29063694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117273700-G-A

29063701-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117273693-G-C

29063718-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117273679-T-A

29063762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117273636-A-G

29064690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117272965-A-G

29064740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117272916-C-T

29064785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117272879-G-T

29064866-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117272794-T-G

29064943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117272734-A-G

29065369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117272185-T-C

29065479-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117272039-G-C

29065617-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117271911-G-C

29065641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117271889-G-A

29065691-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117271839-C-G

29065729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117271801-T-C

29065760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117271771-G-A

29065760-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117271771-G-C

http://identifiers.org/hco/3/GRCh38#29065766-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117271765-A-C

29065809-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117271723-T-A

29066009-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117271557-A-T

29066064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117271491-G-A

http://identifiers.org/hco/3/GRCh38#29066168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117271391-C-A

29066190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117271348-A-G

http://identifiers.org/hco/3/GRCh38#29066237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117271308-C-A

29066251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117271288-A-G

29066412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117271123-G-A

29066475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117271050-A-G

29066503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117271019-G-A

29066639-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117270706-C-G

29066851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117270479-C-T

29066907-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117270428-T-G

29067702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117268823-T-C

29067802-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117268722-G-C

29067970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117268573-G-T

29068088-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117268436-G-C

29068120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117268408-C-T

29068720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117267880-A-G

29068912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117267680-T-C

29068912-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117267680-T-G

29072434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117267406-C-T

29072504-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117267328-G-C

http://identifiers.org/hco/3/GRCh38#29072592-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117267248-A-C

29072601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117267241-A-G

29072736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117267117-T-C

29072803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117267048-T-C

29073111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117266755-T-C

29075321-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117266178-G-C

29075366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117266149-G-A

29075388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117266127-T-C

29075415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117266099-G-T

29075774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117265695-G-T

29075835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117265635-G-A

29075857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117265613-G-A

29076094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117265376-T-C

29076094-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117265376-T-G

29076142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117265324-C-T

29076513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117264923-T-C

29076549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117264883-A-G

29078373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117263758-C-T

29079304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117262271-T-C

29079350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117262226-G-A

29079462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117262152-G-T

29079557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117262064-G-A

29079643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117261976-T-C

29080031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117261605-G-A

29080031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117261605-G-T

29080109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117261527-A-G

29080153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117261484-T-C

29080205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117261267-A-G

http://identifiers.org/hco/3/GRCh38#29080347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117260970-C-A

http://identifiers.org/hco/3/GRCh38#29080677-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117260712-A-C

29080677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117260712-A-G

29080753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117260645-A-G

29080761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117260637-G-A

29080839-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117260593-T-A

29080839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117260593-T-C

http://identifiers.org/hco/3/GRCh38#29081043-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117260427-A-C

http://identifiers.org/hco/3/GRCh38#29081127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117260349-C-A

29081811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117259071-T-C

29083948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117258515-A-G

http://identifiers.org/hco/3/GRCh38#29084165-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117258301-A-C

29104154-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117253629-T-G

29104155-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117253628-T-G

29104157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117253626-G-T

29104453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117252971-A-G

29104457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117252967-G-A

29104457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117252967-G-T

29104640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117252806-A-G

29104914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117252535-C-T

29104954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117252497-T-C

29105061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117252436-G-A

29114026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117249311-A-G

http://identifiers.org/hco/3/GRCh38#29114152-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117249198-A-C

29114152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117249198-A-G

29114207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117249139-G-A

29114460-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117248926-A-T

29114541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117248845-T-C

29127810-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117245197-C-G

29127870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117245154-G-A

29127956-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117245076-G-C

29127989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117245046-G-A

29128025-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117245013-T-A

29128025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117245013-T-C

http://identifiers.org/hco/3/GRCh38#29128103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117244553-C-A

29128113-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117244543-T-A

29128137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117244519-G-A

29128353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117244306-A-G

29128452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117244206-T-C

29128494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117244161-T-C

29128528-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117244128-C-G

29128646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117244007-C-T

29128823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117243770-C-T

29128879-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117243715-T-A

29128879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117243715-T-C

29128972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117243623-A-G

29129034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117241931-C-T

29129080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117241885-G-A

http://identifiers.org/hco/3/GRCh38#29129090-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117241875-A-C

29129093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117241872-G-A

29129327-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117241650-T-A

29129330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117241647-A-G

29133334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117240146-T-C

29133395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117240090-A-G

http://identifiers.org/hco/3/GRCh38#29133432-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117240056-A-C

29133432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117240056-A-G

29133481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117240005-G-A

29133507-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117239995-G-C

29133507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117239995-G-T

29133546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117239964-A-G

29133929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117239564-C-T

http://identifiers.org/hco/3/GRCh38#29133950-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117239544-A-C

29134072-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117239439-T-G

29134170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117239369-T-C

29134472-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117239076-T-A

29135180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117237470-G-A

http://identifiers.org/hco/3/GRCh38#29135225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117237429-C-A

29135227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117237427-T-C

29136106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117237012-G-A

29136192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117236898-A-G

29136227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117236862-G-A

29136291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117236803-G-A

29137374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117236695-C-T

29137467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117236632-C-T

29137636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117236452-T-C

http://identifiers.org/hco/3/GRCh38#29137841-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117236294-A-C

29138135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117235410-C-T

29138153-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117235394-C-G

29138228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117235317-C-T

29138353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117235191-T-C

http://identifiers.org/hco/3/GRCh38#29138398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117235147-C-A

29138492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117235053-T-C

29138555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117234986-G-T

29138639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117234906-G-A

29138639-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117234906-G-C

http://identifiers.org/hco/3/GRCh38#29139344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117231297-C-A

http://identifiers.org/hco/3/GRCh38#29139346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117231295-C-A

29140232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117230371-G-A

29140242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117230361-G-A

29140320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117230319-G-A

29140327-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117230312-A-T

29140437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117230199-G-A

29140443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117230193-A-G

29140590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117230057-A-G

29140641-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117230009-T-A

29140655-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117229996-G-C

29140743-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117229882-C-G

29141794-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117228296-C-G

29141915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117228166-T-C

29141976-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117228064-C-G

29141979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117228061-T-C

29142308-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117227561-C-G

29142651-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117227208-G-C

29142651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117227208-G-T

29142739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117227119-C-T

29142819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117227034-C-T

29143384-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117226620-G-C

29143465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117226551-C-T

29143887-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117225673-C-G

29143891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117225669-A-G

29143974-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117225591-T-A

29144025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117225165-G-A

29144073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117225121-T-C

29144425-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117224794-A-T

29144494-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117224742-A-T

29144628-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117224652-C-G

29144628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117224652-C-T

29144693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117223757-G-A

29144761-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117223692-A-T

29144817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117223638-C-T

http://identifiers.org/hco/3/GRCh38#29144828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117223629-C-A

29144828-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117223629-C-G

29144850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117223611-T-C

29144911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117223550-C-T

29144989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117223472-C-T

29145078-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117223387-T-A

29145260-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117223204-T-G

http://identifiers.org/hco/3/GRCh38#29145417-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117223043-A-C

29145417-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117223043-A-T

29145797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117222649-G-A

29145852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117222593-C-T

29145947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117222498-C-T

29146024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117222423-T-C

29146110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117222373-C-T

29146169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117222315-T-C

29146191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117222293-G-T

29147481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117221992-T-C

29147786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117221738-A-G

29148263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117220088-C-T

http://identifiers.org/hco/3/GRCh38#29148868-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117219648-A-C

29148868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117219648-A-G

29148869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117219647-T-C

http://identifiers.org/hco/3/GRCh38#29148886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117219620-C-A

29149157-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117219352-A-T

29149536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117218483-C-T

29149641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117218398-T-C

29150324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117217510-G-T

29150402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117217418-G-A

29150601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117217227-A-G

29150811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117217003-G-A

29150864-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117216955-A-T

29151165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117215983-A-G

29151443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117215689-T-C

http://identifiers.org/hco/3/GRCh38#29151463-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117215669-A-C

29151463-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117215669-A-T

29151541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117215597-G-A

29151838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117215314-C-T

29151933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117215239-T-C

29153068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117212738-G-A

29153215-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117212592-T-G

29153358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117212446-G-A

29153489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117212278-T-C

29153656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117211942-T-C

29153740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117211384-A-G

29153808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117211320-C-T

29153966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117211213-G-A

29154010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117211178-G-A

29154162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117211033-C-T

29154860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117210980-G-T

29155068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117210807-C-T

29155069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117210806-G-A

29155385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117210202-C-T

29155576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117209954-T-C

29155630-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117209881-T-A

29155630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117209881-T-C

29156273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117209226-C-T

29157093-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117207649-G-C

29157262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117207484-G-A

29157262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117207484-G-T

29157266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117207480-G-T

29157267-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117207479-T-G

29157385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117207380-T-C

29157554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117207258-G-A

29157692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117207122-A-G

29158717-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117206097-A-T

http://identifiers.org/hco/3/GRCh38#29158853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117205972-C-A

29158853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117205972-C-T

29158986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117205852-C-T

29159119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117205733-C-T

29165249-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117199847-C-G

29165306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117199790-G-A

29165428-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117199716-C-G

http://identifiers.org/hco/3/GRCh38#29165682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117199494-C-A

29165684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117199492-G-T

29165697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117199479-C-T

29165699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117199477-T-C

29165763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117199426-T-C

29165808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117199385-G-A

29167955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117196230-A-G

29168048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117196154-C-T

http://identifiers.org/hco/3/GRCh38#29168111-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117196092-A-C

29168146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117196057-T-C

29168356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117195421-T-C

29168861-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117194972-T-A

29168861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117194972-T-C

29168890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117194942-A-G

29169185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117194675-A-G

29170629-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117192524-A-T

29170745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117192409-A-G

29170797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117192346-C-T

29171104-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117192088-C-G

29171104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117192088-C-T

http://identifiers.org/hco/3/GRCh38#29171131-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117192066-A-C

29171243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117191081-T-C

29171296-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117191052-T-G

29171889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117190483-C-T

29172165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117190180-A-G

29173454-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117189131-C-G

29173472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117189113-G-A

29173472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117189113-G-T

http://identifiers.org/hco/3/GRCh38#29173493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117189093-C-A

http://identifiers.org/hco/3/GRCh38#29173672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117188920-C-A

http://identifiers.org/hco/3/GRCh38#29173789-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117188793-A-C

29173789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117188793-A-G

29174225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: -A-G

29174321-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: -T-A

29174614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: -G-A

29174812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: -G-A

29174827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: -C-T

29174874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: -A-G

http://identifiers.org/hco/3/GRCh38#29175006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: -C-A

29175013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: -T-C

http://identifiers.org/hco/3/GRCh38#29175052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: -C-A

29175076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: -C-T

29176305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117186887-A-G

29176336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117186856-T-C

29176379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117186814-C-T

29176490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117186658-G-T

29176511-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117186577-C-G

29176511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117186577-C-T

29176842-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117186213-G-C

29176898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117186152-G-A

29176898-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117186152-G-C

29176927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117186137-T-C

29176951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117186113-T-C

29177058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117186000-T-C

29177074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117185984-G-A

http://identifiers.org/hco/3/GRCh38#29178729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117184099-C-A

29179695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117183935-T-C

29179842-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117183801-A-T

29181664-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117182781-G-C

29182060-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117182489-T-G

29182302-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117182255-T-G

29182336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117182221-G-A

29182400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117182155-T-C

29182709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117181849-A-G

http://identifiers.org/hco/3/GRCh38#29182806-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117181775-A-C

29182989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 117181595-A-G

29183073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 117181511-G-T

29183138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117181446-C-T

29183163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117181421-G-T

29183174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117181418-G-A

29183174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117181418-G-T

http://identifiers.org/hco/3/GRCh38#29183262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117181358-C-A

29183273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117181347-G-A

29183273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117181347-G-T

29183363-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117181267-T-A

29183371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117181259-G-A

http://identifiers.org/hco/3/GRCh38#29183536-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117181080-A-C

29183668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117180968-G-A

29183759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117180891-T-C

29183987-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117180716-T-G

29184263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117180470-T-C

29185076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117178875-C-T

29185106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117178848-G-T

29185138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117178819-A-G

29185138-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117178819-A-T

29185225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117178739-G-T

http://identifiers.org/hco/3/GRCh38#29185411-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117178598-A-C

29185418-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117178591-T-A

29185567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117178438-A-G

29185602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117178399-C-T

http://identifiers.org/hco/3/GRCh38#29185603-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117178398-A-C

29186337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117177667-G-A

29186518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117177502-A-G

29186559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117177470-T-C

29186899-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117177160-C-G

29186899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117177160-C-T

http://identifiers.org/hco/3/GRCh38#29187200-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117176387-A-C

29187294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117176301-G-A

http://identifiers.org/hco/3/GRCh38#29187328-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117176267-A-C

29187362-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117176234-G-C

29187367-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117176229-A-T

29187516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117175491-A-G

29196851-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117170561-T-A

29196990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117170421-A-G

29197000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117170411-A-G

29197000-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117170411-A-T

29197063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117170347-A-G

29197146-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117170282-G-C

29197150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117170278-T-C

29197178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117170254-T-C

http://identifiers.org/hco/3/GRCh38#29197238-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117170192-A-C

29197350-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117170084-A-T

29197367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117170068-A-G

29197384-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117170051-T-A

http://identifiers.org/hco/3/GRCh38#29197391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117170044-C-A

29197391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117170044-C-T

29198460-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117168997-G-C

29198574-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117168890-T-G

29198635-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117168826-T-A

29198635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117168826-T-C

29198684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117168777-G-A

29198803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117168654-G-A

http://identifiers.org/hco/3/GRCh38#29200049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117166322-C-A

29200049-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 117166322-C-G

29200098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 117166275-A-G

http://identifiers.org/hco/3/GRCh38#29200114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117166259-C-A

29200159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 117166214-G-A

29200159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 117166214-G-T

http://identifiers.org/hco/3/GRCh38#29200360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117166023-C-A

29200360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 117166023-C-T

29200477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 117165648-A-G

29200502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 117165623-T-C

29200581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 117165542-T-C

29200603-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 117165520-T-A

29200603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 117165520-T-C

29200632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 117165512-T-C

29200659-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 117165486-A-T

29200728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117165417-T-C

29200733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117165412-A-G

29200733-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117165412-A-T

29200736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117165409-A-G

29200991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117164457-A-G

http://identifiers.org/hco/3/GRCh38#29200992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117164456-C-A

29200992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117164456-C-T

29201025-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117164424-G-C

29201215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117164228-A-G

29201371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117164089-G-T

29201520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117163980-A-G

http://identifiers.org/hco/3/GRCh38#29201524-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117163976-A-C

29201676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117163890-G-A

29201676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117163890-G-T

29201829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117163835-G-A

29202231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117163431-A-G

http://identifiers.org/hco/3/GRCh38#29202546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117162986-C-A

29202583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117162949-C-T

29202811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117162723-A-G

29202976-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117162386-A-T

http://identifiers.org/hco/3/GRCh38#29203423-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117161971-A-C

29203473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117161924-C-T

29203591-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117161827-G-C

29203708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117161706-G-A

29203730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117161684-C-T

http://identifiers.org/hco/3/GRCh38#29203786-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117161624-A-C

29203786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117161624-A-G

29203786-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117161624-A-T

29204333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117160748-A-G

http://identifiers.org/hco/3/GRCh38#29204520-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117160572-A-C

29204788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117160429-G-T

29204914-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117160302-T-A

29204944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117160272-T-C

29205512-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117159308-T-G

29205591-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117159173-T-A

29205591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117159173-T-C

http://identifiers.org/hco/3/GRCh38#29205749-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117159042-A-C

29205749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117159042-A-G

29205846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117158943-A-G

29207087-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117151877-G-C

29207244-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117151729-C-G

29207252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117151721-A-G

29208338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117151488-T-C

29208403-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117151420-T-A

29208427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117151397-C-T

29208465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117151368-G-A

http://identifiers.org/hco/3/GRCh38#29208506-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117151327-A-C

29208562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117151268-T-C

29208722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117150786-T-C

29208876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117150624-G-T

29208977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117150521-A-G

29209133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117150364-C-T

http://identifiers.org/hco/3/GRCh38#29209197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117150299-C-A

29209197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117150299-C-T

29209267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117150227-A-G

29209408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117150051-C-T

29209791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117149675-A-G

29209811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117149646-T-C

29210151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117149038-T-C

29210501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117148639-A-G

29210851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117147954-T-C

29211037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117147768-A-G

29211078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117147726-T-C

29211364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117147484-G-A

29211368-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117147480-C-G

29211594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117147233-T-C

29211630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117147197-C-T

29211640-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117147191-T-G

29211677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117147152-C-T

29212945-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117146814-C-G

29213271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117146510-A-G

29213410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117146371-C-T

29213517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117146210-A-G

29213523-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117146204-C-G

29213532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117146172-G-A

29213740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117145828-A-G

29213770-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117145798-A-T

29214013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117145557-G-A

29214027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117145544-C-T

29218651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117143213-A-G

29218713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117143154-T-C

29218742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117143123-A-G

29218837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117143022-A-G

29218837-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117143022-A-T

29218847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117143012-A-G

29218849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117143010-A-G

29218974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117142886-T-C

29219235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117142639-A-G

29219239-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117142635-T-G

29219473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117142401-T-C

29219482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117142392-G-A

29220314-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117141502-A-T

29223219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117139369-G-T

29223293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117139304-T-C

29223408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117139204-G-A

29223408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117139204-G-T

29223668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117138881-C-T

29223758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117138777-A-G

29227264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117138005-C-T

29227525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117137741-C-T

29227539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117137727-A-G

29227539-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117137727-A-T

29227862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117136719-A-G

29227928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117136665-G-A

29228143-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117136454-G-C

29228246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117136355-C-T

29228344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117136256-T-C

http://identifiers.org/hco/3/GRCh38#29228377-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117136224-A-C

29228377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117136224-A-G

29228479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117136150-A-G

29228678-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117135974-A-T

29229014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117135495-G-A

29229021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117135481-A-G

29229035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117135467-A-G

http://identifiers.org/hco/3/GRCh38#29229203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117135296-C-A

29229238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117135268-G-T

29229285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117135218-A-G

29229398-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117135103-T-A

29229461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117135039-A-G

29229475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117135022-A-G

29229566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117134931-A-G

29229585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117134912-T-C

29229587-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117134910-T-G

29229639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117134859-A-G

29229640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117134858-C-T

29229785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117134705-A-G

29229861-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117134627-A-T

29229878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117134610-C-T

29229933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117134549-A-G

29229933-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117134549-A-T

29229941-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117134541-G-C

29229941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117134541-G-T

http://identifiers.org/hco/3/GRCh38#29229961-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117134521-A-C

29229991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117134493-A-G

29230021-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117134463-T-G

29230029-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117134455-G-C

29230123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117134356-A-G

29230164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117134317-A-G

29230238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117134196-T-C

29230254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117134178-G-A

29230256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117134176-A-G

29232479-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117130602-C-G

29232479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117130602-C-T

29236301-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117128645-C-G

29236357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117128589-A-G

29236423-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117128519-G-C

29237158-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117127816-T-G

29237954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117127235-G-A

29237970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117127219-C-T

29238170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117127031-A-G

29240272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117125391-T-C

29240355-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117125319-C-G

http://identifiers.org/hco/3/GRCh38#29240404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117125181-C-A

29240404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117125181-C-T

29240407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117125178-C-T

29240408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117125177-C-T

29240427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117125150-A-G

29240445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117125132-C-T

29240551-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117125021-T-A

29240569-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117125003-T-G

29240816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117124776-C-T

29240939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117124669-T-C

29240946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117124662-A-G

29242303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117123489-A-G

29242725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117123079-T-C

29244371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117121188-A-G

29244439-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117121113-T-A

29244513-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117121058-A-T

29244608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117120980-G-A

29244613-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117120975-G-C

29244653-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117120941-T-G

29244698-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117120897-A-T

http://identifiers.org/hco/3/GRCh38#29245726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117120602-C-A

29245870-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117120489-A-T

29248912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 117119136-A-G

29248942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 117119106-T-C

29248943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 117119105-T-C

29248943-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 117119105-T-G

29248959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 117119089-A-G

29248959-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 117119089-A-T

29249582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 117118803-G-T

29249623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 117118771-G-A

29249623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 117118771-G-T

http://identifiers.org/hco/3/GRCh38#29249729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117118686-C-A

29249731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 117118684-A-G

29249888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 117118527-G-A

http://identifiers.org/hco/3/GRCh38#29249966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117118448-C-A

29249966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 117118448-C-T

29250089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 117118322-A-G

http://identifiers.org/hco/3/GRCh38#29250245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117118164-C-A

29251585-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 117114157-T-G

29251592-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 117114150-T-G

29252138-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 117113931-T-G

29252241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 117113837-T-C

29253153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117112935-G-A

http://identifiers.org/hco/3/GRCh38#29253259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117112826-C-A

29253559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117111579-T-C

http://identifiers.org/hco/3/GRCh38#29253709-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117111437-A-C

29253710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117111436-T-C

29253726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117111410-G-T

29253736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117111400-G-A

29253816-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117110951-T-A

29253876-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117110913-T-G

29254261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117110412-A-G

29254517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117109892-A-G

29254534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117109874-A-G

29254538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117109870-A-G

29254571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117109837-G-A

29254571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117109837-G-T

29254905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117109521-A-G

http://identifiers.org/hco/3/GRCh38#29255138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117108701-C-A

29255306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117108540-A-G

29255326-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117108519-C-G

29255495-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117108348-C-G

29255639-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117108223-C-G

29255681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117108191-A-G

29255779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117108092-A-G

29259569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117105021-T-C

http://identifiers.org/hco/3/GRCh38#29259625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117104965-C-A

29259803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117104777-T-C

29259955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117104640-T-C

29259956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117104639-G-A

29259977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117104618-G-A

29260058-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117104531-T-G

29260084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117104507-G-A

29260084-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117104507-G-C

29260084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117104507-G-T

29260126-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117104481-T-G

29260316-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117104300-G-C

29260585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117104034-G-A

29260601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117104014-A-G

29263021-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 117102123-G-C

29263129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 117102010-C-T

29265254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117095342-C-T

29265452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117094401-C-T

29265559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117094286-A-G

29265670-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117094199-C-G

29265764-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117094104-T-A

29265810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117094057-A-G

29265878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117093987-G-A

http://identifiers.org/hco/3/GRCh38#29265927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117093937-C-A

29265927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117093937-C-T

29265999-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117093871-C-G

29266183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117093705-G-A

29266192-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117093696-G-C

29266304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117093591-A-G

29266434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117093450-A-G

29266460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117093424-A-G

29266550-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117093338-C-G

29266668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117093238-T-C

29266846-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117093075-T-G

29267184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117092412-A-G

29267407-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117092187-C-G

29267546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117092054-C-T

29267842-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117091798-A-T

29268020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117091619-G-A

29268090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117091551-G-A

29268679-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117090497-C-G

29268679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117090497-C-T

29268941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117090309-G-A

29269403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117090050-T-C

29269466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117089986-A-G

29269803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117089675-C-T

29270116-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117089242-C-G

29270116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117089242-C-T

29270262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117089105-A-G

29270366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117088965-G-A

29270525-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117088901-A-T

29270817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117088652-A-G

http://identifiers.org/hco/3/GRCh38#29270906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117088578-C-A

29270957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117088526-G-A

29271022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117088466-T-C

29271413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117087578-T-C

29271513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117087478-A-G

29277679-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117085575-C-G

29277754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117085508-A-G

29277832-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117085429-A-T

29278373-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117084540-C-G

29278672-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117084242-G-C

29278792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117084138-G-T

29278793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117084137-T-C

29279092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117083657-G-A

29279213-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117083577-T-G

29279394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117083455-G-A

29279496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117083373-A-G

29279683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117083165-C-T

http://identifiers.org/hco/3/GRCh38#29279762-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117083022-A-C

29279984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 117082679-C-T

29280090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117082575-C-T

29280396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117082251-T-C

29280429-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117082221-A-T

29280556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117082105-T-C

29280566-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117082095-C-G

http://identifiers.org/hco/3/GRCh38#29280718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117081920-C-A

29280718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117081920-C-T

http://identifiers.org/hco/3/GRCh38#29280856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117081765-C-A

http://identifiers.org/hco/3/GRCh38#29280965-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117081647-A-C

29281025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117081587-G-A

29281166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 117081448-C-T

29281250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 117081350-A-G

29281250-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 117081350-A-T

29281404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 117081188-G-T

http://identifiers.org/hco/3/GRCh38#29281435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117081153-C-A

29281435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 117081153-C-T

29281522-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117081042-T-A

29281522-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117081042-T-G

http://identifiers.org/hco/3/GRCh38#29281817-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117080727-A-C

29282236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117080313-G-A

29282408-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117080119-G-C

29282658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117079857-G-A

29282763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117079764-C-T

29283022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117079503-T-C

29283154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117079371-A-G

29283275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117079251-C-T

29283488-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117078994-G-C

29283605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117078837-G-A

29283712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117078730-A-G

29283976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117078505-A-G

29284212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117078275-A-G

29284567-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117077894-T-G

29284755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117077728-G-A

29285118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117077310-A-G

29285178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117077255-G-T

http://identifiers.org/hco/3/GRCh38#29285342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117077198-C-A

29285373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117077161-A-G

29285420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117077112-A-G

29285495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117077045-A-G

29285527-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117077017-T-A

29285578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117076978-G-T

29285606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117076952-G-A

29285606-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117076952-G-C

29285686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117076884-T-C

29286307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117076220-C-T

29286309-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117076218-T-G

29286342-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117076185-G-C

http://identifiers.org/hco/3/GRCh38#29286498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117076059-C-A

29286536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117076031-T-C

http://identifiers.org/hco/3/GRCh38#29286571-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117075998-A-C

29286576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117075993-A-G

http://identifiers.org/hco/3/GRCh38#29286935-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117075512-A-C

29287489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117074922-C-T

29287617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117074797-T-C

http://identifiers.org/hco/3/GRCh38#29287882-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117074151-A-C

29287972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117074070-G-A

29288286-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117073730-C-G

29288328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117073691-G-A

29288328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117073691-G-T

29288403-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117073623-C-G

29288584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117073459-T-C

29288815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117073244-C-T

29288850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117073211-C-T

29288853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117073208-T-C

29288915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117073120-T-C

29290273-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117071958-T-A

29290286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117071942-G-A

29290286-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117071942-G-C

29290346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117071881-T-C

29290507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117071713-G-A