29287040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40362910-T-C

http://identifiers.org/hco/19/GRCh38#29287064-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40362934-A-C

29287064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40362934-A-G

29287089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40362959-A-G

http://identifiers.org/hco/19/GRCh38#29287215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40363087-C-A

29287215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40363087-C-T

http://identifiers.org/hco/19/GRCh38#29287245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40363116-C-A

29287259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40363130-C-T

29287292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40363161-G-A

29287321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40363186-G-T

29287520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40363367-A-G

29287558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40363406-G-A

29287558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40363406-G-T

29287724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40363575-C-T

29288056-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40364850-T-G

29288253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40365041-C-T

29288511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40365280-A-G

29288925-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40365676-C-G

http://identifiers.org/hco/19/GRCh38#29289050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40365790-C-A

29289050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40365790-C-T

29289986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40367302-G-A

29290011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40367326-C-T

29290136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40367420-A-G

29290180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40367461-C-T

29290189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40367471-G-A

29290189-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40367471-G-C

29290532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40367813-G-A

29290659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40367949-C-T

29290687-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40367977-A-T

29291138-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40368568-T-G

29291579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40368958-G-T

29291590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40368969-G-A

29291650-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40369021-T-G

29291662-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40369033-A-T

29291969-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40369340-T-A

29292028-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40369462-C-G

29292028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40369462-C-T

29293041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40370508-G-A

29293041-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40370508-G-C

29293041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40370508-G-T

29293082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40370544-G-A

http://identifiers.org/hco/19/GRCh38#29293239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40370693-C-A

29293424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40370869-G-A

29293567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40370995-G-A

29293633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40371052-C-T

29293786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40371201-C-T

29293807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40371204-A-G

29293877-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40371274-T-G

29293985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40371373-G-A

29294385-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40371759-T-G

29294387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40371761-G-A

29294387-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40371761-G-C

29294399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40371773-C-T

29294404-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40371783-C-G

29294404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40371783-C-T

29294579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40371897-G-T

29294766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40372030-T-C

29295789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40372918-G-A

29296122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40373210-C-T

29296364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40373451-G-A

29296578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40373648-G-A

29296624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40373715-T-C

29296764-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40373842-G-C

29296844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40373919-G-A

29296844-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40373919-G-C

http://identifiers.org/hco/19/GRCh38#29296973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40375947-C-A

29296973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40375947-C-T

29297114-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40376066-C-G

29297158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40376120-G-T

29297212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40376153-T-C

29297293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40376217-G-A

29297410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40376299-G-A

http://identifiers.org/hco/19/GRCh38#29297646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40376533-C-A

29297646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40376533-C-T

29297670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40376547-G-A

29297672-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40376549-G-C

29297746-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40376632-A-T

29298054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40377018-G-A

29301409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40378232-G-A

http://identifiers.org/hco/19/GRCh38#29301428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40378251-C-A

29301444-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40378268-A-T

29301465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40378297-A-G

29301506-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40378377-C-G

29301506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40378377-C-T

http://identifiers.org/hco/19/GRCh38#29301778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40378667-C-A

29301779-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40378668-T-A

29301896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40378786-T-C

29301978-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40378887-T-A

29302016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40378927-G-A

29302050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40378960-C-T

29302280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40379150-C-T

29302374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40379229-C-T

29302557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40383103-G-T

29302673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40383225-G-A

29302714-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40383266-T-A

29302760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40383295-C-T

29307662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40385237-G-A

29307662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40385237-G-T

29309350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40386516-G-A

29309962-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40387094-C-G

29310130-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40387270-T-G

29310308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40387422-C-T

29310353-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40387467-G-C

29310467-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40387554-T-A

29310527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40387655-A-G

29311509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40388364-A-G

29311783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40388591-G-A

29311798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40388606-G-A

29311971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40388772-A-G

29311974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40388775-A-G

29313305-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40389804-T-G

29313340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40389847-G-A

29313974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40390364-G-A

29314073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40390464-T-C

29314288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40390700-G-A

29314376-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40390792-G-C

29314456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40390865-G-T

http://identifiers.org/hco/19/GRCh38#29314622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40391018-C-A

29314694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40391087-A-G

29314842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40391242-G-A

29314842-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40391242-G-C

29314938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40391323-G-A

29314957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40391342-G-A

29314957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40391342-G-T

29315002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40391387-A-G

29315199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40391576-G-A

29315212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40391590-G-A

29315398-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40391764-T-G

29315431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40391794-G-A

http://identifiers.org/hco/19/GRCh38#29315448-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40391809-A-C

29315448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40391809-A-G

29316199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40392633-A-G

29316283-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40392713-C-G

29317196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40396066-A-G

29318044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40396440-C-T

29318059-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40396455-G-C

29318059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40396455-G-T

29318068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40396465-A-G

29318253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40396639-C-T

29318417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40396819-G-A

29318625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40396978-C-T

29319320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40399397-A-G

29319333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40399410-G-T

29319356-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40399431-T-A

29319356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40399431-T-C

http://identifiers.org/hco/19/GRCh38#29319804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40399869-C-A

29319888-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40399969-C-G

29320023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40401072-T-C

29320182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40401192-C-T

29320369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40401394-T-C

29320480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40401503-C-T

29320646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40401666-C-T

29320815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40401832-G-A

29320843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40401857-G-A

29321052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40402047-C-T

29321240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40402262-C-T

29321265-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40402296-G-C

29321302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40402337-G-A

29321305-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40402340-A-T

29321335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40402392-G-A

http://identifiers.org/hco/19/GRCh38#29321338-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40402395-A-C

29321374-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40402416-A-T

29321398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40402442-T-C

29321947-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40403034-C-G

29321980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40403067-G-A

29322030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40403117-C-T

http://identifiers.org/hco/19/GRCh38#29322037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40403124-C-A

29322037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40403124-C-T

29322044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40403131-G-A

29322044-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40403131-G-C

29324498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40408703-A-G

29324519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40408724-G-A

29324519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40408724-G-T

29324575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40408775-G-A

29325749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40408983-A-G

29325751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40408986-T-C

29325756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40408991-G-T

29326248-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40409458-A-T

29326403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40409616-C-T

29326526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40409730-C-T

29326673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40409844-T-C

http://identifiers.org/hco/19/GRCh38#29326688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40409852-C-A

29328611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40411223-G-A

29328776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40411362-C-T

29328806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40411393-C-T

29328857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40411425-A-G

29328877-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40411446-A-T

29329035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40411606-G-A

29329170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40411740-G-A

29329273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40411817-G-T

29329279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40411822-C-T

29329440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40411964-A-G

29329479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40412005-A-G

http://identifiers.org/hco/19/GRCh38#29329504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#40412032-C-A

29329504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40412032-C-T

29329612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40412142-T-C

29329612-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40412142-T-G

29329642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40412173-A-G

http://identifiers.org/hco/19/GRCh38#29330031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40412796-C-A

29330169-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40412896-C-G

29330281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40413006-T-C

http://identifiers.org/hco/19/GRCh38#29330293-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40413018-A-C

29330293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40413018-A-G

29330293-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40413018-A-T

29330318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40413042-C-T

29330319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40413043-T-C

29330488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40413196-T-C

29330645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40413335-C-T

29330807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40413468-C-T

29330814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40413475-T-C

29330837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40413501-C-T

29331109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40413703-T-C

http://identifiers.org/hco/19/GRCh38#29331546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40413957-C-A

29331546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40413957-C-T

29331604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40413999-G-T

29331698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40414086-T-C

29331740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40414128-G-A

29331796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40414180-G-A

29331796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40414180-G-T

29332062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40414457-T-C

29332062-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40414457-T-G

http://identifiers.org/hco/19/GRCh38#29332472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40415476-C-A

29332507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40415512-T-C

29332573-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40415581-G-C

29332638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40415636-C-T

29332675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40415669-T-C

29332900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40415889-G-A

29333400-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40416071-C-G

29333400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40416071-C-T

29334252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40419468-T-C

29334634-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40419830-G-C

29335248-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40419965-A-T

29335386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40420106-A-G

29335390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40420110-G-A

29335395-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40420115-A-T

29335461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40420184-G-A

29335472-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40420195-A-T

29335551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40420260-G-T

29336688-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40422458-T-A

29336711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40422481-A-G

29336743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40422506-T-C

29336744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40422507-G-A

29336889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40422617-G-A

29336889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40422617-G-T

http://identifiers.org/hco/19/GRCh38#29337002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40422695-C-A

29337002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40422695-C-T

29337081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40422773-G-A

29337098-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40422808-G-C

29337324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40422935-G-T

29337330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40422941-G-T

29337413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40423027-G-A

29337563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40423178-A-G

29337627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40423238-T-C

29337668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40423279-G-A

29338913-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40425788-T-G

29339191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40426048-G-A

29339444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40426346-G-A

29339446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40426350-G-T

29339671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40426478-C-T

29339722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40426521-T-C

29339722-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40426521-T-G

29339723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40426522-G-A

29339724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40426523-C-T

29339740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40426536-A-G

29339801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40426595-G-A

29339985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40427102-G-A

29340027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40427144-C-T

29367149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40438261-C-T

29367194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40438303-A-G

http://identifiers.org/hco/19/GRCh38#29367272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40438351-C-A

29367272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40438351-C-T

29367522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40438585-G-A

29367626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40438691-T-C

29367627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40438692-G-T

29367643-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40438711-T-A

29367643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40438711-T-C

http://identifiers.org/hco/19/GRCh38#29367786-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40438814-A-C

29367843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40438870-C-T

29367863-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40438890-C-G

29367863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40438890-C-T

29367867-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40438894-T-G

29367872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40438899-C-T

29367876-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40438903-T-A

29367878-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40438905-C-G

http://identifiers.org/hco/19/GRCh38#29367948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40439283-C-A

29367948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40439283-C-T

29367985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40439327-G-A

29368068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40439408-A-G

29368129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40439469-T-C

29368185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40439524-G-T

29368188-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40439527-C-G

29368268-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40439571-T-G

29370509-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40440754-G-C

29370509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40440754-G-T

29370571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40440811-C-T

29371784-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40441454-G-C

http://identifiers.org/hco/19/GRCh38#29371835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40441489-C-A

29371890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40441546-G-A

29371890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40441546-G-T

29371891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40441547-G-A

29371994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40441646-C-T

29374950-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40443349-G-C

29374980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40443379-C-T

29374991-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40443390-T-G

29375001-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40443400-T-A

29375001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40443400-T-C

29375017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40443416-C-T

29375032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40443431-C-T

29375488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40443591-C-T

29375503-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40443606-C-G

29375660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40443853-G-A

29375905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40444097-C-T

29376020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40444223-A-G

29376948-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40444779-C-G

http://identifiers.org/hco/19/GRCh38#29376953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40444784-C-A

29377446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40445211-A-G

29377477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40445244-C-T

http://identifiers.org/hco/19/GRCh38#29377657-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40445516-A-C

29378321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40446127-A-G

29378507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40446309-T-C

29378552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40446347-A-G

29378658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40446450-C-T

29378698-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40446490-G-C

29379286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40446999-G-A

29379325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40447038-G-A

29379537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40448625-C-T

29379634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40448722-G-T

29379674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40448759-G-T

29382708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40450881-C-T

29382726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40450899-G-T

29382853-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40451031-T-G

29383895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40451377-C-T

29383926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40451409-A-G

29384130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40451595-C-T

http://identifiers.org/hco/19/GRCh38#29384205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40451666-C-A

29384241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40451702-G-A

29384243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40451704-G-A

29384251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40451712-G-T

29384268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40451730-G-A

29386941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40454328-C-T

29386959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40454343-C-T

29387044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40454395-G-T

29387152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40454492-G-A

29387357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40454700-C-T

29387432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40454770-G-A

29389159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40455092-C-T

29389178-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40455114-C-G

29389239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40455176-G-A

29389290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40455226-T-C

29389290-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40455226-T-G

29389325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40455255-C-T

29389368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40455294-A-G

29389561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40455491-G-T

29389637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40455565-G-A

29389684-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40455613-C-G

29389684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40455613-C-T

29389779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40455706-C-T

29389805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40455732-A-G

http://identifiers.org/hco/19/GRCh38#29396746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40458859-C-A

http://identifiers.org/hco/19/GRCh38#29396750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40458863-C-A

29396804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40458914-A-G

29396804-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40458914-A-T

29396817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40458927-A-G

http://identifiers.org/hco/19/GRCh38#29396827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40458930-C-A

http://identifiers.org/hco/19/GRCh38#29396882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40458986-C-A

29396882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40458986-C-T

http://identifiers.org/hco/19/GRCh38#29396883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40458987-C-A

29396883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40458987-C-T

http://identifiers.org/hco/19/GRCh38#29397044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40459133-C-A

29397074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40459163-G-T

29397163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 40459252-G-A

29397163-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 40459252-G-C

http://identifiers.org/hco/19/GRCh38#29397266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40459353-C-A

http://identifiers.org/hco/19/GRCh38#29397302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40459389-C-A

29397302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40459389-C-T

29397464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40459578-G-T

http://identifiers.org/hco/19/GRCh38#29397581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40459682-C-A

29397581-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40459682-C-G

29397581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40459682-C-T

29397593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40459695-G-T

29397604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40459706-C-T

29398031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40459963-G-A

29398051-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40459983-C-G

29398051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40459983-C-T

http://identifiers.org/hco/19/GRCh38#29398150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40460081-C-A

29398244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40460169-C-T

29398321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40460233-G-A

http://identifiers.org/hco/19/GRCh38#29398427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40460314-C-A

29398515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40460383-T-C

29398523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40460391-A-G

29398565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40460407-G-T

29398609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40460444-T-C

http://identifiers.org/hco/19/GRCh38#29398663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40460485-C-A

29398663-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40460485-C-G

29398663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40460485-C-T

29398989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40461104-G-T

29399005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40461120-G-A

29399066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40461166-G-A

29399082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40461180-G-A

29399082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40461180-G-T

29399243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40461322-C-T

29399305-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40461370-A-T

29399411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40461470-T-C

29399493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40461552-G-A

29399572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40461633-T-C

29399581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40461642-C-T

29399585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40461647-T-C

29399606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40461674-G-A

29400598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40461917-G-T

29400666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40462041-G-A

29400677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40462052-G-A

29400725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40462095-C-T

29400744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40462124-G-A

29400803-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40462155-A-T

29400921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40462267-G-A

29400921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40462267-G-T

29400935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40462280-C-T

29400936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40462285-G-A

29401035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40462378-G-A

29401112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40462456-G-A

29401256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40462609-C-T

29401266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40462619-A-G

29401343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40462705-C-T

29401351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40462713-G-A

29401428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40462820-C-T

29401554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40462916-C-T

29401561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40462923-C-T

29401822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40464022-G-A

29402020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40464213-G-A

29402315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40464472-G-A

29402527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40464667-C-T

29402558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40464696-C-T

29402691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40464838-C-T

29402831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40464970-G-A

http://identifiers.org/hco/19/GRCh38#29402854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40464979-C-A

29403565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40465342-C-T

29403708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40465487-G-A

29403974-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40465908-C-G

29403997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40465930-G-A

29404022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40465955-G-A

29404964-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40469796-G-C

29405104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40469929-G-A

29405364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40470194-C-T

29407376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40470402-G-A

29407396-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40470430-G-C

29407549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40470577-A-G

29407596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40470624-T-C

29407932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40470946-G-A

29407932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40470946-G-T

29408005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40471021-C-T

29408261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40471277-G-A

29408261-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40471277-G-C

29408369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40471378-T-C

29408466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40471464-T-C

29408513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40471515-G-A

29408559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40471558-T-C

29408605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40471585-A-G

29408605-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40471585-A-T

29408735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40471728-G-A

29408768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40471749-G-A

http://identifiers.org/hco/19/GRCh38#29408936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40471920-C-A

29409161-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40472156-C-G

29409161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40472156-C-T

29409267-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40472247-C-G

29409338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40472325-C-T

29409351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40472337-G-A

29409351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40472337-G-T

29409357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40472343-G-A

29409357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40472343-G-T

29409367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40472351-G-A

29409419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40472436-G-A

29409419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40472436-G-T

29409460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40472470-C-T

29409530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40472545-C-T

29409594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40472615-A-G

29409735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40472770-G-T

29409828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40472834-C-T

29409918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40472920-T-C

29409994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40472990-T-C

29410195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40473170-T-C

29410380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40473845-C-T

29410480-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40473929-G-C

29410482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40473931-G-T

29410861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40474339-G-A

29410875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40474353-T-C

29411034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40474534-C-T

29411085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40474586-G-A

29411134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40474617-C-T

29411166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40474649-C-T

29411167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40474650-G-A

http://identifiers.org/hco/19/GRCh38#29411338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40474759-C-A

29411338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40474759-C-T

29411339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40474760-G-A

29411417-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40474837-C-G

29411417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40474837-C-T

29411426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40474846-T-C

29411585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40475003-G-A

29416560-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40476116-T-G

29416964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40476500-C-T

29416981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40476517-G-A

29417248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40476718-C-T

29417291-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40476757-C-G

29417361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40476849-G-A

29417395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40476887-T-C

http://identifiers.org/hco/19/GRCh38#29417510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40476993-C-A

http://identifiers.org/hco/19/GRCh38#29417597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40477087-C-A

29417625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40477115-G-A

29417625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40477115-G-T

29417746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40477184-G-A

29417815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40477253-G-A

29417894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40477286-C-T

29418068-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40477429-G-C

29418082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40477443-T-C

http://identifiers.org/hco/19/GRCh38#29418212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40477572-C-A

29421172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40477681-A-G

29421176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40477685-T-C

29421320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40477817-G-A

29421387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40477896-G-T

29421759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40478235-G-T

http://identifiers.org/hco/19/GRCh38#29421891-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40478348-A-C

29421930-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40478386-C-G

29421930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40478386-C-T

29421963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40478438-C-T

29422050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40478503-G-A

29422094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40478559-G-A

29422096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40478561-C-T

29422144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40478606-T-C

29422170-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40478631-A-T

http://identifiers.org/hco/19/GRCh38#29422242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40478697-C-A

29422447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40478916-A-G

29423185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40479367-T-C

29423274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40479450-C-T

29423556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40479771-G-T

29424172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40480242-A-G

29424228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40480280-T-C

http://identifiers.org/hco/19/GRCh38#29424247-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40480297-A-C

29424483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40480526-G-A

29424499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40480546-G-A

29424576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40480607-C-T

29424731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40480679-C-T

29424747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40480695-C-T

29424787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40480734-T-C

29424835-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40480753-C-G

29424956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40480846-T-C

29424964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40480854-C-T

29424966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40480856-G-A

29424969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40480859-T-C

29425058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40480928-C-T

29425121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40480958-C-T

29425219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40481042-T-C

29425340-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40481184-G-C

29425342-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40481186-C-G

29425399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40481242-C-T

29425459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40481297-G-A

29425459-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40481297-G-C

29427705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40483042-G-A

http://identifiers.org/hco/19/GRCh38#29427748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40483081-C-A

29427951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40483206-A-G

29428550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40483859-C-T

29428733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 40484004-G-A

29428843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40484098-A-G

29428886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40484146-G-A

29428886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40484146-G-T

29428902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40484163-T-C

29428902-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40484163-T-G

http://identifiers.org/hco/19/GRCh38#29428925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40484185-C-A

29428925-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40484185-C-G

29428925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40484185-C-T

29429045-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40484721-C-G

29429086-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40484761-C-G

29429087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40484762-A-G

29429214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40484888-G-A

29429381-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40485027-C-G

29429381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40485027-C-T

29429435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40485078-G-A

29429435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40485078-G-T

http://identifiers.org/hco/19/GRCh38#29429504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40485134-C-A

29429504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40485134-C-T

29429566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40485180-G-A

29429576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40485190-C-T

29429612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40485220-G-A

29429636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40485245-G-A

29431593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40480134-C-T

29436643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40491994-G-A

29436679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40492030-T-C

29437015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40492381-G-A

29437099-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40492464-A-T

29437332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40492668-G-A

29437332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40492668-G-T

29445309-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40500731-T-G

29445371-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40500793-A-T

http://identifiers.org/hco/19/GRCh38#29445415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40500829-C-A

29445415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40500829-C-T

29445588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40500995-G-T

29445674-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40501080-A-T

29445695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40501101-G-A

29446355-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40501164-C-G

29446421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40501229-C-T

29446480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40501292-C-T

29446527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40501328-G-A

29446595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40501396-T-C

29446599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40501400-G-A

29446680-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40501480-G-C

29446707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40501505-C-T

29447051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40501821-G-A

29447113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40501862-A-G

http://identifiers.org/hco/19/GRCh38#29447303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40501980-C-A

29447561-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40502117-T-A

29447561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40502117-T-C

29447561-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40502117-T-G

29447570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40502126-C-T

29447575-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40502131-T-A

http://identifiers.org/hco/19/GRCh38#29447579-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40502135-A-C

29447579-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40502135-A-T

29447785-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40502281-C-G

http://identifiers.org/hco/19/GRCh38#29447909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40502365-C-A

29447932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40502388-G-A

29447932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40502388-G-T

29447962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40502418-G-A

http://identifiers.org/hco/19/GRCh38#29448287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40503323-C-A

29448287-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40503323-C-G

29448290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40503326-G-T

http://identifiers.org/hco/19/GRCh38#29448361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40503393-C-A

29448847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40503473-G-A

http://identifiers.org/hco/19/GRCh38#29448938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40503564-C-A

29448964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40503937-A-G

http://identifiers.org/hco/19/GRCh38#29449064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40504031-C-A

29449064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40504031-C-T

29449067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40504034-C-T

29449208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40504178-G-A

29449212-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40504182-G-C

29449297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40504270-T-C

29449464-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40504427-T-G

29450496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40505314-C-T

29450516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40505336-C-T

http://identifiers.org/hco/19/GRCh38#29450523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40505343-C-A

29450702-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40505544-C-G

29450702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40505544-C-T

29450992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40505832-C-T

29451084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40505892-G-A

http://identifiers.org/hco/19/GRCh38#29451092-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40505900-A-C

29451144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40505960-G-A

29466484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40510067-C-T

29466485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40510068-C-T

http://identifiers.org/hco/19/GRCh38#29466516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40510097-C-A

29466854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40510394-A-G

29466973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40510504-G-A

29466987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40510521-A-G

29466991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40510525-G-A

29467202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40510763-C-T

29467397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40510969-C-T

29467398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40510970-C-T

29467491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40511071-A-G

29467797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40511498-G-A

29467797-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40511498-G-C

29467855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40511591-T-C

29467924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40511659-T-C

29468046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40511771-T-C

29468069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40511794-A-G

29468089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40511807-G-A

29468089-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40511807-G-C

http://identifiers.org/hco/19/GRCh38#29468168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40512719-C-A

29475107-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40514119-T-G

29475259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40514244-A-G

29475497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40514490-G-A

29475606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40514597-C-T

29475637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40514631-A-G

http://identifiers.org/hco/19/GRCh38#29475696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40514690-C-A

29476264-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40516456-C-G

29476301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40516498-G-A

29476334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40516525-T-C

29476347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40516544-G-A

29476556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40516747-A-G

29476669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40516858-T-C

29476765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40516950-C-T

29476820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40516994-A-G

29476832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40517006-G-A

29476877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40517052-T-C

29476889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40517064-T-C

29483162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40517992-G-T

29483346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40518165-A-G

29483490-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40518305-C-G

http://identifiers.org/hco/19/GRCh38#29483837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40519251-C-A

29483935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40519346-G-A

http://identifiers.org/hco/19/GRCh38#29483940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40519351-C-A

29484100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40519535-A-G

29484175-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40519606-C-G

29488030-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40522520-C-G

29488030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40522520-C-T

29488125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40522614-T-C

29488144-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40522636-A-T

29488339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40522822-T-C

29488395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40522873-T-C

29488573-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40523045-A-T

http://identifiers.org/hco/19/GRCh38#29488612-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40523084-A-C

29489604-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40523311-G-C

29489762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40523469-T-C

29489773-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40523480-G-C

29489773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40523480-G-T

29489819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40523539-C-T

29489824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40523544-C-T

29489825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40523545-G-A

29489825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40523545-G-T

29489945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40523630-C-T

29489999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40523681-G-A

29489999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40523681-G-T

29490098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40523789-G-T

http://identifiers.org/hco/19/GRCh38#29490176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40523869-C-A

29490187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40523880-G-A

29490816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40524349-C-T

29496687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40527455-T-C

29496690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40527458-G-A

29496691-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40527459-G-C

29496752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40527521-C-T

http://identifiers.org/hco/19/GRCh38#29496910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40527655-C-A

29496910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40527655-C-T

29497239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40527907-T-C

29497533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40528126-T-C

29497588-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40528181-G-C

29497762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40528292-G-T

29497916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40528424-G-A

29498055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40528566-C-T

29498106-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40528619-C-G

29498106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40528619-C-T

29498249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40528739-A-G

29499020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40530137-T-C

29499020-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40530137-T-G

29499083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40530201-G-A

29499155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40530275-A-G

29499197-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40530317-C-G

29499226-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40530351-G-C

29499455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40530587-C-T

29502242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40531092-G-A

29502278-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40531122-T-A

29502281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40531125-A-G

29502371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40531221-T-C

http://identifiers.org/hco/19/GRCh38#29502609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40531434-C-A

http://identifiers.org/hco/19/GRCh38#29502801-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40531627-A-C

29502801-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40531627-A-T

29502892-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40531724-C-G

29502892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40531724-C-T

29502914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40531741-A-G

http://identifiers.org/hco/19/GRCh38#29503041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40531867-C-A

29503124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40531939-G-A

http://identifiers.org/hco/19/GRCh38#29503317-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40532132-A-C

29503585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40532411-G-A

29503585-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40532411-G-C

29503977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40533478-C-T

29504393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40533912-G-A

29504393-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40533912-G-C

29504589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40534094-G-A

29504708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40534159-C-T

29504822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40534229-G-A

http://identifiers.org/hco/19/GRCh38#29504911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40534291-C-A

29504911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40534291-C-T

29505080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40534364-G-A

29505393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40534672-C-T

29505565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40534880-G-T

http://identifiers.org/hco/19/GRCh38#29506838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40535470-C-A

http://identifiers.org/hco/19/GRCh38#29507437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40536231-C-A

29507567-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40536342-G-C

http://identifiers.org/hco/19/GRCh38#29507623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#40536398-C-A

http://identifiers.org/hco/19/GRCh38#29507649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40536424-C-A

29507649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40536424-C-T

29508008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40536816-G-A

http://identifiers.org/hco/19/GRCh38#29508020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40536828-C-A

29508020-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40536828-C-G

29508020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40536828-C-T

29508033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40536841-G-A

29508033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40536841-G-T

29508042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40536850-G-A

29508065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40536872-A-G

29508200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40536990-G-A

29508687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40537473-T-C

29508719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40537502-A-G

http://identifiers.org/hco/19/GRCh38#29508918-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40537686-A-C

29508967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40537738-G-A

29508967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40537738-G-T

29508974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40537745-A-G

29509012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40537802-G-T

29509027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40537817-T-C

29509046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40537838-A-G

29509106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40537893-G-A

29509106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40537893-G-T

29509124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40537911-T-C

29509129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40537916-G-A

29509129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40537916-G-T

http://identifiers.org/hco/19/GRCh38#29509209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40537986-C-A

29509209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40537986-C-T

http://identifiers.org/hco/19/GRCh38#29511100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40538353-C-A

29511122-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40538373-A-T

http://identifiers.org/hco/19/GRCh38#29515958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40540141-C-A

29515958-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40540141-C-G

29515958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40540141-C-T

29515959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40540142-G-A

29516017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40540198-T-C

29516051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40540235-G-A

29516057-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40540241-A-T

29516058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40540242-A-G

29516119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40540302-G-A

29516119-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40540302-G-C

29516218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40540399-G-A

29516437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40540595-G-A

29516503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40540661-G-A

29516549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40540708-A-G

29516649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40540824-A-G

29516687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40540884-C-T

29516695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40540892-G-A

29516768-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40540959-C-G

29517056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40541173-G-A

29517246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40541359-A-G

29517246-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40541359-A-T

29517376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40541472-A-G

29517393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40541489-A-G

29517405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40541501-C-T

29517447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40541542-G-A

http://identifiers.org/hco/19/GRCh38#29517500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40541598-C-A

29517719-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40541791-C-G

29517852-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40542036-C-G

29517903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40542086-G-A

29518416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40542551-T-C

29518895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40543009-G-A

29519228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40543095-G-T

29519353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40543133-T-C

http://identifiers.org/hco/19/GRCh38#29519469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40543222-C-A

29519605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40543343-G-T

29519681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40543409-G-A

29519681-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40543409-G-C

29519681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40543409-G-T

29519691-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40543419-C-G

29519699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40543427-A-G

29519724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40543452-A-G

29519803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40543532-A-G

http://identifiers.org/hco/19/GRCh38#29519808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40543537-C-A

29519828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40543558-T-C

29519829-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40543559-G-C

29520125-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40543811-T-A

29520387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40543924-G-T

29520388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40543925-C-T

29520514-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40544058-T-A

29520662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40544202-G-A

http://identifiers.org/hco/19/GRCh38#29521201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40544704-C-A

29521245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40544747-A-G

29521245-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40544747-A-T

29521262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40544763-G-A

29521272-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40544771-G-C

29521425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40544891-C-T

http://identifiers.org/hco/19/GRCh38#29521525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40544964-C-A

29521737-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40545187-G-C

29521820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40545256-C-T

http://identifiers.org/hco/19/GRCh38#29523472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40545799-C-A

29523567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40545888-G-A

29523726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40546022-G-A

29523777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40546069-G-T

29523835-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40546121-G-C

29523842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40546128-C-T

29523961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40546219-G-A

29524058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40546328-A-G

29524183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40546479-G-A

29524377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40546664-C-T

29524570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40546840-C-T

29524725-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40546941-C-G

29524725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40546941-C-T

29524892-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40547107-T-A

29525077-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40547249-C-G

29525265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40547459-G-T

29525309-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40547506-G-T

29525323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40547522-A-G

http://identifiers.org/hco/19/GRCh38#29525336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40547535-C-A

http://identifiers.org/hco/19/GRCh38#29525440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#40547639-C-A

29525451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 40547650-G-A

http://identifiers.org/hco/19/GRCh38#29525503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#40547700-C-A

29525614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 40547810-C-T

http://identifiers.org/hco/19/GRCh38#29525680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40547878-C-A

29525680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40547878-C-T

29525691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40547889-A-G

http://identifiers.org/hco/19/GRCh38#29525721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40547918-C-A

29525721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27615
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40547918-C-T