http://identifiers.org/hco/5/GRCh38#17089686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#25519002-C-A

17089777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25518933-G-A

17089844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25518899-C-T

17090371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25517793-C-T

17090447-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25517717-C-G

17090464-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25517700-G-C

17092263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25515667-T-C

17092319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25515609-G-A

17092370-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25515565-A-T

17092466-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25515470-G-C

17092708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25515240-A-G

17092830-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25515132-T-G

17096489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25511007-A-G

17096643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25510865-G-A

17096647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25510861-A-G

17096750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25510761-C-T

17096751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25510760-A-G

17096995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25510478-G-T

17097019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25510454-G-A

http://identifiers.org/hco/5/GRCh38#17097025-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#25510448-A-C

17097048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25510426-A-G

17098880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25509150-T-C

http://identifiers.org/hco/5/GRCh38#17099054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#25509008-C-A

17099054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25509008-C-T

17099217-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25508885-A-T

17099247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25508857-G-A

17099412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25508718-C-T

17103438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25506935-G-T

17103463-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25506910-T-A

http://identifiers.org/hco/5/GRCh38#17103493-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#25506883-A-C

17103641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25506744-C-T

http://identifiers.org/hco/5/GRCh38#17103907-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#25506007-A-C

17103921-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25505993-G-C

17106055-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25505413-C-G

17106108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25505367-G-A

17106244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25505231-A-G

17106342-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25505134-T-G

http://identifiers.org/hco/5/GRCh38#17109955-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#25504883-A-C

17109991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25504849-G-A

17110353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25504664-T-C

17110425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25504592-C-T

17110438-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25504579-G-C

17110440-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25504577-G-C

17110440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25504577-G-T

17110474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25504536-T-C

17110511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25504498-A-G

17110621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25504303-C-T

17110780-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25504183-T-A

17110780-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25504183-T-G

http://identifiers.org/hco/5/GRCh38#17110823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#25504140-C-A

17110823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25504140-C-T

17110878-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25504088-T-A

17111089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25503882-C-T

17111320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25503679-G-A

17111342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25503658-G-A

17111964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25502896-G-A

17112006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25502862-A-G

http://identifiers.org/hco/5/GRCh38#17112026-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#25502846-A-C

17113969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25500876-T-C

http://identifiers.org/hco/5/GRCh38#17113987-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#25500842-A-C

17114096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25500741-A-G

17114214-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25500395-T-G

17114382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25500225-T-C

17114428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25500180-A-G

17114447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25500161-T-C

17114537-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25500069-T-G

17114672-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25499953-T-A

17114690-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25499935-T-G

17115077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25499507-A-G

http://identifiers.org/hco/5/GRCh38#17115145-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#25499443-A-C

17115190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25499403-G-T

17115319-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25499275-G-C

17115319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25499275-G-T

17115463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25499173-C-T

17115517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25499120-C-T

17115542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25499097-A-G

http://identifiers.org/hco/5/GRCh38#17115662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#25498989-C-A

17115695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25498958-C-T

17116084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25498606-A-G

17116126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25498564-C-T

17116310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25498405-A-G

17116319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25498392-A-G

17117791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25497977-G-A

17117877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25497892-C-T

17117963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25497818-C-T

17118053-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25497728-A-T

17118068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25497713-G-A

http://identifiers.org/hco/5/GRCh38#17118516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#25497615-C-A

17118528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25497603-T-C

17118962-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25497217-A-T

http://identifiers.org/hco/5/GRCh38#17118989-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#25497190-A-C

17118989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25497190-A-G

17119056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25497109-G-A

17119940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25496556-C-T

17119960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25496537-C-T

17120036-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25496464-G-C

17120100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25496433-G-A

17120278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25496254-G-A

17120389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25496149-T-C

17120403-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25496135-T-G

17120414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25496123-C-T

http://identifiers.org/hco/5/GRCh38#17120642-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#25495900-A-C

17120662-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25495880-C-G

17121831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25495257-G-A

17121837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25495251-G-A

17122021-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25495066-C-G

17122124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25494939-G-A

17122282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25494820-C-T

17122309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25494789-C-T

17122329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25494769-C-T

17122351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25494745-C-T

17122420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25494681-C-T

17122522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25494604-G-T

17123128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25493980-C-T

17123154-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25493952-C-G

17123157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25493949-G-A

17123157-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25493949-G-C

17123159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25493947-T-C

17123208-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25493915-T-G

17123242-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25493880-T-G

17124134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25493422-C-T

17124296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25493235-C-T

17124389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25493145-A-G

17124500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25493033-G-A

17124585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25492949-T-C

17124590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25492944-C-T

17124612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25492929-G-A

17124625-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25492917-C-G

17125927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25492446-C-T

17125976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25492395-A-G

17126079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25492281-C-T

17128149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25491071-T-C

17128225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25490997-C-T

17128258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25490964-C-T

17128342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25490885-A-G

17128473-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25490745-A-T

17129260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25490200-G-T

17129270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25490193-A-G

17129286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25490177-C-T

17129423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25490012-C-T

http://identifiers.org/hco/5/GRCh38#17129435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#25490000-C-A

17129515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25489907-A-G

http://identifiers.org/hco/5/GRCh38#17129654-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#25489766-A-C

17129864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25489555-C-T

17129887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25489531-G-A

http://identifiers.org/hco/5/GRCh38#17131127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: -C-A

17131246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: -T-C

17131266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: -G-A

17131266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: -G-T

17131607-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25487443-A-T

17131659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25487391-G-T

17131671-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25487379-T-A

17131677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25487373-G-A

17131677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25487373-G-T

http://identifiers.org/hco/5/GRCh38#17131682-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#25487368-A-C

http://identifiers.org/hco/5/GRCh38#17131852-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#25486985-A-C

17132048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25486814-G-T

17132131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25486727-A-G

17132197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25486661-A-G

17132786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25486393-C-T

17132929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25486254-C-T

17132950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25486233-G-A

17132955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25486228-T-C

17133039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25486152-C-T

17133201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25485914-A-G

17133234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25485881-G-A

17133234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25485881-G-T

17133481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25485626-A-G

17133501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25485593-T-C

17135191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25484512-T-C

17135312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25484409-A-G

17135317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25484404-A-G

17135364-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25484324-C-G

17136752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25483461-T-C

17137882-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25482892-T-A

http://identifiers.org/hco/5/GRCh38#17139156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#25482080-C-A

17139186-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25482055-A-T

17139201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25482040-G-T

17139206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25482035-C-T

17139263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25481986-G-A

http://identifiers.org/hco/5/GRCh38#17139271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#25481978-C-A

17139271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25481978-C-T

17139273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25481976-C-T

17139301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25481948-T-C

17139416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25481837-A-G

17139700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25481573-A-G

17139784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25481527-G-A

17139784-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25481527-G-C

17140025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25481446-G-T

17140062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25481412-G-A

17140118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25481357-G-A

17141913-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25480152-C-G

17142059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25480014-G-A

17142203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25479870-G-A

17142203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25479870-G-T

17142397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25479333-T-C

http://identifiers.org/hco/5/GRCh38#17142406-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#25479324-A-C

17142460-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25479273-T-A

17142460-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25479273-T-G

17142541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25479192-T-C

17142560-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25479173-T-G

17142620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25479113-A-G

17143423-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25478829-T-A

17143561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25478682-C-T

17143678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25478565-G-A

17143684-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25478559-T-G

17143782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25478467-G-A

17144567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25477715-G-A

17144567-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25477715-G-C

17144689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25477609-A-G

17144692-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25477606-A-T

17145233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25476124-C-T

17145874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25475807-G-A

17145900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25475776-C-T

17145937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25475741-C-T

17146218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25475472-A-G

17146234-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25475456-C-G

17147309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25474195-C-T

17147310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25474194-A-G

17147326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25474180-A-G

17147534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25474000-G-A

17151727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25472661-G-A

17151758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25472638-G-A

17151818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25472574-G-A

17151849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25472543-C-T

17152062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25472318-C-T

17152112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25472270-A-G

http://identifiers.org/hco/5/GRCh38#17152429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#25471980-C-A

17152429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25471980-C-T

17152483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25471911-C-T

17152592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25471622-T-C

17152663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25471558-C-T

17152797-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25471442-T-G

17152800-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25471439-G-C

17152821-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25471418-C-G

17152822-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25471417-T-A

17152822-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25471417-T-G

17152864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25471381-T-C

17152922-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25471345-C-G

17152927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25471340-T-C

17157932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25470192-C-T

17157990-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25470142-A-T

17157991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25470141-T-C

17158003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25470129-G-A

17158211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25469923-G-A

17158451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25469700-A-G

17159129-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25469383-C-G

17159253-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25469247-C-G

17159253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25469247-C-T

17159270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25469233-T-C

17159977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25468733-A-G

17159978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25468732-T-C

http://identifiers.org/hco/5/GRCh38#17159979-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#25468731-A-C

17160935-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25468327-A-T

17161004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25468271-A-G

17161722-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25467894-T-G

17161976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25467623-A-G

17161993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25467606-G-A

17163087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25465571-A-G

17167062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25463075-T-C

17167105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25463033-A-G

17167225-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25462923-T-G

17167465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25462733-A-G

17167517-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25462690-T-G

17167523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25462684-A-G

17167833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25461813-G-A

17167949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25461680-A-G

17168246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25461373-A-G

17168260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25461361-G-A

17168339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25461294-C-T

17168396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25461238-G-A

17168396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25461238-G-T

17168473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25461164-A-G

17168556-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25461105-C-G

17169183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25460563-C-T

17169895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25459865-G-A

http://identifiers.org/hco/5/GRCh38#17170041-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#25459729-A-C

17170041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25459729-A-G

17170041-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25459729-A-T

17170468-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25459608-A-T

17170513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25459563-A-G

17178297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25454111-C-T

17178298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25454110-G-A

17178299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25454109-G-A

17178447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25453980-C-T

17178547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25453888-A-G

17178670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25453798-A-G

http://identifiers.org/hco/5/GRCh38#17178934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#25453679-C-A

http://identifiers.org/hco/5/GRCh38#17179149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#25453501-C-A

17180891-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25451524-T-A

17181169-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25451258-T-A

17181338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25451117-A-G

17181387-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25451078-C-G

http://identifiers.org/hco/5/GRCh38#17181501-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#25450974-A-C

17181574-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25450920-G-C

17181667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25450837-G-A

17181726-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25450782-G-C

17181805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25450707-T-C

17181836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25450667-C-T

17182605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25449723-A-G

17183096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25449281-G-A

17183308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25449064-G-T

17183466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25448920-G-A

http://identifiers.org/hco/5/GRCh38#17184030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#25448304-C-A

17184088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25448246-T-C

17184137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25448197-C-T

17184551-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25447841-A-T

17184681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25447615-A-G

17184741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25447552-C-T

http://identifiers.org/hco/5/GRCh38#17184815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#25447481-C-A

17185710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25446456-A-G

17185768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25446378-G-A

17185822-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25446329-G-C

17186550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25445607-G-A

17186804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25445407-C-T

17186833-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25445377-C-G

17186945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25445196-C-T

17187092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25445067-C-T

17187496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25444515-G-T

17187524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25444487-C-T

17187607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25444402-C-T

17187653-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25444356-C-G

17188147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25443899-G-A

17188327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25443716-C-T

17189350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25442505-G-A

17189584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25442254-A-G

17189585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25442253-T-C

17189816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25442058-A-G

17189818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25442056-G-A

17189827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25442047-G-A

17189834-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25442040-G-T

17190083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25441839-C-T

17190280-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25441630-G-C

17190380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25441558-C-T

17190424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25441514-A-G

17190466-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25441474-G-C

17190504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25441429-T-C

17190505-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25441428-T-A

http://identifiers.org/hco/5/GRCh38#17190542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#25441379-C-A

17190545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25441376-G-T

17190610-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25441312-C-G

17190610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25441312-C-T

17190714-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25441209-T-G

17191418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25441184-G-A

17191507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25441097-G-A

17192229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25440947-G-A

17192285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25440889-C-T

17192625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25440598-A-G

17192865-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25440453-T-G

http://identifiers.org/hco/5/GRCh38#17192905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#25440420-C-A

17192905-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25440420-C-G

17193011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25440328-C-T

17193828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25439251-T-C

17193944-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25439172-T-G

17194386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25438738-G-A

17194386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25438738-G-T

17194392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25438732-G-A

17194392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25438732-G-T

http://identifiers.org/hco/5/GRCh38#17194492-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#25438634-A-C

17194492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25438634-A-G

17194738-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25438406-G-C

17194867-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25437739-C-G

17195186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25437455-A-G

17195187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25437454-T-C

17195193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25437448-T-C

17195198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25437443-G-A

17195259-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25435942-C-G

17195259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25435942-C-T

17195290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25435912-C-T

17195300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25435902-A-G

17195303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25435895-G-T

17195330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25435869-G-A

17195562-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25435659-C-G

17195735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25435508-C-T

17195785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25435451-G-A

17195796-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25435440-C-G

17195796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25435440-C-T

17199661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25432994-T-C

http://identifiers.org/hco/5/GRCh38#17199680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#25432904-C-A

17199730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25432857-G-T

17199820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25432768-T-C

17200031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25432607-G-A

17200068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25432571-G-A

17200162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25432494-C-T

17200183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25432477-A-G

17200515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25432139-A-G

17203463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25428899-T-C

17205381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25427095-A-G

17205837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25426650-A-G

17205914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25426568-T-C

17206147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25426151-A-G

17206173-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25426127-T-G

17206265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25426049-T-C

17206360-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25425961-A-T

17206392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25425929-G-A

17208842-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25424988-T-G

17210207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25420663-A-G

17210243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25420629-G-A

17210279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25420592-C-T

17210309-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25420565-G-T

17210922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25420343-G-A

http://identifiers.org/hco/5/GRCh38#17210997-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#25420264-A-C

17211017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25420244-G-A

http://identifiers.org/hco/5/GRCh38#17211844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#25418620-C-A

17211918-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25418585-T-A

17211918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25418585-T-C

17211935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25418568-C-T

17211993-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25418522-T-A

17212036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25418466-G-T

http://identifiers.org/hco/5/GRCh38#17213047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#25418347-C-A

17213125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25418283-T-C

17213194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25418224-G-A

17213238-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25418180-T-G

http://identifiers.org/hco/5/GRCh38#17213286-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#25418133-A-C

17213541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25417904-G-A

17213619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25417680-A-G

17213619-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25417680-A-T

17214366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25416938-C-T

17214415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25416877-C-T

17214491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25416802-G-A

17215541-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25415757-G-C

17215697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25415723-T-C

17215796-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25415643-T-G

http://identifiers.org/hco/5/GRCh38#17216167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#25415173-C-A

17216167-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 25415173-C-G

17216254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 25415077-G-A

http://identifiers.org/hco/5/GRCh38#17216275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#25415056-C-A

17216275-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 25415056-C-G

17216587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 25414737-C-T

http://identifiers.org/hco/5/GRCh38#17216626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#25414711-C-A

17216626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 25414711-C-T

17216656-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 25414683-T-A

17216656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 25414683-T-C

17216689-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 25414646-T-A

17216689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 25414646-T-C

http://identifiers.org/hco/5/GRCh38#17216720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#25414617-C-A

http://identifiers.org/hco/5/GRCh38#17216801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#25414535-C-A

17216801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 25414535-C-T

17216802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 25414534-A-G

17216802-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 25414534-A-T

http://identifiers.org/hco/5/GRCh38#17216813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#25414522-C-A

17216869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 25414465-G-A

17216869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 25414465-G-T

17217034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 25414294-G-A

17217160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 25414214-G-A

17217160-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 25414214-G-T