http://identifiers.org/hco/9/GRCh38#35406881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#43267283-C-A

http://identifiers.org/hco/9/GRCh38#35406886-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43267288-A-C

35406886-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43267288-A-T

35406887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43267289-A-G

35406930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43267329-G-A

http://identifiers.org/hco/9/GRCh38#35406996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43267422-C-A

35406996-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43267422-C-G

35407234-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43267727-C-G

35407289-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43267769-T-A

35407545-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43268177-G-C

35407594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43268235-C-T

35407670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43268301-G-A

35407677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43268308-A-G

35407681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43268312-G-A

35407955-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43268702-C-G

35407955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43268702-C-T

35408768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43291500-T-C

35408854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43291587-T-C

35408877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43291610-A-G

35408935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: non coding transcript exon variant
orthologous variants: 43291665-T-C

35409030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43291794-G-A

35409030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43291794-G-T

35409051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43291820-T-C

35409053-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43291822-T-A

35409087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43291906-G-A

35409117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43291957-G-T

35409207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43292044-C-T

http://identifiers.org/hco/9/GRCh38#35409276-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43292127-A-C

35409299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43292149-C-T

35409304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43292154-C-T

35409850-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43292303-C-G

35409852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43292305-A-G

35410003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43292458-A-G

35413900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43293335-A-G

35413974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43293415-A-G

35414271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43293797-G-A

35414355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43293906-A-G

35414559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43294092-A-G

35414663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43294199-G-A

35414784-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43294460-C-G

35414789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43294465-A-G

35415074-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43294685-A-T

35415155-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43294778-T-G

35415166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43294789-C-T

35415181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43294804-G-A

35415275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43294898-A-G

35432388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43295954-A-G

http://identifiers.org/hco/9/GRCh38#35432528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43296087-C-A

35432555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43296112-A-G

35432602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43296158-G-A

35432615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43296171-A-G

35433612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43302494-G-T

35433643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43302525-G-A

http://identifiers.org/hco/9/GRCh38#35433644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43302526-C-A

35433644-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43302526-C-G

35433645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43302527-C-T

35433671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43302548-G-T

35433688-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43302563-T-G

35433694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43302569-T-C

35433859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43302705-T-C

35433867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43302713-A-G

35433907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43302749-C-T

35434195-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43303028-T-A

35434259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43303090-T-C

35434536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43303556-T-C

35434542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43303562-A-G

35434590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43303599-A-G

35434854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43303824-C-T

35435063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43304187-T-C

http://identifiers.org/hco/9/GRCh38#35437718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43304587-C-A

35437735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43304606-G-T

35437973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43304838-G-A

http://identifiers.org/hco/9/GRCh38#35438180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43305034-C-A

35438223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43305051-C-T

35438297-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43305118-G-C

35438390-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43305220-A-T

35438433-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43305455-T-A

35438500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43305518-G-A

http://identifiers.org/hco/9/GRCh38#35438517-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43305535-A-C

35438517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43305535-A-G

http://identifiers.org/hco/9/GRCh38#35438587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43305596-C-A

35438663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43305667-G-T

35438863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43305859-G-A

35438864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43305860-C-T

http://identifiers.org/hco/9/GRCh38#35438884-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43305883-A-C

35438884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43305883-A-G

http://identifiers.org/hco/9/GRCh38#35438902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43305901-C-A

http://identifiers.org/hco/9/GRCh38#35438906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43305905-C-A

35438906-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43305905-C-G

35438948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43305944-T-C

35439002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43305985-T-C

35439027-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43306010-G-C

35439028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43306011-G-T

http://identifiers.org/hco/9/GRCh38#35439034-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43306017-A-C

35439039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43306022-G-A

35439041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43306024-C-T

http://identifiers.org/hco/9/GRCh38#35439064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43306043-C-A

http://identifiers.org/hco/9/GRCh38#35439109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43306082-C-A

35439179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43306139-T-C

35439213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43306170-G-A

35439213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43306170-G-T

35439297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43306263-T-C

http://identifiers.org/hco/9/GRCh38#35439364-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43306315-A-C

35439364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43306315-A-G

35439425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43306381-G-T

35439502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43306452-G-A

35439596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43307781-T-C

35439653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43307823-A-G

http://identifiers.org/hco/9/GRCh38#35439680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43307850-C-A

35439680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43307850-C-T

35439697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43307869-T-C

35439787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43307962-A-G

35439849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43308023-C-T

http://identifiers.org/hco/9/GRCh38#35439856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43308030-C-A

35439856-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43308030-C-G

35440020-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43308179-T-A

http://identifiers.org/hco/9/GRCh38#35440034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43308185-C-A

http://identifiers.org/hco/9/GRCh38#35440195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43308325-C-A

35440380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43308476-G-T

35440381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43308477-T-C

35440436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: non coding transcript exon variant
orthologous variants: 43308532-G-A

35440436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: non coding transcript exon variant
orthologous variants: 43308532-G-T

35440445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: non coding transcript exon variant
orthologous variants: 43308541-G-T

35440486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43308582-G-T

35440627-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43309663-T-G

35440761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43309788-A-G

35440783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43309810-C-T

35440816-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43309843-C-G

35440826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43309853-C-T

35440848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43309877-G-A

35440973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43309984-A-G

35441071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43310050-G-A

35441762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43310366-A-G

35443220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43310643-G-A

35443230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43310653-G-A

35443232-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43310655-T-A

35443232-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43310655-T-G

35443247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43310670-A-G

35443255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43310678-G-A

35443257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43310680-G-A

35443263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43310686-A-G

35443322-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43310753-A-T

35443366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43310851-G-A

35443374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43310859-G-A

35443424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43310909-G-T

35443443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43310921-C-T

35443444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43310922-G-A

35443455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43310933-G-A

35444001-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43311027-A-T

35444002-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43311028-A-T

35444017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43311043-G-A

35444252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43311312-G-A

35444252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43311312-G-T

35444265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43311326-G-T

35444270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43311331-A-G

35444433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: non coding transcript exon variant
orthologous variants: 43311504-A-G

35444473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43311544-G-T

35444476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43311546-T-C

35444484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43311557-G-T

35444501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43311571-G-T

http://identifiers.org/hco/9/GRCh38#35444541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43311611-C-A

35444616-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43311686-T-A

35444727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43311818-T-C

http://identifiers.org/hco/9/GRCh38#35444827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43311913-C-A

http://identifiers.org/hco/9/GRCh38#35444977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43312047-C-A

35444982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43312052-A-G

35444982-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43312052-A-T

35445230-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43312543-T-A

35446125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43320337-C-T

35446259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43320443-G-T

35446276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43320460-T-C

35446438-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: non coding transcript exon variant
orthologous variants: 43320625-A-T

35446512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43320698-A-G

35446705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43320876-T-C

35447090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43322288-G-A

35447113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43322311-A-G

35447279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: non coding transcript exon variant
orthologous variants: 43322456-A-G

http://identifiers.org/hco/9/GRCh38#35447345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43322522-C-A

35447345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: non coding transcript exon variant
orthologous variants: 43322522-C-T

35447395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43322572-C-T

35447401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43322585-C-T

35447417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43322604-G-A

35447417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43322604-G-T

35447434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43322621-G-T

35447466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43322653-G-A

http://identifiers.org/hco/9/GRCh38#35447475-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43322662-A-C

35447601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43322757-T-C

35447773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43322918-G-A

http://identifiers.org/hco/9/GRCh38#35447981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43323149-C-A

35447981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43323149-C-T

35448072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43323559-C-T

35448694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43324185-G-A

35448749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43324245-A-G

35448749-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43324245-A-T

35448783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43324270-A-G

35448965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43324448-G-A

http://identifiers.org/hco/9/GRCh38#35448992-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43324475-A-C

35449131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43324561-G-T

35449324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43324721-A-G

35449324-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43324721-A-T

http://identifiers.org/hco/9/GRCh38#35449334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43324727-C-A

http://identifiers.org/hco/9/GRCh38#35449387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43324759-C-A

35449387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43324759-C-T

http://identifiers.org/hco/9/GRCh38#35449456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43324827-C-A

35449456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43324827-C-T

35449500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43324871-A-G

35449530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43324901-C-T

http://identifiers.org/hco/9/GRCh38#35449604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43324960-C-A

35449604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43324960-C-T

35449651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43324999-G-T

35451150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43325029-T-C

35451203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43325082-A-G

35451205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43325084-G-T

35451306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43325172-C-T

35451344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43325207-C-T

35451404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43325267-G-A

35451556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43325409-A-G

35451863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43330042-G-T

35451962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43330249-A-G

35452036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43330318-C-T

35452175-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43330481-A-T

35468817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43333801-C-T

35468842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43333825-G-A

35468860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43333843-G-A

http://identifiers.org/hco/9/GRCh38#35468921-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43333903-A-C

35469003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43334002-T-C

http://identifiers.org/hco/9/GRCh38#35469008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43334007-C-A

35469008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43334007-C-T

35469120-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43334137-A-T

35469328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43334345-G-T

35469401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43334416-G-A

35469539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43334696-A-G

35469539-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43334696-A-T

35469559-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43334716-C-G

35469567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43334724-C-T

35469640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43334791-C-T

35469763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43334881-A-G

35470638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43342107-G-A

35470821-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43342267-G-C

35470824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43342270-G-A

35470947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43342365-G-T

35471092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: non coding transcript exon variant
orthologous variants: 43342509-C-T

http://identifiers.org/hco/9/GRCh38#35471161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#43342578-C-A

35471161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 43342578-C-T

35471182-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43342599-G-C

35471232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43342649-T-C

http://identifiers.org/hco/9/GRCh38#35471239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43342655-C-A

35471335-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43342741-T-A

http://identifiers.org/hco/9/GRCh38#35471348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43342754-C-A

http://identifiers.org/hco/9/GRCh38#35473099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43343637-C-A

35473190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43343716-A-G

35473198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43343724-T-C

35473484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43343983-G-A

35473534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43344015-T-C

35473785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43344487-G-A

35473906-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43344583-G-C

35473910-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43344587-G-C

http://identifiers.org/hco/9/GRCh38#35474928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43351188-C-A

35475028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43351261-T-C

35475040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43351276-G-A

35475040-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43351276-G-C

35475068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43351305-G-A

35475251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43351483-G-A

35477035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43368846-T-C

35477112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43368883-C-T

35477177-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43368944-G-C

http://identifiers.org/hco/9/GRCh38#35477363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#43369076-C-A

35477442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43369132-A-G

35477468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43369158-C-T

35477502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43369192-G-A

35477530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43369218-G-A

35477530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43369218-G-T

35477894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43369278-G-A

35477894-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43369278-G-C

35478096-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43369475-G-T

35478110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43369504-A-G

35478123-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43369517-T-A

35478123-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43369517-T-G

35478126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43369520-G-T

35478135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43369529-G-A

35478135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43369529-G-T

35478162-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43369551-T-A

35478192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43369581-G-T

35478357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43369746-T-C

35478740-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43369918-T-G

35478753-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43369930-G-C

35478754-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43369931-A-T

35478802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43369978-G-A

35478808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43369984-G-T

35479757-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43370337-G-C

35479764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43370344-T-C

http://identifiers.org/hco/9/GRCh38#35479771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43370351-C-A

35479771-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43370351-C-G

35479771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43370351-C-T

http://identifiers.org/hco/9/GRCh38#35479788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43370368-C-A

35479788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43370368-C-T

35479813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43370393-A-G

35479851-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43370429-C-G

35479851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43370429-C-T

http://identifiers.org/hco/9/GRCh38#35479884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43370446-C-A

http://identifiers.org/hco/9/GRCh38#35479931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43370493-C-A

35479931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: non coding transcript exon variant
orthologous variants: 43370493-C-T

35480022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: non coding transcript exon variant
orthologous variants: 43370553-T-C

35480033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: non coding transcript exon variant
orthologous variants: 43370564-G-A

35480033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: non coding transcript exon variant
orthologous variants: 43370564-G-T

35480035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: non coding transcript exon variant
orthologous variants: 43370566-G-A

35480035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: non coding transcript exon variant
orthologous variants: 43370566-G-T

35480279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: non coding transcript exon variant
orthologous variants: 43370810-G-T

35480323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43370853-G-A

35480323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43370853-G-T

35480324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43370854-G-A

35480324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43370854-G-T

35480367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43370871-G-T

35480369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43370873-G-A

35480410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43370914-G-A

35480410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43370914-G-T

35480450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43370951-T-C

http://identifiers.org/hco/9/GRCh38#35480517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43371018-C-A

35480537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43371038-G-A

35480537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43371038-G-T

35480630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43371132-G-A

35480641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43371144-A-G

35480936-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43371632-A-T

35480975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43371668-C-T

http://identifiers.org/hco/9/GRCh38#35481417-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43372039-A-C

35481417-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43372039-A-T

35481470-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43372189-A-T

35481695-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43372497-A-T

35481709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43372510-T-C

35481721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43372522-G-A

35481730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43372531-T-C

35481866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: non coding transcript exon variant
orthologous variants: 43372664-T-C

http://identifiers.org/hco/9/GRCh38#35481986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43372784-C-A

35482247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: non coding transcript exon variant
orthologous variants: 43373045-A-G

35482426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: non coding transcript exon variant
orthologous variants: 43373173-G-T

35482540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: non coding transcript exon variant
orthologous variants: 43373258-T-C

35482579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: non coding transcript exon variant
orthologous variants: 43373297-T-C

35482583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27245
most severe consequence: non coding transcript exon variant
orthologous variants: 43373301-G-T