.org/hco/11/GRCh38#122807926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40928070-C-A

122807926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40928070-C-T

122807933-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40928063-A-T

122807946-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40928051-G-C

122807946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40928051-G-T

122808195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40927872-T-C

http://identifiers.org/hco/11/GRCh38#122808202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40927865-C-A

122808279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40927788-G-T

122808281-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40927786-T-A

122808281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40927786-T-C

122808312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40927755-A-G

122808312-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40927755-A-T

122808370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40927703-C-T

122808548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40927611-G-A

122808558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40927601-G-A

122808754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40927424-G-A

122808754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40927424-G-T

122808781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40927394-G-A

122808865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40927276-T-C

122809394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40926628-G-T

122809529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40926514-T-C

122809684-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40926394-T-G

122809690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40926390-A-G

http://identifiers.org/hco/11/GRCh38#122809706-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40926374-A-C

122810075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40926000-A-G

122810075-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40926000-A-T

122810416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40925692-T-C

122810445-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40925663-T-G

http://identifiers.org/hco/11/GRCh38#122810461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40925653-C-A

122810512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40925599-C-T

http://identifiers.org/hco/11/GRCh38#122810617-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40925525-A-C

122810617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40925525-A-G

122810879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40925221-T-C

http://identifiers.org/hco/11/GRCh38#122810903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40925197-C-A

122810903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40925197-C-T

http://identifiers.org/hco/11/GRCh38#122810937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40925163-C-A

122811236-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40924858-T-G

122811259-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40924835-A-T

http://identifiers.org/hco/11/GRCh38#122812134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40924656-C-A

http://identifiers.org/hco/11/GRCh38#122812305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40924516-C-A

http://identifiers.org/hco/11/GRCh38#122812402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40924429-C-A

122812518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40924286-T-C

122812657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40924137-T-C

122812672-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40924123-G-C

122812672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40924123-G-T

http://identifiers.org/hco/11/GRCh38#122812682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40924113-C-A

http://identifiers.org/hco/11/GRCh38#122812732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40924076-C-A

http://identifiers.org/hco/11/GRCh38#122812791-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40924034-A-C

122813189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40923624-G-A

122813230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40923584-G-T

122813396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40923427-G-A

122813396-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40923427-G-C

122813474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40923359-T-C

122813688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40923155-G-A

122813688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40923155-G-T

122814063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40922820-G-T

http://identifiers.org/hco/11/GRCh38#122814072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40922811-C-A

http://identifiers.org/hco/11/GRCh38#122814164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40922722-C-A

122814217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40922669-T-C

122814354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40922520-G-A

122814354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40922520-G-T

122814366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40922508-C-T

122814371-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40922503-G-C

122814371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40922503-G-T

122814388-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29884
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40922486-A-T